المؤلفون: Crotti, L, Spazzolini, C, Nyegaard, M, Overgaard, MT, Kotta, MC, Dagradi, F, Sala, L, Aiba, T, Ayers, MD, Baban, A, Barc, J, Beach, CM, Behr, ER, Bos, JM, Cerrone, M, Covi, P, Cuneo, B, Denjoy, I, Donner, B, Elbert, A, Eliasson, H, Etheridge, SP, Fukuyama, M, Girolami, F, Hamilton, R, Horie, M, Iascone, M, Jaimez, JJ, Jensen, HK, Kannankeril, PJ, Kaski, JP, Makita, N, Munoz-Esparza, C, Odland, HH, Ohno, S, Papagiannis, J, Porretta, AP, Prandstetter, C, Probst, V, Robyns, T, Rosenthal, E, Roses-Noguer, F, Sekarski, N, Singh, A, Spentzou, G, Stute, F, Tfelt-Hansen, J, Till, J, Tobert, KE, Vinocur, JM, Webster, G, Wilde, AAM, Wolf, CM, Ackerman, MJ, Schwartz, PJ

المصدر: European heart journal. 44(35):3357-3370

مصطلحات موضوعية: Medicin och hälsovetenskap

الوصول الحر: http://kipublications.ki.se/Default.aspx?queryparsed=id:153391881Test

المؤلفون: Walsh R., Lahrouchi N., Tadros R., Kyndt F., Glinge C., Postema P. G., Amin A. S., Nannenberg E. A., Ware J. S., Whiffin N., Mazzarotto F., Skoric-Milosavljevic D., Krijger C., Arbelo E., Babuty D., Barajas-Martinez H., Beckmann B. M., Bezieau S., Bos J. M., Breckpot J., Campuzano O., Castelletti S., Celen C., Clauss S., Corveleyn A., Crotti L., Dagradi F., de Asmundis C., Denjoy I., Dittmann S., Ellinor P. T., Ortuno C. G., Giustetto C., Gourraud J. -B., Hazeki D., Horie M., Ishikawa T., Itoh H., Kaneko Y., Kanters J. K., Kimoto H., Kotta M. -C., Krapels I. P. C., Kurabayashi M., Lazarte J., Leenhardt A., Loeys B. L., Lundin C., Makiyama T., Mansourati J., Martins R. P., Mazzanti A., Morner S., Napolitano C., Ohkubo K., Papadakis M., Rudic B., Molina M. S., Sacher F., Sahin H., Sarquella-Brugada G., Sebastiano R., Sharma S., Sheppard M. N., Shimamoto K., Shoemaker M. B., Stallmeyer B., Steinfurt J., Tanaka Y., Tester D. J., Usuda K., van der Zwaag P. A., Van Dooren S., Van Laer L., Winbo A., Winkel B. G., Yamagata K., Zumhagen S., Volders P. G. A., Lubitz S. A., Antzelevitch C., Platonov P. G., Odening K. E., Roden D. M., Roberts J. D., Skinner J. R., Tfelt-Hansen J., van den Berg M. P., Olesen M. S., Lambiase P. D., Borggrefe M., Hayashi K., Rydberg A., Nakajima T., Yoshinaga M., Saenen J. B., Kaab S., Brugada P., Robyns T., Giachino D. F., Ackerman M. J., Brugada R., Brugada J., Gimeno J. R., Hasdemir C., Guicheney P., Priori S. G., Schulze-Bahr E., Makita N., Schwartz P. J., Shimizu W., Aiba T., Schott J. -J., Redon R., Ohno S., Probst V., Arnaout A. A., Amelot M., Anselme F., Billon O., Defaye P., Dupuis J. -M., Jesel L., Laurent G., Maury P., Pasquie J. -L., Wiart F., Behr E. R., Barc J., Bezzina C. R.

