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20082021

Research activity per year

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ADJUNCT INSTRUCTOR | Psychiatry

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Dive into the research topics where Abidemi Adegbola is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
  • 1 Similar Profiles
  • PTPN4 germline variants result in aberrant neurodevelopment and growth

    Chmielewska, J. J., Burkardt, D., Granadillo, J. L., Slaugh, R., Morgan, S., Rotenberg, J., Keren, B., Mignot, C., Escobar, L., Turnpenny, P., Zuteck, M., Seaver, L. H., Ploski, R., Dziembowska, M., Wynshaw-Boris, A. & Adegbola, A., 8 Jul 2021, In: Human Genetics and Genomics Advances. 2, 3, 100033.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    6 Scopus citations
  • Disruption of CTNND2, encoding delta-catenin, causes a penetrant attention deficit disorder and myopia

    Adegbola, A., Lutz, R., Nikkola, E., Strom, S. P., Picker, J. & Wynshaw-Boris, A., 22 Oct 2020, In: Human Genetics and Genomics Advances. 1, 1, 100007.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    13 Scopus citations
  • Concise Review: Induced Pluripotent Stem Cell Models for Neuropsychiatric Diseases

    Adegbola, A., Bury, L. A., Fu, C., Zhang, M. & Wynshaw-Boris, A., Dec 2017, In: Stem cells translational medicine. 6, 12, p. 2062-2070 9 p.

    Research output: Contribution to journalReview articlepeer-review

    Open Access
    19 Scopus citations
  • Monoallelic expression of the human FOXP2 speech gene

    Adegbola, A. A., Cox, G. F., Bradshaw, E. M., Hafler, D. A., Gimelbrant, A. & Chess, A., 2 Jun 2015, In: Proceedings of the National Academy of Sciences of the United States of America. 112, 22, p. 6848-6854 7 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    33 Scopus citations
  • Redefining the MED13L syndrome

    Adegbola, A., Musante, L., Callewaert, B., Maciel, P., Hu, H., Isidor, B., Picker-Minh, S., Le Caignec, C., Chiaie, B. D., Vanakker, O., Menten, B., Dheedene, A., Bockaert, N., Roelens, F., Decaestecker, K., Silva, J., Soares, G., Lopes, F., Najmabadi, H. & Kahrizi, K. & 12 others, Cox, G. F., Angus, S. P., Staropoli, J. F., Fischer, U., Suckow, V., Bartsch, O., Chess, A., Ropers, H. H., Wienker, T. F., Hübner, C., Kaindl, A. M. & Kalscheuer, V. M., 22 Oct 2015, In: European Journal of Human Genetics. 23, 10, p. 1308-1317 10 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    74 Scopus citations