Asymptotic properties of affected-sib-pair linkage analysisHOLMANS, P.American journal of human genetics. 1993, Vol 52, Num 2, pp 362-374, issn 0002-9297Article

Allowing for genotyping error in analysis of unmatched case-control studiesRICE, K. M; HOLMANS, P.Annals of human genetics. 2003, Vol 67, Num 2, pp 165-174, issn 0003-4800, 10 p.Article

Efficient strategies for genome scanning using maximum-likelihood affected-sib-pair analysisHOLMANS, P; CRADDOCK, N.American journal of human genetics. 1997, Vol 60, Num 3, pp 657-666, issn 0002-9297Article

Efficiency of typing unaffected relatives in an affected-sib-pair linkage study with single-locus and multiple tightly linked markersHOLMANS, P; CLAYTON, D.American journal of human genetics. 1995, Vol 57, Num 5, pp 1221-1232, issn 0002-9297Article

Bayesian trio models for association in the presence of genotyping errorsBEMARDINELLI, L; BERZUINI, C; SEAMAN, S et al.Genetic epidemiology. 2004, Vol 26, Num 1, pp 70-80, issn 0741-0395, 11 p.Article

Altered form of subuni 6 of mitochondrial ATP synthase complex in oligomycin-resistant mutants of chinese hamster ovary cellsHOLMANS, P. L; BREEN, G. A. M.Somatic cell and molecular genetics. 1987, Vol 13, Num 4, pp 347-353, issn 0740-7750Article

Increased expression of the dnaA gene has no effect on DNA replication in a dnaA⁺ strain of Escherichia coliCHURCHWARD, G; HOLMANS, P; BREMER, H et al.MGG. Molecular & general genetics. 1983, Vol 192, Num 3, pp 506-508, issn 0026-8925Article

Autosome search for schizophrenia susceptibility genes in multiply affected familiesREES, M. I; FENTON, I; MANT, R et al.Molecular psychiatry. 1999, Vol 4, Num 4, pp 353-359, issn 1359-4184Article

The T-cell receptor β locus and susceptibility to multiple sclerosisWOOD, N. W; SAWCER, S. J; KELLAR-WOOD, H. F et al.Neurology. 1995, Vol 45, Num 10, pp 1859-1863, issn 0028-3878Article

Genome-wide association study of recurrent early-onset major depressive disorderSHI, J; POTASH, J. B; JOHNSON, J. K et al.Molecular psychiatry. 2011, Vol 16, Num 2, pp 193-201, issn 1359-4184, 9 p.Article

Genome-wide scan of bipolar disorder in 65 pedigrees: supportive evidence for linkage at 8q24, 18q22, 4q32, 2p12, and 13q12MCINNIS, M. G; LAN, T-H; HUO, Y et al.Molecular psychiatry. 2003, Vol 8, Num 3, pp 288-298, issn 1359-4184, 11 p.Article

Genetic variability at the amyloid-β precursor protein locus may contribute to the risk of late-onset Alzheimer's diseaseWAVRANT-DE VRIEZE, F; CROOK, R; WU, W et al.Neuroscience letters. 1999, Vol 269, Num 2, pp 67-70, issn 0304-3940Article

The butyrylcholinesterase K variant and susceptibility to Alzheimer's diseaseKEHOE, P. G; WILLIAMS, H; HOLMANS, P et al.Journal of medical genetics. 1998, Vol 35, Num 12, pp 1034-1035, issn 0022-2593Article

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGCHAMSHERE, M. L; WALTERS, Jtr; RILEY, B et al.Molecular psychiatry. 2013, Vol 18, Num 6, pp 708-712, issn 1359-4184, 5 p.Article

A full genome scan for late onset Alzheimer's diseaseKEHOE, P; VRIEZE, F. W.-D; LOVESTONE, S et al.Human molecular genetics (Print). 1999, Vol 8, Num 2, pp 237-245, issn 0964-6906Article

No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's diseaseWAVRANT-DEVRIEZE, F; RUDRASINGHAM, V; PEREZ-TUR, J et al.Neuroscience letters. 1999, Vol 262, Num 2, pp 137-139, issn 0304-3940Article

A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophreniaWILLIAMS, J; SPURLOCK, G; MESZAROS, K et al.Molecular psychiatry. 1998, Vol 3, Num 2, pp 141-149, issn 1359-4184Article

Association of the angiotensin I converting enzyme gene deletion polymorphism with early onset of ESRF in PKD1 adult polycystic kidney diseaseBABOOLAL, K; RAVINE, D; DANIELS, J et al.Kidney international. 1997, Vol 52, Num 3, pp 607-613, issn 0085-2538Conference Paper

No linkage between multiple sclerosis and the T cell receptor α chain locusEOLI, M; WOOD, N. W; KELLAR-WOOD, H. F et al.Journal of the neurological sciences. 1994, Vol 124, Num 1, pp 32-37, issn 0022-510XArticle

Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studiesSHYN, S. I; SHI, J; SCHEFTNER, W. A et al.Molecular psychiatry. 2011, Vol 16, Num 2, pp 202-215, issn 1359-4184, 14 p.Article

No Evidence That Rare Coding Variants in ZNF804A Confer Risk of SchizophreniaDWYER, S; WILLIAMS, H; HOLMANS, P et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2010, Vol 153, Num 8, pp 1411-1416, issn 1552-4841, 6 p.Article

Testing for Gene × Environment Interaction Effects in Attention Deficit Hyperactivity Disorder and Associated Antisocial BehaviorLANGLEY, K; TURIC, D; RICE, F et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2008, Vol 147, Num 1, pp 49-53, issn 1552-4841, 5 p.Article

Genome-Wide Scan in 124 Indonesian Sib-Pair Families With Schizophrenia Reveals Genome-Wide Significant Linkage to a Locus on Chromosome 3p26-21IRMANSYAH; SCHWAB, S. G; WILDENAUER, D. B et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2008, Vol 147, Num 7, pp 1245-1252, issn 1552-4841, 8 p.Article

Familial phenotype differences in PKD1HATEBOER, N; LAZAROU, L. P; WILLIAMS, A. J et al.Kidney international. 1999, Vol 56, Num 1, pp 34-40, issn 0085-2538Article

Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case―control sampleGREEN, E. K; HAMSHERE, M; PURCELL, S et al.Molecular psychiatry. 2013, Vol 18, Num 12, pp 1302-1307, issn 1359-4184, 6 p.Article