المساهمون: Walsh R., Lahrouchi N., Tadros R., Kyndt F., Glinge C., Postema P.G., Amin A.S., Nannenberg E.A., Ware J.S., Whiffin N., Mazzarotto F., Skoric-Milosavljevic D., Krijger C., Arbelo E., Babuty D., Barajas-Martinez H., Beckmann B.M., Bezieau S., Bos J.M., Breckpot J., Campuzano O., Castelletti S., Celen C., Clauss S., Corveleyn A., Crotti L., Dagradi F., de Asmundis C., Denjoy I., Dittmann S., Ellinor P.T., Ortuno C.G., Giustetto C., Gourraud J.-B., Hazeki D., Horie M., Ishikawa T., Itoh H., Kaneko Y., Kanters J.K., Kimoto H., Kotta M.-C., Krapels I.P.C., Kurabayashi M., Lazarte J., Leenhardt A., Loeys B.L., Lundin C., Makiyama T., Mansourati J., Martins R.P., Mazzanti A., Morner S., Napolitano C., Ohkubo K., Papadakis M., Rudic B., Molina M.S., Sacher F., Sahin H., Sarquella-Brugada G., Sebastiano R., Sharma S., Sheppard M.N., Shimamoto K., Shoemaker M.B., Stallmeyer B., Steinfurt J., Tanaka Y., Tester D.J., Usuda K., van der Zwaag P.A., Van Dooren S., Van Laer L., Winbo A., Winkel B.G., Yamagata K., Zumhagen S., Volders P.G.A., Lubitz S.A., Antzelevitch C., Platonov P.G., Odening K.E., Roden D.M., Roberts J.D., Skinner J.R., Tfelt-Hansen J., van den Berg M.P., Olesen M.S., Lambiase P.D., Borggrefe M., Hayashi K., Rydberg A., Nakajima T., Yoshinaga M., Saenen J.B., Kaab S., Brugada P., Robyns T., Giachino D.F.

مصطلحات موضوعية: ACMG/AMP guideline, Brugada, LQTS, variant interpretation

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32893267; info:eu-repo/semantics/altIdentifier/wos/WOS:000566661000001; volume:23; issue:1; firstpage:47; lastpage:58; numberofpages:12; journal:GENETICS IN MEDICINE; http://hdl.handle.net/2318/1766442Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85090223596; https://www.nature.com/articles/s41436-020-00946-5Test

الإتاحة: https://doi.org/10.1038/s41436-020-00946-5Test
http://hdl.handle.net/2318/1766442Test
https://www.nature.com/articles/s41436-020-00946-5Test

المؤلفون: Kozek K., Wada Y., Sala L., Denjoy I., Egly C., O'Neill M. J., Aiba T., Shimizu W., Makita N., Ishikawa T., Crotti L., Spazzolini C., Kotta M. -C., Dagradi F., Castelletti S., Pedrazzini M., Gnecchi M., Leenhardt A., Salem J. -E., Ohno S., Zuo Y., Glazer A. M., Mosley J. D., Roden D. M., Knollmann B. C., Blume J. D., Extramiana F., Schwartz P. J., Horie M., Kroncke B. M.

المساهمون: Kozek, K, Wada, Y, Sala, L, Denjoy, I, Egly, C, O'Neill, M, Aiba, T, Shimizu, W, Makita, N, Ishikawa, T, Crotti, L, Spazzolini, C, Kotta, M, Dagradi, F, Castelletti, S, Pedrazzini, M, Gnecchi, M, Leenhardt, A, Salem, J, Ohno, S, Zuo, Y, Glazer, A, Mosley, J, Roden, D, Knollmann, B, Blume, J, Extramiana, F, Schwartz, P, Horie, M, Kroncke, B

مصطلحات موضوعية: genetic variation, heterozygote, ion channel, long QT syndrome, phenotype

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34309407; info:eu-repo/semantics/altIdentifier/wos/WOS:000686019100005; volume:14; issue:4; firstpage:495; lastpage:505; numberofpages:11; journal:CIRCULATION; http://hdl.handle.net/10281/390668Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85113773646

