Complement Factor H Deficiency

Complement Factor H Deficiency is a rare genetic disorder characterized by impaired regulation of the alternative complement pathway due to mutations in the complement factor H protein, leading to uncontrolled complement activation and increased risk of autoimmune and inflammatory conditions such as atypical hemolytic uremic syndrome.

522

Publications

49.1K

Citations

3K

Authors

889

Institutions

Publications per year

2017–2026

101

Variants

Cfh Deficiency

Authors

3K

  1. VF
    Véronique Frémeaux‐Bacchi

    Hôpital Européen Georges-Pompidou, France

    32 publications · 4.8K citations

    28

    h-index

  2. PF
    Peter F. Zipfel

    Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI), Germany

    32 publications · 4.4K citations

    28

    h-index

  3. SR
    Santiago Rodrı́guez de Córdoba

    Centro de Investigaciones Biológicas Margarita Salas, Spain

    24 publications · 2.6K citations

    23

    h-index

  4. MC
    Matthew C. Pickering

    Imperial College London, United Kingdom

    30 publications · 2.9K citations

    23

    h-index

  5. TH
    Timothy H.J. Goodship

    Newcastle University, United Kingdom

    22 publications · 4.3K citations

    22

    h-index

1–5 of 3K

Venues

  1. Journal of the American Society of Nephrology

    32 publications · 4.5K citations

    31

    h-index

  2. Pediatric Nephrology

    26 publications · 1.1K citations

    20

    h-index

  3. Investigative Ophthalmology & Visual Science

    IOVS · 19 publications · 744 citations

    17

    h-index

  4. Kidney International

    17 publications · 1.9K citations

    16

    h-index

  5. PubMed

    Repository · 22 publications · 929 citations

    15

    h-index

1–5