Projects per year
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Dive into the research topics where Melissa P. Wasserstein is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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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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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 Access3 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 Access -
Detection of mosaic variants using genome sequencing in a large pediatric cohort
Odgis, J. A., Gallagher, K. M., Rehman, A. U., Marathe, P. N., Bonini, K. E., Sebastin, M., Di Biase, M., Brown, K., Kelly, N. R., Ramos, M. A., Thomas-Wilson, A., Guha, S., Okur, V., Ganapathi, M., Elkhoury, L., Edelmann, L., Zinberg, R. E., Abul-Husn, N. S., Diaz, G. A., Greally, J. M., & 6 others, Mar 2023, In: American Journal of Medical Genetics, Part A. 191, 3, p. 699-710 12 p.Research output: Contribution to journal › Article › peer-review
3 Scopus citations -
Olipudase alfa enzyme replacement therapy for acid sphingomyelinase deficiency (ASMD): sustained improvements in clinical outcomes after 6.5 years of treatment in adults
Lachmann, R. H., Diaz, G. A., Wasserstein, M. P., Armstrong, N. M., Yarramaneni, A., Kim, Y. & Kumar, M., Dec 2023, In: Orphanet Journal of Rare Diseases. 18, 1, 94.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations -
The TeleKidSeq pilot study: incorporating telehealth into clinical care of children from diverse backgrounds undergoing whole genome sequencing
Sebastin, M., Odgis, J. A., Suckiel, S. A., Bonini, K. E., Di Biase, M., Brown, K., Marathe, P., Kelly, N. R., Ramos, M. A., Rodriguez, J. E., Aguiñiga, K. L., Lopez, J., Maria, E., Rodriguez, M. A., Yelton, N. M., Cunningham-Rundles, C., Gallagher, K., McDonald, T. V., McGoldrick, P. E., Robinson, M., & 15 others, Dec 2023, In: Pilot and Feasibility Studies. 9, 1, 47.Research output: Contribution to journal › Article › peer-review
Open Access3 Scopus citations