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	Title	Author(s)	Issue Date
	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
	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
	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
	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
	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
	Program Report: GENECOUNTING support programs Journal:Annals of Human Genetics	Curtis, D Knight, J Sham, PC	2006
	Quantitative trait locus analysis of candidate gene alleles associated with attention deficit hyperactivity disorder (ADHD) in five genes: DRD4, DAT1, DRD5, SNAP-25, and 5HT1B Journal:American Journal of Medical Genetics - Neuropsychiatric Genetics	Mill, J Xu, X Ronald, A Curran, S Price, T Knight, J Craig, I Sham, P Plomin, R Asherson, P	2005
	SNPs, microarrays and pooled DNA: Identification of four loci associated with mild mental impairment in a sample of 6000 children Journal:Human Molecular Genetics	Butcher, LM Meaburn, E Knight, J Sham, PC Schalkwyk, LC Craig, IW Plomin, R	2005
	Software for generating liability distributions for pedigrees conditional on their observed disease states and covariates Journal:Genetic Epidemiology	Campbell, DD Sham, PC Knight, J Wickham, H Landau, S	2010
	TTF-1 and RET promoter SNPs: Regulation of RET transcription in Hirschsprung's disease Journal:Human Molecular Genetics	GarciaBarcelo, M Ganster, RW Lui, VCH Leon, TYY So, MT Lau, AMF Fu, M Sham, MH Knight, J Zannini, MS Sham, PC Tam, PKH	2005
	Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration Journal:Human Molecular Genetics	Simpson, CL Lemmens, R Miskiewicz, K Broom, WJ Hansen, VK van Vught, PWJ Landers, JE Sapp, P van Den Bosch, L Knight, J Neale, BM Turner, MR Veldink, JH Ophoff, RA Tripathi, VB Beleza, A Shah, MN Proitsi, P Van Hoecke, A Carmeliet, P Horvitz, HR Leigh, PN Shaw, CE van den Berg, LH Sham, PC Powell, JF Verstreken, P Brown Jr, RH Robberecht, W AlChalabi, A	2009
	Whole genome linkage scan of recurrent depressive disorder from the depression network study Journal:Human Molecular Genetics	Mcguffin, P Knight, J Breen, G Brewster, S Boyd, PR Craddock, N Gill, M Korszun, A Maier, W Middleton, L Mors, O Owen, MJ Perry, J Preisig, M Reich, T Rice, J Rietschel, M Jones, L Sham, P Farmer, AE	2005

Showing results 15 to 26 of 26 < previous