Assistant Professor of Biomedical Sciences
In addition to his academic roles at Quinnipiac and Weill Cornell, Dr. Wolujewicz is a Research Affiliate at the Connecticut Agricultural Experiment Station, collaborating on genomic and epidemiological surveillance efforts related to vector-borne diseases with direct public health relevance.
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 students for careers in biomedical research, data science, and translational science through training in modern experimental and computational methodologies.
The Wolujewicz Lab integrates computational genomics, biomedical data science, and machine learning approaches to investigate the genetic architecture of complex neurological and neurodevelopmental disorders, including neural tube defects, while also developing metagenomic strategies for vector-borne pathogen detection and public health surveillance.
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
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)