|
humans |
56 |
|
genetic predisposition to disease |
51 |
|
schizophrenia |
48 |
|
asian continental ancestry group - genetics |
47 |
|
female |
47 |
|
genotype |
47 |
|
polymorphism, single nucleotide |
47 |
|
male |
46 |
|
adult |
41 |
|
genome-wide association study |
37 |
|
middle aged |
35 |
|
polymorphism, single nucleotide - genetics |
34 |
|
depression |
29 |
|
aged |
28 |
|
chinese |
28 |
|
genetic association |
28 |
|
genetics |
27 |
|
mendelian randomization |
26 |
|
risk factors |
26 |
|
single nucleotide polymorphism |
25 |
|
association |
23 |
|
psychosis |
23 |
|
controlled study |
22 |
|
risk factor |
22 |
|
vitamin d |
22 |
|
cell adhesion molecules - genetics |
21 |
|
gene frequency |
21 |
|
young adult |
21 |
|
gwas |
20 |
|
atrial fibrillation |
19 |
|
coronary artery disease |
19 |
|
first episode |
19 |
|
adolescent |
18 |
|
antigens, cd - genetics |
18 |
|
whole-exome sequencing |
18 |
|
epidemiology |
17 |
|
hong kong |
17 |
|
mri |
17 |
|
prevalence |
17 |
|
animals |
16 |
|
case-control studies |
16 |
|
child |
16 |
|
copy number variation |
16 |
|
human |
16 |
|
promoter regions, genetic |
16 |
|
cross-sectional studies |
15 |
|
gene identification |
15 |
|
gene locus |
15 |
|
l-lactate dehydrogenase - blood |
15 |
|
linkage disequilibrium |
15 |
|
major clinical study |
15 |
|
mice |
15 |
|
neuregulin-1 - genetics |
15 |
|
alleles |
14 |
|
asian |
14 |
|
asian continental ancestry group |
14 |
|
chemicals and cas registry numbers |
14 |
|
china |
14 |
|
cohort studies |
14 |
|
gene expression |
14 |
|
genetic variation |
14 |
|
hypertension |
14 |
|
magnetic resonance imaging |
14 |
|
age factors |
13 |
|
bile duct atresia |
13 |
|
cancer susceptibility genes |
13 |
|
chromosome 10q |
13 |
|
early-age onset |
13 |
|
gene function |
13 |
|
genetic susceptibility |
13 |
|
genome-wide association |
13 |
|
hepatocellular carcinoma |
13 |
|
hirschsprung disease |
13 |
|
hirschsprung disease - genetics |
13 |
|
lipocalin-2 |
13 |
|
magnetic resonance imaging - methods |
13 |
|
meta-analysis |
13 |
|
mst1r |
13 |
|
nasopharyngeal carcinoma |
13 |
|
priority journal |
13 |
|
receptors, cell surface - genetics |
13 |
|
recurrence |
13 |
|
remission |
13 |
|
risk prediction |
13 |
|
secondary prevention |
13 |
|
sex factors |
13 |
|
animal tissue |
12 |
|
anorectal malformation |
12 |
|
anxiety |
12 |
|
body mass index |
12 |
|
chromosome aberration |
12 |
|
cos cells |
12 |
|
cost-effectiveness |
12 |
|
disease progression |
12 |
|
ephrin-a2 - genetics |
12 |
|
evaluation |
12 |
|
first-episode psychosis |
12 |
|
gene expression regulation, neoplastic |
12 |
|
gene mapping |
12 |
|
genetic predisposition to disease - genetics |
12 |
|
gwa |
12 |
|
haplotypes |
12 |
|
ischemic stroke |
12 |
|
lupus erythematosus, systemic - genetics |
12 |
|
mental health |
12 |
|
mutation - genetics |
12 |
|
mutations |
12 |
|
myocardial infarction |
12 |
|
ret |
12 |
|
severe acute respiratory syndrome - blood - genetics |
12 |
|
sle |
12 |
|
snp |
12 |
|
survival |
12 |
|
uhrf1bp1 |
12 |
|
wnt signaling pathway |
12 |
|
antigens, cd3 - genetics |
11 |
|
bmd |
11 |
|
cd247 |
11 |
|
china - epidemiology |
11 |
|
databases, genetic |
11 |
|
ethnic group |
11 |
|
gene mutation |
11 |
|
genetic polymorphism |
11 |
|
genetic predisposition |
11 |
|
genome-wide association studies |
11 |
|
genomics |
11 |
|
heterozygote |
11 |
|
human tissue |
11 |
|
kw034 - copy number/structural variation |
11 |
|
lupus erythematosus, systemic - genetics - immunology |
11 |
|
nucleotide sequence |
11 |
|
odds ratio |
11 |
|
pleiotropy |
11 |
|
polymorphism, genetic |
11 |
|
psychotic disorders |
11 |
|
sars |
11 |
|
schizophrenic psychology |
11 |
|
systemic lupus erythematosus |
11 |
|
whole exome sequencing |
11 |
|
25-hydroxyvitamin d |
10 |
|
adipocyte |
10 |
|
algorithms |
10 |
|
b-type natriuretic peptide |
10 |
|
bone density - genetics |
10 |
|
brain - pathology |
10 |
|
cardiac troponin |
10 |
|
cell adhesion molecules - genetics - metabolism |
10 |
|
cluster analysis |
10 |
|
delusional disorder |
10 |
|
diffusion tensor imaging |
10 |
|
dopamine |
10 |
|
endophenotype |
10 |
|
exome chip |
10 |
|
f-dopa |
10 |
|
fibroblast growth factor |
10 |
|
first-episode schizophrenia |
10 |
|
genome scan |
10 |
|
genotype-phenotype correlations |
10 |
|
intracellular signaling peptides and proteins - genetics |
10 |
|
lactate dehydrogenase |
10 |
|
lumbar disc degeneration |
10 |
|
lupus erythematosus, systemic - enzymology - genetics |
10 |
|
mapping complex traits |
10 |
|
negative symptoms |
10 |
|
positron emission tomography |
10 |
|
protein binding - genetics |
10 |
|
psychiatric status rating scales |
10 |
|
rare complex disease |
10 |
|
striatal dopamine capacity synthesis |
10 |
|
type 2 diabetes |
10 |
|
type 2 diabetes mellitus |
10 |
|
vitamin d-binding protein |
10 |
|
association study |
9 |
|
cancer |
9 |
|
cardiovascular disease |
9 |
|
chromosomes, human, pair 6 - genetics |
9 |
|
development |
9 |
|
early intervention |
9 |
|
expression quantitative trait loci |
9 |
|
fractional anisotropy |
9 |
|
fracture |
9 |
|
gene |
9 |
|
genetic correlation |
9 |
|
linkage |
9 |
|
lumbar vertebrae |
9 |
|
mutation |
9 |
|
natural selection |
9 |
|
obesity |
9 |
|
prognosis |
9 |
|
rare variants |
9 |
|
receptors, calcitriol - genetics |
9 |
|
schizophrenia - pathology |
9 |
|
severity of illness index |
9 |
|
sex disparity |
9 |
|
software |
9 |
|
young-onset ischemic stroke |
9 |
|
adiponectin - blood - genetics |
8 |
|
allelic imbalance |
8 |
|
asian continental ancestry group - ethnology |
8 |
|
bioinformatics |
8 |
|
bipolar disorder |
8 |
|
blood pressure - genetics |
8 |
|
brain - ultrastructure |
8 |
|
cell adhesion molecules - genetics - physiology |
8 |
|
cell differentiation - physiology |
8 |
|
computational biology |
8 |
|
corpus striatum |
8 |
|
cyclin a2 |
8 |
|
degeneration |
8 |
|
degenerative disc disease |
8 |
|
diabetic retinopathy |
8 |
|
disc |
8 |
|
disease models, animal |
8 |
|
disease susceptibility |
8 |
|
dna mutational analysis |
8 |
|
drug-naive |
8 |
|
duration of untreated psychosis |
8 |
|
employment |
8 |
|
family health |
8 |
|
gene deletion |
8 |
|
gene duplication |
8 |
|
gene expression regulation |
8 |
|
gene frequency - genetics |
8 |
|
genetic variants |
8 |
|
genetics, population |
8 |
|
haplotype |
8 |
|
hbv integration |
8 |
|
hcc |
8 |
|
hedgehog proteins - genetics - metabolism |
8 |
|
heritability |
8 |
|
hirschsprung disease - genetics - physiopathology |
8 |
|
homozygote |
8 |
|
hong kong - epidemiology |
8 |
|
hypertension - blood - genetics |
8 |
|
insr |
8 |
|
insulin resistance - genetics |
8 |
|
intervertebral |
8 |
|
intervertebral disc degeneration |
8 |
|
kw080 - genome-wide association |
8 |
|
lectins, c-type - genetics |
8 |
|
long-term outcome |
8 |
|
long-term outcomes |
8 |
|
lumbar |
8 |
|
maternal age |
8 |
|
maternal exposure |
8 |
|
medical sciences |
8 |
|
models, genetic |
8 |
|
multivariate analysis |
8 |
|
nasopharyngeal neoplasms - genetics |
8 |
|
neuroglia - cytology - physiology |
8 |
|
obesity - genetics |
8 |
|
panss |
8 |
|
pedigree |
8 |
|
phenotyping |
8 |
|
polygenic score |
8 |
|
potassium channels, inwardly rectifying - genetics |
8 |
|
predictors |
8 |
|
prenatal exome |
8 |
|
proliferative diabetic retinopathy |
8 |
|
promoter regions, genetic - genetics |
8 |
|
prospective studies |
8 |
|
prospective study |
8 |
|
proteins - genetics |
8 |
|
raclopride |
8 |
|
receptors, notch - genetics - metabolism |
8 |
|
relapse |
8 |
|
sars virus - isolation and purification - pathogenicity |
8 |
|
schizophrenia - genetics |
8 |
|
severe acute respiratory syndrome - physiopathology - virology |
8 |
|
sight-threatening diabetic retinopathy |
8 |
|
single nucleotide polymorphisms |
8 |
|
single-nucleotide polymorphism |
8 |
|
splicing |
8 |
|
temporal lobe - ultrastructure |
8 |
|
variants of unknown clinical significance |
8 |
|
5' untranslated regions - genetics |
7 |
|
adolescent idiopathic scoliosis |
7 |
|
age distribution |
7 |
|
als |
7 |
|
amino acid substitution |
7 |
|
amino acid substitution - genetics |
7 |
|
antigens, cd11b - genetics |
7 |
|
antipsychotic agents - pharmacology - therapeutic use |
7 |
|
asian continental ancestry group - ethnology - genetics |
7 |
|
behavior, animal |
7 |
|
biological markers |
7 |
|
bone mineral density |
7 |
|
bone/joint abnormalities |
7 |
|
c-reactive protein |
7 |
|
cardiovascular diseases |
7 |
|
cartilage |
7 |
|
cartilage diseases - genetics |
7 |
|
causality |
7 |
|
cd209 |
7 |
|
cell line |
7 |
|
cer1 |
7 |
|
charcot-marie-tooth |
7 |
|
charcot-marie-tooth disease - genetics - pathology - physiopathology |
7 |
|
chromosome mapping - methods |
7 |
|
cognitive structure |
7 |
|
col4a5 |
7 |
|
col4a6 |
7 |
|
complex traits and polygenic disorders |
7 |
|
connexins - genetics |
7 |
|
content-dependent process |
7 |
|
dc-sign |
7 |
|
de novo mutations |
7 |
|
diabetes |
7 |
|
directed differentiation |
7 |
|
dna - metabolism |
7 |
|
dna probes - genetics |
7 |
|
early psychosis |
7 |
|
electromyography |
7 |
|
electrophoretic mobility shift assay |
7 |
|
ens |
7 |
|
environment |
7 |
|
epidemiological study |
7 |
|
exome |
7 |
|
extracellular matrix proteins - chemistry - genetics |
7 |
|
extracellular matrix proteins - genetics - physiology |
7 |
|
fatty acid-binding proteins - blood |
7 |
|
follow-up studies |
7 |
|
gene library |
7 |
|
genetic diseases, x-linked - genetics |
7 |
|
genetic mapping |
7 |
|
genetic variation - genetics |
7 |
|
gjb1 (connexin32) |
7 |
|
gonosomal mosaicism |
7 |
|
han chinese |
7 |
|
haplotypes - genetics |
7 |
|
health surveys |
7 |
|
hela cells |
7 |
|
human induced pluripotent stem cells |
7 |
|
incidence |
7 |
|
intervertebral disc - pathology |
7 |
|
intervertebral disc disease |
7 |
|
intervertebral disk |
7 |
|
intervertebral disk displacement - complications - epidemiology - genetics |
7 |
|
interview, psychological |
7 |
|
isolated diffuse oesophageal leiomyomatosis |
7 |
|
japan |
7 |
|
kw040 - development |
7 |
|
kw065 - gastrointestinal system |
7 |
|
kw099 - malformation |
7 |
|
