MARIA SABATER MOLINA

Sabater Molina M, Nicolas Rocamora E, Bendicho AI, Vazquez EG, Zorio E, Rodriguez FD, Gil Ortuno C, Rodriguez AI, Sanchez-Lopez AJ, Jara Rubio R, Moreno-Docon A, Marcos PJ, Garcia Pavia P, Villa RB, Gimeno Blanes JR. Polymorphisms in ACE, ACE2, AGTR1 genes and severity of COVID-19 disease. PLoS One. 2022 Feb 4;17(2):e0263140. doi: 10.1371/journal.pone.0263140. eCollection 2022. PubMed PMID: 35120165; PubMed Central PMCID: PMC8815985.

AÑO: 2022; IF: 3.7

35120165

Barc J, Tadros R, Glinge C, Chiang DY, Jouni M, Simonet F, Jurgens SJ, Baudic M, Nicastro M, Potet F, Offerhaus JA, Walsh R, Choi SH, Verkerk AO, Mizusawa Y, Anys S, Minois D, Arnaud M, Duchateau J, Wijeyeratne YD, Muir A, Papadakis M, Castelletti S, Torchio M, Ortuno CG, Lacunza J, Giachino DF, Cerrato N, Martins RP, Campuzano O, Van Dooren S, Thollet A, Kyndt F, Mazzanti A, Clementy N, Bisson A, Corveleyn A, Stallmeyer B, Dittmann S, Saenen J, Noel A, Honarbakhsh S, Rudic B, Marzak H, Rowe MK, Federspiel C, Le Page S, Placide L, Milhem A, Barajas-Martinez H, Beckmann BM, Krapels IP, Steinfurt J, Winkel BG, Jabbari R, Shoemaker MB, Boukens BJ, Skoric-Milosavljevic D, Bikker H, Manevy F, Lichtner P, Ribases M, Meitinger T, Muller-Nurasyid M; KORA-Study Group; Veldink JH, van den Berg LH, Van Damme P, Cusi D, Lanzani C, Rigade S, Charpentier E, Baron E, Bonnaud S, Lecointe S, Donnart A, Le Marec H, Chatel S, Karakachoff M, Bezieau S, London B, Tfelt-Hansen J, Roden D, Odening KE, Cerrone M, Chinitz LA, Volders PG, van de Berg MP, Laurent G, Faivre L, Antzelevitch C, Kaab S, Arnaout AA, Dupuis JM, Pasquie JL, Billon O, Roberts JD, Jesel L, Borggrefe M, Lambiase PD, Mansourati J, Loeys B, Leenhardt A, Guicheney P, Maury P, Schulze-Bahr E, Robyns T, Breckpot J, Babuty D, Priori SG, Napolitano C; Nantes Referral Center for inherited cardiac arrhythmia; de Asmundis C, Brugada P, Brugada R, Arbelo E, Brugada J, Mabo P, Behar N, Giustetto C, Molina MS, Gimeno JR, Hasdemir C, Schwartz PJ, Crotti L, McKeown PP, Sharma S, Behr ER, Haissaguerre M, Sacher F, Rooryck C, Tan HL, Remme CA, Postema PG, Delmar M, Ellinor PT, Lubitz SA, Gourraud JB, Tanck MW, George AL Jr, MacRae CA, Burridge PW, Dina C, Probst V, Wilde AA, Schott JJ, Redon R, Bezzina CR. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nat Genet. 2022 Mar;54(3):232-239. doi: 10.1038/s41588-021-01007-6. Epub 2022 Feb 24. Erratum In: Nat Genet. 2022 May;54(5):735. PubMed PMID: 35210625; PubMed Central PMCID: PMC9376964.

AÑO: 2022; IF: 30.8

35210625

Guler MN, Tscheiller NM, Sabater-Molina M, Gimeno JR, Nebigil CG. Evidence for reciprocal network interactions between injured hearts and cancer. Front Cardiovasc Med. 2022 Jul 15;9:929259. doi: 10.3389/fcvm.2022.929259. eCollection 2022. PubMed PMID: 35911555; PubMed Central PMCID: PMC9334681.

AÑO: 2022; IF: 3.6

35911555

Martinez-Campelo L, Cruz R, Blanco-Verea A, Moscoso I, Ramos-Luis E, Lage R, Alvarez-Barredo M, Sabater-Molina M, Penafiel-Verdu P, Jimenez-Jaimez J, Rodriguez-Manero M, Brion M. Searching for genetic modulators of the phenotypic heterogeneity in Brugada syndrome. PLoS One. 2022 Mar 1;17(3):e0263469. doi: 10.1371/journal.pone.0263469. eCollection 2022. PubMed PMID: 35231055; PubMed Central PMCID: PMC8887717.

AÑO: 2022; IF: 3.7

35231055

Sanchez-Campillo M, Pastor-Fajardo MT, Sabater-Molina M, Lopez-Andreo MJ, Larque E. Critical Steps for Human Gut Exfoliome RNA Profiling Analysis Using Non-Invasive Stool Samples. Ann Nutr Metab. 2022;78(2):80-90. doi: 10.1159/000520968. Epub 2021 Nov 17. PubMed PMID: 34788767.

AÑO: 2022; IF: 3.9

34788767