Ambroise Wonkam

Also affiliated with University of Cape Town, Johns Hopkins Medicine, The Coordinating Center

MedicineBiochemistry, Genetics and Molecular BiologyNeuroscience

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 2%percentile

3.3Author DataRank

Indexed papers

6in 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 6 indexed papers 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 86 papers — median percentile 58. 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

High-depth African genomes inform human migration and health

Nature(2020)10.1038/s41586-020-2859-7

N/A

0.889DataRank · unranked

374 citations

Shaun Aron, Laura R. Botigué, Dhriti Sengupta, Gerrit Botha, Taoufik Bensellak +62 more

Systematic Review of the Economic Evaluation of Returning Incidental Findings in Genomic Research

Frontiers in Public Health(2021)10.3389/fpubh.2021.697381

N/A

0.811DataRank · unranked

9 citations

John E. Ataguba, Jantina de Vries, Ambroise Wonkam, Mayara Fontes Marx

Evolutionary history of sickle-cell mutation: implications for global genetic medicine

Human Molecular Genetics(2021)10.1093/hmg/ddab004

N/A

0.675DataRank · unranked

89 citations

Ambroise Wonkam, Kevin Esoh

The Sickle Cell Disease Ontology: recent development and expansion of the universal sickle cell knowledge representation

Database(2022)10.1093/database/baac014

Top 36%

0.540DataRank

Top 36%9 citations

Jade Hotchkiss, Victoria Nembaware, Ambroise Wonkam, Nicola Mulder, Gaston K. Mazandu

Looking ahead: ethical and social challenges of somatic gene therapy for sickle cell disease in Africa

Gene Therapy(2023)10.1038/s41434-023-00429-7

N/A

0.483DataRank · unranked

24 citations

Obiageli Nnodu, Patrick Ohiani Moru, Akpaka A Kalu, Bénido Impouma, Marsha Treadwell +2 more

Development of the sickle Pan-African research consortium registry in Tanzania: opportunity to harness data science for sickle cell disease

Frontiers in Hematology(2023)10.3389/frhem.2023.1040720

Top 40%

0.480DataRank

Top 40%14 citations

Raphael Zozimus Sangeda, Upendo Masamu, Eliah Kazumali, Agnes Jonathan, Michael Msangawale +18 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

Variants of LRP2 , encoding a multifunctional cell‐surface endocytic receptor, associated with hearing loss and retinal dystrophy

Clinical Genetics(2023)10.1111/cge.14312

N/A

0.477DataRank · unranked

23 citations

Rizwan Yousaf, Shoujun Gu, Sayaka Inagaki, Amy Turriff, Keith Pelstring +22 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

Perceptions and preferences for genetic testing for sickle cell disease or trait: a qualitative study in Cameroon, Ghana and Tanzania

European Journal of Human Genetics(2024)10.1038/s41431-024-01553-7

N/A

0.449DataRank · unranked

19 citations

Karen Kengne Kamga, Marsha Treadwell, Jemima Dennis-Antwi, Kofi A. Anie, Daima Bukini +3 more

Sickle Cell Disease in Africa: SickleInAfrica Registry in Ghana, Nigeria and Tanzania

eJHaem(2025)10.1002/jha2.70044

Top 44%

0.425DataRank

Top 44%10 citations

Wilson Mupfururirwa, Reuben Chianumba, Evans Xorse Amuzu, Daniel Kandonga, Victoria Nembaware +19 more

Establishing a database for sickle cell disease patient mapping and survival tracking: The sickle pan-african research consortium Nigeria example

Frontiers in Genetics(2022)10.3389/fgene.2022.1041462

Top 44%

0.423DataRank

Top 44%11 citations

Anazoeze Jude Madu, Reuben Chianumba, Hezekiah Isa, Isaac Olanrewaju, Samuel Osagie +10 more

Genome-wide association study identifies novel candidate malaria resistance genes in Cameroon

Human Molecular Genetics(2023)10.1093/hmg/ddad026

N/A

0.373DataRank · unranked

11 citations

Tobias O. Apinjoh, Alfred Amambua‐Ngwa, Steven Ger Nyanjom, Emile R. Chimusa, Lucas Amenga–Etego +3 more

