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

Year Number of Results
2000 1
2001 2
2004 1
2005 3
2007 9
2008 10
2009 1
2010 1
2011 1
2017 2
2019 2
2020 1
2024 0

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32 results

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Page 1
Gene symbol: SCN5A.
Crotti L, Ferrandi C, Insolia R, Pedrazzini M, Andreoli E, Veia A, Crimi G, Agnetti A, De Ferrari GM, Schwartz PJ. Crotti L, et al. Among authors: ferrandi c. Hum Genet. 2007 Feb;120(6):913. Hum Genet. 2007. PMID: 17438610 No abstract available.
Gene symbol: SCN5A.
Crotti L, Ferrandi C, Insolia R, Pedrazzini M, Tosin L, Veia A, Turco A, De Ferrari GM, Schwartz PJ. Crotti L, et al. Among authors: ferrandi c. Hum Genet. 2007 Feb;120(6):911-2. Hum Genet. 2007. PMID: 17438607 No abstract available.
Exome sequences and multi-environment field trials elucidate the genetic basis of adaptation in barley.
Bustos-Korts D, Dawson IK, Russell J, Tondelli A, Guerra D, Ferrandi C, Strozzi F, Nicolazzi EL, Molnar-Lang M, Ozkan H, Megyeri M, Miko P, Çakır E, Yakışır E, Trabanco N, Delbono S, Kyriakidis S, Booth A, Cammarano D, Mascher M, Werner P, Cattivelli L, Rossini L, Stein N, Kilian B, Waugh R, van Eeuwijk FA. Bustos-Korts D, et al. Among authors: ferrandi c. Plant J. 2019 Sep;99(6):1172-1191. doi: 10.1111/tpj.14414. Epub 2019 Jun 27. Plant J. 2019. PMID: 31108005 Free PMC article.
Gene symbol: KCNH2. Disease: Long QT syndrome.
Crotti L, Pedrazzini M, Insolia R, Ferrandi C, Cuoretti A, Celano G, Gandolfi E, Dagradi F, Schwartz PJ. Crotti L, et al. Among authors: ferrandi c. Hum Genet. 2008 Jun;123(5):541. Hum Genet. 2008. PMID: 20960616 Free article. No abstract available.
Cardiac potassium channel dysfunction in sudden infant death syndrome.
Rhodes TE, Abraham RL, Welch RC, Vanoye CG, Crotti L, Arnestad M, Insolia R, Pedrazzini M, Ferrandi C, Vege A, Rognum T, Roden DM, Schwartz PJ, George AL Jr. Rhodes TE, et al. Among authors: ferrandi c. J Mol Cell Cardiol. 2008 Mar;44(3):571-81. doi: 10.1016/j.yjmcc.2007.11.015. Epub 2007 Dec 7. J Mol Cell Cardiol. 2008. PMID: 18222468 Free PMC article.
Gene symbol: KCNH2.
Crotti L, Pedrazzini M, Ferrandi C, Insolia R, Tosin L, Vicentini A, Turco A, De Ferrari GM, Schwartz PJ. Crotti L, et al. Among authors: ferrandi c. Hum Genet. 2007 Feb;120(6):912. Hum Genet. 2007. PMID: 17438608 No abstract available.
Gene symbol: KCNQ1.
Crotti L, Insolia R, Pedrazzini M, Ferrandi C, Tosin L, Moncalvo C, Turco A, Agnetti A, De Ferrari GM, Schwartz PJ. Crotti L, et al. Among authors: ferrandi c. Hum Genet. 2007 Feb;120(6):912. Hum Genet. 2007. PMID: 17438609 No abstract available.
Cardiac sodium channel dysfunction in sudden infant death syndrome.
Wang DW, Desai RR, Crotti L, Arnestad M, Insolia R, Pedrazzini M, Ferrandi C, Vege A, Rognum T, Schwartz PJ, George AL Jr. Wang DW, et al. Among authors: ferrandi c. Circulation. 2007 Jan 23;115(3):368-76. doi: 10.1161/CIRCULATIONAHA.106.646513. Epub 2007 Jan 8. Circulation. 2007. PMID: 17210841
KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.
Crotti L, Lundquist AL, Insolia R, Pedrazzini M, Ferrandi C, De Ferrari GM, Vicentini A, Yang P, Roden DM, George AL Jr, Schwartz PJ. Crotti L, et al. Among authors: ferrandi c. Circulation. 2005 Aug 30;112(9):1251-8. doi: 10.1161/CIRCULATIONAHA.105.549071. Epub 2005 Aug 22. Circulation. 2005. PMID: 16116052
32 results