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
- 10 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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Center of Excellence in Precision Medicine and Population Health
Cox, N., Miller-hughes, S., Weiss, R. E., Wilkins, C. H., Lima, M., Carrasquillo, O., Kripalani, S., Haas, D., Denny, J. & Griffith, D.
National Institute on Minority Health and Health Disparities
5/19/16 → 3/31/21
Project: Research project
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Pediatric Endocrinology Research Training Grant
National Institute of Diabetes and Digestive and Kidney Diseases
7/1/04 → 6/30/19
Project: Research project
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Nuclear cofactors in Human Thyroid Disease
National Center for Research Resources
7/15/03 → 5/31/07
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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Measurement of reverse triiodothyronine level and the triiodothyronine to reverse triiodothyronine ratio in dried blood spot samples at birth may facilitate early detection of monocarboxylate transporter 8 deficiency
Iwayama, H., Kakita, H., Iwasa, M., Adachi, S., Takano, K., Kikuchi, M., Fujisawa, Y., Osaka, H., Yamada, Y., Okumura, A., Hirani, K., Weiss, R. E. & Refetoff, S., Sep 1 2021, In: Thyroid. 31, 9, p. 1316-1321 6 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Novel DIO1 Gene Mutation Acting as Phenotype Modifier for Novel Compound Heterozygous TPO Gene Mutations Causing Congenital Hypothyroidism
Furman, A., Hannoush, Z., Echegoyen, F. B., Dumitrescu, A., Refetoff, S. & Weiss, R. E., Oct 1 2021, In: Thyroid. 31, 10, p. 1589-1591 3 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
6 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