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THBS1 is a new autosomal recessive non-syndromic hearing impairment gene.
Bharadwaj T, Acharya A, Khan FU, Khan S, Ullah I, Schrauwen I, Ahmad W, Leal SM. Bharadwaj T, et al. Among authors: acharya a. BMC Med Genomics. 2024 Dec 18;17(1):291. doi: 10.1186/s12920-024-02060-w. BMC Med Genomics. 2024. PMID: 39696404 Free PMC article.
Vaccines for immunological defense against traumatic brain injury.
Lintecum K, Thumsi A, Dunn K, Druschel L, Chimene S, Prieto DF, Simmons A, Mantri S, Esrafili A, Swaminathan SJ, Trivedi M, Manjre S, Willingham C, Kizeev G, Davila A, Inamdar S, Mangal JL, Suresh AP, Kasthuri NM, Jaggarapu MMCS, Appel N, Khodaei T, Ng ND, Sundem A, Pathak S, Bjorklund G, Balmer T, Newbern J, Capadona J, Stabenfeldt SE, Acharya AP. Lintecum K, et al. Among authors: acharya ap. bioRxiv [Preprint]. 2024 Dec 5:2024.12.02.626331. doi: 10.1101/2024.12.02.626331. bioRxiv. 2024. PMID: 39677609 Free PMC article. Preprint.
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: acharya a. 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.
Bart syndrome with musculoskeletal deformity: a rare case report.
Pokhrel S, Niraula Z, Ghimire P, Ale Magar S, Acharya A, Awal K. Pokhrel S, et al. Among authors: acharya a. Ann Med Surg (Lond). 2024 Nov 13;86(12):7465-7468. doi: 10.1097/MS9.0000000000002732. eCollection 2024 Dec. Ann Med Surg (Lond). 2024. PMID: 39649920 Free PMC article.
1,323 results