Genomic Scientist | PhD in Human Genetics
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I recently defended my PhD in Human Genetics at Northwestern University, where I studied the genetic basis of polycystic ovary syndrome (PCOS). With a strong foundation in variant interpretation, NGS sequencing technologies, and clinical genomics, I bring both technical expertise and a deep commitment to patient-centered science. I’ve also led science communication and advocacy efforts through my work with a rare disease nonprofit.
I’m now seeking opportunities where I can contribute to advancing diagnostic genetics and improving the lives of patients and families.
From 2019 to 2025, I conducted my PhD research in Human Genetics at Northwestern University, investigating the genetic architecture of polycystic ovary syndrome (PCOS). I worked extensively with whole-exome sequencing data, curated candidate genes, and interpreted over 100 genetic variants. In 2023, I also completed an internship at a clinical molecular diagnostics lab, where I participated in variant interpretation meetings and gained exposure to clinical reporting workflows.
I earned my PhD in Human Genetics from Northwestern University in 2025, where my research focused on the genetic architecture of polycystic ovary syndrome (PCOS). I also hold a Bachelor of Arts in Biology from Lawrence University, which I completed in 2018.