Mitochondrial Deafness

Mitochondrial Deafness is a sensorineural hearing impairment resulting from pathogenic mutations in mitochondrial DNA or nuclear genes affecting mitochondrial function, distinguished by its matrilineal inheritance pattern and association with oxidative phosphorylation deficits in cochlear cells.

299

Publications

19.9K

Citations

1.7K

Authors

609

Institutions

Publications per year

2017–2026

36

Authors

1.7K

  1. MG
    Min‐Xin Guan

    Cincinnati Children's Hospital Medical Center, United States

    51 publications · 4K citations

    35

    h-index

  2. NF
    Nathan Fischel‐Ghodsian

    Cedars-Sinai Medical Center, United States

    20 publications · 2.8K citations

    18

    h-index

  3. YQ
    Yaping Qian

    Cincinnati Children's Hospital Medical Center, United States

    13 publications · 1.1K citations

    13

    h-index

  4. RL
    Ronghua Li

    Ningbo University, China

    12 publications · 1.6K citations

    12

    h-index

  5. JZ
    Jing Zheng

    Zhejiang University, China

    12 publications · 636 citations

    11

    h-index

1–5 of 1.7K

Venues

  1. Biochemical and Biophysical Research Communications

    BBRC · 23 publications · 852 citations

    20

    h-index

  2. Nucleic Acids Research

    12 publications · 866 citations

    12

    h-index

  3. Journal of Biological Chemistry

    JBC · 11 publications · 672 citations

    11

    h-index

  4. Mitochondrion

    11 publications · 528 citations

    11

    h-index

  5. Human Mutation

    10 publications · 638 citations

    10

    h-index

1–5