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Page 1
Case Report: Whole Exome Sequencing Identifies Compound Heterozygous Variants in TSFM Gene Causing Juvenile Hypertrophic Cardiomyopathy.
Yang JO, Shaybekyan H, Zhao Y, Kang X, Fishbein GA, Khanlou N, Alejos JC, Halnon N, Satou G, Biniwale R, Lee H, Van Arsdell G, Nelson SF, Touma M; UCLA Clinical Genomics Center; UCLA Congenital Heart Defects-BioCore Faculty. Yang JO, et al. Among authors: halnon n. Front Cardiovasc Med. 2022 Jan 6;8:798985. doi: 10.3389/fcvm.2021.798985. eCollection 2021. Front Cardiovasc Med. 2022. PMID: 35071363 Free PMC article.
Gene-environment regulatory circuits of right ventricular pathology in tetralogy of fallot.
Zhao Y, Kang X, Gao F, Guzman A, Lau RP, Biniwale R, Wadehra M, Reemtsen B, Garg M, Halnon N, Quintero-Rivera F, Van Arsdell G, Coppola G, Nelson SF, Touma M; UCLA Congenital Heart Defects BioCore Faculty. Zhao Y, et al. Among authors: halnon n. J Mol Med (Berl). 2019 Dec;97(12):1711-1722. doi: 10.1007/s00109-019-01857-y. Epub 2019 Dec 13. J Mol Med (Berl). 2019. PMID: 31834445 Free PMC article.
Online self-report data for duchenne muscular dystrophy confirms natural history and can be used to assess for therapeutic benefits.
Wang RT, Silverstein Fadlon CA, Ulm JW, Jankovic I, Eskin A, Lu A, Rangel Miller V, Cantor RM, Li N, Elashoff R, Martin AS, Peay HL, Halnon N, Nelson SF. Wang RT, et al. Among authors: halnon n. PLoS Curr. 2014 Oct 17;6:ecurrents.md.e1e8f2be7c949f9ffe81ec6fca1cce6a. doi: 10.1371/currents.md.e1e8f2be7c949f9ffe81ec6fca1cce6a. PLoS Curr. 2014. PMID: 25635234 Free PMC article.
Cardiac MRI biomarkers for Duchenne muscular dystrophy.
Magrath P, Maforo N, Renella P, Nelson SF, Halnon N, Ennis DB. Magrath P, et al. Among authors: halnon n. Biomark Med. 2018 Nov;12(11):1271-1289. doi: 10.2217/bmm-2018-0125. Epub 2018 Nov 30. Biomark Med. 2018. PMID: 30499689 Free PMC article. Review.
Home use of a compact, 12‑lead ECG recording system for newborns.
Lin HJ, Lan YT, Silka MJ, Halnon NJ, Villa-Lopez E, Arenas N, Escobedo F, Montoya R, Valdez S, Rajabi Shishvan O, Sedano S, Marr EH, Lauzon M, Moosa AS, Ko KJ, Shoji EC, Clark AM, Smith LM, Criley JM, Grody WW, Chen YI, Taylor KD, Guo X, Soyata T, Rotter JI, Chien T, Chou P, Chang RK. Lin HJ, et al. Among authors: halnon nj. J Electrocardiol. 2019 Mar-Apr;53:89-94. doi: 10.1016/j.jelectrocard.2019.01.086. Epub 2019 Jan 25. J Electrocardiol. 2019. PMID: 30716528 Free PMC article. Clinical Trial.
Recessive ciliopathy mutations in primary endocardial fibroelastosis: a rare neonatal cardiomyopathy in a case of Alstrom syndrome.
Zhao Y, Wang LK, Eskin A, Kang X, Fajardo VM, Mehta Z, Pineles S, Schmidt RJ, Nagiel A, Satou G, Garg M, Federman M, Reardon LC, Lee SL, Biniwale R, Grody WW, Halnon N, Khanlou N, Quintero-Rivera F, Alejos JC, Nakano A, Fishbein GA, Van Arsdell GS, Nelson SF, Touma M. Zhao Y, et al. Among authors: halnon n. J Mol Med (Berl). 2021 Nov;99(11):1623-1638. doi: 10.1007/s00109-021-02112-z. Epub 2021 Aug 13. J Mol Med (Berl). 2021. PMID: 34387706 Free PMC article.
Whole-Exome Sequencing Identifies Homozygote Nonsense Variants in LMOD2 Gene Causing Infantile Dilated Cardiomyopathy.
Sono R, Larrinaga TM, Huang A, Makhlouf F, Kang X, Su J, Lau R, Arboleda VA, Biniwale R, Fishbein GA, Khanlou N, Si MS, Satou GM, Halnon N, Ucla Congenital Heart Defects-BioCore Faculty, Van Arsdell GS, Gregorio CC, Nelson S, Touma M. Sono R, et al. Among authors: halnon n. Cells. 2023 May 23;12(11):1455. doi: 10.3390/cells12111455. Cells. 2023. PMID: 37296576 Free PMC article.
53 results