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

Year Number of Results
2002 1
2003 1
2004 1
2006 2
2008 1
2009 3
2011 6
2012 6
2013 4
2014 5
2015 4
2016 6
2017 2
2018 4
2019 4
2020 3
2021 2
2022 3
2024 0

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Page 1
A Review of Recent Developments in Turner Syndrome Research.
Huang AC, Olson SB, Maslen CL. Huang AC, et al. Among authors: maslen cl. J Cardiovasc Dev Dis. 2021 Oct 23;8(11):138. doi: 10.3390/jcdd8110138. J Cardiovasc Dev Dis. 2021. PMID: 34821691 Free PMC article. Review.
Recent Advances in Placenta-Heart Interactions.
Maslen CL. Maslen CL. Front Physiol. 2018 Jun 14;9:735. doi: 10.3389/fphys.2018.00735. eCollection 2018. Front Physiol. 2018. PMID: 29962966 Free PMC article. Review.
Cardiovascular Outcomes in Aortopathy: GenTAC Registry of Genetically Triggered Aortic Aneurysms and Related Conditions.
Holmes KW, Markwardt S, Eagle KA, Devereux RB, Weinsaft JW, Asch FM, LeMaire SA, Maslen CL, Song HK, Milewicz DM, Prakash SK, Guo D, Morris SA, Pyeritz RE, Milewski RC, Ravekes WJ, Dietz HC, Shohet RV, Silberbach M, Roman MJ; GenTAC Investigators. Holmes KW, et al. Among authors: maslen cl. J Am Coll Cardiol. 2022 May 31;79(21):2069-2081. doi: 10.1016/j.jacc.2022.03.367. J Am Coll Cardiol. 2022. PMID: 35618343 Free PMC article.
DNA Methylation Analysis of Turner Syndrome BAV.
Gutierrez J, Davis BA, Nevonen KA, Ward S, Carbone L, Maslen CL. Gutierrez J, et al. Among authors: maslen cl. Front Genet. 2022 May 31;13:872750. doi: 10.3389/fgene.2022.872750. eCollection 2022. Front Genet. 2022. PMID: 35711915 Free PMC article.
The genetic basis of Turner syndrome aortopathy.
Corbitt H, Gutierrez J, Silberbach M, Maslen CL. Corbitt H, et al. Among authors: maslen cl. Am J Med Genet C Semin Med Genet. 2019 Mar;181(1):117-125. doi: 10.1002/ajmg.c.31686. Epub 2019 Feb 16. Am J Med Genet C Semin Med Genet. 2019. PMID: 30770620 Free PMC article.
Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms.
Burnicka-Turek O, Steimle JD, Huang W, Felker L, Kamp A, Kweon J, Peterson M, Reeves RH, Maslen CL, Gruber PJ, Yang XH, Shendure J, Moskowitz IP. Burnicka-Turek O, et al. Among authors: maslen cl. Hum Mol Genet. 2016 Jul 15;25(14):3011-3028. doi: 10.1093/hmg/ddw155. Epub 2016 Jun 23. Hum Mol Genet. 2016. PMID: 27340223 Free PMC article.
Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects.
Ramachandran D, Zeng Z, Locke AE, Mulle JG, Bean LJ, Rosser TC, Dooley KJ, Cua CL, Capone GT, Reeves RH, Maslen CL, Cutler DJ, Feingold E, Sherman SL, Zwick ME. Ramachandran D, et al. Among authors: maslen cl. G3 (Bethesda). 2015 Jul 20;5(10):1961-71. doi: 10.1534/g3.115.019943. G3 (Bethesda). 2015. PMID: 26194203 Free PMC article.
50 results