Ambroise Wonkam

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 59

Top Venues

Genes

Disease models & mechanisms

Molecular genetics & genomic medicine

Experimental biology and medicine (Maywood, N.J.)

University of Cape Town Department of Medicine (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

University of Cape Town Department of Medicine Apr 01 2009

South Africa

PHD :: Division of Human Genetics

Publications

Emma Wiener, Laura Cottino, Gerrit Botha, Oscar Asanya Nyangiri, Harry Noyes, Annette MacLeod, David Jakubosky, Clement Adebamowo, Phillip Awadalla, Guida Landouré, Mogomotsi Matshaba, Enock Matovu, Michelle Ramsay, Gustave Simo, Martin Chitolongo Simuunza, Caroline T Tiemessen, Ambroise Wonkam, Venesa Sahibdeen, Amanda Krause, Stephen Tollman, Scott Hazelhurst, null null
An assessment of the genomic structural variation landscape in Sub-Saharan African populations. Research square (2024)
Stephen Tollman, Emma Wiener, Laura Cottino, Gerrit Botha, Oscar Asanya Nyangiri, Harry Noyes, Annette MacLeod, David Jakubosky, Clement Adebamowo, Phillip Awadalla, Guida Landouré, Mogomotsi Matshaba, Enock Matovu, Michelle Ramsay, Gustave Simo, Martin Chitolongo Simuunza, Caroline T Tiemessen, Ambroise Wonkam, Venesa Sahibdeen, Amanda Krause, Scott Hazelhurst
An assessment of the genomic structural variation landscape in Sub-Saharan African populations. Research square (2024)
Stephen Tollman, Emma Wiener, Laura Cottino, Gerrit Botha, Oscar Asanya Nyangiri, Harry Noyes, Annette MacLeod, David Jakubosky, Clement Adebamowo, Phillip Awadalla, Guida Landouré, Mogomotsi Matshaba, Enock Matovu, Michelle Ramsay, Gustave Simo, Martin Chitolongo Simuunza, Caroline T Tiemessen, Ambroise Wonkam, Venesa Sahibdeen, Amanda Krause, Scott Hazelhurst
An assessment of the genomic structural variation landscape in Sub-Saharan African populations. Research square (2024)
Nchangwi Syntia Munung, Karen Kengne Kamga, Marsha J Treadwell, Jemima Dennis-Antwi, Kofi A Anie, Daima Bukini, Julie Makani, Ambroise Wonkam
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 : EJHG (2024)
Nchangwi Syntia Munung, Karen Kengne Kamga, Marsha J Treadwell, Jemima Dennis-Antwi, Kofi A Anie, Daima Bukini, Julie Makani, Ambroise Wonkam
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 : EJHG (2024)
Nchangwi Syntia Munung, Karen Kengne Kamga, Marsha J Treadwell, Jemima Dennis-Antwi, Kofi A Anie, Daima Bukini, Julie Makani, Ambroise Wonkam
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 : EJHG (2024)
Musalula Sinkala, Gaone Retshabile, Phelelani Thokozani Mpangase, Salia Bamba, Modibo K Goita, Victoria Nembaware, Samar S M Elsheikh, Jeannine M Heckmann, Kevin Kum Esoh, Mogomotsi Matshaba, Clement A Adebamowo, Sally N Adebamowo, Ofon E Amih, Ambroise Wonkam, Michelle Ramsay, Nicola M Mulder
Mapping Epigenetic Gene Variant Dynamics: Comparative Analysis of Frequency, Functional Impact and Trait Associations in African and European Populations. medRxiv : the preprint server for health sciences (2024)
Ambroise Wonkam
The future of sickle cell disease therapeutics rests in genomics. Disease models & mechanisms 16 (2) (2023)
Elvis Twumasi Aboagye, Samuel Mawuli Adadey, Edmond Wonkam-Tingang, Lucas Amenga-Etego, Gordon A Awandare, Ambroise Wonkam
Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment. Genes 14 (2) (2023)
Ambroise Wonkam
The future of sickle cell disease therapeutics rests in genomics. Disease models & mechanisms 16 (2) (2023)
Kevin Kum Esoh, Tobias O Apinjoh, Alfred Amambua-Ngwa, Steven G Nyanjom, Emile R Chimusa, Lucas Amenga-Etego, Ambroise Wonkam, Eric A Achidi
Genome-wide association study identifies novel candidate malaria resistance genes in Cameroon. Human molecular genetics (2023)
Dimpho Ralefala, Mary Kasule, Olivia P Matshabane, Ambroise Wonkam, Mogomotsi Matshaba, Jantina de Vries
Participant views on practical considerations for feedback of individual genetic research results: a case study from Botswana. Global bioethics = Problemi di bioetica 34 (1) (2023)
Ambroise Wonkam
The future of sickle cell disease therapeutics rests in genomics. Disease models & mechanisms 16 (2) (2023)
Ambroise Wonkam
The future of sickle cell disease therapeutics rests in genomics. Disease models & mechanisms 16 (2) (2023)
Ambroise Wonkam
The future of sickle cell disease therapeutics rests in genomics. Disease models & mechanisms 16 (2) (2023)
Elvis Twumasi Aboagye, Samuel Mawuli Adadey, Edmond Wonkam-Tingang, Lucas Amenga-Etego, Gordon A Awandare, Ambroise Wonkam
Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment. Genes 14 (2) (2023)
Ambroise Wonkam
The future of sickle cell disease therapeutics rests in genomics. Disease models & mechanisms 16 (2) (2023)
Elvis Twumasi Aboagye, Samuel Mawuli Adadey, Edmond Wonkam-Tingang, Lucas Amenga-Etego, Gordon A Awandare, Ambroise Wonkam
Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment. Genes 14 (2) (2023)
Elvis Twumasi Aboagye, Samuel Mawuli Adadey, Edmond Wonkam-Tingang, Lucas Amenga-Etego, Gordon A Awandare, Ambroise Wonkam
Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment. Genes 14 (2) (2023)
Rabia Faridi, Rizwan Yousaf, Shoujun Gu, Sayaka Inagaki, Amy E Turriff, Keith Pelstring, Bin Guan, Amelia Naik, Andrew J Griffith, Samuel Mawuli Adadey, Elvis Twumasi Aboagye, Gordon Akanzuwine Awandare, Robert J Morell, Ekaterini Tsilou, Amanda G Noyes, Laura Anne Goodell Sulmonte, Ambroise Wonkam, Isabelle Schrauwen, Regie Lyn P Santos-Cortez, Hela Azaiez, Carmen C Brewer, Sheikh Riazuddin, Robert B Hufnagel, Michael Hoa, Wadih M Zein, J Karl de Dios, Thomas B Friedman
Variants of LRP2, encoding a multifunctional cell-surface endocytic receptor, associated with hearing loss and retinal dystrophy. Clinical genetics (2023)
Ambroise Wonkam
The future of sickle cell disease therapeutics rests in genomics. Disease models & mechanisms 16 (2) (2023)
Ambroise Wonkam
New mutations predict clinical manifestation of complex traits. Nature reviews. Genetics 23 (7) (2022)
Abdoulaye Yalcouyé, Kevin Esoh, Landouré Guida, Ambroise Wonkam
Current profile of Charcot-Marie-Tooth disease in Africa: A systematic review. Journal of the peripheral nervous system : JPNS 27 (2) (2022)
Cornelius Olukunle Ewuoso, Benjamin E Berkman, Ambroise Wonkam, Jantina de Vries
Should institutions fund the feedback of individual findings in genomic research? Journal of medical ethics (2022)
Giorgio Sirugo, Ambroise Wonkam
Beyond Race: A Wake-up Call for Drug Therapy Informed by Genotyping. Annals of internal medicine 175 (8) (2022)
