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Year Number of Results
2018 2
2020 2
2021 3
2022 6
2023 3
2024 0

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15 results

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Page 1
Hearing loss in Africa: current genetic profile.
Adadey SM, Wonkam-Tingang E, Aboagye ET, Quaye O, Awandare GA, Wonkam A. Adadey SM, et al. Among authors: aboagye et. Hum Genet. 2022 Apr;141(3-4):505-517. doi: 10.1007/s00439-021-02376-y. Epub 2021 Oct 5. Hum Genet. 2022. PMID: 34609590 Free PMC article. Review.
Childhood Hearing Impairment in Senegal.
Dia Y, Loum B, Dieng YJKB, Diop JPD, Adadey SM, Aboagye ET, Ba SA, Touré AA, Niang F, Diaga Sarr P, Tidiane Ly CA, Sène ARG, Kock C, Bassier R, Popel K, Ndiaye Diallo R, Wonkam A, Diallo BK. Dia Y, et al. Among authors: aboagye et. Genes (Basel). 2023 Feb 23;14(3):562. doi: 10.3390/genes14030562. Genes (Basel). 2023. PMID: 36980833 Free PMC article.
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: aboagye et. Clin Genet. 2023 Jun;103(6):699-703. doi: 10.1111/cge.14312. Epub 2023 Mar 13. Clin Genet. 2023. PMID: 36807241
Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes.
Wonkam A, Adadey SM, Schrauwen I, Aboagye ET, Wonkam-Tingang E, Esoh K, Popel K, Manyisa N, Jonas M, deKock C, Nembaware V, Cornejo Sanchez DM, Bharadwaj T, Nasir A, Everard JL, Kadlubowska MK, Nouel-Saied LM, Acharya A, Quaye O, Amedofu GK, Awandare GA, Leal SM. Wonkam A, et al. Among authors: aboagye et. Commun Biol. 2022 Apr 19;5(1):369. doi: 10.1038/s42003-022-03326-8. Commun Biol. 2022. PMID: 35440622 Free PMC article.
GJB2 Is a Major Cause of Non-Syndromic Hearing Impairment in Senegal.
Dia Y, Adadey SM, Diop JPD, Aboagye ET, Ba SA, De Kock C, Ly CAT, Oluwale OG, Sène ARG, Sarr PD, Diallo BK, Diallo RN, Wonkam A. Dia Y, et al. Among authors: aboagye et. Biology (Basel). 2022 May 23;11(5):795. doi: 10.3390/biology11050795. Biology (Basel). 2022. PMID: 35625523 Free PMC article.
Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment.
Adadey SM, Schrauwen I, Aboagye ET, Bharadwaj T, Esoh KK, Basit S, Acharya A, Nouel-Saied LM, Liaqat K, Wonkam-Tingang E, Mowla S, Awandare GA, Ahmad W, Leal SM, Wonkam A. Adadey SM, et al. Among authors: aboagye et. J Hum Genet. 2021 Dec;66(12):1169-1175. doi: 10.1038/s10038-021-00954-6. Epub 2021 Jul 5. J Hum Genet. 2021. PMID: 34226616 Free PMC article.
15 results