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Genetic analyses in multiplex families confirms chromosome 5q35 as a risk locus for Alzheimer's Disease in individuals of African Ancestry.
Nuytemans K, Rajabli F, Jean-Francois M, Kurup JT, Adams LD, Starks TD, Whitehead PL, Kunkle BW, Caban-Holt A, Haines JL, Cuccaro ML, Vance JM, Byrd GS, Beecham GW, Reitz C, Pericak-Vance MA; NIA-LOAD Family-Based Study; Alzheimer’s Disease Sequencing Project. Nuytemans K, et al. Among authors: vance jm. Neurobiol Aging. 2024 Jan;133:125-133. doi: 10.1016/j.neurobiolaging.2023.10.010. Epub 2023 Oct 31. Neurobiol Aging. 2024. PMID: 37952397 Free article.
A novel mutation in the von Hippel-Lindau gene.
Loeb DB, Pericak-Vance MA, Stajich JM, Vance JM. Loeb DB, et al. Among authors: vance jm. Hum Mol Genet. 1994 Aug;3(8):1423-4. doi: 10.1093/hmg/3.8.1423. Hum Mol Genet. 1994. PMID: 7987327 No abstract available.
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutation.
Stajich JM, Gilchrist JM, Lennon F, Lee A, Yamaoka L, Rosi B, Gaskell PC, Pritchard M, Donald L, Roses AD, Vance JM, Pericak-Vance MA. Stajich JM, et al. Among authors: vance jm. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S75-81. doi: 10.1016/s0960-8966(97)00087-4. Neuromuscul Disord. 1997. PMID: 9392021
281 results