H.B. Ginjaar - Concepedia

Author

H.B. Ginjaar

Leiden University Medical Center

Also Known As

H B Ginjaar, H. B. Ginjaar, H. Ginjaar, H.B Ginjaar, H.B. Ginjaar, HB Ginjaar

Publications

2.3K

Citations

H-Index

Concepts

All Affiliations

Leiden University Medical Center Leiden University Radboud University Nijmegen Amsterdam UMC Location University of Amsterdam Radboud University Medical Center

About

H.B. Ginjaar is an author at Leiden University Medical Center specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	13	936
2	Cell Biology	2	2	51
3	Health Sciences	1	1	52
4	Social Sciences	1	1	116
5	Biostatistics	1	1	152

H.B. Ginjaar

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications. Johan T. den Dunnen, P.M. Grootscholten, Egbert Bakker, PubMed	1989	505
Calpainopathy—A Survey of Mutations and Polymorphisms Isabelle Richard, Carinne Roudaut, Amets Sáenz, The American Journal of Human Genetics Genetic DisorderGeneticsGenetic EpidemiologyPathologyGenetic Variation	1999	206
Duplications in theDMD gene Stefan J. White, Annemieke Aartsma‐Rus, Kevin M. Flanigan, Human Mutation	2006	158
Serum matrix metalloproteinase-9 (MMP-9) as a biomarker for monitoring disease progression in Duchenne muscular dystrophy (DMD) Vishna Devi Nadarajah, Maaike van Putten, P. Garrood, Neuromuscular Disorders Biomarker (Medicine)Prognostic BiomarkersDisease ProgressionDuchenne Muscular DystrophyMedicine	2011	152
Dystrophin levels and clinical severity in Becker muscular dystrophy patients J.C. van den Bergen, Beatrijs Wokke, Annika Janson, Journal of Neurology Neurosurgery & Psychiatry	2013	121
Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new <i>CACNA1A</i> mutation E. E. Kors, Atle Melberg, Kaate R. J. Vanmolkot, Neurology Neurological DisorderGeneticsSwedish FamilyEarly Onset AtaxiaEpilepsy	2004	116
The clinical spectrum of limb girdle muscular dystrophy A survey in the Netherlands Anneke J. van der Kooi, P. G. Barth, H. F. M. Busch, Brain	1996	96
Recurrence risk due to germ line mosaicism: Duchenne and Becker muscular dystrophy A. Helderman-van den Enden, Renate de Jong, Johan T. den Dunnen, Clinical Genetics	2009	94
Redefining the clinical phenotypes of non-dystrophic myotonic syndromes J. Trip, Gea Drost, H.B. Ginjaar, Journal of Neurology Neurosurgery & Psychiatry	2009	90
Limb-girdle muscular dystrophy in the Netherlands: Gene defect identified in half the families Anneke J. van der Kooi, W. Frankhuizen, P. G. Barth, Neurology Muscle TissueRare DiseasesMendelian DisorderDutch Cross-sectional StudyGenetic Disorder	2007	69

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