Fabiana Scornik, PhD - Publications

Affiliations: 
Masonic Medical Research Laboratory, Utica, Frankfort, NY, United States 

23 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Martínez-Moreno R, Carreras D, Sarquella-Brugada G, Pérez GJ, Selga E, Scornik FS, Brugada R. Loss of sodium current caused by a Brugada syndrome-associated variant is determined by patient-specific genetic background. Heart Rhythm. PMID 38008367 DOI: 10.1016/j.hrthm.2023.11.019  0.592
2023 Martínez-Moreno R, Pérez-Serra A, Selga E, Carreras D, Aran B, Kuebler B, Scornik FS, Pérez GJ, Brugada R. Generation of the induced pluripotent stem cell line ESi108-A from a familial atrial fibrillation patient. Stem Cell Research. 73: 103239. PMID 37922745 DOI: 10.1016/j.scr.2023.103239  0.522
2022 Martínez-Moreno R, Carreras D, Aran B, Kuebler B, Sarquella-Brugada G, Brugada R, Pérez GJ, Scornik FS, Selga E. Generation of four induced pluripotent stem cell lines from a family harboring a single nucleotide variant in SCN5A. Stem Cell Research. 63: 102847. PMID 35772296 DOI: 10.1016/j.scr.2022.102847  0.586
2022 Martínez-Moreno R, Pérez-Serra A, Carreras D, Aran B, Kuebler B, Brugada R, Scornik FS, Pérez GJ, Selga E. Generation of an induced pluripotent stem cell line from a healthy Caucasian male. Stem Cell Research. 60: 102717. PMID 35231795 DOI: 10.1016/j.scr.2022.102717  0.514
2021 Carreras D, Martinez-Moreno R, Pinsach-Abuin ML, Santafe MM, Gomà P, Brugada R, Scornik FS, Pérez GJ, Pagans S. Epigenetic Changes Governing Expression in Denervated Skeletal Muscle. International Journal of Molecular Sciences. 22. PMID 33803193 DOI: 10.3390/ijms22052755  0.506
2020 Martinez-Moreno R, Selga E, Riuró H, Carreras D, Parnes M, Srinivasan C, Wangler MF, Pérez GJ, Scornik FS, Brugada R. An Variant Affects Both Cardiac-Type (Na1.5) and Brain-Type (Na1.1) Sodium Currents and Contributes to Complex Concomitant Brain and Cardiac Disorders. Frontiers in Cell and Developmental Biology. 8: 528742. PMID 33134290 DOI: 10.3389/fcell.2020.528742  0.536
2020 Martinez-Moreno R, Carreras D, Selga E, Sarquella-Brugada G, Brugada R, Perez GJ, Scornik FS. Comparative Study of the Effects of an SCN5A Mutation within a Family Diagnosed with Brugada Syndrome using iPS-CM Biophysical Journal. 118: 500a. DOI: 10.1016/j.bpj.2019.11.2759  0.501
2020 Carreras D, Martinez-Moreno R, Selga E, Brugada R, Scornik FS, Perez GJ. CPVT-Associated Mutation P.G357S-RYR2 Promotes a Gain of Function in Patient-Specific Induced Pluripotent Stem Cell-Derived Cardiomyocytes (iPS-CM) Biophysical Journal. 118: 255a. DOI: 10.1016/j.bpj.2019.11.1488  0.523
2019 Yeste M, Llavanera M, Pérez G, Scornik F, Puig-Parri J, Brugada R, Bonet S, Pinart E. Elucidating the Role of K Channels during In Vitro Capacitation of Boar Spermatozoa: Do SLO1 Channels Play a Crucial Role? International Journal of Molecular Sciences. 20. PMID 31847486 DOI: 10.3390/ijms20246330  0.483
2019 Santori M, Gil R, Blanco-Verea A, Riuró H, Díaz-Castro Ó, López-Abel B, Brugada R, Carracedo Á, Pérez GJ, Scornik FS, Brion M. Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillation. Forensic Science International. Genetics. 43: 102159. PMID 31522018 DOI: 10.1016/j.fsigen.2019.102159  0.468
2019 Cuyàs E, Gumuzio J, Lozano-Sánchez J, Carreras D, Verdura S, Llorach-Parés L, Sanchez-Martinez M, Selga E, Pérez GJ, Scornik FS, Brugada R, Bosch-Barrera J, Segura-Carretero A, Martin ÁG, Encinar JA, et al. Extra Virgin Olive Oil Contains a Phenolic Inhibitor of the Histone Demethylase LSD1/KDM1A. Nutrients. 11. PMID 31331073 DOI: 10.3390/nu11071656  0.429
