The Human Gut Microbiome: Ecology and Recent Evolutionary ChangesWALTER, Jens; LEY, Ruth.Annual review of microbiology. 2011, Vol 65, pp 411-429, issn 0066-4227, 19 p.Article

Revisiting human primary immunodeficienciesCASANOVA, Jean-Laurent; FIESCHI, Claire; ZHANG, Shen-Ying et al.Journal of internal medicine. 2008, Vol 264, Num 2, pp 115-127, issn 0954-6820, 13 p.Article

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Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosisGBADEGESIN, Rasheed A; LAVIN, Peter J; OTTATI, Carolina et al.Kidney international. 2012, Vol 81, Num 1, pp 94-99, issn 0085-2538, 6 p.Article

Human subjects are protected from mast cell tryptase deficiency despite frequent inheritance of loss-of-function mutationsTRIVEDI, Neil N; TAMRAZ, Bani; CHU, Catherine et al.Journal of allergy and clinical immunology. 2009, Vol 124, Num 5, pp 1099-1105, issn 0091-6749, 7 p.Article

Genotype―phenotype correlation in 440 patients with NPHP-related ciliopathiesCHAKI, Moumita; HOEFELE, Julia; ALLEN, Susan J et al.Kidney international. 2011, Vol 80, Num 11, pp 1239-1245, issn 0085-2538, 7 p.Article

Mycobacterium tuberculosis, macrophages, and the innate immune response : does common variation matter?BERRINGTON, William R; HAWN, Thomas R.Immunological reviews. 2007, Vol 219, pp 167-186, issn 0105-2896, 20 p.Article

Population history and its impact on medical genetics in QuebecLABERGE, A.-M; MICHAUD, J; RICHTER, A et al.Clinical genetics. 2005, Vol 68, Num 4, pp 287-301, issn 0009-9163, 15 p.Article

A founder BRCA2 mutation in non-Afrikaner breast cancer patients of the Western Cape of South AfricaVAN DER MERWE, N. C; HAMEL, N; SCHNEIDER, S.-R et al.Clinical genetics. 2012, Vol 81, Num 2, pp 179-184, issn 0009-9163, 6 p.Article

The Behavioral Phenotype of Mowat-Wilson SyndromeEVANS, Elizabeth; EINFELD, Stewart; MOWAT, David et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 2, pp 358-366, issn 1552-4825, 9 p.Article

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Heredity versus Environment in Tuberculosis in Twins : The 1950s United Kingdom Prophit Survey-Simonds and Comstock RevisitedVAN DER EIJK, Ellen A; VAN DE VOSSE, Esther; VANDENBROUCKE, Jan P et al.American journal of respiratory and critical care medicine. 2007, Vol 176, Num 12, pp 1281-1288, issn 1073-449X, 8 p.Article

Sweet taste preferences are partly genetically determined : identification of a trait locus on chromosome 16KESKITALO, Kaisu; KNAAPILA, Antti; KALLELA, Mikko et al.The American journal of clinical nutrition. 2007, Vol 86, Num 1, pp 55-63, issn 0002-9165, 9 p.Article

Mapping of an autosomal dominant gene for Dupuytren's contracture to chromosome 16q in a Swedish familyHU, F. Z; NYSTROM, A; PRESTON, R. A et al.Clinical genetics. 2005, Vol 68, Num 5, pp 424-429, issn 0009-9163, 6 p.Article

Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3VERBEEK, D. S; VAN DE WARRENBURG, B. P; WESSELING, P et al.Brain. 2004, Vol 127, pp 2551-2557, issn 0006-8950, 7 p., 11Article

Applying systems biology in drug discovery and developmentGALIZZI, Jean-Pierre; LOCKHART, Brian Paul; BRIL, Antoine et al.Drug metabolism and drug interactions. 2013, Vol 28, Num 2, pp 67-78, issn 0792-5077, 12 p.Article

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Environmental setting of human migrations in the circum-Pacific regionPOPE, Kevin O; TERRELL, John E.Journal of biogeography. 2008, Vol 35, Num 1, pp 1-21, issn 0305-0270, 21 p.Article

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Personal genetics: regulatory framework in Europe from a service provider's perspectiveGRIMALDI, Keith A; LOOK, Markus P; SCIOLI, G. Antonio et al.European journal of human genetics. 2011, Vol 19, Num 4, pp 382-388, issn 1018-4813, 7 p.Article

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Genomics, divination, racecraft. Commentary and Author's replyPALMIE, Stephan; ABU EL-HAJ, Nadia; GOODMAN, Alan H et al.American ethnologist. 2007, Vol 34, Num 2, pp 205-251, issn 0094-0496, 47 p.Article