Amanda Openshaw, MS, LCGC

Phone: 800-242-2787 ext. 3429

Specialties

• Genetics
• Constitutional FISH
• Cytogenetics
• Genomic SNP microarray
• Maternal serum screening

Education

• Master’s Degree—Genetic Counseling, University of Michigan

Certification/Affiliations

• American Board of Genetic Counseling

Research Interests

• Laboratory stewardship (utilization management) for genetic testing
• Genetics research protocols
• Genetics education

Recent Publications

• Ballout RA, Dickerson C, Wick MJ, et al. Int22h1/Int22h2-mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features. Hum Mutat. 2020;41(7):1238-1249.
• Dugan SL, Panza E, Openshaw A, et al. Delineation of the 9q31 deletion syndrome: Genomic microarray characterization of two patients with overlapping deletions. Am J Med Genet A. 2018;176(12):2901-2906.
• Paulraj P, Palumbos JC, Openshaw A, et al. Multiple congenital anomalies and global developmental delay in a patient with interstitial 6q25.2q26 deletion: a diagnostic odyssey. Cytogenet Genome Res. 2018;156(4):191-196.