Genetic approaches to studying common diseases and complex traitsHIRSCHHORN, Joel N.Pediatric research. 2005, Vol 57, Num 5, pp 74-77, issn 0031-3998, 4 p., 2Article

Genome-wide association studies : potential next steps on a genetic journeyMCCARTHY, Mark I; HIRSCHHORN, Joel N.Human molecular genetics (Print). 2008, Vol 17, issn 0964-6906, R156-R165, NS2Article

Association StudiesMCCARTHY, Mark I; HIRSCHHORN, Joel N.Human molecular genetics (Print). 2008, Vol 17, issn 0964-6906, 87 p., NS2Serial Issue

Gencrypt: one-way cryptographic hashes to detect overlapping individuals across samplesTURCHIN, Michael C; HIRSCHHORN, Joel N.Bioinformatics (Oxford. Print). 2012, Vol 28, Num 6, pp 886-888, issn 1367-4803, 3 p.Article

The regulation of direct-to-consumer genetic testsKAYE, Jane.Human molecular genetics (Print). 2008, Vol 17, issn 0964-6906, R180-R183, NS2Article

Genome-wide association studies for common diseases and complex traitsHIRSCHHORN, Joel N; DALY, Mark J.Nature reviews. Genetics (Print). 2005, Vol 6, Num 2, pp 95-108, issn 1471-0056, 14 p.Article

Extending genome-wide association studies to copy-number variationMCCARROLL, Steven A.Human molecular genetics (Print). 2008, Vol 17, issn 0964-6906, R135-R142, NS2Article

Pedigree analysis of constitutional delay of growth and maturation: Determination of familial aggregation and inheritance patternsSEDLMEYER, Ines L; HIRSCHHORN, Joel N; PALMERT, Mark R et al.The Journal of clinical endocrinology and metabolism. 2002, Vol 87, Num 12, pp 5581-5586, issn 0021-972X, 6 p.Article

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common diseaseLOHMUELLER, Kirk E; PEARCE, Celeste L; PIKE, Malcolm et al.Nature genetics. 2003, Vol 33, Num 2, pp 177-182, issn 1061-4036, 6 p.Article

Metabolic and cardiovascular traits : an abundance of recently identified common genetic variantsMOHLKE, Karen L; BOEHNKE, Michael; ABECASIS, Goncalo R et al.Human molecular genetics (Print). 2008, Vol 17, issn 0964-6906, R102-R108, NS2Article

Autoimmune diseases : insights from genome-wide association studiesLETTRE, Guillaume; RIOUX, John D.Human molecular genetics (Print). 2008, Vol 17, issn 0964-6906, R116-R121, NS2Article

Accounting for ancestry : population substructure and genome-wide association studiesCHAO TIAN; GREGERSEN, Peter K; SELDIN, Michael F et al.Human molecular genetics (Print). 2008, Vol 17, issn 0964-6906, R143-R150, NS2Article

Genome-wide association studies : implications for multiethnic samplesCOOPER, Richard S; TAYO, Bamidele; XIAOFENG ZHU et al.Human molecular genetics (Print). 2008, Vol 17, issn 0964-6906, R151-R155, NS2Article

Common genetic variation in eight genes of the GH/IGF1 axis does not contribute to adult height variationLETTRE, Guillaume; BUTLER, Johannah L; ARDLIE, Kristin G et al.Human genetics. 2007, Vol 122, Num 2, pp 129-139, issn 0340-6717, 11 p.Article

Pharmacogenomics : candidate gene identification, functional validation and mechanismsLIEWEI WANG; WEINSHILBOUM, Richard M.Human molecular genetics (Print). 2008, Vol 17, issn 0964-6906, R174-R179, NS2Article

Lactose and Lactase-Who Is Lactose Intolerant and Why?MONTGOMERY, Robert K; KRASINSKI, Stephen D; HIRSCHHORN, Joel N et al.Journal of pediatric gastroenterology and nutrition. 2007, Vol 45, issn 0277-2116, S131-S137, SUP2Article

Detection of regulatory variation in mouse genesCOWLES, Christopher R; HIRSCHHORN, Joel N; ALTSHULER, David et al.Nature genetics. 2002, Vol 32, Num 3, pp 432-437, issn 1061-4036, 6 p.Article

Genome-wide association studies in cancerEASTON, Douglas F; EELES, Rosalind A.Human molecular genetics (Print). 2008, Vol 17, issn 0964-6906, R109-R115, NS2Article

Using gene expression to investigate the genetic basis of complex disordersNICA, Alexandra C; DERMITZAKIS, Emmanouil T.Human molecular genetics (Print). 2008, Vol 17, issn 0964-6906, R129-R134, NS2Article

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traitsJIAN YANG; FERREIRA, Teresa; FRAYLING, Timothy M et al.Nature genetics. 2012, Vol 44, Num 4, pp 369-375, issn 1061-4036, 7 p.Article

An age-dependent diet-modified effect of the PPARγ Pro12Ala polymorphism in childrenDEDOUSSIS, George V; MANIOS, Yannis; HIRSCHHORN, Joel N et al.Metabolism, clinical and experimental. 2011, Vol 60, Num 4, pp 467-473, issn 0026-0495, 7 p.Article

Comprehensive Evaluation of ESR2 Variation and Ovarian Cancer RiskPEARCE, Celeste Leigh; NEAR, Aimee M; BUTLER, Johannah L et al.Cancer epidemiology, biomarkers & prevention. 2008, Vol 17, Num 2, pp 393-396, issn 1055-9965, 4 p.Article

Investigation of the estrogen receptor-α gene with type 2 diabetes and/or nephropathy in african-american and european-american populationsGALLAGHER, Carla J; KEENE, Keith L; SALE, Michèle M et al.Diabetes (New York, NY). 2007, Vol 56, Num 3, pp 675-684, issn 0012-1797, 10 p.Article

Comprehensive association testing of common mitochondrial DNA variation in metabolic diseaseSAXENA, Richa; DE BAKKER, Paul I. W; ARDLIE, Kristin G et al.American journal of human genetics. 2006, Vol 79, Num 1, pp 54-61, issn 0002-9297, 8 p.Article

Conserved noncoding sequences are selectively constrained and not mutation cold spotsDRAKE, Jared A; BIRD, Christine; HIRSCHHORN, Joel N et al.Nature genetics. 2006, Vol 38, Num 2, pp 223-227, issn 1061-4036, 5 p.Article