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Nature Genetics|May 20, 2020
Quantifying genetic effects on disease mediated by assayed gene expression levelsDouglas W Yao, Luke J O'Connor, Alkes L Price, et al.Nature Genetics|May 20, 2020
Cas9 activates the p53 pathway and selects for p53-inactivating mutationsOana M Enache, Veronica Rendo, Mai Abdusamad, et al.Nature Genetics|May 20, 2020
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analysesHaoyu Zhang, Thomas U Ahearn, Julie Lecarpentier, et al.Nature Genetics|November 5, 2022
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritisKazuyoshi Ishigaki, Saori Sakaue, Chikashi Terao, et al.Nature Genetics|February 16, 2005
Complex trait analysis of gene expression uncovers polygenic and pleiotropic networks that modulate nervous system functionElissa J Chesler, Lu Lu, Siming Shou, et al.Nature Genetics|February 16, 2005
Uncovering regulatory pathways that affect hematopoietic stem cell function using 'genetical genomics'Leonid Bystrykh, Ellen Weersing, Bert Dontje, et al.Nature Genetics|February 26, 2004
Systematic generation of high-resolution deletion coverage of the Drosophila melanogaster genomeAnnette L Parks, Kevin R Cook, Marcia Belvin, et al.Nature Genetics|March 29, 2005
Genome-wide strategies for detecting multiple loci that influence complex diseasesJonathan Marchini, Peter Donnelly, Lon R CardonNature Genetics|April 12, 2005
Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesionHugo Vega, Quinten Waisfisz, Miriam Gordillo, et al.Nature Genetics|April 20, 2005
Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebsShalini Jadeja, Ian Smyth, Jolanta E Pitera, et al.Pageof 745