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The physicians in our directory are members of a Children’s Health hospital medical staff or are credentialed by Children’s Health for managed care participation. Some physicians are employed by Children’s Health, some are employed elsewhere, and some maintain an independent medical practice. There is no fee for being listed in our directory. The physicians populating your search results are selected based on the criteria that you provide and are then listed alphabetically. If a physician is no longer on a Children’s Health medical staff or participating in a Children’s Health managed care agreement, he/she would not be eligible to be listed in our directory.

Kathleen Sanders Wilson, MD $$

Pathologist

Professor at UT Southwestern Medical Center

Languages Spoken:
English
UT Southwestern Pediatric Group

Education and Training

Medical School
University of Texas Southwestern Medical Center (1991)
Residency
UT Southwestern Medical Center at Dallas (1994), Pathology
UT Southwestern Medical Center at Dallas (1992), Pathology
Fellowship
UT Southwestern Medical Center at Dallas (1997), Clinical Cytogenetics
Board Certification
American Board of Pathology/Clinical Pathology
  • Research Interests

    • Cytogenomic microarray analysis play in elucidating the pathogenetic events of both constitutional and acquired (neoplastic) disorders
    • Fluorescence in situ hybridization
    • Role of clinical genetic diagnostic technologies of conventional cytogenetic analysis
  • Publications

    • Cytogenetic and Cytogenomic Microarray Characterization of Chromothripsis in Chromosome 8 Affecting MOZ/NCOA2 (TIF2), FGFR1, RUNX1T1, and RUNX1 in a Pediatric Acute Myeloid Leukemia. Koduru PR, Wilson K, Wen J, Garcia R, Patel S, Monaghan SA Journal of pediatric hematology/oncology 2017 Jan
    • JAK-STAT6 Pathway Inhibitors Block Eotaxin-3 Secretion by Epithelial Cells and Fibroblasts from Esophageal Eosinophilia Patients: Promising Agents to Improve Inflammation and Prevent Fibrosis in EoE. Cheng E, Zhang X, Wilson KS, Wang DH, Park JY, Huo X, Yu C, Zhang Q, Spechler SJ, Souza RF PloS one 2016 11 6 e0157376
    • Novel r(2)(p25q31) Cytogenetic Abnormality in a Pediatric Patient With Acute Leukemia of Ambiguous Lineage. Kim J, Bu L, Koduru PR, Wilson KS, Fuda FS, Kumar KR, Timmons CF, Slone TL, Luu HS Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 2014 Dec
    • Therapy-induced Secondary Acute Myeloid Leukemia With t(11;19)(q23;p13.1) in a Pediatric Patient With Relapsed Acute Promyelocytic Leukemia. Dang DN, Morris HD, Feusner JH, Koduru P, Wilson K, Timmons CF, Cavalier M, Luu HS Journal of pediatric hematology/oncology 2014 Jun
    • Response to Mariani Et al.: A second report of PARK2 duplication and developmental delay. Scheuerle AE, Wilson KS American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2013 Jul 162 5 484
    • The clinical consequences of hemizygosity across 2 MB of 10q23 are restricted to Cowden syndrome. Lewis CM, Bu D, Sarode V, Robinson L, Wilson KS, Viscusi RK, Eng C, Euhus DM Breast cancer research and treatment 2012 Dec 136 3 911-8
    • High-resolution array CGH identifies common mechanisms that drive embryonal rhabdomyosarcoma pathogenesis., Paulson V, Chandler G, Rakheja D, Galindo R, Wilson K, Amatruda JF, Cameron S. Genes Chromosom Cancer 2011 50 397-408.
    • College of American Pathologists/American College of Medical Genetics proficiency testing for constitutional cytogenomic microarray analysis., Brothman AR, Dolan MM, Goodman BK, Park JP, Persons DL, Saxe DF, Tepperberg JH, Tsuchiya KD, Van Dyke DL, Wilson KS, Wolff DJ, Theil KS. Genet in Med 2011 13 765-769.
    • PARK2 copy number aberrations in two children presenting with autism spectrum disorder: Further support of an association and possible evidence for a new microdeletion/microduplication syndrome., Scheuerle A and Wilson K. Am J Med Genet Part B Neuropsychiatr Genet 2011 156B 413-420.
    • The interface of Medicare coverage decision-making and emerging molecular-based laboratory testing., Burken MI, Wilson KS, Heller K, Pratt VM, Schoonmaker MM, Seifter E. Genet in Med 2009 11 225-231.
    • A bcr3/short form PML/RARα transcript in an acute promyelocytic leukemia resulted from a derivative chromosome 17 due to submicroscopic insertion of PML gene into RARα locus., Wang H-Y, Ding J, Vasef MA, Wilson KS. Am J Clin Path 2009 131 64-71.
  • Professional Activities

    • American College of Medical Genetics (2002)
    • College of American Pathologists (1993)
    • American Medical Association (1991)
    • Dallas County Medical Society (1991)
    • Texas Medical Association (1991)
  • Awards and Honors

    • Doximity Recognition - Top M.D. by Consumers Checkbook (2017)
    • Outstanding Teacher in Genetics: Pre-Clinical Teaching Award - UT Southwestern Class of 2015 (2012)
    • Guide to America's Top Pathologists - Consumers' Research Council of America (2007-present) (2007)
    • Outstanding Teacher in Pathology - UT Southwestern Class of 2009 (2007)
    • Small Group Teaching Award in Pathology - UT Southwestern Class of 2009 (2007)
    • Favorite Teacher Recognition in Pathology - UT Southwestern Class of 2007 (2005)
    • Guide to America's Top Physicians - Consumers' Research Council of America (2004-present) (2004)
    • Amherst College: Graduation with Honors - B.A., magna cum laude (1986)
    • Aston L. Clarke Research Fellowship - UT Southwestern Medical Center at Dallas (1985)

Where I Provide Care: