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Nature Genetics|February 19, 2008
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizuresAndrew J Sharp, Heather C Mefford, Kelly Li, et al.Nature Genetics|February 19, 2008
Regulatory changes underlying expression differences within and between Drosophila speciesPatricia J Wittkopp, Belinda K Haerum, Andrew G ClarkNature Genetics|January 8, 2008
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysmAnna Helgadottir, Gudmar Thorleifsson, Kristinn P Magnusson, et al.Nature Genetics|January 8, 2008
Deficiency or inhibition of oxygen sensor Phd1 induces hypoxia tolerance by reprogramming basal metabolismJulián Aragonés, Martin Schneider, Katie Van Geyte, et al.Nature Genetics|February 11, 2014
Mutation-dependent recessive inheritance of NPHS2-associated steroid-resistant nephrotic syndromeKálmán Tory, Dóra K Menyhárd, Stéphanie Woerner, et al.Nature Genetics|February 27, 2014
Stem cell fate regulation by dynein motor protein Lis1Britta Will, Ulrich SteidlNature Genetics|March 12, 2014
Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disabilityKatrina Tatton-Brown, Sheila Seal, Elise Ruark, et al.Nature Genetics|March 25, 2014
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4Pilar Ramos, Anthony N Karnezis, David W Craig, et al.Nature Genetics|February 14, 2017
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biasesHolly A F Stessman, Bo Xiong, Bradley P Coe, et al.Nature Genetics|January 31, 2017
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular riskHelen R Warren, Evangelos Evangelou, Claudia P Cabrera, et al.Pageof 744