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Page 1
Biomarkers.
Roberts AC, Ooteghem KV, McIlroy B, Culum I, Beyer KB, Thai V, Aulakh N, Li J, Dunne C, Lim A, Swartz RH, Finger E, Maher AC, Okonkwo OC, Goldstein F, Huentelman MJ, Geula C, Rogalski EJ. Roberts AC, et al. Among authors: huentelman mj. Alzheimers Dement. 2024 Dec;20 Suppl 2:e089381. doi: 10.1002/alz.089381. Alzheimers Dement. 2024. PMID: 39785625
Public Health.
Branch AE, McQuail J, Kaczorowski CC, Foster TC, Disterhoft JF, Huentelman MJ, Rapp PR, Barnes CA. Branch AE, et al. Among authors: huentelman mj. Alzheimers Dement. 2024 Dec;20 Suppl 7:e087235. doi: 10.1002/alz.087235. Alzheimers Dement. 2024. PMID: 39784985
Developing Topics.
Ghisays V, Khajouei E, Piras I, Goradia DD, Malek-Ahmadi MH, Chen Y, Naymik M, Saner D, Su Y, Huentelman MJ, Karnes JH, Reiman EM. Ghisays V, et al. Among authors: huentelman mj. Alzheimers Dement. 2024 Dec;20 Suppl 8:e094631. doi: 10.1002/alz.094631. Alzheimers Dement. 2024. PMID: 39783441
Duchenne Muscular Dystrophy in Two Half-Brothers Due to Inherited 306 Kb Inverted Insertion of 10p15.1 into Intron 44 of the Dp427m Transcript of the DMD Gene.
Jepsen WM, Fazenbaker A, Ramsey K, Bonfitto A, Naymik M, Turner B, Sloan J, Tiwari N, Bernes SM, Neilson DE, Sanchez-Castillo M, Huentelman MJ, Narayanan V. Jepsen WM, et al. Among authors: huentelman mj. Int J Mol Sci. 2024 Nov 6;25(22):11922. doi: 10.3390/ijms252211922. Int J Mol Sci. 2024. PMID: 39595988 Free PMC article.
Amyloid-β predominant Alzheimer's disease neuropathologic change.
Kovacs GG, Katsumata Y, Wu X, Aung KZ, Fardo DW, Forrest SL; Alzheimer's Disease Genetics Consortium; Nelson PT. Kovacs GG, et al. Brain. 2024 Oct 17:awae325. doi: 10.1093/brain/awae325. Online ahead of print. Brain. 2024. PMID: 39417691
Phenome-Wide Association of APOE Alleles in the All of Us Research Program.
Khajouei E, Ghisays V, Piras IS, Martinez KL, Naymik M, Ngo P, Tran TC, Denny JC, Wheeler TJ, Huentelman MJ, Reiman EM, Karnes JH. Khajouei E, et al. Among authors: huentelman mj. medRxiv [Preprint]. 2024 Sep 4:2024.09.04.24313010. doi: 10.1101/2024.09.04.24313010. medRxiv. 2024. PMID: 39281754 Free PMC article. Preprint.
Snyder-Robinson syndrome presenting with learning disability, epilepsy, and osteoporosis: a novel SMS gene variant.
Leung M, Sanchez-Castillo M, Belnap N, Naymik M, Bonfitto A, Sloan J, Hassett K, Jepsen WM, Sankaramoorthy A, Stewart TM, Foley JR, Rangasamy S, Huentelman MJ, Narayanan V, Ramsey K. Leung M, et al. Among authors: huentelman mj. Rare. 2024;2:100017. doi: 10.1016/j.rare.2023.100017. Epub 2023 Dec 13. Rare. 2024. PMID: 38770537 Free PMC article.
228 results