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Dolores González‐Morón

Observed names: D González-Morón, D. González-Morón, DOLORES GONZÁLEZ-MORÓN, Dolores Gonzales Moron, Dolores Gonzalez-Moron, Dolores Gonzalez-Morón, Dolores Gonzalez‐Moron, Dolores González-Morón, Gonzalez- Moron D
Observed institutions: Consejo Nacional de Investigaciones Científicas y Técnicas, Austral University, Universidad de Buenos Aires, Centre Hospitalier Universitaire Vaudois, Hospital Ramos Mejía, Centro de Investigación Médica Aplicada, Universidad de Navarra, University of Lausanne
ORCID: 0000-0002-8508-1342
Observed ORCID: 0000-0002-8508-1342
OpenAlex ID: A5073454147
Optical coherence tomography as a biomarker of neurodegeneration in multiple sclerosis: A review
2018 · Ricardo Alonso, Dolores Gonzalez-Moron, et al. · Multiple Sclerosis and Related Disorders · 98
Whole exome sequencing in neurogenetic odysseys: An effective, cost- and time-saving diagnostic approach
2018 · Marta Córdoba, Sergio Alejandro Rodriguez-Quiroga, et al. · PLoS ONE · 90
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Computational classifiers for predicting the short-term course of Multiple sclerosis
2011 · Bartolome Bejarano, Mariangela Bianco, et al. · BMC Neurology · 67
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Whole Genome Sequencing Reveals a De Novo SHANK3 Mutation in Familial Autism Spectrum Disorder
2015 · Sergio I. Nemirovsky, Marta Córdoba, et al. · PLoS ONE · 55
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Identification of a somatic mutation in the RHEB gene through high depth and ultra-high depth next generation sequencing in a patient with Hemimegalencephaly and drug resistant Epilepsy
2018 · Valeria Salinas, Patricia Vega, et al. · European Journal of Medical Genetics · 34
Serotonin transporter gene variation and refractory mesial temporal epilepsy with hippocampal sclerosis
2009 · Marcelo Andrés Kauffman, Damián Consalvo, et al. · Epilepsy Research · 31
Germline and somatic mutations in cortical malformations: Molecular defects in Argentinean patients with neuronal migration disorders
2017 · Dolores González-Morón, Sebastián Vishnopolska, et al. · PLoS ONE · 26
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Argentinian clinical genomics in a leukodystrophies and genetic leukoencephalopathies cohort: Diagnostic yield in our first 9 years
2019 · Leila Cohen, Analisa Manín, et al. · Annals of Human Genetics · 16
Neurogenetics in Argentina: diagnostic yield in a personalized research based clinic
2015 · SERGIO ALEJANDRO RODRÍGUEZ-QUIROGA, MARTA CORDOBA, et al. · Genetics Research · 16
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The odyssey of complex neurogenetic disorders: From undetermined to positive
2020 · Valeria Salinas, Patricia Vega, et al. · American Journal of Medical Genetics Part C Seminars in Medical Genetics · 15
TNFSFR1A R92Q mutation, autoinflammatory symptoms and multiple sclerosis in a cohort from Argentina
2011 · Marcelo A. Kauffman, Dolores Gonzalez-Morón, et al. · Molecular Biology Reports · 13
Overwhelming genetic heterogeneity and exhausting molecular diagnostic process in chronic and progressive ataxias: facing it up with an algorithm, a gene, a panel at a time
2020 · J. Perez Maturo, L. Zavala, et al. · Journal of Human Genetics · 12
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Cerebrotendinous Xanthomatosis Revealed in Drug-Resistant Epilepsy Diagnostic Workup
2011 · Marcelo Andrés Kauffman, Dolores Gonzalez-Morón, et al. · The American Journal of the Medical Sciences · 12
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Craniofacial features of POLR3-related leukodystrophy caused by biallelic variants in POLR3A, POLR3B and POLR1C
2023 · Amytice Mirchi, Simon-Pierre Guay, et al. · Journal of Medical Genetics · 11
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Progressive external ophthalmoplegia (PEO) due to a mutation in the C10orf2 (PEO1) gene mimicking a myasthenic crisis
2013 · Dolores Gonzalez-Moron, Jose Bueri, et al. · BMJ Case Reports · 10
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Huntington’s disease masquerading as spinocerebellar ataxia
2013 · Sergio Alejandro Rodríguez-Quiroga, Dolores Gonzalez-Morón, et al. · BMJ Case Reports · 10
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Diagnosis of mitochondrial disorders applying massive pyrosequencing
2012 · Marcelo Andrés Kauffman, Dolores González-Morón, et al. · Molecular Biology Reports · 8
A Family with Late‐Onset and Predominant Choreic Niemann Pick Type C: A Treatable Piece in the Etiological Puzzle of Choreas
2020 · Sergio Rodriguez‐Quiroga, Lucia Zavala, et al. · Movement Disorders Clinical Practice · 6
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Timely diagnosis of Wilson's disease using whole exome sequencing
2015 · Sergio A. Rodríguez-Quiroga, Julieta Rosales, et al. · Parkinsonism & Related Disorders · 6
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[The broad phenotypic spectrum of SCA-3: hereditary spastic paraplegia].
2013 · Sergio A Rodríguez-Quiroga, Dolores González-Morón, et al. · PubMed · 5
Whole Exome Sequencing in Neurogenetic Diagnostic Odysseys: An Argentinian Experience
2016 · M Córdoba, SA Rodriguez-Quiroga, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 3
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POLR3-Related Leukodystrophy: A Qualitative Study on Parents’ Experiences With the Health Care System
2025 · Adam Le, Kelly-Ann Thibault, et al. · Pediatric Neurology · 2
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Holmes Tremor‐Like Phenotype in DYT1 Dystonia
2018 · Sergio Rodriguez‐Quiroga, Dolores Gonzalez‐Moron, et al. · Movement Disorders Clinical Practice · 2
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Clinical effectiveness of an inteferon beta 1a biosimilar: Results from an open-label, multicenter, observational study
2011 · Marcelo Kauffman, Gonzalez- Moron D, et al. · Journal of Bioequivalence & Bioavailability · 2
Niemann Pick Type C as Presentation of Huntington-Like Syndrome (P4.043)
2018 · Lucia Zavala, Nelida Susana Garretto, et al. · Neurology · 1
Works count: 31
Citation count: 551
H-index: 12
I10-index: 16
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