Kevin Esoh

842 total citations · 1 hit paper
26 papers, 478 citations indexed

About

Kevin Esoh is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Kevin Esoh has authored 26 papers receiving a total of 478 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 8 papers in Sensory Systems and 6 papers in Genetics. Recurrent topics in Kevin Esoh's work include Hearing, Cochlea, Tinnitus, Genetics (8 papers), vaccines and immunoinformatics approaches (3 papers) and Cancer-related molecular mechanisms research (3 papers). Kevin Esoh is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (8 papers), vaccines and immunoinformatics approaches (3 papers) and Cancer-related molecular mechanisms research (3 papers). Kevin Esoh collaborates with scholars based in South Africa, United States and Ghana. Kevin Esoh's co-authors include Ambroise Wonkam, Robert Adamu Shey, Stephen Mbigha Ghogomu, Cabirou Mounchili Shintouo, Jacob Souopgui, Luc Vanhamme, Derrick Neba Nebangwa, Francis N. Nkemngo, Guida Landouré and Isabelle Schrauwen and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Human Molecular Genetics.

In The Last Decade

Kevin Esoh

23 papers receiving 471 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

In-silico design of a multi-epitope vaccine candidate against onchocerciasis and related filarial diseases

2019 263 citations Robert Adamu Shey, Stephen Mbigha Ghogomu et al. Scientific Reports profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kevin Esoh South Africa	10	339	116	116	84	53	26	478
Ryan McCormack United States	14	243 0.7×	89 0.8×	15 0.1×	204 2.4×	35 0.7×	26	591
Brooke Harmon United States	11	139 0.4×	167 1.4×	31 0.3×	92 1.1×	14 0.3×	16	443
H. Bunschoten Netherlands	11	152 0.4×	64 0.6×	73 0.6×	106 1.3×	15 0.3×	14	505
Thibaut Pelat France	20	516 1.5×	150 1.3×	415 3.6×	208 2.5×	9 0.2×	34	952
Daniel M. Kozink United States	10	90 0.3×	71 0.6×	81 0.7×	206 2.5×	31 0.6×	12	516
H. J. Wellensiek Germany	9	285 0.8×	237 2.0×	26 0.2×	223 2.7×	49 0.9×	21	751
Christin M. Hong United States	6	300 0.9×	197 1.7×	122 1.1×	241 2.9×	6 0.1×	9	799
Angeline Lim Singapore	13	210 0.6×	196 1.7×	145 1.3×	105 1.3×	7 0.1×	17	573
Debra A. Barnes United States	13	185 0.5×	85 0.7×	31 0.3×	251 3.0×	12 0.2×	19	708
Lucía Moro Argentina	16	352 1.0×	210 1.8×	33 0.3×	54 0.6×	28 0.5×	48	783

Countries citing papers authored by Kevin Esoh

Since Specialization

Citations

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

Fields of papers citing papers by Kevin Esoh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kevin Esoh

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

All Works

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20 of 20 papers shown

Esoh, Kevin, et al.. (2025). Enhancing Large-Scale Pharmacogenetic Studies in African Populations for Clinical Care and Drug Development. The Annual Review of Pharmacology and Toxicology. 66(1). 171–190.

Esoh, Kevin, et al.. (2025). Parasite-resistant variants in African genomes: implications for global genetic medicine. Trends in Parasitology. 41(7). 536–546.

Schrauwen, Isabelle, Anushree Acharya, Rachel Latanich, et al.. (2024). Whole-exome sequencing reveals known and candidate genes for hearing impairment in Mali. Human Genetics and Genomics Advances. 6(1). 100391–100391.

