Judith M.A. Verhagen

Author

Also Known As

J M A Verhagen, J Verhagen, J. M. A. Verhagen, J.M. Verhagen, J.M.A. Verhagen, Judith M A Verhagen, Judith M Verhagen, Judith M. A. Verhagen, Judith M.A. Verhagen, Judith MA Verhagen

Publications

2.6K

Citations

H-Index

Concepts

All Affiliations

Erasmus MC Radboud University Nijmegen University Medical Center Groningen University Medical Center Utrecht Erasmus University Rotterdam

About

Judith M.A. Verhagen is an author at Erasmus MC specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	14	1.3K
2	Public Health	3	3	105
3	Social Sciences	2	2	171
4	Biology	1	1	25
5	Epidemiology	1	1	57

Judith M.A. Verhagen

Publications

2.4K

Citations

H-Index

Page 1

	Year	Citations
Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis Ingrid M.B.H. van de Laar, Rogier A. Oldenburg, Gerard Pals, Nature Genetics Cartilage DegenerationOsteoarthritisPathologySyndromic FormAortic Aneurysms	2011	663
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
A mutation update on the LDS-associated genes<i>TGFB2/3</i>and<i>SMAD2/3</i> Dorien Schepers, Giada Tortora, Hiroko Morisaki, Human Mutation	2018	160
ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm Russell A. Gould, Hamza Aziz, Courtney E. Woods, Nature Genetics	2018	148
Cardiovascular malformations caused by NOTCH1 mutations do not keep left: data on 428 probands with left-sided CHD and their families Wilhelmina S. Kerstjens‐Frederikse, Ingrid M.B.H. van de Laar, Yvonne J. Vos, Genetics in Medicine	2016	140
A Mutation in the Golgi Qb-SNARE Gene GOSR2 Causes Progressive Myoclonus Epilepsy with Early Ataxia Mark Corbett, Michael Schwake, Melanie Bahlo, The American Journal of Human Genetics Molecular NeuroscienceNeurological DisorderMedicineGeneticsEarly Ataxia	2011	123
Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor Elisabeth Gillis, Ajay Kumar, Ilse Luyckx, Frontiers in Physiology	2017	107
Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric Cardiomyopathy Rowida Almomani, Judith M.A. Verhagen, Johanna C. Herkert, Journal of the American College of Cardiology CardiomyopathyGeneticsBiallelic Truncating MutationsPathologyMedicine	2016	102
‘North Sea’ progressive myoclonus epilepsy: phenotype of subjects with GOSR2 mutation Lysa Boissé Lomax, Marta A. Bayly, Helle Hjalgrim, Brain Gosr2 MutationRare DiseasesNeurological DisorderProgressive Myoclonus EpilepsyNorth Sea	2013	80
Phenotypic variability of atypical 22q11.2 deletions not including<i>TBX1</i> Judith M.A. Verhagen, Karin E. M. Diderich, Grétel Oudesluijs, American Journal of Medical Genetics Part A Interstitial DeletionsGeneticsPathologyMolecular GeneticsDisease Gene Identification	2012	67

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