Naseem Uddin, M.D.
Assistant Professor

Medical School

Karachi Medical and Dental College (1999)

Internship

Aga Khan University, Pakistan (2000), Medical/surgical

Residency

UT Southwestern Medical Center (2007), Anatomic & Clinical Pathology

Fellowship

UT Southwestern Medical Center (2008), Pediatric Pathology

Fellowship

UT Southwestern Medical Center (2009), Cytogenetics

Fellowship

University of UTAH Program (2010), Cytogenetics

• Gene Fusions in Pediatric Neoplasms
• Placenta Acreta Spectrum

Featured Publications

Second instance of co-occurring 22q11.2 deletion syndrome and Williams syndrome.

Uhles CL, Barnes S, Uddin N, Umaña LA, Am J Med Genet A 2021 Jul

Congenital Myenteric Hypoganglionosis.

Kapur RP, Bellizzi AM, Bond S, Chen H, Han JS, LeGallo RD, Midgen C, Poulin AA, Uddin N, Warren M, Velázquez Vega JE, Zuppan CW, Am J Surg Pathol 2021 Jan

Development and Clinical Validation of a Multiplex Gene Fusion Assay.

García R, Patel N, Uddin N, Y Park J, Lab Med 2020 Feb

Homozygous NEK8 Mutations in Siblings with Neonatal Cholestasis Progressing to End Stage Liver, Renal and Cardiac Disease.

Hassan S, Wolf MTF, Umaña LA, Malik S, Uddin N, Andersen J, Aqul A, J. Pediatr. Gastroenterol. Nutr. 2019 Oct

Multimodal depiction of a rare immature gastric teratoma from fetus to infant.

Beavers AJ, Khan A, Uddin N, Weakley DL, Setoodeh S, Pfeifer CM Radiol Case Rep 2019 Mar 14 3 372-376

Congenital infantile fibrosarcoma mimicking a cutaneous vascular lesion: a case report and review of the literature.

Enos T, Hosler GA, Uddin N, Mir A J. Cutan. Pathol. 2016 Nov

Epidermoid cyst of the uvula in a child.

Daram S, Ulualp SO, Uddin N SAGE Open Med Case Rep 2016 4 2050313X16683629

IKBKG Mutation With Incontinentia Pigmenti and Ring-Enhancing Encephalopathy.

Eksambe D, Agim N, Uddin N, Gotway G, Pascual JM JAMA Neurol 2015 Dec 72 12 1533-5

Constitutional trisomy 8 mosaicism in a healthy bone marrow donor: confirmation of first reported donor origin trisomy 8.

Uddin N, Williams MS, South ST Am. J. Hematol. 2010 Dec 85 12 974-6

Acute myeloid leukemia with inv(16) with CBFB-MYH11, 3'CBFB deletion, variant t(9;22) with BCR-ABL1, and del(7)(q22q32) in a pediatric patient: case report and literature review.

Tirado CA, Valdez F, Klesse L, Karandikar NJ, Uddin N, Arbini A, Fustino N, Collins R, Patel S, Smart RL, Garcia R, Doolittle J, Chen W Cancer Genet. Cytogenet. 2010 Jul 200 1 54-9

• American College of Medical Genetics and Genomics (2020)
• Cancer Genomics Consortium (2020)
• Society for Pediatric Pathology (2011)
• The American Cytogenetics Conference (2010)
• The American Society of Human Genetics (2009)
• College of American Pathologists (2003)