Roy E Weiss

  • 8408 Citations
1976 …2021

Research output per year

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Projects

  • 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, 3

    Research output: Contribution to journalArticle

  • 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 journalArticle

  • 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 journalArticle

  • 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 journalArticle

  • 3 Scopus citations