George W. Padberg - Concepedia

Author

George W. Padberg

Also Known As

Aad Tibben, G PADBERG, G Padberg, G W Padberg, G. PADBERG, G. Padberg, G. W. A. M. Padberg, G. W. PADBERG, G. W. Padberg, G. W.A.M. Padberg

372

Publications

13.8K

Citations

H-Index

161

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center Leiden University Leiden University Medical Center Fred Hutch Cancer Center

About

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

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	33	50	7.1K
2	Health Sciences	11	11	727
3	Public Health	3	3	136
4	Arts	2	2	98
5	Natural Sciences	1	1	13

George W. Padberg

108

Publications

12.8K

Citations

H-Index

Page 1

	Year	Citations
Treatment of single brain metastasis: Radiotherapy alone or combined with neurosurgery Charles J. Vecht, Hanny Haaxma‐Reiche, Evert M. Noordijk, Annals of Neurology	1993	1K
A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy Richard J.L.F. Lemmers, Patrick J. van der Vliet, Rinse Klooster, Science Facioscapulohumeral Muscular DystrophyDevelopmental BiologyMendelian DisorderFshd PatientsGenetic Disorder	2010	756
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy Cisca Wijmenga, Jane Hewitt, Lodewijk A. Sandkuijl, Nature Genetics ChromatinMendelian DisorderGenetic DisorderGeneticsMolecular Biology	1992	662
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2 Richard J.L.F. Lemmers, Rabi Tawil, Lisa M. Petek, Nature Genetics Rare DiseasesDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	2012	641
The choice of treatment of single brain metastasis should be based on extracranial tumor activity and age Evert M. Noordijk, Charles J. Vecht, Hanny Haaxma-Reiche, International Journal of Radiation OncologyBiologyPhysics Neuro-oncologyExtracranial Tumor ActivityGliomaSingle Brain MetastasisMedicine	1994	634
FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit Judith C. T. van Deutekom, Cisca Wljmenga, Esther A.E.Van Tlenhoven, Human Molecular Genetics	1993	525
Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy Petra G.M. van Overveld, Richard J F L Lemmers, Lodewijk A. Sandkuijl, Nature Genetics GeneticsMolecular BiologyDegenerative DiseaseMedicineNeurogenetics	2003	404
Population-based incidence and prevalence of facioscapulohumeral dystrophy Johanna C.W. Deenen, Hisse Arnts, Silvère M. van der Maarel, Neurology	2014	368
Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element Jan Gabriëls, M.-C. Beckers, Hao Ding, Gene Developmental BiologyMendelian DisorderPutative GeneGenetic DisorderGenetics	1999	342
Novel PTEN mutations in patients with Cowden disease: absence of clear genotype–phenotype correlations Marcel Nelen, Hannie Kremer, Irene B. M. Konings, European Journal of Human Genetics Cowden DiseaseGeneticsPathogenesisPathologyMolecular Medicine	1999	342

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