Edmond Wonkam‐Tingang

National Human Genome Research Institute

NeuroscienceBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 3%percentile

1.2Author DataRank

Indexed papers

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Hearing Impairment Overview in Africa: the Case of Cameroon

Genes(2020)10.3390/genes11020233

Top 17%

1.2DataRank

Top 17%37 citations

Jean Jacques Noubiap, Jean Valentin F. Fokouo, O. Gabriel, Séraphin Nguefack, Emile R. Chimusa +2 more

Papers

Driven by 15 papers — median percentile 83. Top paper: “Hearing Impairment Overview in Africa: the Case of Cameroon”.

Hearing Impairment Overview in Africa: the Case of Cameroon

Genes(2020)10.3390/genes11020233

Top 17%

1.2DataRank

Top 17%37 citations

Jean Jacques Noubiap, Jean Valentin F. Fokouo, O. Gabriel, Séraphin Nguefack, Emile R. Chimusa +2 more

Hearing loss in Africa: current genetic profile

Human Genetics(2021)10.1007/s00439-021-02376-y

N/A

0.477DataRank · unranked

23 citations

Edmond Wonkam‐Tingang, Elvis Twumasi Aboagye, Osbourne Quaye, Gordon A. Awandare, Ambroise Wonkam +1 more

Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes

Communications Biology(2022)10.1038/s42003-022-03326-8

N/A

0.464DataRank · unranked

21 citations

Samuel Mawuli Adadey, Isabelle Schrauwen, Elvis Twumasi Aboagye, Edmond Wonkam‐Tingang, Kevin Esoh +17 more

Cell-based analysis of CLIC5A and SLC12A2 variants associated with hearing impairment in two African families

Frontiers in Genetics(2022)10.3389/fgene.2022.924904

N/A

0.208DataRank · unranked

3 citations

Edmond Wonkam‐Tingang, Leonardo Alves de Souza Rios, Elvis Twumasi Aboagye, Kevin Esoh, Noluthando Manyisa +5 more

A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family

Experimental Biology and Medicine(2021)10.1177/1535370221999746

N/A

0DataRank · unranked

14 citations

Isabelle Schrauwen, Kevin Esoh, Thashi Bharadwaj, Liz M. Nouel‐Saied, Anushree Acharya +4 more

Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment

Journal of Human Genetics(2021)10.1038/s10038-021-00954-6

N/A

0DataRank · unranked

14 citations

Isabelle Schrauwen, Elvis Twumasi Aboagye, Thashi Bharadwaj, Kevin Esoh, Sulman Basit +10 more

Knowledge and Challenges Associated With Hearing Impairment in Affected Individuals From Cameroon (Sub-Saharan Africa)

Frontiers in Rehabilitation Sciences(2021)10.3389/fresc.2021.726761

N/A

0DataRank · unranked

9 citations

Karen Kengne Kamga, Samuel Mawuli Adadey, Séraphin Nguefack, Carmen De Kock, Nchangwi Syntia Munung +2 more

A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family

Genes(2021)10.3390/genes12111765

N/A

0DataRank · unranked

9 citations

Isabelle Schrauwen, Leonardo Alves de Souza Rios, Shaheen Mowla, Cedrik Tekendo‐Ngongang, Kalinka Popel +11 more

Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment

Genes(2023)10.3390/genes14020399

N/A

0DataRank · unranked

18 citations

Samuel Mawuli Adadey, Edmond Wonkam‐Tingang, Lucas Amenga–Etego, Gordon A. Awandare, Ambroise Wonkam +1 more

Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertension

JCI Insight(2024)10.1172/jci.insight.172152

N/A

0DataRank · unranked

4 citations

Edmond Wonkam‐Tingang, Monesha Gupta‐Malhotra, S. Shahrukh Hashmi, Yixing Han, Aarti Jajoo +19 more

Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment

Genes(2020)10.3390/genes11111249

N/A

0DataRank · unranked

20 citations

Isabelle Schrauwen, Kevin Esoh, Thashi Bharadwaj, Liz M. Nouel‐Saied, Anushree Acharya +6 more

Bi-Allelic MARVELD2 Variant Identified with Exome Sequencing in a Consanguineous Multiplex Ghanaian Family Segregating Non-Syndromic Hearing Loss

International Journal of Molecular Sciences(2025)10.3390/ijms26073337

N/A

0DataRank · unranked

0 citations

Samuel Mawuli Adadey, Leonardo Alves de Souza Rios, Kevin Esoh, Edmond Wonkam‐Tingang, Lettilia Xhakaza +9 more

Cascade Testing for Fragile X Syndrome in a Rural Setting in Cameroon (Sub-Saharan Africa)

Genes(2020)10.3390/genes11020136

N/A

0DataRank · unranked

14 citations

Séraphin Nguefack, Khuthala Minka, Edmond Wonkam‐Tingang, Alina Esterhuizen, Syntia Nchangwi Munung +3 more

DMD‐related muscular dystrophy in Cameroon: Clinical and genetic profiles

Molecular Genetics & Genomic Medicine(2020)10.1002/mgg3.1362

N/A

0DataRank · unranked

11 citations

Séraphin Nguefack, Alina Esterhuizen, David Chelo, Ambroise Wonkam, Edmond Wonkam‐Tingang

Sickle cell disease in sub-Saharan Africa: transferable strategies for prevention and care

The Lancet Haematology(2021)10.1016/s2352-3026(21)00191-5

N/A

0DataRank · unranked

78 citations

Edmond Wonkam‐Tingang, Ambroise Wonkam, Kevin Esoh

Edmond Wonkam‐Tingang

Indexed papers

Top data-sharing exemplar

Papers