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Page 1
Molecular convergence of risk variants for congenital heart defects leveraging a regulatory map of the human fetal heart.
Ma XR, Conley SD, Kosicki M, Bredikhin D, Cui R, Tran S, Sheth MU, Qiu WL, Chen S, Kundu S, Kang HY, Amgalan D, Munger CJ, Duan L, Dang K, Rubio OM, Kany S, Zamirpour S, DePaolo J, Padmanabhan A; Birth Defects Research Laboratory; Olgin J, Damrauer S, Andersson R, Gu M, Priest JR, Quertermous T, Qiu X, Rabinovitch M, Visel A, Pennacchio L, Kundaje A, Glass IA, Gifford CA, Pirruccello JP, Goodyer WR, Engreitz JM. Ma XR, et al. Among authors: kany s. medRxiv [Preprint]. 2024 Nov 22:2024.11.20.24317557. doi: 10.1101/2024.11.20.24317557. medRxiv. 2024. PMID: 39606363 Free PMC article. Preprint.
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience.
Jurgens SJ, Rämö JT, Kramarenko DR, Wijdeveld LFJM, Haas J, Chaffin MD, Garnier S, Gaziano L, Weng LC, Lipov A, Zheng SL, Henry A, Huffman JE, Challa S, Rühle F, Verdugo CD, Krijger Juárez C, Kany S, van Orsouw CA, Biddinger K, Poel E, Elliott AL, Wang X, Francis C, Ruan R, Koyama S, Beekman L, Zimmerman DS, Deleuze JF, Villard E, Trégouët DA, Isnard R; FinnGen; VA Million Veteran Program; HERMES Consortium; Boomsma DI, de Geus EJC, Tadros R, Pinto YM, Wilde AAM, Hottenga JJ, Sinisalo J, Niiranen T, Walsh R, Schmidt AF, Choi SH, Chang KM, Tsao PS, Matthews PM, Ware JS, Lumbers RT, van der Crabben S, Laukkanen J, Palotie A, Amin AS, Charron P, Meder B, Ellinor PT, Daly M, Aragam KG, Bezzina CR. Jurgens SJ, et al. Among authors: kany s. Nat Genet. 2024 Nov 21. doi: 10.1038/s41588-024-01975-5. Online ahead of print. Nat Genet. 2024. PMID: 39572784
Rare Genetic Variants in LDLR, APOB, and PCSK9 Are Associated With Aortic Stenosis.
Rämö JT, Jurgens SJ, Kany S, Choi SH, Wang X, Smirnov AN, Friedman SF, Maddah M, Khurshid S, Ellinor PT, Pirruccello JP. Rämö JT, et al. Among authors: kany s. Circulation. 2024 Nov 26;150(22):1767-1780. doi: 10.1161/CIRCULATIONAHA.124.070982. Epub 2024 Sep 2. Circulation. 2024. PMID: 39222019
Rare coding variant analysis for human diseases across biobanks and ancestries.
Jurgens SJ, Wang X, Choi SH, Weng LC, Koyama S, Pirruccello JP, Nguyen T, Smadbeck P, Jang D, Chaffin M, Walsh R, Roselli C, Elliott AL, Wijdeveld LFJM, Biddinger KJ, Kany S, Rämö JT, Natarajan P, Aragam KG, Flannick J, Burtt NP, Bezzina CR, Lubitz SA, Lunetta KL, Ellinor PT. Jurgens SJ, et al. Among authors: kany s. Nat Genet. 2024 Sep;56(9):1811-1820. doi: 10.1038/s41588-024-01894-5. Epub 2024 Aug 29. Nat Genet. 2024. PMID: 39210047
Electrocardiogram-Based Artificial Intelligence to Discriminate Cardioembolic Stroke and Stratify Risk of Atrial Fibrillation After Stroke.
Khurshid S, Friedman SF, Kany S, Mahajan R, Turner AC, Lubitz SA, Maddah M, Ellinor PT, Anderson CD. Khurshid S, et al. Among authors: kany s. Circ Arrhythm Electrophysiol. 2024 Oct;17(10):e012959. doi: 10.1161/CIRCEP.124.012959. Epub 2024 Aug 28. Circ Arrhythm Electrophysiol. 2024. PMID: 39193715 No abstract available.
56 results