Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation

Journal: Nature Communications

Published: 2018-09-14

DOI: 10.1038/s41467-018-05714-3

Affiliations: 29

Authors: 31

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Institutions FC
Department of Human Genetics, Leiden University, Netherlands 0.16
Department of Genetics, RUG, Netherlands 0.10
Genomics Coordination Centre (GCC), RUG, Netherlands 0.06
University of Exeter Medical School (UEMS), United Kingdom (UK) 0.06
Department of Biomedical Data Sciences, Leiden University, Netherlands 0.06
Department of Internal Medicine, Erasmus MC, Netherlands 0.05
Department of Molecular Epidemiology, Leiden University, Netherlands 0.05
Department of Twin Research and Genetic Epidemiology, KCL, United Kingdom (UK) 0.05
Institute of Epidemiology II (EPI II), HMGU, Germany 0.05
MRC Integrative Epidemiology Unit (IEU), UoB, United Kingdom (UK) 0.05
SURFsara, Netherlands 0.03
Neuroscience Campus Amsterdam (NCA), VU University Amsterdam, Netherlands 0.03
Genetic Epidemiology Unit, Erasmus MC, Netherlands 0.03
Bristol Medical School, UoB, United Kingdom (UK) 0.02
School for Cardiovascular Diseases (CARIM), UM, Netherlands 0.02
Centre for Genomics and Oncological Research (GENYO), Spain 0.02
Department of Medical Statistics and BioInformatics (MSBI), Leiden University, Netherlands 0.02
UMC Utrecht Brain Center Rudolf Magnus, Netherlands 0.02
UMC Utrecht Department of Neurology, Netherlands 0.02
Department of Biological Psychology, VU University Amsterdam, Netherlands 0.02
Department of Internal Medicine, Maastricht UMC+, Netherlands 0.02
Department of Psychiatry, VU University Amsterdam, Netherlands 0.02
Department of Clinical Chemistry (AKC), Erasmus MC, Netherlands 0.02
Research Unit of Molecular Epidemiology (AME), HMGU, Germany 0.02
Medizinische Klinik und Poliklinik I, LMU, Germany 0.01
Institute of Genetic Epidemiology (IGE), HMGU, Germany 0.01
Munich Heart Alliance (MHA), Germany 0.01

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