Kathleen S. Wilson, M.D.

Publications:

Tonk VS, Wilson KS, Timmons CF, Schneider NR. Trisomy 2, trisomy 20, and del(17p) as sole chromosomal abnormalities in three cases of hepatoblastoma. Genes Chromosom Cancer 1994;11:199-202.
Wilson KS, Timmons CF, Hilton DS, Weinberg AG, Tonk VS. Letter to the editor: Chromosomal instability in hereditary tyrosinemia Type 1. Pediatr Pathol 1994;14:1055-1057.
Wilson KS, Maroney SA, Gander RM. The family pet as an unlikely source of group A beta-hemolytic streptococcal infection in humans. Pediatr Infect Dis J 1995;14:372-375.
Tonk VS, Wilson KS, Timmons CF, Schneider NR, Tomlinson GE. Renal cell carcinoma with translocation (X;1): Further evidence for a cytogenetically defined subtype. Cancer Genet Cytogenet 1995;81:72-75.
Hoang MP, Wilson KS, Schneider NR, Timmons CF. Case report of a 22-week fetus with 47,XXX karyotype and multiple lower mesodermal defects. Pediatr Devel Pathol 1999;2:58-61.
Morales CP, Holt SE, Ouellette M, Kaur KJ, Yan Y, Wilson KS, White MA, Wright WE, Shay JW. Absence of cancer-associated changes in human fibroblasts immortalized with telomerase. Nature Genet 1999;21:115-118.
Ferber D. Immortalized cells seem cancer-free so far. (Karyotype publication) Science 1999;283:154-155.
McDaniel LD, Prueitt R, Probst LC, Wilson KS, Tomkins D, Wilson GN, Schultz RA. Novel assay for Roberts syndrome assigns variable phenotypes to one complementation group. Am J Med Genet 2000;93:223-229.
Sinkre P, Perry A, Cai D, Raghavan R, Watson M, Wilson KS, Rogers BB. Deletion of the NF2 region in both meningioma and juxtaposed meningioangiomatosis, a case report supporting a neoplastic relationship. Pediatr Devel Pathol 2001;4:568-572.
Wilson KS, McKenna RW, Kroft SH, Dawson DB, Ansari Q, Schneider NR. Primary effusion lymphomas (PEL) exhibit complex and recurrent cytogenetic abnormalities. Br J Haematol 2002;116:113-121.
Willis MS, Wilson KS. Chronic myelogenous leukemia. Lab Med 2002;33:203-207.
Wilson, KS, Cooley LD, Dewald G, Du E, Mascarello JT, Park JP, Persons DL, Rao KW, Vance GH, Wolff DJ. Conventional Cytogenetics Participant Summary Report. Survey CY-A 2003. Northfield, IL: College of American Pathologists: 2003.
Wilson KS, Cooley LD, Dewald G, Du E, Mascarello JT, Park JP, Persons DL, Rao KW, Vance GH, Wolff DJ. Fluorescence in situ hybridization (FISH) for Congenital Abnormalities Participant Summary Report. Survey CYG-A 2003. Northfield, IL: College of American Pathologists: 2003.
Rakheja D, Wilson KS, Rogers B. Dysmorphic villi mimicking partial mole in a case with del(18)(q21). Pediatr Devel Pathol 2004;7:546-548.
Rakheja D, Wilson KS, Meehan JJ, Schultz RA, Maale GE, Timmons CF. Extrapleural benign solitary fibrous tumor in the shoulder of a 9-year old girl: case report and review of the literature. Pediatr Devel Pathol 2004;7:653-660.
Butcher BW, Wilson KS, Kroft S, Collins RH, Bhushan V. Acute leukemia with B-lymphoid and myeloid differentiation associated with an inv(5)(q13q33) in the adult patient. Cancer Genet Cytogenet 2005;157:62-66.
Rakheja D, Wilson KS, Meehan JJ, Schultz RA, Gomez AM. “Proximal-type” and classic epithelioid sarcomas represent a clinicopathologic continuum: A case report. Pediatr Develop Pathol 2005;8:105-114.
