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Year | Number of Results |
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2023 | 4 |
2024 | 1 |
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Page 1
Underrepresentation of Diverse Ancestries Drives Uncertainty in Genetic Variants Found in Cardiomyopathy-Associated Genes.
JACC Adv. 2024 Feb;3(2):100767. doi: 10.1016/j.jacadv.2023.100767. Epub 2023 Dec 15.
JACC Adv. 2024.
PMID: 38464909
Free PMC article.
Nonsense Variant PRDM16-Q187X Causes Impaired Myocardial Development and TGF-β Signaling Resulting in Noncompaction Cardiomyopathy in Humans and Mice.
Sun B, Rouzbehani OMT, Kramer RJ, Ghosh R, Perelli RM, Atkins S, Fatahian AN, Davis K, Szulik MW, Goodman MA, Hathaway MA, Chi E, Word TA, Tunuguntla H, Denfield SW, Wehrens XHT, Whitehead KJ, Abdelnasser HY, Warren JS, Wu M, Franklin S, Boudina S, Landstrom AP.
Sun B, et al.
Circ Heart Fail. 2023 Dec;16(12):e010351. doi: 10.1161/CIRCHEARTFAILURE.122.010351. Epub 2023 Dec 19.
Circ Heart Fail. 2023.
PMID: 38113297
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DiscoVari: A Web-Based Precision Medicine Tool for Predicting Variant Pathogenicity in Cardiomyopathy- and Channelopathy-Associated Genes.
Kurzlechner LM, Kishnani S, Chowdhury S, Atkins SL, Moya-Mendez ME, Parker LE, Rosamilia MB, Tadros HJ, Pace LA, Patel V, Chahal CAA, Landstrom AP.
Kurzlechner LM, et al.
Circ Genom Precis Med. 2023 Aug;16(4):317-327. doi: 10.1161/CIRCGEN.122.003911. Epub 2023 Jul 6.
Circ Genom Precis Med. 2023.
PMID: 37409478
Free article.
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Induced Pluripotent Stem Cell-Based Modeling of Single-Ventricle Congenital Heart Diseases.
Parker LE, Kurzlechner LM, Landstrom AP.
Parker LE, et al.
Curr Cardiol Rep. 2023 May;25(5):295-305. doi: 10.1007/s11886-023-01852-3. Epub 2023 Mar 17.
Curr Cardiol Rep. 2023.
PMID: 36930454
Free PMC article.
Review.
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