Gerard W. Hensels - Concepedia

Concepedia

Author

Gerard W. Hensels

Amsterdam UMC Location University of Amsterdam

Also Known As

G W Hensels, G. W. Hensels, G.W. Hensels, Gerard W. Hensels

13

Publications

1.1K

Citations

12

H-Index

27

Concepts

All Affiliations

Amsterdam UMC Location University of Amsterdam Radboud University Nijmegen University of Amsterdam

GW

About

Gerard W. Hensels is an author at Amsterdam UMC Location University of Amsterdam specializing in genetics, medicine, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	888
2	Molecular Genetics	5	5	172
3	Cell Biology	2	2	196
4	Natural Sciences	1	1	25
5	Molecular Biology	1	1	25

Gerard W. Hensels

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12

Publications

1.1K

Citations

12

H-Index

	Year	Citations
The peripheral myelin gene PMP–22/GAS–3 is duplicated in Charcot–Marie–Tooth disease type 1A Linda J. Valentijn, Pieter A. Bolhuis, Ina Zorn, Nature Genetics GeneticsExperimental NeuropathologyPathologyDegenerative DiseasePeripheral Nerves	1992	317
Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot–Marie–Tooth disease type 1B Tanja Kulkens, Pieter A. Bolhuis, Ruud A. Wolterman, Nature Genetics Neurodegenerative DiseasesGenetic DisorderGeneticsPathologyDegenerative Disease	1993	184
De-novo mutation in hereditary motor and sensory neuropathy type I Jessica E. Hoogendijk, Gerard W. Hensels, Emiel A. M. Janssen, The Lancet Rare DiseasesHereditary MotorMendelian DisorderGenetic DisorderMedicine	1992	161
Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28. Pieter A. Bolhuis, Gerard W. Hensels, Theo J.M. Hulsebos, PubMed	1991	143
Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1) Emiel A. M. Janssen, Stephan Kemp, Gerard W. Hensels, Human Genetics Mendelian DisorderConnexin32 Gene MutationsMedicineGeneticsPathogenesis	1997	58
Alternatively sized duplication in Charcot — Marie — Tooth disease type 1A Linda J. Valentijn, Frank Baas, Ina Zorn, Human Molecular Genetics Journal Article AlternativelyNetherlands SearchGeneticsNeuroepidemiologyOral Hygiene	1993	54
Hypokinesia and presenile dementia in a Dutch family with a novel insertion in the prion protein gene Willem A. van Gool, Gerard W. Hensels, Edo M Hoogerwaard, Brain	1995	48
Genetic localization of Bethlem myopathy G. Joost Jöbsis, P. A. Bolhuis, J.M. Boers, Neurology Rare DiseasesMendelian DisorderBethlem Myopathy FamiliesBethlem MyopathyGenetics	1996	44
The duplication in Charcot-Marie-Tooth disease type 1a spans at least 1100 kb on chromosome 17p11.2 Jessica E. Hoogendijk, Gerard W. Hensels, Ina Zorn, Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyLeast 1100	1991	33
Allelic heterogeneity in hereditary motor and sensory neuropathy type la (Charcot‐Marie‐Tooth disease type 1a) Jessica E. Hoogendijk, Emiel A. M. Janssen, A.A.W.M. Gabreëls‐Festen, Neurology	1993	31

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