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Institution

Yuri Zarate

TitleAssociate Professor
InstitutionUniversity of Arkansas for Medical Sciences
DepartmentPediatrics, College of Medicine
DivisionPeds Genetics
Address ACH Administration
1900 Maryland Street
Mail Slot # 512-22
Little Rock AR 72202
Phone501-364-2971
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    Other Positions
    TitleAssistant Professor
    InstitutionUniversity of Arkansas for Medical Sciences
    DepartmentGenetics, College of Medicine
    DivisionGenetics Faculty


    Collapse Overview 

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    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Helm BM, Powis Z, Prada CE, Casasbuenas-Alarcon OL, Balmakund T, Schaefer GB, Kahler SG, Kaylor J, Winter S, Zarate YA, Schrier Vergano SA. The role of IQSEC2 in syndromic intellectual disability: Narrowing the diagnostic odyssey. Am J Med Genet A. 2017 Oct; 173(10):2814-2820. PMID: 28815955.
      View in: PubMed
    2. Zarate YA, Steinraths M, Matthews A, Smith W, Sun A, Wilson LC, Brain C, Allgove J, Jacobs B, Fish JL, Powell CM, Wasserman W, Van Karnebeek C, Wakeling EL, Ma NS. Bone health and SATB2-associated syndrome. Clin Genet. 2017 Aug 08. PMID: 28787087.
      View in: PubMed
    3. Hills JA, Zarate YA, Danylchuk NR, Lepard T, Chen JC, Collins RT. Advanced cardiovascular imaging in Williams syndrome: Abnormalities, usefulness, and strategy for use. Am J Med Genet A. 2017 May; 173(5):1194-1199. PMID: 28332295.
      View in: PubMed
    4. Zarate YA, Kalsner L, Basinger A, Jones JR, Li C, Szybowska M, Xu ZL, Vergano S, Caffrey AR, Gonzalez CV, Dubbs H, Zackai E, Millan F, Telegrafi A, Baskin B, Person R, Fish JL, Everman DB. Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome. Clin Genet. 2017 Oct; 92(4):423-429. PMID: 28139846.
      View in: PubMed
    5. Sellars EA, Balmakund T, Bosanko K, Nichols BL, Kahler SG, Zarate YA. Severe Metabolic Acidosis and Hepatopathy due to Leukoencephalopathy with Thalamus and Brainstem Involvement and High Lactate. Neuropediatrics. 2017 Apr; 48(2):108-110. PMID: 27875839.
      View in: PubMed
    6. Zarate YA, Fish JL. SATB2-associated syndrome: Mechanisms, phenotype, and practical recommendations. Am J Med Genet A. 2017 Feb; 173(2):327-337. PMID: 27774744.
      View in: PubMed
    7. Zarate YA, Jones JR, Jones MA, Millan F, Juusola J, Vertino-Bell A, Schaefer GB, Kruer MC. Lessons from a pair of siblings with BPAN. Eur J Hum Genet. 2016 Jul; 24(7):1095. PMID: 27307113.
      View in: PubMed
    8. Zarate YA, Bhoj E, Kaylor J, Li D, Tsurusaki Y, Miyake N, Matsumoto N, Phadke S, Escobar L, Irani A, Hakonarson H, Schrier Vergano SA. SMARCE1, a rare cause of Coffin-Siris Syndrome: Clinical description of three additional cases. Am J Med Genet A. 2016 Aug; 170(8):1967-73. PMID: 27264197.
      View in: PubMed
    9. Zarate YA, Kaylor JA, Bosanko K, Lau S, Vargas J, Gao H. First clinical report of an infant with microcephaly and CASC5 mutations. Am J Med Genet A. 2016 Aug; 170(8):2215-8. PMID: 27149178.
      View in: PubMed
    10. Zarate YA, Clingenpeel R, Sellars EA, Tang X, Kaylor JA, Bosanko K, Linam LE, Byers PH. COL1A1 and COL1A2 sequencing results in cohort of patients undergoing evaluation for potential child abuse. Am J Med Genet A. 2016 Jul; 170(7):1858-62. PMID: 27090748.
      View in: PubMed
    11. Samanta D, Bosanko KB, Zarate YA. An infant with ash-leaf and café au lait spots: a case of double phakomatosis. Acta Neurol Belg. 2017 03; 117(1):323-324. PMID: 27043227.
