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Clinical utility of exome sequencing in infantile heart failure.
Ritter A, Bedoukian E, Berger JH, Copenheaver D, Gray C, Krantz I, Izumi K, Juusola J, Leonard J, Lin K, Medne L, Santani A, Skraban C, Yang S, Ahrens-Nicklas RC. Ritter A, et al. Among authors: berger jh. Genet Med. 2020 Feb;22(2):423-426. doi: 10.1038/s41436-019-0654-3. Epub 2019 Sep 17. Genet Med. 2020. PMID: 31527676 Free PMC article.
Variants in NAA15 cause pediatric hypertrophic cardiomyopathy.
Ritter A, Berger JH, Deardorff M, Izumi K, Lin KY, Medne L, Ahrens-Nicklas RC. Ritter A, et al. Among authors: berger jh. Am J Med Genet A. 2021 Jan;185(1):228-233. doi: 10.1002/ajmg.a.61928. Epub 2020 Oct 26. Am J Med Genet A. 2021. PMID: 33103328 Free PMC article.
Disruption of cardiac thin filament assembly arising from a mutation in LMOD2: A novel mechanism of neonatal dilated cardiomyopathy.
Ahrens-Nicklas RC, Pappas CT, Farman GP, Mayfield RM, Larrinaga TM, Medne L, Ritter A, Krantz ID, Murali C, Lin KY, Berger JH, Yum SW, Carreon CK, Gregorio CC. Ahrens-Nicklas RC, et al. Among authors: berger jh. Sci Adv. 2019 Sep 4;5(9):eaax2066. doi: 10.1126/sciadv.aax2066. eCollection 2019 Sep. Sci Adv. 2019. PMID: 31517052 Free PMC article.
Editorial Comment.
Baker BH, Berger JH. Baker BH, et al. Among authors: berger jh. J Urol. 2023 Dec;210(6):853-854. doi: 10.1097/JU.0000000000003680.01. Epub 2023 Oct 5. J Urol. 2023. PMID: 37795816 No abstract available.
34 results