الإتاحة: https://doi.org/10.1161/CIRCGEN.120.003289Test
http://hdl.handle.net/10281/390668Test

المؤلفون: Lahrouchi N, Tadros R, Crotti L, Mizusawa Y, Postema PG, Beekman L, Walsh R, Hasegawa K, Barc J, Ernsting M, Turkowski KL, Mazzanti A, Beckmann BM, Shimamoto K, Diamant UB, Wijeyeratne YD, Kucho Y, Robyns T, Ishikawa T, Arbelo E, Christiansen M, Winbo A, Jabbari R, Lubitz SA, Steinfurt J, Rudic B, Loeys B, Shoemaker MB, Weeke PE, Pfeiffer R, Davies B, Andorin A, Hofman N, Dagradi F, Pedrazzini M, Tester DJ, Bos JM, Sarquella-Brugada G, Campuzano Ó, Platonov PG, Stallmeyer B, Zumhagen S, Nannenberg EA, Veldink JH, van den Berg LH, Al-Chalabi A, Shaw CE, Shaw PJ, Morrison KE, Andersen PM, Müller-Nurasyid M, Cusi D, Barlassina C, Galan P, Lathrop M, Munter M, Werge T, Ribasés M, Aung T, Khor CC, Ozaki M, Lichtner P, Meitinger T, van Tintelen JP, Hoedemaekers Y, Denjoy I, Leenhardt A, Napolitano C, Shimizu W, Schott JJ, Gourraud JB, Makiyama T, Ohno S, Itoh H, Krahn AD, Antzelevitch C, Roden DM, Saenen J, Borggrefe M, Odening KE, Ellinor PT, Tfelt-Hansen J, Skinner JR, van den Berg MP, Olesen MS, Brugada J, Brugada R, Makita N, Breckpot J, Yoshinaga M, Behr ER, Rydberg A, Aiba T, Kääb S, Priori SG, Guicheney P, Tan HL, Newton-Cheh C, Ackerman MJ, Schwartz PJ, Schulze-Bahr E, Probst V, Horie M, Wilde AA, Tanck MWT, Bezzina CR.

المساهمون: Lahrouchi, N, Tadros, R, Crotti, L, Mizusawa, Y, Postema, P, Beekman, L, Walsh, R, Hasegawa, K, Barc, J, Ernsting, M, Turkowski, K, Mazzanti, A, Beckmann, B, Shimamoto, K, Diamant, U, Wijeyeratne, Y, Kucho, Y, Robyns, T, Ishikawa, T, Arbelo, E, Christiansen, M, Winbo, A, Jabbari, R, Lubitz, S, Steinfurt, J, Rudic, B, Loeys, B, Shoemaker, M, Weeke, P, Pfeiffer, R, Davies, B, Andorin, A, Hofman, N, Dagradi, F, Pedrazzini, M, Tester, D, Bos, J, Sarquella-Brugada, G, Campuzano, Ó, Platonov, P, Stallmeyer, B, Zumhagen, S, Nannenberg, E, Veldink, J, van den Berg, L, Al-Chalabi, A, Shaw, C, Shaw, P, Morrison, K, Andersen, P, Müller-Nurasyid, M, Cusi, D, Barlassina, C, Galan, P, Lathrop, M, Munter, M, Werge, T, Ribasés, M, Aung, T, Khor, C, Ozaki, M, Lichtner, P, Meitinger, T, van Tintelen, J, Hoedemaekers, Y, Denjoy, I, Leenhardt, A, Napolitano, C, Shimizu, W, Schott, J, Gourraud, J, Makiyama, T, Ohno, S, Itoh, H, Krahn, A, Antzelevitch, C, Roden, D, Saenen, J, Borggrefe, M, Odening, K, Ellinor, P, Tfelt-Hansen, J, Skinner, J, van den Berg, M, Olesen, M, Brugada, J, Brugada, R, Makita, N, Breckpot, J, Yoshinaga, M, Behr, E, Rydberg, A, Aiba, T, Kääb, S, Priori, S, Guicheney, P, Tan, H, Newton-Cheh, C, Ackerman, M, Schwartz, P

