• 1163 Citations
  • 16 h-Index
19942019
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Research Output 1994 2019

  • 1163 Citations
  • 16 h-Index
  • 33 Article
  • 2 Chapter
2019
Acute Myeloid Leukemia
Gene Amplification
docetaxel
Leukemia
Breast Neoplasms
2018

Copy number variations in a population with prune belly syndrome

Iqbal, N. S., Jascur, T. A., Harrison, S., Chen, C., Arevalo, M. K., Wong, D., Sanchez, E., Grimsby, G., Wilson, K. & Baker, L. A., Jan 1 2018, (Accepted/In press) In : American Journal of Medical Genetics, Part A.

Research output: Contribution to journalArticle

Prune Belly Syndrome
Population
Myotonia Congenita
Polymerase Chain Reaction
X-Linked Genes
2017
Chromosomes, Human, Pair 8
Acute Myeloid Leukemia
Cytogenetics
Pediatrics
Genes
2016
20 Citations (Scopus)
non-specific protein-tyrosine kinase
Eosinophilic Esophagitis
esophageal diseases
Janus Kinases
eosinophilia
2015
Chromosome Aberrations
Leukemia
Pediatrics
Clonal Evolution
Blood Cell Count
2014

A Neurologic Gene Map

Kayani, S. N., Wilson, K. S. & Rosenberg, R. N., Nov 13 2014, Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease: Fifth Edition. Elsevier Inc., p. 1333-1400 68 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Nervous System
Databases
Genes
Public Sector
Genomic Structural Variation

Therapy-induced secondary acute myeloid leukemia with t(11;19)(q23;p13.1) in a pediatric patient with relapsed acute promyelocytic leukemia

Dang, D. N., Morris, H. D., Feusner, J. H., Koduru, P., Wilson, K., Timmons, C. F., Cavalier, M. & Luu, H. S., Nov 8 2014, In : Journal of Pediatric Hematology/Oncology. 36, 8, p. e546-e548

Research output: Contribution to journalArticle

Acute Promyelocytic Leukemia
Acute Myeloid Leukemia
Pediatrics
Anthracyclines
Chromosome Aberrations
2013
2 Citations (Scopus)
DNA Copy Number Variations
Chromosome Deletion
Gene Duplication
Ubiquitin-Protein Ligases
Pervasive Child Development Disorders

The cytogenetics of solid tumors

Cooley, L. D. & Wilson, K. S., Jan 1 2013, The Principles of Clinical Cytogenetics, Third Edition. Springer New York, p. 371-411 41 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Cytogenetics
Tumors
Chromosomes
Pediatrics
Neoplasms
2012

The clinical consequences of hemizygosity across 2 MB of 10q23 are restricted to Cowden syndrome

Lewis, C. M., Bu, D., Sarode, V., Robinson, L., Wilson, K. S., Viscusi, R. K., Eng, C. & Euhus, D. M., Dec 2012, In : Breast Cancer Research and Treatment. 136, 3, p. 911-918 8 p.

Research output: Contribution to journalArticle

Multiple Hamartoma Syndrome
Megalencephaly
Papilloma
Breast
Fathers
2011
9 Citations (Scopus)

College of American Pathologists/American College of Medical Genetics proficiency testing for constitutional cytogenomic microarray analysis

Brothman, A. R., Dolan, M. M., Goodman, B. K., Park, J. P., Persons, D. L., Saxe, D. F., Tepperberg, J. H., Tsuchiya, K. D., Van Dyke, D. L., Wilson, K. S., Wolff, D. J. & Theil, K. S., Sep 2011, In : Genetics in Medicine. 13, 9, p. 765-769 5 p.

Research output: Contribution to journalArticle

Microarray Analysis
DNA
Pathologists
Cytogenetics
Technology
73 Citations (Scopus)

High-resolution array CGH identifies common mechanisms that drive embryonal rhabdomyosarcoma pathogenesis

Paulson, V., Chandler, G., Rakheja, D., Galindo, R. L., Wilson, K. S., Amatruda, J. F. & Cameron, S., Jun 2011, In : Genes Chromosomes and Cancer. 50, 6, p. 397-408 12 p.

Research output: Contribution to journalArticle

Embryonal Rhabdomyosarcoma
Neoplasms
Comparative Genomic Hybridization
Rhabdomyosarcoma
Receptor Protein-Tyrosine Kinases
2010
21 Citations (Scopus)

Malignant transformation of non-neoplastic Barrett's epithelial cells through well-defined genetic manipulations

Zhang, X., Yu, C., Wilson, K., Zhang, H. Y., Melton, S. D., Huo, X., Wang, D. H., Genta, R. M., Spechler, S. J. & Souza, R. F., 2010, In : PLoS One. 5, 9, p. 1-11 11 p., e13093.

