Jessica E. Hoogendijk

Author

Also Known As

Esther Brusse, J E Hoogendijk, J Hoogendijk, J. E. Hoogendijk, J. Hoogendijk, J.E Hoogendijk, J.E. Hoogendijk, Jessica E Hoogendijk, Jessica E. Hoogendijk, Jessica Hoogendijk

152

Publications

5.7K

Citations

H-Index

Concepts

All Affiliations

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

About

Jessica E. Hoogendijk is an author at University Medical Center Utrecht specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	28	3.4K
2	Health Sciences	1	1	79
3	Natural Sciences	1	1	25
4	Public Health	1	1	210
5	Social Sciences	1	1	18

Jessica E. Hoogendijk

Publications

4.8K

Citations

H-Index

Page 1

	Year	Citations
119th ENMC international workshop: Trial design in adult idiopathic inflammatory myopathies, with the exception of inclusion body myositis, 10–12 October 2003, Naarden, The Netherlands Jessica E. Hoogendijk, Anthony A. Amato, Bryan Lecky, Neuromuscular Disorders RheumatologyAutoimmune DiseaseEnmc International WorkshopRheumatic DiseasesClinical Trials	2004	914
Identical point mutations of PMP–22 in Trembler–J mouse and Charcot–Marie–Tooth disease type 1A Linda J. Valentijn, Frank Baas, Ruud A. Wolterman, Nature Genetics Mendelian DisorderGenetic DisorderGeneticsPathogenesisMolecular Biology	1992	420
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
Long-term outcome in polymyositis and dermatomyositis I. M. Bronner, M. F. G. van der Meulen, Marjolein Visser, Annals of the Rheumatic Diseases	2006	213
Epidemiology of inclusion body myositis in the Netherlands: A nationwide study Umesh A. Badrising, Marion L. C. Maat–Schieman, Sjoerd G. van Duinen, Neurology Motor Neuron DiseaseMedicineClinical EpidemiologyDiagnosisErroneous Diagnosis	2000	210
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
Changes in vasopressin cells of the rat suprachiasmatic nucleus with aging Benno Roozendaal, Willem A. van Gool, Dick F. Swaab, Brain Research Pituitary GlandNeuroanatomyPhysiologyNeuroendocrine MechanismVasopressin Cells	1987	175
International consensus on a proposed score system for muscle biopsy evaluation in patients with juvenile dermatomyositis: A tool for potential use in clinical trials Lucy R. Wedderburn, Hemlata Varsani, Charles K.-C. Li, Arthritis Care & Research	2007	164
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
Two divergent types of nerve pathology in patients with different P sub 0 mutations in Charcot-Marie-Tooth disease Anneke Gabreëls-Festen, Jessica E. Hoogendijk, P.H.S. Meijerink, Neurology	1996	149

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