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Maria Serrano is an assistant professor at Boston University, focusing her research on understanding shared cellular molecular mechanisms in neurodevelopment and vasculogenesis within the context of rare diseases and their epigenetic basis. Her work notably includes the investigation of Kabuki Syndrome, linked to mutations in the KMT2D gene, and the discovery that KMT2D has a direct role in modulating Notch signaling, providing insights into cardiovascular phenotypes. Dr. Serrano utilizes zebrafish models to study the dynamics of KMT2D, having established a stable null KMT2D zebrafish mutant line that has revealed multiple novel cardiovascular features over time. Her research interests encompass non-canonical epigenetic mechanisms governing neuronal differentiation and blood vessel patterning, aiming to bridge basic research with clinical practice and support interdisciplinary collaborations in the rare diseases field. Dr. Serrano is committed to fostering diversity, equity, and inclusion within her lab and the scientific community, mentoring underrepresented students in STEM and striving to cultivate an inclusive environment that respects diverse backgrounds, especially guiding first-generation students through the complexities of academia.
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