Sergio Córdova

951 total citations
12 papers, 441 citations indexed

About

Sergio Córdova is a scholar working on Genetics, Psychiatry and Mental health and Rheumatology. According to data from OpenAlex, Sergio Córdova has authored 12 papers receiving a total of 441 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Psychiatry and Mental health and 6 papers in Rheumatology. Recurrent topics in Sergio Córdova's work include Genetics and Neurodevelopmental Disorders (8 papers), Epilepsy research and treatment (7 papers) and Glycogen Storage Diseases and Myoclonus (6 papers). Sergio Córdova is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Epilepsy research and treatment (7 papers) and Glycogen Storage Diseases and Myoclonus (6 papers). Sergio Córdova collaborates with scholars based in Mexico, Honduras and United States. Sergio Córdova's co-authors include Marco T. Medina, P Loiseau, Jean‐François Dartigues, S Cohadon, B Duché, Antonio V. Delgado‐Escueta, José M. Serratosa, Ma. Elisa Alonso, Óscar H. Del Brutto and R S Sparkes and has published in prestigious journals such as Epilepsia, Neuroscience Letters and Epilepsy Research.

In The Last Decade

Sergio Córdova

12 papers receiving 418 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sergio Córdova Mexico 10 284 176 142 120 89 12 441
Marie-Odile Livet France 13 161 0.6× 257 1.5× 45 0.3× 127 1.1× 182 2.0× 20 631
Gregorio Pineda Spain 5 252 0.9× 156 0.9× 131 0.9× 97 0.8× 118 1.3× 6 408
Rebekka Kretz Germany 12 403 1.4× 111 0.6× 169 1.2× 261 2.2× 123 1.4× 16 627
Dianela Claps Italy 12 301 1.1× 135 0.8× 98 0.7× 167 1.4× 92 1.0× 15 473
H Gerken Germany 11 348 1.2× 115 0.7× 185 1.3× 151 1.3× 70 0.8× 25 523
Noriyuki Akasaka Japan 14 214 0.8× 245 1.4× 122 0.9× 122 1.0× 175 2.0× 27 566
B. Dalla Bernardina Italy 11 354 1.2× 60 0.3× 158 1.1× 135 1.1× 126 1.4× 16 509
Nienke E. Verbeek Netherlands 18 351 1.2× 392 2.2× 152 1.1× 136 1.1× 308 3.5× 23 777
Paola Diadori Canada 10 179 0.6× 109 0.6× 147 1.0× 114 0.9× 86 1.0× 16 425
Katsuyuki Fukushima Japan 8 352 1.2× 161 0.9× 228 1.6× 131 1.1× 231 2.6× 14 567

Countries citing papers authored by Sergio Córdova

Since Specialization
Citations

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

Fields of papers citing papers by Sergio Córdova

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sergio Córdova. 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 Sergio Córdova. The network helps show where Sergio Córdova may publish in the future.

Co-authorship network of co-authors of Sergio Córdova

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

All Works

12 of 12 papers shown
1.
Suzuki, Toshimitsu, Antonio V. Delgado‐Escueta, María Elisa Alonso, et al.. (2006). Mutation analyses of genes on 6p12-p11 in patients with juvenile myoclonic epilepsy. Neuroscience Letters. 405(1-2). 126–131. 11 indexed citations
2.
Delgado‐Escueta, Antonio V., Dongsheng Bai, Julia N. Bailey, et al.. (2003). Recent Developments in the Quest for Myoclonic Epilepsy Genes. Epilepsia. 44(s11). 13–26. 14 indexed citations
3.
Suzuki, Toshimitsu, Ryoji Morita, Yoshihisa Sugimoto, et al.. (2002). Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11–p12: LRRC1, GCLC, KIAA0057 and CLIC5. Epilepsy Research. 50(3). 265–275. 10 indexed citations
4.
Bai, Dongsheng, María Elisa Alonso, Marco T. Medina, et al.. (2002). Juvenile myoclonic epilepsy: Linkage to chromosome 6p12 in Mexico families. American Journal of Medical Genetics. 113(3). 268–274. 28 indexed citations
5.
Delgado‐Escueta, Antonio V., Dongsheng Bai, Julia N. Bailey, et al.. (2002). Epilepsia mioclínica juvenil del cromosoma 6p12: Avances clínicos y genéticos. Revista de Neurología. 35(1). 82–82. 1 indexed citations
6.
Córdova, Sergio, et al.. (2000). Fixed, Dilated Pupils in the ICU: Another Recoverable Cause. Anaesthesia and Intensive Care. 28(1). 91–93. 5 indexed citations
7.
Delgado‐Escueta, Antonio V., Marco T. Medina, José M. Serratosa, et al.. (1999). Mapping and positional cloning of common idiopathic generalized epilepsies: juvenile myoclonus epilepsy and childhood absence epilepsy.. PubMed. 79. 351–74. 36 indexed citations
8.
Delgado‐Escueta, Antonio V., Manyee Gee, José M. Serratosa, et al.. (1996). Juvenile myoclonic epilepsy in chromosome 6p12-p11: Locus heterogeneity and recombinations. American Journal of Medical Genetics. 63(3). 438–446. 54 indexed citations
9.
Delgado‐Escueta, Antonio V., et al.. (1995). Juvenile myoclonic epilepsy locus in chromosome 6p21.2-p11: linkage to convulsions and electroencephalography trait.. PubMed. 57(2). 368–81. 99 indexed citations
10.
Medina, Marco T., et al.. (1993). Effect of Anticysticercal Treatment on the Prognosis of Epilepsy in Neurocysticercosis: A Pilot Trial. Epilepsia. 34(6). 1024–1027. 32 indexed citations
11.
Córdova, Sergio, et al.. (1989). Acquired Epileptic Aphasia (the Landau‐Kleffner Syndrome) Due to Neurocysticercosis. Epilepsia. 30(5). 569–572. 46 indexed citations
12.
Loiseau, P, B Duché, Sergio Córdova, Jean‐François Dartigues, & S Cohadon. (1988). Prognosis of Benign Childhood Epilepsy with Centrotemporal Spikes: A Foliow‐Up Study of 168 Patients. Epilepsia. 29(3). 229–235. 105 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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