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Nature Genetics|March 15, 2011
Genome-wide association study identifies susceptibility loci for IgA nephropathyAli G Gharavi, Krzysztof Kiryluk, Murim Choi, et al.Nature Genetics|March 15, 2011
Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosisGeorge F Mells, James A B Floyd, Katherine I Morley, et al.Nature Genetics|February 14, 1998
Mice with gene targetted prion protein alterations show that Prnp, Sinc and Prni are congruentR C Moore, J Hope, P A McBride, et al.Nature Genetics|February 14, 1998
Localisation of a gene implicated in a severe speech and language disorderS E Fisher, F Vargha-Khadem, K E Watkins, et al.Nature Genetics|February 14, 1998
SOX10 mutations in patients with Waardenburg-Hirschsprung diseaseV Pingault, N Bondurand, K Kuhlbrodt, et al.Nature Genetics|February 14, 1998
Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with retinitis pigmentosaS A Hagstrom, M A North, P L Nishina, et al.Nature Genetics|September 1, 1997
DMBT1, a new member of the SRCR superfamily, on chromosome 10q25.3-26.1 is deleted in malignant brain tumoursJ Mollenhauer, S Wiemann, W Scheurlen, et al.Nature Genetics|September 1, 1997
Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1J T Thomas, M W Kilpatrick, K Lin, et al.Nature Genetics|September 1, 1997
A deletion in the bovine myostatin gene causes the double-muscled phenotype in cattleL Grobet, L J Martin, D Poncelet, et al.Nature Genetics|September 1, 1997
Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neuronsU Albrecht, J S Sutcliffe, B M Cattanach, et al.Pageof 744