Elias Gbeha

1.1k total citations
10 papers, 393 citations indexed

About

Elias Gbeha is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Elias Gbeha has authored 10 papers receiving a total of 393 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Elias Gbeha's work include RNA modifications and cancer (2 papers), Evolution and Genetic Dynamics (2 papers) and Hemoglobinopathies and Related Disorders (2 papers). Elias Gbeha is often cited by papers focused on RNA modifications and cancer (2 papers), Evolution and Genetic Dynamics (2 papers) and Hemoglobinopathies and Related Disorders (2 papers). Elias Gbeha collaborates with scholars based in Canada, Benin and United Kingdom. Elias Gbeha's co-authors include Philip Awadalla, Jean‐Christophe Grenier, Youssef Idaghdour, Alan Hodgkinson, Vanessa Bruat, Jean-Philippe Goulet, Ambaliou Sanni, Julie Hussin, Mohamed Chérif Rahimy and Jacklyn Quinlan and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Elias Gbeha

10 papers receiving 388 citations

Peers

Elias Gbeha
Michael D. Kessler United States
Rakesh Tamang India
Baofeng Huang China
Silvia Gravina United States
Gail C. Ekman United States
Antoine Molaro United States
Arvind Babu United States
Simone Ecker United Kingdom
David A. Skerrett‐Byrne Australia
Ana S. Quina Portugal
Michael D. Kessler United States
Elias Gbeha
Citations per year, relative to Elias Gbeha Elias Gbeha (= 1×) peers Michael D. Kessler

Countries citing papers authored by Elias Gbeha

Since Specialization
Citations

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

Fields of papers citing papers by Elias Gbeha

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elias Gbeha

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

All Works

10 of 10 papers shown
1.
Favé, Marie‐Julie, Fabien C. Lamaze, David Soave, et al.. (2018). Gene-by-environment interactions in urban populations modulate risk phenotypes. Nature Communications. 9(1). 827–827. 80 indexed citations
2.
Peischl, Stephan, Isabelle Dupanloup, Adrien Foucal, et al.. (2017). Relaxed Selection During a Recent Human Expansion. Genetics. 208(2). 763–777. 42 indexed citations
3.
Diawara, Aïssatou, Elias Gbeha, Philip Awadalla, et al.. (2016). Comparative Analysis of Iron Homeostasis in Sub-Saharan African Children with Sickle Cell Disease and Their Unaffected Siblings. Frontiers in Pediatrics. 4. 8–8. 7 indexed citations
4.
Hodgkinson, Alan, Jean‐Christophe Grenier, Elias Gbeha, & Philip Awadalla. (2016). A haplotype-based normalization technique for the analysis and detection of allele specific expression. BMC Bioinformatics. 17(1). 364–364. 5 indexed citations
5.
Hussin, Julie, Alan Hodgkinson, Youssef Idaghdour, et al.. (2015). Recombination affects accumulation of damaging and disease-associated mutations in human populations. Nature Genetics. 47(4). 400–404. 56 indexed citations
6.
Quinlan, Jacklyn, Youssef Idaghdour, Jean-Philippe Goulet, et al.. (2014). Genomic architecture of sickle cell disease in West African children. Frontiers in Genetics. 5. 26–26. 12 indexed citations
7.
Hodgkinson, Alan, Youssef Idaghdour, Elias Gbeha, et al.. (2014). High-Resolution Genomic Analysis of Human Mitochondrial RNA Sequence Variation. Science. 344(6182). 413–415. 74 indexed citations
8.
Idaghdour, Youssef, Jacklyn Quinlan, Jean-Philippe Goulet, et al.. (2012). Evidence for additive and interaction effects of host genotype and infection in malaria. Proceedings of the National Academy of Sciences. 109(42). 16786–16793. 70 indexed citations
9.
Lefebvre, J, Claudia Moreau, Elias Gbeha, et al.. (2011). An X-Linked Haplotype of Neandertal Origin Is Present Among All Non-African Populations. Molecular Biology and Evolution. 28(7). 1957–1962. 34 indexed citations
10.
Sirois, Francine, Elias Gbeha, Ambaliou Sanni, et al.. (2008). Ethnic Differences in the Frequency of the Cardioprotective C679X PCSK9 Mutation in a West African Population. Genetic Testing. 12(3). 377–380. 13 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