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Nature Genetics|October 27, 2004
Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthaseMichael A Simpson, Harold Cross, Christos Proukakis, et al.Nature Genetics|October 27, 2004
Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studiesShin Lin, Aravinda Chakravarti, David J CutlerNature Genetics|October 27, 2004
Mechanisms and convergence of compensatory evolution in mammalian mitochondrial tRNAsAndrew D Kern, Fyodor A KondrashovNature Genetics|June 1, 2005
TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal functionJochen Reiser, Krishna R Polu, Clemens C Möller, et al.Nature Genetics|February 28, 2006
Analysis of the human protein interactome and comparison with yeast, worm and fly interaction datasetsT K B Gandhi, Jun Zhong, Suresh Mathivanan, et al.Nature Genetics|February 28, 2006
Mutations in different components of FGF signaling in LADD syndromeEdyta Rohmann, Han G Brunner, Hülya Kayserili, et al.Nature Genetics|February 28, 2006
High mutation rates have driven extensive structural polymorphism among human Y chromosomesSjoerd Repping, Saskia K M van Daalen, Laura G Brown, et al.Nature Genetics|February 28, 2006
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosisMatthew J Greenway, Peter M Andersen, Carsten Russ, et al.Nature Genetics|September 28, 2005
A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosisMatthew R Lincoln, Alexandre Montpetit, M Zameel Cader, et al.Nature Genetics|September 28, 2005
A whole-genome admixture scan finds a candidate locus for multiple sclerosis susceptibilityDavid Reich, Nick Patterson, Philip L De Jager, et al.Pageof 744