Jan Willem R. Pott - Concepedia

Author

Jan Willem R. Pott

Also Known As

J. W. Pott, Jan W. Pott, Jan W. R. Pott, Jan W.R. Pott, Jan Willem Pott, Jan Willem R Pott, Jan Willem R. Pott, Yvonne de Jong-Hesse

Publications

819

Citations

H-Index

Concepts

All Affiliations

University of Groningen University Medical Center Groningen Radboud University Medical Center Bartiméus Radboud University Nijmegen

About

Jan Willem R. Pott is an author at University of Groningen specializing in ophthalmology, medicine, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	455
2	Neurology	3	3	281
3	Molecular Biology	1	1	174
4	Molecular Medicine	1	1	213
5	Neuroscience	1	1	34

Jan Willem R. Pott

Publications

663

Citations

H-Index

Page 1

	Year	Citations
International Consensus Statement on the Clinical and Therapeutic Management of Leber Hereditary Optic Neuropathy Valério Carelli, Michele Carbonelli, I.F.M. de Coo, Journal of Neuro-Ophthalmology Ocular DiseaseNeurological DisorderOptic NerveNeurobiology Of DiseaseLeber Hereditary Optic Neuropathy	2017	213
Defects in RGS9 or its anchor protein R9AP in patients with slow photoreceptor deactivation Koji Nishiguchi, Michael A. Sandberg, Aart C. Kooijman, Nature Protein Quality ControlPhotoreceptor CellSignal TransductionOphthalmologyMolecular Biology	2003	174
De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone Monochromacy Elena Buena‐Atienza, Klaus Rüther, Britta Baumann, Scientific Reports	2016	36
Leber’s hereditary optic neuropathy and vitamin B12 deficiency Jan Willem R. Pott, Kwok H. Wong Graefe s Archive for Clinical and Experimental Ophthalmology Ocular DiseaseOphthalmologyGenetic DisorderOptic NeuropathyLeber Hereditary Optic Neuropathy	2006	34
A Girl Without a Chiasm: Electrophysiologic and MRI Evidence for the Absence of Crossing Optic Nerve Fibers in a Girl With a Congenital Nystagmus Nomdo M. Jansonius, Ton M. van der Vliet, Frans W. Cornelissen, Journal of Neuro-Ophthalmology Mri EvidenceOphthalmologyNeuroanatomyPediatricsOptic Neuropathy	2001	34
Stargardt disease: monitoring incidence and diagnostic trends in the Netherlands using a nationwide disease registry Esmee H. Runhart, Patty P.A. Dhooge, Magda A. Meester‐Smoor, Acta Ophthalmologica	2021	32
Novel membrane frizzled‐related protein gene mutation as cause of posterior microphthalmia resulting in high hyperopia with macular folds Rosemarie A. Wasmann, Jolien S. Klein Wassink‐Ruiter, Olof Sundin, Acta Ophthalmologica	2013	27
Impact of Bevacizumab on Visual Function, Tumor Size, and Toxicity in Pediatric Progressive Optic Pathway Glioma: A Retrospective Nationwide Multicentre Study Carlien A. M. Bennebroek, J. van Zwol, Giorgio L. Porro, Cancers	2022	26
Clinical outcomes of treatment with idebenone in Leber's hereditary optic neuropathy in the Netherlands: A national cohort study Judith A. M. van Everdingen, Jan Willem R. Pott, Noël J.C. Bauer, Acta Ophthalmologica	2022	24
Impact of upper blepharoplasty, with or without orbicularis oculi muscle removal, on tear film dynamics and dry eye symptoms: A randomized controlled trial M.H.J. Hollander, Jan Willem R. Pott, Konstantina Delli, Acta Ophthalmologica	2021	22

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