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Whole-exome sequencing reveals known and candidate genes for hearing impairment in Mali.
Yalcouyé A, Schrauwen I, Traoré O, Bamba S, Aboagye ET, Acharya A, Bharadwaj T, Latanich R, Esoh K, Fortes-Lima CA, de Kock C, Jonas M, Maiga ADB, Cissé CAK, Sangaré MA, Guinto CO, Landouré G, Leal SM, Wonkam A. Yalcouyé A, et al. Among authors: esoh k. HGG Adv. 2024 Dec 10;6(1):100391. doi: 10.1016/j.xhgg.2024.100391. Online ahead of print. HGG Adv. 2024. PMID: 39663698 Free article.
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.
Nnodu OE, Munung NS, Chirande L, Chunda-Liyoka C, Kiguli S, Sarfo FS, Touré BA, Balandya E, Guindo A, Kuona P, Esoh K, Jonas M, Nwegbu M, Masamu U, Morrice J, Moru PO, Bitoungui VN, Nembaware V, Nkya S, Tshilolo L, Makani J, Wonkam A, Peprah E; SickleInAfrica Consortium. Nnodu OE, et al. Among authors: esoh k. BMJ Open. 2024 Nov 7;14(11):e089056. doi: 10.1136/bmjopen-2024-089056. BMJ Open. 2024. PMID: 39515852 Free article.
Mapping Epigenetic Gene Variant Dynamics: Comparative Analysis of Frequency, Functional Impact and Trait Associations in African and European Populations.
Sinkala M, Retshabile G, Mpangase PT, Bamba S, Goita MK, Nembaware V, Elsheikh SSM, Heckmann J, Esoh K, Matshaba M, Adebamowo CA, Adebamowo SN, Amih OE, Wonkam A, Ramsay M, Mulder N. Sinkala M, et al. Among authors: esoh k. medRxiv [Preprint]. 2024 Aug 12:2024.08.11.24311816. doi: 10.1101/2024.08.11.24311816. medRxiv. 2024. PMID: 39185519 Free PMC article. Preprint.
Novel variant in CADM3 causes Charcot-Marie-Tooth disease.
Yalcouyé A, Rebelo AP, Cissé L, Rives L, Bamba S, Cogan J, Esoh K, Diarra S, Ezell KM, Taméga A, Guinto CO, Dohrn MF, Hamid R, Fischbeck KH, Zuchner S, Landouré G. Yalcouyé A, et al. Among authors: esoh k. Brain Commun. 2023 Sep 5;5(5):fcad227. doi: 10.1093/braincomms/fcad227. eCollection 2023. Brain Commun. 2023. PMID: 38074074 Free PMC article.
A monoallelic variant in EYA1 is associated with Branchio-Otic syndrome in a Malian family.
Yalcouyé A, Traoré O, Diarra S, Schrauwen I, Esoh K, Kadlubowska MK, Bharadwaj T, Adadey SM, Kéita M, Guinto CO, Leal SM, Landouré G, Wonkam A. Yalcouyé A, et al. Among authors: esoh k. Mol Genet Genomic Med. 2022 Jul;10(7):e1995. doi: 10.1002/mgg3.1995. Epub 2022 Jun 14. Mol Genet Genomic Med. 2022. PMID: 35698919 Free PMC article.
Five Priorities of African Genomics Research: The Next Frontier.
Wonkam A, Munung NS, Dandara C, Esoh KK, Hanchard NA, Landoure G. Wonkam A, et al. Among authors: esoh kk. Annu Rev Genomics Hum Genet. 2022 Aug 31;23:499-521. doi: 10.1146/annurev-genom-111521-102452. Epub 2022 May 16. Annu Rev Genomics Hum Genet. 2022. PMID: 35576571 Free article. Review.
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