Zarate YA - Search Results

1

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

2

Bi-allelic variants in INTS11 are associated with a complex neurological disorder.

Tepe B, Macke EL, Niceta M, Weisz Hubshman M, Kanca O, Schultz-Rogers L, Zarate YA, Schaefer GB, Granadillo De Luque JL, Wegner DJ, Cogne B, Gilbert-Dussardier B, Le Guillou X, Wagner EJ, Pais LS, Neil JE, Mochida GH, Walsh CA, Magal N, Drasinover V, Shohat M, Schwab T, Schmitz C, Clark K, Fine A, Lanpher B, Gavrilova R, Blanc P, Burglen L, Afenjar A, Steel D, Kurian MA, Prabhakar P, Gößwein S, Di Donato N, Bertini ES; Undiagnosed Diseases Network; Wangler MF, Yamamoto S, Tartaglia M, Klee EW, Bellen HJ. Tepe B, et al. Among authors: zarate ya. Am J Hum Genet. 2023 May 4;110(5):774-789. doi: 10.1016/j.ajhg.2023.03.012. Epub 2023 Apr 12. Am J Hum Genet. 2023. PMID: 37054711 Free PMC article.

3

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.

4

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

5

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

6

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

7

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.

8

COL1A1 and COL1A2 sequencing results in cohort of patients undergoing evaluation for potential child abuse.

Zarate YA, Clingenpeel R, Sellars EA, Tang X, Kaylor JA, Bosanko K, Linam LE, Byers PH. Zarate YA, et al. Am J Med Genet A. 2016 Jul;170(7):1858-62. doi: 10.1002/ajmg.a.37664. Epub 2016 Apr 19. Am J Med Genet A. 2016. PMID: 27090748

9

Severe Metabolic Acidosis and Hepatopathy due to Leukoencephalopathy with Thalamus and Brainstem Involvement and High Lactate.

Sellars EA, Balmakund T, Bosanko K, Nichols BL, Kahler SG, Zarate YA. Sellars EA, et al. Among authors: zarate ya. Neuropediatrics. 2017 Apr;48(2):108-110. doi: 10.1055/s-0036-1593984. Epub 2016 Nov 22. Neuropediatrics. 2017. PMID: 27875839

10

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

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