Ana Gorostidi - Concepedia

Author

Ana Gorostidi

Biogipuzkoa Health Research Institute ORCID

Also Known As

A. Gorostidi, Alazne Gabilondo, Alexis Brice, Ana Gorostidi, Frederico Simões do Couto, Gabriel Miltenberger, Giorgio Giaccone, Gorostidi, Ana, Juan José Poza, María de Arriba

Publications

3.1K

Citations

H-Index

Concepts

All Affiliations

Biogipuzkoa Health Research Institute Biomedical Research Networking Center on Neurodegenerative Diseases University of the Basque Country University College London Instituto de Salud Carlos III

About

Ana Gorostidi is an author at Biogipuzkoa Health Research Institute specializing in medicine, neuropathology, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	21	1.2K
2	Social Sciences	5	5	223
3	Cell Biology	4	4	285
4	Natural Sciences	2	2	119
5	Engineering	1	1	19

Ana Gorostidi

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study Emma L. van der Ende, Lieke Meeter, Jackie M. Poos, The Lancet Neurology Alzheimer's DiseaseGenetic Frontotemporal DementiaOphthalmologyDementiaMulticentre Cohort Study	2019	179
The LRRK2 G2019S mutant exacerbates basal autophagy through activation of the MEK/ERK pathway José Manuel Bravo‐San Pedro, Mireia Niso‐Santano, Rubén Gómez‐Sánchez, Cellular and Molecular Life Sciences Cell AutophagyMitophagySignal TransductionSignaling PathwayCell Regulation	2012	177
Alzheimer’s disease cerebrospinal fluid biomarker in cognitively normal subjects Jon B. Toledo, Henrik Zetterberg, Argonde C. van Harten, Brain	2015	139
Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementia Oriol Dols‐Icardo, María J. Bullido, Pau Pástor, Neurobiology of Aging Alzheimer's DiseaseDementiaPathologyRisk FactorVascular Dementia	2013	119
LRRK2 G2019S and R1441G mutations associated with Parkinson’s disease are common in the Basque Country, but relative prevalence is determined by ethnicity Ana Gorostidi, Javier Ruiz‐Martínez, Adolfo López de Munaín, Neurogenetics R1441g MutationsGenetic DisorderParkinson DiseaseGeneticsGenetic Epidemiology	2008	79
Neuropathology of Parkinson's disease with the R1441G mutation in <i>LRRK2</i> J.F. Martí-Massó, Javier Ruiz‐Martínez, Maria J. Bolaño, Movement Disorders Corticobasal DegenerationNeurological DisorderPathologySocial SciencesNeurobiology Of Disease	2009	73
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population‐Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight Sara Bandrés‐Ciga, Sarah Ahmed, Marya S. Sabir, Movement Disorders	2019	70
Mutations in Progranulin Gene: Clinical, Pathological, and Ribonucleic Acid Expression Findings Adolfo López de Munaín, Ainhoa Alzualde, Ana Gorostidi, Biological Psychiatry Mendelian DisorderGenetic DisorderMedicineGeneticsProteomics	2008	65
Functional network resilience to pathology in presymptomatic genetic frontotemporal dementia Timothy Rittman, Robin Borchert, Simon Jones, Neurobiology of Aging	2019	62
Differential early subcortical involvement in genetic FTD within the GENFI cohort Martina Bocchetta, Emily Todd, Georgia Peakman, NeuroImage Clinical	2021	62

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