Omar A Abdul-Rahman, MD

  • Phone402-559-6328
  • Source: Scopus
  • Calculated based on no. of publications stored in Pure and citations from Scopus
20042021

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  • Effect of Whole-Genome Sequencing on the Clinical Management of Acutely Ill Infants with Suspected Genetic Disease: A Randomized Clinical Trial

    Krantz, I. D., Medne, L., Weatherly, J. M., Wild, K. T., Biswas, S., Devkota, B., Hartman, T., Brunelli, L., Fishler, K. P., Abdul-Rahman, O., Euteneuer, J. C., Hoover, D., Dimmock, D., Cleary, J., Farnaes, L., Knight, J., Schwarz, A. J., Vargas-Shiraishi, O. M., Wigby, K., Zadeh, N. & 23 others, Shinawi, M., Wambach, J. A., Baldridge, D., Cole, F. S., Wegner, D. J., Urraca, N., Holtrop, S., Mostafavi, R., Mroczkowski, H. J., Pivnick, E. K., Ward, J. C., Talati, A., Brown, C. W., Belmont, J. W., Ortega, J. L., Robinson, K. D., Brocklehurst, W. T., Perry, D. L., Ajay, S. S., Hagelstrom, R. T., Bennett, M., Rajan, V. & Taft, R. J., 2021, (Accepted/In press) In: JAMA Pediatrics.

    Research output: Contribution to journalArticlepeer-review

    Open Access
  • Estimating the community prevalence, child traits, and maternal risk factors of fetal alcohol spectrum disorders (FASD) from a random sample of school children

    May, P. A., Hasken, J. M., Hooper, S. R., Hedrick, D. M., Jackson-Newsom, J., Mullis, C. E., Dobyns, E., Kalberg, W. O., Buckley, D., Robinson, L. K., Abdul-Rahman, O., Adam, M. P., Manning, M. A., Jewett, T. & Hoyme, H. E., Oct 1 2021, In: Drug and Alcohol Dependence. 227, 108918.

    Research output: Contribution to journalArticlepeer-review

  • Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome

    Sheppard, S. E., Campbell, I. M., Harr, M. H., Gold, N., Li, D., Bjornsson, H. T., Cohen, J. S., Fahrner, J. A., Fatemi, A., Harris, J. R., Nowak, C., Stevens, C. A., Grand, K., Au, M., Graham, J. M., Sanchez-Lara, P. A., Campo, M. D., Jones, M. C., Abdul-Rahman, O., Alkuraya, F. S. & 83 others, Bassetti, J. A., Bergstrom, K., Bhoj, E., Dugan, S., Kaplan, J. D., Derar, N., Gripp, K. W., Hauser, N., Innes, A. M., Keena, B., Kodra, N., Miller, R., Nelson, B., Nowaczyk, M. J., Rahbeeni, Z., Ben-Shachar, S., Shieh, J. T., Slavotinek, A., Sobering, A. K., Abbott, M. A., Allain, D. C., Amlie-Wolf, L., Au, P. Y. B., Bedoukian, E., Beek, G., Barry, J., Berg, J., Bernstein, J. A., Cytrynbaum, C., Chung, B. H. Y., Donoghue, S., Dorrani, N., Eaton, A., Flores-Daboub, J. A., Dubbs, H., Felix, C. A., Fong, C. T., Fung, J. L. F., Gangaram, B., Goldstein, A., Greenberg, R., Ha, T. K., Hersh, J., Izumi, K., Kallish, S., Kravets, E., Kwok, P. Y., Jobling, R. K., Knight Johnson, A. E., Kushner, J., Lee, B. H., Levin, B., Lindstrom, K., Manickam, K., Mardach, R., McCormick, E., McLeod, D. R., Mentch, F. D., Minks, K., Muraresku, C., Nelson, S. F., Porazzi, P., Pichurin, P. N., Powell-Hamilton, N. N., Powis, Z., Ritter, A., Rogers, C., Rohena, L., Ronspies, C., Schroeder, A., Stark, Z., Starr, L., Stoler, J., Suwannarat, P., Velinov, M., Weksberg, R., Wilnai, Y., Zadeh, N., Zand, D. J., Falk, M. J., Hakonarson, H., Zackai, E. H. & Quintero-Rivera, F., Jun 2021, In: American Journal of Medical Genetics, Part A. 185, 6, p. 1649-1665 17 p.

    Research output: Contribution to journalArticlepeer-review

  • Fetal alcohol spectrum disorders: current state of diagnosis and treatment

    Gomez, D. A. & Abdul-Rahman, O. A., Dec 1 2021, In: Current Opinion in Pediatrics. 33, 6, p. 570-575 6 p.

    Research output: Contribution to journalArticlepeer-review

  • TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathy

    Whitman, M. C., Barry, B. J., Robson, C. D., Facio, F. M., Van Ryzin, C., Chan, W. M., Lehky, T. J., Thurm, A., Zalewski, C., King, K. A., Brewer, C., Almpani, K., Lee, J. S., Delaney, A., FitzGibbon, E. J., Lee, P. R., Toro, C., Paul, S. M., Abdul-Rahman, O. A., Webb, B. D. & 16 others, Jabs, E. W., Moller, H. U., Larsen, D. A., Antony, J. H., Troedson, C., Ma, A., Ragnhild, G., Wirgenes, K. V., Tham, E., Kvarnung, M., Maarup, T. J., MacKinnon, S., Hunter, D. G., Collins, F. S., Manoli, I. & Engle, E. C., Dec 2021, In: Human genetics. 140, 12, p. 1709-1731 23 p.

    Research output: Contribution to journalArticlepeer-review