Projects per year
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Collaborations and top research areas from the last five years
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NY ScreenPlus: A Comprehensive, Flexible, Multi-disorder Newborn Screening Program
Wasserstein, M. M. P. & Wasserstein, M. P.
National Institute of Child Health and Human Development
9/4/12 → 7/31/24
Project: Research project
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Incorporating genomics into the clinical care of diverse NYC children
8/4/17 → 5/31/22
Project: Research project
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Incorporating genomics into the clinical care of diverse NYC children
Kenny, E. E., Gelb, B. D., Horowitz, C. R. & Wasserstein, M. P.
National Human Genome Research Institute
8/4/17 → 5/31/18
Project: Research project
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LSDs:A Pilot NBS and Examination of the Associated Ethical Legal & Social Issues
Wasserstein, M. P., Rose, S. A. & Rose, S. A.
9/4/12 → 7/31/21
Project: Research project
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SAFETY, EFFICACY & PHARMACOKINETICS OF MYOZYME IN PATIENTS WITH POMPE DISEASE
National Center for Research Resources
3/1/07 → 2/29/08
Project: Research project
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Physician services and costs after disclosure of diagnostic sequencing results in the NYCKidSeq program
Berkalieva, A., Kelly, N. R., Fisher, A., Hohmann, S. F., Sebastin, M., Di Biase, M., Bonini, K. E., Marathe, P., Odgis, J. A., Suckiel, S. A., Ramos, M. A., Rhodes, R., Abul-Husn, N. S., Greally, J. M., Horowitz, C. R., Wasserstein, M. P., Kenny, E. E., Gelb, B. D. & Ferket, B. S., Jan 2024, In: Genetics in Medicine. 26, 1, 101011.Research output: Contribution to journal › Article › peer-review
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ScreenPlus: A comprehensive, multi-disorder newborn screening program
Kelly, N. R., Orsini, J. J., Goldenberg, A. J., Mulrooney, N. S., Boychuk, N. A., Clarke, M. J., Paleologos, K., Martin, M. M., McNeight, H., Caggana, M., Bailey, S. M., Eiland, L. R., Ganesh, J., Kupchik, G., Lumba, R., Nafday, S., Stroustrup, A., Gelb, M. H. & Wasserstein, M. P., Mar 2024, In: Molecular Genetics and Metabolism Reports. 38, 101037.Research output: Contribution to journal › Article › peer-review
Open Access -
The motivation and process for developing a consortium-wide time and motion study to estimate resource implications of innovations in the use of genome sequencing to inform patient care
Hoban, H. G., Yip, T. A., Chau, J. C., Bensen, J. T., Desrosiers, L. R., Finnila, C. R., Hindorff, L. A., Kelly, N. R., Lynch, F. L., Rolf, B. A., Smith, H. S., Wasserstein, M. P. & Hassmiller Lich, K., Jan 2024, In: Clinical and Translational Science. 17, 1, e13635.Research output: Contribution to journal › Short survey › peer-review
Open Access -
Are we prepared to deliver gene-targeted therapies for rare diseases?
Yu, T. W., Kingsmore, S. F., Green, R. C., MacKenzie, T., Wasserstein, M., Caggana, M., Gold, N. B., Kennedy, A., Kishnani, P. S., Might, M., Brooks, P. J., Morris, J. A., Parisi, M. A. & Urv, T. K., Mar 2023, In: American Journal of Medical Genetics, Part C: Seminars in Medical Genetics. 193, 1, p. 7-12 6 p.Research output: Contribution to journal › Comment/debate › peer-review
Open Access4 Scopus citations -
Consensus clinical management guidelines for acid sphingomyelinase deficiency (Niemann–Pick disease types A, B and A/B)
Geberhiwot, T., Wasserstein, M., Wanninayake, S., Bolton, S. C., Dardis, A., Lehman, A., Lidove, O., Dawson, C., Giugliani, R., Imrie, J., Hopkin, J., Green, J., de Vicente Corbeira, D., Madathil, S., Mengel, E., Ezgü, F., Pettazzoni, M., Sjouke, B., Hollak, C., Vanier, M. T., & 2 others , Dec 2023, In: Orphanet Journal of Rare Diseases. 18, 1, 85.Research output: Contribution to journal › Article › peer-review
Open Access4 Scopus citations