Wonkam A - Search Results

1

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

Faridi R, Yousaf R, Gu S, Inagaki S, Turriff AE, Pelstring K, Guan B, Naik A, Griffith AJ, Adadey SM, Aboagye ET, Awandare GA, Morell RJ, Tsilou E, Noyes AG, Sulmonte LAG, Wonkam A, Schrauwen I, Leal SM, Azaiez H, Brewer CC, Riazuddin S, Hufnagel RB, Hoa M, Zein WM, de Dios JK, Friedman TB. Faridi R, et al. Among authors: wonkam a. Clin Genet. 2023 Jun;103(6):699-703. doi: 10.1111/cge.14312. Epub 2023 Mar 13. Clin Genet. 2023. PMID: 36807241

2

Targeted genomic enrichment and massively parallel sequencing identifies novel nonsyndromic hearing impairment pathogenic variants in Cameroonian families.

Lebeko K, Sloan-Heggen CM, Noubiap JJ, Dandara C, Kolbe DL, Ephraim SS, Booth KT, Azaiez H, Santos-Cortez RL, Leal SM, Smith RJ, Wonkam A. Lebeko K, et al. Among authors: wonkam a. Clin Genet. 2016 Sep;90(3):288-90. doi: 10.1111/cge.12799. Epub 2016 Jun 1. Clin Genet. 2016. PMID: 27246798 Free PMC article.

3

Public Health Burden of Hearing Impairment and the Promise of Genomics and Environmental Research: A Case Study in Ghana, Africa.

Adadey SM, Awandare G, Amedofu GK, Wonkam A. Adadey SM, et al. Among authors: wonkam a. OMICS. 2017 Nov;21(11):638-646. doi: 10.1089/omi.2017.0145. OMICS. 2017. PMID: 29140768 Free PMC article. Review.

4

Genomics and Epigenomics of Congenital Heart Defects: Expert Review and Lessons Learned in Africa.

Thomford NE, Dzobo K, Yao NA, Chimusa E, Evans J, Okai E, Kruszka P, Muenke M, Awandare G, Wonkam A, Dandara C. Thomford NE, et al. Among authors: wonkam a. OMICS. 2018 May;22(5):301-321. doi: 10.1089/omi.2018.0033. OMICS. 2018. PMID: 29762087 Free PMC article. Review.

5

GJB2 and GJB6 Mutations in Non-Syndromic Childhood Hearing Impairment in Ghana.

Adadey SM, Manyisa N, Mnika K, de Kock C, Nembaware V, Quaye O, Amedofu GK, Awandare GA, Wonkam A. Adadey SM, et al. Among authors: wonkam a. Front Genet. 2019 Sep 18;10:841. doi: 10.3389/fgene.2019.00841. eCollection 2019. Front Genet. 2019. PMID: 31620164 Free PMC article.

6

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

Tingang Wonkam E, Chimusa E, Noubiap JJ, Adadey SM, F Fokouo JV, Wonkam A. Tingang Wonkam E, et al. Among authors: wonkam a. Genes (Basel). 2019 Oct 25;10(11):844. doi: 10.3390/genes10110844. Genes (Basel). 2019. PMID: 31731535 Free PMC article.

7

The Hearing Impairment Ontology: A Tool for Unifying Hearing Impairment Knowledge to Enhance Collaborative Research.

Hotchkiss J, Manyisa N, Adadey SM, Oluwole OG, Wonkam E, Mnika K, Yalcouye A, Nembaware V, Haendel M, Vasilevsky N, Mulder NJ, Jupp S, Wonkam A, Mazandu GK. Hotchkiss J, et al. Among authors: wonkam e, wonkam a. Genes (Basel). 2019 Nov 21;10(12):960. doi: 10.3390/genes10120960. Genes (Basel). 2019. PMID: 31766582 Free PMC article.

8

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

Adadey SM, Tingang Wonkam E, Twumasi Aboagye E, Quansah D, Asante-Poku A, Quaye O, Amedofu GK, Awandare GA, Wonkam A. Adadey SM, et al. Among authors: wonkam a. Genes (Basel). 2020 Jan 27;11(2):132. doi: 10.3390/genes11020132. Genes (Basel). 2020. PMID: 32012697 Free PMC article.

9

GJB4 and GJC3 variants in non-syndromic hearing impairment in Ghana.

Adadey SM, Esoh KK, Quaye O, Amedofu GK, Awandare GA, Wonkam A. Adadey SM, et al. Among authors: wonkam a. Exp Biol Med (Maywood). 2020 Sep;245(15):1355-1367. doi: 10.1177/1535370220931035. Epub 2020 Jun 11. Exp Biol Med (Maywood). 2020. PMID: 32524838 Free PMC article.

10

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

Wonkam-Tingang E, Schrauwen I, Esoh KK, Bharadwaj T, Nouel-Saied LM, Acharya A, Nasir A, Adadey SM, Mowla S, Leal SM, Wonkam A. Wonkam-Tingang E, et al. Among authors: wonkam a. Genes (Basel). 2020 Oct 23;11(11):1249. doi: 10.3390/genes11111249. Genes (Basel). 2020. PMID: 33114113 Free PMC article.

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