lectins, c-type - genetics - metabolism |
7 |
|
likelihood functions |
7 |
|
lipids |
7 |
|
long-term follow-up |
7 |
|
longitudinal |
7 |
|
lupus erythematosus, systemic - ethnology - genetics |
7 |
|
matrix metalloproteinase 1 - genetics |
7 |
|
microscopy, electron, transmission |
7 |
|
multi-method approach |
7 |
|
mutation detection |
7 |
|
nephritis - ethnology - genetics |
7 |
|
neural conduction - genetics - physiology |
7 |
|
neural crest |
7 |
|
neuregulin 1 |
7 |
|
neuropathy |
7 |
|
next generation sequencing |
7 |
|
non-coding region |
7 |
|
notochord-like cells (ncls) |
7 |
|
nuclear proteins - metabolism |
7 |
|
nucleus pulposus (np)-like cells |
7 |
|
osteoarthritis |
7 |
|
paternal age |
7 |
|
peripheral nerves - pathology - physiopathology - ultrastructure |
7 |
|
point mutation - genetics |
7 |
|
polymorphism |
7 |
|
predictive value of tests |
7 |
|
prevention |
7 |
|
pyrophosphatases - genetics - physiology |
7 |
|
quantitative trait loci |
7 |
|
questionnaires |
7 |
|
real-world |
7 |
|
receptors, cell surface - genetics - metabolism |
7 |
|
regression analysis |
7 |
|
reproducibility of results |
7 |
|
schizophrenia - drug therapy - pathology |
7 |
|
schizophrenia - drug therapy - physiopathology |
7 |
|
sequence analysis |
7 |
|
sp1 transcription factor - genetics |
7 |
|
spinal diseases - genetics |
7 |
|
transcription factor ap-2 - genetics |
7 |
|
transfection |
7 |
|
v266l |
7 |
|
variant prioritization |
7 |
|
vertebral disk displumbar vertebrae |
7 |
|
youth |
7 |
|
5' untranslated region |
6 |
|
adiponectin |
6 |
|
adiponectin - genetics |
6 |
|
adipose tissue - chemistry |
6 |
|
adrenomedullin |
6 |
|
adults |
6 |
|
affective psychoses |
6 |
|
aged, 80 and over |
6 |
|
alzheimer's disease |
6 |
|
anti-psychotics |
6 |
|
anxiety disorders |
6 |
|
arhgap4 |
6 |
|
back pain - diagnosis - epidemiology |
6 |
|
biological markers - blood - metabolism |
6 |
|
biomarkers |
6 |
|
biomedicine |
6 |
|
blood glucose - analysis |
6 |
|
blood pressure |
6 |
|
bone density |
6 |
|
brain - drug effects - metabolism - pathology |
6 |
|
burkholderia pseudomallei |
6 |
|
cancer stem cell |
6 |
|
cancer stemness |
6 |
|
carrier proteins - genetics |
6 |
|
caudate |
6 |
|
cell adhesion molecules - blood |
6 |
|
child, preschool |
6 |
|
choledochal cyst |
6 |
|
chromosome 8p |
6 |
|
chromosomes, human, pair 9 |
6 |
|
clustering |
6 |
|
col9a2 |
6 |
|
col9a3 |
6 |
|
collagen |
6 |
|
collagen type ix - genetics |
6 |
|
communityolder |
6 |
|
complete |
6 |
|
computer simulation |
6 |
|
covid-19 |
6 |
|
cytokines - genetics |
6 |
|
data mining |
6 |
|
de novo |
6 |
|
developmental |
6 |
|
diabetes mellitus, type 2 - diagnosis - ethnology - genetics |
6 |
|
disease outbreaks |
6 |
|
dna-binding proteins - genetics - metabolism |
6 |
|
drug naïve |
6 |
|
dysglycemia |
6 |
|
environmental stressors |
6 |
|
erbb4 |
6 |
|
excess life-years lost |
6 |
|
exon |
6 |
|
fibrinogen |
6 |
|
fibrinogen - genetics - metabolism |
6 |
|
founder mutation |
6 |
|
fractures, bone - genetics |
6 |
|
gamma-glutamyltransferase - blood - metabolism |
6 |
|
gene cluster |
6 |
|
genes |
6 |
|
genetic disease |
6 |
|
genetic epidemiology |
6 |
|
genome |
6 |
|
genome, human |
6 |
|
genome-wide haplotype association mapping (ham) |
6 |
|
ggt |
6 |
|
glucose intolerance - blood - genetics |
6 |
|
hepatitis b |
6 |
|
homeostasis |
6 |
|
hong kong - epidemiology - ethnology |
6 |
|
human genetics |
6 |
|
hyperglycaemia |
6 |
|
hypertension - blood - enzymology - epidemiology |
6 |
|
hypertension - blood - epidemiology - genetics |
6 |
|
hypertension - blood - ethnology - genetics - physiopathology |
6 |
|
hypertension - epidemiology |
6 |
|
hypertriglyceridemia - epidemiology |
6 |
|
igt |
6 |
|
immunohistochemistry |
6 |
|
impaired glucose tolerance |
6 |
|
in situ hybridization |
6 |
|
inflammation |
6 |
|
insulin |
6 |
|
insulin resistance |
6 |
|
interleukin-6 |
6 |
|
interleukin-6 - blood - genetics |
6 |
|
internal medicine |
6 |
|
intervertebral disc displacement - diagnosis - epidemiology |
6 |
|
intervertebral disc displacement - epidemiology - genetics |
6 |
|
intervertebral disc herniation |
6 |
|
lateral ventricles |
6 |
|
life expectancy |
6 |
|
lifetime prevalence |
6 |
|
linkage analysis |
6 |
|
liver carcinogenesis |
6 |
|
liver function test |
6 |
|
locomotion |
6 |
|
lod score |
6 |
|
longitudinal studies |
6 |
|
loss of heterozygosity |
6 |
|
low back pain |
6 |
|
lumbar vertebrae - pathology |
6 |
|
lumbar vertebrae - pathology - radiography |
6 |
|
major depressive episode |
6 |
|
mecp2 |
6 |
|
memory |
6 |
|
mental disorders / epidemiology |
6 |
|
metabolic diseases |
6 |
|
metabolic syndrome x - blood - epidemiology - etiology |
6 |
|
metabolic syndrome x - genetics |
6 |
|
metabolism |
6 |
|
mice, inbred c57bl |
6 |
|
mice, inbred strains |
6 |
|
models, biological |
6 |
|
molecular medicine |
6 |
|
naturalistic |
6 |
|
neuronal plasticity - drug effects |
6 |
|
obesity - epidemiology |
6 |
|
obesity - genetics - metabolism |
6 |
|
osteoblasts - metabolism |
6 |
|
osteoporosis - genetics - metabolism |
6 |
|
p6-c4 |
6 |
|
pacbio rs ii |
6 |
|
patterns of degeneration |
6 |
|
pharmacy and pharmacology environmental studies |
6 |
|
polymorphism, restriction fragment length |
6 |
|
population based study |
6 |
|
population surveys |
6 |
|
population-based |
6 |
|
power |
6 |
|
prediabetic state - diagnosis - ethnology - genetics |
6 |
|
premature mortality |
6 |
|
prepulse inhibition |
6 |
|
proto-oncogene proteins - genetics - metabolism |
6 |
|
psychiatric disorders |
6 |
|
quality control |
6 |
|
rare variants association |
6 |
|
receptors, cell surface - blood |
6 |
|
renbp |
6 |
|
replication |
6 |
|
retrospective studies |
6 |
|
reverse transcriptase polymerase chain reaction |
6 |
|
sciatica - diagnosis - epidemiology |
6 |
|
sequence analysis, dna |
6 |
|
sex distribution |
6 |
|
single nucleotide |
6 |
|
single-cell sequencing |
6 |
|
social unrest |
6 |
|
southern chinese women |
6 |
|
spinal |
6 |
|
spinal diseases - etiology - genetics - pathology |
6 |
|
stenosis |
6 |
|
stressful life events |
6 |
|
suicide |
6 |
|
taq i |
6 |
|
taq polymerase - genetics |
6 |
|
temporal trends |
6 |
|
toxicology and environmental safety |
6 |
|
trp2 |
6 |
|
trp3 |
6 |
|
tspyl2 |
6 |
|
tumor heterogeneity |
6 |
|
vitamin d receptor |
6 |
|
youth mental health |
6 |
|
γ-glutamyl transaminase |
6 |
|
adiposity - physiology |
5 |
|
alk |
5 |
|
alzheimer disease - genetics |
5 |
|
antipsychotic agents - therapeutic use |
5 |
|
antipsychotics |
5 |
|
area under curve |
5 |
|
atherosclerosis |
5 |
|
autophagy |
5 |
|
binding sites - genetics |
5 |
|
biological markers - blood |
5 |
|
blood glucose - metabolism |
5 |
|
bone density - genetics - physiology |
5 |
|
brain - pathology - physiopathology |
5 |
|
bronchiectasis |
5 |
|
candidate gene approach |
5 |
|
candidate genes |
5 |
|
carcinoma, hepatocellular - mortality - pathology - surgery |
5 |
|
carcinoma, non-small-cell lung - genetics |
5 |
|
carotid artery diseases - diagnosis |
5 |
|
carotid intima-media thickness |
5 |
|
cds |
5 |
|
cell adhesion molecules |
5 |
|
chi-square distribution |
5 |
|
cholesterol |
5 |
|
chromosomes, human, pair 1 |
5 |
|
chromosomes, human, pair 11 |
5 |
|
chromosomes, human, pair 14 |
5 |
|
chromosomes, human, pair 3 - genetics |
5 |
|
cognition |
5 |
|
complex traits: theory and methods |
5 |
|
computational biology - methods |
5 |
|
copy number variant |
5 |
|
crispr/cas9 |
5 |
|
cystic fibrosis |
5 |
|
cytoskeletal proteins - genetics |
5 |
|
depressive disorder, major - diagnosis - epidemiology - psychology |
5 |
|
diabetes mellitus |
5 |
|
diabetes mellitus - blood - drug therapy - epidemiology |
5 |
|
diffusion |
5 |
|
diffusion magnetic resonance imaging |
5 |
|
disease-free survival |
5 |
|
egfr |
5 |
|
endocrinology |
5 |
|
endophenotypes |
5 |
|
epilepsy - genetics |
5 |
|
europe |
5 |
|
exome sequencing |
5 |
|
extracellular matrix proteins - genetics |
5 |
|
f11 receptor |
5 |
|
family history |
5 |
|
fatty-acid-binding proteins |
5 |
|
females |
5 |
|
femur - metabolism |
5 |
|
fractures, bone - epidemiology - genetics |
5 |
|
gastrointestinal system |
5 |
|
gene expression regulation - physiology |
5 |
|
gene polymorphism |
5 |
|
gene-environment interaction |
5 |
|
genes, tumor suppressor |
5 |
|
genetic linkage |
5 |
|
genetic linkage - genetics |
5 |
|
genetic markers |
5 |
|
genetic testing |
5 |
|
genome sequencing |
5 |
|
genotype-phenotype correlation |
5 |
|
glycogen storage disease type iib |
5 |
|
glycosylated hemoglobin a |
5 |
|
gtp-binding proteins - genetics - immunology |
5 |
|
health care workers |
5 |
|
health personnel - psychology |
5 |
|
health personnel - statistics and numerical data |
5 |
|
hemoglobin a, glycosylated - metabolism |
5 |
|
hirschsprung disease - genetics - metabolism |
5 |
|
homeodomain proteins - genetics |
5 |
|
hscr |
5 |
|
hyperglycemia - genetics |
5 |
|
hypertension - ethnology - genetics |
5 |
|
hypertension - genetics - physiopathology |
5 |
|
hypoglycemic agents - therapeutic use |
5 |
|
image processing, computer-assisted |
5 |
|
immunity, innate |
5 |
|
infectious disease outbreak |
5 |
|
insulin - blood |
5 |
|
intercellular signaling peptides and proteins - genetics |
5 |
|
interferon-alpha - immunology |
5 |
|
interferon-beta - immunology |
5 |
|
kras |
5 |
|
kw020 - characterization of disorders |
5 |
|
kw024 - chromosomal deletions |
5 |
|
kw039 - delineation of diseases |
5 |
|
kw078 - genome scan |
5 |
|
latent tgf-beta binding proteins - genetics |
5 |
|
liver embryo |
5 |
|
liver neoplasms - mortality - pathology - surgery |
5 |
|
long-term psychological distress |
5 |
|
lumbosacral region - anatomy & histology |
5 |
|
lung adenocarcinomas |
5 |
|
lung neoplasms - genetics |
5 |
|
major depressive disorder |
5 |
|
mapk7 |
5 |
|
mendelian disease |
5 |
|
metabolic syndrome |
5 |
|
metabolic syndrome x - blood |
5 |
|
microarray |
5 |
|
nerve net - pathology - physiopathology |
5 |
|
network |
5 |
|
neurogenetics |
5 |
|
never medicated |
5 |
|
nuclear proteins - genetics |
5 |
|
nuclear proteins - genetics - metabolism |
