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Nature Genetics|August 11, 1998
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1BR H Wallace, D W Wang, R Singh, et al.Nature Genetics|August 11, 1998
A retinoblastoma-binding protein that affects cell-cycle control and confers transforming abilityJ T Woitach, M Zhang, C H Niu, et al.Nature Genetics|August 11, 1998
Replication focus-forming activity 1 and the Werner syndrome gene productH Yan, C Y Chen, R Kobayashi, et al.Nature Genetics|August 11, 1998
Functional analysis of human MLH1 mutations in Saccharomyces cerevisiaeH Shimodaira, N Filosi, H Shibata, et al.Nature Genetics|August 11, 1998
A mouse model for hereditary thyroid dysgenesis and cleft palateM De Felice, C Ovitt, E Biffali, et al.Nature Genetics|September 25, 2012
Recurrent somatic TET2 mutations in normal elderly individuals with clonal hematopoiesisLambert Busque, Jay P Patel, Maria E Figueroa, et al.Nature Genetics|September 18, 2012
Rapid variance components-based method for whole-genome association analysisGulnara R Svishcheva, Tatiana I Axenovich, Nadezhda M Belonogova, et al.Nature Genetics|September 11, 2012
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagusZhan Su, Laura J Gay, Amy Strange, et al.Nature Genetics|September 11, 2012
Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotoniaMagdalena Zimoń, Jonathan Baets, Leonardo Almeida-Souza, et al.Nature Genetics|June 26, 2012
De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephalyJeong Ho Lee, My Huynh, Jennifer L Silhavy, et al.Pageof 744