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Paper Details

Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences.
Hum Genomics
9
2021
Author NameAffiliation
Indraniel DasMcDonnell Genome Institute, Washington University School of Medicine
David E LarsonMcDonnell Genome Institute, Washington University School of Medicine
David E LarsonWashington University School of Medicine
Aki S HavulinnaInstitute for Molecular Medicine Finland (FIMM), University of Helsinki
Aki S HavulinnaFinnish Institute for Health and Welfare (THL)
Charleston W K ChiangCenter for Genetic Epidemiology, Keck School of Medicine, University of Southern California
Charleston W K ChiangUniversity of Southern California
Nelson B FreimerCenter for Neurobehavioral Genetics, Jane and Terry Semel Institute for Neuroscience and Human Behavior, University of California Los Angeles
Aarno PalotieInstitute for Molecular Medicine Finland (FIMM), University of Helsinki
Aarno PalotieMassachusetts General Hospital
Aarno PalotieBroad Institute of MIT and Harvard
Samuli RipattiInstitute for Molecular Medicine Finland (FIMM), University of Helsinki
Samuli RipattiBroad Institute of MIT and Harvard
Samuli RipattiUniversity of Helsinki
Johanna KuusistoUniversity of Eastern Finland
Johanna KuusistoKuopio University Hospital
Michael BoehnkeDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan School of Public Health ann arbor
Markku LaaksoUniversity of Eastern Finland
Markku LaaksoKuopio University Hospital
Adam E LockeMcDonnell Genome Institute, Washington University School of Medicine
Adam E LockeWashington University School of Medicine
Nathan O StitzielMcDonnell Genome Institute, Washington University School of Medicine
Nathan O StitzielWashington University School of Medicine
Nathan O StitzielWashington University School of Medicine
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