Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.


The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

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
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 9
2022 8
2023 4

Text availability

Article attribute

Article type

Publication date

Search Results

113 results

Results by year

Filters applied: . Clear all
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.
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.
Association of Damaging Variants in Genes With Increased Cancer Risk Among Patients With Congenital Heart Disease.
Morton SU, Shimamura A, Newburger PE, Opotowsky AR, Quiat D, Pereira AC, Jin SC, Gurvitz M, Brueckner M, Chung WK, Shen Y, Bernstein D, Gelb BD, Giardini A, Goldmuntz E, Kim RW, Lifton RP, Porter GA Jr, Srivastava D, Tristani-Firouzi M, Newburger JW, Seidman JG, Seidman CE. Morton SU, et al. Among authors: tristani firouzi m. JAMA Cardiol. 2021 Apr 1;6(4):457-462. doi: 10.1001/jamacardio.2020.4947. JAMA Cardiol. 2021. PMID: 33084842 Free PMC article.
The Long and Short of It: Insights Into the Short QT Syndrome.
Tristani-Firouzi M. Tristani-Firouzi M. J Am Coll Cardiol. 2014 Apr 8;63(13):1309-1310. doi: 10.1016/j.jacc.2013.11.021. Epub 2013 Dec 11. J Am Coll Cardiol. 2014. PMID: 24333498 Free article. No abstract available.
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.
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.
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.
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.
Family Screening After Sudden Death in a Population-Based Study of Children.
Kannankeril PJ, Shoemaker MB, Fountain D, Roden DM, Yandell M, Tristani-Firouzi M, Etheridge SP, Webster G, George AL, McNally EM, MacLeod H, Burns KM. Kannankeril PJ, et al. Among authors: tristani firouzi m. Pediatrics. 2022 Apr 1;149(4):e2021054432. doi: 10.1542/peds.2021-054432. Pediatrics. 2022. PMID: 35284934 Free PMC article.
113 results