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Amjad Farooq

Associate Professor

  • 2774 Citations
19962019

Research output per year

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Projects

Structural and Functional Studies of the Novel DBD Domain of MKP5

Farooq, A.

National Institutes of Health

8/1/08 → 5/31/14

Project: Research project

    • Research Output

    • 2774 Citations
    • 76 Article
    • 7 Letter
    • 5 Review article
    • 2 Comment/debate

    Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss

    Li, C., Bademci, G., Subasioglu, A., Diaz-Horta, O., Zhu, Y., Liu, J., Mitchell, T. G., Abad, C., Seyhan, S., Duman, D., Cengiz, F. B., Tokgoz-Yilmaz, S., Blanton, S. H., Farooq, A., Walz, K., Zhai, R. G. & Tekin, M., Jan 22 2019, In : Proceedings of the National Academy of Sciences of the United States of America. 116, 4, p. 1347-1352 6 p.

    Research output: Contribution to journal › Article

    • 2 Scopus citations

    Interplay between HGAL and Grb2 proteins regulates B-cell receptor signaling

    Jiang, X., Lu, X., Zhang, Y., Lacaria, L., Schuchardt, B. J., Mikles, D. C., Magistri, M., García-Ramírez, I., Sanchez-Garcia, I., Farooq, A., Verdun, R. E., Abdulreda, M. H., Moy, V. T. & Lossos, I. S., Aug 13 2019, In : Blood Advances. 3, 15, p. 2286-2297 12 p.

    Research output: Contribution to journal › Article

    Open Access

    • Novel variant p.E269K confirms causative role of PLS1 mutations in autosomal dominant hearing loss

    Diaz-Horta, O., Bademci, G., Tokgoz-Yilmaz, S., Guo, S., Zafeer, F., Sineni, C. J., Duman, D., Farooq, A. & Tekin, M., Jan 1 2019, (Accepted/In press) In : Clinical Genetics.

    Research output: Contribution to journal › Article

    • Erratum: SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency (Brain (2018) 141 (662-672) DOI: 10.1093/brain/awx369)

    Rebelo, A., Dimah, S., Pereira, C., Farooq, A., Huff, T., Abreu, L., Moraes, C., Mnatsakanova, D., Mathews, K., Yang, H., Schon, E., Zuchner, S. & Shy, M., Apr 1 2018, In : Brain. 141, 4, e32.

    Research output: Contribution to journal › Comment/debate

    • SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency

    Rebelo, A. P., Saade, D., Pereira, C. V., Farooq, A., Huff, T. C., Abreu, L., Moraes, C. T., Mnatsakanova, D., Mathews, K., Yang, H., Schon, E. A., Zuchner, S. L. & Shy, M. E., Mar 1 2018, In : Brain. 141, 3, p. 662-672 11 p.

    Research output: Contribution to journal › Article

    • 17 Scopus citations