asian continental ancestry group - genetics |
27 |
single nucleotide polymorphism |
24 |
genome-wide association study |
23 |
female |
21 |
genotype |
21 |
male |
21 |
genetic association |
19 |
genetic predisposition to disease |
19 |
controlled study |
17 |
copy number variation |
15 |
gene identification |
15 |
gene locus |
15 |
human |
15 |
major clinical study |
15 |
neuregulin-1 - genetics |
15 |
asian |
14 |
association |
14 |
polymorphism, single nucleotide |
14 |
bile duct atresia |
13 |
chinese |
13 |
chromosome 10q |
13 |
gene frequency |
13 |
gene function |
13 |
genetic susceptibility |
13 |
hirschsprung disease |
13 |
hirschsprung disease - genetics |
13 |
humans |
13 |
priority journal |
13 |
risk factor |
13 |
risk factors |
13 |
adult |
12 |
animal tissue |
12 |
anorectal malformation |
12 |
chromosome aberration |
12 |
ephrin-a2 - genetics |
12 |
gwa |
12 |
lupus erythematosus, systemic - genetics |
12 |
middle aged |
12 |
ret |
12 |
sle |
12 |
uhrf1bp1 |
12 |
wnt signaling pathway |
12 |
aged |
11 |
antigens, cd3 - genetics |
11 |
case-control studies |
11 |
cd247 |
11 |
cos cells |
11 |
epidemiology |
11 |
ethnic group |
11 |
gene expression |
11 |
gene mapping |
11 |
gene mutation |
11 |
genetic predisposition |
11 |
genetics |
11 |
gwas |
11 |
human tissue |
11 |
kw034 - copy number/structural variation |
11 |
lupus erythematosus, systemic - genetics - immunology |
11 |
mutation - genetics |
11 |
nucleotide sequence |
11 |
systemic lupus erythematosus |
11 |
whole exome sequencing |
11 |
polymorphism, single nucleotide - genetics |
10 |
rare complex disease |
10 |
young adult |
10 |
amino acid substitution |
9 |
asian-specific |
9 |
exome-chip association analysis |
9 |
expression quantitative trait loci |
9 |
natural selection |
9 |
pax4 |
9 |
type 2 diabetes |
9 |
adiponectin - blood - genetics |
8 |
blood pressure - genetics |
8 |
body mass index |
8 |
cell differentiation - physiology |
8 |
cyclin a2 |
8 |
degeneration |
8 |
development |
8 |
disc |
8 |
gene deletion |
8 |
gene duplication |
8 |
gene expression regulation |
8 |
hbv integration |
8 |
hedgehog proteins - genetics - metabolism |
8 |
hepatocellular carcinoma |
8 |
hirschsprung disease - genetics - physiopathology |
8 |
hypertension - blood - genetics |
8 |
intervertebral |
8 |
kw080 - genome-wide association |
8 |
lumbar |
8 |
mri |
8 |
neuroglia - cytology - physiology |
8 |
receptors, notch - genetics - metabolism |
8 |
splicing |
8 |
amino acid substitution - genetics |
7 |
animals |
7 |
c-reactive protein |
7 |
cardiovascular diseases |
7 |
col4a5 |
7 |
col4a6 |
7 |
complex traits and polygenic disorders |
7 |
de novo mutations |
7 |
ens |
7 |
gene |
7 |
gonosomal mosaicism |
7 |
hong kong |
7 |
isolated diffuse oesophageal leiomyomatosis |
7 |
kw040 - development |
7 |
kw065 - gastrointestinal system |
7 |
kw099 - malformation |
7 |
multivariate analysis |
7 |
mutations |
7 |
neural crest |
7 |
neuregulin 1 |
7 |
rare variants |
7 |
schizophrenia |
7 |
schizophrenia - genetics |
7 |
single-nucleotide polymorphism |
7 |
v266l |
7 |
5' untranslated region |
6 |
adolescent |
6 |
adrenomedullin |
6 |
age factors |
6 |
aged, 80 and over |
6 |
alanine |
6 |
anorectal malformations |
6 |
arhgap4 |
6 |
asian continental ancestry group |
6 |
biological markers |
6 |
biological markers - blood - metabolism |
6 |
blood pressure |
6 |
carcinoma, papillary - genetics - metabolism - pathology |
6 |
cell adhesion molecules - blood |
6 |
cell proliferation |
6 |
cell transformation, neoplastic - genetics - metabolism |
6 |
