GeneDx

Biopharma Commercial Executive

Warsaw Breakage Syndrome Foundation

The Mission of the Warsaw Breakage Syndrome is to promote community, research, and advocacy.

Founder

Librarey

Where rare disease families find and share resources

Co-Founder and Chief Momvocate

Comend

The digital space empowering families. Join other families with rare conditions to share support and collaborate on research.

Chief Rare Mom

Associate Business Development Liaison

Project Manager

Virginia Commonwealth University School of Medicine

Research assistant and project coordinator working in a breast cancer lab. Over 5 years experience in research project management and data analysis. Skilled in project development, scheduling, task prioritizing, data documentation and trouble-shooting.

Research Assistant and Project Coordinator

Randolph-Macon College

During my time at Randolph-Macon I worked in the lab of Dr. Traci Stevens. The Stevens lab primarily focuses on characterizing the molecular pathways that Abl uses to regulate actin-based processes in vivo, using the fruit fly as a model system. Currently the lab is exploring the roles of candidate genes in Abl signaling pathways and carrying out a genomic screen to identify novel components of Abl signaling pathways that regulate cell shape changes and cell migration during development. Specifically, I designed an experiment to identify new genes that genetically interact with Bcr-Abl, a fusion gene that was previously shown to cause changes in cell morphology, in the epithelium of fruit flies during development.

Undergraduate Research Assistant

Participated in a summer research fellowship and where I was able to continue my research on identifying genes that genetically interact with Bcr-Abl in the epithelium of fruit flies during development.

Schapiro Undergraduate Research Fellow

Business Development professional with CRO industry specialty lab experience. Scientific expertise in genetics, cancer biology, and molecular biology. 

Twin mom, rare mom, heart mom, & genetics enthusiast.  In 2021 my son was diagnosed with Warsaw Breakage Syndrome and at the time there were less than 25 documented cases worldwide. Founder of the Warsaw Breakage Syndrome Foundation, where our mission is to create community, drive research, and lead advocacy for patients with Warsaw Breakage Syndrome. 

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Sierra Phillips

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