Christine Verellen‐Dumoulin

Author

Also Known As

CHRISTINE VERELLEN-DUMOULIN, Christine Verellen-Dumoulin, Christine Verellen‐Dumoulin, Christine Verellen–Dumoulin, Dimphna van Reijen, Dominique Van Paemel, Jacek Zaremba, Marie-Claude Léonard, Verellen-Dumoulin, C., Wim Vandenberghe

Publications

5.8K

Citations

H-Index

Concepts

All Affiliations

Institute of Pathology and Genetics Inserm University Medical Center Groningen UCLouvain Newcastle University

About

Christine Verellen‐Dumoulin is an author at Institute of Pathology and Genetics specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	22	2K
2	Health Sciences	3	3	142
3	Natural Sciences	1	1	29
4	Public Health	1	1	59
5	Social Sciences	1	1	18

Christine Verellen‐Dumoulin

Publications

4.3K

Citations

H-Index

Page 1

	Year	Citations
Identification of mutations in the α3(IV) and α4(IV) collagen genes in autosomal recessive Alport syndrome Toshio Mochizuki, Henny H. Lemmink, Mariko Mariyama, Nature Genetics Mendelian DisorderGenetic DisorderGeneticsCollagen GenesPathology	1994	510
Deletion of KDM6A, a Histone Demethylase Interacting with MLL2, in Three Patients with Kabuki Syndrome Damien Lederer, Bernard Grisart, M. Cristina Digilio, The American Journal of Human Genetics	2011	371
CNGA3 Mutations in Hereditary Cone Photoreceptor Disorders Bernd Wissinger, Daphne Gamer, Herbert Jägle, The American Journal of Human Genetics Photoreceptor CellOphthalmologyGenetic DisorderGeneticsCnga3 Mutations	2001	321
Long term trends in prevalence of neural tube defects in Europe: population based study Babak Khoshnood, Maria Loane, Hermien E. K. de Walle, BMJ	2015	243
A Cluster of Mutations in the UMOD Gene Causes Familial Juvenile Hyperuricemic Nephropathy with Abnormal Expression of Uromodulin Karin Dahan, Olivier Devuyst, Michèle Smaers, Journal of the American Society of Nephrology	2003	220
Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data Breidge Boyle, Marie‐Claude Addor, Larraitz Arriola, Archives of Disease in Childhood Fetal & Neonatal	2017	210
Mutations in <i>FKBP10</i> cause recessive osteogenesis imperfecta and bruck syndrome Brian Kelley, Fransiska Malfait, Luisa Bonafé, Journal of Bone and Mineral Research	2010	185
Trends in congenital anomalies in Europe from 1980 to 2012 Joan K. Morris, Anna Springett, Ruth Greenlees, PLoS ONE	2018	158
Intracranial aneurysms in autosomal dominant polycystic kidney disease Dominique Chauveau, Yves Pirson, Christine Verellen‐Dumoulin, Kidney International GlomerulonephritisIntracranial AneurysmsMedicineKidney FailureNeurology	1994	145
Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome Renata Lúcia Leite Ferreira de Lima, Sarah A. Hoper, Michella Ghassibe‐Sabbagh, Genetics in Medicine Mendelian DisorderGenetic DisorderGeneticsPathogenesisGenetic Epidemiology	2009	141

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