G.W. Padberg - Concepedia

Author

G.W. Padberg

Also Known As

G Padberg, G W A M Padberg, G W Padberg, G. Padberg, G. W. A. M. Padberg, G. W. PADBERG, G. W. Padberg, G.W. Padberg, George W Padberg, George W. Padberg

Publications

2.1K

Citations

H-Index

Concepts

All Affiliations

Radboud University Nijmegen Leiden University Dana-Farber Cancer Institute University of Amsterdam Centre National de la Recherche Scientifique

About

G.W. Padberg is an author at Radboud University Nijmegen specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	1.3K
2	Molecular Biology	2	2	84
3	Arts	1	1	101
4	Health Sciences	1	1	28
5	Kinesiology	1	1	28

G.W. Padberg

Publications

1.9K

Citations

H-Index

Page 1

	Year	Citations
Localization of the gene for Cowden disease to chromosome 10q22–23 Marcel Nelen, G.W. Padberg, E Peeters, Nature Genetics Cowden DiseaseGeneticsPathogenesisPathologyMolecular Genetics	1996	669
Diagnostic criteria for facioscapulohumeral muscular dystrophy G.W. Padberg, Peter Lunt, Manuela C. Koch, Neuromuscular Disorders DiagnosisMotor DisorderMedicineOrthopaedic SurgeryNeuromusculoskeletal Disorder	1991	218
Clinical features of facioscapulohumeral muscular dystrophy 2 Jessica C. de Greef, Richard J.L.F. Lemmers, Pilar Camaño, Neurology	2010	179
Linkage of Autosomal Dominant Hearing Loss to the Short Arm of Chromosome 1 in Two Families Paul Coucke, Guy Van Camp, Bulantrisna Djoyodiharjo, New England Journal of Medicine	1994	135
Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15 Guy Van Camp, Paul Coucke, Wendy Balemans, Human Molecular Genetics Non-syndromic Hearing LossGeneticsGenetic EpidemiologyMolecular GeneticsDisease Gene Identification	1995	101
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
Differential loss of heterozygosity in the region of the Cowden locus within 10q22-23 in follicular thyroid adenomas and carcinomas. Deborah J. Marsh, Zimu Zheng, Jan Zedenius, PubMed Somatic VariantCytogeneticsCowden DiseaseGeneticsMedicine	1997	72
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
Loss of heterozygosity in human breast carcinomas in the ataxia telangiectasia, Cowden disease and BRCA1 gene regions F Kerangueven, François Eisinger, Tetsuro Noguchi, Oncogene Brca1 Gene RegionsTumor BiologyGenome InstabilitySomatic VariantGenetic Disorder	1997	62
Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases. Egbert Bakker, M J van der Wielen, Els Voorhoeve, Journal of Medical Genetics Genetic TestingGeneticsDiagnosisMolecular BiologyPathology	1996	61

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