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Page 1
Genetic and clinical characterization of a novel FH founder mutation in families with hereditary leiomyomatosis and renal cell cancer syndrome.
Sánchez-Heras AB, Dámaso E, Castillejo A, Robledo M, Teulé A, Lázaro C, Sánchez-Martínez R, Zúñiga Á, López-Fernández A, Balmaña J, Robles L, Ramon Y Cajal T, Castillejo MI, Ibañez RP, Sevila CM, Sánchez-Mira A, Escandell I, Gómez L, Berbel P, Soto JL. Sánchez-Heras AB, et al. Among authors: zuniga a. Orphanet J Rare Dis. 2024 Jan 26;19(1):26. doi: 10.1186/s13023-024-03017-z. Orphanet J Rare Dis. 2024. PMID: 38279137 Free PMC article.
Population Digital Health: Continuous Health Monitoring and Profiling at Scale.
Hossein Motlagh N, Zuniga A, Thi Nguyen N, Flores H, Wang J, Tarkoma S, Prosperi M, Helal S, Nurmi P. Hossein Motlagh N, et al. Among authors: zuniga a. Online J Public Health Inform. 2024 Nov 20;16:e60261. doi: 10.2196/60261. Online J Public Health Inform. 2024. PMID: 39565687 Free PMC article.
Identification of targetable epigenetic vulnerabilities in uveal melanoma.
Yenisehirli G, Borges S, Braun SS, Zuniga AN, Quintana GI, Kutsnetsoff JN, Rodriguez S, Adis EV, Lopez S, Dollar JJ, Stathias V, Volmar CH, Karaca E, Brothers S, Bilbao D, Harbour JW, Correa ZM, Kurtenbach S. Yenisehirli G, et al. Among authors: zuniga an. bioRxiv [Preprint]. 2024 Oct 11:2024.10.11.617464. doi: 10.1101/2024.10.11.617464. bioRxiv. 2024. PMID: 39416076 Free PMC article. Preprint.
332 results