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Nature Genetics|October 4, 2000
Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19M Constância, W Dean, S Lopes, et al.Nature Genetics|May 1, 1993
A new locus for autosomal dominant retinitis pigmentosa on chromosome 7pC F Inglehearn, S A Carter, T J Keen, et al.Nature Genetics|June 30, 2001
PAX6 haploinsufficiency causes cerebral malformation and olfactory dysfunction in humansS M Sisodiya, S L Free, K A Williamson, et al.Nature Genetics|March 10, 2001
Open-reading-frame sequence tags (OSTs) support the existence of at least 17,300 genes in C. elegansJ Reboul, P Vaglio, N Tzellas, et al.Nature Genetics|July 31, 2012
NMNAT1 mutations cause Leber congenital amaurosisMarni J Falk, Qi Zhang, Eiko Nakamaru-Ogiso, et al.Nature Genetics|June 2, 2015
Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsiaSusanne Kohl, Ditta Zobor, Wei-Chieh Chiang, et al.Nature Genetics|August 1, 1996
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosisJ N Feder, A Gnirke, W Thomas, et al.Nature Genetics|October 27, 2014
Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathyCarol-Anne Martin, Ilyas Ahmad, Anna Klingseisen, et al.Nature Genetics|September 17, 2013
Identification of a rare coding variant in complement 3 associated with age-related macular degenerationXiaowei Zhan, David E Larson, Chaolong Wang, et al.Nature Genetics|December 23, 2015
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variantsLars G Fritsche, Wilmar Igl, Jessica N Cooke Bailey, et al.Pageof 2