2019 Sendfeld F, Selga E, Scornik FS, Pérez GJ, Mills NL, Brugada R. Experimental Models of Brugada syndrome. International Journal of Molecular Sciences. 20. PMID 31032819 DOI: 10.3390/ijms20092123  0.579
2019 Martinez-Moreno R, Selga E, Sarquella-Brugada G, Brugada R, Perez G, Scornik F. Cardiac Sodium Current is Severely Impaired in Induced Pluripotent Stem Cell-Derived Cardiomyocytes from Brugada Syndrome Patients Biophysical Journal. 116: 390a-391a. DOI: 10.1016/J.BPJ.2018.11.2114  0.341
2017 Selga E, Sendfeld F, Martinez-Moreno R, Medine CN, Tura-Ceide O, Wilmut SI, Pérez GJ, Scornik FS, Brugada R, Mills NL. Sodium channel current loss of function in induced pluripotent stem cell-derived cardiomyocytes from a Brugada syndrome patient. Journal of Molecular and Cellular Cardiology. PMID 29024690 DOI: 10.1016/j.yjmcc.2017.10.002  0.607
2015 Peeters U, Scornik F, Riuró H, Pérez G, Komurcu-Bayrak E, Van Malderen S, Pappaert G, Tarradas A, Pagans S, Daneels D, Breckpot K, Brugada P, Bonduelle M, Brugada R, Van Dooren S. Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome. Circulation Journal : Official Journal of the Japanese Circulation Society. 79: 2118-29. PMID 26179811 DOI: 10.1253/circj.CJ-15-0164  0.588
2015 Wangüemert F, Bosch Calero C, Pérez C, Campuzano O, Beltran-Alvarez P, Scornik FS, Iglesias A, Berne P, Allegue C, Ruiz Hernandez PM, Brugada J, Pérez GJ, Brugada R. Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 12: 1636-43. PMID 25814417 DOI: 10.1016/j.hrthm.2015.03.033  0.519
2014 Riuró H, Campuzano O, Arbelo E, Iglesias A, Batlle M, Pérez-Villa F, Brugada J, Pérez GJ, Scornik FS, Brugada R. A missense mutation in the sodium channel β1b subunit reveals SCN1B as a susceptibility gene underlying long QT syndrome. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 11: 1202-9. PMID 24662403 DOI: 10.1016/j.hrthm.2014.03.044  0.39
2013 Riuró H, Beltran-Alvarez P, Tarradas A, Selga E, Campuzano O, Vergés M, Pagans S, Iglesias A, Brugada J, Brugada P, Vázquez FM, Pérez GJ, Scornik FS, Brugada R. A missense mutation in the sodium channel β2 subunit reveals SCN2B as a new candidate gene for Brugada syndrome. Human Mutation. 34: 961-6. PMID 23559163 DOI: 10.1002/humu.22328  0.414
2013 Tarradas A, Selga E, Beltran-Alvarez P, Pérez-Serra A, Riuró H, Picó F, Iglesias A, Campuzano O, Castro-Urda V, Fernández-Lozano I, Pérez GJ, Scornik FS, Brugada R. A novel missense mutation, I890T, in the pore region of cardiac sodium channel causes Brugada syndrome. Plos One. 8: e53220. PMID 23308164 DOI: 10.1371/journal.pone.0053220  0.38
2013 Medine C, Perez G, Sendfeld F, Scornik F, Mills N, Wilmut I, Tura O. 264 CHARACTERISATION OF CARDIOMYOCYTES DERIVED FROM HUMAN INDUCED PLURIPOTENT STEM (IPS) CELLS Heart. 99: A139.2-A139. DOI: 10.1136/Heartjnl-2013-304019.264  0.376
2004 Antzelevitch C, Belardinelli L, Wu L, Fraser H, Zygmunt AC, Burashnikov A, Di Diego JM, Fish JM, Cordeiro JM, Goodrow RJ, Scornik F, Perez G. Electrophysiologic properties and antiarrhythmic actions of a novel antianginal agent. Journal of Cardiovascular Pharmacology and Therapeutics. 9: S65-83. PMID 15378132 DOI: 10.1177/107424840400900106  0.47
1993 Scornik FS, Codina J, Birnbaumer L, Toro L. Modulation of coronary smooth muscle KCa channels by Gs alpha independent of phosphorylation by protein kinase A. The American Journal of Physiology. 265: H1460-5. PMID 8238435  0.457
1992 Scornik FS, Toro L. U46619, a thromboxane A2 agonist, inhibits KCa channel activity from pig coronary artery. The American Journal of Physiology. 262: C708-13. PMID 1550211  0.481
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