5 |
|
nucleic acid hybridization |
5 |
|
obesity - blood |
5 |
|
obesity - ethnology - genetics |
5 |
|
oncofetal proteins |
5 |
|
oncogene proteins - genetics - metabolism |
5 |
|
oncogenic mutations |
5 |
|
osteoporosis |
5 |
|
outbreak |
5 |
|
pelvic bones - metabolism |
5 |
|
physical chromosome mapping - methods |
5 |
|
polygenic risk |
5 |
|
posttraumatic symptoms |
5 |
|
proteomic profiling |
5 |
|
proteomics |
5 |
|
proto-oncogene proteins c-ret |
5 |
|
proto-oncogene proteins c-ret - genetics |
5 |
|
raindance |
5 |
|
rare variant |
5 |
|
receptor protein-tyrosine kinases - genetics - metabolism |
5 |
|
replication study |
5 |
|
resistin - genetics |
5 |
|
rs11190870 |
5 |
|
sars virus - immunology |
5 |
|
schizophrenia, first-episode |
5 |
|
scoliosis - genetics |
5 |
|
severe acute respiratory syndrome |
5 |
|
severe acute respiratory syndrome - epidemiology - psychology |
5 |
|
severe acute respiratory syndrome - genetics - immunology |
5 |
|
sickness impact profile |
5 |
|
southern chinese |
5 |
|
spectrometry, mass, matrix-assisted laser desorption-ionization |
5 |
|
spine - anatomy & histology - physiology |
5 |
|
stress |
5 |
|
stress disorders, post-traumatic - diagnosis - epidemiology - etiology |
5 |
|
stress disorders, post-traumatic - diagnosis - epidemiology - psychology |
5 |
|
striato-thalamic volume |
5 |
|
structural |
5 |
|
survivors - psychology - statistics and numerical data |
5 |
|
targeted resequencing |
5 |
|
trafficking defects |
5 |
|
transcription factors - genetics |
5 |
|
transcription factors - genetics - metabolism |
5 |
|
treatment outcome |
5 |
|
united states - epidemiology |
5 |
|
variant annotation |
5 |
|
wga |
5 |
|
whole genome association |
5 |
|
working memory |
5 |
|
x-linked vacuolar cardiomyopathy and myopathy |
5 |
|
zebrafish |
5 |
|
ace |
4 |
|
adhd |
4 |
|
alen |
4 |
|
ann |
4 |
|
anterior cingulate cortex |
4 |
|
antipsychotic agents - administration and dosage - pharmacology - therapeutic use |
4 |
|
apoe |
4 |
|
atp2b4 |
4 |
|
autistic disorder - complications |
4 |
|
autistic disorder - diagnosis - etiology - pathology |
4 |
|
base sequence |
4 |
|
binding sites |
4 |
|
biochemical genetics |
4 |
|
blood pressure measurement |
4 |
|
brain - growth and development |
4 |
|
brain structure |
4 |
|
calcium transient |
4 |
|
calcium-binding proteins - genetics |
4 |
|
cancer proteome |
4 |
|
carcinoma, hepatocellular - genetics |
4 |
|
cart |
4 |
|
caudal regression |
4 |
|
cdx1 |
4 |
|
cell type-specific |
4 |
|
chromosome 1q |
4 |
|
chromosome 2q |
4 |
|
chromosome 5q |
4 |
|
chromosome mapping - statistics & numerical data |
4 |
|
chromosomes, human, y - genetics |
4 |
|
classification |
4 |
|
cognitive decline |
4 |
|
collagen type i - genetics |
4 |
|
colorectal cancer |
4 |
|
colorectal neoplasms - genetics |
4 |
|
complex disease |
4 |
|
complex traits |
4 |
|
congenital abnormalities - diagnosis - pathology |
4 |
|
copy number/structural variation |
4 |
|
copy-number variation |
4 |
|
databases - nucleic acid |
4 |
|
deletion |
4 |
|
discriminant analysis |
4 |
|
disease-susceptible gene |
4 |
|
dna mutational analysis - methods |
4 |
|
dna, mitochondrial - genetics |
4 |
|
dti |
4 |
|
epigenome |
4 |
|
esophageal carcinoma |
4 |
|
estrogen receptor alpha - genetics |
4 |
|
estrogen receptor beta - genetics |
4 |
|
european continental ancestry group - genetics |
4 |
|
familial aggregation |
4 |
|
familial spastic paraplegia |
4 |
|
family |
4 |
|
fractures, bone - complications - genetics - physiopathology |
4 |
|
frontal lobe - pathology |
4 |
|
gene expression profiling - instrumentation - methods |
4 |
|
gene regulatory networks - genetics |
4 |
|
genetic |
4 |
|
genetic association studies |
4 |
|
genetic loci |
4 |
|
genetic predisposition to disease - epidemiology |
4 |
|
head - abnormalities - pathology |
4 |
|
health service utilization |
4 |
|
heart failure |
4 |
|
homeodomain proteins - metabolism |
4 |
|
homozygosity mapping |
4 |
|
identification of disease genes |
4 |
|
induced pluripotent stem cells |
4 |
|
information storage and retrieval - methods |
4 |
|
internet |
4 |
|
intervertebral disc degeneration - genetics - physiopathology |
4 |
|
intervertebral disk - metabolism - pathology - physiopathology |
4 |
|
intervertebral disk displacement - genetics - metabolism - physiopathology |
4 |
|
joint effect |
4 |
|
kw075 - genetic mapping |
4 |
|
kw078 – genome scan |
4 |
|
kw083 - genotype-phenotype correlations |
4 |
|
kw086 – identification of disease genes |
4 |
|
kw087 - immune system |
4 |
|
kw117 - mutation detection |
4 |
|
kw139 - polymorphism |
4 |
|
ldl-c |
4 |
|
ldl-receptor related proteins - genetics |
4 |
|
linkage disequilibrium analysis |
4 |
|
liver neoplasms - genetics |
4 |
|
longitudinal study |
4 |
|
low back pain - genetics - physiopathology |
4 |
|
low density lipoprotein receptor-related protein-5 |
4 |
|
lumbar disk degeneration |
4 |
|
machine learning |
4 |
|
massively parallel sequencing |
4 |
|
mental disorders |
4 |
|
meta-analysis as topic |
4 |
|
metabolic side effects |
4 |
|
micrornas - genetics - metabolism |
4 |
|
microsatellite repeats |
4 |
|
mir-122 |
4 |
|
mitochondrial |
4 |
|
molecular basis of mendelian disorders |
4 |
|
mri scan |
4 |
|
neuritic elongation |
4 |
|
neurodegeneration |
4 |
|
neuroleptic naive |
4 |
|
nrg3 |
4 |
|
oligonucleotide array sequence analysis - instrumentation - methods |
4 |
|
organogenesis |
4 |
|
osteoporotic fractures - genetics - physiopathology |
4 |
|
periostin |
4 |
|
pharmacy and pharmacology psychology |
4 |
|
pmca |
4 |
|
population-based linkage |
4 |
|
pro-neuronal survival |
4 |
|
ptpn21 |
4 |
|
putamen |
4 |
|
putamen - drug effects - pathology |
4 |
|
quantitative trait, heritable |
4 |
|
receptors, calcium-sensing - genetics |
4 |
|
recessive mutation |
4 |
|
regional index: eurasia |
4 |
|
regulatory variant |
4 |
|
sacral agenesis |
4 |
|
sample selection |
4 |
|
schizophrenia - diagnosis - etiology - pathology |
4 |
|
schizophrenia - diagnosis - genetics |
4 |
|
schizophrenia - genetics - pathology |
4 |
|
second-generation antipsychotics |
4 |
|
selection - genetic |
4 |
|
sex differences |
4 |
|
snps |
4 |
|
spinal fractures - genetics - physiopathology |
4 |
|
spine |
4 |
|
statins |
4 |
|
statistical genetics |
4 |
|
study design |
4 |
|
subphenotypes |
4 |
|
subtraction analysis |
4 |
|
susceptibility |
4 |
|
transforming growth factor beta - genetics |
4 |
|
tumor suppressor gene |
4 |
|
twin studies |
4 |
|
vertebral fracture |
4 |
|
vitamin d binding protein |
4 |
|
vitamin d insufficiency |
4 |
|
voxel-based analysis |
4 |
|
voxel-based morphometry |
4 |
|
ageing |
3 |
|
alcohol consumption |
3 |
|
allele |
3 |
|
alu |
3 |
|
analysis of variance |
3 |
|
antimicrobial resistance |
3 |
|
arrhythmias |
3 |
|
asian continental ancestry group - genetics - statistics and numerical data |
3 |
|
asians |
3 |
|
attention |
3 |
|
biomarker |
3 |
|
bone and bones - anatomy & histology |
3 |
|
bone size |
3 |
|
candidate gene |
3 |
|
carbapenemases |
3 |
|
cardiac enhancers |
3 |
|
case-control |
3 |
|
causal inference |
3 |
|
cellular neuroscience |
3 |
|
chromatin state |
3 |
|
chromosome mapping |
3 |
|
chromosomes, human, 16-18 |
3 |
|
chromosomes, human, pair 17 - genetics |
3 |
|
cognition disorders - diagnosis - genetics |
3 |
|
comorbidity |
3 |
|
complex human traits |
3 |
|
confidence intervals |
3 |
|
corpus callosum |
3 |
|
crohn disease - genetics |
3 |
|
cspg5 |
3 |
|
databases, factual |
3 |
|
degradome |
3 |
|
dermatoglyphics |
3 |
|
developmental neuroscience |
3 |
|
diabetes mellitus, type 2 - genetics |
3 |
|
disease susceptibility loci |
3 |
|
dna - chemistry - metabolism |
3 |
|
esr2 |
3 |
|
evolution, molecular |
3 |
|
expressed sequence tags |
3 |
|
factor analysis, statistical |
3 |
|
family study |
3 |
|
femur - injuries - metabolism |
3 |
|
fibrosis |
3 |
|
fractures, bone - etiology - genetics |
3 |
|
fto |
3 |
|
function validation |
3 |
|
functional enrichment |
3 |
|
functional prediction |
3 |
|
gamma-aminobutyric acid |
3 |
|
gender |
3 |
|
gene coverage |
3 |
|
gene density |
3 |
|
generalized ld score regression |
3 |
|
genetic architecture |
3 |
|
genetic predisposition to disease - ethnology - genetics |
3 |
|
genome - genetics |
3 |
|
genomics - methods |
3 |
|
genotype-by-sex interaction |
3 |
|
glutamate |
3 |
|
great britain - epidemiology |
3 |
|
guanine nucleotide binding protein |
3 |
|
gwas summary statistics |
3 |
|
health behavior |
3 |
|
hepatitis b virus |
3 |
|
herpesvirus 4, human - classification - genetics - isolation & purification |
3 |
|
high-throughput assay |
3 |
|
hypertension - genetics |
3 |
|
immune response |
3 |
|
incompatibility groups |
3 |
|
inheritance patterns |
3 |
|
intelligence |
3 |
|
interaction |
3 |
|
intermediate phenotypes |
3 |
|
intervertebral disc |
3 |
|
ion transport |
3 |
|
knowledge-based genetic association |
3 |
|
kw008 - bioinformatics |
3 |
|
lassosum |
3 |
|
ldpred2 |
3 |
|
liability threshold model |
3 |
|
linkage disequilibrium blocks |
3 |
|
long qt syndrome |
3 |
|
matrisome |
3 |
|
megaprs |
3 |
|
memory disorders - diagnosis - genetics |
3 |
|
mental retardation - diagnosis - genetics |
3 |
|
minisatellite repeats |
3 |
|
mitogen activated protein kinase |
3 |
|
models, statistical |
3 |
|
molecular interaction |
3 |
|
nasopharyngeal neoplasms - virology |
3 |
|
ndm-1 |
3 |
|
nedd4l |
3 |
|
neuregulin-1 |
3 |
|
neurodegenerative diseases |
3 |
|
neuropsychological tests |
3 |
|
neuroticism |
3 |
|
noncoding variants |
3 |
|
nonnegativity |
3 |
|
notch signaling pathway |
3 |
|
obesity. type 2 diabetes |
3 |
|
obstetric complications |
3 |
|
osteoporosis - blood - ethnology - genetics |
3 |
|
osteoporosis - complications - genetics |
3 |
|
osteoporosis - epidemiology - genetics |
3 |
|
osteoprotegerin |
3 |
|
osteoprotegerin - blood - genetics |
3 |
|
paralyses, familial periodic - ethnology - etiology - genetics |
3 |
|
partition heritability |
3 |
|
personality - genetics |
3 |
|
personality inventory |
3 |
|
plasmids |
3 |
|
polygenic risk scores |
3 |
|
polygenic scores |
3 |
|
