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Nature Genetics|March 2, 2011
Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndromeLouise S Bicknell, Sarah Walker, Anna Klingseisen, et al.Nature Genetics|March 2, 2011
Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1David R Goudie, Mariella D'Alessandro, Barry Merriman, et al.Nature Genetics|March 30, 2011
Next-generation association studies for complex traitsEleftheria ZegginiNature Genetics|March 2, 2021
Transcription factor competition at the γ-globin promoters controls hemoglobin switchingNan Liu, Shuqian Xu, Qiuming Yao, et al.Nature Genetics|July 31, 2019
CELA2A mutations predispose to early-onset atherosclerosis and metabolic syndrome and affect plasma insulin and platelet activationFatemehsadat Esteghamat, James S Broughton, Emily Smith, et al.Nature Genetics|July 31, 2019
Functional dissection of the Sox9-Kcnj2 locus identifies nonessential and instructive roles of TAD architectureAlexandra Despang, Robert Schöpflin, Martin Franke, et al.Nature Genetics|July 31, 2019
Accurate estimation of SNP-heritability from biobank-scale data irrespective of genetic architectureKangcheng Hou, Kathryn S Burch, Arunabha Majumdar, et al.Nature Genetics|August 2, 2019
Mapping cis-regulatory chromatin contacts in neural cells links neuropsychiatric disorder risk variants to target genesMichael Song, Xiaoyu Yang, Xingjie Ren, et al.Nature Genetics|August 2, 2019
DNA cross-link repair safeguards genomic stability during premeiotic germ cell developmentRoss J Hill, Gerry P CrossanNature Genetics|April 18, 2024
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorderCaroline M Nievergelt, Adam X Maihofer, Elizabeth G Atkinson, et al.Pageof 744