      View in: PubMed
    12. Zarate YA, Jones JR, Jones MA, Millan F, Juusola J, Vertino-Bell A, Schaefer GB, Kruer MC. Lessons from a pair of siblings with BPAN. Eur J Hum Genet. 2016 Jul; 24(7):1080-3. PMID: 26577041.
      View in: PubMed
    13. Zarate YA, Sellars E, Lepard T, Tang X, Collins RT. Aortic dilation, genetic testing, and associated diagnoses. Genet Med. 2016 Apr; 18(4):356-63. PMID: 26133393.
      View in: PubMed
    14. Zarate YA, Sellars E, Lepard T, Carlo WF, Tang X, Collins RT. Aortic dilation in pediatric patients. Eur J Pediatr. 2015 Dec; 174(12):1585-92. PMID: 26070999.
      View in: PubMed
    15. 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. Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing. Am J Med Genet A. 2015 May; 167A(5):1026-32. PMID: 25885067.
      View in: PubMed
    16. Zarate YA, Bosanko KA, Bhoj E, Ganetzky R, Starr LJ, Zackai EH, Schaefer GB. Phenotypic modifications of patients with full chromosome aneuploidies and concurrent suspected or confirmed second diagnoses. Am J Med Genet A. 2015 Sep; 167A(9):2168-75. PMID: 25914130.
      View in: PubMed
    17. Zarate YA, Farrell JM, Alfaro MP, Elhassan NO. STAR syndrome is part of the differential diagnosis of females with anorectal malformations. Am J Med Genet A. 2015 Aug; 167A(8):1940-3. PMID: 25845904.
      View in: PubMed
    18. Campbell CL, Collins RT, Zarate YA. Severe neonatal presentation of Kleefstra syndrome in a patient with hypoplastic left heart syndrome and 9q34.3 microdeletion. Birth Defects Res A Clin Mol Teratol. 2014 Dec; 100(12):985-90. PMID: 25380126.
      View in: PubMed
    19. Kaylor J, Alfaro M, Ishwar A, Sailey C, Sawyer J, Zarate YA. Molecular and cytogenetic evaluation of a patient with ring chromosome 13 and discordant results. Cytogenet Genome Res. 2014; 144(2):104-8. PMID: 25377780.
      View in: PubMed
    20. Zarate YA, Shur N, Robin A, Garnica AD, Quintos JB, Schaefer GB. Persistent congenital hyperinsulinism in two patients with Beckwith-Wiedemann syndrome due to mosaic uniparental disomy 11p. J Pediatr Endocrinol Metab. 2014 Sep; 27(9-10):951-5. PMID: 24756053.
      View in: PubMed
    21. Collins RT, Phomakay V, Zarate YA, Tang X. Impact of aortic aneurysm on hospitalizations in patients with marfan syndrome: a multi-institutional study. Pediatr Cardiol. 2015 Jan; 36(1):132-9. PMID: 25096902.
      View in: PubMed
    22. Zarate YA, Bosanko KA, Jarasvaraparn C, Vengoechea J, McDonough EM. Description of the first case of adenomyomatosis of the gallbladder in an infant. Case Rep Pediatr. 2014; 2014:248369. PMID: 25024860; PMCID: PMC4082867.
    23. Zarate YA, Lepard T, Sellars E, Kaylor JA, Alfaro MP, Sailey C, Schaefer GB, Collins RT. Cardiovascular and genitourinary anomalies in patients with duplications within the Williams syndrome critical region: phenotypic expansion and review of the literature. Am J Med Genet A. 2014 Aug; 164A(8):1998-2002. PMID: 24844942.
      View in: PubMed
    24. Zarate YA, Bell C, Schaefer GB. Radioulnar Synostosis and Brain Abnormalities in a Patient With 17q21.31 Microdeletion Involving EFTUD2. Cleft Palate Craniofac J. 2015 Mar; 52(2):237-9. PMID: 24805776.
      View in: PubMed
    25. Zarate YA, Bell C, Schaefer B. Description of another case of 3q26.33-3q27.2 microdeletion supports a recognizable phenotype. Eur J Med Genet. 2013 Nov; 56(11):624-5. PMID: 24055528.
      View in: PubMed
    26. Zarate YA, Lichty AW, Champion KJ, Clarkson LK, Holden KR, Matheus MG. Unique cerebrovascular anomalies in Noonan syndrome with RAF1 mutation. J Child Neurol. 2014 Aug; 29(8):NP13-7. PMID: 23877478.
