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Results by year

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

Year Number of Results
1998 3
1999 1
2000 1
2001 1
2002 2
2003 1
2004 3
2005 5
2006 5
2007 6
2008 2
2009 5
2010 3
2011 12
2012 15
2013 11
2014 8
2015 7
2016 8
2017 7
2018 8
2019 13
2020 7
2021 9
2022 3
2023 1

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127 results

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Page 1
A Platform for Generation of Chamber-Specific Cardiac Tissues and Disease Modeling.
Zhao Y, Rafatian N, Feric NT, Cox BJ, Aschar-Sobbi R, Wang EY, Aggarwal P, Zhang B, Conant G, Ronaldson-Bouchard K, Pahnke A, Protze S, Lee JH, Davenport Huyer L, Jekic D, Wickeler A, Naguib HE, Keller GM, Vunjak-Novakovic G, Broeckel U, Backx PH, Radisic M. Zhao Y, et al. Among authors: broeckel u. Cell. 2019 Feb 7;176(4):913-927.e18. doi: 10.1016/j.cell.2018.11.042. Epub 2019 Jan 24. Cell. 2019. PMID: 30686581 Free PMC article.
The ENTPD1 promoter polymorphism -860 A > G (rs3814159) is associated with increased gene transcription, protein expression, CD39/NTPDase1 enzymatic activity, and thromboembolism risk.
Maloney JP, Branchford BR, Brodsky GL, Cosmic MS, Calabrese DW, Aquilante CL, Maloney KW, Gonzalez JR, Zhang W, Moreau KL, Wiggins KL, Smith NL, Broeckel U, Di Paola J. Maloney JP, et al. Among authors: broeckel u. FASEB J. 2017 Jul;31(7):2771-2784. doi: 10.1096/fj.201600344R. Epub 2017 Mar 16. FASEB J. 2017. PMID: 28302652 Free PMC article.
Genes for left ventricular hypertrophy.
Arnett DK, de las Fuentes L, Broeckel U. Arnett DK, et al. Among authors: broeckel u. Curr Hypertens Rep. 2004 Feb;6(1):36-41. doi: 10.1007/s11906-004-0009-5. Curr Hypertens Rep. 2004. PMID: 14972088 Review.
The future of genetic case-control studies.
Schork NJ, Fallin D, Thiel B, Xu X, Broeckel U, Jacob HJ, Cohen D. Schork NJ, et al. Among authors: broeckel u. Adv Genet. 2001;42:191-212. doi: 10.1016/s0065-2660(01)42023-2. Adv Genet. 2001. PMID: 11037322 Review.
Toward the etiologies of congenital heart diseases.
Pelech AN, Broeckel U. Pelech AN, et al. Among authors: broeckel u. Clin Perinatol. 2005 Dec;32(4):825-44, vii. doi: 10.1016/j.clp.2005.09.005. Clin Perinatol. 2005. PMID: 16325664 Review.
Incorporating G6PD genotyping to identify patients with G6PD deficiency.
Morris SA, Crews KR, Hayden RT, Takemoto CM, Yang W, Baker DK, Broeckel U, Relling MV, Haidar CE. Morris SA, et al. Among authors: broeckel u. Pharmacogenet Genomics. 2022 Apr 1;32(3):87-93. doi: 10.1097/FPC.0000000000000456. Pharmacogenet Genomics. 2022. PMID: 34693927 Free PMC article.
127 results