Wilson KS, Dewald G, Van Dyke DL, Dowling PK, Mascarello JT, Persons DL, Rao KW, Theil KS, Thomsen JA, Vance GH, Wolff DJ. Conventional Cytogenetics Participant Summary Report. Survey CY-B 2005. Northfield, IL: College of American Pathologists: 2005.
Wilson KS, Dewald G, Van Dyke DL, Dowling PK, Mascarello JT, Persons DL, Rao KW, Theil KS, Thomsen JA, Vance GH, Wolff DJ. Fluorescence in situ hybridization (FISH) for Neoplastic Disorders Participant Summary Report. Survey CYF-A 2005. Northfield, IL: College of American Pathologists: 2005.
Xu Y, McKenna RW, Wilson KS, Karandikar NJ, Schultz RA, Kroft SH. Immunophenotypic identification of acute myeloid leukemia with monocytic differentiation. Leukemia 2006; 20:1321-1324.
Persons DL, Tubbs RR, Cooley LD, Dewald GW, Dowling PK, Du E, Mascarello JT, Rao KW, Wilson KS, Wolff DJ, Habegger-Vance G. HER-2 fluorescence in situ hybridization: results from the survey program of the College of American Pathologists. Arch Pathol Lab Med 2006;130:325-331.
Wilson KS, Dowling PK, Mascarello JT, Persons DL, Saxe DF, Thiel KS, Thomsen JA, Tsuchiya KD, Van Dyke DL, Wolff DJ. Fluorescence in situ hybridization (FISH), Paraffin embedded tissues, Participant Summary Report. Survey CYL 2006. Northfield, IL: College of American Pathologists: 2006.
Wilson KS, Dowling PK, Mascarello JT, Persons DL, Saxe DF, Thiel KS, Thomsen JA, Tsuchiya KD, Van Dyke DL, Wolff DJ. Conventional Cytogenetics Participant Summary Report. Survey CY-C 2006. Northfield, IL: College of American Pathologists: 2006.
Wilson KS, Brothman A, Dowling PK, Goodman B, Persons DL, Saxe DF, Thiel KS, Tsuchiya KD, Van Dyke DL, Wolff DJ. Fluorescence in situ hybridization (FISH), Hematolymphoid and constitutional disorders, Participant Summary Report. Survey CYF-A 2007. Northfield, IL: College of American Pathologists: 2007.
Wang H-Y, Wilson KS,McKenna RW, Karandiker N, Xu Y. An extranodal nasal natural killer/T-cell lymphoma with isochromosome 7q10 as the sole cytogenetic aberration was initially diagnosed via bone marrow biopsy. Arch Pathol Lab Med 2007;131:1709-1714.
Rakheja D, Goldman S, Wilson KS, Lenarsky C, Weinthal J, Schultz RA. Translocation (4;19)(q35;q13.1) associated primitive round cell sarcoma: report of a case and review of the literature. Pediatr Dev Pathol 2008;11(3):239-44.
Wang H-Y, Ding J, Vasef MA, Wilson KS. A bcr3/short form PML/RARa transcript in an acute promyelocytic leukemia resulted from a derivative chromosome 17 due to submicroscopic insertion of PML gene into RARa locus. Am J Clin Path 2009;131:64-71.
Burken MI, Wilson KS, Heller K, Pratt VM, Schoonmaker MM, Seifter E. The interface of Medicare coverage decision-making and emerging molecular-based laboratory testing. Genetics in Medicine 2009;11:225-231.

Abstracts:

Tonk VS, Wilson KS, Timmons CJ, Schneider NR. Trisomy 2, trisomy 20, and del(17p) as sole chromosomal abnormalities in three cases of hepatoblastoma. Am J Hum Genet 1993;A53 (suppl):#360. 1993 American Society of Human Genetics Meeting.
Wilson KS, Tonk VS, Bartlett BL, McKenna RW, Schneider NR. Chronic myeloid leukemia with a complex variant translocation misinterpreted by conventional cytogenetics but clarified by fluorescence in situ hybridization (FISH). 1994 Texas Society of Pathologists Meeting.
Cheo DL, Hammer R, Nieves L, Wilson KS, Friedberg EC. Mouse models of human nucleotide excision repair/transcription deficiency syndromes. J Cell Biochem 1995;21A:295. 1994 Keystone DNA Repair Symposium.
