Haplogroup-specific Mutations
Haplogroup-Specific Mutations is a genetic marker category consisting of mitochondrial DNA variants that are uniquely shared among individuals within a particular haplogroup and serve to distinguish that lineage from other related lineages in the human maternal phylogeny.
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Institutions
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2017–2026
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Corinna Herrnstadt, Joanna L. Elson, Eoin Fahy et al. · The American Journal of Human Genetics · 2002 · 534 citations · Full text
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Cincinnati Children's Hospital Medical Center, United States
11 publications · 514 citations
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Wenzhou Medical University
Wenzhou, China
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Chinese Academy of Sciences
Beijing, China
11 h-index
55 publications
5.3K citations
University of Pavia
Pavia, Italy
10 h-index
33 publications
3K citations

Cincinnati Children's Hospital Medical Center
Cincinnati, United States
10 h-index
32 publications
2K citations
Inserm
Paris, France
10 h-index
54 publications
1.7K citations
Kunming Institute of Zoology
Kunming, China
9 h-index
42 publications
4.6K citations

Zhejiang University
Hangzhou, China
8 h-index
28 publications
871 citations
University of California, Irvine
Irvine, United States
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3K citations
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17 publications · 853 citations
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Repository · 11 publications · 1.1K citations
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FSI · 9 publications · 364 citations
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EJHG · 8 publications · 521 citations
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