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Nature Genetics|February 15, 2001
A nuclear-mitochondrial DNA interaction affecting hearing impairment in miceK R Johnson, Q Y Zheng, Y Bykhovskaya, et al.Nature Genetics|January 9, 2023
Multimodal single-cell and whole-genome sequencing of small, frozen clinical specimensYiping Wang, Joy Linyue Fan, Johannes C Melms, et al.Nature Genetics|January 9, 2023
SPICEMIX enables integrative single-cell spatial modeling of cell identityBenjamin Chidester, Tianming Zhou, Shahul Alam, et al.Nature Genetics|January 2, 2026
A breakage-replication/fusion process explains complex rearrangements and segmental DNA amplificationCheng-Zhong Zhang, Carlos Mendez-Dorantes, Kathleen H Burns, et al.Nature Genetics|May 1, 1995
Cloning of the gene for ocular albinism type 1 from the distal short arm of the X chromosomeM T Bassi, M V Schiaffino, A Renieri, et al.Nature Genetics|May 1, 1995
Evidence for a susceptibility locus for schizophrenia on chromosome 6pter-p22S Wang, C E Sun, C A Walczak, et al.Nature Genetics|May 1, 1995
The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1A Benomar, L Krols, G Stevanin, et al.Nature Genetics|May 1, 1995
Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3pL G Gouw, C D Kaplan, J H Haines, et al.Nature Genetics|November 1, 1995
Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complexC G Bönnemann, R Modi, S Noguchi, et al.Nature Genetics|November 1, 1995
A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneityR E Straub, C J MacLean, F A O'Neill, et al.Pageof 744