Wilson Marques - Concepedia

Author

Wilson Marques

Also Known As

Coelho Rodrigues, JERUSA SMID, Jon Infante, Júnior, Wilson Marques, Leonardo M. Kebbe, Leopoldo Perez de Isla, Marques Jr, Wilson, Marques, Wilson, Mathieu, Martial, Oswaldo Marques Jr

426

Publications

7.1K

Citations

H-Index

147

Concepts

All Affiliations

Universidade de São Paulo Universidade de Ribeirão Preto Universidade Federal de São Paulo Universidade Estadual de Campinas (UNICAMP)University College London

About

Wilson Marques is an author at Universidade de São Paulo specializing in medicine, neurology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	49	3.5K
2	Health Sciences	11	11	586
3	Social Sciences	5	5	127
4	Natural Sciences	3	3	80
5	Public Health	2	2	32

Wilson Marques

102

Publications

6.2K

Citations

H-Index

Page 1

	Year	Citations
Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature Gillian Rice, Paul R. Kasher, Gabriella Forte, Nature Genetics Autoimmune DiseaseGenetic DisorderGeneticsPathogenesisImmunology	2012	916
Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia Andrea Cortese, Roberto Simone, Roisin Sullivan, Nature Genetics Biallelic ExpansionNeurological DisorderGenetic DisorderIntronic RepeatLate-onset Ataxia	2019	564
Multi-system neurological disease is common in patients with OPA1 mutations Patrick Yu‐Wai‐Man, Philip G. Griffiths, Gráinne S. Gorman, Brain	2010	437
Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study Gillian Rice, Gabriella Forte, Marcin Szynkiewicz, The Lancet Neurology Genetic DisorderAicardi-goutières SyndromeGeneticsMedicineImmunology	2013	425
PNPLA6 mutations cause Boucher-Neuhäuser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum Matthis Synofzik, Michael Gonzalez, Charles Marques Lourenço, Brain Corticobasal DegenerationGeneticsPathologyPnpla6 MutationsMolecular Genetics	2013	221
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion Andrea Cortese, Stefano Tozza, Wai Yan Yau, Brain Vestibular Areflexia SyndromeMotor DysfunctionNeurological DisorderCorticobasal DegenerationPathology	2020	213
Alteration of Ganglioside Biosynthesis Responsible for Complex Hereditary Spastic Paraplegia Amir Boukhris, Rebecca Schüle, José Leal Loureiro, The American Journal of Human Genetics MedicinePhysiologyGanglioside Biosynthesis ResponsibleNeurologyCentral Nervous System	2013	178
Eplontersen for Hereditary Transthyretin Amyloidosis With Polyneuropathy Teresa Coelho, Wilson Marques, Noel R. Dasgupta, JAMA	2023	171
Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study David Adams, Michael Polydefkis, Alejandra González‐Duarte, The Lancet Neurology Alzheimer's DiseaseOpen-label Extension StudyMedicineHereditary Transthyretin-mediated AmyloidosisNeurology	2020	154
Damage to the Superior Gluteal Nerve after Direct Lateral Approach to the Hip Celso Hermínio Ferraz Picado, Wilson Marques Clinical Orthopaedics and Related Research MedicineOsteoarthritisOrthopaedicsElectromyographySurgery	2006	109

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