HKU Scholars Hub: Browsing DSpace

Browsing by Author Knight, J

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 中

or enter first few letters:

Showing results 1 to 20 of 26 next >

Title	Author(s)	Issue Date	Views
Age at onset in sod1-mediated amyotrophic lateral sclerosis shows familiality Journal:Neurogenetics	Fogh, I Rijsdijk, F Andersen, PM Sham, PC Knight, J Neale, B McKennaYasek, D Silani, V Brown Jr, RH Powell, JF AlChalabi, A	2007	165
The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: Association signals in DRD4, DAT1 and 16 other genes Journal:Molecular Psychiatry	Brookes, K Xu, X Chen, W Zhou, K Neale, B Lowe, N Aneey, R Franke, B Gill, M Ebstein, R Buitelaar, J Sham, P Campbell, D Knight, J Andreou, P Altink, M Arnold, R Boer, F Buschgens, C Butler, L Christiansen, H Feldman, L Fleischman, K Fliers, E HoweForbes, R Goldfarb, A Heise, A Gabriëls, I KornLubetzki, I Marco, R Medad, S Minderaa, R Mulas, F Müller, U Mulligan, A Rabin, K Rommelse, N Sethna, V Sorohan, J Uebel, H Psychogiou, L Weeks, A Barrett, R Craig, I Banaschewski, T SonugaBarke, E Eisenberg, J Kuntsi, J Manor, I McGuffin, P Miranda, A Oades, RD Plomin, R Roeyers, H Rothenberger, A Sergeant, J Steinhausen, HC Taylor, E Thompson, M Faraone, SV Asherson, P Johansson, L	2006	192
Application of multi-locus analytical methods to identify interacting loci in case-control studies Journal:Annals of Human Genetics	Vermeulen, SHHM Den Heijer, M Sham, P Knight, J	2007	135
Association of the serotonin transporter gene, neuroticism and smoking behaviours Journal:Journal of Human Genetics	O'Gara, C Knight, J Stapleton, J Luty, J Neale, B Nash, M HeuzoDiaz, P Hoda, F Cohen, S Sutherland, G Collier, D Sham, P Ball, D McGuffin, P Craig, I	2008	150
Biological insights from 108 schizophrenia-associated genetic loci Journal:Nature	Ripke, S Neale, BM Corvin, A Walters, JTR Farh, KH Holmans, PA Lee, P Bulik-Sullivan, B Collier, DA Huang, HL Pers, TH Julia, A Kahn, RS Kalaydjieva, L Karachanak-Yankova, S Karjalainen, J Kavanagh, D Keller, MC Kennedy, JL Khrunin, A Kim, YJ Agartz, I Klovins, J Knowles, JA Konte, B Kucinskas, V Kucinskiene, ZA Kuzelova-Ptackova, H Kahler, AK Laurent, C Lee, CKJ Lee, SH Agerbo, E Legge, SE Lerer, B Li, M Li, T Liang, KY Lieberman, J Limborska, S Loughland, CM Lubinski, J Lonnqvist, J Albus, M Macek Jr, M Magnusson, PKE Maher, BS Maler, W Mallet, J Marsal, S Mattheisen, M Mattingsdal, M McCarley, RW McDonald, C Alexander, M Mclntosh, AM Meier, S Meijer, CJ Melegh, B Melle, I Mesholam-Gately, RI Metspalu, A Michie, PT Milani, L Milanova, V Amin, F Mokrab, Y Morris, DW Mors, O Murphy, KC Murray, RM Myin-Germeys, I Muller-Myhsok, B Melis, M Nenadic, I Nertney, DA Bacanu, SA Nestadt, G Nicodemus, KK Nikitina-Zake, L Nisenbaum, L Nordin, A O'Callaghan, E O'Dushlaine, C O'Neill, FA Oh, SY Olincy, A Begemann, M Olsen, L Van Os, J Psychosis Endophenotypes International Consortium, 'Pantelis, C Papadimitriou, GN Papiol, S Parkhomenko, E Pato, MT Paunio, T Pejovic-Milovancevic, M Belliveau Jr, RA Perkins, DO Pietilainen, O Pimm, J Pocklington, AJ Powell, J Price, A Pulver, AE Purcell, SM Quested, D Rasmussen, HB Bene, J Reichenberg, A Reimers, MA Richards, AL Roffman, JL Roussos, P Ruderier, DM Salomaa, V Sanders, AR Schall, U Schubert, CR Bergen, SE Schulze, TG Schwab, SG