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Nature Genetics|November 17, 2020
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factorsMark K Bakker, Rick A A van der Spek, Wouter van Rheenen, et al.Nature Genetics|May 28, 2021
Radiotherapy is associated with a deletion signature that contributes to poor outcomes in patients with cancerEmre Kocakavuk, Kevin J Anderson, Frederick S Varn, et al.Nature Genetics|February 26, 2020
Chromatin interaction analyses elucidate the roles of PRC2-bound silencers in mouse developmentChew Yee Ngan, Chee Hong Wong, Harianto Tjong, et al.Nature Genetics|February 7, 2020
Disruption of chromatin folding domains by somatic genomic rearrangements in human cancerKadir C Akdemir, Victoria T Le, Sahaana Chandran, et al.Nature Genetics|March 7, 2020
Lysine 4 of histone H3.3 is required for embryonic stem cell differentiation, histone enrichment at regulatory regions and transcription accuracyMaja Gehre, Daria Bunina, Simone Sidoli, et al.Nature Genetics|July 5, 2022
Multiomic atlas with functional stratification and developmental dynamics of zebrafish cis-regulatory elementsDamir Baranasic, Matthias Hörtenhuber, Piotr J Balwierz, et al.Nature Genetics|June 2, 2014
A molecular basis for classic blond hair color in EuropeansCatherine A Guenther, Bosiljka Tasic, Liqun Luo, et al.Nature Genetics|March 17, 2015
Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migrationJames Curtis, Yang Luo, Helen L Zenner, et al.Nature Genetics|March 26, 2015
Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemiaLeila Noetzli, Richard W Lo, Alisa B Lee-Sherick, et al.Nature Genetics|March 31, 2015
Targeted disruption of DNMT1, DNMT3A and DNMT3B in human embryonic stem cellsJing Liao, Rahul Karnik, Hongcang Gu, et al.Pageof 744