polymorphism, single nucleotide - physiology |
3 |
|
population |
3 |
|
population admixture |
3 |
|
population stratification |
3 |
|
protein expression |
3 |
|
protein-serine-threonine kinases - genetics |
3 |
|
proteome |
3 |
|
proton magnetic resonance spectroscopy |
3 |
|
prs-cs |
3 |
|
psychopathology |
3 |
|
qtl |
3 |
|
quantitative genetics |
3 |
|
quantitative trait association |
3 |
|
quantitative trait loci - genetics - physiology |
3 |
|
random forest |
3 |
|
rare disease |
3 |
|
recombination |
3 |
|
regulatory elements, transcriptional |
3 |
|
sampling studies |
3 |
|
sbayesr |
3 |
|
set-based association test |
3 |
|
silac |
3 |
|
simulation |
3 |
|
sm/j |
3 |
|
snp heritability |
3 |
|
socioeconomic factors |
3 |
|
statistics, nonparametric |
3 |
|
tdt |
3 |
|
tetralogy of fallot |
3 |
|
thyrotoxicosis - complications - ethnology - genetics |
3 |
|
transcription factors - chemistry - genetics - metabolism |
3 |
|
transcriptional gene regulation |
3 |
|
transmission/disequilibrium test |
3 |
|
tryptophan hydroxylase |
3 |
|
twins |
3 |
|
unidimensional scaling |
3 |
|
variance component |
3 |
|
variants |
3 |
|
verbal behavior |
3 |
|
wes |
3 |
|
wgs |
3 |
|
"endophenotypes" |
2 |
|
2de |
2 |
|
5-ht(2a) |
2 |
|
5-htt |
2 |
|
a-b ridge count |
2 |
|
accuracy |
2 |
|
achievement |
2 |
|
acoustic stimulation |
2 |
|
actionable mutation |
2 |
|
adh2 |
2 |
|
admixture |
2 |
|
affective disorder |
2 |
|
age at onset |
2 |
|
age of onset |
2 |
|
aggression |
2 |
|
allelic association |
2 |
|
anxiety - diagnosis - epidemiology - genetics - psychology |
2 |
|
ap3s1 gene |
2 |
|
asthma |
2 |
|
attention deficit disorder with hyperactivity - genetics |
2 |
|
autism |
2 |
|
bdnf |
2 |
|
bias correction |
2 |
|
biasedness |
2 |
|
bic |
2 |
|
binary traits |
2 |
|
bioinformatics prioritization |
2 |
|
bioinformatics tool |
2 |
|
biology |
2 |
|
bipolar affective disorder |
2 |
|
bipolar disorder - diagnosis - epidemiology - genetics |
2 |
|
bipolar disorder - diagnosis - genetics |
2 |
|
bipolar disorder - diagnosis - genetics - psychology |
2 |
|
bipolar disorder - genetics |
2 |
|
brain - abnormalities |
2 |
|
brain - physiopathology |
2 |
|
brain chemistry - genetics |
2 |
|
brain damage, chronic - diagnosis - etiology - psychology |
2 |
|
breast neoplasms - diagnosis - genetics |
2 |
|
cannabis use |
2 |
|
catecholamines |
2 |
|
censoring |
2 |
|
cerebral asymmetry |
2 |
|
cerebral ventricles - abnormalities |
2 |
|
chinese population |
2 |
|
chinese setting |
2 |
|
chromosome 12 |
2 |
|
chromosomes, human, pair 12 |
2 |
|
chromosomes, human, pair 15 - genetics |
2 |
|
chromosomes, human, pair 22 |
2 |
|
chromosomes, human, pair 22 - genetics |
2 |
|
clozapine - therapeutic use |
2 |
|
clu polymorphisms |
2 |
|
coalescence |
2 |
|
cognitive ability |
2 |
|
cognitive functioning |
2 |
|
commd7 gene |
2 |
|
common variants |
2 |
|
computational retinal microvasculature biomarkers (crmb) |
2 |
|
constraints |
2 |
|
covariate-modulated false discovery rate |
2 |
|
cross-phenotype association |
2 |
|
csf1 gene |
2 |
|
data integration |
2 |
|
data interpretation, statistical |
2 |
|
databases, nucleic acid |
2 |
|
dbsnp |
2 |
|
deg analysis |
2 |
|
dementia |
2 |
|
demography |
2 |
|
depression - diagnosis - epidemiology - genetics - psychology |
2 |
|
depressive disorder - genetics |
2 |
|
diagnostic and statistical manual of mental disorders |
2 |
|
disease outbreaks - statistics & numerical data |
2 |
|
diseases in twins |
2 |
|
diseases in twins - diagnosis - epidemiology - genetics |
2 |
|
diseases in twins - genetics |
2 |
|
disinhibition |
2 |
|
dna - analysis |
2 |
|
dna - genetics |
2 |
|
dna - genetics - isolation & purification |
2 |
|
dna pooling |
2 |
|
dna primers |
2 |
|
dna primers - genetics |
2 |
|
dopamine plasma membrane transport proteins - genetics |
2 |
|
dose-dependent |
2 |
|
drd4 |
2 |
|
drug response prediction |
2 |
|
early detection of cancer |
2 |
|
early onset |
2 |
|
early-onset schizophrenia |
2 |
|
electroencephalography |
2 |
|
england - epidemiology |
2 |
|
epidemiologic methods |
2 |
|
epilepsy |
2 |
|
epilepsy, generalized - genetics |
2 |
|
epistasis |
2 |
|
eqtls |
2 |
|
event-related potentials, p300 - physiology |
2 |
|
exons |
2 |
|
experimental errors |
2 |
|
extended pedigree |
2 |
|
extreme selection |
2 |
|
factor analysis |
2 |
|
familial risk |
2 |
|
family characteristics |
2 |
|
first-episode |
2 |
|
first-episode patients |
2 |
|
frontal lobe dysfunction |
2 |
|
functional annotation |
2 |
|
functional connectivity |
2 |
|
functional laterality - physiology |
2 |
|
gamma oscillation |
2 |
|
genes, dominant |
2 |
|
genetic association studies - methods |
2 |
|
genetic data |
2 |
|
genetic diseases, inborn - genetics |
2 |
|
genetic heterogeneity |
2 |
|
genetic markers - genetics |
2 |
|
genetic sharing |
2 |
|
genetic techniques |
2 |
|
genetic testing - methods |
2 |
|
genetics, medical - methods |
2 |
|
genome search |
2 |
|
genome-wide |
2 |
|
genome-wide association study - statistics and numerical data |
2 |
|
genome-wide snps |
2 |
|
genomic coordinate |
2 |
|
genomic restricted maximum likelihood |
2 |
|
genomics - statistics & numerical data |
2 |
|
genotype error |
2 |
|
germany |
2 |
|
gestational age |
2 |
|
great britain |
2 |
|
haplotype estimation |
2 |
|
hapmap |
2 |
|
hbv |
2 |
|
health status |
2 |
|
height |
2 |
|
heroin dependence |
2 |
|
heterogeneity |
2 |
|
highly variable gene |
2 |
|
hippocampus |
2 |
|
hospitalization |
2 |
|
ibd mapping |
2 |
|
identical by descent (ibd) |
2 |
|
identity-by-descent (ibd) |
2 |
|
immunology |
2 |
|
impulsivity |
2 |
|
infant, newborn |
2 |
|
influenza |
2 |
|
influenza a virus |
2 |
|
influenza, human - complications - epidemiology |
2 |
|
influenza, human - epidemiology |
2 |
|
instrumental variables |
2 |
|
interviews as topic |
2 |
|
introns - genetics |
2 |
|
k-mode |
2 |
|
kw052 - epilepsy |
2 |
|
kw080 - genome sequencing |
2 |
|
kw101 - mapping complex traits |
2 |
|
kw118 - mutation detection |
2 |
|
kw124 - neurogenetics |
2 |
|
ld |
2 |
|
least squares problem |
2 |
|
linear models |
2 |
|
linear regression |
2 |
|
linkage disequilibrium - genetics |
2 |
|
linkage disequilibrium score regression |
2 |
|
linkage equilibrium |
2 |
|
logistic models |
2 |
|
logistic regression |
2 |
|
london |
2 |
|
maldi-tof ms |
2 |
|
markov chain monte carlo |
2 |
|
mathematical computing |
2 |
|
mathematics |
2 |
|
matrix-vector multiplication |
2 |
|
medical informatics - methods |
2 |
|
medical sciences - psychiatry and neurology |
2 |
|
membrane glycoproteins - genetics |
2 |
|
membrane transport proteins |
2 |
|
memory performance |
2 |
|
mendelian randomisation |
2 |
|
mental disorders - epidemiology - genetics |
2 |
|
meta-analysis with shared subjects |
2 |
|
methodology |
2 |
|
microsatellite repeats - genetics |
2 |
|
minisatellite repeats - genetics |
2 |
|
missense mutation |
2 |
|
model-fitting |
2 |
|
modifier genes |
2 |
|
molecular sequence data |
2 |
|
monoamine oxidase - genetics |
2 |
|
monte carlo method |
2 |
|
mood disorders - diagnosis - genetics |
2 |
|
motivation |
2 |
|
multilocus test |
2 |
|
mx |
2 |
|
nerve tissue proteins |
2 |
|
nerve tissue proteins - genetics |
2 |
|
neural perturbation |
2 |
|
neurocognitive deficit |
2 |
|
neurodevelopment |
2 |
|
neurogenetics and neurodegeneration |
2 |
|
neuropsychological deficits |
2 |
|
neuropsychology |
2 |
|
neurotransmitter |
2 |
|
nonparametric maximum likelihood |
2 |
|
nuclear family |
2 |
|
onset age |
2 |
|
optical coherence tomography angiography (octa) |
2 |
|
orthopedics and traumatology |
2 |
|
p300 |
2 |
|
parallel computation |
2 |
|
parenting |
2 |
|
path analysis |
2 |
|
pedigree error |
2 |
|
personality assessment |
2 |
|
personality development |
2 |
|
personality inventory - statistics & numerical data |
2 |
|
personality trait |
2 |
|
phenotype |
2 |
|
polygenic risk score |
2 |
|
polymerase chain reaction |
2 |
|
polymorphism, genetic - genetics |
2 |
|
polymorphism, single-stranded conformational |
2 |
|
population surveillance |
2 |
|
potassium channels - genetics |
2 |
|
potassium channels, calcium-activated |
2 |
|
power calculation |
2 |
|
precision medicine |
2 |
|
pregnancy |
2 |
|
pregnancy complications, infectious - epidemiology |
2 |
|
prenatal exposure delayed effects |
2 |
|
product partition model with covariates (ppmx) |
2 |
|
prostatic neoplasms - diagnosis - genetics |
2 |
|
protein interaction maps |
2 |
|
protein profiling |
2 |
|
psychiatric genetics |
2 |
|
psychiatric status rating scales - statistics & numerical data |
2 |
|
psychiatric traits |
2 |
|
psychoses |
2 |
|
psychotic disorders - diagnosis - epidemiology - genetics |
2 |
|
psychotic disorders - diagnosis - genetics - psychology |
2 |
|
psychotic disorders - genetics |
2 |
|
qtl association |
2 |
|
qtl association analyses |
2 |
|
quantitative trait |
2 |
|
quantitative trait loci (qtl) |
2 |
|
quantitative trait loci - genetics |
2 |
|
radio frequency |
2 |
|
reaction time - genetics |
2 |
|
receptor, serotonin, 5-ht1b - genetics |
2 |
|
receptor, serotonin, 5-ht2a |
2 |
|
receptor, serotonin, 5-ht2c - genetics |
2 |
|
receptors, dopamine d2 - genetics |
2 |
|
receptors, dopamine d4 |
2 |
|
receptors, gaba-a - genetics |
2 |
|
receptors, serotonin - genetics |
2 |
|
reference values |
2 |
|
refsnp (rs) id |
2 |
|
registries |
2 |
|
regression |
2 |
|
relatives |
2 |
|
repetitive sequences, nucleic acid - genetics |
2 |
|
residence characteristics |
2 |
|
retinal imaging |
2 |
|
retinal vein occlusion |
2 |
|
rgs4 |
2 |
|
risk |
2 |
|
risk assessment |
2 |
|
risk-taking |
2 |
|
schizoaffective disorder |
2 |
|
schizophrenia - diagnosis - epidemiology |
2 |
|
schizophrenia - diagnosis - epidemiology - genetics |
2 |
|
schizophrenia - diagnosis - etiology |
2 |
|
schizophrenia - diagnosis - genetics - physiopathology |
2 |
|
schizophrenia - drug therapy - genetics |
2 |
|
schizophrenia - epidemiology |
2 |
|
schizophrenia - epidemiology - etiology |
2 |
|
schizophrenia - epidemiology - genetics |
2 |
|
schizophrenia - ethnology - genetics |
2 |
|
schizophrenia - etiology |
2 |
|
