Education History
| Fellowship |
Harvard Medical School |
Fellow |
|---|---|---|
| Fellowship |
University of North Carolina |
Fellow |
| Doctoral Training |
Wesleyan University |
PhD |
| Graduate Training |
University of Maine - Orono |
MS |
| Undergraduate |
University of Maine - Orono |
BS |
Selected Publications
Journal Article
- Herriges JC, Dugan SLLamb AN (2019). Clinical and molecular cytogenetic characterization of a novel 10q interstitial deletion: a case report and review of the literature. . Mol Cytogenet, 12(doi:10.1186/s13039-019-0430-8), 20.
- Herriges JC, Arch EM, Burgio PA, Baldwin EE, LaGrave D, Lamb AN, Toydemir RM (2018). Delineating the Clinical Spectrum Associated With Xq25q26.2 Duplications: Report of 2 Families and Review of the Literature. J Child Neurol, 34(2), 86-93. (Read full article)
- 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 CL (2018). Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar. Hum Mutat, 39(11), 1650-1659. (Read full article)
- Lamb AN, Rosenfeld JA, Coppinger J, Dodge ET, Dabell MP, Torchia BS, Ravnan JB, Shaffer LG, Ballif BC (2012). Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysis. Genet Med, 14(11), 914-21. (Read full article)
- Donnenfeld AE, Lamb AN (2003). Cytogenetics and molecular cytogenetics in prenatal diagnosis. Clin Lab Med, 23(2), 457-80. (Read full article)
- Huang B, Ning Y, Lamb AN, Sandlin CJ, Jamehdor M, Ried T, Bartley J (1998). Identification of an unusual marker chromosome by spectral karyotyping. Am J Med Genet, 80(4), 368-72. (Read full article)