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ArticlesPeer ReviewedFull Text
Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment
Author / Creator:Adadey, Samuel M. ; Schrauwen, Isabelle ; Aboagye, Elvis Twumasi ; Bharadwaj, Thashi ; Esoh, Kevin K. ; Basit, Sulman ; Acharya, Anushree ; Nouel-Saied, Liz M. ; Liaqat, Khurram ; Wonkam-Tingang, Edmond ; Mowla, Shaheen ; Awandare, Gordon A. ; Ahmad, Wasim ; Leal, Suzanne M. ; Wonkam, Ambroise
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2021-12, Vol.66 (12), p.1169-1175
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ArticlesPeer ReviewedFull Text
DMD‐related muscular dystrophy in Cameroon: Clinical and genetic profiles
Author / Creator:Wonkam‐Tingang, Edmond ; Nguefack, Séraphin ; Esterhuizen, Alina I. ; Chelo, David ; Wonkam, Ambroise
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2020-08, Vol.8 (8), p.e1362-n/a
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ArticlesPeer ReviewedFull Text
Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes
Author / Creator:Wonkam, Ambroise ; Adadey, Samuel Mawuli ; Schrauwen, Isabelle ; Aboagye, Elvis Twumasi ; Wonkam-Tingang, Edmond ; Esoh, Kevin ; Popel, Kalinka ; Manyisa, Noluthando ; Jonas, Mario ; deKock, Carmen ; Nembaware, Victoria ; Cornejo Sanchez, Diana M. ; Bharadwaj, Thashi ; Nasir, Abdul ; Everard, Jenna L. ; Kadlubowska, Magda K. ; Nouel-Saied, Liz M. ; Acharya, Anushree ; Quaye, Osbourne ; Amedofu, Geoffrey K. ; Awandare, Gordon A. ; Leal, Suzanne M.
Publisher:London: Nature Publishing Group UK
Journal title:Communications biology, 2022-04, Vol.5 (1), p.369-16, Article 369
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ArticlesPeer ReviewedFull Text
Hearing loss in Africa: current genetic profile
Author / Creator:Adadey, Samuel Mawuli ; Wonkam-Tingang, Edmond ; Aboagye, Elvis Twumasi ; Quaye, Osbourne ; Awandare, Gordon A. ; Wonkam, Ambroise
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Human genetics, 2022-04, Vol.141 (3-4), p.505-517
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ArticlesPeer ReviewedFull Text
Bi-Allelic MARVELD2 Variant Identified with Exome Sequencing in a Consanguineous Multiplex Ghanaian Family Segregating Non-Syndromic Hearing Loss
Author / Creator:Twumasi Aboagye, Elvis ; Adadey, Samuel Mawuli ; Alves de Souza Rios, Leonardo ; Esoh, Kevin K. ; Wonkam-Tingang, Edmond ; Xhakaza, Lettilia ; De Kock, Carmen ; Schrauwen, Isabelle ; Amenga-Etego, Lucas ; Lang, Dirk ; Awandare, Gordon A. ; Leal, Suzanne M. ; Mowla, Shaheen ; Wonkam, Ambroise
Publisher:Switzerland: MDPI AG
Journal title:International journal of molecular sciences, 2025-04, Vol.26 (7), p.3337
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ArticlesPeer ReviewedFull Text
Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment
Author / Creator:Aboagye, Elvis Twumasi ; Adadey, Samuel Mawuli ; Wonkam-Tingang, Edmond ; Amenga-Etego, Lucas ; Awandare, Gordon A. ; Wonkam, Ambroise
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2023-02, Vol.14 (2), p.399
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ArticlesPeer ReviewedFull Text
GJB2 and GJB6 Mutations in Hereditary Recessive Non-Syndromic Hearing Impairment in Cameroon
Author / Creator:Tingang Wonkam, Edmond ; Chimusa, Emile ; Noubiap, Jean Jacques ; Adadey, Samuel Mawuli ; F. Fokouo, Jean Valentin ; Wonkam, Ambroise
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2019-10, Vol.10 (11), p.844
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ArticlesPeer ReviewedFull Text
Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden
