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Rare genetic coding variants associated with human longevity and protection against age-related diseases.
Lin JR, Sin-Chan P, Napolioni V, Torres GG, Mitra J, Zhang Q, Jabalameli MR, Wang Z, Nguyen N, Gao T; Regeneron Genetics Center; Laudes M, Görg S, Franke A, Nebel A, Greicius MD, Atzmon G, Ye K, Gorbunova V, Ladiges WC, Shuldiner AR, Niedernhofer LJ, Robbins PD, Milman S, Suh Y, Vijg J, Barzilai N, Zhang ZD. Lin JR, et al. Among authors: jabalameli mr. Nat Aging. 2021 Sep;1(9):783-794. doi: 10.1038/s43587-021-00108-5. Epub 2021 Sep 13. Nat Aging. 2021. PMID: 37117627
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia.
Lin JR, Zhao Y, Jabalameli MR, Nguyen N, Mitra J; International 22q11.DS Brain and Behavior Consortium; Swillen A, Vorstman JAS, Chow EWC, van den Bree M, Emanuel BS, Vermeesch JR, Owen MJ, Williams NM, Bassett AS, McDonald-McGinn DM, Gur RE, Bearden CE, Morrow BE, Lachman HM, Zhang ZD. Lin JR, et al. Among authors: jabalameli mr. Mol Psychiatry. 2023 May;28(5):2071-2080. doi: 10.1038/s41380-023-02009-y. Epub 2023 Mar 3. Mol Psychiatry. 2023. PMID: 36869225
Unravelling genetic components of longevity.
Jabalameli MR, Zhang ZD. Jabalameli MR, et al. Nat Aging. 2022 Jan;2(1):5-6. doi: 10.1038/s43587-021-00162-z. Nat Aging. 2022. PMID: 37118361 No abstract available.
21 results