      View in: PubMed
    27. Zarate YA, Lichty AW, Champion KJ, Clarkson LK, Holden KR, Matheus MG. Unique Cerebrovascular Anomalies in Noonan Syndrome With RAF1 Mutation. J Child Neurol. 2013.
    28. Zarate YA, Dwivedi A, Bartel FO, Bellomo MA, Cathey SS, Champaigne NL, Clarkson LK, Dupont BR, Everman DB, Geer JS, Gordon BC, Lichty AW, Lyons MJ, Rogers RC, Saul RA, Schroer RJ, Skinner SA, Stevenson RE. Clinical utility of the X-chromosome array. Am J Med Genet A. 2013 Jan; 161A(1):120-30. PMID: 23208842.
      View in: PubMed
    29. Zarate YA, Zhan H, Jones JR. Infrequent Manifestations of Kabuki Syndrome in a Patient with Novel MLL2 Mutation. Mol Syndromol. 2012 Oct; 3(4):180-4. PMID: 23239960; PMCID: PMC3507269.
    30. Prada CE, Zarate YA, Hopkin RJ. Genetic causes of macroglossia: diagnostic approach. Pediatrics. 2012 Feb; 129(2):e431-7. PMID: 22250026.
      View in: PubMed
    31. Prada CE, Zarate YA, Hagenbuch S, Lovell A, Schorry EK, Hopkin RJ. Lethal presentation of neurofibromatosis and Noonan syndrome. Am J Med Genet A. 2011 Jun; 155A(6):1360-6. PMID: 21567923.
      View in: PubMed
    32. Zarate YA, Dwivedi A, Bartel FO, Corning K, Dupont BR. 47, XY, +der(Y),t(X;Y)(p21.1;p11.2): a unique case of XY sex reversal. Am J Med Genet A. 2011 Feb; 155A(2):386-91. PMID: 21271659.
      View in: PubMed
    33. Zarate YA, Putnam PE, Saal HM. Intestinal malrotation in a patient with Pfeiffer syndrome type 2. Cleft Palate Craniofac J. 2010 Nov; 47(6):638-41. PMID: 20509766.
      View in: PubMed
    34. Zarate YA, Martin LJ, Hopkin RJ, Bender PL, Zhang X, Saal HM. Evaluation of growth in patients with isolated cleft lip and/or cleft palate. Pediatrics. 2010 Mar; 125(3):e543-9. PMID: 20142284.
      View in: PubMed
    35. Zarate YA, Patterson L, Yin H, Hopkin RJ. A case of minimal change disease in a Fabry patient. Pediatr Nephrol. 2010 Mar; 25(3):553-6. PMID: 19876652.
      View in: PubMed
    36. Zarate YA, Mena R, Martin LJ, Steele P, Tinkle BT, Hopkin RJ. Experience with hemihyperplasia and Beckwith-Wiedemann syndrome surveillance protocol. Am J Med Genet A. 2009 Aug; 149A(8):1691-7. PMID: 19610116.
      View in: PubMed
    37. Zarate YA, Hopkin RJ. Twin-twin transfusion resulting in fetal cell contamination in Beckwith-Wiedemann syndrome. Am J Med Genet A. 2009 Jul; 149A(7):1569-70. PMID: 19533777.
      View in: PubMed
    38. Zarate YA, Pacheco MC, Bove KE, Gorlin R, Zhao H, Hopkin RJ. Phenotypic and microscopic description of a new case of Ermine phenotype. Am J Med Genet A. 2009 Jun; 149A(6):1253-6. PMID: 19449401.
      View in: PubMed
    39. Zarate YA, Hopkin RJ. Fabry's disease. Lancet. 2008 Oct 18; 372(9647):1427-35. PMID: 18940466.
      View in: PubMed
    40. Sutherell J, Zarate Y, Tinkle BT, Markham LW, Cripe LH, Hyland JC, Witte D, Hopkin RJ, Hinton RB. Novel fibrillin 1 mutation in a case of neonatal Marfan syndrome: the increasing importance of early recognition. Congenit Heart Dis. 2007 Sep-Oct; 2(5):342-6. PMID: 18377451.
      View in: PubMed
    41. Zarate YA, Kogan JM, Schorry EK, Smolarek TA, Hopkin RJ. A new case of de novo 11q duplication in a patient with normal development and intelligence and review of the literature. Am J Med Genet A. 2007 Feb 01; 143A(3):265-70. PMID: 17219392.
      View in: PubMed
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