Concepedia

Martin Digweed

MD

Statistics

Publications

52

Citations

5K

H-Index

30

Active since

1981

Affiliations

Charité - Universitätsmedizin Berlin(Current)

Humboldt-Universität zu Berlin

Freie Universität Berlin

University of Würzburg

Charles University

Martin Digweed is an author at Charité - Universitätsmedizin Berlin specializing in genetics, life sciences, and genetic disorders.

Publications per year

1981–2020

52

Publications

52

Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome

Raymonda Varon, Christine Vissinga, Matthias Platzer et al. · Cell · 1998 · 1.1K citations · Full text

, , +10

Human Fanconi anemia monoubiquitination pathway promotes homologous DNA repair

Koji Nakanishi, Yun‐Gui Yang, Andrew J. Pierce et al. · Proceedings of the National Academy of Sciences · 2005 · 389 citations · Full text

, , +17

The Fanconi anaemia group G gene FANCG is identical with XRCC9

Johan P. de Winter, Quinten Waisfisz, Martin A. Rooimans et al. · Nature Genetics · 1998 · 355 citations

, , +5

Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita

Tom Vulliamy, Richard Beswick, Michael Kirwan et al. · Proceedings of the National Academy of Sciences · 2008 · 330 citations · Full text

, , +16

Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK)

André Reis, Hans-Christian Hennies, Lutz Langbein et al. · Nature Genetics · 1994 · 251 citations

, , +8

1–5 of 52