Beatrice Schuster - Concepedia

Author

Beatrice Schuster

University of Würzburg

Also Known As

Beatrice Schuster

Publications

1.4K

Citations

H-Index

Concepts

All Affiliations

University of Würzburg Vrije Universiteit Amsterdam Amsterdam UMC Location Vrije Universiteit Amsterdam Heinrich Heine University Düsseldorf Centre for Biomedical Network Research on Rare Diseases

About

Beatrice Schuster is an author at University of Würzburg specializing in molecular genetics, genetics, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	1.3K
2	Molecular Genetics	6	6	1.3K
3	Molecular Biology	5	5	1.3K
4	Natural Sciences	2	2	525
5	Engineering	1	1	25

Beatrice Schuster

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Mutation of the RAD51C gene in a Fanconi anemia–like disorder Fiona Vaz, Helmut Hanenberg, Beatrice Schuster, Nature Genetics Genetic DisorderGeneticsMolecular BiologyMolecular GeneticsRad51c Gene	2010	402
Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia Massimo Bogliolo, Beatrice Schuster, Chantal Stoepker, The American Journal of Human Genetics Genome InstabilityGenetic DisorderGeneticsMolecular BiologyDna-repair Endonuclease Xpf	2013	303
SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype Chantal Stoepker, Karolina Hain, Beatrice Schuster, Nature Genetics Genetic DisorderNatural SciencesGeneticsProtein GeneticsMolecular Biology	2011	295
A Histone-Fold Complex and FANCM Form a Conserved DNA-Remodeling Complex to Maintain Genome Stability Zhijiang Yan, Mathieu Delannoy, Ling Chen, Molecular Cell ChromatinFancm FormChromatin StructureChromatin RemodelingMedicine	2010	230
Genotyping of Fanconi Anemia Patients by Whole Exome Sequencing: Advantages and Challenges Kerstin Knies, Beatrice Schuster, Najim Ameziane, PLoS ONE BioinformaticsFanconi AnemiaLong-read SequencingMedicineGenetics	2012	39
On the role of FAN1 in Fanconi anemia Juan Pablo Trujillo‐Quintero, Leonardo Mina, Roser Pujol, Blood	2012	34
Whole Exome Sequencing Reveals Uncommon Mutations in the Recently Identified Fanconi Anemia Gene<i>SLX</i><i>4</i>/<i>FANCP</i> Beatrice Schuster, Kerstin Knies, Chantal Stoepker, Human Mutation Fanconi AnemiaGenome InstabilityEngineeringSomatic VariantGenetic Disorder	2012	25
Hepatoblastoma in a 4‐year‐old girl with Fanconi anaemia Sascha Kopic, Katharina Eirich, Beatrice Schuster, Acta Paediatrica	2010	24

Page 1