Author / Creator:Adadey, Samuel Mawuli ; Wonkam-Tingang, Edmond ; Twumasi Aboagye, Elvis ; Nayo-Gyan, Daniel Wonder ; Boatemaa Ansong, Maame ; Quaye, Osbourne ; Awandare, Gordon A. ; Wonkam, Ambroise
Publisher:Switzerland: MDPI
Journal title:Life (Basel, Switzerland), 2020-10, Vol.10 (11), p.258
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ArticlesPeer ReviewedFull Text
Hearing Impairment Overview in Africa: the Case of Cameroon
Author / Creator:Wonkam Tingang, Edmond ; Noubiap, Jean Jacques ; F. Fokouo, Jean Valentin ; Oluwole, Oluwafemi Gabriel ; Nguefack, Séraphin ; Chimusa, Emile R. ; Wonkam, Ambroise
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2020-02, Vol.11 (2), p.233
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ArticlesPeer ReviewedFull Text
A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family
Author / Creator:Manyisa, Noluthando ; Schrauwen, Isabelle ; de Souza Rios, Leonardo Alves ; Mowla, Shaheen ; Tekendo-Ngongang, Cedrik ; Popel, Kalinka ; Esoh, Kevin ; Bharadwaj, Thashi ; Nouel-Saied, Liz M. ; Acharya, Anushree ; Nasir, Abdul ; Wonkam-Tingang, Edmond ; Kock, Carmen de ; Dandara, Collet ; Leal, Suzanne M. ; Wonkam, Ambroise
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2021-11, Vol.12 (11), p.1765
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ArticlesPeer ReviewedFull Text
Cascade Testing for Fragile X Syndrome in a Rural Setting in Cameroon (Sub-Saharan Africa)
Author / Creator:Kengne Kamga, Karen ; Nguefack, Séraphin ; Minka, Khuthala ; Wonkam Tingang, Edmond ; Esterhuizen, Alina ; Nchangwi Munung, Syntia ; De Vries, Jantina ; Wonkam, Ambroise
Publisher:Switzerland: MDPI
Journal title:Genes, 2020-01, Vol.11 (2), p.136
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ArticlesPeer ReviewedFull Text
Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment
Author / Creator:Wonkam-Tingang, Edmond ; Schrauwen, Isabelle ; Esoh, Kevin K. ; Bharadwaj, Thashi ; Nouel-Saied, Liz M. ; Acharya, Anushree ; Nasir, Abdul ; Adadey, Samuel M. ; Mowla, Shaheen ; Leal, Suzanne M. ; Wonkam, Ambroise
Publisher:MDPI AG
Journal title:Genes, 2020-11, Vol.11 (11), p.1249
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ArticlesPeer ReviewedFull Text
Enhancing Genetic Medicine: Rapid and Cost-Effective Molecular Diagnosis for a GJB2 Founder Mutation for Hearing Impairment in Ghana
Author / Creator:M. Adadey, Samuel ; Tingang Wonkam, Edmond ; Twumasi Aboagye, Elvis ; Quansah, Darius ; Asante-Poku, Adwoa ; Quaye, Osbourne ; K. Amedofu, Geoffrey ; A. Awandare, Gordon ; Wonkam, Ambroise
Publisher:Switzerland: MDPI
Journal title:Genes, 2020-01, Vol.11 (2), p.132
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Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment

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

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

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Hearing loss in Africa: current genetic profile

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

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

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GJB2 and GJB6 Mutations in Hereditary Recessive Non-Syndromic Hearing Impairment in Cameroon

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Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden

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Hearing Impairment Overview in Africa: the Case of Cameroon

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

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

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

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

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