Marianne de Visser - Concepedia

Author

Marianne de Visser

Also Known As

Albert Hofman, Anneke van der Kooi, M de Visser, M. De Visser, M. de Visser, Marianne De Visser, Marianne Visser, Marianne de Visser, Muriel Visser

139

Publications

9.2K

Citations

H-Index

Concepts

All Affiliations

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

About

Marianne de Visser is an author at University Medical Center Utrecht specializing in medicine, neurology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	26	33	3.4K
2	Health Sciences	5	5	154
3	Public Health	4	4	219
4	Social Sciences	1	1	17
5	Anatomy	1	1	35

Marianne de Visser

Publications

Citations

H-Index

Page 1

	Year	Citations
Safety and efficacy of eculizumab in anti-acetylcholine receptor antibody-positive refractory generalised myasthenia gravis (REGAIN): a phase 3, randomised, double-blind, placebo-controlled, multicentre study James F. Howard, Kimiaki Utsugisawa, Michael Benatar, The Lancet Neurology Multicentre StudyPharmacologyMedicineMyasthenia GravisNeuromuscular Blockade	2017	745
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis Michael A. van Es, Jan H. Veldink, Christiaan G. J. Saris, Nature Genetics Genome-wide Association StudyNeurodegenerative DiseasesAmyotrophic Lateral SclerosisGeneticsGenetic Epidemiology	2009	402
Evidence for an oligogenic basis of amyotrophic lateral sclerosis Marka van Blitterswijk, Michael A. van Es, Eric A. M. Hennekam, Human Molecular Genetics	2012	344
A randomized sequential trial of creatine in amyotrophic lateral sclerosis Geert Jan Groeneveld, Jan H. Veldink, Ingeborg van der Tweel, Annals of Neurology	2003	283
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis Kevin P. Kenna, Perry T.C. van Doormaal, Annelot M. Dekker, Nature Genetics Neurodegenerative DiseasesAmyotrophic Lateral SclerosisNeurological DisorderNeurologyNeuroscience	2016	278
Population based epidemiology of amyotrophic lateral sclerosis using capture-recapture methodology Mark Huisman, Sonja W. de Jong, Perry T.C. van Doormaal, Journal of Neurology Neurosurgery & Psychiatry	2011	275
Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contractures G. Joost Jöbsis, H Keizers, Jeroen Vreijling, Nature Genetics RheumatologyMendelian DisorderAutoimmune DiseaseGenetic DisorderBethlem Myopathy	1996	249
Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophy. J. M. Cobben, Gerrit van der Steege, P.M. Grootscholten, PubMed	1995	217
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
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia Russell L. McLaughlin, Dick Schijven, Wouter van Rheenen, Nature Communications	2017	154

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