schizophrenia - genetics - physiopathology |
2 |
|
schizophrenia - physiopathology |
2 |
|
schizotypal personality disorder - diagnosis - genetics |
2 |
|
scrna-seq |
2 |
|
seasons |
2 |
|
seldi-tof proteinchip |
2 |
|
selection |
2 |
|
selective genotyping |
2 |
|
sensitivity and specificity |
2 |
|
sequence analysis, dna - methods |
2 |
|
sequence deletion |
2 |
|
sequence variant |
2 |
|
serotonin |
2 |
|
serotonin - metabolism |
2 |
|
serotonin plasma membrane transport proteins |
2 |
|
sert |
2 |
|
serum lipids |
2 |
|
serum markers |
2 |
|
siblings |
2 |
|
sibs |
2 |
|
sibships |
2 |
|
single nucleotide polymorphism (snp) |
2 |
|
single nucleotide polymorphisms (snp) |
2 |
|
single-cell rna seq |
2 |
|
skm-snp |
2 |
|
small-conductance calcium-activated potassium channels |
2 |
|
smoothing |
2 |
|
social adjustment |
2 |
|
social behavior |
2 |
|
social cognition |
2 |
|
social environment |
2 |
|
sociology |
2 |
|
spinocerebellar ataxias |
2 |
|
stability |
2 |
|
statistical model |
2 |
|
statistics |
2 |
|
statistics as topic |
2 |
|
subspace clustering |
2 |
|
substance-related disorders - genetics |
2 |
|
subtyping |
2 |
|
susceptibility genes |
2 |
|
symptom dimensions |
2 |
|
syndrome |
2 |
|
taiwan |
2 |
|
targeted cancer therapy |
2 |
|
targeted maximum likelihood estimation |
2 |
|
time factors |
2 |
|
torque |
2 |
|
transcriptome-wide association studies (twas) |
2 |
|
transcriptome-wide association study |
2 |
|
transfer learning |
2 |
|
transglutaminase 6 |
2 |
|
trinucleotide repeats |
2 |
|
tryptophan hydroxylase - genetics |
2 |
|
tumor biomarkers |
2 |
|
twin |
2 |
|
twin studies as topic |
2 |
|
twins - genetics |
2 |
|
twins, dizygotic |
2 |
|
twins, dizygotic - genetics |
2 |
|
twins, monozygotic |
2 |
|
twins, monozygotic - genetics |
2 |
|
variance components |
2 |
|
variance explained |
2 |
|
vegetation |
2 |
|
vulnerability |
2 |
|
wales - epidemiology |
2 |
|
within-subject analysis |
2 |
|
young-onset hypertension |
2 |
|
(schizophrenia) |
1 |
|
22q11 |
1 |
|
3' untranslated regions |
1 |
|
3' untranslated regions - genetics |
1 |
|
5-ht |
1 |
|
5-ht(2a) receptor gene |
1 |
|
5-ht-2a |
1 |
|
5-ht2a |
1 |
|
5-ht2c receptor |
1 |
|
5ht1b |
1 |
|
6p |
1 |
|
acoustic stimulation - methods |
1 |
|
acute disease |
1 |
|
acute schizophrenia |
1 |
|
adaptation, psychological |
1 |
|
addiction |
1 |
|
adiposity |
1 |
|
adjustment disorders - diagnosis - etiology - psychology |
1 |
|
administration, inhalation |
1 |
|
adolescence |
1 |
|
adolescent psychology |
1 |
|
affect |
1 |
|
affected sib-pair analysis |
1 |
|
affective disorders, psychotic - diagnosis - genetics - psychology |
1 |
|
affective disorders, psychotic - epidemiology - etiology |
1 |
|
affective disorders, psychotic - genetics |
1 |
|
affective psychosis |
1 |
|
africa - ethnology |
1 |
|
african americans - psychology |
1 |
|
african americans - psychology - statistics & numerical data |
1 |
|
african continental ancestry group |
1 |
|
african continental ancestry group - genetics |
1 |
|
aging |
1 |
|
agoraphobia - diagnosis - genetics |
1 |
|
alcohol dehydrogenase - genetics |
1 |
|
alcohol drinking - epidemiology |
1 |
|
alcohol policy |
1 |
|
alcoholism |
1 |
|
alcoholism - diagnosis - epidemiology - psychology |
1 |
|
alcoholism - genetics |
1 |
|
alcoholism - psychology |
1 |
|
aldehyde dehydrogenase |
1 |
|
allele frequency |
1 |
|
allelic assocation |
1 |
|
alternative splicing - genetics |
1 |
|
alzheimer disease - epidemiology - genetics - physiopathology |
1 |
|
amino acid sequence |
1 |
|
amphetamine |
1 |
|
amphetamine-related disorders |
1 |
|
amphetamine-related disorders - diagnosis - epidemiology - psychology |
1 |
|
amphetamine-related disorders - epidemiology - genetics |
1 |
|
amphetamine-related disorders - etiology - genetics |
1 |
|
amygdala - abnormalities - physiopathology |
1 |
|
amyotrophic lateral sclerosis |
1 |
|
amyotrophic lateral sclerosis - genetics |
1 |
|
angelman syndrome - genetics |
1 |
|
angiotensin ii type i receptor gene |
1 |
|
anorexia nervosa - etiology - genetics - psychology |
1 |
|
anticipation |
1 |
|
anticonvulsants - therapeutic use |
1 |
|
antipsychotic |
1 |
|
antipsychotic agents - metabolism - therapeutic use |
1 |
|
antipsychotic agents - pharmacology |
1 |
|
antisocial personality disorder - diagnosis - epidemiology - psychology |
1 |
|
anxiety - diagnosis - epidemiology |
1 |
|
anxiety - etiology |
1 |
|
anxiety disorders - diagnosis - epidemiology - psychology |
1 |
|
anxiety disorders - diagnosis - genetics |
1 |
|
anxiety disorders - genetics |
1 |
|
apolipoprotein e |
1 |
|
apolipoproteins e - genetics |
1 |
|
arousal |
1 |
|
arousal - physiology |
1 |
|
arvcf |
1 |
|
asd |
1 |
|
asian high-income region |
1 |
|
assessment |
1 |
|
association mapping |
1 |
|
asymmetry |
1 |
|
attention deficit disorder with hyperactivity - classification - genetics |
1 |
|
attention deficit disorder with hyperactivity - diagnosis - genetics - |
1 |
|
attention deficit disorder with hyperactivity - epidemiology - genetics |
1 |
|
attention deficit disorder with hyperactivity - epidemiology - genetics - psychology |
1 |
|
attention deficit disorder with hyperactivity - genetics - pathology |
1 |
|
attention deficit disorder with hyperactivity - genetics - psychology |
1 |
|
attention deficit hyperactivity disorder |
1 |
|
attention deficit hyperactivity disorder (adhd) |
1 |
|
attention-deficit hyperactivity disorder (adhd) |
1 |
|
attitude |
1 |
|
attitude to health |
1 |
|
australia |
1 |
|
autistic disorder - diagnosis - genetics |
1 |
|
autistic disorder - epidemiology |
1 |
|
autistic disorder - epidemiology - virology |
1 |
|
autoimmune diseases - diagnosis - genetics - psychology |
1 |
|
autoimmune diseases - epidemiology |
1 |
|
autoimmune disorder |
1 |
|
autoimmunity |
1 |
|
autoradiography |
1 |
|
base composition |
1 |
|
basic helix-loop-helix leucine zipper transcription factors |
1 |
|
behavior |
1 |
|
behaviour genetics |
1 |
|
behavioural disorder |
1 |
|
behavioural genomics |
1 |
|
belgium |
1 |
|
benzodiazepines |
1 |
|
bias (epidemiology) |
1 |
|
binge drinking |
1 |
|
biochemical |
1 |
|
biological evolution |
1 |
|
biological marker |
1 |
|
biological marker and endophenotype |
1 |
|
biological pathways |
1 |
|
biometry |
1 |
|
biostatistics |
1 |
|
biostatistics - methods |
1 |
|
bipolar |
1 |
|
bipolar disorder - diagnosis |
1 |
|
bipolar disorder - diagnosis - epidemiology - genetics - psychology |
1 |
|
bipolar disorder - diagnosis - epidemiology - psychology |
1 |
|
bipolar disorder - diagnosis - etiology - psychology |
1 |
|
bipolar disorder - diagnosis - genetics - physiopathology - psychology |
1 |
|
bipolar disorder - diagnosis - prevention & control - psychology |
1 |
|
bipolar disorder - diagnosis - therapy |
1 |
|
bipolar disorder - drug therapy - prevention & control - psychology |
1 |
|
bipolar disorder - drug therapy - prevention & control - therapy |
1 |
|
bipolar disorder - enzymology - genetics |
1 |
|
bipolar disorder - epidemiology - physiopathology - psychology |
1 |
|
bipolar disorder - epidemiology - psychology |
1 |
|
bipolar disorder - ethnology - genetics |
1 |
|
bipolar disorder - etiology - genetics |
1 |
|
bipolar disorder - genetics - metabolism |
1 |
|
bipolar disorder - genetics - physiopathology |
1 |
|
bipolar disorder - genetics - psychology |
1 |
|
bipolar disorder - pathology |
1 |
|
bipolar disorder - psychology |
1 |
|
bipolar i disorder |
1 |
|
birth complications |
1 |
|
birth order |
1 |
|
birth rate |
1 |
|
birthweight |
1 |
|
blood pressure - genetics - physiology |
1 |
|
blue mountains eye study |
1 |
|
bmi |
1 |
|
body height |
1 |
|
brain - anatomy & histology |
1 |
|
brain - anatomy & histology - growth & development |
1 |
|
brain - blood supply - radiography |
1 |
|
brain - drug effects - physiopathology |
1 |
|
brain - metabolism |
1 |
|
brain - physiology |
1 |
|
brain anatomy |
1 |
|
brain damage, chronic - genetics - psychology |
1 |
|
brain diseases - ethnology |
1 |
|
brain expression |
1 |
|
brain infarction - genetics - physiopathology |
1 |
|
brain ischemia - genetics - physiopathology |
1 |
|
brain mapping |
1 |
|
brain morphology |
1 |
|
brain networks |
1 |
|
bronchopneumonia - complications - epidemiology - psychology |
1 |
|
cacna1a |
1 |
|
calcium channels - genetics |
1 |
|
calpain - genetics |
1 |
|
candidate locus |
1 |
|
cannabinoids - metabolism |
1 |
|
canonical correlation analysis |
1 |
|
cardiometabolic |
1 |
|
caregivers - education - psychology |
1 |
|
caregivers - psychology |
1 |
|
carer |
1 |
|
carers |
1 |
|
caribbean region - ethnology |
1 |
|
carrier proteins - biosynthesis - genetics |
1 |
|
carrier proteins - genetics - physiology |
1 |
|
case-control association analysis |
1 |
|
case-control design |
1 |
|
case-control study |
1 |
|
catchment area (health) |
1 |
|
catechol o-methyltransferase - genetics |
1 |
|
catechol o-methyltransferase - genetics - metabolism |
1 |
|
catecholamine |
1 |
|
cell line, tumor |
1 |
|
central nervous system stimulants - poisoning |
1 |
|
central nervous system stimulants - toxicity |
1 |
|
cerebellum |
1 |
|
cerebral cortex |
1 |
|
cerebral cortex - pathology |
1 |
|
cerebral cortex - physiopathology |
1 |
|
cerebral ventricles - anatomy & histology |
1 |
|
cerebral ventricles - pathology |
1 |
|
characterization |
1 |
|
chickenpox - complications - epidemiology - psychology |
1 |
|
child and adolescent mental health |
1 |
|
child development |
1 |
|
child of impaired parents - psychology |
1 |
|
childhood experience |
1 |
|
childhood schizotypy |
1 |
|
childhood trauma |
1 |
|
cholesterol - blood |
1 |
|
chrfam7a |
1 |
|
chrna7 |
1 |
|
chromatography, high pressure liquid |
1 |
|
chromosome 15 |
1 |
|
chromosome 22 |
1 |
|
chromosome 6p |
1 |
|
chromosome deletion |
1 |
|
chromosome mapping - methods - statistics & numerical data |
1 |
|
chromosome x |
1 |
|
chromosomes, artificial, bacterial - genetics |
1 |
|
chromosomes, human - genetics |
1 |
|
chromosomes, human, pair 1 - genetics |
1 |
|
chromosomes, human, pair 12 - genetics |
1 |
|
chromosomes, human, pair 13 |
1 |
|
