Ernie M.H.F. Bongers

Author

Also Known As

E Bongers, E M Bongers, E M H F Bongers, E. Bongers, E. M. H. F. Bongers, E.M.H.F. Bongers, ERNIE M H F BONGERS, ERNIE M.H.F. BONGERS, ESLUNG group, Ernie Bongers

105

Publications

8.3K

Citations

H-Index

110

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center University Medical Center Utrecht University Medical Center Groningen Amsterdam UMC Location Vrije Universiteit Amsterdam

About

Ernie M.H.F. Bongers is an author at Radboud University Nijmegen specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	32	38	3.7K
2	Social Sciences	3	3	200
3	Health Sciences	2	2	61
4	Natural Sciences	2	2	340
5	Public Health	1	1	108

Ernie M.H.F. Bongers

Publications

6.5K

Citations

H-Index

Page 1

	Year	Citations
Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes Heather C. Mefford, Andrew J. Sharp, Carl Baker, New England Journal of Medicine	2008	803
Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm Mark E. Lindsay, Dorien Schepers, Nikhita Bolar, Nature Genetics Thoracic Aortic AneurysmSyndromic PresentationDevelopmental BiologyPathologyVascular Biology	2012	454
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome Bregje W.M. van Bon, Heather C. Mefford, Björn Menten, Journal of Medical Genetics	2009	366
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 the pre-replication complex cause Meier-Gorlin syndrome Louise S. Bicknell, Ernie M.H.F. Bongers, Andrea Leitch, Nature Genetics Mendelian DisorderGenetic DisorderGeneticsDna ReplicationMolecular Genetics	2011	250
Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome David A. Koolen, Jamie M. Kramer, Kornelia Neveling, Nature Genetics ChromatinGenome InstabilityGene Deletion DataChromatin StructureMicrodeletion Syndrome	2012	238
Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome Nathalie Van der Aa, Liesbeth Rooms, Geert Vandeweyer, European Journal of Medical Genetics Developmental BiologyGenetic DisorderGeneticsPathogenesisPathology	2009	215
<i>TBX4</i> mutations (small patella syndrome) are associated with childhood-onset pulmonary arterial hypertension Wilhelmina S. Kerstjens‐Frederikse, Ernie M.H.F. Bongers, Marcus T.R. Roofthooft, Journal of Medical Genetics	2013	202
Mutations in the Human TBX4 Gene Cause Small Patella Syndrome Ernie M.H.F. Bongers, Pascal H. G. Duijf, Sylvia E. C. van Beersum, The American Journal of Human Genetics Genetic DisorderGeneticsPathologyMedicineOrthopaedic Surgery	2004	181
Renal cancer and pneumothorax risk in Birt–Hogg–Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families Arjan C. Houweling, Lieke Gijezen, Marianne A. Jonker, British Journal of Cancer	2011	162

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