Hennie T. Brüggenwirth

Author

Also Known As

Bruggenwirth H, Bruggenwirth, Hennie T., H Brüggenwirth, H. Brüggenwirth, H. T. Bruggenwirth, H. T. Brüggenwirth, H.T. Brüggenwirth, Hennie T. Bruggenwirth, Hennie B.R. Brüggenwirth, Hennie Bruggenwirth

117

Publications

Citations

H-Index

Concepts

All Affiliations

Erasmus MC Erasmus University Rotterdam Radboud University Nijmegen Radboud University Medical Center Erasmus MC - Sophia Children’s Hospital

About

Hennie T. Brüggenwirth is an author at Erasmus MC specializing in medicine, genetics, and endocrinology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	20	1.4K
2	Public Health	6	6	429
3	Health Sciences	3	3	148
4	Engineering	1	1	84
5	Natural Sciences	1	1	11

Hennie T. Brüggenwirth

Publications

3.5K

Citations

H-Index

Page 1

	Year	Citations
Dynamic assembly of end-joining complexes requires interaction between Ku70/80 and XRCC4 Pierre‐Olivier Mari, Bogdan I. Florea, Stephan P. Persengiev, Proceedings of the National Academy of Sciences	2006	396
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies Claire Redin, Harrison Brand, Ryan L. Collins, Nature Genetics Human Congenital AnomaliesDevelopmental AnomalyDevelopmental BiologyCytogeneticsGenomic Landscape	2016	346
Mutations in a TGF-β Ligand, TGFB3, Cause Syndromic Aortic Aneurysms and Dissections Aida M. Bertoli‐Avella, Elisabeth Gillis, Hiroko Morisaki, Journal of the American College of Cardiology	2015	290
Genotype<i>Versus</i>Phenotype in Families with Androgen Insensitivity Syndrome Annemie L. M. Boehmer, Hennie T. Brüggenwirth, Cissy van Assendelft, The Journal of Clinical Endocrinology & Metabolism InfertilityPhenotypic VariationGenetic DisorderGeneticsAndrogen Insensitivity Syndrome	2001	287
Phenotypic spectrum of the SMAD3-related aneurysms–osteoarthritis syndrome Ingrid M.B.H. van de Laar, Denise van der Linde, E.H. Oei, Journal of Medical Genetics	2011	249
Different types of V(D)J recombination and end-joining defects in DNA double-strand break repair mutant mammalian cells Nicole S. Verkaik, Rebecca E. E. Esveldt–van Lange, Diana van Heemst, European Journal of Immunology	2002	186
Mucopolysaccharidosis type IIIA: Clinical spectrum and genotype‐phenotype correlations M. J. Valstar, Sanne Neijs, Hennie T. Brüggenwirth, Annals of Neurology	2010	185
Survival and prognostic factors in BRCA1-associated breast cancer Cecile T.M. Brekelmans, Caroline Seynaeve, M. Menke-Pluymers, Annals of Oncology Breast OncologyMedicinePathologyBreast CancerBrca1-associated Breast Cancer	2005	134
Mucopolysaccharidosis type IIIB may predominantly present with an attenuated clinical phenotype M. J. Valstar, Hennie T. Brüggenwirth, Renske Olmer, Journal of Inherited Metabolic Disease	2010	124
Mosaicism due to a Somatic Mutation of the Androgen Receptor Gene Determines Phenotype in Androgen Insensitivity Syndrome1 Paul‐Martin Holterhus, Hennie T. Brüggenwirth, Olaf Hiort, The Journal of Clinical Endocrinology & Metabolism	1997	87

Page 1