Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1984 1
1985 1
1986 3
1987 1
1990 1
1992 2
1993 4
1994 3
1995 2
1996 2
1997 1
1998 1
1999 4
2000 6
2001 1
2002 5
2003 6
2004 8
2005 8
2006 6
2007 9
2008 11
2009 10
2010 6
2011 5
2012 16
2013 13
2014 12
2015 17
2016 15
2017 17
2018 19
2019 21
2020 27
2021 32
2022 4
Text availability
Article attribute
Article type
Publication date

Search Results

267 results
Results by year
Filters applied: . Clear all
Page 1
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.
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. Lahrouchi N, et al. Among authors: makita n. Circulation. 2020 Jul 28;142(4):324-338. doi: 10.1161/CIRCULATIONAHA.120.045956. Epub 2020 May 20. Circulation. 2020. PMID: 32429735 Free PMC article.
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls.
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 JB, Hazeki D, Horie M, Ishikawa T, Itoh H, Kaneko Y, Kanters JK, Kimoto H, Kotta MC, 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 JJ, Redon R, Ohno S, Probst V; Nantes Referral Center for inherited cardiac arrhythmia, Behr ER, Barc J, Bezzina CR. Walsh R, et al. Among authors: makita n. Genet Med. 2021 Jan;23(1):47-58. doi: 10.1038/s41436-020-00946-5. Epub 2020 Sep 7. Genet Med. 2021. PMID: 32893267 Free PMC article.
V2 vasopressin receptor mutations.
Makita N, Manaka K, Sato J, Iiri T. Makita N, et al. Vitam Horm. 2020;113:79-99. doi: 10.1016/bs.vh.2019.08.012. Epub 2019 Sep 13. Vitam Horm. 2020. PMID: 32138955 Review.
Neuroendocrine manifestations of Erdheim-Chester disease.
Manaka K, Sato J, Makita N. Manaka K, et al. Among authors: makita n. Handb Clin Neurol. 2021;181:137-147. doi: 10.1016/B978-0-12-820683-6.00010-5. Handb Clin Neurol. 2021. PMID: 34238453 Review.
Inherited bradyarrhythmia: A diverse genetic background.
Ishikawa T, Tsuji Y, Makita N. Ishikawa T, et al. Among authors: makita n. J Arrhythm. 2016 Oct;32(5):352-358. doi: 10.1016/j.joa.2015.09.009. Epub 2015 Nov 19. J Arrhythm. 2016. PMID: 27761158 Free PMC article. Review.
Cardiac connexins, mutations and arrhythmias.
Delmar M, Makita N. Delmar M, et al. Among authors: makita n. Curr Opin Cardiol. 2012 May;27(3):236-41. doi: 10.1097/HCO.0b013e328352220e. Curr Opin Cardiol. 2012. PMID: 22382502 Review.
Letter to the Editor.
Ishikawa T, Makita N, Aoki H, Saida Y. Ishikawa T, et al. Among authors: makita n. J Vet Intern Med. 2017 Jul;31(4):967-968. doi: 10.1111/jvim.14781. Epub 2017 Jun 19. J Vet Intern Med. 2017. PMID: 28626919 Free PMC article. No abstract available.
Pathological Features of Lamin Cardiomyopathy.
Kawano H, Ishimatsu T, Kawamura K, Ishijima M, Hayashi T, Ishikawa T, Makita N, Maemura K. Kawano H, et al. Among authors: makita n. Circ J. 2020 Jun 25;84(7):1193. doi: 10.1253/circj.CJ-20-0187. Epub 2020 Apr 25. Circ J. 2020. PMID: 32336741 Free article. No abstract available.
267 results