Research output: Contribution to journalArticle

genetic engineering
Barrett Esophagus
T-cells
epithelial cells
esophagus
2009
3 Citations (Scopus)
Acute Promyelocytic Leukemia
Chromosomes, Human, Pair 17
Insertional Mutagenesis
Chromosomes, Human, Pair 15
Interphase
7 Citations (Scopus)

The interface of Medicare coverage decision-making and emerging molecular-based laboratory testing.

Burken, M. I., Wilson, K. S., Heller, K., Pratt, V. M., Schoonmaker, M. M. & Seifter, E., Apr 2009, In : Genetics in medicine : official journal of the American College of Medical Genetics. 11, 4, p. 225-231 7 p.

Research output: Contribution to journalArticle

Medicare
Decision Making
Molecular Diagnostic Techniques
Confusion
Health Policy
2008
29 Citations (Scopus)

Translocation (4;19)(q35;q13.1)-associated primitive round cell sarcoma: Report of a case and review of the literature

Rakheja, D., Goldman, S., Wilson, K. S., Lenarsky, C., Weinthal, J. & Schuttz, R. A., May 2008, In : Pediatric and Developmental Pathology. 11, 3, p. 239-244 6 p.

Research output: Contribution to journalArticle

Primitive Neuroectodermal Tumors
Sarcoma
Ewing's Sarcoma
Diagnostic Errors
Cytogenetics
2007
3 Citations (Scopus)

An extranodal nasal natural killer/T-cell lymphoma with isochromosome 7q10 as the sole cytogenetic aberration was initially diagnosed via bone marrow biopsy

Wang, H. Y., Wilson, K. S., McKenna, R. W., Xu, Y. & Karandikar, N., Nov 2007, In : Archives of Pathology and Laboratory Medicine. 131, 11, p. 1709-1714 6 p.

Research output: Contribution to journalArticle

Isochromosomes
Natural Killer T-Cells
T-Cell Lymphoma
Nose
Chromosome Aberrations
2006
40 Citations (Scopus)

HER-2 fluorescence in situ hybridization: Results from the Survey Program of the College of American Pathologists

Persons, D. L., Tubbs, R. R., Cooley, L. D., Dewald, G. W., Dowling, P. K., Du, E., Mascarello, J. T., Rao, K. W., Wilson, K. S., Wolff, D. J. & Habegger-Vance, G., Mar 2006, In : Archives of Pathology and Laboratory Medicine. 130, 3, p. 325-331 7 p.

Research output: Contribution to journalArticle

Fluorescence In Situ Hybridization
Breast Neoplasms
erbB-2 Genes
Pathologists
Surveys and Questionnaires
19 Citations (Scopus)

Immunophenotypic identification of acute myeloid leukemia with monocytic differentiation [15]

Xu, Y., McKenna, R. W., Wilson, K. S., Karandikar, N. J., Schultz, R. A. & Kroft, S. H., Jul 2006, In : Leukemia. 20, 7, p. 1321-1324 4 p.

Research output: Contribution to journalArticle

Immunophenotyping
Myeloid Leukemia
Acute Disease
Acute Myeloid Leukemia
Monocytes
2005
6 Citations (Scopus)

Acute leukemia with B-lymphoid and myeloid differentiation associated with an inv(5)(q13q33) in an adult patient

Butcher, B. W., Wilson, K. S., Kroft, S. H., Collins, R. H. & Bhushan, V., Feb 2005, In : Cancer Genetics and Cytogenetics. 157, 1, p. 62-66 5 p.

Research output: Contribution to journalArticle

Biphenotypic Acute Leukemia
Leukemia
Chromosome Aberrations
Chromosomes, Human, Pair 5
Hematologic Neoplasms
17 Citations (Scopus)

"Proximal-type" and classic epithelioid sarcomas represent a clinicopathologic continuum: Case report

Rakheja, D., Wilson, K. S., Meehan, J., Schultz, R. A. & Gomez, A. M., Feb 2005, In : Pediatric and Developmental Pathology. 8, 1, p. 105-114 10 p.

Research output: Contribution to journalArticle

Sarcoma
Tetraploidy
Karyotype
Cytogenetics
Hand
2004

Dysmorphic villi mimicking partial mole in a case with del(18)(q21)

Rakheja, D., Wilson, K. S. & Rogers, B. B., Nov 2004, In : Pediatric and Developmental Pathology. 7, 5, p. 546-548 3 p.

Research output: Contribution to journalArticle

Chromosome Aberrations
Chorionic Villi
Triploidy
Hydatidiform Mole
Tetraploidy
17 Citations (Scopus)

Extrapleural benign solitary fibrous tumor in the shoulder of a 9-year-old girl: Case report and review of the literature

Rakheja, D., Wilson, K. S., Meehan, J. J., Schultz, R. A., Maale, G. E. & Timmons, C. F., Dec 2004, In : Pediatric and Developmental Pathology. 7, 6, p. 653-660 8 p.

