Anneke B. Oostra - Concepedia

Concepedia

Author

Anneke B. Oostra

Amsterdam UMC Location Vrije Universiteit Amsterdam

Also Known As

A B Oostra, A OOSTRA, A. B. Oostra, A.B. Oostra, Anneke B Oostra, Anneke B. Oostra, Anneke Oostra, Anneke B. Oostra, Oostra, Anneke B.

54

Publications

4.3K

Citations

28

H-Index

56

Concepts

All Affiliations

Amsterdam UMC Location Vrije Universiteit Amsterdam University of Amsterdam The Netherlands Cancer Institute Vrije Universiteit Amsterdam University of Würzburg

AB

About

Anneke B. Oostra is an author at Amsterdam UMC Location Vrije Universiteit Amsterdam specializing in medicine, genetics, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	19	2.4K
2	Natural Sciences	5	5	664
3	Health Sciences	3	3	303
4	Public Health	1	1	51
5	Biochemistry	1	1	18

Anneke B. Oostra

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37

Publications

4.3K

Citations

28

H-Index

	Year	Citations
A novel ubiquitin ligase is deficient in Fanconi anemia Amom Ruhikanta Meetei, Johan P. de Winter, Annette L. Medhurst, Nature Genetics Novel Ubiquitin LigaseGeneticsHematologyMolecular BiologyMolecular Genetics	2003	568
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
Evidence for at Least Eight Fanconi Anemia Genes Hans Joenje, Anneke B. Oostra, Mario Wijker, The American Journal of Human Genetics BiologyGenetic DisorderMedicineGeneticsMolecular Genetics	1997	284
Oxygen-dependence of chromosomal aberrations in Fanconi's anaemia Hans Joenje, Fré Arwert, Aldur W. Eriksson, Nature BiologyChromatinCell DivisionCytogeneticsGenetics	1981	276
Warsaw Breakage Syndrome, a Cohesinopathy Associated with Mutations in the XPD Helicase Family Member DDX11/ChlR1 Petra van der Lelij, Krystyńa Chrzańowska, Barbara C. Godthelp, The American Journal of Human Genetics Mendelian DisorderWarsaw Breakage SyndromeGenetic DisorderGeneticsPathogenesis	2010	270
Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes Marieke Levitus, Martin A. Rooimans, Jûrgen Steltenpool, Blood	2003	240
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
Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance. Jerome R. Lo Ten Foe, M. L. Kwee, Martin A. Rooimans, PubMed	1997	203
Somatic Mosaicism in Fanconi Anemia: Molecular Basis and Clinical Significance Jerome R. Lo Ten Foe, M. L. Kwee, Martin A. Rooimans, European Journal of Human Genetics	1997	196
FAAP100 is essential for activation of the Fanconi anemia‐associated DNA damage response pathway Ling Chen, Masamichi Ishiai, Abdullah Mahmood Ali, The EMBO Journal	2007	174

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