Rebelo, Adriana, Lassana Cissé, Lynette Rives, et al.. (2023). Novel variant in CADM3 causes Charcot–Marie–Tooth disease. Brain Communications. 5(5). fcad227–fcad227. 2 indexed citations

Esoh, Kevin, Tobias O. Apinjoh, Alfred Amambua‐Ngwa, et al.. (2023). Genome-wide association study identifies novel candidate malaria resistance genes in Cameroon. Human Molecular Genetics. 32(12). 1946–1958. 5 indexed citations

Adadey, Samuel Mawuli, Kevin Esoh, Anushree Acharya, et al.. (2022). A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana. BMC Medical Genomics. 15(1). 237–237. 4 indexed citations

Adadey, Samuel Mawuli, Kevin Esoh, Carmen De Kock, et al.. (2022). Cell-based analysis of CLIC5A and SLC12A2 variants associated with hearing impairment in two African families. Frontiers in Genetics. 13. 924904–924904. 1 indexed citations

Asante-Poku, Adwoa, Stephen Osei-Wusu, Samuel Yaw Aboagye, et al.. (2022). Genetic Analysis of TB Susceptibility Variants in Ghana Reveals Candidate Protective Loci in SORBS2 and SCL11A1 Genes. Frontiers in Genetics. 12. 729737–729737. 5 indexed citations

Shey, Robert Adamu, Stephen Mbigha Ghogomu, Derrick Neba Nebangwa, et al.. (2022). Rational design of a novel multi-epitope peptide-based vaccine against Onchocerca volvulus using transmembrane proteins. Frontiers in Tropical Diseases. 3. 2 indexed citations

10.

Esoh, Kevin, et al.. (2022). Current profile of Charcot‐Marie‐Tooth disease in Africa: A systematic review. Journal of the Peripheral Nervous System. 27(2). 100–112. 8 indexed citations

11.

Adadey, Samuel Mawuli, Kevin Esoh, Mario Jonas, et al.. (2022). Age Estimate of GJB2-p.(Arg143Trp) Founder Variant in Hearing Impairment in Ghana, Suggests Multiple Independent Origins across Populations. Biology. 11(3). 476–476. 7 indexed citations

12.

Wonkam, Ambroise, Nchangwi Syntia Munung, Collet Dandara, et al.. (2022). Five Priorities of African Genomics Research: The Next Frontier. Annual Review of Genomics and Human Genetics. 23(1). 499–521. 16 indexed citations

13.

Esoh, Kevin, et al.. (2021). Sickle cell disease in sub-Saharan Africa: transferable strategies for prevention and care. The Lancet Haematology. 8(10). e744–e755. 28 indexed citations

14.

Adadey, Samuel Mawuli, Isabelle Schrauwen, Kevin Esoh, et al.. (2021). Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment. Journal of Human Genetics. 66(12). 1169–1175. 10 indexed citations

15.

Ouso, Daniel O., et al.. (2021). Open Science in Kenya: Where Are We?. SHILAP Revista de lepidopterología. 6. 669675–669675. 12 indexed citations

16.

Esoh, Kevin, Tobias O. Apinjoh, Steven Ger Nyanjom, et al.. (2021). Fine scale human genetic structure in three regions of Cameroon reveals episodic diversifying selection. Scientific Reports. 11(1). 1039–1039. 3 indexed citations

17.

Shey, Robert Adamu, Stephen Mbigha Ghogomu, Cabirou Mounchili Shintouo, et al.. (2021). Computational Design and Preliminary Serological Analysis of a Novel Multi-Epitope Vaccine Candidate Against Onchocerciasis and Related Filarial Diseases. Pathogens. 10(2). 99–99. 19 indexed citations

18.

Schrauwen, Isabelle, Shaheen Mowla, Cedrik Tekendo‐Ngongang, et al.. (2021). A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family. Genes. 12(11). 1765–1765. 7 indexed citations

19.

Adadey, Samuel Mawuli, et al.. (2020). GJB4andGJC3variants in non-syndromic hearing impairment in Ghana. Experimental Biology and Medicine. 245(15). 1355–1367. 4 indexed citations

20.

Shey, Robert Adamu, Stephen Mbigha Ghogomu, Kevin Esoh, et al.. (2019). In-silico design of a multi-epitope vaccine candidate against onchocerciasis and related filarial diseases. Scientific Reports. 9(1). 4409–4409. 263 indexed citations breakdown →

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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