Paloma González-Pérez

Author

University of Massachusetts Chan Medical School ORCID

Also Known As

P. Gonzalez-Perez, Paloma Gonzalez-Perez, Paloma Gonzalez‐Perez, Paloma González-Pérez

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

University of Massachusetts Chan Medical School Harvard University Duke University Massachusetts General Hospital Hospital Universitario Virgen del Rocío

About

Paloma González-Pérez is an author at University of Massachusetts Chan Medical School specializing in medicine, genetics, and neurodegenerative diseases.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	1.1K
2	Neurology	3	3	518
3	Molecular Biology	1	1	76
4	Neuroscience	1	1	299
5	Pathology	1	1	299

Paloma González-Pérez

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis Chi-Hong Wu, Claudia Fallini, Nicola Ticozzi, Nature Neurodegenerative DiseasesAmyotrophic Lateral SclerosisDevelopmental BiologyProfilin 1Genetic Disorder	2012	594
EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans Annelies Van Hoecke, Lies Schoonaert, Robin Lemmens, Nature Medicine Neurodegenerative DiseasesAmyotrophic Lateral SclerosisNeurological DisorderDisease ModifierPathology	2012	299
ERBB4 Mutations that Disrupt the Neuregulin-ErbB4 Pathway Cause Amyotrophic Lateral Sclerosis Type 19 Yuji Takahashi, Y. Fukuda, Jun Yoshimura, The American Journal of Human Genetics Neurodegenerative DiseasesAmyotrophic Lateral SclerosisErbb4 MutationsGeneticsNeurology	2013	143
<scp>ALS</scp> ‐linked protein disulfide isomerase variants cause motor dysfunction Ute Woehlbier, Alicia Colombo, Mirva J. Saaranen, The EMBO Journal	2016	114
Peripheral arterial disease in patients with stages IV and V chronic renal failure Ana Tereza Gomes Guerrero, Rafael Montes, José Manuel Muñoz-Terol, Nephrology Dialysis Transplantation	2006	84
Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patients Paloma González-Pérez, Ute Woehlbier, Ru-Ju Chian, Gene Neurodegenerative DiseasesAmyotrophic Lateral SclerosisGeneticsMolecular BiologyNeurochemical Biomarkers	2015	76
Novel mutation in <i>VCP</i> gene causes atypical amyotrophic lateral sclerosis Paloma González-Pérez, Elizabeth T. Cirulli, Vivian E. Drory, Neurology	2012	71
Phenotypic variability in a Spanish family with a Caveolin-3 mutation Paloma González-Pérez, P. Gallano, Lidia González‐Quereda, Journal of the Neurological Sciences Genetic DisorderMedicineGeneticsEvolutionary BiologyGenetic Variation	2008	25
Antisense oligonucleotide and adjuvant exercise therapy reverse fatigue in old mice with myotonic dystrophy Ningyan Hu, Eun Joo Kim, Layal Antoury, Molecular Therapy — Nucleic Acids	2020	23
Frequency and type of cancers in myotonic dystrophy: A retrospective cross‐sectional study Eleonora S. D’Ambrosio, Kathy Chuang, William S. David, Muscle & Nerve	2023	12

Page 1