Christopher M. Gómez

9.9k total citations · 1 hit paper
158 papers, 6.7k citations indexed

About

Christopher M. Gómez is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Christopher M. Gómez has authored 158 papers receiving a total of 6.7k indexed citations (citations by other indexed papers that have themselves been cited), including 113 papers in Molecular Biology, 103 papers in Cellular and Molecular Neuroscience and 68 papers in Neurology. Recurrent topics in Christopher M. Gómez's work include Genetic Neurodegenerative Diseases (97 papers), Mitochondrial Function and Pathology (72 papers) and Ion channel regulation and function (30 papers). Christopher M. Gómez is often cited by papers focused on Genetic Neurodegenerative Diseases (97 papers), Mitochondrial Function and Pathology (72 papers) and Ion channel regulation and function (30 papers). Christopher M. Gómez collaborates with scholars based in United States, Canada and Australia. Christopher M. Gómez's co-authors include David P. Richman, S. H. Subramony, Susan Perlman, Lawrence J. Schut, Leroy Hood, Randall M. Thompson, H. Brent Clark, Khalaf Bushara, Xiaofei Du and Vipin Kumar and has published in prestigious journals such as Nature, New England Journal of Medicine and Cell.

In The Last Decade

Christopher M. Gómez

153 papers receiving 6.6k citations

Hit Papers

International Cooperative... 1997 2026 2006 2016 1997 250 500 750 1000

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Christopher M. Gómez 3.7k 3.5k 2.4k 708 619 158 6.7k
Koujiro Tohyama 1.7k 0.5× 2.6k 0.7× 1.2k 0.5× 1.1k 1.5× 660 1.1× 81 5.9k
Corinna Bürger 2.7k 0.7× 2.3k 0.7× 1.6k 0.7× 479 0.7× 736 1.2× 66 6.3k
Jaap J. Plomp 2.6k 0.7× 2.8k 0.8× 2.5k 1.0× 305 0.4× 248 0.4× 91 6.1k
Imaharu Nakano 2.6k 0.7× 2.1k 0.6× 3.7k 1.5× 1.3k 1.8× 249 0.4× 238 7.0k
Matteo Caleo 1.8k 0.5× 2.4k 0.7× 1.4k 0.6× 1.0k 1.4× 258 0.4× 141 6.3k
Lucio Santoro 1.6k 0.4× 2.9k 0.8× 3.5k 1.5× 999 1.4× 375 0.6× 254 7.0k
Marina Mata 2.0k 0.6× 2.9k 0.8× 753 0.3× 414 0.6× 178 0.3× 125 5.9k
Matthias Klugmann 3.6k 1.0× 3.3k 1.0× 465 0.2× 1.0k 1.4× 211 0.3× 99 7.4k
Owain W. Howell 1.8k 0.5× 1.9k 0.5× 1.2k 0.5× 1.8k 2.6× 411 0.7× 58 7.0k
John Forsayeth 3.6k 1.0× 2.7k 0.8× 1.2k 0.5× 259 0.4× 336 0.5× 118 6.6k

Countries citing papers authored by Christopher M. Gómez

Since Specialization
Citations

This map shows the geographic impact of Christopher M. Gómez'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 Christopher M. Gómez with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christopher M. Gómez more than expected).

Fields of papers citing papers by Christopher M. Gómez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher M. Gómez. 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 Christopher M. Gómez. The network helps show where Christopher M. Gómez may publish in the future.