Age Estimate of GJB2-p.(Arg143Trp) Founder Variant in Hearing Impairment in Ghana, Suggests Multiple Independent Origins across Populations

Biology(2022)10.3390/biology11030476

N/A

0.373DataRank · unranked

11 citations

Samuel Mawuli Adadey, Kevin Esoh, Mario Jonas, Carmen De Kock, Lucas Amenga–Etego +3 more

Acceptability, barriers and facilitators of using dried blood spots-point-of-care testing for sickle cell disease in Africa: an implementation science protocol for a multinational qualitative study

BMJ Open(2024)10.1136/bmjopen-2024-089056

N/A

0.373DataRank · unranked

11 citations

Nchangwi Syntia Munung, Lulu Chirande, Catherine Chunda‐Liyoka, Sarah Kiguli, Fred Stephen Sarfo +18 more

Genomics and Health Data Governance in Africa: Democratize the Use of Big Data and Popularize Public Engagement

The Hastings Center Report(2024)10.1002/hast.4933

N/A

0.360DataRank · unranked

10 citations

Charmaine Royal, Carmen De Kock, Gordon A. Awandare, Victoria Nembaware, Séraphin Nguefack +3 more

MECP2 duplication syndrome in a patient from Cameroon

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61510

N/A

0.312DataRank · unranked

7 citations

Sophie Dahoun, Séraphin Nguefack, Isabelle Moix, Stefania Gimelli, Huguette Zambo +4 more

Priorities for sickle cell disease global research and implementation

The Lancet(2024)10.1016/s0140-6736(24)01400-4

N/A

0.312DataRank · unranked

7 citations

Nchangwi Syntia Munung, Aldiouma Guindo, Obiageli Nnodu, Ambroise Wonkam

Childhood Hearing Impairment in Senegal

Genes(2023)10.3390/genes14030562

N/A

0.293DataRank · unranked

5 citations

Birame Loum, Yaay Joor Koddu Biigé Dieng, Jean Pascal Demba Diop, Samuel Mawuli Adadey, Elvis Twumasi Aboagye +13 more

Whole exome sequencing reveals a biallelic frameshift mutation in GRXCR2 in hearing impairment in Cameroon

Molecular Genetics & Genomic Medicine(2021)10.1002/mgg3.1609

N/A

0.292DataRank · unranked

6 citations

Kamogelo Lebeko, Shaheen Mowla, Jean Jacques Noubiap, Mike Chong, Guillaume Paré +1 more

“Iron”ing out hemophagocytosis through PIEZO1

Cell(2021)10.1016/j.cell.2021.01.038

N/A

0.292DataRank · unranked

6 citations

Ambroise Wonkam, Neil A. Hanchard

Barriers to sickle cell disease care: a biopsychosocial analysis mapped to the standards of care guidelines by the sickle pan African research consortium

Journal of Public Health(2025)10.1093/pubmed/fdaf147

N/A

0.292DataRank · unranked

6 citations

Vhuthu Raphunga, Achuma Mashalaba, Arthemon Nguweneza, Kambe Banda, Vivian Paintsil +3 more

Should institutions fund the feedback of individual findings in genomic research?

Journal of Medical Ethics(2022)10.1136/medethics-2021-107992

N/A

0.292DataRank · unranked

6 citations

Benjamin E. Berkman, Ambroise Wonkam, Jantina de Vries, Cornelius Ewuoso

GJB1 variants in Charcot‐Marie‐Tooth disease X‐linked type 1 in Mali

Journal of the Peripheral Nervous System(2022)10.1111/jns.12486

N/A

0.269DataRank · unranked

5 citations

Seybou Hassane Diallo, Lassana Cissé, Mamadou Karembé, Salimata Diallo, Thomas Coulibaly +8 more

Clinical characteristics and risk factors of relative systemic hypertension and hypertension among sickle cell patients in Cameroon

Frontiers in Medicine(2022)10.3389/fmed.2022.924722

N/A

0.269DataRank · unranked

5 citations

Valentina Josiane Ngo Bitoungui, Khuthala Mnika, Gaston K. Mazandu, Victoria Nembaware, André Pascal Kengne +2 more

Advancing genetic services in African healthcare: Challenges, opportunities, and strategic insights from a scoping review