Research output: Contribution to journalArticle

Solitary Fibrous Tumors
Cytogenetic Analysis
Karyotype
Neoplasms
2002

Chronic myelogenous leukemia

Willis, M. S. & Wilson, K. S., 2002, In : Laboratory Medicine. 33, 3, p. 203-207 5 p.

Research output: Contribution to journalArticle

Leukemia, Myelogenous, Chronic, BCR-ABL Positive
40 Citations (Scopus)

Primary effusion lymphomas exhibit complex and recurrent cytogenetic abnormalities

Wilson, K. S., Mckenna, R. W., Kroft, S. H., Dawson, D. B., Ansari, Q. & Schneider, N. R., 2002, In : British Journal of Haematology. 116, 1, p. 113-121 9 p.

Research output: Contribution to journalArticle

Primary Effusion Lymphoma
Chromosome Aberrations
Trisomy
Cell Line
Chromosomes, Human, Pair 1
2001
20 Citations (Scopus)

Deletion of the NF2 region in both meningioma and juxtaposed meningioangiomatosis: Case report supporting a neoplastic relationship

Sinkre, P., Perry, A., Cai, D., Raghavan, R., Watson, M., Wilson, K. & Barton Rogers, B., 2001, In : Pediatric and Developmental Pathology. 4, 6, p. 568-572 5 p.

Research output: Contribution to journalArticle

Meningioma
Neurofibromatosis 2
Christianity
Fluorescence In Situ Hybridization
2000
15 Citations (Scopus)

Novel assay for Roberts syndrome assigns variable phenotypes to one complementation group

McDaniel, L. D., Prueitt, R., Probst, L. C., Wilson, K. S., Tomkins, D., Wilson, G. N. & Schultz, R. A., Jun 12 2000, In : American Journal of Medical Genetics. 93, 3, p. 223-229 7 p.

Research output: Contribution to journalArticle

Phenotype
Heterochromatin
Cleft Lip
Cleft Palate
Metaphase
1999
650 Citations (Scopus)

Absence of cancer-associated changes in human fibroblasts immortalized with telomerase

Morales, C. P., Holt, S. E., Ouellette, M., Kaur, K. J., Yan, Y., Wilson, K. S., White, M. A., Wright, W. E. & Shay, J. W., Jan 1999, In : Nature Genetics. 21, 1, p. 115-118 4 p.

Research output: Contribution to journalArticle

Telomerase
Fibroblasts
Neoplasms
Telomere Shortening
Cell Aging
19 Citations (Scopus)

Case report of a 22-week fetus with 47,XXX karyotype and multiple lower mesodermal defects

Hoang, M. P., Wilson, K. S., Schneider, N. R. & Timmons, C. F., Jan 1999, In : Pediatric and Developmental Pathology. 2, 1, p. 58-61 4 p.

Research output: Contribution to journalArticle

Single Umbilical Artery
Karyotype
Ovary
Spine
Fetus
1995
50 Citations (Scopus)

Renal cell carcinoma with translocation (X;1) Further evidence for a cytogenetically defined subtype

Tonk, V., Wilson, K. S., Timmons, C. F., Schneider, N. R. & Tomlinson, G. E., 1995, In : Cancer Genetics and Cytogenetics. 81, 1, p. 72-75 4 p.

Research output: Contribution to journalArticle

Renal Cell Carcinoma
Karyotype
30 Citations (Scopus)

The family pet as an unlikely source of group A beta-hemolytic streptococcal infection in humans

Wilson, K. S., Maroney, S. A. & Gander, R. M., 1995, In : Pediatric Infectious Disease Journal. 14, 5, p. 372-375 4 p.

Research output: Contribution to journalArticle

Streptococcal Infections
Pets
Pharyngitis
Streptococcus
Bacitracin
1994
6 Citations (Scopus)

Chromosomal instability in hereditary tyrosinemia type i

Wilson, K. S., Timmons, C. F., Hilton, D. S., Weinbug, A. & Tonk, V., 1994, In : Fetal and Pediatric Pathology. 14, 6, p. 1055-1057 3 p.

Research output: Contribution to journalArticle

Inborn Errors Amino Acid Metabolism
Tyrosinemias
Chromosomal Instability
Acute Disease
Preschool Children

Glandular inclusions in inguinal hernia sacs: A clinicopatholoical study of six cases

Mierau, G. W. & Wilson, K. S., 1994, In : Fetal and Pediatric Pathology. 14, 6, p. 1051-1054 4 p.

Research output: Contribution to journalArticle

Inguinal Hernia
36 Citations (Scopus)

Trisomy 2, trisomy 20, and del(17p) as sole chromosomal abnormalities in three cases of hepatoblastoma

Tonk, V. S., Wilson, K. S., Timmons, C. F. & Schneider, N. R., 1994, In : Genes Chromosomes and Cancer. 11, 3, p. 199-202 4 p.

Research output: Contribution to journalArticle

Hepatoblastoma
Trisomy
Chromosome Aberrations
Karyotype
Chromosomes