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Nature Genetics|October 1, 1996
Identification of an essential nonneuronal function of neurotrophin 3 in mammalian cardiac developmentM J Donovan, R Hahn, L Tessarollo, et al.Nature Genetics|October 1, 1996
Epilepsy and brain abnormalities in mice lacking the Otx1 geneD Acampora, S Mazan, V Avantaggiato, et al.Nature Genetics|April 4, 2006
Systematic identification of human mitochondrial disease genes through integrative genomicsSarah Calvo, Mohit Jain, Xiaohui Xie, et al.Nature Genetics|April 4, 2006
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studiesSusan Service, Joseph DeYoung, Maria Karayiorgou, et al.Nature Genetics|December 7, 2007
Psoriasis is associated with increased beta-defensin genomic copy numberEdward J Hollox, Ulrike Huffmeier, Patrick L J M Zeeuwen, et al.Nature Genetics|December 25, 2007
Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signalingElen Griffith, Sarah Walker, Carol-Anne Martin, et al.Nature Genetics|December 25, 2007
Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2Uwe Kornak, Ellen Reynders, Aikaterini Dimopoulou, et al.Nature Genetics|December 25, 2007
Closing gaps in the human genome with fosmid resources generated from multiple individualsDonald Bovee, Yang Zhou, Eric Haugen, et al.Nature Genetics|January 8, 2008
Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypesMasayo Kagami, Yoichi Sekita, Gen Nishimura, et al.Nature Genetics|January 8, 2008
Ultraconservation identifies a small subset of extremely constrained developmental enhancersAxel Visel, Shyam Prabhakar, Jennifer A Akiyama, et al.Pageof 745