Paul A. Levy

Phone718-741-2323
Emailplevymontefioreorg

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15 Article
4 Review article
1 Short survey

Consensus recommendations for the classification and long-term follow up of infants who screen positive for Krabbe Disease
Thompson-Stone, R., Ream, M. A., Gelb, M., Matern, D., Orsini, J. J., Levy, P. A., Rubin, J. P., Wenger, D. A., Burton, B. K., Escolar, M. L. & Kurtzberg, J., Sep 1 2021, In: Molecular Genetics and Metabolism. 134, 1-2, p. 53-59 7 p.
Research output: Contribution to journal › Article › peer-review

Open Access
13 Scopus citations
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders
CAUSES Study & SPARK Consortium, Dec 1 2021, In: Genome Medicine. 13, 1, 63.
Research output: Contribution to journal › Article › peer-review

Open Access
47 Scopus citations
The future of newborn screening for lysosomal disorders
Wasserstein, M. P., Orsini, J. J., Goldenberg, A., Caggana, M., Levy, P. A., Breilyn, M. & Gelb, M. H., Aug 24 2021, In: Neuroscience Letters. 760, 136080.
Research output: Contribution to journal › Article › peer-review

Open Access
19 Scopus citations
Trisomies
Levy, P. A. & Marion, R., Feb 2018, In: Pediatrics in review. 39, 2, p. 104-106 3 p.
Research output: Contribution to journal › Article › peer-review

7 Scopus citations
221 newborn-screened neonates with medium-chain acyl-coenzyme A dehydrogenase deficiency: Findings from the Inborn Errors of Metabolism Collaborative
Bentler, K., Zhai, S., Elsbecker, S. A., Arnold, G. L., Burton, B. K., Vockley, J., Cameron, C. A., Hiner, S. J., Edick, M. J., Berry, S. A., Thomas, J., Dodge, M., Singh, R., Lakshman, S., Coakley, K., Stembridge, A., Russi, A. S., Phillips, E., Burton, B. & Edano, C. & 61 others, Shrestha, S., Hoganson, G., Dwyer, L., Hainline, B., Romie, S., Hainline, S., Asamoah, A., Goodin, K., Rajakaruna, C., Jackson, K., Hamosh, A., Vernon, H., Smith, N., Ahmad, A., Lipinski, S., Feldman, G., Berry, S., Elsbecker, S., Bentler, K., Font-Montgomery, E., Peck, D., Pena, L. D. M., Koeberl, D. D., Jiang, Y. H., Kishnani, P. S., Rizzo, W., Dawson, M., Ambrose, N., Levy, P., Kronn, D., Fong, C. T., D'Aco, K., Hart, T., Erbe, R., Samons, M., Leslie, N., Powers, R., Bartholomew, D., Goff, M., vanCalcar, S., Hansen, J., Arnold, G., Walsh-Vockley, C., Rhead, W., Dimmock, D., Engelking, P., Bird, C., Swan, A., Schwoerer, J. S., Henry, S., Narumanchi, T. C., Hummel, M., Wilkins, J., Davis-Keppen, L., Stein, Q., Loman, R., Cameron, C., Edick, M. J., Hiner, S. J., Justice, K. & Zhai, S., Sep 1 2016, In: Molecular Genetics and Metabolism. 119, 1-2, p. 75-82 8 p.
Research output: Contribution to journal › Article › peer-review

Open Access
15 Scopus citations

Paul A. Levy, M.D.

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Collaborations and top research areas from the last five years

Dive into details

Consensus recommendations for the classification and long-term follow up of infants who screen positive for Krabbe Disease

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders

The future of newborn screening for lysosomal disorders

Trisomies

221 newborn-screened neonates with medium-chain acyl-coenzyme A dehydrogenase deficiency: Findings from the Inborn Errors of Metabolism Collaborative

Paul A. Levy, M.D.

Fingerprint

Collaborations and top research areas from the last five years

Publications

Consensus recommendations for the classification and long-term follow up of infants who screen positive for Krabbe Disease

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders

The future of newborn screening for lysosomal disorders

Trisomies

221 newborn-screened neonates with medium-chain acyl-coenzyme A dehydrogenase deficiency: Findings from the Inborn Errors of Metabolism Collaborative