Caleb Rogers

Assistant Professor

  • Source: Scopus
  • Calculated based on no. of publications stored in Pure and citations from Scopus

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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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  • Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1

    Koczkowska, M., Callens, T., Chen, Y., Gomes, A., Hicks, A. D., Sharp, A., Johns, E., Uhas, K. A., Armstrong, L., Bosanko, K. A., Babovic-Vuksanovic, D., Baker, L., Basel, D. G., Bengala, M., Bennett, J. T., Chambers, C., Clarkson, L. K., Clementi, M., Cortés, F. M., Cunningham, M. & 88 others, D'Agostino, M. D., Delatycki, M. B., Digilio, M. C., Dosa, L., Esposito, S., Fox, S., Freckmann, M. L., Fauth, C., Giugliano, T., Giustini, S., Goetsch, A., Goldberg, Y., Greenwood, R. S., Griffis, C., Gripp, K. W., Gupta, P., Haan, E., Hachen, R. K., Haygarth, T. L., Hernández-Chico, C., Hodge, K., Hopkin, R. J., Hudgins, L., Janssens, S., Keller, K., Kelly-Mancuso, G., Kochhar, A., Korf, B. R., Lewis, A. M., Liebelt, J., Lichty, A., Listernick, R. H., Lyons, M. J., Maystadt, I., Martinez Ojeda, M., McDougall, C., McGregor, L. K., Melis, D., Mendelsohn, N., Nowaczyk, M. J. M., Ortenberg, J., Panzer, K., Pappas, J. G., Pierpont, M. E., Piluso, G., Pinna, V., Pivnick, E. K., Pond, D. A., Powell, C. M., Rogers, C., Ruhrman Shahar, N., Rutledge, S. L., Saletti, V., Sandaradura, S. A., Santoro, C., Schatz, U. A., Schreiber, A., Scott, D. A., Sellars, E. A., Sheffer, R., Siqveland, E., Slopis, J. M., Smith, R., Spalice, A., Stockton, D. W., Streff, H., Theos, A., Tomlinson, G. E., Tran, G., Trapane, P. L., Trevisson, E., Ullrich, N. J., Van den Ende, J., Schrier Vergano, S. A., Wallace, S. E., Wangler, M. F., Weaver, D. D., Yohay, K. H., Zackai, E., Zonana, J., Zurcher, V., Claes, K. B. M., Eoli, M., Martin, Y., Wimmer, K., De Luca, A., Legius, E. & Messiaen, L. M., Jan 1 2020, In: Human mutation. 41, 1, p. 299-315 17 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    15 Scopus citations
  • KMT2B-related disorders: Expansion of the phenotypic spectrum and long-term efficacy of deep brain stimulation

    Cif, L., Demailly, D., Lin, J. P., Barwick, K. E., Sa, M., Abela, L., Malhotra, S., Chong, W. K., Steel, D., Sanchis-Juan, A., Ngoh, A., Trump, N., Meyer, E., Vasques, X., Rankin, J., Allain, M. W., Applegate, C. D., Isfahani, S. A., Baleine, J., Balint, B. & 91 others, Bassetti, J. A., Baple, E. L., Bhatia, K. P., Blanchet, C., Burglen, L., Cambonie, G., Seng, E. C., Bastaraud, S. C., Cyprien, F., Coubes, C., d’Hardemare, V., Doja, A., Dorison, N., Doummar, D., Dy-Hollins, M. E., Farrelly, E., Fitzpatrick, D. R., Fearon, C., Fieg, E. L., Fogel, B. L., Forman, E. B., Fox, R. G., Gahl, W. A., Galosi, S., Gonzalez, V., Graves, T. D., Gregory, A., Hallett, M., Hasegawa, H., Hayflick, S. J., Hamosh, A., Hully, M., Jansen, S., Jeong, S. Y., Krier, J. B., Krystal, S., Kumar, K. R., Laurencin, C., Lee, H., Lesca, G., François, L. L., Lynch, T., Mahant, N., Martinez-Agosto, J. A., Milesi, C., Mills, K. A., Mondain, M., Morales-Briceno, H., Ostergaard, J. R., Pal, S., Pallais, J. C., Pavillard, F., Perrigault, P. F., Petersen, A. K., Polo, G., Poulen, G., Rinne, T., Roujeau, T., Rogers, C., Roubertie, A., Sahagian, M., Schaefer, E., Selim, L., Selway, R., Sharma, N., Signer, R., Soldatos, A. G., Stevenson, D. A., Stewart, F., Tchan, M., Verma, I. C., de Vries, B. B. A., Wilson, J. L., Wong, D. A., Zaitoun, R., Zhen, D., Znaczko, A., Dale, R. C., de Gusmão, C. M., Friedman, J., Fung, V. S. C., King, M. D., Mohammad, S. S., Rohena, L., Waugh, J. L., Toro, C., Raymond, F. L., Topf, M., Coubes, P., Gorman, K. M. & Kurian, M. A., 2020, In: Brain. 143, 11, p. 3242-3261 20 p.

    Research output: Contribution to journalArticlepeer-review

    2 Scopus citations
  • A new NBIA patient from Turkey with homozygous C19ORF12 mutation

    Kasapkara, Ç. S., Tümer, L., Gregory, A., Ezgü, F., İnci, A., Derinkuyu, B. E., Fox, R., Rogers, C. & Hayflick, S., Dec 1 2019, In: Acta Neurologica Belgica. 119, 4, p. 623-625 3 p.

    Research output: Contribution to journalLetterpeer-review

    2 Scopus citations
  • Looking deep into the eye-of-the-tiger in pantothenate kinase-associated neurodegeneration

    Lee, J. H., Gregory, A., Hogarth, P., Rogers, C. & Hayflick, S. J., Mar 1 2018, In: American Journal of Neuroradiology. 39, 3, p. 583-588 6 p.

    Research output: Contribution to journalArticlepeer-review

    6 Scopus citations
  • MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder

    University of Washington Center for Mendelian Genomics, Dec 1 2016, In: American Journal of Human Genetics. 99, 6, p. 1229-1244 16 p.

    Research output: Contribution to journalArticlepeer-review

    39 Scopus citations
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