Learn more about our Clinical Microarray and ExomeNext coming together to optimize Genetic Diagnosis.
Melissa Parra, MS, CG
Kelly D.F. Gonzalez MS, CGC
Visit our secure online portal to start your order.
AmbryPort Login or Create an AccountConfidently guiding patient care through reliable results
Finding answers through superior variant interpretation
Understanding human disease through innovation, research, and partnerships
Offering anonymous, no-cost genetic testing and confidential genetic counseling to patients suspected of having or clinically diagnosed with hATTR amyloidosis through the hATTR Compass program
Choose an option below to order
your kit and start your genetic testing
Will insurance cover my patient's genetic test?
Click HereWhy partner with us?
Learn MoreWe are driven to give healthcare providers the most advanced testing information available so you can determine the best treatment options for your patients.
Learn more about our Clinical Microarray and ExomeNext coming together to optimize Genetic Diagnosis.
Melissa Parra, MS, CG
Kelly D.F. Gonzalez MS, CGC
Senior Manager of Clinical Diagnostics
Ms. Parra, M.S., CGC joined the client services department at Ambry Genetics in 2010. She obtained her Bachelor of Science degree in Molecular Genetics from the University of California, Davis in 1997 and Master of Science degree in Genetic Counseling from California State University, Northridge in 2005. In her current position, Ms. Parra assists clients with test coordination, result reporting and interpretation. Her specialty within the department is in chromosome microarray analysis and the NextGen sequencing panel for X-linked mental retardation.
Senior Manager of Clinical Genomics
Kelly Farwell Gonzalez received a B.A. in Psychobiology from Scripps College (the Claremont Colleges) and a M.S. in Genetic Counseling from the University of Arizona. Prior to her graduate studies, she spent several years in a research lab studying DNA mutagenesis. She later worked for more than four years as a senior genetic counselor at the Molecular Diagnostic Laboratory at City of Hope, where she continued her involvement in research, most of which focused on Li-Fraumeni Syndrome (LFS). She has more than 15 peer-reviewed publications in molecular genetics and has been an invited lecturer at several scientific meetings. Driven by her interest in new molecular technologies, Ms. Farwell Gonzalez joined Ambry in 2009 to lead the genomic services group where she gained expertise in multiple sequencing platforms and DNA/RNA enrichment techniques. Ms. Farwell Gonzalez currently leads Ambry's emerging clinical genomics offerings, most notably, the Clinical Diagnostic Exome, which allows her to draw on her expertise in next-gen sequencing, DNA mutagenesis, and genetic counseling.
Subscribe to receive notifications for future webinars.
Subscribe