chromosomes, human, pair 13 - genetics |
1 |
|
chromosomes, human, pair 17 |
1 |
|
chromosomes, human, pair 22 - chemistry - genetics |
1 |
|
chromosomes, human, pair 4 - genetics |
1 |
|
chromosomes, human, pair 6 |
1 |
|
chronic and negative symptoms |
1 |
|
chronic disease |
1 |
|
cigarette consumption |
1 |
|
clinical characteristics |
1 |
|
clockdelta19 mouse |
1 |
|
cloning, molecular |
1 |
|
clozapine |
1 |
|
clozapine - metabolism - pharmacology - therapeutic use |
1 |
|
clozapine - pharmacology |
1 |
|
clozapine - pharmacology - therapeutic use |
1 |
|
clozapine response |
1 |
|
cognition disorders - diagnosis - epidemiology |
1 |
|
cognition disorders - genetics |
1 |
|
cognition disorders - psychology |
1 |
|
cognitive deficits |
1 |
|
cognitive function |
1 |
|
cognitive therapy |
1 |
|
cognitive therapy - methods |
1 |
|
cohort effect |
1 |
|
cohort study |
1 |
|
collagen type xi - genetics - metabolism |
1 |
|
collagen type xviii - genetics - metabolism |
1 |
|
combined analysis |
1 |
|
combined modality therapy |
1 |
|
commingling |
1 |
|
common variant |
1 |
|
communicable diseases - complications - epidemiology - psychology |
1 |
|
compensatory |
1 |
|
competing risks |
1 |
|
complex |
1 |
|
complex disease genetics |
1 |
|
complex phenotypes |
1 |
|
comt |
1 |
|
comt gene |
1 |
|
comt-schizophrenia |
1 |
|
concordant |
1 |
|
conditional heritability |
1 |
|
confounding |
1 |
|
consanguinity |
1 |
|
consistency |
1 |
|
contingency table analysis |
1 |
|
contingent negative variation - genetics |
1 |
|
coping |
1 |
|
cornea - pathology |
1 |
|
cornell medical index |
1 |
|
coronary disease - genetics |
1 |
|
coronary heart disease |
1 |
|
cortical interneurons |
1 |
|
cost-effective design |
1 |
|
covariates |
1 |
|
cross-cultural comparison |
1 |
|
cyp2d6 |
1 |
|
cytochrome p-450 cyp1a2 |
1 |
|
cytochrome p-450 cyp2d6 |
1 |
|
cytochrome p-450 cyp2d6 - genetics - metabolism |
1 |
|
cytochrome p-450 enzyme system - genetics |
1 |
|
cytokine |
1 |
|
d-amino-acid oxidase - genetics - metabolism |
1 |
|
dar locus |
1 |
|
darier disease - genetics |
1 |
|
dat |
1 |
|
dat1 |
1 |
|
data collection - methods - standards |
1 |
|
database |
1 |
|
decision making - physiology |
1 |
|
defries-fulker analysis |
1 |
|
delirium, dementia, amnestic, cognitive disorders - classification - diagnosis - genetics - psychology |
1 |
|
delirium, dementia, amnestic, cognitive disorders - diagnosis - epidemiology - genetics |
1 |
|
delirium, dementia, amnestic, cognitive disorders - diagnosis - epidemiology - psychology |
1 |
|
delirium, dementia, amnestic, cognitive disorders - diagnosis - etiology - psychology |
1 |
|
delirium, dementia, amnestic, cognitive disorders - diagnosis - genetics - psychology |
1 |
|
delirium, dementia, amnestic, cognitive disorders - epidemiology - etiology |
1 |
|
delirium, dementia, amnestic, cognitive disorders - epidemiology - etiology - psychology |
1 |
|
delirium, dementia, amnestic, cognitive disorders - etiology |
1 |
|
delirium, dementia, amnestic, cognitive disorders - etiology - psychology |
1 |
|
delirium, dementia, amnestic, cognitive disorders - genetics - psychology |
1 |
|
delusions - classification - diagnosis - psychology |
1 |
|
delusions - diagnosis - epidemiology - etiology |
1 |
|
delusions - etiology |
1 |
|
delusions - genetics |
1 |
|
dementia - epidemiology - genetics |
1 |
|
dementia - psychology |
1 |
|
dementia concerns |
1 |
|
denmark - epidemiology |
1 |
|
depression - diagnosis |
1 |
|
depression - diagnosis - epidemiology |
1 |
|
depression - diagnosis - genetics |
1 |
|
depression - epidemiology - psychology |
1 |
|
depression - etiology |
1 |
|
depression - etiology - genetics |
1 |
|
depression - genetics - metabolism |
1 |
|
depression/genetics |
1 |
|
depressive disorder - diagnosis - epidemiology - genetics |
1 |
|
depressive disorder - diagnosis - epidemiology - psychology |
1 |
|
depressive disorder - diagnosis - genetics |
1 |
|
depressive disorder - diagnosis - genetics - therapy |
1 |
|
depressive disorder - diagnosis - psychology |
1 |
|
depressive disorder - epidemiology - genetics |
1 |
|
depressive disorder - epidemiology - psychology |
1 |
|
depressive disorder - genetics - psychology |
1 |
|
depressive disorder - physiopathology - prevention & control - psychology |
1 |
|
depressive disorder, major - diagnosis - epidemiology - etiology |
1 |
|
depressive disorder, major - psychology |
1 |
|
developmental and epileptic encephalopathy |
1 |
|
developmental disabilities - epidemiology |
1 |
|
developmental disabilities - epidemiology - physiopathology |
1 |
|
df analysis |
1 |
|
dfna22 |
1 |
|
diabetes mellitus, type 1 - epidemiology |
1 |
|
diagnosis |
1 |
|
diagnostic categories |
1 |
|
dickkopf |
1 |
|
dimension |
1 |
|
dimensions |
1 |
|
discordant |
1 |
|
discrimination (psychology) |
1 |
|
disease |
1 |
|
disease locus mapping |
1 |
|
disease notification - statistics & numerical data |
1 |
|
disease pedigree |
1 |
|
disease susceptibility - psychology |
1 |
|
diseases in twins - diagnosis - genetics |
1 |
|
diseases in twins - diagnosis - genetics - physiopathology - psychology |
1 |
|
diseases in twins - genetics - psychology |
1 |
|
disorders of sex development - genetics |
1 |
|
distortion |
1 |
|
dkk |
1 |
|
dna |
1 |
|
dna - analysis - genetics |
1 |
|
dna - analysis - genetics - metabolism |
1 |
|
dna - blood |
1 |
|
dna - chemistry - genetics |
1 |
|
dna glycosylases |
1 |
|
dna methylation |
1 |
|
dna pool |
1 |
|
dna transposable elements |
1 |
|
dna transposable elements - genetics |
1 |
|
dna, satellite - analysis |
1 |
|
dna-binding proteins |
1 |
|
dna-binding proteins - genetics |
1 |
|
dominance, cerebral - genetics - physiology |
1 |
|
dopamine - genetics |
1 |
|
dopamine - metabolism |
1 |
|
dopamine plasma membrane transport proteins |
1 |
|
dopamine receptors |
1 |
|
dopamine system |
1 |
|
dopamine transporter gene |
1 |
|
double-blind method |
1 |
|
drd2 |
1 |
|
drd3 |
1 |
|
drd4 receptor gene, association study, childhood behavior |
1 |
|
drd5 |
1 |
|
drug abuse |
1 |
|
drug resistance - genetics |
1 |
|
dsm-5 disorders |
1 |
|
dynamic states |
1 |
|
dysbindin |
1 |
|
dysthymic disorder - diagnosis - genetics |
1 |
|
dystrobrevin |
1 |
|
echo-planar imaging - methods |
1 |
|
economic risk |
1 |
|
educational status |
1 |
|
effect size transformation |
1 |
|
effective heritability |
1 |
|
elastic net |
1 |
|
electrocardiography |
1 |
|
electroconvulsive therapy |
1 |
|
electroencephalography - methods |
1 |
|
electrooculography |
1 |
|
electrophoresis, agar gel |
1 |
|
electrophoresis, capillary - methods |
1 |
|
em algorithm |
1 |
|
endothelium |
1 |
|
england |
1 |
|
enzyme activation |
1 |
|
epidemiologic factors |
1 |
|
epileptic encephalopathy |
1 |
|
epistasis, genetic |
1 |
|
epistatic gene-gene interaction |
1 |
|
eqtl |
1 |
|
erps |
1 |
|
ethnic difference |
1 |
|
european continental ancestry group |
1 |
|
european continental ancestry group - genetics - psychology |
1 |
|
european continental ancestry group - psychology |
1 |
|
european continental ancestry group - psychology - statistics & numerical data |
1 |
|
event related potentials |
1 |
|
event-related potentials, p300 - drug effects - physiology |
1 |
|
event-related potentials, p300 - genetics - physiology |
1 |
|
evoked potentials - drug effects - physiology |
1 |
|
evoked potentials - genetics |
1 |
|
evoked potentials - physiology |
1 |
|
evoked potentials, auditory - genetics |
1 |
|
evoked potentials, auditory - genetics - physiology |
1 |
|
expansion |
1 |
|
experimental economics |
1 |
|
eye movements - genetics |
1 |
|
eye movements - physiology |
1 |
|
factor |
1 |
|
factor score |
1 |
|
false negative reactions |
1 |
|
false positive reactions |
1 |
|
familial loading |
1 |
|
familiality |
1 |
|
family - psychology |
1 |
|
family environment |
1 |
|
family history score |
1 |
|
family studies |
1 |
|
family trios |
1 |
|
famine |
1 |
|
father-child relations |
1 |
|
fathers |
1 |
|
fatigue |
1 |
|
fatigue - epidemiology - psychology |
1 |
|
fatigue syndrome, chronic - diagnosis - epidemiology - psychology |
1 |
|
femur neck - physiopathology |
1 |
|
first episode psychosis |
1 |
|
fluorescence |
1 |
|
fluorometry |
1 |
|
focal epilepsy |
1 |
|
forecast |
1 |
|
forecasting |
1 |
|
founder effect |
1 |
|
frontal lobe - anatomy & histology |
1 |
|
frontal lobe - physiopathology |
1 |
|
fronto-occipital |
1 |
|
functional laterality |
1 |
|
functional mri |
1 |
|
functional psychosis |
1 |
|
gender difference |
1 |
|
gender differences |
1 |
|
gene counting |
1 |
|
gene dosage |
1 |
|
gene enrichment |
1 |
|
gene expression - genetics |
1 |
|
gene expression profiling |
1 |
|
gene pool |
1 |
|
gene targeting - methods |
1 |
|
gene-counting |
1 |
|
gene-environment correlation |
1 |
|
general pedigrees |
1 |
|
genes, dominant - genetics |
1 |
|
genes, overlapping - genetics |
1 |
|
genes, recessive |
1 |
|
genetic association analyses |
1 |
|
genetic composite scores |
1 |
|
genetic correlation matrix |
1 |
|
genetic counseling |
1 |
|
genetic diseases, inborn |
1 |
|
genetic disposition |
1 |
|
genetic generalized epilepsy |
1 |
|
genetic liability |
1 |
|
genetic models |
1 |
|
genetic nurture |
1 |
|
genetic overlap |
1 |
|
genetic predisposition to disease - genetics - psychology |
1 |
|
genetic predisposition to disease. |
1 |
|
genetic risk prediction |
1 |
|
genetic testing - economics - methods |
1 |
|
genetic testing - statistics and numerical data |
1 |
|
genetic variation - drug effects |
1 |
|
genetic vulnerability |
1 |
|
genetics, behavioral |
1 |
|
genetics, behavioral - methods |
1 |
|
genetics, population - statistics & numerical data |
1 |
|
genome wide association studies |
1 |
|
genome-wide association study - methods |
1 |
|
genomic control |
1 |
|
genomic imprinting |
1 |
|
genotype-environment correlation |
1 |
|
genotype-environment interaction |
1 |
|
genotyping |
1 |
|
gerontology |
1 |
|
gibbs sampler |
1 |
|
gilles de la tourette syndrome |
1 |
|
glaucoma - genetics |
1 |
|
glaucoma, open-angle - genetics |
1 |
|
glycoproteins - genetics |
1 |
|
glycosidase |
1 |
|
goals |
