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Nature Genetics|October 1, 1992
Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187A de la Chapelle, R Tolvanen, G Boysen, et al.Nature Genetics|January 1, 2004
Complete sequencing and characterization of 21,243 full-length human cDNAsToshio Ota, Yutaka Suzuki, Tetsuo Nishikawa, et al.Nature Genetics|January 1, 2004
Chromosome stability, in the absence of apoptosis, is critical for suppression of tumorigenesis in Trp53 mutant miceGeng Liu, John M Parant, Gene Lang, et al.Nature Genetics|January 1, 2004
Epigenetic regulation of telomere length in mammalian cells by the Suv39h1 and Suv39h2 histone methyltransferasesMarta García-Cao, Roderick O'Sullivan, Antoine H F M Peters, et al.Nature Genetics|January 1, 2004
Meiotic pairing and imprinted X chromatin assembly in Caenorhabditis elegansChristopher J Bean, Christine E Schaner, William G KellyNature Genetics|December 3, 2003
Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosisGeorge Papanikolaou, Mark E Samuels, Erwin H Ludwig, et al.Nature Genetics|January 13, 2004
Sequencing of a rice centromere uncovers active genesKiyotaka Nagaki, Zhukuan Cheng, Shu Ouyang, et al.Nature Genetics|October 31, 2007
A gene harvest revealing the archeology and complexity of human diseaseEnrico Petretto, Edison T Liu, Timothy J AitmanNature Genetics|June 19, 2007
A new multipoint method for genome-wide association studies by imputation of genotypesJonathan Marchini, Bryan Howie, Simon Myers, et al.Nature Genetics|June 19, 2007
Toward simpler and faster genome-wide mutagenesis in miceSen Wu, Guoxin Ying, Qiang Wu, et al.Pageof 742