Paloma González-Pérez

1.5k total citations
13 papers, 247 citations indexed

About

Paloma González-Pérez is a scholar working on Neurology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Paloma González-Pérez has authored 13 papers receiving a total of 247 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Neurology, 6 papers in Molecular Biology and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Paloma González-Pérez's work include Neurogenetic and Muscular Disorders Research (4 papers), Parkinson's Disease Mechanisms and Treatments (4 papers) and Genetic Neurodegenerative Diseases (4 papers). Paloma González-Pérez is often cited by papers focused on Neurogenetic and Muscular Disorders Research (4 papers), Parkinson's Disease Mechanisms and Treatments (4 papers) and Genetic Neurodegenerative Diseases (4 papers). Paloma González-Pérez collaborates with scholars based in United States, Spain and Chile. Paloma González-Pérez's co-authors include Robert H. Brown, Peter C. Sapp, Ana Carolina Ruíz-Fernández, Ru-Ju Chian, Guy A. Rouleau, Claudio Hetz, Patrick A. Dion, Hussein Daoud, Ute Woehlbier and Claire S. Leblond and has published in prestigious journals such as Neurology, Gene and Neurobiology of Disease.

In The Last Decade

Paloma González-Pérez

13 papers receiving 238 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Paloma González-Pérez United States 8 92 85 70 61 52 13 247
Stayko Sarafov Bulgaria 9 215 2.3× 68 0.8× 37 0.5× 29 0.5× 40 0.8× 20 297
Raphael M. Buzzi Switzerland 11 90 1.0× 79 0.9× 36 0.5× 29 0.5× 18 0.3× 22 281
Junko Fujitake Japan 10 303 3.3× 69 0.8× 86 1.2× 32 0.5× 25 0.5× 22 414
Claudia Stancanelli Italy 10 251 2.7× 28 0.3× 61 0.9× 38 0.6× 24 0.5× 17 314
Bianca M. de Graaf Netherlands 9 301 3.3× 41 0.5× 32 0.5× 135 2.2× 94 1.8× 15 458
Monica Gagliardi Italy 9 99 1.1× 70 0.8× 18 0.3× 46 0.8× 23 0.4× 33 257
Saori Morozumi Japan 9 65 0.7× 202 2.4× 31 0.4× 87 1.4× 17 0.3× 17 330
Marie‐Laure Martin‐Négrier France 12 178 1.9× 85 1.0× 30 0.4× 73 1.2× 14 0.3× 22 305
Alessia Perna Italy 11 130 1.4× 54 0.6× 19 0.3× 124 2.0× 11 0.2× 36 303
Ulf Drugge Sweden 11 328 3.6× 118 1.4× 101 1.4× 89 1.5× 29 0.6× 26 501

Countries citing papers authored by Paloma González-Pérez

Since Specialization
Citations

This map shows the geographic impact of Paloma González-Pérez's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Paloma González-Pérez with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Paloma González-Pérez more than expected).

Fields of papers citing papers by Paloma González-Pérez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paloma González-Pérez. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Paloma González-Pérez. The network helps show where Paloma González-Pérez may publish in the future.

Co-authorship network of co-authors of Paloma González-Pérez

This figure shows the co-authorship network connecting the top 25 collaborators of Paloma González-Pérez. A scholar is included among the top collaborators of Paloma González-Pérez based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Paloma González-Pérez. Paloma González-Pérez is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

13 of 13 papers shown
1.
González-Pérez, Paloma, et al.. (2023). Cancer and Myotonic Dystrophy. Journal of Clinical Medicine. 12(5). 1939–1939. 10 indexed citations
2.
González-Pérez, Paloma, et al.. (2023). Parent-of-Origin Effect on the Age at Symptom Onset in Myotonic Dystrophy Type 2. Neurology Genetics. 9(3). e200073–e200073. 2 indexed citations
3.
David, William S., et al.. (2023). Frequency and type of cancers in myotonic dystrophy: A retrospective cross‐sectional study. Muscle & Nerve. 68(2). 142–148. 9 indexed citations
4.
González-Pérez, Paloma, et al.. (2022). Neuropathic Pain as Main Manifestation of POLG-Related Disease: A Case Report. Frontiers in Neurology. 13. 846110–846110. 1 indexed citations
5.
González-Pérez, Paloma, et al.. (2020). Clinical and electrophysiological evaluation of myasthenic features in an alpha-dystroglycanopathy cohort (FKRP-predominant). Neuromuscular Disorders. 30(3). 213–218. 4 indexed citations
6.
Kim, Eun Joo, et al.. (2020). Antisense oligonucleotide and adjuvant exercise therapy reverse fatigue in old mice with myotonic dystrophy. Molecular Therapy — Nucleic Acids. 23. 393–405. 18 indexed citations
7.
González-Pérez, Paloma, Matthew Torre, Jeffrey Helgager, & Anthony A. Amato. (2019). Proximal muscle weakness. Practical Neurology. 19(4). 321–325. 2 indexed citations
8.
González-Pérez, Paloma, Marcelo Correia, Arístides A. Capizzano, & Harold P. Adams. (2016). Isolated cortical vein thrombosis in autoimmune polyglandular syndrome type 2. Neurology. 86(13). 1262–1263. 2 indexed citations
9.
González-Pérez, Paloma, Ute Woehlbier, Ru-Ju Chian, et al.. (2015). Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patients. Gene. 566(2). 158–165. 58 indexed citations
10.
González-Pérez, Paloma, Yubing Lu, Ru-Ju Chian, et al.. (2012). Association of UBQLN1 mutation with Brown–Vialetto–Van Laere syndrome but not typical ALS. Neurobiology of Disease. 48(3). 391–398. 17 indexed citations
11.
González-Pérez, Paloma, Elizabeth T. Cirulli, Vivian E. Drory, et al.. (2012). Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosis. Neurology. 79(22). 2201–2208. 47 indexed citations
12.
González-Pérez, Paloma, P. Gallano, Lidia González‐Quereda, et al.. (2008). Phenotypic variability in a Spanish family with a Caveolin-3 mutation. Journal of the Neurological Sciences. 276(1-2). 95–98. 15 indexed citations
13.
González-Pérez, Paloma, et al.. (2006). Peripheral arterial disease in patients with stages IV and V chronic renal failure. Nephrology Dialysis Transplantation. 21(12). 3525–3531. 62 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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2026