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

Year Number of Results
1996 4
1997 2
1998 2
1999 1
2001 4
2002 3
2003 5
2004 3
2005 5
2006 6
2007 4
2008 6
2009 2
2010 4
2011 5
2012 2
2013 7
2014 6
2015 2
2016 2
2017 6
2018 6
2019 3
2020 10
2021 8
2022 0
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100 results
Results by year
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Page 1
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.
Jin SC, Homsy J, Zaidi S, Lu Q, Morton S, DePalma SR, Zeng X, Qi H, Chang W, Sierant MC, Hung WC, Haider S, Zhang J, Knight J, Bjornson RD, Castaldi C, Tikhonoa IR, Bilguvar K, Mane SM, Sanders SJ, Mital S, Russell MW, Gaynor JW, Deanfield J, Giardini A, Porter GA Jr, Srivastava D, Lo CW, Shen Y, Watkins WS, Yandell M, Yost HJ, Tristani-Firouzi M, Newburger JW, Roberts AE, Kim R, Zhao H, Kaltman JR, Goldmuntz E, Chung WK, Seidman JG, Gelb BD, Seidman CE, Lifton RP, Brueckner M. Jin SC, et al. Among authors: tristani firouzi m. Nat Genet. 2017 Nov;49(11):1593-1601. doi: 10.1038/ng.3970. Epub 2017 Oct 9. Nat Genet. 2017. PMID: 28991257 Free PMC article.
Genomic analyses implicate noncoding de novo variants in congenital heart disease.
Richter F, Morton SU, Kim SW, Kitaygorodsky A, Wasson LK, Chen KM, Zhou J, Qi H, Patel N, DePalma SR, Parfenov M, Homsy J, Gorham JM, Manheimer KB, Velinder M, Farrell A, Marth G, Schadt EE, Kaltman JR, Newburger JW, Giardini A, Goldmuntz E, Brueckner M, Kim R, Porter GA Jr, Bernstein D, Chung WK, Srivastava D, Tristani-Firouzi M, Troyanskaya OG, Dickel DE, Shen Y, Seidman JG, Seidman CE, Gelb BD. Richter F, et al. Among authors: tristani firouzi m. Nat Genet. 2020 Aug;52(8):769-777. doi: 10.1038/s41588-020-0652-z. Epub 2020 Jun 29. Nat Genet. 2020. PMID: 32601476 Free PMC article. Clinical Trial.
Systems Analysis Implicates WAVE2 Complex in the Pathogenesis of Developmental Left-Sided Obstructive Heart Defects.
Edwards JJ, Rouillard AD, Fernandez NF, Wang Z, Lachmann A, Shankaran SS, Bisgrove BW, Demarest B, Turan N, Srivastava D, Bernstein D, Deanfield J, Giardini A, Porter G, Kim R, Roberts AE, Newburger JW, Goldmuntz E, Brueckner M, Lifton RP, Seidman CE, Chung WK, Tristani-Firouzi M, Yost HJ, Ma'ayan A, Gelb BD. Edwards JJ, et al. Among authors: tristani firouzi m. JACC Basic Transl Sci. 2020 Apr 8;5(4):376-386. doi: 10.1016/j.jacbts.2020.01.012. eCollection 2020 Apr. JACC Basic Transl Sci. 2020. PMID: 32368696 Free PMC article.
Expanding the phenotype of CACNA1C mutation disorders.
Gakenheimer-Smith L, Meyers L, Lundahl D, Menon SC, Bunch TJ, Sawyer BL, Tristani-Firouzi M, Etheridge SP. Gakenheimer-Smith L, et al. Among authors: tristani firouzi m. Mol Genet Genomic Med. 2021 Jun;9(6):e1673. doi: 10.1002/mgg3.1673. Epub 2021 Apr 1. Mol Genet Genomic Med. 2021. PMID: 33797204 Free PMC article.
Kir 2.1 channelopathies: the Andersen-Tawil syndrome.
Tristani-Firouzi M, Etheridge SP. Tristani-Firouzi M, et al. Pflugers Arch. 2010 Jul;460(2):289-94. doi: 10.1007/s00424-010-0820-6. Epub 2010 Mar 21. Pflugers Arch. 2010. PMID: 20306271 Review.
hERG potassium channels and cardiac arrhythmia.
Sanguinetti MC, Tristani-Firouzi M. Sanguinetti MC, et al. Among authors: tristani firouzi m. Nature. 2006 Mar 23;440(7083):463-9. doi: 10.1038/nature04710. Nature. 2006. PMID: 16554806 Review.
Andersen-Tawil syndrome: an ever-expanding phenotype?
Tristani-Firouzi M. Tristani-Firouzi M. Heart Rhythm. 2006 Nov;3(11):1351-2. doi: 10.1016/j.hrthm.2006.08.015. Epub 2006 Aug 24. Heart Rhythm. 2006. PMID: 17074643 No abstract available.
The history and geographic distribution of a KCNQ1 atrial fibrillation risk allele.
Hateley S, Lopez-Izquierdo A, Jou CJ, Cho S, Schraiber JG, Song S, Maguire CT, Torres N, Riedel M, Bowles NE, Arrington CB, Kennedy BJ, Etheridge SP, Lai S, Pribble C, Meyers L, Lundahl D, Byrnes J, Granka JM, Kauffman CA, Lemmon G, Boyden S, Scott Watkins W, Karren MA, Knight S, Brent Muhlestein J, Carlquist JF, Anderson JL, Chahine KG, Shah KU, Ball CA, Benjamin IJ, Yandell M, Tristani-Firouzi M. Hateley S, et al. Among authors: tristani firouzi m. Nat Commun. 2021 Nov 8;12(1):6442. doi: 10.1038/s41467-021-26741-7. Nat Commun. 2021. PMID: 34750360 Free PMC article.
100 results