Alias, L, de Heredia, ML, Luna, S, Cliville, N, Gonzalez-Quereda, L, Gallano, P, de Juan, J, Pujol, A, Diez, S, Boronat, S, Orus, C, Lasa, A, Venegas, MD. Case report: De novo pathogenic variant in WFS1 causes Wolfram-like syndrome debuting with congenital bilateral deafness. Frontiers in Genetics. 2022; 13DOI:10.3389/fgene.2022.998898. PMID:36330437. IF:3.700(Q2/4D).

Caneiro-Queija, B, Raposeiras-Roubin, S, Adamo, M, Freixa, X, Arzamendi, D, Benito-Gonzalez, T, Montefusco, A, Pascual, I, Nombela-Franco, L, Rodes-Cabau, J, Shuvy, M, Portoles-Hernandez, A, Godino, C, Haberman, D, Lupi, L, Regueiro, A, Li, CH, Fernandez-Vazquez, F, Frea, S, Avanzas, P, Tirado-Conte, G, Paradis, JM, Peretz, A, Monivas, V, Baz, JA, Galasso, M, Branca, L, Sanchis, L, Asmarats, L, Garrote-Coloma, C, Angelini, F, Leon, V, de Agustin, JA, Alperi, A, Beeri, R, Maccagni, G, Sabate, M, Fernandez-Peregrina, E, Gualis, J, Bocchino, PP, Curello, S, Iniguez-Romo, A, Estevez-Loureiro, R. Prognostic Impact of Nutritional Status After Transcatheter Edge-to-Edge Mitral Valve Repair: The MIVNUT Registry. Journal of the American Heart Association. 2022; 11(20)DOI:10.1161/JAHA.121.023121. PMID:36216434. IF:5.400(Q2/3D).

Huang, TY, Chen, J, Muller-Edenborn, B, Mayer, L, Eichenlaub, M, Weidmann, ZM, Allgeier, J, Bohnen, M, Lehrmann, H, Trenk, D, Schoechlin, S, Westermann, D, Arentz, T, Jadidi, A. Validating left atrial fractionation and low-voltage substrate during atrial fibrillation and sinus rhythm-A high-density mapping study in persistent atrial fibrillation. Frontiers in Cardiovascular Medicine. 2022; 9DOI:10.3389/fcvm.2022.1000027. PMID:36330001. IF:3.600(Q2/5D).

Thibord, F, Klarin, D, Brody, JA, Chen, MH, Levin, MG, Chasman, DI, Goode, EL, Hveem, K, Teder-Laving, M, Martinez-Perez, A, Aissi, D, Daian-Bacq, D, Ito, K, Natarajan, P, Lutsey, PL, Nadkarni, GN, de Vries, PS, Cuellar-Partida, G, Wolford, BN, Pattee, JW, Kooperberg, C, Braekkan, SK, Li-Gao, RF, Saut, N, Sept, C, Germain, M, Judy, RL, Wiggins, KL, Ko, D, O'Donnell, CJ, Taylor, KD, Giulianini, F, De Andrade, M, Nost, TH, Boland, A, Empana, JP, Koyama, S, Gilliland, T, Do, R, Huffman, JE, Wang, X, Zhou, W, Soria, JM, Souto, JC, Pankratz, N, Haessler, J, Hindberg, K, Rosendaal, FR, Turman, C, Olaso, R, Kember, RL, Bartz, TM, Lynch, JA, Heckbert, SR, Armasu, SM, Brumpton, B, Smadja, DM, Jouven, X, Komuro, I, Clapham, KR, Loos, RJF, Willer, CJ, Sabater-Lleal, M, Pankow, JS, Reiner, AP, Morelli, VM, Ridker, PM, Vlieg, AV, Deleuze, JF, Kraft, P, Rader, DJ, Lee, KM, Psaty, BM, Skogholt, AH, Emmerich, J, Suchon, P, Rich, SS, Vy, HT, Tang, WH, Jackson, RD, Hansen, JB, Morange, PE, Kabrhel, C, Tregouet, DA, Damrauer, SM, Johnson, AD, Smith, NL. Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors. CIRCULATION. 2022; 146(16)DOI:10.1161/CIRCULATIONAHA.122.059675. PMID:36154123. IF:37.800(Q1/1D).