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100439

N/A

0.241DataRank · unranked

4 citations

Pallissa Fonkam Marlyse, Séraphin Nguefack, Ambroise Wonkam, Karen Kengne Kamga

The Ugandan sickle Pan-African research consortium registry: design, development, and lessons

BMC Medical Informatics and Decision Making(2024)10.1186/s12911-024-02618-9

Top 61%

0.241DataRank

Top 61%4 citations

Henry Mutegeki, Daudi Jjingo, Deogratias Munube, Ruth Namazzi, Robert Opoka +13 more

Modelling the mortality of sickle cell disease in Africa

The Lancet Haematology(2021)10.1016/s2352-3026(21)00268-4

N/A

0.213DataRank · unranked

2 citations

André Pascal Kengne, Ambroise Wonkam

Participant views on practical considerations for feedback of individual genetic research results: a case study from Botswana

Global Bioethics(2023)10.1080/11287462.2023.2192329

N/A

0.208DataRank · unranked

3 citations

Mary Kasule, Olivia P. Matshabane, Ambroise Wonkam, Mogomotsi Matshaba, Jantina de Vries +1 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

Evolutionary Analyses and Identification of Rare Pathogenic Variant in The MCPH1 BRCT3 Domain Broaden Its Role in Non-syndromic Hearing Impairment

Research Square(2022)10.21203/rs.3.rs-1815312/v1

N/A

0.165DataRank · unranked

2 citations

Kili James, Ambroise Wonkam, Oluwafemi Gabriel Oluwole

Whole-exome sequencing reveals known and candidate genes for hearing impairment in Mali

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100391

N/A

0.104DataRank · unranked

1 citations

Isabelle Schrauwen, Oumou Traoré, Salia Bamba, Elvis Twumasi Aboagye, Anushree Acharya +14 more

Craniofacial, dental, and molecular features of Pyle disease in a South African child

BDJ Open(2022)10.1038/s41405-022-00120-w

N/A

0DataRank · unranked

5 citations

Imaan Amina Roomaney, Chandre Oosterwyk, Noluthando Manyisa, Christian Domilongo Bope, Gloudi Agenbag +2 more

A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana

BMC Medical Genomics(2022)10.1186/s12920-022-01391-w

N/A

0DataRank · unranked

5 citations

Elvis Twumasi Aboagye, Kevin Esoh, Anushree Acharya, Thashi Bharadwaj, Nicole S. Lin +6 more

Preferences and expectations of feedback of individual genetic research results in African genomics: Views of South African parents of children with neurodevelopmental disorders

Open Research Africa(2022)10.12688/openresafrica.13594.1

N/A

0DataRank · unranked

3 citations

Cleo A Albertus, Marlyn C. Faure, Dimpho Ralefala, Kirsten A. Donald, Ambroise Wonkam +2 more

Feeding back of individual genomic results in Botswana: mapping opportunities and challenges

Research Square(2022)10.21203/rs.3.rs-1524983/v1

N/A

0DataRank · unranked

0 citations

Mogomotsi Matshaba, Ambroise Wonkam, Jantina de Vries, Mary Kasule

The future of sickle cell disease therapeutics rests in genomics

Disease Models & Mechanisms(2023)10.1242/dmm.049765

N/A

0DataRank · unranked

22 citations

Ambroise Wonkam

Caught between pity, explicit bias, and discrimination: a qualitative study on the impact of stigma on the quality of life of persons living with sickle cell disease in three African countries

Quality of Life Research(2023)10.1007/s11136-023-03533-8

N/A

0DataRank · unranked

21 citations

Marsha Treadwell, Karen Kengne Kamga, Jemima Dennis-Antwi, Kofi A. Anie, Daima Bukini +3 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

Leveraging our common African origins to understand human evolution and health

Cell Genomics(2023)10.1016/j.xgen.2023.100278

N/A

0DataRank · unranked

12 citations

Adebowale Adeyemo, Ambroise Wonkam

Feeding back of individual genetic results in Botswana: mapping opportunities and challenges

BMC Medical Ethics(2023)10.1186/s12910-023-00912-1

N/A

0DataRank · unranked

0 citations

Mogomotsi Matshaba, Ambroise Wonkam, Jantina de Vries, Mary Kasule

Data protection legislation in Africa and pathways for enhancing compliance in big data health research

