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Dive into the research topics where Caleb Rogers is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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  • Missense variant in RBM10 associated with mild and non-lethal form of TARP syndrome

    Potter, A. B., O'Brien, T. D., Kulkarni, A., McCabe, S., Matthews, K., Kovak, K., Rogers, C., Richards, C. S. & Moore, S., 2023, (Accepted/In press) In: Clinical Genetics.

    Research output: Contribution to journalLetterpeer-review

  • Six new cases of CRB2-related syndrome and a review of clinical findings in 28 reported patients

    Adutwum, M., Hurst, A., Mirzaa, G., Kushner, J. D., Rogers, C., Khalek, N., Cristancho, A. G., Burrill, N., Seifert, M. E., Scarano, M. I., Schnur, R. E. & Slavotinek, A., Jan 2023, In: Clinical Genetics. 103, 1, p. 97-102 6 p.

    Research output: Contribution to journalArticlepeer-review

    2 Scopus citations
  • Consolidation of the clinical and genetic definition of a SOX4- related neurodevelopmental syndrome

    Angelozzi, M., Karvande, A., Molin, A. N., Ritter, A. L., Leonard, J. M. M., Savatt, J. M., Douglass, K., Myers, S. M., Grippa, M., Tolchin, D., Zackai, E., Donoghue, S., Hurst, A. C. E., Descartes, M., Smith, K., Velasco, D., Schmanski, A., Crunk, A., Tokita, M. J., De Lange, I. M., & 28 othersVan Gassen, K., Robinson, H., Guegan, K., Suri, M., Patel, C., Bournez, M., Faivre, L., Tran-Mau-Them, F., Baker, J., Fabie, N., Weaver, K., Shillington, A., Hopkin, R. J., Barge-Schaapveld, D. Q. C. M., Ruivenkamp, C. A. L., Bökenkamp, R., Vergano, S., Seco Moro, M. N., Díaz De Bustamante, A., Misra, V. K., Kennelly, K., Rogers, C., Friedman, J., Wigby, K. M., Lenberg, J., Graziano, C., Ahrens-Nicklas, R. C. & Lefebvre, V., Mar 1 2022, In: Journal of medical genetics. 59, 11, p. 1058-1068 11 p.

    Research output: Contribution to journalArticlepeer-review

    3 Scopus citations
  • Consensus clinical management guideline for beta-propeller protein-associated neurodegeneration

    BPAN Guideline Contributing Author Group, Dec 2021, In: Developmental Medicine and Child Neurology. 63, 12, p. 1402-1409 8 p.

    Research output: Contribution to journalReview articlepeer-review

    Open Access
    11 Scopus citations
  • 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 othersBassetti, 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

    21 Scopus citations