Mário Campos

582 total citations
40 papers, 376 citations indexed

About

Mário Campos is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Mário Campos has authored 40 papers receiving a total of 376 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 17 papers in Genetics and 10 papers in Neurology. Recurrent topics in Mário Campos's work include Genetics and Neurodevelopmental Disorders (11 papers), Autism Spectrum Disorder Research (10 papers) and Parkinson's Disease Mechanisms and Treatments (9 papers). Mário Campos is often cited by papers focused on Genetics and Neurodevelopmental Disorders (11 papers), Autism Spectrum Disorder Research (10 papers) and Parkinson's Disease Mechanisms and Treatments (9 papers). Mário Campos collaborates with scholars based in Brazil, United Kingdom and Germany. Mário Campos's co-authors include Cíntia Barros Santos-Rebouças, Márcia Mattos Gonçalves Pimentel, Jussara Mendonça dos Santos, Verônica Marques Zembrzuski, Pedro Hernán Cabello, Ana Carolina Proença da Fonseca, Denise Hack Nicaretta, João Santos Pereira, Ana Lúcia Zuma de Rosso and Giselda Maria Kalil de Cabello and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurobiology of Aging and Neuroscience Letters.

In The Last Decade

Mário Campos

38 papers receiving 366 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mário Campos Brazil 12 160 154 119 83 59 40 376
Stephanie R. Villa United States 8 73 0.5× 167 1.1× 50 0.4× 109 1.3× 42 0.7× 8 363
Zhongdong Lin China 10 84 0.5× 133 0.9× 29 0.2× 51 0.6× 30 0.5× 23 321
Alfonso Oyarzábal Spain 11 79 0.5× 242 1.6× 76 0.6× 72 0.9× 38 0.6× 18 452
Kristin Barañano United States 9 237 1.5× 228 1.5× 42 0.4× 165 2.0× 49 0.8× 21 536
Stefano Cattaneo Italy 10 97 0.6× 203 1.3× 70 0.6× 122 1.5× 90 1.5× 18 401
Noora Putkonen Finland 5 57 0.4× 249 1.6× 44 0.4× 65 0.8× 136 2.3× 5 482
Madina Makhmutova United States 7 78 0.5× 215 1.4× 16 0.1× 84 1.0× 42 0.7× 11 400
Hannah C. Saternos United States 8 65 0.4× 145 0.9× 22 0.2× 38 0.5× 125 2.1× 12 325
Bernabé I. Bustos United States 10 100 0.6× 232 1.5× 57 0.5× 102 1.2× 85 1.4× 20 364
Zarazuela Zolkipli‐Cunningham United States 14 79 0.5× 406 2.6× 32 0.3× 51 0.6× 64 1.1× 25 566