chemicals and cas registry numbers |
6 |
child |
6 |
choledochal cyst |
6 |
cross-sectional studies |
6 |
de novo |
6 |
dysglycemia |
6 |
electrophoretic mobility shift assay |
6 |
exome |
6 |
exon |
6 |
fibrinogen |
6 |
fibrinogen - genetics - metabolism |
6 |
gamma-glutamyltransferase - blood - metabolism |
6 |
gene cluster |
6 |
gene expression regulation, neoplastic |
6 |
germ-line mutation |
6 |
ggt |
6 |
gli3 |
6 |
goiter, nodular - genetics - metabolism - pathology |
6 |
han chinese |
6 |
haplotype |
6 |
haplotypes |
6 |
hong kong - epidemiology |
6 |
hong kong - epidemiology - ethnology |
6 |
hypertension |
6 |
hypertension - blood - enzymology - epidemiology |
6 |
hypertension - blood - epidemiology - genetics |
6 |
hypertension - blood - ethnology - genetics - physiopathology |
6 |
immunoblotting |
6 |
insulin resistance - genetics |
6 |
interleukin-6 |
6 |
interleukin-6 - blood - genetics |
6 |
lipocalin-2 |
6 |
liver function test |
6 |
luciferases - diagnostic use |
6 |
mecp2 |
6 |
medical sciences |
6 |
neoplasm staging |
6 |
nuclear proteins - genetics - metabolism |
6 |
pharmacy and pharmacology environmental studies |
6 |
polymorphism |
6 |
predictive value of tests |
6 |
prevalence |
6 |
questionnaires |
6 |
rare variants association |
6 |
rats |
6 |
receptors, cell surface - blood |
6 |
regression analysis |
6 |
renbp |
6 |
reverse transcriptase polymerase chain reaction |
6 |
sex factors |
6 |
shh |
6 |
signal transduction - genetics |
6 |
single nucleotide |
6 |
single nucleotide polymorphisms |
6 |
thyroid gland - cytology - metabolism |
6 |
thyroid neoplasms - genetics - metabolism - pathology |
6 |
toxicology and environmental safety |
6 |
transcription factors - genetics - metabolism |
6 |
transcription, genetic |
6 |
up-regulation |
6 |
valine |
6 |
γ-glutamyl transaminase |
6 |
age distribution |
5 |
blood glucose - metabolism |
5 |
carrier proteins - genetics |
5 |
cds |
5 |
cell adhesion molecules |
5 |
cell adhesion molecules - genetics |
5 |
cholesterol |
5 |
chromosomes, human, pair 9 |
5 |
cohort studies |
5 |
complex traits: theory and methods |
5 |
copy number variant |
5 |
cytoskeletal proteins - genetics |
5 |
diabetes mellitus |
5 |
diabetes mellitus - blood - drug therapy - epidemiology |
5 |
endocrinology |
5 |
epilepsy - genetics |
5 |
f11 receptor |
5 |
gastrointestinal system |
5 |
gene polymorphism |
5 |
genetic mapping |
5 |
genome sequencing |
5 |
genome-wide association |
5 |
genotype-phenotype correlation |
5 |
glycosylated hemoglobin a |
5 |
hemoglobin a, glycosylated - metabolism |
5 |
hscr |
5 |
hypertension - ethnology - genetics |
5 |
hypertension - genetics - physiopathology |
5 |
hypoglycemic agents - therapeutic use |
5 |
insulin - blood |
5 |
kw020 - characterization of disorders |
5 |
kw024 - chromosomal deletions |
5 |
kw039 - delineation of diseases |
5 |
kw078 - genome scan |
5 |
models, genetic |
5 |
network |
5 |
neurogenetics |
5 |
nuclear proteins - genetics |
5 |
obesity |
5 |
obesity - ethnology - genetics |
5 |
physical chromosome mapping - methods |
5 |
prognosis |
5 |
proto-oncogene proteins c-ret - genetics |
5 |
raindance |
5 |
rare variant |
5 |
receptors, cell surface - genetics |
5 |
retrospective studies |
5 |
sex distribution |
5 |
snp |
5 |
targeted resequencing |
5 |
united states - epidemiology |
5 |
wga |
5 |
whole genome association |
5 |
ace |
4 |
alzheimer disease - genetics |
4 |
alzheimer's disease |
4 |
apoe |
4 |
binding sites |
4 |
blood pressure measurement |
4 |
bone density - genetics |
4 |
calcium-binding proteins - genetics |