Wilson KS, Schultz RA, Schneider NR, Wilson GN, Evans GA. Molecular cytogenetic characterization of partial 11q trisomy in a child. Am J Hum Genet 1997;A143(suppl):#815.
1997 American Society of Human Genetics Meeting.
Wilson KS, Kroft SH, McKenna RW, Schneider NR. Cytogenetics of primary effusion lymphoma (HHV-8-positive body-cavity-based lymphoma). Am J Hum Genet 1998;A92(suppl):#503.
1998 American Society of Human Genetics Meeting.
Washington LT, Kroft SK, Wilson KS, Schneider NR, Aquino DB. CD56 expression by neutrophils associated with myeloid disorders. 1999 Texas Society of Pathologists Meeting.
Chenal M, Graham M, Wilson KS, Marley E, Hynan L. Treatment of patients with Burkitt lymphoma with and without HIV infection. 2000 Tenth Annual Mayo Clinic Jacksonville Hematology/Oncology Review.
Spiekerman J, Jester JV, Wilson KS, Schneider NR, Cohen D, Couchman J. Cytogenetic studies of telomerase transfected cell lines of the human cornea. J Ass Genet Tech 2000;26:153. 2000 Association of Genetic Technologists Meeting.
Wilson KS, McKenna RW, Kroft SH, Dawson DB, Schneider NR. Primary effusion lymphomas (PEL) exhibit complex and recurrent cytogenetic abnormalities. Mod Pathol 2001;11(suppl)183A:#1075. 2001 United States and Canadian Academy of Pathology Annual Meeting.
Tubbs RR, Nagle R, Hammond E, DeLellis R, His E, Linden M, Ormsby A, Pettigrew N, Rickert R, Said J, Bayer-Garner I, Roche P, Habegger-Vance G, Brothman A, Persons D, Wilson KS, Mascarello J, Rao K, Herrmann ME, Cooley L, Dewald G, Park J. Use of tissue MIDI-arrays for HER2 quality assurance: A College of American Pathologists feasibility study. Lab Invest 2003;83:50A and Mod Pathol 2003;16:50A. 2003 United States and Canadian Academy of Pathology Annual Meeting.
Maleki A, Bober M, Tiongson C, Elder F, Wilson KS. Infant with a de novo complex chromosomal rearrangement involving chromosomes 3, 5, 6, 7, 10 and 18 and a minimum of ten breakpoints. Genet Med 2004;6:324(#165). 2004 American College of Medical Genetics Meeting.
Schultz R, Duncan C, Elder F, Wilson KS , Read C, Garcia N, McDaniel L. Refinements in multiplex ligation-dependent probe amplification (MLPA) yield a robust, cost-efficient, high-throughput technology to assess genomic imbalance in pediatric populations. 2004 American Society of Human Genetics Annual Meeting Archive, Program #933.
URL:http://www.ashg.org/cgi-bin/ashg04s/ashg04
Xu Y, McKenna RW, Wilson KS, Karandikar NJ, Schultz RA, Kroft SH. Immunophenotypic identification of acute myeloid leukemia with monocytic differentiation. Mod Pathol 2005;18 (Suppl 1):258A. 2004 United States and Canadian Academy of Pathology Annual Meeting.
Schultz RA, Tomlinson GE, Rakheja D, Chen T, Schneider NR, Wilson KS, Echebiri C, Hirschman BA, Brothman AR, Eis P, Richmond TA, Selzer RR, Feusner JH, Malogolowkin M, Stallings RL, Children's Oncology Group. A role for the developmental gene NOTCH2 in hepatoblastoma. 2006 American Society of Human Genetics Annual Meeting
Seegmiller A, Maleki A, Wilson KS, Karandikar NJ. Characterization of B-cell lymphomas with C-MYC rearrangement in a background of complex cytogenetic abnormalities. Poster #198. 2008 USCAP Annual Meeting.
Arnold MA, Wilson KS, Arbini AA, Doolittle J, Chen W. Acute B-lineage leukemia with t(9;11)(p22;q23) involving MLL rearrangement is associated with a mature immunophenotype and aggressive clinical behavior. Poster #203 2009 USCAP Annual Meeting.
