Projects per year
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Dive into the research topics where Roy E Weiss is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Projects
- 5 Finished
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Center of Excellence in Precision Medicine and Population Health
5/19/16 → 3/31/21
Project: Research project
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HEMATOPOIESIS IN RETROVIRUS INFECTED SIMIANS
Weiss, R. E., Weiss, R. E., Weiss, R. E., Rosenberg, I., Weiss, N. M., Goldberg, L., Schuster, C., Rabinovich, C. E., Kremser, C., Buse, J., Solway, J., Josephson, M., Asplin, J., Herbst, A. L., Lashner, B., Mazzone, T., Kreiter, M., Dewit, H., Brown, F. D., Scoeller, D., Rajfer, S., Pononsky, K., Richman, D., Douglas, F. L., Baron, J. M., Thistlethwaite, J. R., Meltzer, H. Y., Johanson, C. E., Chelmickaschorr, E. V. A., Arcilla, R., Zacny, J., Roos, R. P., Polansky, K., Scany, A. M., Tartof, D., Davidson, N., Lichtor, J. L., Knowles, J. B., Jonas, R. B., January, C., Hall, J., Roizan, N., Voke, T., Cara, J., Cuttler, L., Senay, E., Beebe, C. A., Loy, G., Palonsky, K. S., Huttenlocher, P., Barron, W. M., Aycinena, P., Kaplan, E., Benca, R., Antel, J., Murphy, M. B., Degroot, L., Baker, A. L., Schueller, D., Cohen, L., Burstein, S., Robertson, G. L., Roizen, N., Fellner, S. K., Samuels, B., Sommerfeld, E., Lau, K., Kaplan, E., Landau, R., Kirschner, B., Saper, C., Hopkins, J., Reder, A. T., Jones, T., Fang, V. S., Berkelhammer, C., Rose, R. P., Apfelbaum, J., Jonghorbani, M., Schuette, S., Pliskin, N., Scanu, A., Sarne, D., Moll, G. W., Goldman, M., Crayton, J., Sitrin, M., Golomb, H., Richards, J., Jaspar, J., Little, A. G., Jaspan, J. B., Bergenstal, R., Rubenstein, A. H., Roizen, M., Lang, R., Cura, J., Rolzen, M., Lindheimer, M., Chait, L., Whitington, P., King, D., Yost, M., Hellman, S., Arnason, B., Mani, S., Sarpong, S., Johnson, D., Draganich, L. F., McClintock, M., Ndukwu, I., Getz, G. S., Keenan, K. E., Steele, G., Murray, P., Kindler, H., Conjeevaram, H., Olopade, O., McNally, B., Ratain, M., Kyle, J., King, A., Yuan, C., Vogelzang, N., Ehrenpreis, E., Cook, E., Weir, B., [No Value], F. L., Vokes, T., Madara, J., Reimann, K., Vokes, E., Woodle, E. S., Covert, R., Ehrman, D., Lauderdale, D., Gajewski, T., Ober, C., McBurnett, K., Clark, M., Brady, L., Rosenfield, R., Brady, L., Ober, C., Hanauer, S. B., McBurnett, K., Keenan, K. E., Murray, P., van Cauter, E. V. E., Kindler, H., Rabinovich, C. D., Conjeevaram, H., Lauderdale, D., Refetoff, S., Schilsky, R., Olopade, O., Bell, G., Ehrman, D., Polonsky, K., McNally, B., De, H., Barnes, R., Ehramann, D., Ratain, M., Cho, J., Clark, M., Gajewski, T., Kyle, J., King, A., Yuan, C., Vogelzang, N., Ehrenpreis, E., Cook, E., Favus, M., Ehrmann, D., David, F., Refetoff, S., Sokoloff, M., Phillipson, L., Hall, J. B., Radovick, S., Vogelzang, N., Kim, K., Dachman, A., Owley, T., Alverdy, J. C., Mc Closkey, M., Te, H., Rosenfield, R., Garfinkel, M., Cocca, E. F., McConville, J., Ober, C., White, S., van Cauter, E. V. E., McNally, E., Royce, L., Lipton, R. B., De, H., Cho, J., Penev, P., King, A., Yuan, C., Ehrmann, D., Brendler, C., Philipson, L. H., Lopez, J., Reutrakul, S., Faxon, D. P., Favus, M., Burnett, D., Utset, T., Ratain, M., Sperling, A. I., Stephenson, M., Lahn, B., Noth, I., Phan, K. L., Refetoff, S., Pannain, S., Nicolae, D. L., Gomberg-Maitland, M., Bell, G., [No Value], N. J., Burnet, D., Tasali, E., Olopade, F., Clark, M., Favus, M., Maitland, M. L., Le Grange, D., Kusher, R., Byrne, M., Clarke, B., Umans, J., Ober, C., Aikens, J., Herold, K., Schoeller, D. A., Gerber, G., Lichtor, J., Wagner-Weiner, L., Yurk, H., Scholler, D., Albert, D., Fleming, G., Bartosh, S., Kushner, R. F., Foss, J., Rosenfield, R. L., Hanauer, S., Favus, M. J., van Cauter, E. V. E., Rabinovich, C. D., Refetoff, S., Schilsky, R., Bell, G., Polonsky, K., De, H., Barnes, R. B., Ehramann, D., Cho, J. & Ehrmann, D.
12/1/78 → 2/28/11
Project: Research project
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Early diagnosis and treatment of an infant with a novel thyroid hormone receptor a gene (pC380SfsX9) mutation
Furman, A. E., Dumitrescu, A. M., Refetoff, S. & Weiss, R. E., Jun 2021, In: Thyroid. 31, 6, p. 922-932 11 p.Research output: Contribution to journal › Article › peer-review
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Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by MCT8 Gene Mutation
Refetoff, S., Pappa, T., Williams, M. K., Matheus, M. G., Liao, X. H., Hansen, K., Nicol, L., Pierce, M., Blasco, P. A., Jensen, M. W., Bernal, J., Weiss, R. E., Dumitrescu, A. M. & Lafranchi, S., May 2021, In: Thyroid. 31, 5, p. 713-720 8 p.Research output: Contribution to journal › Article › peer-review
2 Scopus citations -
Central Congenital Hypothyroidism Caused by a Novel Mutation, C47W, in the Cysteine Knot Region of TSHβ
Ebrhim, R. S., Bruellman, R. J., Watanabe, Y., Creech, M. K., Abdullah, M. A., Dumitrescu, A. M., Refetoff, S. & Weiss, R. E., Jun 2020, In: Hormone Research in Paediatrics. 92, 6, p. 390-394 5 p.Research output: Contribution to journal › Article › peer-review
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Clinical and Molecular Analysis in 2 Families With Novel Compound Heterozygous SBP2 (SECISBP2) Mutations
Fu, J., Korwutthikulrangsri, M., Gönç, E. N., Sillers, L., Liao, X. H., Alikaşifoǧlu, A., Kandemir, N., Menucci, M. B., Burman, K. D., Weiss, R. E. & Dumitrescu, A. M., Jan 8 2020, In: Journal of Clinical Endocrinology and Metabolism. 105, 3, dgz169.Research output: Contribution to journal › Article › peer-review
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Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism
Bruellman, R. J., Watanabe, Y., Ebrhim, R. S., Creech, M. K., Abdullah, M. A., Dumitrescu, A. M., Refetoff, S. & Weiss, R. E., May 1 2020, In: The Journal of clinical endocrinology and metabolism. 105, 5Research output: Contribution to journal › Article › peer-review
3 Scopus citations