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Page 1
The impact of common and rare genetic variants on bradyarrhythmia development.
Weng LC, Rämö JT, Jurgens SJ, Khurshid S, Chaffin M, Hall AW, Morrill VN, Wang X, Nauffal V, Sun YV, Beer D, Lee S, Nadkarni GN, Duong T, Wang B, Czuba T, Austin TR, Yoneda ZT, Friedman DJ, Clayton A, Hyman MC, Judy RL, Skanes AC, Orland KM, Treu TM, Oetjens MT, Alonso A, Soliman EZ, Lin H, Lunetta KL, van der Pals J, Issa TZ, Nafissi NA, May HT, Leong-Sit P, Roselli C, Choi SH; FinnGen; Million Veteran Program; Regeneron Genetics Center; Khan HR, Knight S, Karlsson Linnér R, Bezzina CR, Ripatti S, Heckbert SR, Gaziano JM, Loos RJF, Psaty BM, Smith JG, Benjamin EJ, Arking DE, Rader DJ, Shah SH, Roden DM, Damrauer SM, Eckhardt LL, Roberts JD, Cutler MJ, Shoemaker MB, Haggerty CM, Cho K, Palotie A, Wilson PWF, Ellinor PT, Lubitz SA. Weng LC, et al. Among authors: orland km. Nat Genet. 2025 Jan;57(1):53-64. doi: 10.1038/s41588-024-01978-2. Epub 2025 Jan 2. Nat Genet. 2025. PMID: 39747593 Free PMC article.
Dynamic role of hormones on Brugada syndrome phenotype.
Vrtikapa D, Krasowski AA, Orland KM, Eckhardt LL. Vrtikapa D, et al. Among authors: orland km. HeartRhythm Case Rep. 2024 Aug 14;10(11):843-846. doi: 10.1016/j.hrcr.2024.08.010. eCollection 2024 Nov. HeartRhythm Case Rep. 2024. PMID: 39664676 Free PMC article. No abstract available.
Examination of the Pediatric Cervical Spine Under Anesthesia.
Montgomery BK, Orland K, Wilson TA, Chen W, Shirley OC, Segar A, Field AJ, Crawford HA. Montgomery BK, et al. Among authors: orland k. Cureus. 2024 Jul 15;16(7):e64623. doi: 10.7759/cureus.64623. eCollection 2024 Jul. Cureus. 2024. PMID: 39156372 Free PMC article.
Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias.
Weng LC, Khurshid S, Hall AW, Nauffal V, Morrill VN, Sun YV, Rämö JT, Beer D, Lee S, Nadkarni G, Johnson R, Andreasen L, Clayton A, Pullinger CR, Yoneda ZT, Friedman DJ, Hyman MC, Judy RL, Skanes AC, Orland KM, Jordà P, Treu TM, Oetjens MT, Subbiah R, Hartmann JP, May HT, Kane JP, Issa TZ, Nafissi NA, Leong-Sit P, Dubé MP, Roselli C, Choi SH; FinnGen, Million Veteran Program, Regeneron Genetics Center; Tardif JC, Khan HR, Knight S, Svendsen JH, Walker B, Karlsson Linnér R, Gaziano JM, Tadros R, Fatkin D, Rader DJ, Shah SH, Roden DM, Marcus GM, Loos RJF, Damrauer SM, Haggerty CM, Cho K, Palotie A, Olesen MS, Eckhardt LL, Roberts JD, Cutler MJ, Shoemaker MB, Wilson PWF, Ellinor PT, Lubitz SA. Weng LC, et al. Among authors: orland km. Circ Genom Precis Med. 2024 Jun;17(3):e004320. doi: 10.1161/CIRCGEN.123.004320. Epub 2024 May 28. Circ Genom Precis Med. 2024. PMID: 38804128
An Analysis of Scoliosis in Autism Spectrum Disorder.
Orland K, Harvey K, Klinkerman LN, Corrales A, Jamnik A, Zale C, Jo CH, Rathjen K, McIntosh A, Petrasic J, Sucato DJ, Ramo B, Johnson M, Brooks JT. Orland K, et al. J Pediatr Orthop. 2023 Nov-Dec 01;43(10):e804-e808. doi: 10.1097/BPO.0000000000002497. Epub 2023 Aug 23. J Pediatr Orthop. 2023. PMID: 37609890
Elucidation of ALG10B as a Novel Long-QT Syndrome-Susceptibility Gene.
Zhou W, Ye D, Tester DJ, Bains S, Giudicessi JR, Haglund-Turnquist CM, Orland KM, January CT, Eckhardt LL, Maginot KR, Ackerman MJ. Zhou W, et al. Among authors: orland km. Circ Genom Precis Med. 2023 Apr;16(2):e003726. doi: 10.1161/CIRCGEN.122.003726. Epub 2023 Feb 22. Circ Genom Precis Med. 2023. PMID: 37071726 Free PMC article.
30 results