Abdoulaye Yalcouyé, Oumou Traoré, Salimata Diarra, Isabelle Schrauwen, Kevin Esoh, Magda Kamila Kadlubowska, Thashi Bharadwaj, Samuel Mawuli Adadey, Mohamed Kéita, Cheick O Guinto, Suzanne M Leal, Guida Landouré, Ambroise Wonkam
A monoallelic variant in EYA1 is associated with Branchio-Otic syndrome in a Malian family. Molecular genetics & genomic medicine 10 (7) (2022)
Yacouba Dia, Samuel Mawuli Adadey, Jean Pascal Demba Diop, Elvis Twumasi Aboagye, Seydi Abdoul Ba, Carmen De Kock, Cheikh Ahmed Tidjane Ly, Oluwafemi Gabriel Oluwale, Andrea Regina Gnilane Sène, Pierre Diaga Sarr, Bay Karim Diallo, Rokhaya Ndiaye Diallo, Ambroise Wonkam
GJB2 Is a Major Cause of Non-Syndromic Hearing Impairment in Senegal. Biology 11 (5) (2022)
Gaston Kuzamunu Mazandu, Jade Hotchkiss, Victoria Nembaware, Ambroise Wonkam, Nicola Mulder
The Sickle Cell Disease Ontology: recent development and expansion of the universal sickle cell knowledge representation. Database : the journal of biological databases and curation 2022 (2022)
Noluthando Manyisa, Samuel Mawuli Adadey, Edmond Wonkam-Tingang, Abdoulaye Yalcouye, Ambroise Wonkam
Hearing Impairment in South Africa and the Lessons Learned for Planetary Health Genomics: A Systematic Review. Omics : a journal of integrative biology 26 (1) (2022)
Cornelius Olukunle Ewuoso, Luis Cordeiro Rodrigues, Ambroise Wonkam, Jantina de Vries
Addressing exploitation and inequities in open science: A relational perspective. Developing world bioethics (2022)
Mary Kasule, Mogomotsi Matshaba, Erisa Sabakaki Mwaka, Ambroise Wonkam, Jantina de Vries
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, epidemiology and genomics 2022 (2022)
Abdoulaye Yalcouyé, Seybou H Diallo, Lassana Cissé, Mamadou Karembé, Salimata Diallo, Thomas Coulibaly, Salimata Diarra, Dramane Coulibaly, Mohamed Keita, Cheick O Guinto, Kenneth H Fischbeck, Ambroise Wonkam, Guida Landouré, null null
GJB1 variants in Charcot-Marie-Tooth disease X-linked type 1 in Mali. Journal of the peripheral nervous system : JPNS 27 (2) (2022)
Arthemon Nguweneza, Chandré Oosterwyk, Kambe Banda, Victoria Nembaware, Gaston Mazandu, Andre Pascal Kengne, Ambroise Wonkam
Factors associated with blood pressure variation in sickle cell disease patients: a systematic review and meta-analyses. Expert review of hematology 15 (4) (2022)
Ambroise Wonkam, Samuel Mawuli Adadey, Isabelle Schrauwen, Elvis Twumasi Aboagye, Edmond Wonkam-Tingang, Kevin Kum Esoh, Kalinka Popel, Noluthando Manyisa, Mario Jonas, Carmen deKock, Victoria Nembaware, Diana M Cornejo Sanchez, Thashi Bharadwaj, Abdul Nasir, Jenna L Everard, Magda K Kadlubowska, Liz M Nouel-Saied, Anushree Acharya, Osbourne Quaye, Geoffrey K Amedofu, Gordon Akanzuwine Awandare, Suzanne M Leal
Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes. Communications biology 5 (1) (2022)
Ambroise Wonkam, Kamogelo Lebeko, Shaheen Mowla, Jean Jacques Noubiap, Mike Chong, Guillaume Pare
Whole exome sequencing reveals a biallelic frameshift mutation in GRXCR2 in hearing impairment in Cameroon. Molecular genetics & genomic medicine 9 (3) (2021)
Karen Kengne Kamga, Jantina De Vries, Séraphin Nguefack, Nchangwi Syntia Munung, Ambroise Wonkam
