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Common variants near MC4R are associated with fat mass, weight and risk of obesityLOOS, Ruth J. F; LINDGREN, Cecilia M; BERNDT, Sonja I et al.Nature genetics. 2008, Vol 40, Num 6, pp 768-775, issn 1061-4036, 8 p.Article

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's diseaseBARRETT, Jeffrey C; HANSOUL, Sarah; BITTON, Alain et al.Nature genetics. 2008, Vol 40, Num 8, pp 955-962, issn 1061-4036, 8 p.Article

Linkage Disequilibrium Mapping of the Replicated Type 2 Diabetes Linkage Signal on Chromosome 1qPROKOPENKO, Inga; ZEGGINI, Eleftheria; FRAYLING, Timothy M et al.Diabetes (New York, NY). 2009, Vol 58, Num 7, pp 1704-1709, issn 0012-1797, 6 p.Article

Posterior polymorphous corneal dystrophy in czech families maps to chromosome 20 and excludes the VSX1 geneGWILLIAM, Rhian; LISKOVA, Petra; EBENEZER, Neil D et al.Investigative ophthalmology & visual science. 2005, Vol 46, Num 12, pp 4480-4484, issn 0146-0404, 5 p.Article

Transcript-specific, single-nucleotide polymorphism discovery and linkage analysis in hexaploid bread wheat (Triticum aestivum L.)ALLEN, Alexandra M; BARKER, Gary L. A; WAITE, Darren et al.Plant biotechnology journal (Print). 2011, Vol 9, Num 9, pp 1086-1099, issn 1467-7644, 14 p.Article

A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortiumSORANZO, Nicole; SPECTOR, Tim D; SALO, Perttu et al.Nature genetics. 2009, Vol 41, Num 11, pp 1182-1190, issn 1061-4036, 9 p.Article

Genome-wide and fine-resolution association analysis of malaria in West AfricaJALLOW, Muminatou; YIK YING TEO; SIRUGO, Giorgio et al.Nature genetics. 2009, Vol 41, Num 6, pp 657-665, issn 1061-4036, 9 p.Article

Genomic organization of human CDS2 and evaluation as a candidate gene for corneal hereditary endothelial dystrophy 2 on chromosome 20p13HALFORD, Stephanie; INGLIS, Suzanne; GWILLIAM, Rhian et al.Experimental eye research. 2002, Vol 75, Num 5, pp 619-623, issn 0014-4835, 5 p.Article

Abdominal Aortic Aneurysm Is Associated with a Variant in Low-Density Lipoprotein Receptor-Related Protein 1BOWN, Matthew J; JONES, Gregory T; CHILD, Anne H et al.American journal of human genetics. 2011, Vol 89, Num 5, pp 619-627, issn 0002-9297, 9 p.Article

Mosaic 22q13 deletions : evidence for concurrent mosaic segmental isodisomy and gene conversionBONAGLIA, Maria Clara; GIORDA, Roberto; DUNHAM, Ian et al.European journal of human genetics. 2009, Vol 17, Num 4, pp 426-433, issn 1018-4813, 8 p.Article

Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's diseaseFISHER, Sheila A; TREMELLING, Mark; BARRETT, Jeffrey C et al.Nature genetics. 2008, Vol 40, Num 6, pp 710-712, issn 1061-4036, 3 p.Article

Newly identified genetic risk variants for celiac disease related to the immune responseHUNT, Karen A; ZHERNAKOVA, Alexandra; GWILLIAM, Rhian et al.Nature genetics. 2008, Vol 40, Num 4, pp 395-402, issn 1061-4036, 8 p.Article

A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21VAN HEEL, David A; FRANKE, Lude; FEIGHERY, Con et al.Nature genetics. 2007, Vol 39, Num 7, pp 827-829, issn 1061-4036, 3 p.Article