1 |
|
gray matter |
1 |
|
gweis |
1 |
|
hallucinations - classification - diagnosis - psychology |
1 |
|
hallucinations - diagnosis - epidemiology - etiology |
1 |
|
hallucinations - genetics |
1 |
|
han chinese, linkage disequilibrium |
1 |
|
haplotype analysis |
1 |
|
haplotype association |
1 |
|
haplotype clustering |
1 |
|
haseman-elston |
1 |
|
hazard ratio |
1 |
|
health care surveys |
1 |
|
health knowledge, attitudes, practice |
1 |
|
health services for the aged - standards |
1 |
|
health status indicators |
1 |
|
hearing loss |
1 |
|
helix-loop-helix motifs |
1 |
|
heroin - administration & dosage |
1 |
|
heroin dependence - genetics |
1 |
|
heterozygote detection |
1 |
|
hierarchical model |
1 |
|
high-throughput screening assays - methods |
1 |
|
hippocampus - abnormalities - physiopathology |
1 |
|
hippocampus - pathology |
1 |
|
histiocytosis, non-langerhans-cell - genetics |
1 |
|
history, 20th century |
1 |
|
hla |
1 |
|
hla antigens |
1 |
|
hla antigens - genetics |
1 |
|
hla-b antigens - genetics |
1 |
|
hla-dq alpha-chains |
1 |
|
hla-dq antigens - genetics |
1 |
|
hla-dq beta-chains |
1 |
|
hla-dr antigens - genetics |
1 |
|
hla-drb1 chains |
1 |
|
hospitalization - statistics & numerical data |
1 |
|
hospitals, psychiatric |
1 |
|
hsc70 heat-shock proteins |
1 |
|
hsp70 heat-shock proteins - genetics - metabolism |
1 |
|
human accelerated region |
1 |
|
human chromosome 22 |
1 |
|
human genetics -- statistical methods. |
1 |
|
human leucocyte antigen (hla) |
1 |
|
huntington disease - diagnosis - epidemiology - genetics - psychology |
1 |
|
huntington's disease |
1 |
|
hydroxylation |
1 |
|
hyperprolineamia |
1 |
|
idiopathic generalised epilepsy (ige) |
1 |
|
illness-specific |
1 |
|
image interpretation, computer-assisted |
1 |
|
image processing, computer-assisted - methods |
1 |
|
immunization programs |
1 |
|
immunogenetics |
1 |
|
imputation |
1 |
|
india |
1 |
|
individualised treatment effect |
1 |
|
infant |
1 |
|
inflamattion |
1 |
|
influenza, human - complications |
1 |
|
influenza, human - complications - diagnosis - epidemiology |
1 |
|
influenza, human - epidemiology - mortality |
1 |
|
influenze |
1 |
|
injections |
1 |
|
inpatient |
1 |
|
inpatients |
1 |
|
insulin dependent diabetes mellitus (iddm) |
1 |
|
integrated |
1 |
|
intellectual disability - etiology |
1 |
|
intellectual disability - genetics |
1 |
|
intelligence - genetics |
1 |
|
intelligence tests |
1 |
|
interaction contrast ratio |
1 |
|
interaction effects |
1 |
|
international classification of diseases |
1 |
|
intraocular pressure |
1 |
|
intraocular pressure - genetics |
1 |
|
intronic |
1 |
|
iq |
1 |
|
ireland - epidemiology |
1 |
|
iv drug use |
1 |
|
jumping to conclusions |
1 |
|
key word |
1 |
|
knowledge |
1 |
|
labor, obstetric |
1 |
|
language |
1 |
|
lasso |
1 |
|
late onset alzheimer's disease |
1 |
|
late paraphrenia |
1 |
|
late-infancy |
1 |
|
latent variable score |
1 |
|
lateral class analysis |
1 |
|
lateral ventricles - pathology |
1 |
|
ld maps |
1 |
|
length of stay |
1 |
|
liability scale |
1 |
|
liability-threshold model |
1 |
|
life change events |
1 |
|
linkage study |
1 |
|
lithium |
1 |
|
local false discovery rate |
1 |
|
local heritability |
1 |
|
locus heterogeneity |
1 |
|
logic regression |
1 |
|
logit scale |
1 |
|
london - epidemiology |
1 |
|
low density lipoprotein receptor-related protein-5 - genetics |
1 |
|
low-frequency / rare variant |
1 |
|
lumbar vertebrae - physiopathology |
1 |
|
lymphocyte activation - immunology |
1 |
|
lymphocytes |
1 |
|
magnetic resonance imaging - statistics & numerical data |
1 |
|
major depression |
1 |
|
major histocompatibility complex - genetics |
1 |
|
mania |
1 |
|
mania-like behavior |
1 |
|
manic depression |
1 |
|
manic-depressive illness |
1 |
|
maoa gene |
1 |
|
maob gene |
1 |
|
marginal heritability |
1 |
|
marijuana abuse - epidemiology - psychology |
1 |
|
marital status |
1 |
|
markov chains |
1 |
|
matched-pair analysis |
1 |
|
maternal behavior - psychology |
1 |
|
maternal welfare |
1 |
|
maximum likelihood estimation |
1 |
|
mdr |
1 |
|
mean diffusivity |
1 |
|
measles - complications - epidemiology |
1 |
|
measles vaccine - administration & dosage - adverse effects |
1 |
|
measles-mumps-rubella vaccine - administration & dosage - adverse effects |
1 |
|
mediation |
1 |
|
medical records |
1 |
|
membrane glycoproteins |
1 |
|
membrane glycoproteins - biosynthesis - genetics |
1 |
|
membrane glycoproteins - genetics - physiology |
1 |
|
membrane proteins - genetics |
1 |
|
membrane transport proteins - genetics |
1 |
|
mental disorders - complications |
1 |
|
mental disorders - genetics |
1 |
|
mental disorders - psychology |
1 |
|
mental health services - standards |
1 |
|
mental retardation |
1 |
|
metaanalysis |
1 |
|
methamphetamine |
1 |
|
methamphetamine - poisoning |
1 |
|
methamphetamine - toxicity |
1 |
|
methionine |
1 |
|
methyltransferases - genetics |
1 |
|
mice, inbred balb c |
1 |
|
micro-arrays |
1 |
|
microcirculation - physiopathology |
1 |
|
microfilament proteins - genetics - metabolism |
1 |
|
microsatellites |
1 |
|
mid-pregnancy |
1 |
|
mild mental impairment |
1 |
|
mismatch negativity |
1 |
|
missingness |
1 |
|
mitochondrial membrane transport proteins - genetics |
1 |
|
mixed function oxygenases - genetics |
1 |
|
mixed-radix number |
1 |
|
mixture |
1 |
|
mmn |
1 |
|
model-free |
1 |
|
model-free association analysis |
1 |
|
models, molecular |
1 |
|
models, neurological |
1 |
|
models, psychological |
1 |
|
models, theoretical |
1 |
|
mog |
1 |
|
molecular diagnosis |
1 |
|
molecular genetics |
1 |
|
molecular signatures |
1 |
|
monoamine oxidase |
1 |
|
monoamine oxidase a |
1 |
|
mood disorders - complications - genetics - psychology |
1 |
|
mood disorders - epidemiology - genetics - metabolism |
1 |
|
morbidity |
1 |
|
morphometry |
1 |
|
mother-child relations |
1 |
|
mothers - psychology |
1 |
|
motor neuron disease |
1 |
|
motor neuron disease - genetics |
1 |
|
mpic |
1 |
|
multifactorial |
1 |
|
multiplex families |
1 |
|
multipoint ibd-sharing |
1 |
|
multivariate genetic analysis |
1 |
|
myelin proteins |
1 |
|
myelin-associated glycoprotein - genetics |
1 |
|
myo6 |
1 |
|
myopia - genetics |
1 |
|
myopia - genetics - pathology |
1 |
|
n-glycosyl hydrolases - metabolism |
1 |
|
nek4 |
1 |
|
nerve tissue proteins - genetics - metabolism |
1 |
|
netherlands |
1 |
|
neural networks (computer) |
1 |
|
neurocognition |
1 |
|
neuroeconomics |
1 |
|
neuroleptics |
1 |
|
neurological soft signs |
1 |
|
neurophysiology |
1 |
|
neuropsychiatric disorders |
1 |
|
neuroscience |
1 |
|
neurosis |
1 |
|
neurotic disorders - diagnosis |
1 |
|
neurotic disorders - diagnosis - epidemiology |
1 |
|
neurotic disorders - diagnosis - genetics |
1 |
|
neurotic disorders - diagnosis - psychology |
1 |
|
neurotic disorders - psychology |
1 |
|
neurotransmitter receptors |
1 |
|
nitrates - blood |
1 |
|
nitric oxide |
1 |
|
nitric oxide synthase |
1 |
|
nitric oxide synthase - genetics |
1 |
|
nitric oxide synthase type iii |
1 |
|
nitrites - blood |
1 |
|
noradrenaline |
1 |
|
norepinephrine |
1 |
|
norepinephrine plasma membrane transport proteins |
1 |
|
nucleus accumbens |
1 |
|
number |
1 |
|
number theory |
1 |
|
object attachment |
1 |
|
obstetric complication |
1 |
|
obstetric labor complications - diagnosis |
1 |
|
obstetric labor complications - diagnosis - etiology - psychology |
1 |
|
obstetric labor complications - epidemiology - psychology |
1 |
|
occupations |
1 |
|
ocd |
1 |
|
ohio |
1 |
|
olanzapine |
1 |
|
oligonucleotide array sequence analysis |
1 |
|
oligonucleotide array sequence analysis - methods |
1 |
|
online tool |
1 |
|
open-angle glaucoma |
1 |
|
opiates |
1 |
|
opioids |
1 |
|
optic disk - pathology |
1 |
|
optic nerve diseases - genetics |
1 |
|
orthomyxoviridae - genetics |
1 |
|
orthomyxoviridae infections - pathology |
1 |
|
osteoporosis - genetics |
1 |
|
outcome assessment (health care) |
1 |
|
oxidoreductases - genetics |
1 |
|
p50 |
1 |
|
p50 erps |
1 |
|
pakistan |
1 |
|
pandas |
1 |
|
panic disorder |
1 |
|
panic disorder - diagnosis - genetics |
1 |
|
parallel ica |
1 |
|
paranoid disorders - diagnosis - epidemiology - etiology |
1 |
|
parent-child relations |
1 |
|
parental genetic effect |
1 |
|
parenting - psychology |
1 |
|
parents |
1 |
|
patient admission |
1 |
|
patient admission - statistics & numerical data |
1 |
|
patient admission - statistics & numerical data - trends |
1 |
|
patient compliance |
1 |
|
patient education as topic |
1 |
|
patient readmission |
1 |
|
pc12 cells |
1 |
|
penetrance |
1 |
|
periodicals as topic - statistics & numerical data |
1 |
|
permutation test |
1 |
|
permutation tests |
1 |
|
personality disorders - classification - diagnosis - genetics - psychology |
1 |
|
personality disorders - diagnosis - epidemiology |
1 |
|
pharmacogenetics |
1 |
|
pharmacokinetics |
1 |
|
phenocopies |
1 |
|
phobic disorders - diagnosis - genetics |
1 |
|
phospholipases a - genetics |
1 |
|
phospholipases a2 |
1 |
|
phosphoproteins - genetics |
1 |
|
photic stimulation |
1 |
|
physical health |
1 |
|
pilot projects |
1 |
|
pirenzepine - analogs & derivatives - pharmacokinetics - therapeutic use |
1 |
|
pirenzepine - analogs & derivatives - therapeutic use |
1 |
|
pla2 |
1 |
|
plasma |
1 |
|
pleasure |
1 |
|
pleiotropic gene |
1 |
|
point mutation |
1 |
|
poisson distribution |
1 |
|
polygenic model |
1 |
|
polymorphism information content |
1 |
|
polymorphism, genetic - drug effects |
1 |
|
polymorphisms |
1 |
|
pooling |
1 |
|
positive symptoms |
1 |
|
prader-willi syndrome - genetics |
1 |
|
prediction |
1 |
|
pregnancy complications - epidemiology |
1 |
|
pregnancy complications - epidemiology - psychology |
1 |
|
premorbid |
1 |
|
prenatal |
1 |
|
prenatal care |
1 |
|
prenatal fetal development |
1 |
|
primary health care |
1 |
|
principal component analysis |
1 |
|
prisons |
1 |
|
prkca |
1 |
|
probability |
1 |
|
procollagen-lysine, 2-oxoglutarate 5-dioxygenase - genetics - metabolism |
1 |
|
prodrome |
1 |
|
prognostic modelling |
1 |
|
proline oxidase - genetics |
1 |
|
