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.

236

Publications

13.9K

Citations

1.7K

Authors

722

Institutions

Publications per year

2017–2026

25

Authors

1.7K

  1. DC
    Douglas C. Wallace

    Emory University, United States

    13 publications · 1.7K citations

    12

    h-index

  2. AT
    Antonio Torroni

    University of Pavia, Italy

    11 publications · 1.7K citations

    11

    h-index

  3. MG
    Min‐Xin Guan

    Cincinnati Children's Hospital Medical Center, United States

    11 publications · 514 citations

    11

    h-index

  4. YY
    Yong‐Gang Yao

    Kunming Institute of Zoology, China

    8 publications · 736 citations

    8

    h-index

  5. AA
    Alessandro Achilli

    University of Pavia, Italy

    8 publications · 962 citations

    8

    h-index

1–5 of 1.7K

Venues

  1. PLoS ONE

    17 publications · 853 citations

    17

    h-index

  2. PubMed

    Repository · 11 publications · 1.1K citations

    11

    h-index

  3. Forensic Science International Genetics

    FSI · 9 publications · 364 citations

    9

    h-index

  4. Mitochondrion

    9 publications · 496 citations

    9

    h-index

  5. European Journal of Human Genetics

    EJHG · 8 publications · 521 citations

    8

    h-index

1–5