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Lei Zhang, PhD, FACMG

TitleDirector, Cytogenetics Laboratory
InstitutionChildren's Mercy Kansas City
DepartmentLaboratory Genetics and Genomics
Address2401 Gillham Rd
Kansas City MO 64108
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    Other Positions
    TitleAssociate Professor
    InstitutionUniversity of Missouri-Kansas City
    DepartmentPathology


    Collapse Biography 
    Collapse education and training
    Herbei Medical University, Shijiazhuang, ChinaMD1986
    Peking Union Medical College, Beijing, ChinaPhD1998
    Virginia Commonwealth University, Richmond, VAFellowship2007Clinical Cytogenetics
    Children's Mercy Hospital, Baltimore, MDFellowship2021Laboratory Genetics and Genomics

    Collapse Bibliography 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
    List All   |   Timeline
    1. Repnikova EA, Zhang L, Orr BA, Roberts J, Zinkus T, Gener M, Kats A. Focal cortical dysplasia type IIIb associated with a KRAS-mutant ganglioglioma. Cancer Genet. 2024 Nov; 288-289:1-4. PMID: 39146656.
      View in: PubMed
    2. Cooley LD, Lansdon LA, Laurence K, Herriges JC, Zhang L, Repnikova EA, Joyce J, Thakor P, Warren L, Smith SC, Yoo B, Gener M, Ginn KF, Farooqi MS. Integrated genetic profiling of archival pediatric high-grade glial tumors and reassessment with 2021 WHO classification of paediatric CNS tumours. Cancer Genet. 2023 06; 274-275:10-20. PMID: 36917897.
      View in: PubMed
    3. Lansdon LA, Cadieux-Dion M, Herriges JC, Johnston J, Yoo B, Alaimo JT, Thiffault I, Miller N, Cohen ASA, Repnikova EA, Zhang L, Farooqi MS, Farrow EG, Saunders CJ. Clinical Validation of Genome Reference Consortium Human Build 38 in a Laboratory Utilizing Next-Generation Sequencing Technologies. Clin Chem. 2022 09 01; 68(9):1177-1183. PMID: 35869940.
      View in: PubMed
    4. Cadieux-Dion M, Farrow E, Thiffault I, Cohen ASA, Welsh H, Bartik L, Schwager C, Engleman K, Zhou D, Zhang L, Repnikova E, Amudhavalli SM, Saunders CJ. Phenotypic expansion and variable expressivity in individuals with JARID2-related intellectual disability: A case series. Clin Genet. 2022 08; 102(2):136-141. PMID: 35533077.
      View in: PubMed
    5. Bartik LE, Hughes SS, Tracy M, Feldt MM, Zhang L, Arganbright J, Kaye A. 22q11.2 duplications: Expanding the clinical presentation. Am J Med Genet A. 2022 03; 188(3):779-787. PMID: 34845825.
      View in: PubMed
    6. Lansdon LA, Chen D, Rush ET, Engleman K, Zhang L, Saunders CJ, Oroszi G. A novel likely pathogenic variant in a patient with Hermansky-Pudlak syndrome. Cold Spring Harb Mol Case Stud. 2021 10; 7(5). PMID: 34362826.
      View in: PubMed
    7. Lansdon LA, Cadieux-Dion M, Yoo B, Miller N, Cohen ASA, Zellmer L, Zhang L, Farrow EG, Thiffault I, Repnikova EA, Cooley LD, Alaimo JT, Porath B, Herriges JC, Saunders CJ, Farooqi MS. Factors Affecting Migration to GRCh38 in Laboratories Performing Clinical Next-Generation Sequencing. J Mol Diagn. 2021 05; 23(5):651-657. PMID: 33631350.
      View in: PubMed
    8. Zhang L, Brown LE, Bowen LM, McCarthy LC, Cooley LD, Repnikova E, Gener MA, Garola R, August KJ, Hays JA, Zwick DL, Li W. Application of 2016 WHO classification in the diagnosis of paediatric high-grade MYC-negative mature B-cell lymphoma with Burkitt-like morphological features. J Clin Pathol. 2020 Sep; 73(9):563-570. PMID: 31964683.
      View in: PubMed
    9. Ahmed AA, Zhang L, Reddivalla N, Hetherington M. Neuroblastoma in children: Update on clinicopathologic and genetic prognostic factors. Pediatr Hematol Oncol. 2017 Apr; 34(3):165-185. PMID: 28662353.
      View in: PubMed
    10. Zhang L, Cooley LD, Chandratre SR, Ahmed A, Jacobson JD. A Newborn with Genital Ambiguity, 45,X/46,XY Mosaicism, a Jumping Chromosome Y, and Congenital Adrenal Hyperplasia. Case Rep Endocrinol. 2013; 2013:747898. PMID: 24251047.
      View in: PubMed
    11. Septer S, Zhang L, Lawson CE, Cocjin J, Attard T, Ardinger HH. Aggressive juvenile polyposis in children with chromosome 10q23 deletion. World J Gastroenterol. 2013; 19(14):2286-92. PMID: 23599658.
      View in: PubMed
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