Health Research Policy and Systems(2024)10.1186/s12961-024-01230-7

N/A

0DataRank · unranked

25 citations

Ciara Staunton, Otshepeng Mazibuko, P. J. Wall, Ambroise Wonkam, Nchangwi Syntia Munung

Human genetics and genomics as a unifying factor for harmony and progress in Africa: a report from the 12th African Society of Human Genetics meeting in Bamako, Mali

Pan African Medical Journal(2024)10.11604/pamj.2024.49.19.41189

N/A

0DataRank · unranked

1 citations

Abdoulaye Yalcouyé, Djénéba Dabitao, Oumar Samassékou, Victoria Nembaware, Fousseyni Kané +10 more

Mapping Epigenetic Gene Variant Dynamics: Comparative Analysis of Frequency, Functional Impact and Trait Associations in African and European Populations

medRxiv(2024)10.1101/2024.08.11.24311816

N/A

0DataRank · unranked

0 citations

Gaone Retshabile, Phelelani Thokozani Mpangase, Salia Bamba, Modibo K. Goita, Victoria Nembaware +11 more

Harnessing genomics and translational research to improve health in Africa: a report of the 13th African Society of Human Genetics meeting in Dar es Salaam, Tanzania

Pan African Medical Journal(2024)10.11604/pamj.2024.49.79.42550

N/A

0DataRank · unranked

0 citations

Siana Nkya, Mohamed Zahir Alimohamed, Kilaza Samson, Grantina Modern, Michèle Ramsay +5 more

Parasite-resistant variants in African genomes: implications for global genetic medicine

Trends in Parasitology(2025)10.1016/j.pt.2025.05.007

N/A

0DataRank · unranked

2 citations

Abdoulaye Yalcouyé, Ambroise Wonkam, Kevin Esoh

The Diverse Genetic Landscape of Hearing Impairment in South African Families

Clinical Genetics(2025)10.1111/cge.14765

N/A

0DataRank · unranked

3 citations

Anushree Acharya, Noluthando Manyisa, Elvis Twumasi Aboagye, Ramses Peigou Wonkam, Lettilia Xhakaza +6 more

Etiologies of Early-Onset Hearing Impairment in Rwanda

Genes(2025)10.3390/genes16030257

N/A

0DataRank · unranked

1 citations

Léon Mutesa, C. Muhizi, Isaie Ncogoza, Elvis Twumasi Aboagye, Norbert Dukuze +4 more

Exome sequencing revealed a novel homozygous variant in TRMT61 A in a multiplex family with atypical Cornelia de Lange Syndrome from Rwanda

BMC Medical Genomics(2025)10.1186/s12920-025-02153-0

N/A

0DataRank · unranked

1 citations

Abdoulaye Yalcouyé, Elvis Twumasi Aboagye, Lettilia Xhakaza, Kalinka Popel, Norbert Dukuze +7 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

The Identification and Classification of Novel Genetic Variants in the MCPH1 Gene Suggest Association with Non-Syndromic Hearing Impairment

OBM Genetics(2025)10.21926/obm.genet.2502299

N/A

0DataRank · unranked

0 citations

Kili James, Ambroise Wonkam, Oluwafemi G. Oluwole

Author Index Vol. 13, No. 7–8, 2010

Public Health Genomics(2010)10.1159/000322612

N/A

0DataRank · unranked

0 citations

T.E. Jayaratne, Poupak Javaher, Elisabeth Nyoungui, L. Ioannou, John Massie +103 more

Genetics of Waardenburg Syndrome in Africa: A Systematic Review

International Journal of Molecular Sciences(2025)10.3390/ijms27010127

N/A

0DataRank · unranked

0 citations

Ramses Peigou Wonkam, Carmen De Kock, Collet Dandara, Ambroise Wonkam, Elvis Twumasi Aboagye

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

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

Whole exome sequencing reveals pathogenic variants inMYO3A,MYO15AandCOL9A3and differential frequencies in ancestral alleles in hearing impairment genes among individuals from Cameroon

Human Molecular Genetics(2020)10.1093/hmg/ddaa225

N/A

0DataRank · unranked

13 citations

Noluthando Manyisa, Christian Domilongo Bope, Collet Dandara, Emile R. Chimusa, Ambroise Wonkam

