| Title | Author(s) | Year | View Count |  | Software for generating liability distributions for pedigrees conditional on their observed disease states and covariates | Campbell, DD; Sham, PC; Knight, J; Wickham, H; Landau, S | 2010 | 95 |
| Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration | 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 | 160 |
| Association of the serotonin transporter gene, neuroticism and smoking behaviours | 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 | 148 |
| Differential methylation of the X-chromosome is a possible source of discordance for bipolar disorder female monozygotic twins | 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 | 158 |
| DSM-IV combined type ADHD shows familial association with sibling trait scores: A sampling strategy for QTL linkage | 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 | 233 |
| CLUMPHAP: A simple tool for performing haplotype-based association analysis | Knight, J; Curtis, D; Sham, PC | 2008 | 136 |
| Age at onset in sod1-mediated amyotrophic lateral sclerosis shows familiality | Fogh, I; Rijsdijk, F; Andersen, PM; Sham, PC; Knight, J; Neale, B; McKennaYasek, D; Silani, V; Brown Jr, RH; Powell, JF; AlChalabi, A | 2007 | 114 |
| Application of multi-locus analytical methods to identify interacting loci in case-control studies | Vermeulen, SHHM; Den Heijer, M; Sham, P; Knight, J | 2007 | 135 |
| Investigation of the ability of haplotype association and logistic regression to identify associated susceptibility loci | North, BV; Sham, PC; Knight, J; Martin, ER; Curtis, D | 2006 | 81 |
| The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: Association signals in DRD4, DAT1 and 16 other genes | 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 | 179 |
| Design and analysis of association studies using pooled DNA from large twin samples | Knight, J; Sham, P | 2006 | 77 |
| Program Report: GENECOUNTING support programs | Curtis, D; Knight, J; Sham, PC | 2006 | 94 |
| 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, P | 2006 | 31 |
| 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, A | 2005 | 30 |
| TTF-1 and RET promoter SNPs: Regulation of RET transcription in Hirschsprung's disease | 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 | 200 |
| 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, A | 2005 | 59 |
| SNPs, microarrays and pooled DNA: Identification of four loci associated with mild mental impairment in a sample of 6000 children | Butcher, LM; Meaburn, E; Knight, J; Sham, PC; Schalkwyk, LC; Craig, IW; Plomin, R | 2005 | 36 |
| 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 | Mill, J; Xu, X; Ronald, A; Curran, S; Price, T; Knight, J; Craig, I; Sham, P; Plomin, R; Asherson, P | 2005 | 40 |
| DNA pooling analysis of 21 norepinephrine transporter gene SNPs with attention deficit hyperactivity disorder: No evidence for association | Xu, X; Knight, J; Brookes, K; Mill, J; Sham, P; Craig, I; Taylor, E; Asherson, P | 2005 | 43 |
| 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 | Curtis, D; Knight, J; Sham, PC | 2005 | 35 |
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