4 |
caudal regression |
4 |
chromosome 1q |
4 |
chromosome 2q |
4 |
chromosome 5q |
4 |
cognitive decline |
4 |
computational biology - methods |
4 |
copy-number variation |
4 |
founder mutation |
4 |
fractures, bone - complications - genetics - physiopathology |
4 |
gene-environment interaction |
4 |
genomics |
4 |
homozygosity mapping |
4 |
intercellular signaling peptides and proteins - genetics |
4 |
joint effect |
4 |
kw117 - mutation detection |
4 |
kw139 - polymorphism |
4 |
population-based linkage |
4 |
psychosis |
4 |
quantitative trait, heritable |
4 |
recessive mutation |
4 |
sacral agenesis |
4 |
sample selection |
4 |
algorithms |
3 |
alleles |
3 |
biomedicine |
3 |
chromosome mapping - methods |
3 |
cognition |
3 |
cognition disorders - diagnosis - genetics |
3 |
colorectal cancer |
3 |
colorectal neoplasms - genetics |
3 |
cspg5 |
3 |
depression |
3 |
endophenotypes |
3 |
environment |
3 |
erbb4 |
3 |
european continental ancestry group - genetics |
3 |
gene sequence |
3 |
genetic |
3 |
genetic epidemiology |
3 |
high-throughput assay |
3 |
human genetics |
3 |
interaction |
3 |
intermediate phenotypes |
3 |
internal medicine |
3 |
kw008 - bioinformatics |
3 |
linkage disequilibrium analysis |
3 |
memory disorders - diagnosis - genetics |
3 |
memory impairment |
3 |
mental retardation - diagnosis - genetics |
3 |
metabolic diseases |
3 |
molecular medicine |
3 |
neuregulin-1 |
3 |
pedigree |
3 |
personality inventory |
3 |
polygenic risk scores |
3 |
protein ret |
3 |
quantitative trait association |
3 |
quantitative trait loci |
3 |
rare disease |
3 |
replication |
3 |
sampling studies |
3 |
schizophrenia - diagnosis - genetics |
3 |
schizophrenic psychology |
3 |
sleep |
3 |
sleep duration |
3 |
statistical genetics |
3 |
study design |
3 |
wes |
3 |
wgs |
3 |
adh2 |
2 |
admixture |
2 |
aggression |
2 |
alcohol consumption |
2 |
allele |
2 |
analysis of variance |
2 |
anxiety |
2 |
anxiety - diagnosis - epidemiology - genetics - psychology |
2 |
ap3s1 gene |
2 |
association study |
2 |
asthma |
2 |
bdnf |
2 |
biology |
2 |
breast neoplasms - diagnosis - genetics |
2 |
cardiovascular disease |
2 |
case control study |
2 |
chromosomal mapping |
2 |
chromosome mapping - statistics & numerical data |
2 |
classification |
2 |
coalescence |
2 |
commd7 gene |
2 |
comorbidity |
2 |
computer simulation |
2 |
csf1 gene |
2 |
databases, factual |
2 |
depression - diagnosis - epidemiology - genetics - psychology |
2 |
dna pooling |
2 |
early detection of cancer |
2 |
endophenotype |
2 |
epilepsy |
2 |
epilepsygene expression |
2 |
experimental errors |
2 |
extended pedigree |
2 |
factor analysis, statistical |
2 |
family |
2 |
genetic architecture |
2 |
genetic association studies |
2 |
genetic sharing |
2 |
genetic variation |
2 |
genome scan |
2 |
genome-wide |
2 |
genome-wide association study - statistics and numerical data |
2 |
genotype error |
2 |
great britain - epidemiology |
2 |
haplotype estimation |
2 |
heritability |
2 |
identical by descent (ibd) |
2 |
identity-by-descent (ibd) |
2 |
kw052 - epilepsy |
2 |
kw080 - genome sequencing |
2 |
kw101 - mapping complex traits |
2 |
kw118 - mutation detection |
2 |
kw124 - neurogenetics |
2 |
liability threshold model |
2 |
linkage |
2 |
linkage disequilibrium |
2 |
longitudinal |
2 |
markov chain monte carlo |
2 |
methodology |
2 |
model-fitting |
2 |
mx |
2 |
neurogenetics and neurodegeneration |
2 |
neuroticism |
2 |
pedigree error |
2 |
personality - genetics |
2 |
polygenic risk score |
2 |
population stratification |
2 |
population surveillance |
