Research output per year
Research output per year
Personal profile
Primary fields of research
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Current research
Identification of novel cilia and centrosomal genes in consanguineous Pakistani families with primary microcephaly.
Search for cilia-associated lethality genes associated with early embryonic loss in consanguineous families from Pakistan.
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Dive into the research topics where Muhammad Farooq is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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A novel in-frame mutation in CLN3 leads to Juvenile neuronal ceroid lipofuscinosis in a large Pakistani family
Sher, M., Farooq, M., Abdullah, U., Ali, Z., Faryal, S., Zakaria, M., Ullah, F., Bukhari, H., Møller, R. S., Tommerup, N. & Baig, S. M., 2 Sept 2019, In: International Journal of Neuroscience. p. 890-895 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
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A novel mutation in CDK5RAP2 gene causes primary microcephaly with speech impairment and sparse eyebrows in a consanguineous Pakistani family
Abdullah, U., Farooq, M., Mang, Y., Marriam Bakhtiar, S., Fatima, A., Hansen, L., Kjaer, K. W., Larsen, L. A., Faryal, S., Tommerup, N. & Mahmood Baig, S., Dec 2017, In: European Journal of Medical Genetics. 60, 12, p. 627-630 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Genome-Wide Supported Risk Variants in MIR137, CACNA1C, CSMD1, DRD2, and GRM3 Contribute to Schizophrenia Susceptibility in Pakistani Population
Fatima, A., Farooq, M., Abdullah, U., Tariq, M., Mustafa, T., Iqbal, M., Tommerup, N. & Mahmood Baig, S., Sept 2017, In: Psychiatry Investigation. 14, 5, p. 687-692 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Homozygous mutation in the NPHP3 gene causing foetal nephronophthisis
Abdullah, U., Farooq, M., Fatima, A., Tauseef, W., Sarwar, Y., Nuri, M., Tommerup, N. & Baig, S. M., Oct 2017, In: Nephrology. 22, 10, p. 818-820 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Mutation of the planar cell polarity gene VANGL1 in adolescent idiopathic scoliosis
Andersen, M. R., Farooq, M., Rasmussen, K. K., Kjaer, K. W., Simony, A., Christensen, S. T. & Larsen, L. A., 15 Jun 2017, In: Spine. 42, 12, p. E702–E707 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
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A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family
Farooq, M., Fatima, A., Mang, Y., Hansen, L., Kjaer, K. W., Baig, S. M., Larsen, L. A. & Tommerup, N., 1 Mar 2016, In: Journal of Human Genetics. 61, 3, p. 271-273 3 p.Research output: Contribution to journal › Comment/debate › Research › peer-review
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Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies
Møller, R. S., Larsen, L. H. G., Johannesen, K. M., Talvik, I., Talvik, T., Vaher, U., Miranda, M. J., Farooq, M., Nielsen, J. E. K., Svendsen, L. L., Kjelgaard, D. B., Linnet, K. M., Hao, Q., Uldall, P., Frangu, M., Tommerup, N., Baig, S. M., Abdullah, U., Born, A. P., Gellert, P., & 12 others, 1 Sept 2016, In: Molecular Syndromology. 7, 4, p. 210-219 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Microduplications encompassing the Sonic Hedgehog Limb Enhancer ZRS are Associated with Haas Type Polysyndactyly and Laurin-Sandrow Syndrome
Lohan, S., Spielmann, M., Doelken, S. C., Flöttmann, R., Farooq, M., Baig, S. M., Wajid, M., Hülsemann, W., Habenicht, R., Kjaer, K. W., Patil, S. J., Girisha, K. M., Abarca-Barriga, H. H., Mundlos, S. & Klopocki, E., Oct 2014, In: Clinical Genetics. 86, 4, p. 318-325 8 p.Research output: Contribution to journal › Journal article › Research › peer-review