Schultz RA, Shaffer LG, Bejjani BA, Ballif BC, Sulpizio S, Byerly S, McDaniel LD, Weaver C, Wilson KS, Pascual JM. Microarray analysis in Glucose Transporter Type I Deficiency and other disorders associated with epilepsy. Signature Genomics 2009 Annual Meeting.
Schultz RA, Rosenfeld JA, Bejjani BA, LG Shaffer, Lamb A, Torchia B, Ballif BC, Sulpizio S, Byerly S, McDaniel LD, Ma Q, Nitui M, Rogers BB, Wilson KS, Pascual JM. Array CGH is a useful diagnostic tool in the investigation and molecular classification of epilepsy. American College of Medical Genetics 2010 Annual Meeting.

Book Chapters:

Cooley LD and Wilson KS. "Conventional and molecular cytogenetics of neoplasia," (Chapter 19) in Abeloff: Clinical Oncology, 4th ed., Abeloff MD (ed.), Elsevier Churchill Livingstone Press: Philadelphia, Pennsylvania, 2008.
Wilson, KS. "Chromosome analysis of hematopoietic diseases," (Chapter 38) in Clinical Laboratory Hematology, 2nd ed., McKenzie SB (ed.) Prentice Hall Press: Birmingham, Alabama, 2009.

Invited Lectures:

Chronic myeloid leukemia with a complex variant translocation misinterpreted by conventional cytogenetics but clarified by fluorescence in situ hybridization (FISH). 1994 Progress in Clinical Pathology Annual Meeting. Department of Pathology, U.T. Southwestern. 9-24-94.
Translocation (6;9)(p23;q34) in acute myeloid leukemia: A distinct clinical and morphologic entity. 1996 Progress in Clinical Pathology Annual Meeting. Department of Pathology, U.T. Southwestern. 10-18-96.
Genetics: A medical perspective. Baylor Health Care System Foundation, Caduceus Society, Baylor University Medical Center at Dallas. 11-14-96.
Human cytogenetic methods and nomenclature. University of North Texas, Cytogenetics Course (graduate level), 1-4-97.
Human cytogenetic methods and nomenclature: Application of fluorescence in situ hybridization (FISH) to human disorders. University of North Texas, Medical Genetics Course (graduate level), 9-25-97.
Molecular cytogenetics and prognostic significance of the t(12;21)(p13;q22) in pediatric acute lymphoblastic leukemia. 1997 Progress in Clinical Pathology Annual Meeting. Department of Pathology, U.T. Southwestern. 10-10-97.
Fluorescence in situ hybridization (FISH): Clinical cases. Baylor DNA Diagnostics Laboratory, Baylor College of Medicine, Houston, TX. 10-10-97.
Conventional cytogenetic and molecular cytogenetic techniques and applications to human disorders. University of North Texas, Medical Genetics Course (graduate level), 9-17-98.
Science Teacher Access to Resources at Southwestern (STARS) mini-symposium: Chromosomal disorders. U.T. Southwestern. 1-21-99.
Monitoring Philadelphia-chromosome-positive cells in patients with chronic myeloid leukemia who are treated with alpha-interferon. 1999 Progress in Clinical Pathology Annual Meeting. Department of Pathology, U.T. Southwestern. 3-5-99.
Using fluorescence in situ hybridization (FISH) to diagnose genetic disorders (a STARS student visit, L.D. Bell High School). U.T. Southwestern. 5-4-99.
American Medical Womens' Association panel participant - Women in medicine. U.T. Southwestern. 9-21-99.
Cytogenetics and applications to human disease. University of North Texas, Medical Genetics Course (graduate level), 9-29-99.
Chromosomal disorders (a STARS student visit, Woodrow Wilson High School). U. T. Southwestern. 9-29-99.
Cytogenetics of primary effusion lymphoma. Department of Pathology Grand Rounds, M.D. Anderson Cancer Center, Houston, TX. 2-18-00.
Philadelphia-chromosome-positive acute lymphoblastic leukemia, status post bone marrow transplantation. 2000 Progress in Clinical Pathology Annual Meeting. Department of Pathology, U.T. Southwestern. 3-3-00.
Molecular cytogenetics - Beyond karyotyping (a STARS student visit, L.D. Bell High School, Advanced Placement Biology). U.T. Southwestern. 4-25-00.
