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William B Dobyns

1979 …2021

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Expertise related to UN Sustainable Devlopment Goals

In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):

  • SDG 3 - Good Health and Well-being

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  • A dyadic approach to the delineation of diagnostic entities in clinical genomics

    Biesecker, L. G., Adam, M. P., Alkuraya, F. S., Amemiya, A. R., Bamshad, M. J., Beck, A. E., Bennett, J. T., Bird, L. M., Carey, J. C., Chung, B., Clark, R. D., Cox, T. C., Curry, C., Dinulos, M. B. P., Dobyns, W. B., Giampietro, P. F., Girisha, K. M., Glass, I. A., Graham, J. M., Gripp, K. W. & 27 others, Haldeman-Englert, C. R., Hall, B. D., Innes, A. M., Kalish, J. M., Keppler-Noreuil, K. M., Kosaki, K., Kozel, B. A., Mirzaa, G. M., Mulvihill, J. J., Nowaczyk, M. J. M., Pagon, R. A., Retterer, K., Rope, A. F., Sanchez-Lara, P. A., Seaver, L. H., Shieh, J. T., Slavotinek, A. M., Sobering, A. K., Stevens, C. A., Stevenson, D. A., Tan, T. Y., Tan, W. H., Tsai, A. C., Weaver, D. D., Williams, M. S., Zackai, E. & Zarate, Y. A., Jan 7 2021, In: American Journal of Human Genetics. 108, 1, p. 8-15 8 p.

    Research output: Contribution to journalReview articlepeer-review

  • Cell-free DNA as a diagnostic analyte for molecular diagnosis of vascular malformations

    Zenner, K., Jensen, D. M., Cook, T. T., Dmyterko, V., Bly, R. A., Ganti, S., Mirzaa, G. M., Dobyns, W. B., Perkins, J. A. & Bennett, J. T., Jan 2021, In: Genetics in Medicine. 23, 1, p. 123-130 8 p.

    Research output: Contribution to journalArticlepeer-review

  • Cobblestone malformation in LAMA2 congenital muscular dystrophy (MDC1A)

    Jayakody, H., Zarei, S., Nguyen, H., Dalton, J., Chen, K., Hudgins, L., Day, J., Withrow, K., Pandya, A., Teasley, J., Dobyns, W. B., Mathews, K. D. & Moore, S. A., 2021, In: Journal of neuropathology and experimental neurology. 79, 9, p. 998-1010 13 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
  • Defining the phenotypical spectrum associated with variants in TUBB2A

    Brock, S., Vanderhasselt, T., Vermaning, S., Keymolen, K., Régal, L., Romaniello, R., Wieczorek, D., Storm, T. M., Schaeferhoff, K., Hehr, U., Kuechler, A., Krägeloh-Mann, I., Haack, T. B., Kasteleijn, E., Schot, R., Mancini, G. M. S., Webster, R., Mohammad, S., Leventer, R. J., Mirzaa, G. & 5 others, Dobyns, W. B., Bahi-Buisson, N., Meuwissen, M., Jansen, A. C. & Stouffs, K., Jan 1 2021, In: Journal of medical genetics. 58, 1, p. 33-40 8 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
  • Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior

    Harris, H. K., Nakayama, T., Lai, J., Zhao, B., Argyrou, N., Gubbels, C. S., Soucy, A., Genetti, C. A., Suslovitch, V., Rodan, L. H., Tiller, G. E., Lesca, G., Gripp, K. W., Asadollahi, R., Hamosh, A., Applegate, C. D., Turnpenny, P. D., Simon, M. E. H., Volker-Touw, C. M. L., Gassen, K. L. I. V. & 61 others, Binsbergen, E. V., Pfundt, R., Gardeitchik, T., Vries, B. B. A. D., Immken, L. D. L., Buchanan, C., Willing, M., Toler, T. L., Fassi, E., Baker, L., Vansenne, F., Wang, X., Ambrus, J. L., Fannemel, M., Posey, J. E., Agolini, E., Novelli, A., Rauch, A., Boonsawat, P., Fagerberg, C. R., Larsen, M. J., Kibaek, M., Labalme, A., Poisson, A., Payne, K. K., Walsh, L. E., Aldinger, K. A., Balciuniene, J., Skraban, C., Gray, C., Murrell, J., Bupp, C. P., Pascolini, G., Grammatico, P., Broly, M., Küry, S., Nizon, M., Rasool, I. G., Zahoor, M. Y., Kraus, C., Reis, A., Iqbal, M., Uguen, K., Audebert-Bellanger, S., Ferec, C., Redon, S., Baker, J., Wu, Y., Zampino, G., Syrbe, S., Brosse, I., Jamra, R. A., Dobyns, W. B., Cohen, L. L., Blomhoff, A., Mignot, C., Keren, B., Courtin, T., Agrawal, P. B., Beggs, A. H. & Yu, T. W., 2021, (Accepted/In press) In: Genetics in Medicine.

    Research output: Contribution to journalArticlepeer-review

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