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Genetic architectures of psychiatric disorders: the emerging picture and its implicationsSULLIVAN, Patrick F; DALY, Mark J; O'DONOVAN, Michael et al.Nature reviews. Genetics (Print). 2012, Vol 13, Num 8, pp 537-551, issn 1471-0056, 15 p.Article

Genetic Mapping in Human DiseaseALTSHULER, David; DALY, Mark J; LANDER, Eric S et al.Science (Washington, D.C.). 2008, Vol 322, Num 5903, pp 881-888, issn 0036-8075, 8 p.Article

Genetic variation in laboratory mice : User's guide to the mouseWADE, Claire M; DALY, Mark J.Nature genetics. 2005, Vol 37, Num 11, pp 1175-1180, issn 1061-4036, 6 p.Article

WHAP : haplotype-based association analysisPURCELL, Shaun; DALY, Mark J; SHAM, Pak C et al.Bioinformatics (Oxford. Print). 2007, Vol 23, Num 2, pp 255-256, issn 1367-4803, 2 p.Article

Parental phenotypes in family-based association analysisPURCELL, Shaun; SHAM, Pak; DALY, Mark J et al.American journal of human genetics. 2005, Vol 76, Num 2, pp 249-259, issn 0002-9297, 11 p.Article

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The value of gene-based selection of tag SNPs in genome-wide association studiesWILTSHIRE, Steven; DE BAKKER, Paul I. W; DALY, Mark J et al.European journal of human genetics. 2006, Vol 14, Num 11, pp 1209-1214, issn 1018-4813, 6 p.Article

Heritability and Genome-Wide Association Study to Assess Genetic Differences between Advanced Age-related Macular Degeneration SubtypesSOBRIN, Lucia; RIPKE, Stephan; RAYCHAUDHURI, Soumya et al.Ophthalmology (Rochester, MN). 2012, Vol 119, Num 9, pp 1874-1885, issn 0161-6420, 12 p.Article

Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degenerationYI YU; BHANGALE, Tushar R; REYNOLDS, Robyn et al.Human molecular genetics (Print). 2011, Vol 20, Num 18, pp 3699-3709, issn 0964-6906, 11 p.Article

Next-Generation Sequencing Strategies Enable Routine Detection of Balanced Chromosome Rearrangements for Clinical Diagnostics and Genetic ResearchTALKOWSKI, Michael E; ERNST, Carl; YIPING SHEN et al.American journal of human genetics. 2011, Vol 88, Num 4, pp 469-481, issn 0002-9297, 13 p.Article

High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiencyCALVO, Sarah E; TUCKER, Elena J; REDMAN, Michelle C et al.Nature genetics. 2010, Vol 42, Num 10, pp 851-858, issn 1061-4036, 8 p.Article

Common body mass index-associated variants confer risk of extreme obesityCOTSAPAS, Chris; SPELIOTES, Elizabeth K; VOIGHT, Benjamin F et al.Human molecular genetics (Print). 2009, Vol 18, Num 18, pp 3502-3507, issn 0964-6906, 6 p.Article

Disruption of Neurexin 1 Associated with Autism Spectrum DisorderKIM, Hyung-Goo; KISHIKAWA, Shotaro; DESCARTES, Maria et al.American journal of human genetics. 2008, Vol 82, Num 1, pp 199-207, issn 0002-9297, 9 p.Article

Evidence of transmission ratio distortion of DLG5 R30Q variant in general and implication of an association with crohn disease in menFRIEDRICHS, Frauke; BRESCIANINI, Sonia; RIOUX, John D et al.Human genetics. 2006, Vol 119, Num 3, pp 305-311, issn 0340-6717, 7 p.Article

Haplotype structure of TNFRSF5-TNFSF5 (CD40-CDD0L) and association analysis in systemic lupus erythematosusCHADHA, Sapna; MILLER, Katie; FARWELL, Lisa et al.European journal of human genetics. 2005, Vol 13, Num 5, pp 669-676, issn 1018-4813, 8 p.Article

Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defectMONSUUR, Alienke J; DE BAKKER, Paul I. W; DIOSDADO, Begona et al.Nature genetics. 2005, Vol 37, Num 12, pp 1341-1344, issn 1061-4036, 4 p.Article

Genetic association of Alzheimer's disease with multiple polymorphisms in alpha-2-macroglobulinSAUNDERS, Aleister J; BERTRAM, Lars; ALBERT, Marilyn S et al.Human molecular genetics (Print). 2003, Vol 12, Num 21, pp 2765-2776, issn 0964-6906, 12 p.Article

zCall: a rare variant caller for array-based genotypingGOLDSTEIN, Jacqueline I; CRENSHAW, Andrew; SCHIZOPHRENIA CONSORTIUM, Swedish et al.Bioinformatics (Oxford. Print). 2012, Vol 28, Num 19, pp 2543-2545, issn 1367-4803, 3 p.Article

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The landscape of somatic copy-number alteration across human cancersBEROUKHIM, Rameen; MERMEL, Craig H; MC HENRY, Kevin T et al.Nature (London). 2010, Vol 463, Num 7283, pp 899-905, issn 0028-0836, 7 p.Article

A high-density association screen of 155 ion transport genes for involvement with common migraineNYHOLT, Dale R; LAFORGE, K. Steven; MONTGOMERY, Grant W et al.Human molecular genetics (Print). 2008, Vol 17, Num 21, pp 3318-3331, issn 0964-6906, 14 p.Article

Biases and reconciliation in estimates of linkage disequilibrium in the human genomePE'ER, Itsik; CHRETIEN, Yves R; DE BAKKER, Paul I. W et al.American journal of human genetics. 2006, Vol 78, Num 4, pp 588-603, issn 0002-9297, 16 p.Article