Explanatory models for the cause of Fragile X Syndrome in rural Cameroon. Journal of genetic counseling 30 (6) (2021)
Biobele J Brown, Anazoeze Madu, Raphael Z Sangeda, Siana Nkya, Emmanuel Peprah, Vivian Paintsil, Bruno P Mmbando, Joyce Gyamfi, Chide E Okocha, Samuel A Asala, Victoria Nembaware, Mario Jonas, Andre P Kengne, Emile R Chimusa, Arthemon Nguweneza, Hezekiah A Isa, Uche Nnebe-Agumadu, Adekunle D Adekile, Alex Osei-Akoto, Kwaku Ohene-Frempong, Emmanuel Balandya, Obiageli Eunice Nnodu, Ambroise Wonkam, Julie Makani, null null
Utilization of Pneumococcal Vaccine and Penicillin Prophylaxis in Sickle Cell Disease in Three African Countries: Assessment among Healthcare Providers in SickleInAfrica. Hemoglobin 45 (3) (2021)
Charmaine D M Royal, Michael Babyak, Nirmish R Shah, Shantanu Srivatsa, Kearsley A Stewart, Paula Tanabe, Ambroise Wonkam, Monika Rani Asnani
Sickle cell disease is a global prototype for integrative research and healthcare. Advanced genetics (Hoboken, N.J.) 2 (1) (2021)
Samuel M Adadey, Isabelle Schrauwen, Elvis Twumasi Aboagye, Thashi Bharadwaj, Kevin Kum Esoh, Sulman Basit, Anushree Acharya, Liz M Nouel-Saied, Khurram Liaqat, Edmond Wonkam-Tingang, Shaheen Mowla, Gordon A Awandare, Wasim Ahmad, Regie Lyn P Santos-Cortez, Ambroise Wonkam
Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment. Journal of human genetics 66 (12) (2021)
Edmond Wonkam-Tingang, Isabelle Schrauwen, Kevin Kum Esoh, Thashi Bharadwaj, Liz M Nouel Saied, Anushree Acharya, Abdul Nasir, Suzanne M Leal, Ambroise Wonkam
A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family. Experimental biology and medicine (Maywood, N.J.) 246 (13) (2021)
Arinao Ndadza, Sarudzai Muyambo, Pindile Mntla, Ambroise Wonkam, Emile Chimusa, Andre Pascal Kengne, Mpiko Ntsekhe, Collet Dandara
Profiling of warfarin pharmacokinetics-associated genetic variants: Black Africans portray unique genetic markers important for an African specific warfarin pharmacogenetics-dosing algorithm. Journal of thrombosis and haemostasis : JTH 19 (12) (2021)
Samuel Mawuli Adadey, Edmond Wonkam-Tingang, Elvis Twumasi Aboagye, Osbourne Quaye, Gordon A Awandare, Ambroise Wonkam
Hearing loss in Africa: current genetic profile. Human genetics (2021)
Charmaine D M Royal, Michael Babyak, Nirmish R Shah, Shantanu Srivatsa, Kearsley A Stewart, Paula Tanabe, Ambroise Wonkam, Monika Rani Asnani
Sickle cell disease is a global prototype for integrative research and healthcare. Advanced genetics (Hoboken, N.J.) 2 (1) (2021)
Karen Kengne Kamga, Nchangwi Syntia Munung, Séraphin Nguefack, Ambroise Wonkam, Jantina De Vries
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 9 (3) (2021)
Dimpho Ralefala, Mary Kasule, Ambroise Wonkam, Mogomotsi Matshaba, Jantina de Vries
Should Feedback of Individual Results be Integrated into the Consent Process in African Genomics? Participants' Views from an HIV-TB Genomics Research Project in Botswana. AJOB empirical bioethics (2021)
Noluthando Manyisa, Isabelle Schrauwen, Leonardo Alves de Souza Rios, Shaheen Mowla, Cedrik Tekendo-Ngongang, Kalinka Popel, Kevin Kum Esoh, Thashi Bharadwaj, Liz M Nouel Saied, Anushree Acharya, Abdul Nasir, Edmond Wonkam-Tingang, Carmen de Kock, Collet Dandara, Suzanne M Leal, Ambroise Wonkam