Genetic discrimination in the workplace - Panel discussion. Hugh O’ Brian Youth Leadership Conference. University of Texas at Dallas. 6-17-00.
Cytogenetics of primary effusion lymphoma. U.T. Southwestern Pathology Department Seminar series. 9-12-00.
Cytogenetic techniques. University of North Texas Medical Genetics Course (graduate level), 9-13-00.
Diagnostic applications of molecular cytogenetics. 2001 Progress in Clinical Pathology Annual Meeting. Department of Pathology, U. T. Southwestern. 2-23-01.
Acute promyelocytic leukemia and PML/RARA gene rearrangements. 2001 Progress in Clinical Pathology Annual Meeting. Department of Pathology, U.T. Southwestern. 2-23-01.
Life as an academic physician. American Medical Womens’ Association guest lecturer. 4-27-01.
Human cytogenetics. University of North Texas, Medical Genetics Course (graduate level) U. T. Southwestern. 9-12-01.
Practical cytogenetics and applications to human disease (a STARS teacher visit). U.T. Southwestern. 9-22-01.
American Medical Womens’ Association panel participant - Women in medicine. U.T. Southwestern. 11-27-01.
Core binding factor leukemias. 2002 Progress in Clinical Pathology Annual Meeting. Department of Pathology, U.T. Southwestern. 4-12-02.
American Medical Womens’ Association panel participant - Women in medicine. U.T. Southwestern. 10-1-02.
Molecular cytogenetics and the evaluation of neoplasia. Charles A. Sammons Cancer Center, Baylor University Medical Center at Dallas. 2-14-03.
Chronic myeloid leukemia and imatinib mesylate (Gleevec). 2003 Progress in Clinical Pathology Annual Meeting. Department of Pathology, U.T. Southwestern. 4-21-03.
American Medical Womens’ Association Banquet and Officer Dinner - Featured Speaker. UT Southwestern. 4-14-04.
American Medical Womens’ Association panel participant - Women in medicine. U.T. Southwestern. 9-15-04.
Recurrent Cytogenetic Aberrations in Pediatric Leukemias. UTSW Pediatric Hematology/Oncology Grand Rounds. Children’s Medical Center. 2-15-05.
American Medical Womens’ Association Banquet and Officer Dinner - Featured Speaker. UT Southwestern. 4-21-05.
American Medical Womens’ Association panel participant - Women in medicine. U.T. Southwestern. 9-21-05.
Texas Scottish Rite Hospital, Center for Excellence in Spine Research Meeting. Benefits of evaluation, genetic testing and counseling for the orthopedic patient/family. 4-19-06.
American Medical Womens’ Association Banquet and Officer Dinner - Featured Speaker. UT Southwestern. 5-23-06.
Molecular cytogenetics of pediatric cancer: recent clinical cases from Cook Children's Medical Center. Cook Children's Medical Center Hematology/Oncology Tumor Board Conference, Fort Worth, Texas. 6-6-06.
Molecular cytogenetics in 2006: from the basics to the cutting edge. North Texas Society of Pathology, Dallas, Texas 9-14-06.
Getting Paid: The Pursuit of Local and National Coverage Decisions. The Association for Molecular Pathology (AMP) Annual Meeting, Orlando, Florida, 11-19-06.
Commencement Address to the Graduating Class of 2007. Trinity Valley High School, Fort Worth,Texas. 5-19-2007.
Update on Reimbursement for Genetic Services from a Local and National Coverage Determination Perspective. Molecular Cluster Meeting, College of American Pathologists, Council on Scientific Affairs 8-10-07.
Diagnosing and Treating Cancer: Molecular Cytogenetics in the Post-Genome Era. Inaugural Speaker of the Dr. Gordon W. Dewald Lectureship. The Association of Genetic Technologists Annual Meeting, 6-14-08.
Genetic Diagnostics: Privacy, Confidentiality, Discrimination, and Commercialization. Southern Methodist University, Dedman School of Law, 2-16-09.
Cytogenomic Microarray Analysis CPT coding. Cytogenetic Resource Committee of the College of American Pathologists and American College of Medical Genetics, 1-31-2010.