مصطلحات موضوعية: genome-wide association study, inheritance pattern, long QT syndrome, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, BIO/18 - GENETICA, MED/01 - STATISTICA MEDICA

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32429735; info:eu-repo/semantics/altIdentifier/wos/WOS:000562745400012; volume:142; issue:4; firstpage:324; lastpage:338; numberofpages:15; journal:CIRCULATION; http://hdl.handle.net/10281/298086Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85088849122

الإتاحة: https://doi.org/10.1161/CIRCULATIONAHA.120.045956Test
http://hdl.handle.net/10281/298086Test

المؤلفون: Wijeyeratne Y. D., Tanck M. W., Mizusawa Y., Batchvarov V., Barc J., Crotti L., Bos J. M., Tester D. J., Muir A., Veltmann C., Ohno S., Page S. P., Galvin J., Tadros R., Muggenthaler M., Raju H., Denjoy I., Schott J. -J., Gourraud J. -B., Skoric-Milosavljevic D., Nannenberg E. A., Redon R., Papadakis M., Kyndt F., Dagradi F., Castelletti S., Torchio M., Meitinger T., Lichtner P., Ishikawa T., Wilde A. A. M., Takahashi K., Sharma S., Roden D. M., Borggrefe M. M., McKeown P. P., Shimizu W., Horie M., Makita N., Aiba T., Ackerman M. J., Schwartz P. J., Probst V., Bezzina C. R., Behr E. R.

المساهمون: Wijeyeratne, Y, Tanck, M, Mizusawa, Y, Batchvarov, V, Barc, J, Crotti, L, Bos, J, Tester, D, Muir, A, Veltmann, C, Ohno, S, Page, S, Galvin, J, Tadros, R, Muggenthaler, M, Raju, H, Denjoy, I, Schott, J, Gourraud, J, Skoric-Milosavljevic, D, Nannenberg, E, Redon, R, Papadakis, M, Kyndt, F, Dagradi, F, Castelletti, S, Torchio, M, Meitinger, T, Lichtner, P, Ishikawa, T, Wilde, A, Takahashi, K, Sharma, S, Roden, D, Borggrefe, M, Mckeown, P, Shimizu, W, Horie, M, Makita, N, Aiba, T, Ackerman, M, Schwartz, P, Probst, V, Bezzina, C, Behr, E

مصطلحات موضوعية: Brugada syndrome, genetics, human, penetrance, phenotype, risk score, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, BIO/18 - GENETICA

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33164571; info:eu-repo/semantics/altIdentifier/wos/WOS:000598974000004; volume:13; issue:6; firstpage:599; lastpage:608; numberofpages:10; journal:CIRCULATION; http://hdl.handle.net/10281/298048Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85097964476

الإتاحة: https://doi.org/10.1161/CIRCGEN.120.002911Test
http://hdl.handle.net/10281/298048Test

