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Nature Genetics|November 6, 2001
A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2S E Holmes, E O'Hearn, A Rosenblatt, et al.Nature Genetics|November 6, 2001
Genome scanning with array CGH delineates regional alterations in mouse islet carcinomasG Hodgson, J H Hager, S Volik, et al.Nature Genetics|August 31, 2001
The power of public access: the human genome project and the scientific processJ QuackenbushNature Genetics|August 31, 2001
Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndromeB Moghadaszadeh, N Petit, C Jaillard, et al.Nature Genetics|September 8, 2001
Identifying regulatory networks by combinatorial analysis of promoter elementsY Pilpel, P Sudarsanam, G M ChurchNature Genetics|November 1, 2001
Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndromeH M Hoffman, J L Mueller, D H Broide, et al.Nature Genetics|November 1, 2001
Epigenetic silencing of CD4 in T cells committed to the cytotoxic lineageY R Zou, M J Sunshine, I Taniuchi, et al.Nature Genetics|November 1, 2001
The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNAH Mandel, R Szargel, V Labay, et al.Nature Genetics|November 1, 2001
Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathyA Saada, A Shaag, H Mandel, et al.Nature Genetics|November 1, 2001
Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locusE Verpy, S Masmoudi, I Zwaenepoel, et al.Pageof 745