Manuel Holtgrewe
9PUBLICATIONS
47CO-AUTHORS
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Publications (9)
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|May 20, 2024
REEV: review, evaluate and explain variants.Dzmitry Hramyka, Henrike Lisa Sczakiel, Max Xiaohang Zhao
|Apr 09, 2024
Loss-of-function variants affecting the STAGA complex component SUPT7L cause a developmental disorder with generalized lipodystrophy.Johannes Kopp, Leonard A Koch, Hristiana Lyubenova
|Jul 27, 2023
SODAR: managing multiomics study data and metadata.Mikko Nieminen, Oliver Stolpe, Mathias Kuhring
|Oct 30, 2022
Integration of Hi-C with short and long-read genome sequencing reveals the structure of germline rearranged genomes.Robert Schöpflin, Uirá Souto Melo, Hossein Moeinzadeh
|Jul 25, 2022
Pathogenic Variants in Cardiomyopathy Disorder Genes Underlie Pediatric Myocarditis-Further Impact of Heterozygous Immune Disorder Gene Variants?Franziska Seidel, Kai Thorsten Laser, Karin Klingel
|Jun 25, 2022
ClearCNV: CNV calling from NGS panel data in the presence of ambiguity and noise.Vinzenz May, Leonard Koch, Björn Fischer-Zirnsak
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Frequent Collaborators
4 joint publications
Björn Fischer-Zirnsak
4 joint publications
Stefan Mundlos
3 joint publications
Dominik Seelow
3 joint publications
Uwe Kornak
2 joint publications
Jirko Kühnisch
2 joint publications
Dieter Beule
2 joint publications
Mikko Nieminen
2 joint publications
Sabine Klaassen
2 joint publications
Guido Vogt
2 joint publications
Nadja Ehmke