promoter regions, genetic - physiology |
1 |
|
prospect theory |
1 |
|
protein kinase c-alpha - genetics |
1 |
|
psychiatric |
1 |
|
psychiatric department, hospital |
1 |
|
psychiatry |
1 |
|
psychiatry - statistics & numerical data |
1 |
|
psychological tests |
1 |
|
psychometrics |
1 |
|
psychomotor disorders - epidemiology - physiopathology |
1 |
|
psychoses, substance-induced - diagnosis - epidemiology - psychology |
1 |
|
psychotic depression |
1 |
|
psychotic disorders - classification - diagnosis - epidemiology - psychology |
1 |
|
psychotic disorders - classification - diagnosis - genetics - psychology |
1 |
|
psychotic disorders - diagnosis |
1 |
|
psychotic disorders - diagnosis - epidemiology - psychology |
1 |
|
psychotic disorders - diagnosis - ethnology - genetics |
1 |
|
psychotic disorders - diagnosis - genetics - physiopathology |
1 |
|
psychotic disorders - diagnosis - psychology - therapy |
1 |
|
psychotic disorders - enzymology - genetics |
1 |
|
psychotic disorders - epidemiology - etiology |
1 |
|
psychotic disorders - epidemiology - genetics - psychology |
1 |
|
psychotic disorders - ethnology - psychology |
1 |
|
psychotic disorders - etiology |
1 |
|
psychotic disorders - etiology - genetics |
1 |
|
psychotic disorders - etiology - psychology |
1 |
|
psychotic disorders - genetics - physiopathology |
1 |
|
psychotic disorders - psychology |
1 |
|
psychotic-like experiences |
1 |
|
psychotropic drugs - therapeutic use |
1 |
|
publishing - statistics & numerical data |
1 |
|
pyramidal cell disarray |
1 |
|
pyramidal cells - pathology |
1 |
|
qmflink |
1 |
|
qtl linkage |
1 |
|
qtls |
1 |
|
quality of life |
1 |
|
quantitative trait loci (qtls) |
1 |
|
quantitative trait locus (qtl) |
1 |
|
quantitative-tdt (q-tdt) |
1 |
|
r package |
1 |
|
radix sort |
1 |
|
random allocation |
1 |
|
rats |
1 |
|
reaction time - genetics - physiology |
1 |
|
reading |
1 |
|
receptor, angiotensin, type 1 - genetics |
1 |
|
receptor, serotonin, 5-ht1d - genetics |
1 |
|
receptor, serotonin, 5-ht2a - genetics |
1 |
|
receptor, serotonin, 5-ht2c |
1 |
|
receptors, androgen - genetics |
1 |
|
receptors, cannabinoid |
1 |
|
receptors, dopamine d1 - genetics |
1 |
|
receptors, dopamine d3 |
1 |
|
receptors, dopamine d4 - genetics |
1 |
|
receptors, dopamine d5 |
1 |
|
receptors, dopamine d5 - genetics |
1 |
|
receptors, drug - genetics |
1 |
|
receptors, interleukin-2 - blood |
1 |
|
receptors, n-methyl-d-aspartate - genetics |
1 |
|
receptors, nicotinic - genetics |
1 |
|
receptors, serotonin - drug effects - genetics |
1 |
|
recombination, genetic |
1 |
|
recombination, genetic - genetics |
1 |
|
recurrence - prevention & control |
1 |
|
recursive algorithm |
1 |
|
registries - statistics & numerical data |
1 |
|
regulator of g protein signalling |
1 |
|
relative risk |
1 |
|
religion and psychology |
1 |
|
repeat expansion detection |
1 |
|
repeated measures |
1 |
|
replications |
1 |
|
research |
1 |
|
research design |
1 |
|
resting-state functional connectivity |
1 |
|
reward |
1 |
|
reward system |
1 |
|
rgs proteins - genetics |
1 |
|
rheumatoid arthritis |
1 |
|
rich-club organization |
1 |
|
right censoring |
1 |
|
riluzole |
1 |
|
risk assessment - methods |
1 |
|
risk attitude |
1 |
|
risk indicators |
1 |
|
risk predictio |
1 |
|
rna - genetics - metabolism |
1 |
|
rna editing |
1 |
|
saccharomyces cerevisiae proteins |
1 |
|
sample size |
1 |
|
schizoid personality disorder - diagnosis - epidemiology - psychology |
1 |
|
schizophrenia - chemically induced - diagnosis - epidemiology |
1 |
|
schizophrenia - classification - diagnosis |
1 |
|
schizophrenia - classification - diagnosis - genetics |
1 |
|
schizophrenia - classification - epidemiology |
1 |
|
schizophrenia - complications - genetics |
1 |
|
schizophrenia - diagnosis |
1 |
|
schizophrenia - diagnosis - drug therapy |
1 |
|
schizophrenia - diagnosis - epidemiology - etiology |
1 |
|
schizophrenia - diagnosis - ethnology |
1 |
|
schizophrenia - diagnosis - ethnology - etiology |
1 |
|
schizophrenia - diagnosis - ethnology - genetics |
1 |
|
schizophrenia - diagnosis - etiology - genetics |
1 |
|
schizophrenia - diagnosis - immunology |
1 |
|
schizophrenia - drug therapy - enzymology |
1 |
|
schizophrenia - drug therapy - ethnology - genetics |
1 |
|
schizophrenia - enzymology - genetics |
1 |
|
schizophrenia - epidemiology - genetics - history |
1 |
|
schizophrenia - epidemiology - genetics - pathology |
1 |
|
schizophrenia - epidemiology - genetics - physiopathology |
1 |
|
schizophrenia - genetics - metabolism |
1 |
|
schizophrenia - immunology |
1 |
|
schizophrenia, disorganized - classification - diagnosis - psychology |
1 |
|
schizophrenia, paranoid - classification - diagnosis - genetics - psychology |
1 |
|
schizophrenia-spectrum disorder |
1 |
|
schizophrenic language |
1 |
|
schizotypal personality disorder - diagnosis - genetics - psychology |
1 |
|
schizotypal personality disorder - genetics |
1 |
|
schizotypal personality disorder - genetics - psychology |
1 |
|
schizotypy |
1 |
|
school-based survey |
1 |
|
scotland |
1 |
|
scotland - epidemiology |
1 |
|
season of birth |
1 |
|
seasonal affective disorder - genetics |
1 |
|
secondary palmar crease |
1 |
|
segregation |
1 |
|
seizures |
1 |
|
selection bias |
1 |
|
self concept |
1 |
|
self-help groups - standards |
1 |
|
sem |
1 |
|
sensitivity |
1 |
|
sequence alignment |
1 |
|
sequence alignment - methods |
1 |
|
sequence homology, amino acid |
1 |
|
sequencing |
1 |
|
serotonergic transmission |
1 |
|
serotonin - genetics - metabolism |
1 |
|
serotonin antagonists - therapeutic use |
1 |
|
serotonin plasma membrane transport proteins - genetics |
1 |
|
serotonin receptors |
1 |
|
serotonin reuptake transporter |
1 |
|
serotonin transporter |
1 |
|
serotonin transporter gene |
1 |
|
serotonin uptake inhibitors - pharmacokinetics - therapeutic use |
1 |
|
set association method |
1 |
|
sex |
1 |
|
sex characteristics |
1 |
|
sex difference |
1 |
|
sex ratio |
1 |
|
shank genes |
1 |
|
shank3 |
1 |
|
sib pair analysis |
1 |
|
sib-pair analysis |
1 |
|
sib-pair design |
1 |
|
sib-pair method, heterogeneity |
1 |
|
sibling pairs |
1 |
|
sibling relations |
1 |
|
siblings - psychology |
1 |
|
sibship size |
1 |
|
signal processing, computer-assisted |
1 |
|
signal transduction - genetics |
1 |
|
similarities |
1 |
|
single strand conformation polymorphism |
1 |
|
single-nucleotide polymorphism (snp) |
1 |
|
skudriver |
1 |
|
skumix |
1 |
|
slc6a4 |
1 |
|
small-vessel disease |
1 |
|
smoking |
1 |
|
smoking cessation |
1 |
|
snap-25 |
1 |
|
snapit technology |
1 |
|
social class |
1 |
|
soluble interleukin 2 receptor |
1 |
|
spain - epidemiology |
1 |
|
spectrin - genetics |
1 |
|
spectrophotometry |
1 |
|
ssri |
1 |
|
stable schizophrenia |
1 |
|
statistical mapping |
1 |
|
statistical method |
1 |
|
statistical methodology |
1 |
|
statistics as topic - methods |
1 |
|
stress, physiological - physiopathology |
1 |
|
stress, psychological - epidemiology - genetics |
1 |
|
striatum |
1 |
|
stroke |
1 |
|
stroke - epidemiology - genetics |
1 |
|
structural asymmetry |
1 |
|
structural equation modeling |
1 |
|
structural variants |
1 |
|
structure-function coupling |
1 |
|
structured association |
1 |
|
students - psychology |
1 |
|
substance abuse |
1 |
|
substance induced |
1 |
|
subtypes |
1 |
|
suicidal behaviour |
1 |
|
suicide - prevention & control - psychology |
1 |
|
suicide, attempted - prevention & control - psychology |
1 |
|
summary statistics |
1 |
|
superoxide dismutase - genetics |
1 |
|
survival analysis |
1 |
|
sustained attention |
1 |
|
sweden - epidemiology |
1 |
|
symporters - genetics |
1 |
|
symptom |
1 |
|
synaptosomal-associated protein 25 |
1 |
|
synergistic effects |
1 |
|
t-lymphocytes - immunology |
1 |
|
tagging |
1 |
|
tandem repeat |
1 |
|
tandem repeat sequences |
1 |
|
tcf transcription factors |
1 |
|
teaching |
1 |
|
telephone interview |
1 |
|
telephone interviews |
1 |
|
temperament |
1 |
|
temporal lobe - anatomy & histology |
1 |
|
temporal lobe - physiopathology |
1 |
|
terminology as topic |
1 |
|
thalamocortical functional connectivity |
1 |
|
thinking |
1 |
|
third generation sequencing |
1 |
|
third ventricle - pathology |
1 |
|
thyrotoxicosis - epidemiology |
1 |
|
tics |
1 |
|
time series |
1 |
|
tonometry, ocular |
1 |
|
tourette syndrome - genetics - pathology |
1 |
|
trans-activators - genetics |
1 |
|
transcription factor 7-like 2 protein |
1 |
|
transcription factors |
1 |
|
transcriptional activation - genetics |
1 |
|
transcriptome |
1 |
|
transdiagnostic |
1 |
|
transdiagnostic signature |
1 |
|
transmission |
1 |
|
transmission disequilibrium |
1 |
|
transmission disequilibrium test |
1 |
|
transmit |
1 |
|
trauma |
1 |
|
treatment failure |
1 |
|
treatment-refractory |
1 |
|
trend analysis |
1 |
|
trinary numbers |
1 |
|
trinucleotide repeat expansion - genetics |
1 |
|
triplet repeat |
1 |
|
twas |
1 |
|
twin modelling |
1 |
|
twin studies as topic - methods |
1 |
|
twin zygosity |
1 |
|
twins - psychology |
1 |
|
twins, dizygotic - genetics - physiology |
1 |
|
twins, dizygotic - genetics - psychology |
1 |
|
twins, monozygotic - genetics - physiology |
1 |
|
twins, monozygotic - genetics - psychology |
1 |
|
two-dimensional gel electrophoresis (2-dge) |
1 |
|
two-hybrid system techniques |
1 |
|
typical antipsychotics |
1 |
|
tyrosine 3-monooxygenase - deficiency - genetics - physiology |
1 |
|
tyrosine 3-monooxygenase - genetics |
1 |
|
underachievement |
1 |
|
universities |
1 |
|
urban birth |
1 |
|
urban health |
1 |
|
urban population |
1 |
|
user-computer interface |
1 |
|
valine |
1 |
|
valproate |
1 |
|
variance components analysis |
1 |
|
variation (genetics) |
1 |
|
vcfs |
1 |
|
virginia |
1 |
|
virus diseases - complications - congenital |
1 |
|
voltage-gated calcium channel |
1 |
|
wales |
1 |
|
west indies - ethnology |
1 |
|
white line |
1 |
|
white matter |
1 |
|
white matter tract |
1 |
|
winter and city birth |
1 |
|
wnt proteins - genetics - metabolism |
1 |
|
wnt signaling |
1 |
|
x chromosome |
1 |
|
x-chromosome |
1 |
|
y chromosome |
1 |
|
ybx1 |
1 |