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TypeTitleAuthor(s)YearViews
A novel two stage approach for causal effect estimation based on predictions of the response variableCampbell, DD; Landau, S; Sham, PC; Knight, J201325
 
Software for generating liability distributions for pedigrees conditional on their observed disease states and covariatesCampbell, DD; Sham, PC; Knight, J; Wickham, H; Landau, S201092
 
Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degenerationSimpson, 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, A2009171
 
DSM-IV combined type ADHD shows familial association with sibling trait scores: A sampling strategy for QTL linkageChen, 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, P2008237
 
Association of the serotonin transporter gene, neuroticism and smoking behavioursO'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, I2008133
 
CLUMPHAP: A simple tool for performing haplotype-based association analysisKnight, J; Curtis, D; Sham, PC2008127
 
Differential methylation of the X-chromosome is a possible source of discordance for bipolar disorder female monozygotic twinsRosa, 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, IW2008158
 
Age at onset in sod1-mediated amyotrophic lateral sclerosis shows familialityFogh, I; Rijsdijk, F; Andersen, PM; Sham, PC; Knight, J; Neale, B; McKennaYasek, D; Silani, V; Brown Jr, RH; Powell, JF; AlChalabi, A2007106
 
Application of multi-locus analytical methods to identify interacting loci in case-control studiesVermeulen, SHHM; Den Heijer, M; Sham, P; Knight, J2007135
 
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)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, P200676
 
Design and analysis of association studies using pooled DNA from large twin samplesKnight, J; Sham, P200671
 
The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: Association signals in DRD4, DAT1 and 16 other genesBrookes, 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, L2006165
 
Investigation of the ability of haplotype association and logistic regression to identify associated susceptibility lociNorth, BV; Sham, PC; Knight, J; Martin, ER; Curtis, D200676
 
Program Report: GENECOUNTING support programsCurtis, D; Knight, J; Sham, PC200675
 
Whole genome linkage scan of recurrent depressive disorder from the depression network studyMcguffin, 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, AE200589
 
A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays.Simpson, CL; Knight, J; Butcher, LM; Hansen, VK; Meaburn, E; Schalkwyk, LC; Craig, IW; Powell, JF; Sham, PC; AlChalabi, A200581
 
A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarraysSimpson, CL; Knight, J; Butcher, LM; Hansen, VK; Meaburn, E; Schalkwyk, LC; Craig, IW; Powell, JF; Sham, PC; AlChalabi, A200556
 
TTF-1 and RET promoter SNPs: Regulation of RET transcription in Hirschsprung's diseaseGarciaBarcelo, M; Ganster, RW; Lui, VCH; Leon, TYY; So, MT; Lau, AMF; Fu, M; Sham, MH; Knight, J; Zannini, MS; Sham, PC; Tam, PKH2005177
 
Quantitative trait locus analysis of candidate gene alleles associated with attention deficit hyperactivity disorder (ADHD) in five genes: DRD4, DAT1, DRD5, SNAP-25, and 5HT1BMill, J; Xu, X; Ronald, A; Curran, S; Price, T; Knight, J; Craig, I; Sham, P; Plomin, R; Asherson, P200573
 
DNA pooling analysis of 21 norepinephrine transporter gene SNPs with attention deficit hyperactivity disorder: No evidence for associationXu, X; Knight, J; Brookes, K; Mill, J; Sham, P; Craig, I; Taylor, E; Asherson, P200564
 
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