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

Using the Drama of DNA approach to community engagement in genomic research in South Africa: experiences and lessons learnt

AAS Open Research(2020)10.12688/aasopenres.13045.1

N/A

0DataRank · unranked

10 citations

Ambroise Wonkam, Jantina de Vries, Marlyn C. Faure

Building Skills and Resources for Genomics, Epigenetics, and Bioinformatics Research for Africa: Report of the Joint 11th Conference of the African Society of Human Genetics and 12th H3Africa Consortium, 2018

American Journal of Tropical Medicine and Hygiene(2020)10.4269/ajtmh.19-0837

N/A

0DataRank · unranked

11 citations

Bonaventure Mihigo, Robert Tumusime, Mediatrice Uwanyirigira, Jorge da Rocha, M Hayat +12 more

IHP-PING—generating integrated human protein–protein interaction networks on-the-fly

Briefings in Bioinformatics(2020)10.1093/bib/bbaa277

N/A

0DataRank · unranked

10 citations

Christopher Hooper, Kenneth Opap, Funmilayo Makinde, Victoria Nembaware, Nicholas Ekow Thomford +4 more

Enhancing Genetic Medicine: Rapid and Cost-Effective Molecular Diagnosis for a GJB2 Founder Mutation for Hearing Impairment in Ghana

Genes(2020)10.3390/genes11020132

N/A

0DataRank · unranked

8 citations

Edmond Tingang Wonkam, Elvis Twumasi Aboagye, Darius Quansah, Adwoa Asante-Poku, Osbourne Quaye +4 more

Genetic modifiers of long‐term survival in sickle cell anemia

Clinical and Translational Medicine(2020)10.1002/ctm2.152

N/A

0DataRank · unranked

35 citations

Emile R. Chimusa, Khuthala Mnika, Gift D. Pule, Valentina Josiane Ngo Bitoungui, Nicola Mulder +4 more

Lived Experiences of Fragile X Syndrome Caregivers: A Scoping Review of Qualitative Studies

Frontiers in Neurology(2020)10.3389/fneur.2020.00128

N/A

0DataRank · unranked

9 citations

Jantina de Vries, Séraphin Nguefack, Syntia Nchangwi Munung, Ambroise Wonkam, Karen Kengne Kamga

A potential roadmap to overcome the current eastern DRC Ebola virus disease outbreak: From a computational perspective

Scientific African(2020)10.1016/j.sciaf.2020.e00282

N/A

0DataRank · unranked

4 citations

Victoria Nembaware, Nicholas Ekow Thomford, Christian Domilongo Bope, Ousmane Ly, Emile R. Chimusa +2 more

Investigating the missing heritability of fetal haemoglobin level in Africa

British Journal of Haematology(2020)10.1111/bjh.17101

N/A

0DataRank · unranked

2 citations

Ambroise Wonkam

Preferences and Expectations of Feedback of Individual Genetic Research Results in African Genomics: Views of South African Parents of Children With Neurodevelopmental Conditions

Research Square(2020)10.21203/rs.3.rs-107280/v1

N/A

0DataRank · unranked

2 citations

Cleo A Albertus, Marlyn C. Faure, Dimpho Ralefala, Kirsten A. Donald, Ambroise Wonkam +2 more

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

Hearing loss and brain disorders: A review of multiple pathologies

Open Medicine(2021)10.1515/med-2021-0402

N/A

0DataRank · unranked

16 citations

Kili James, Abdoulaye Yalcouyé, Ambroise Wonkam, Oluwafemi Gabriel Oluwole

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

Utilization of Pneumococcal Vaccine and Penicillin Prophylaxis in Sickle Cell Disease in Three African Countries: Assessment among Healthcare Providers in SickleInAfrica

Hemoglobin(2021)10.1080/03630269.2021.1954943

N/A

0DataRank · unranked

12 citations

Anazoeze Jude Madu, Raphael Zozimus Sangeda, Siana Nkya, Emmanuel Peprah, Vivian Paintsil +20 more

