Journal Article |
| Hermetz KE, Surti U, Cody JD, Rudd MK. A recurrent translocation is mediated by homologous recombination between HERV-H elements Mol Cytogenet 2012 Jan;5(1):6-6.
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| Luo Y, Hermetz KE, Jackson JM, Mulle JG, Dodd A, Tsuchiya KD, Ballif BC, Shaffer LG, Cody JD, Ledbetter DH, Martin CL, Rudd MK. Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements Hum Mol Genet 2011 Jul;20(19).
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| Hasi M, Soileau B, Sebold C, Hill A, Hale DE, ODonnell L, Cody JD. The role of the TCF4 gene in the phenotype of individuals with 18q segmental deletions Hum Genet 2011 Jun;130:777-787.
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| White WA, Schatz MP, Cody JD, Sebold C. Ophthalmic Manifestations of Tetrasomy 18p - A series of 25 patients Journal of American Association of Pediatric Ophthalmology and Strabismus 2011 Apr;14(1).
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| Cody JD, Hale DE. Linking chromosome abnormality and copy number variation Am J Med Genet A 2011 Mar;155(3):469-475.
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| Cody JD, Heard P, Hale D. Identification of two novel chromosome regions associated with isolated growth hormone deficiency J Pediatr Endocrinol Metab 2010 Nov;23(11):1159-1164.
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| Sebold C, Roeder E, Zimmerman M, Soileau B, Heard P, Carter E, Schatz M, White WA, Perry B, Reinker K, ODonnell L, Lancaster J, Li J, Hasi M, Hill A, Pankratz L, Hale DE, Cody JD. Tetrasomy 18p: report of the molecular and clinical findings of 43 individuals Am J Med Genet A 2010 Sep;152A(9):2164-2172.
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| ODonnell L, Soileau B, Heard P, Carter E, Sebold C, Gelfond J, Hale DE, Cody JD. Genetic determinants of autism in individuals with deletions of 18q Hum Genet 2010 May;128(2):155-164.
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| Zavala J, Ramirez M, Medina R, Heard P, Carter E, Crandall A, Hale D, Cody J, Escamilla M, Cody JD. Psychiatric syndromes in individuals with chromosome 18 abnormalities Am J Med Genet B Neuropsychiatr Genet 2010 Apr;153B(3):837-845.
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| Cody JD, Carter EM, Sebold C, Heard PL, Hale DE. A gene dosage map of Chromosome 18: a map with clinical utility Genet Med 2009 Nov;11(11):778-782.
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| Heard PL, Carter EM, Crandall AC, Sebold C, Hale DE, Cody JD. High resolution genomic analysis of 18q- using oligo-microarray comparative genomic hybridization (aCGH) Am J Med Genet A 2009 Jun;.
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| Cody JD, Heard PL, Crandall AC, Carter EM, Li J, Hardies LJ, Lancaster J, Perry B, Stratton RF, Sebold C, Schaub RL, Soileau B, Hill A, Hasi M, Fox PT, Hale DE. Narrowing critical regions and determining penetrance for selected 18q- phenotypes Am J Med Genet A 2009 Jun;149A(7):1421-1430.
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| Horbinski C, Carter EM, Heard PL, Sathanoori M, Hu J, Vockley J, Gunn S, Hale DE, Surti U, Cody JD. Molecular and clinical characterization of a recurrent cryptic unbalanced t(4q;18q) resulting in an 18q deletion and 4q duplication Am J Med Genet A 2008 Oct;146A(22):2898-2904.
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Abstract |
| Pankratz L, Hale D, Cody JD. Endocrine Abnormalities in 18 q-: A patient clinical cohort and 21 patient medical record review; 2011 Mar. (Pediatric Endocrine Society of Texas, Oklahoma, Louisiana and Arkansas).
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| Katie Rudd, Jill Mokry, Blake C. Ballif, Christa L. Martin, David H. Ledbetter, Lisa G. Shaffer, Jannine D. Cody, Karen E. HermetZ. Large inverted duplications form via a DNA hairpin intermediate; 2011 Mar. (AM College of Medical Genetic).
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| Cody C, ODonnell L, Soileau B, Riper MV, Stark D, Hale DE, Cody JD. Exploration of the Elements of Resilience and Fragility in Sibling Relationships; 2011 Jan. (UTHSCSA/ IIMS Research Day).
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| Gelfond JA, Pankratz L, Heard P, Carter E, Hale DE, Cody JD. Methodologies for Identifying Dosage Sensitive Genes; 2011 Jan. (UTHSCSA/ IIMS Research Day).
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| Pankratz L, Sebold C, Roeder ER, Zimmerman M, Soileau B, Heard P, Carter E, Schatz M, White WA, Perry B, Reinker K, ODonnell L, Lancaster J, Li J, Hasi M, Hill A, Hale DE, Cody JD. Tetrasomy 18p: Report of the Molecular and Clinical Findings of 43 Individuals; 2011 Jan. (UTHSCSA/ IIMS Research Day).
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| ODonnell L, Soileau B, Heard P, Carter E, Sebold C, Gelfond J, Hale DE, Cody JD. Genetic Determinants of Autism in Individuals with Deletions of 18q-; 2011 Jan. (UTHSCSA/ IIMS Research Day).
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| Sebold CD, Roeder E, Soileau B, Malik A, Neigut D, Hernandez K, Thomas M, Perry B, Fox P, Semrud-Clikeman M, Butcher B, Smith S, ODonnell L, Richards K, Reinker K, Tragus R, Hale DE, Cody JD. Expanding the clinical phenotype of tetrasomy 18p: Platform presentation at the European Society of Human Genetics Annual Meeting. Barcelona, Spain; 2008 Jan. (Eur J Hum Genet 16).
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| Cody JD, Sebold CD, Hale DE. Increasing research through collaboration: Poster presentation at the European Society of Human Genetics Annual Meeting. Barcelona, Spain; 2008 Jan. (Eur J Hum Genet 16 (Supp 3): P09.03).
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| Davis KS, Semrud-Clikeman M, Cody J, ODonnell L, Soileau B. Types of Parenting Stress in Families of Children with Genetic Disorders: Poster presentation at the National Conference in Child Health Psychology; 2008 Jan.
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| Hale DE, Sebold CD, Cody JD. Endocrine abnormalities in 18p-: Poster presentation at the European Society of Human Genetics Annual Meeting. Barcelona, Spain; 2008 Jan. (Eur J Hum Genet 16 (Supp 2): P02.071).
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| ODonnell L, Soileau B, Sebold C, Cody JD. Cognitive and behavioral patterns associated with 18p-: Poster presentation at the European Society of Human Genetics Annual Meeting. Barcelona, Spain; 2008 Jan. (Eur J Hum Genet 16 (Supp 2): P02.070).
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Editorial |
| Cody JD. Reply to letter from Drs. Ledbetter, Saul, and Moeschler Genet Med 2009 Sep;11(9):682-683.
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