Katie Rudd, PhD

Specialties

• Cytogenetics
• Molecular Genetics

Education

• Doctorate Degree—Genetics, Case Western Reserve University
• Fellowship—Postdoctoral, Fred Hutchinson Cancer Research Center
• Fellowship—Clinical Cytogenetics, University of Washington
• Fellowship—Clinical Molecular Genetics, Emory University
• Fellowship—Clinical Molecular Genetics, Duke University Health System

Certifications/Affiliations

• American Board of Medical Genetics and Genomics (Clinical Cytogenetics, Clinical Molecular Genetics)
• New York State Department of Health License—Genetic Testing, Oncology: Molecular and Cellular Tumor Markers, and Cytogenetics
• American Board of Medical Genetics and Genomics, Board of Directors

Research Interests

•  Copy number variation
•  Mechanisms of chromosome rearrangement

Awards

• Basil O’Connor Starter Scholar Research Award

Recent Publications

• Hwang S, Rudd MK, Finch L, et al. VACTERL phenotype with mosaic trisomy 5 and uniparental disomy 5. Am J Med Genet A. 2018;176(2):502-504.
• Rudd MK, Schleede JB, Williams SR, et al. Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomy. Prenat Diagn. 2018;38(12):920-923.