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Nature Genetics|February 28, 2012
Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndromeJeroen K J Van Houdt, Beata Anna Nowakowska, Sérgio B Sousa, et al.Nature Genetics|March 6, 2012
Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesiaHannah M Mitchison, Miriam Schmidts, Niki T Loges, et al.Nature Genetics|September 30, 2008
Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver diseaseStefano Romeo, Julia Kozlitina, Chao Xing, et al.Nature Genetics|September 30, 2008
Genetic control of rice plant architecture under domesticationJian Jin, Wei Huang, Ji-Ping Gao, et al.Nature Genetics|September 30, 2008
Variant between CPT1B and CHKB associated with susceptibility to narcolepsyTaku Miyagawa, Minae Kawashima, Nao Nishida, et al.Nature Genetics|September 30, 2008
Control of a key transition from prostrate to erect growth in rice domesticationLubin Tan, Xianran Li, Fengxia Liu, et al.Nature Genetics|September 17, 2008
MYH9 is a major-effect risk gene for focal segmental glomerulosclerosisJeffrey B Kopp, Michael W Smith, George W Nelson, et al.Nature Genetics|September 17, 2008
Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13Anne Barton, Wendy Thomson, Xiayi Ke, et al.Nature Genetics|September 9, 2008
Common variants of FUT2 are associated with plasma vitamin B12 levelsAditi Hazra, Peter Kraft, Jacob Selhub, et al.Pageof 744