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Allen N. Lamb

Allen N. Lamb, PhD

Languages spoken: English

Academic Information

Departments Adjunct - Pathology

Board Certification

  • American Board of Medical Genetics (Clinical Cytogenetics)

Education History

Undergraduate University of Maine - Orono
BS
Graduate Training University of Maine - Orono
MS
Doctoral Training Wesleyan University
PhD
Fellowship University of North Carolina
Fellow
Fellowship Harvard Medical School
Fellow

Selected Publications

Journal Article

  1. Huang B, Ning Y, Lamb AN, Sandlin CJ, Jamehdor M, Ried T, Bartley (1998). Identification of an unusual marker chromosome by spectral karyotyping. American journal of medical genetics, 80(4), 368-72. (Read full article)
  2. Riggs ER, Nelson T, Merz A, Ackley T, Bunke B, Collins CD, Collinson MN, Fan YS, Goodenberger ML, Golden DM, Haglund-Hazy L, Krgovic D, Lamb AN, Lewis Z, Li G, Liu Y, Meck J, Neufeld-Kaiser W, Runke CK, Sanmann JN, Stavropoulos DJ, Strong E, Su M, Tayeh MK, Kokalj Vokac N, Thorland EC, Andersen E, Martin C (2018). Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar. Human mutation, 39(11), 1650-1659. (Read full article)
  3. Donnenfeld AE, Lamb A (2003). Cytogenetics and molecular cytogenetics in prenatal diagnosis. Clinics in laboratory medicine, 23(2), 457-80. (Read full article)
  4. Herriges JC, Arch EM, Burgio PA, Baldwin EE, LaGrave D, Lamb AN, Toydemir R (2019). Delineating the Clinical Spectrum Associated With Xq25q26.2 Duplications: Report of 2 Families and Review of the Literature. Journal of child neurology, 34(2), 86-93. (Read full article)
  5. Lamb AN, Rosenfeld JA, Coppinger J, Dodge ET, Dabell MP, Torchia BS, Ravnan JB, Shaffer LG, Ballif B (2012). Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysis. Genetics in medicine, 14(11), 914-21. (Read full article)
  6. Herriges JC, Dugan SL, Lamb AN (2019). Clinical and molecular cytogenetic characterization of a novel 10q interstitial deletion: a case report and review of the literature. . Molecular cytogenetics, 12(doi:10.1186/s13039-019-0430-8), 20.