Ana Sánchez‐Monteagudo

Author

Centro de Investigacion Principe Felipe ORCID

Also Known As

A. Sánchez‐Monteagudo, Ana Sánchez-Monteagudo, Ana Sánchez‐Monteagudo

Publications

325

Citations

H-Index

Concepts

All Affiliations

Centro de Investigacion Principe Felipe Instituto de Investigación Sanitaria La Fe Hospital Universitari i Politècnic La Fe Universitat de València Centro de Investigación Biomédica en Red

About

Ana Sánchez‐Monteagudo is an author at Centro de Investigacion Principe Felipe specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	112
2	Public Health	2	2	58
3	Epidemiology	2	2	58
4	Social Sciences	1	1	20
5	Molecular Biology	1	1	29

Ana Sánchez‐Monteagudo

Publications

279

Citations

H-Index

Page 1

	Year	Citations
Distal hereditary motor neuropathies: Mutation spectrum and genotype–phenotype correlation Marina Frasquet, Ricard Rojas‐García, Herminia Argente‐Escrig, European Journal of Neurology	2020	67
A newly distal hereditary motor neuropathy caused by a rare AIFM1 mutation Paula Sancho, Ana Sánchez‐Monteagudo, Antonio Collado, Neurogenetics Rare DiseasesMendelian DisorderNeurological DisorderGenetic DisorderGenetics	2017	34
Genetics of Wilson disease and Wilson‐like phenotype in a clinical series from eastern Spain Ana Sánchez‐Monteagudo, Isabel Sastre, Irene Martínez‐Torres, Clinical Genetics GeneticsGenetic EpidemiologyPathologyMolecular BiologyMolecular Genetics	2020	29
Wilson disease: revision of diagnostic criteria in a clinical series with great genetic homogeneity Luis García‐Villarreal, Andrea Hernández-Ortega, Ana Sánchez‐Monteagudo, Journal of Gastroenterology Mendelian DisorderDiagnostic CriteriaGenetic DisorderGeneticsInherited Metabolic Disease	2020	29
Characterising the phenotype and mode of inheritance of patients with inherited peripheral neuropathies carrying <i>MME</i> mutations Vincenzo Lupo, Marina Frasquet, Ana Sánchez‐Monteagudo, Journal of Medical Genetics	2018	24
Molecular and functional characterization of the BMPR2 gene in Pulmonary Arterial Hypertension Guillermo Pousada, Vincenzo Lupo, Sheila Castro‐Sánchez, Scientific Reports	2017	22
<i>NR4A2</i> Mutations Can Cause Intellectual Disability and Language Impairment With Persistent Dystonia-Parkinsonism Silvia Jesús, Isabel Hinarejos, Fátima Carrillo, Neurology Genetics Nr4a2/nurr1 GeneNeurological DisorderGeneticsSocial SciencesNeurobiology Of Disease	2021	20
Expanding the β-III Spectrin-Associated Phenotypes toward Non-Progressive Congenital Ataxias with Neurodegeneration Paula Sancho, Amparo Andrés-Bordería, Nerea Gorría-Redondo, International Journal of Molecular Sciences	2021	17
Clinical spectrum of <i>BICD2</i> mutations Marina Frasquet, Ángela Flox Camacho, Roger Vílchez, European Journal of Neurology	2020	14
Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias Dolores Martínez‐Rubio, Isabel Hinarejos, Paula Sancho, International Journal of Molecular Sciences	2022	13

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