Scolnick, EM Scott, RJ Seidman, LJ Shi, JX Sigurdsson, E Silagadze, T Silverman, JM Sim, K Bevilacqua, E Slominsky, P Smoller, JW SO, HC Spencer, CCA Stahl, EA Stefansson, H Steinberg, S Stogmann, E Straub, RE Strengman, E Bigdeli, TB Strohmaier, J Stroup, TS Subramaniam, M Suvisaan, J Svrakic, DM Szatkiewicz, JP Soderman, E Thirumalai, S Toncheva, D Tosato, S Black, DW Veijola, J Waddington, J Walsh, D Wang, D Wang, Q Webb, BT Weiser, M Wildenauer, DB Williams, NM Williams, S Bruggeman, R Witt, SH Wolen, AR Wong, EHM Wormley, BK Xi, HS Zai, CC Zheng, XB Zimprich, F Wray, NR Stefansson, K Buccola, NG Visscher, PM Wellcome Trust Case-Control Consortium 2, 'Adolfsson, R Andreassen, OA Blackwood, DHR Bramon, E Buxbaum, JD Borglum, AD Cichon, S Darvasi, A Buckner, RL Domenici, E Ehrenreich, H Esko, T Gejman, PV Gill, M Gurling, H Hultman, CM Lwata, N Jablensky, AV Jonsson, EG Byerley, W Kendler, KS Kirov, G Knight, J Lencz, T Levinson, D Li, QGS Liu, JJ Malhotra, AK McCarroll, SA McQuillin, A Cahn, W Moran, JL Mortensen, PB Mowry, BJ Nothen, MM Ophoff, RA Owen, MJ Palotie, A Pato, CN Petryshen, TL Posthuma, D Cai, GQ Rietschel, M Riley, BP Rujescu, D Sham, PC Sklar, P St Clair, D Weinberger, DR Wendland, JR Werge, T Daly, MJ Campion, D Sullivan, PF O'Donovan, MC Cantor, RM Carr, VJ Carrera, N Catts, SV Chambert, KD Chan, RCK Chen, RYL Chen, EYH Cheng, W Cheung, EFC Chong, SA Cloninger, CR Cohen, D Cohen, N Cormican, P Craddock, N Crowley, JJ Cirtis, D Davidson, M Davis, KL Degenhardt, F Del Favero, J Demontis, D Dikeos, D Dinan, T Djurovic, S Donohoe, G Drapeau, E Duan, J Dudbridge, F Durmishi, N Eichhammer, P Eriksson, J Escott-Price, V Essioux, L Fanous, AH Farrell, MS Frank, J Franke, L Freedman, R Freimer, NB Friedl, M Friedman, JL Fromer, M Genovese, G Georgieva, L Giegling, L Giusti-Rodriguez, P Godard, S Goldstein, JL Golimbet, V Gopal, S Gratten, J Haan, LD Hammer, C Hamshere, ML Hansen, M Hansen, T Haroutunian, V Hartmann, AM Henskens, FA Herms, S Hirschhorn, JN Hoffmann, P Hofman, A Hollegaard, MV Hougaard, DM Ikeda, M Joa, L	2014	131
A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays Journal:Nucleic acids research	Simpson, CL Knight, J Butcher, LM Hansen, VK Meaburn, E Schalkwyk, LC Craig, IW Powell, JF Sham, PC AlChalabi, A	2005	45
CLUMPHAP: A simple tool for performing haplotype-based association analysis Journal:Genetic Epidemiology	Knight, J Curtis, D Sham, PC	2008	180
Design and analysis of association studies using pooled DNA from large twin samples Journal:Behavior Genetics	Knight, J Sham, P	2006	154
Differential methylation of the X-chromosome is a possible source of discordance for bipolar disorder female monozygotic twins Journal:American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics	Rosa, A Picchioni, MM Kalidindi, S Loat, CS Knight, J Toulopoulou, T Vonk, R Van Der Schot, AC Nolen, W Kahn, RS McGuffin, P Murray, RM Craig, IW	2008	168
DNA pooling analysis of 21 norepinephrine transporter gene SNPs with attention deficit hyperactivity disorder: No evidence for association Journal:American Journal of Medical Genetics - Neuropsychiatric Genetics	Xu, X Knight, J Brookes, K Mill, J Sham, P Craig, I Taylor, E Asherson, P	2005	51