Countries citing papers authored by Mário Campos

Since Specialization
Citations

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

Fields of papers citing papers by Mário Campos

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mário Campos

This figure shows the co-authorship network connecting the top 25 collaborators of Mário Campos. A scholar is included among the top collaborators of Mário Campos 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 Mário Campos. Mário Campos 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.
Palhinha, Lohanna, Eliane Lopes Rosado, Verônica Marques Zembrzuski, et al.. (2025). Genomic deletions on 16p11.2 associated with severe obesity in Brazil. Frontiers in Endocrinology. 15. 1495534–1495534.
2.
Palhinha, Lohanna, José Firmino Nogueira Neto, Eliane Lopes Rosado, et al.. (2025). FTO rs17817449 Variant Increases the Risk of Severe Obesity in a Brazilian Cohort: A Case-Control Study. Diabetes Metabolic Syndrome and Obesity. Volume 18. 283–303. 2 indexed citations
3.
4.
Fonseca, Ana Carolina Proença da, Lohanna Palhinha, Verônica Marques Zembrzuski, et al.. (2024). Genetic variants in DBC1, SIRT1, UCP2 and ADRB2 as potential biomarkers for severe obesity and metabolic complications. Frontiers in Genetics. 15. 1363417–1363417. 2 indexed citations
5.
Rosado, Eliane Lopes, Ana Carolina Proença da Fonseca, Marcelo Ribeiro‐Alves, et al.. (2023). A Pilot Study of Dietetic, Phenotypic, and Genotypic Features Influencing Hypertensive Disorders of Pregnancy in Women with Pregestational Diabetes Mellitus. Life. 13(5). 1104–1104.
6.
Fonseca, Ana Carolina Proença da, Pedro Hernán Cabello, Melanie Rodacki, et al.. (2022). Identification of Variants Responsible for Monogenic Forms of Diabetes in Brazil. Frontiers in Endocrinology. 13. 827325–827325. 2 indexed citations
7.
Fonseca, Ana Carolina Proença da, Mário Campos, Verônica Marques Zembrzuski, et al.. (2020). Genetic Variants in the Activation of the Brown-Like Adipocyte Pathway and the Risk for Severe Obesity. Obesity Facts. 13(2). 130–143. 4 indexed citations
8.
Fonseca, Ana Carolina Proença da, Verônica Marques Zembrzuski, Mário Campos, et al.. (2020). Study of LEP, MRAP2 and POMC genes as potential causes of severe obesity in Brazilian patients. Eating and Weight Disorders - Studies on Anorexia Bulimia and Obesity. 26(5). 1399–1408. 16 indexed citations
9.
Campos, Mário, Fabiana B. Kohlrausch, João Régis Ivar Carneiro, et al.. (2020). Identification of a Rare and Potential Pathogenic MC4R Variant in a Brazilian Patient With Adulthood-Onset Severe Obesity. Frontiers in Genetics. 11. 608840–608840. 2 indexed citations
10.
Fonseca, Ana Carolina Proença da, Pedro Hernán Cabello, Melanie Rodacki, et al.. (2020). <p>Identification of the First PAX4-MODY Family Reported in Brazil</p>. Diabetes Metabolic Syndrome and Obesity. Volume 13. 2623–2631. 9 indexed citations
11.
Gubert, Fernanda, Pablo Domizi, Taís Hanae Kasai-Brunswick, et al.. (2019). Generation of patient-specific pluripotent induced stem cell line UFRJi007-A from a Brazilian familial amyotrophic lateral sclerosis patient. Stem Cell Research. 39. 101490–101490. 1 indexed citations
12.
Kupfer, Rosane, et al.. (2019). MODY probability calculator for GCK and HNF1A screening in a multiethnic background population. Archives of Endocrinology and Metabolism. 64(1). 17–23. 11 indexed citations
13.
Campos, Mário, João Santos Pereira, Marco Antônio Araújo Leite, et al.. (2016). Autosomal dominant Parkinson’s disease: Incidence of mutations in LRRK2, SNCA, VPS35 and GBA genes in Brazil. Neuroscience Letters. 635. 67–70. 16 indexed citations
14.
Campos, Mário, et al.. (2015). Levels of mannose-binding lectin in individuals with visceral leishmaniasis in the northeast region of Brazil. Genetics and Molecular Research. 14(4). 19094–19101. 1 indexed citations
15.
Campos, Mário, Ana Lúcia Zuma de Rosso, Denise Hack Nicaretta, et al.. (2012). Exon dosage variations in Brazilian patients with Parkinson's disease: analysis of SNCA, PARKIN, PINK1 and DJ-1 genes.. SHILAP Revista de lepidopterología. 32(3). 173–8. 12 indexed citations
16.
Campos, Mário, Frédérique Ponchel, Sarah M. Churchman, et al.. (2011). A MECP2 missense mutation within the MBD domain in a Brazilian male with autistic disorder. Brain and Development. 33(10). 807–809. 8 indexed citations
17.
Campos, Mário, Ana Lúcia Zuma de Rosso, João Santos Pereira, et al.. (2010). Mutational analysis of GIGYF2, ATP13A2 and GBA genes in Brazilian patients with early-onset Parkinson's disease. Neuroscience Letters. 485(2). 121–124. 19 indexed citations
18.
Campos, Mário, et al.. (2008). A MECP2 mutation in a highly conserved aminoacid causing mental retardation in a male. Brain and Development. 31(2). 176–178. 3 indexed citations
19.
Pimentel, Márcia Mattos Gonçalves, João Santos Pereira, Ana Lúcia Zuma de Rosso, et al.. (2007). A study of LRRK2 mutations and Parkinson's disease in Brazil. Neuroscience Letters. 433(1). 17–21. 29 indexed citations
20.
Santos-Rebouças, Cíntia Barros, et al.. (2006). Lack of FMR3 expression in a male with non-syndromic mental retardation and a microdeletion immediately distal to FRAXE CCG repeat. Neuroscience Letters. 397(3). 245–248. 6 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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