Projects per year
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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.
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Projects
- 1 Finished
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Structural and Functional Studies of the Novel DBD Domain of MKP5
8/1/08 → 5/31/14
Project: Research project
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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., Grace Zhai, R. & 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 › peer-review
3 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 › peer-review
Open Access2 Scopus citations -
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., Dec 1 2019, In: Clinical Genetics. 96, 6, p. 575-578 4 p.Research output: Contribution to journal › Article › peer-review
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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 2018, In: Brain. 141, 4, e32.Research output: Contribution to journal › Comment/debate › peer-review
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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. & Shy, M. E., Mar 1 2018, In: Brain. 141, 3, p. 662-672 11 p.Research output: Contribution to journal › Article › peer-review
22 Scopus citations