Concepedia

Detlev Schindler

DS

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Publications

150

Citations

11.7K

H-Index

55

Active since

1984

Affiliations

University of Würzburg(Current)

Charité - Universitätsmedizin Berlin

Heinrich Heine University Düsseldorf

Medizinische Hochschule Hannover

Centre for Biomedical Network Research on Rare Diseases

Detlev Schindler is an author at University of Würzburg specializing in life sciences, genetics, and genetic disorders.

ORCID

Publications per year

1984–2025

150

Publications

150

Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene

Alfons Meindl, Heide Hellebrand, Constanze Wiek et al. · Nature Genetics · 2010 · 734 citations

, , +16

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer

Sarah Reid, Detlev Schindler, Helmut Hanenberg et al. · Nature Genetics · 2006 · 643 citations

, , +11

Mutation of the RAD51C gene in a Fanconi anemia–like disorder

Fiona Vaz, Helmut Hanenberg, Beatrice Schuster et al. · Nature Genetics · 2010 · 405 citations

, , +12

Mutations in the Pericentrin ( <i>PCNT</i> ) Gene Cause Primordial Dwarfism

Anita Rauch, Christian T. Thiel, Detlev Schindler et al. · Science · 2008 · 397 citations

, , +17

The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia

Orna Levran, Claire Attwooll, Rashida Henry et al. · Nature Genetics · 2005 · 368 citations

, , +9

1–5 of 150