Projects per year
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Projects
Center of Excellence in Precision Medicine and Population Health
5/19/16 → 3/31/21
Project: Research project
Research Output
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., Alikaşifoğlu, A., Kandemir, N., Menucci, M. B., Burman, K. D., Weiss, R. E. & Dumitrescu, A. M., Mar 1 2020, In : The Journal of clinical endocrinology and metabolism. 105, 3Research output: Contribution to journal › Article
Congenital Hypothyroidism due to Oligogenic Mutations in Two Sudanese Families
Watanabe, Y., Bruellman, R. J., Ebrhim, R. S., Abdullah, M. A., Dumitrescu, A. M., Refetoff, S. & Weiss, R. E., Feb 1 2019, In : Thyroid. 29, 2, p. 302-304 3 p.Research output: Contribution to journal › Article
3
Scopus
citations
A Novel Missense Mutation in the SLC5A5 Gene in a Sudanese Family with Congenital Hypothyroidism
Watanabe, Y., Ebrhim, R. S., Abdullah, M. A. & Weiss, R. E., Aug 1 2018, In : Thyroid. 28, 8, p. 1068-1070 3 p.Research output: Contribution to journal › Article
3
Scopus
citations
A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: A case report
Watanabe, Y., Sharwood, E., Goodwin, B., Creech, M. K., Hassan, H. Y., Netea, M. G., Jaeger, M., Dumitrescu, A., Refetoff, S., Huynh, T. & Weiss, R. E., May 2 2018, In : BMC Medical Genetics. 19, 1, 69.Research output: Contribution to journal › Article
3
Scopus
citations