Zarate YA - Search Results

1

Severe neonatal presentation of Kleefstra syndrome in a patient with hypoplastic left heart syndrome and 9q34.3 microdeletion.

Campbell CL, Collins RT 2nd, Zarate YA. Campbell CL, et al. Among authors: zarate ya. Birth Defects Res A Clin Mol Teratol. 2014 Dec;100(12):985-90. doi: 10.1002/bdra.23324. Epub 2014 Nov 7. Birth Defects Res A Clin Mol Teratol. 2014. PMID: 25380126

2

Cardiovascular and genitourinary anomalies in patients with duplications within the Williams syndrome critical region: phenotypic expansion and review of the literature.

Zarate YA, Lepard T, Sellars E, Kaylor JA, Alfaro MP, Sailey C, Schaefer GB, Collins RT 2nd. Zarate YA, et al. Am J Med Genet A. 2014 Aug;164A(8):1998-2002. doi: 10.1002/ajmg.a.36601. Epub 2014 May 20. Am J Med Genet A. 2014. PMID: 24844942 Review.

3

Impact of aortic aneurysm on hospitalizations in patients with marfan syndrome: a multi-institutional study.

Collins RT 2nd, Phomakay V, Zarate YA, Tang X. Collins RT 2nd, et al. Among authors: zarate ya. Pediatr Cardiol. 2015 Jan;36(1):132-9. doi: 10.1007/s00246-014-0976-5. Epub 2014 Aug 6. Pediatr Cardiol. 2015. PMID: 25096902

4

Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing.

Zarate YA, Perry H, Ben-Omran T, Sellars EA, Stein Q, Almureikhi M, Simmons K, Klein O, Fish J, Feingold M, Douglas J, Kruer MC, Si Y, Mao R, McKnight D, Gibellini F, Retterer K, Slavotinek A. Zarate YA, et al. Am J Med Genet A. 2015 May;167A(5):1026-32. doi: 10.1002/ajmg.a.36849. Am J Med Genet A. 2015. PMID: 25885067

5

Aortic dilation in pediatric patients.

Zarate YA, Sellars E, Lepard T, Carlo WF, Tang X, Collins RT 2nd. Zarate YA, et al. Eur J Pediatr. 2015 Dec;174(12):1585-92. doi: 10.1007/s00431-015-2575-8. Epub 2015 Jun 13. Eur J Pediatr. 2015. PMID: 26070999

6

Aortic dilation, genetic testing, and associated diagnoses.

Zarate YA, Sellars E, Lepard T, Tang X, Collins RT 2nd. Zarate YA, et al. Genet Med. 2016 Apr;18(4):356-63. doi: 10.1038/gim.2015.88. Epub 2015 Jul 2. Genet Med. 2016. PMID: 26133393 Free article.

7

SATB2-associated syndrome: Mechanisms, phenotype, and practical recommendations.

Zarate YA, Fish JL. Zarate YA, et al. Am J Med Genet A. 2017 Feb;173(2):327-337. doi: 10.1002/ajmg.a.38022. Epub 2016 Oct 24. Am J Med Genet A. 2017. PMID: 27774744 Free PMC article. Review.

8

Advanced cardiovascular imaging in Williams syndrome: Abnormalities, usefulness, and strategy for use.

Hills JA, Zarate YA, Danylchuk NR, Lepard T, Chen JC, Collins RT 2nd. Hills JA, et al. Among authors: zarate ya. Am J Med Genet A. 2017 May;173(5):1194-1199. doi: 10.1002/ajmg.a.38138. Epub 2017 Mar 22. Am J Med Genet A. 2017. PMID: 28332295

9

Parental-reported neurodevelopmental issues in Loeys-Dietz syndrome.

Collins RT 2nd, Flor JM, Tang X, Bange JM, Zarate YA. Collins RT 2nd, et al. Among authors: zarate ya. Res Dev Disabil. 2018 Dec;83:153-159. doi: 10.1016/j.ridd.2018.08.003. Epub 2018 Sep 10. Res Dev Disabil. 2018. PMID: 30212788

10

Constitutive activation of the PI3K-AKT pathway and cardiovascular abnormalities in an individual with Kosaki overgrowth syndrome.

Zarate YA, Boccuto L, Srikanth S, Pauly R, Ocal E, Balmakund T, Hinkle K, Stefans V, Schaefer GB, Collins RT 2nd. Zarate YA, et al. Am J Med Genet A. 2019 Jun;179(6):1047-1052. doi: 10.1002/ajmg.a.61145. Epub 2019 Apr 2. Am J Med Genet A. 2019. PMID: 30941910 Review.

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