المؤلفون: Walsh, R, Lahrouchi, N, Tadros, R, Kyndt, F, Glinge, C, Postema, PG, Amin, AS, Nannenberg, EA, Ware, JS, Whiffin, N, Mazzarotto, F, Škorić-Milosavljević, D, Krijger, C, Arbelo, E, Babuty, D, Barajas-Martinez, H, Beckmann, BM, Bézieau, S, Bos, JM, Breckpot, J, Campuzano, O, Castelletti, S, Celen, C, Clauss, S, Corveleyn, A, Crotti, L, Dagradi, F, de Asmundis, C, Denjoy, I, Dittmann, S, Ellinor, PT, Ortuño, CG, Giustetto, C, Gourraud, J-B, Hazeki, D, Horie, M, Ishikawa, T, Itoh, H, Kaneko, Y, Kanters, JK, Kimoto, H, Kotta, M-C, Krapels, IPC, Kurabayashi, M, Lazarte, J, Leenhardt, A, Loeys, BL, Lundin, C, Makiyama, T, Mansourati, J, Martins, RP, Mazzanti, A, Mörner, S, Napolitano, C, Ohkubo, K, Papadakis, M, Rudic, B, Molina, MS, Sacher, F, Sahin, H, Sarquella-Brugada, G, Sebastiano, R, Sharma, S, Sheppard, MN, Shimamoto, K, Shoemaker, MB, Stallmeyer, B, Steinfurt, J, Tanaka, Y, Tester, DJ, Usuda, K, van der Zwaag, PA, Van Dooren, S, Van Laer, L, Winbo, A, Winkel, BG, Yamagata, K, Zumhagen, S, Volders, PGA, Lubitz, SA, Antzelevitch, C, Platonov, PG, Odening, KE, Roden, DM, Roberts, JD, Skinner, JR, Tfelt-Hansen, J, van den Berg, MP, Olesen, MS, Lambiase, PD, Borggrefe, M, Hayashi, K, Rydberg, A, Nakajima, T, Yoshinaga, M, Saenen, JB, Kääb, S, Brugada, P, Robyns, T, Giachino, DF, Ackerman, MJ, Brugada, R, Brugada, J, Gimeno, JR, Hasdemir, C, Guicheney, P, Priori, SG, Schulze-Bahr, E, Makita, N, Schwartz, PJ, Shimizu, W, Aiba, T, Schott, J-J, Redon, R, Ohno, S, Probst, V, Nantes Referral Center for inherited cardiac arrhythmia, Behr, ER, Barc, J, Bezzina, CR

وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document

العلاقة: https://openaccess.sgul.ac.uk/id/eprint/112371/3/s41436-020-00946-5.pdfTest; https://openaccess.sgul.ac.uk/id/eprint/112371/1/Arrhythmia_variant_interpretation_manuscript_GiM_FINAL_Figs_Tables.docxTest; Walsh, R; Lahrouchi, N; Tadros, R; Kyndt, F; Glinge, C; Postema, PG; Amin, AS; Nannenberg, EA; Ware, JS; Whiffin, N; et al. Walsh, R; Lahrouchi, N; Tadros, R; Kyndt, F; Glinge, C; Postema, PG; Amin, AS; Nannenberg, EA; Ware, JS; Whiffin, N; Mazzarotto, F; Škorić-Milosavljević, D; Krijger, C; Arbelo, E; Babuty, D; Barajas-Martinez, H; Beckmann, BM; Bézieau, S; Bos, JM; Breckpot, J; Campuzano, O; Castelletti, S; Celen, C; Clauss, S; Corveleyn, A; Crotti, L; Dagradi, F; de Asmundis, C; Denjoy, I; Dittmann, S; Ellinor, PT; Ortuño, CG; Giustetto, C; Gourraud, J-B; Hazeki, D; Horie, M; Ishikawa, T; Itoh, H; Kaneko, Y; Kanters, JK; Kimoto, H; Kotta, M-C; Krapels, IPC; Kurabayashi, M; Lazarte, J; Leenhardt, A; Loeys, BL; Lundin, C; Makiyama, T; Mansourati, J; Martins, RP; Mazzanti, A; Mörner, S; Napolitano, C; Ohkubo, K; Papadakis, M; Rudic, B; Molina, MS; Sacher, F; Sahin, H; Sarquella-Brugada, G; Sebastiano, R; Sharma, S; Sheppard, MN; Shimamoto, K; Shoemaker, MB; Stallmeyer, B; Steinfurt, J; Tanaka, Y; Tester, DJ; Usuda, K; van der Zwaag, PA; Van Dooren, S; Van Laer, L; Winbo, A; Winkel, BG; Yamagata, K; Zumhagen, S; Volders, PGA; Lubitz, SA; Antzelevitch, C; Platonov, PG; Odening, KE; Roden, DM; Roberts, JD; Skinner, JR; Tfelt-Hansen, J; van den Berg, MP; Olesen, MS; Lambiase, PD; Borggrefe, M; Hayashi, K; Rydberg, A; Nakajima, T; Yoshinaga, M; Saenen, JB; Kääb, S; Brugada, P; Robyns, T; Giachino, DF; Ackerman, MJ; Brugada, R; Brugada, J; Gimeno, JR; Hasdemir, C; Guicheney, P; Priori, SG; Schulze-Bahr, E; Makita, N; Schwartz, PJ; Shimizu, W; Aiba, T; Schott, J-J; Redon, R; Ohno, S; Probst, V; Nantes Referral Center for inherited cardiac arrhythmia; Behr, ER; Barc, J; Bezzina, CR (2021) Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls. Genet Med, 23 (1). pp. 47-58. ISSN 1530-0366 https://doi.org/10.1038/s41436-020-00946-5Test SGUL Authors: Behr, Elijah Raphael Papadakis, Michael Sharma, Sanjay Sheppard, Mary Noelle