DSM-IV combined type ADHD shows familial association with sibling trait scores: A sampling strategy for QTL linkage Journal:American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics	Chen, W Zhou, K Sham, P Franke, B Kuntsi, J Campbell, D Fleischman, K Knight, J Andreou, P Arnold, R Altink, M Boer, F Boholst, MJ Buschgens, C Butler, L Christiansen, H Fliers, E HoweForbes, R Gabriëls, I Heise, A KornLubetzki, I Marco, R Medad, S Minderaa, R Müller, UC Mulligan, A Psychogiou, L Rommelse, N Sethna, V Uebel, H McGuffin, P Plomin, R Banaschewski, T Buitelaar, J Ebstein, R Eisenberg, J Gill, M Manor, I Miranda, A Mulas, F Oades, RD Roeyers, H Rothenberger, A Sergeant, J SonugaBarke, E Steinhausen, HC Taylor, E Thompson, M Faraone, SV Asherson, P	2008	182
Endothelial Nitric Oxide Gene Haplotypes and Risk of Cerebral Small-Vessel Disease Journal:Stroke	Hassan, A Gormley, K O'sullivan, M Knight, J Sham, P Vallance, P Bamford, J Markus, H	2004	43
Erratum: The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: Association signals in DRD4, DAT1 and 16 other genes (Molecular Psychiatry (2006) 11, (934-953) DOI: 10.1038/sj.mp.4001869) Journal:Molecular Psychiatry	Brookes, K Xu, X Chen, W Zhou, K Neale, B Lowe, N Anney, R Franke, B Gill, M Ebstein, R Buitelaar, J Sham, P Campbell, D Knight, J Andreou, P Altink, M Arnold, R Boer, F Buschgens, C Butler, L Christiansen, H Feldman, L Fleischman, K Fliers, E HoweForbes, R Goldfarb, A Heise, A Gabriëls, I KornLubetzki, I Johansson, L Marco, R Medad, S Minderaa, R Mulas, F Müller, U Mulligan, A Rabin, K Rommelse, N Sethna, V Sorohan, J Uebel, H Psychogiou, L Weeks, A Barrett, R Craig, I Banaschewski, T SonugaBarke, E Eisenberg, J Kuntsi, J Manor, I Mcguffin, P Miranda, A Oades, RD Plomin, R Roeyers, H Rothenberger, A Sergeant, J Steinhausen, HC Taylor, E Thompson, M Faraone, SV Asherson, P	2006	46
Evidence that RNA editing modulates splice site selection in the 5-HT2C receptor gene Journal:Nucleic Acids Research	Flomen, R Knight, J Sham, P Kerwin, R Makoff, A	2004	50
Haplotype and linkage disequilibrium analysis to characterise a region in the calcium channel gene CACNA1A associated with idiopathic generalised epilepsy Journal:European Journal of Human Genetics	Chioza, B OseiLah, A Nashef, L SuarezMerino, B Wilkie, H Sham, P Knight, J Asherson, P Makoff, AJ	2002	52
Haplotype Association Analysis of Discrete and Continuous Traits Using Mixture of Regression Models Journal:Behavior Genetics	Sham, PC Rijsdijk, FV Knight, J Makoff, A North, B Curtis, D	2004	62
Investigation of the ability of haplotype association and logistic regression to identify associated susceptibility loci Journal:Annals of Human Genetics	North, BV Sham, PC Knight, J Martin, ER Curtis, D	2006	149
A new method of linkage analysis using LOD scores for quantitative traits supports linkage of monoamine oxidase activity to D17S250 in the Collaborative Study on the Genetics of Alcoholism pedigrees Journal:Psychiatric Genetics	Curtis, D Knight, J Sham, PC	2005	59
A novel two stage approach for causal effect estimation based on predictions of the response variable Proceeding/Conference:European Mathematical Genetics Meeting, EMGM 2013 Abstracts Book	Campbell, DD Landau, S Sham, PC Knight, J	2013	52
Program Report: GENECOUNTING support programs Journal:Annals of Human Genetics	Curtis, D Knight, J Sham, PC	2006	151

Showing results 1 to 20 of 26 next >