• 2774 Citations
19962019

Research output per year

If you made any changes in Pure these will be visible here soon.

Fingerprint Dive into the research topics where Amjad Farooq is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Projects

  • 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 journalArticle

  • 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 journalArticle

    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 journalArticle

  • 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 journalComment/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 journalArticle

  • 17 Scopus citations