الإتاحة: https://doi.org/10.1038/s41436-020-00946-5Test
https://openaccess.sgul.ac.uk/id/eprint/112371Test/
https://openaccess.sgul.ac.uk/id/eprint/112371/3/s41436-020-00946-5.pdfTest
https://openaccess.sgul.ac.uk/id/eprint/112371/1/Arrhythmia_variant_interpretation_manuscript_GiM_FINAL_Figs_Tables.docxTest

المؤلفون: O'Neill M. J., Sala L., Denjoy I., Wada Y., Kozek K., Crotti L., Dagradi F., Kotta M. -C., Spazzolini C., Leenhardt A., Salem J. -E., Kashiwa A., Ohno S., Tao R., Roden D. M., Horie M., Extramiana F., Schwartz P. J., Kroncke B. M.

المساهمون: O'Neill, M, Sala, L, Denjoy, I, Wada, Y, Kozek, K, Crotti, L, Dagradi, F, Kotta, M, Spazzolini, C, Leenhardt, A, Salem, J, Kashiwa, A, Ohno, S, Tao, R, Roden, D, Horie, M, Extramiana, F, Schwartz, P, Kroncke, B

مصطلحات موضوعية: Channelopathy, Incomplete Penetrance, Long QT Syndrome, Personalized Medicine, Statistical Genetic

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/36496179; info:eu-repo/semantics/altIdentifier/wos/WOS:000925286200001; volume:25; issue:3 (March 2023); journal:GENETICS IN MEDICINE; https://hdl.handle.net/10281/467709Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85147441238

الإتاحة: https://doi.org/10.1016/j.gim.2022.12.002Test
https://hdl.handle.net/10281/467709Test

المؤلفون: Bos JM, Crotti L, Rohatgi RK, Castelletti S, Dagradi F, Schwartz PJ, Ackerman MJ.

المساهمون: Bos, J, Crotti, L, Rohatgi, R, Castelletti, S, Dagradi, F, Schwartz, P, Ackerman, M

مصطلحات موضوعية: blocker, long QT syndrome, mexiletine, potassium channel, sodium channel, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, BIO/14 - FARMACOLOGIA

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31006312; info:eu-repo/semantics/altIdentifier/wos/WOS:000468492100012; volume:12; issue:5; journal:CIRCULATION. ARRHYTHMIA AND ELECTROPHYSIOLOGY; http://hdl.handle.net/10281/281497Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85065066682

الإتاحة: https://doi.org/10.1161/CIRCEP.118.007280Test
http://hdl.handle.net/10281/281497Test

المؤلفون: Lahrouchi, Najim, Tadros, Rafik, Crotti, Lia, Mizusawa, Yuka, Postema, Pieter G., Beekman, Leander, Walsh, Roddy, Hasegawa, Kanae, Barc, Julien, Ernsting, Marko, Turkowski, Kari L., Mazzanti, Andrea, Beckmann, Britt M., Shimamoto, Keiko, Diamant, U.B., Wijeyeratne, Yanushi D., Kucho, Y., Robyns, T., Ishikawa, T., Arbelo, Elena, Christiansen, M., Winbo, A., Jabbari, R., Lubitz, S.A., Steinfurt, J., Rudic, B., Loeys, B., Shoemaker, M.B., Weeke, P.E., Pfeiffer, R., Davies, B., Andorin, Antoine, Hofman, N., Dagradi, F., Pedrazzini, M., Tester, D.J., Bos, J.M., Sarquella Brugada, Geòrgia, Campuzano Larrea, Oscar, Platonov, P.G.

