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The New England Journal of Medicine|November 13, 2014
Inactivating mutations in NPC1L1 and protection from coronary heart disease, Nathan O Stitziel, Hong-Hee Won, et al.Nature|December 17, 2025
An integrated view of the structure and function of the human 4D nucleomeJob Dekker, Betul Akgol Oksuz, Yang Zhang, et al.Biorxiv : the Preprint Server for Biology|November 1, 2024
An integrated view of the structure and function of the human 4D nucleome, Job Dekker, Betul Akgol Oksuz, et al.Nature|April 20, 2013
The African coelacanth genome provides insights into tetrapod evolutionChris T Amemiya, Jessica Alföldi, Alison P Lee, et al.Nature|October 25, 2008
Somatic mutations affect key pathways in lung adenocarcinomaLi Ding, Gad Getz, David A Wheeler, et al.Molecular Psychiatry|October 23, 2019
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulationJoshua C Bis, Xueqiu Jian, Brian W Kunkle, et al.Molecular Psychiatry|August 16, 2018
Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulationJoshua C Bis, Xueqiu Jian, Brian W Kunkle, et al.Nature|December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionRon Do, Nathan O Stitziel, Hong-Hee Won, et al.Nature|October 15, 2020
Inherited causes of clonal haematopoiesis in 97,691 whole genomesAlexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.Nature|December 13, 2005
Genome sequence, comparative analysis and haplotype structure of the domestic dogKerstin Lindblad-Toh, Claire M Wade, Tarjei S Mikkelsen, et al.Pageof 40