Assistant Professor of Biomedical Sciences
At Quinnipiac, Dr. Wolujewicz teaches undergraduate and graduate courses including Biomedical Genomics, Biotechnology, Computational Biomedicine, and Cellular Basis of Neurobiological Disorders. Through his teaching, mentorship, and research, he is committed to preparing the next generation of scientists with training in cutting-edge biomedical techniques and data-driven discovery.
Dr. Wolujewicz is a recipient of the Timothy M. George Award for Excellence in Neural Tube Defect Research and is an active member of The Society of Birth Defects Research and Prevention. The Wolujewicz Lab integrates computational genomics, biomedical data science, and AI-driven approaches to explore the genetic basis of human disease. His work focuses on genomic contributions to complex neurological disorders, advancing our understanding of the genetic underpinnings of neural tube defects, and developing innovative metagenomic strategies for vector-borne pathogen surveillance and public health applications.
Education
- MS, Rutgers-The State Univ of NJ
- MPH, Rutgers-The State Univ of NJ
- PHD, Cornell University-Ny
- PHD, Cornell University
Areas of Expertise
- Biomedical Genomics
- Biotechnology
- Population Health
- Neurology/Neuroscience
- Computational Biomedicine
Organization
- Biomedical Sciences
Office Location
- The Site 271
Mail Drop
- EC-BMS
Courses
-
BIO 282 Genetics
Fall 2025 -
BMS 312 Biomedical Genomics
Fall 2025 -
BMS 472 Biotechnology
Spring 2026 -
BMS 498 Independent Study in Biomedical Sciences I
Fall 2025 -
BMS 499 Independent Study in Biomedical Sciences II
Fall 2025 -
BMS 556 Seminar in Health Care Disparities
Spring 2026 -
BMS 578 Cellular Basis of Neurobiological Disorders
Fall 2025 -
BMS 622 MED Cross-Listed Selective
Spring 2026 -
BMS 650 Thesis I
Fall 2025
Experience
Quinnipiac University
Assistant Professor of Biomedical Sciences
Hamden, CT
2023 - Present
Quinnipiac University
Assistant Professor of Medical Sciences
North Haven, CT
2023 - Present
Weill Cornell Medical College
Adjunct Assistant Professor of Neuroscience
New York, NY
2023 - Present
Weill Cornell Medical College
Postdoctoral Associate in Neuroscience
New York, NY
2022 - 2023
Selected Publications
Peer Reviewed Presentations
Evidence for Pathogenic Expansions in NTD Case-Parent Trios
Paul Wolujewicz, Vanessa Aguiar-Pulido, Megan Shuguli, Sarah Fazal, Gregory Heuer, Osvaldo M. Mutchinick, Jose Suazo, Pablo Alacron, Adolfo Aguayo Gómez, Richard H. Finnell, Rosa A. Pardo, M. Elizabeth Ross
International Conference on Neural Tube Defects, Vancouver, Canada, University of British Columbia (2024)
Peer Reviewed Journal
Schizophrenia endothelial cells exhibit higher permeability and altered angiogenesis patterns in patient-derived organoids
Isidora Stankovic, Michael Notaras, Paul Wolujewicz, Tyler Lu, Raphael Lis, Margaret Elizabeth Ross, Dilek Colak
Translational Psychiatry (2024)
Peer Reviewed Journal
Integrative computational analyses implicate regulatory genomic elements contributing to spina bifida.
Wolujewicz P, Aguiar-Pulido V, Thareja G, Suhre K, Elemento O, Finnell RH, Ross ME.
Genetics in Medicine Open (2024)
Peer Reviewed Journal
A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephalocele.
Crane-Smith, Z., De Castro, S. C. P., Nikolopoulou, E., Wolujewicz, P., Smedley, D., Lei, Y., Mather, E., Santos, C., Hopkinson, M., Pitsillides, A. A., Genomics England Research Consortium, Finnell, R. H., Ross, M. E., Copp, A. J., & Greene, N. D. E.
32(17) Human molecular genetics 2681–2692 (2023)
Peer Reviewed Journal
Astrocytes derived from ASD individuals alter behavior and destabilize neuronal activity through aberrant Ca2+ signaling.
Allen, M., Huang, B. S., Notaras, M. J., Lodhi, A., Barrio-Alonso, E., Lituma, P. J., Wolujewicz, P., Witztum, J., Longo, F., Chen, M., Greening, D. W., Klann, E., Ross, M. E., Liston, C., & Colak, D.
Molecular psychiatry (2022)
Peer Reviewed Journal
Systems biology analysis of human genomes points to key pathways conferring spina bifida risk.
Aguiar-Pulido, V., Wolujewicz, P., Martinez-Fundichely, A., Elhaik, E., Thareja, G., Abdel Aleem, A., Chalhoub, N., Cuykendall, T., Al-Zamer, J., Lei, Y., El-Bashir, H., Musser, J. M., Al-Kaabi, A., Shaw, G. M., Khurana, E., Suhre, K., Mason, C. E., Elemento, O., Finnell, R. H., & Ross, M. E.
Proceedings of the National Academy of Sciences (2021)
Peer Reviewed Journal
Genome-wide investigation identifies a rare copy-number variant burden associated with human spina bifida.
Wolujewicz P, Aguiar-Pulido V, AbdelAleem A, Nair V, Thareja G, Suhre K, Shaw GM, Finnell RH, Elemento O, Ross ME.
Genetics in Medicine (2021)
Peer Reviewed Journal Article Review
Unraveling the complex genetics of neural tube defects: From biological models to human genomics and back.
Wolujewicz P, Steele JW, Kaltschmidt JA, Finnell RH, Ross ME.
Genesis (2021)