المصدر: Circulation, 2020, vol. 142, núm. 4, p. 324-338 ; Articles publicats (D-CM) ; Lahrouchi N Tadros R Crotti L Mizusawa Y Postema PG Beekman L Walsh R Hasegawa K Barc J Ernsting M Turkowski KL Mazzanti A Beckmann BM Shimamoto K Diamant UB Wijeyeratne YD Kucho Y Robyns T Ishikawa T Arbelo E Christiansen M Winbo A Jabbari R Lubitz SA Steinfurt J Rudic B Loeys B Shoemaker MB Weeke PE Pfeiffer R Davies B Andorin A Hofman N Dagradi F Pedrazzini M Tester DJ Bos JM Sarquella Brugada, Geòrgia Campuzano Larrea, Oscar Platonov PG 2020 Transethnic Genome-Wide Association ....

مصطلحات موضوعية: Genòmica, Genomics, Genomes, Arrítmia, Arrhythmia, Malalties congènites, Genetic disorders

وصف الملف: 15 p.; application/pdf

العلاقة: info:eu-repo/semantics/altIdentifier/issn/0009-7322; info:eu-repo/semantics/altIdentifier/eissn/1524-4539; http://hdl.handle.net/10256/24241Test

الإتاحة: https://doi.org/10.1161/CIRCULATIONAHA.120.045956Test
http://hdl.handle.net/10256/24241Test

المؤلفون: Walsh, Roddy, Lahrouchi, Najim, Tadros, Rafik, Kyndt, Florence, Glinge, C ., Postema, P.G., Amin, Ahmad S., Nannenberg, E.A., Ware, J.S., Whiffin, N., Mazzarotto, F., Korić-Milosavljević, D., Krijger, C., Arbelo, Elena, Babuty, D., Barajas-Martinez, H., Beckmann, B.M., Bézieau, S., Bos, J.M., Breckpot, J., Campuzano Larrea, Oscar, Castelletti, S., Celen, C., Clauss, S., Corveleyn, A., Crotti, Lia, Dagradi, F., de Asmundis, C., Denjoy, Isabelle, Dittmann, S., Ellinor, P.T., Ortuño, C.G., Giustetto, Carla, Gourraud, Jean Baptiste, Hazeki, D., Horie, M., Ishikawa, T., Itoh, H.

المصدر: Genetics in Medicine, 2020, vol. 23, núm. 1, p. 47-58 ; Articles publicats (D-CM) ; Walsh, Roddy Lahrouchi, Najim Tadros, Rafik Kyndt, Florence Glinge C Postema PG Amin AS Nannenberg EA Ware JS Whiffin N Mazzarotto F korić-Milosavljević D Krijger C Arbelo E Babuty D Barajas-Martinez H Beckmann BM Bézieau S Bos JM Breckpot J Campuzano Larrea, Oscar Castelletti S Celen C Clauss S Corveleyn A Crotti L Dagradi F de Asmundis C Denjoy I Dittmann S Ellinor PT Ortuño CG Giustetto C Gourraud JB Hazeki D Horie M Ishikawa T Itoh H 2020 Enhancing rare variant interpretation in ....

وصف الملف: 12 p.; application/pdf

العلاقة: info:eu-repo/semantics/altIdentifier/issn/1098-3600; info:eu-repo/semantics/altIdentifier/eissn/1530-0366; http://hdl.handle.net/10256/24191Test

الإتاحة: https://doi.org/10.1038/s41436-020-00946-5Test
http://hdl.handle.net/10256/24191Test