A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family. Genes 12 (11) (2021)
Edmond Wonkam-Tingang, Isabelle Schrauwen, Kevin Kum Esoh, Thashi Bharadwaj, Liz M Nouel Saied, Anushree Acharya, Abdul Nasir, Samuel Mawuli Adadey, Shaheen Mowla, Suzanne M Leal, Ambroise Wonkam
Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment. Genes 11 (11) (2020)
Oluwafemi Gabriel Oluwole, Kevin Kum Esoh, Edmond Wonkam-Tingang, Noluthando Manyisa, Jean Jacques Noubiap, Emile R Chimusa, Ambroise Wonkam
Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment. Experimental biology and medicine (Maywood, N.J.) 246 (2) (2020)
Ambroise Wonkam, Jantina de Vries
Returning incidental findings in African genomics research. Nature genetics 52 (1) (2020)
Ambroise Wonkam
Investigating the missing heritability of fetal haemoglobin level in Africa. British journal of haematology 191 (5) (2020)
Amy L McGuire, Stacey Gabriel, Sarah A Tishkoff, Ambroise Wonkam, Aravinda Chakravarti, Eileen E M Furlong, Barbara Treutlein, Alexander Meissner, Howard Y Chang, Núria López-Bigas, Eran Segal, Jin-Soo Kim
The road ahead in genetics and genomics. Nature reviews. Genetics 21 (10) (2020)
Edmond Wonkam-Tingang, Séraphin Nguefack, Alina I Esterhuizen, David Chelo, Ambroise Wonkam
DMD-related muscular dystrophy in Cameroon: Clinical and genetic profiles. Molecular genetics & genomic medicine 8 (8) (2020)
Samuel Mawuli Adadey, Edmond Wonkam-Tingang, Elvis Twumasi Aboagye, Daniel Wonder Nayo-Gyan, Maame Boatemaa Ansong, Osbourne Quaye, Gordon A Awandare, Ambroise Wonkam
Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden. Life (Basel, Switzerland) 10 (11) (2020)
Samuel M Adadey, Kevin Kum Esoh, Osbourne Quaye, Geoffrey K Amedofu, Gordon A Awandare, Ambroise Wonkam
GJB4 and GJC3 variants in non-syndromic hearing impairment in Ghana. Experimental biology and medicine (Maywood, N.J.) 245 (15) (2020)
Edmond Wonkam Tingang, Jean Jacques Noubiap, Jean Valentin F Fokouo, Oluwafemi Gabriel Oluwole, Séraphin Nguefack, Emile R Chimusa, Ambroise Wonkam
Hearing Impairment Overview in Africa: the Case of Cameroon. Genes 11 (2) (2020)
Kevin Dzobo, Dimakatso Alice Senthebane, Chelene Ganz, Nicholas Ekow Thomford, Ambroise Wonkam, Collet Dandara
Advances in Therapeutic Targeting of Cancer Stem Cells within the Tumor Microenvironment: An Updated Review. Cells 9 (8) (2020)
Gift Dineo Pule, Valentina Josiane Ngo Bitoungui, Bernard Chetcha Chemegni, Andre Pascal Kengne, Ambroise Wonkam
SAR1a promoter polymorphisms are not associated with fetal hemoglobin in patients with sickle cell disease from Cameroon. BMC research notes 10 (1) (2017)
Amy Geard, Gift D Pule, Bernard Chetcha Chemegni, Valentina J Ngo Bitoungui, Andre P Kengne, Emile R Chimusa, Ambroise Wonkam
Clinical and genetic predictors of renal dysfunctions in sickle cell anaemia in Cameroon. British journal of haematology 178 (4) (2017)
Ambroise Wonkam, Khuthala Mnika, Valentina J Ngo Bitoungui, Bernard Chetcha Chemegni, Emile R Chimusa, Collet Dandara, Andre P Kengne
Clinical and genetic factors are associated with pain and hospitalisation rates in sickle cell anaemia in Cameroon. British journal of haematology 180 (1) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Ambroise Wonkam