2 |
prostatic neoplasms - diagnosis - genetics |
2 |
psychiatric disorders |
2 |
psychiatric genetics |
2 |
psychiatric status rating scales |
2 |
psychopathology |
2 |
qtl |
2 |
qtl association analyses |
2 |
quantitative genetics |
2 |
regulation |
2 |
selection |
2 |
severity of illness index |
2 |
sibs |
2 |
sibships |
2 |
single nucleotide polymorphisms (snp) |
2 |
snps |
2 |
socioeconomic factors |
2 |
software |
2 |
stability |
2 |
statistical model |
2 |
statistics, nonparametric |
2 |
susceptibility |
2 |
tdt |
2 |
twins |
2 |
variance components |
2 |
variance explained |
2 |
vulnerability |
2 |
addiction |
1 |
adolescence |
1 |
adoption |
1 |
adoption - psychology |
1 |
age of onset |
1 |
alcohol abuse |
1 |
antisocial behavior |
1 |
aptitude |
1 |
association analysis |
1 |
atherosclerosis |
1 |
attitude |
1 |
bmi |
1 |
cannabis |
1 |
change |
1 |
child behavior checklist for ages 2-3 |
1 |
child development |
1 |
child, preschool |
1 |
childhood |
1 |
chromosome mapping |
1 |
chromosomes, human, pair 3 - genetics |
1 |
chromosomes, human, pair 9 - genetics |
1 |
cognitive ability |
1 |
colorado |
1 |
conditioning |
1 |
continuity |
1 |
diabetes |
1 |
diallel cross |
1 |
differential heritability |
1 |
differential shared environmentality |
1 |
east asians |
1 |
empirical p-value |
1 |
environment influences |
1 |
externalizing |
1 |
family study |
1 |
gabrg2 |
1 |
general cognitive ability |
1 |
genes |
1 |
genetic counseling |
1 |
genetic influences |
1 |
genetic linkage |
1 |
genetic linkage - genetics |
1 |
genetic variation - genetics |
1 |
genome |
1 |
genome, human - genetics |
1 |
genomewide |
1 |
genomewide association |
1 |
glyca |
1 |
height |
1 |
hla-dr antigens - genetics |
1 |
huntington disease - epidemiology - etiology - genetics |
1 |
huntington disease - epidemiology - genetics |
1 |
huntington's disease |
1 |
hutterite |
1 |
identical by descent |
1 |
inbred strains |
1 |
incomplete diallel |
1 |
infant |
1 |
infant twins |
1 |
inflammation |
1 |
intelligence |
1 |
intelligence - genetics |
1 |
internalizing |
1 |
interval mapping |
1 |
large pedigrees |
1 |
likelihood functions |
1 |
linkage analysis |
1 |
linkage methods |
1 |
linkage study |
1 |
lipid factors |
1 |
lipids - blood - genetics |
1 |
lipoproteins - blood - genetics |
1 |
longitudinal studies |
1 |
marijuana abuse - genetics |
1 |
marker alleles |
1 |
maximum likelihood |
1 |
mhc |
1 |
model fitting |
1 |
modifier genes |
1 |
multiple linear regression |
1 |
multiple regression |
1 |
multiple sclerosis |
1 |
multiple sclerosis - epidemiology - genetics |
1 |
multipoint sib-pair analysis |
1 |
multivariate analyses |
1 |
normality |
1 |
observer variation |
1 |
parents - psychology |
1 |
phenotype |
1 |
pleiotropy |
1 |
population group |
1 |
power simulations |
1 |
qtls |
1 |
quantitative trait loci (qtl) |
1 |
quantitative traits |
1 |
rater bias |
1 |
receptors, n-methyl-d-aspartate - genetics |
1 |
rheumatoid arthritis |
1 |
shyness |
1 |
sib pairs |
1 |
siblings - psychology |
1 |
social environment |
1 |
statistical power |
1 |
statistics as topic |
1 |
temperament |
1 |
trans-activators - genetics |
1 |
trinucleotide repeat |
1 |
trinucleotide repeat expansion |
1 |
twin analysis |
1 |
twins - blood - genetics |
1 |
twins, dizygotic - blood - genetics |
1 |
twins, dizygotic - genetics - psychology |
1 |
twins, monozygotic - blood - genetics |
1 |
twins, monozygotic - genetics - psychology |
1 |
ubiquitin thiolesterase - genetics |
1 |
venezuela - epidemiology |
1 |
weight |
1 |
whole genome scan |
1 |