Personal profile
Education/Academic qualification
Life Sciences, PhD
Award Date: 30 Oct 2006
Fingerprint
Dive into the research topics where Vijay Gupta is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
Projects
- 1 Active
-
QBRI-CORE-000017: Identify and validate genetic, environmental, and molecular risk factors underlying autism and syndromic neurodevelopmental disorders in the Qatari Population and the MENA Region.
Hottenga, J. J. (Lead Principal Investigator), Gupta, V. (Post Doctoral Fellow) & Ben Mahmoud, A. (Post Doctoral Fellow)
1/01/25 → 31/12/27
Project: Experimental Development/Translation Research
-
Recurrent and Novel Pathogenic Variants in Genes Involved with Hearing Loss in the Pakistani Population
Shadab, M., Ben-Mahmoud, A., Martínez Völter, L. N., Abbasi, A. A., Ku, B., Ejaz, A., Latif, Z., Gupta, V., Owrang, D., Jang, M. H., Zhang, Z., Mohammad, R., Houlden, H., Kim, H. G. & Vona, B., Jul 2025, In: Molecular Diagnosis and Therapy. 29, 4, p. 519-537 19 p.Research output: Contribution to journal › Article › peer-review
Open Access1 Link opens in a new tab Citation (Scopus) -
Autosomal recessive non-syndromic hearing loss genes in Pakistan during the previous three decades
Shadab, M., Abbasi, A. A., Ejaz, A., Ben-Mahmoud, A., Gupta, V., Kim, H. G. & Vona, B., Apr 2024, In: Journal of Cellular and Molecular Medicine. 28, 8, e18119.Research output: Contribution to journal › Review article › peer-review
Open Access4 Link opens in a new tab Citations (Scopus) -
Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism
Ghasemi, M. R., Sadeghi, H., Hashemi-Gorji, F., Mirfakhraie, R., Gupta, V., Ben-Mahmoud, A., Bagheri, S., Razjouyan, K., Salehpour, S., Tonekaboni, S. H., Dianatpour, M., Omrani, D., Jang, M. H., Layman, L. C., Miryounesi, M. & Kim, H. G., 5 Aug 2024, In: BMC Medical Genomics. 17, 1, 196.Research output: Contribution to journal › Article › peer-review
Open Access4 Link opens in a new tab Citations (Scopus) -
Genome Sequencing Identifies 13 Novel Candidate Risk Genes for Autism Spectrum Disorder in a Qatari Cohort
Ben-Mahmoud, A., Gupta, V., Abdelaleem, A., Thompson, R., Aden, A., Mbarek, H., Saad, C., Tolefat, M., Alshaban, F., Stanton, L. W. & Kim, H. G., 27 Oct 2024, In: International Journal of Molecular Sciences. 25, 21, 11551.Research output: Contribution to journal › Article › peer-review
Open Access4 Link opens in a new tab Citations (Scopus) -
Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3)
Susgun, S., Ben-Mahmoud, A., Rüschendorf, F., Ku, B., Hussain, S. I., Schulz, S., Puk, O., Biskup, S., Labonne, J. D. J., Don, D. W., Gupta, V., Choi, T. I., Khan, S., Wasif, N., Lacassie, Y., Layman, L. C., Iseri, S. A. U., Kim, C. H. & Kim, H. G., 5 Jan 2024, In: Human Mutation. 2024, 13 p., 5518289.Research output: Contribution to journal › Article › peer-review
Open Access