Etiologies of Childhood Hearing Impairment in Schools for the Deaf in Mali

Frontiers in Pediatrics(2021)10.3389/fped.2021.726776

N/A

0DataRank · unranked

11 citations

Oumou Traoré, Abdoulaye Taméga, Alassane Baneye Maīga, Fousseyni Kané, Oluwafemi G. Oluwole +7 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

Explanatory models for the cause of Fragile X Syndrome in rural Cameroon

Journal of Genetic Counseling(2021)10.1002/jgc4.1440

N/A

0DataRank · unranked

6 citations

Jantina de Vries, Séraphin Nguefack, Nchangwi Syntia Munung, Ambroise Wonkam, Karen Kengne Kamga

Fine scale human genetic structure in three regions of Cameroon reveals episodic diversifying selection

Scientific Reports(2021)10.1038/s41598-020-79124-1

N/A

0DataRank · unranked

6 citations

Tobias O. Apinjoh, Steven Ger Nyanjom, Ambroise Wonkam, Emile R. Chimusa, Lucas Amenga–Etego +3 more

Negotiating political power and stigma around fragile X Syndrome in a rural village in Cameroon: A tale of a royal family and a community

Molecular Genetics & Genomic Medicine(2021)10.1002/mgg3.1615

N/A

0DataRank · unranked

2 citations

Nchangwi Syntia Munung, Séraphin Nguefack, Ambroise Wonkam, Jantina de Vries, Karen Kengne Kamga

An Integrated Platform Supporting Semantic Similarity Score Calculation and Reproducibility

Research Square(2021)10.21203/rs.3.rs-806346/v1

N/A

0DataRank · unranked

0 citations

Kenneth Opap, Funmilayo Makinde, Victoria Nembaware, Francis E. Agamah, Christian Domilongo Bope +4 more

Establishing a Sickle Cell Disease Registry in Africa: Experience From the Sickle Pan-African Research Consortium, Kumasi-Ghana

Frontiers in Genetics(2022)10.3389/fgene.2022.802355

N/A

0DataRank · unranked

33 citations

Evans Xorse Amuzu, Isaac Nyanor, Emmanuel Asafo‐Adjei, Abdul Razak Mohammed, Suraj Abubakar Yawnumah +13 more

Five Priorities of African Genomics Research: The Next Frontier

Annual Review of Genomics and Human Genetics(2022)10.1146/annurev-genom-111521-102452

N/A

0DataRank · unranked

31 citations

Nchangwi Syntia Munung, Collet Dandara, Kevin Esoh, Neil A. Hanchard, Guida Landouré +1 more

Current profile of Charcot‐Marie‐Tooth disease in Africa: A systematic review

Journal of the Peripheral Nervous System(2022)10.1111/jns.12489

N/A

0DataRank · unranked

22 citations

Kevin Esoh, Guida Landouré, Ambroise Wonkam, Abdoulaye Yalcouyé

Addressing exploitation and inequities in open science: A relational perspective

Developing World Bioethics(2022)10.1111/dewb.12378

N/A

0DataRank · unranked

10 citations

Luís Cordeiro‐Rodrigues, Ambroise Wonkam, Jantina de Vries, Cornelius Ewuoso

GJB2 Is a Major Cause of Non-Syndromic Hearing Impairment in Senegal

Biology(2022)10.3390/biology11050795

N/A

0DataRank · unranked

14 citations

Samuel Mawuli Adadey, Jean Pascal Demba Diop, Elvis Twumasi Aboagye, Seydi Abdoul Ba, Carmen De Kock +8 more

Considerations of Autonomy in Guiding Decisions around the Feedback of Individual Genetic Research Results from Genomics Research: Expectations of and Preferences from Researchers in Botswana

Global Health(2022)10.1155/2022/3245206

N/A

0DataRank · unranked

11 citations

Mogomotsi Matshaba, Erisa Mwaka, Ambroise Wonkam, Jantina de Vries, Mary Kasule

The Implementation of Laboratory Information Management System in Multi-Site Genetics Study in Africa: The Challenges and Up-Scaling Opportunities

Journal of Molecular Pathology(2022)10.3390/jmp3040022

N/A

0DataRank · unranked

11 citations

Chandre Oosterwyk, Dominique Anderson, Samuel Mawuli Adadey, Khuthala Mnika, Noluthando Manyisa +13 more

Ambroise Wonkam

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