Co-authorship network of co-authors of Christopher M. Gómez

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher M. Gómez. A scholar is included among the top collaborators of Christopher M. Gómez 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 Christopher M. Gómez. Christopher M. Gómez is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Lin, Chi‐Ying, Theresa A. Boyle, Jeremy D. Schmahmann, et al.. (2024). Early-Life Social Determinants of SCA6 Age at Onset, Severity, and Progression. The Cerebellum. 23(4). 1449–1456.
2.
Rezania, Kourosh, et al.. (2023). Pontine stroke in a patient with Chronic Progressive External Ophthalmoplegia (CPEO): a case report. BMC Neurology. 23(1). 231–231. 2 indexed citations
3.
Gómez, Christopher M., et al.. (2023). Characterization of a chronic cough in cerebellar ataxia, neuropathy, vestibular areflexia syndrome. Laryngoscope Investigative Otolaryngology. 8(3). 730–738. 10 indexed citations
4.
Rummey, Christian, Louise A. Corben, Martin B. Delatycki, et al.. (2022). Natural History of Friedreich Ataxia. Neurology. 99(14). e1499–e1510. 33 indexed citations
5.
Godfrey, Jack D., et al.. (2022). HER2 c-Terminal Fragments Are Expressed via Internal Translation of the HER2 mRNA. International Journal of Molecular Sciences. 23(17). 9549–9549. 3 indexed citations
6.
Pérez, B., Hannah K. Shorrock, Mónica Báñez-Coronel, et al.. (2021). CCG•CGG interruptions in high‐penetrance SCA8 families increase RAN translation and protein toxicity. EMBO Molecular Medicine. 13(11). e14095–e14095. 16 indexed citations
7.
Dubrovsky, Genia, Minh Ly Nguyen, Christopher M. Gómez, et al.. (2021). Parental attitudes towards choosing between operative and nonoperative management of pediatric acute appendicitis. Journal of Pediatric Surgery. 57(8). 1592–1598. 5 indexed citations
8.
Rummey, Christian, John M. Flynn, Louise A. Corben, et al.. (2021). Scoliosis in Friedreich's ataxia: longitudinal characterization in a large heterogeneous cohort. Annals of Clinical and Translational Neurology. 8(6). 1239–1250. 17 indexed citations
9.
Sidtis, John J. & Christopher M. Gómez. (2021). Genotypic Differences in Networks Supporting Regional Predictors of Speech Rate in Spinocerebellar Ataxia: Preliminary Observations. Brain Connectivity. 11(6). 408–417.
10.
Wong, Darice Y., Claudio M. de Gusmão, May Sanyoura, et al.. (2020). Prevalence of RFC1 -mediated spinocerebellar ataxia in a North American ataxia cohort. Neurology Genetics. 6(3). e440–e440. 32 indexed citations
11.
Du, Xiaofei, João L. Carvalho-de-Souza, Willy Carrasquel-Ursulaez, et al.. (2020). Loss-of-function BK channel mutation causes impaired mitochondria and progressive cerebellar ataxia. Proceedings of the National Academy of Sciences. 117(11). 6023–6034. 56 indexed citations
12.
Wong, Darice Y., Claudio M. de Gusmão, May Sanyoura, et al.. (2020). Prevalence of RFC1-Mediated Spinocerebellar Ataxia in a North American Ataxia Cohort. Annals of Neurology. 88. 3 indexed citations
13.
Joers, James M., Dinesh K. Deelchand, Tianmeng Lyu, et al.. (2018). Neurochemical abnormalities in premanifest and early spinocerebellar ataxias. Annals of Neurology. 83(4). 816–829. 53 indexed citations
14.
Sun, Miao, Amy Knight Johnson, Viswateja Nelakuditi, et al.. (2018). Targeted exome analysis identifies the genetic basis of disease in over 50% of patients with a wide range of ataxia-related phenotypes. Genetics in Medicine. 21(1). 195–206. 49 indexed citations
15.
Carvalho-de-Souza, João L., Tomoya Kubota, Xiaofei Du, et al.. (2016). A Missense Mutation in the Selectivity Filter of BK Affects the Channel's Potassium Conductance. Biophysical Journal. 110(3). 449a–449a. 5 indexed citations
16.
Moscovich, Mariana, Michael S. Okun, Christopher G. Favilla, et al.. (2014). Clinical Evaluation of Eye Movements in Spinocerebellar Ataxias. Journal of Neuro-Ophthalmology. 35(1). 16–21. 46 indexed citations
17.
Du, Xiaofei, Jun Wang, Haipeng Zhu, et al.. (2013). Second Cistron in CACNA1A Gene Encodes a Transcription Factor Mediating Cerebellar Development and SCA6. Cell. 154(1). 118–133. 132 indexed citations
18.
Watase, Kei, Curtis F. Barrett, Taisuke Miyazaki, et al.. (2008). Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant Ca V 2.1 channels. Proceedings of the National Academy of Sciences. 105(33). 11987–11992. 122 indexed citations
19.
Maschke, Matthias, Gary W. Oehlert, Susan Perlman, et al.. (2005). Clinical feature profile of spinocerebellar ataxia type 1–8 predicts genetically defined subtypes. Movement Disorders. 20(11). 1405–1412. 44 indexed citations
20.
Gómez, Christopher M., David P. Richman, & Phillip W. Berman. (1979). Monoclonal anti-acetylcholine receptor antibodies: Evidence for multiple pharmacologic specificities. Federation Proceedings. 38. 1 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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