Taibah K - Search Results

1

Genetic association analysis of 77,539 genomes reveals rare disease etiologies.

Greene D; Genomics England Research Consortium; Pirri D, Frudd K, Sackey E, Al-Owain M, Giese APJ, Ramzan K, Riaz S, Yamanaka I, Boeckx N, Thys C, Gelb BD, Brennan P, Hartill V, Harvengt J, Kosho T, Mansour S, Masuno M, Ohata T, Stewart H, Taibah K, Turner CLS, Imtiaz F, Riazuddin S, Morisaki T, Ostergaard P, Loeys BL, Morisaki H, Ahmed ZM, Birdsey GM, Freson K, Mumford A, Turro E. Greene D, et al. Among authors: taibah k. Nat Med. 2023 Mar;29(3):679-688. doi: 10.1038/s41591-023-02211-z. Epub 2023 Mar 16. Nat Med. 2023. PMID: 36928819 Free PMC article.

2

ILDR1: Novel mutation and a rare cause of congenital deafness in the Saudi Arabian population.

Ramzan K, Taibah K, Tahir AI, Al-Tassan N, Berhan A, Khater AM, Al-Hazzaa SA, Al-Owain M, Imtiaz F. Ramzan K, et al. Among authors: taibah k. Eur J Med Genet. 2014 May-Jun;57(6):253-8. doi: 10.1016/j.ejmg.2014.04.004. Epub 2014 Apr 21. Eur J Med Genet. 2014. PMID: 24768815

3

COL4A4-related nephropathy caused by a novel mutation in a large consanguineous Saudi family.

Ramzan K, Imtiaz F, Taibah K, Alnufiee S, Akhtar M, Al-Hazzaa SA, Al-Owain M. Ramzan K, et al. Among authors: taibah k. Int J Pediatr Otorhinolaryngol. 2014 Mar;78(3):427-32. doi: 10.1016/j.ijporl.2013.12.008. Epub 2013 Dec 18. Int J Pediatr Otorhinolaryngol. 2014. PMID: 24398087

4

A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population.

Imtiaz F, Taibah K, Ramzan K, Bin-Khamis G, Kennedy S, Al-Mubarak B, Trabzuni D, Allam R, Al-Mostafa A, Sogaty S, Al-Shaikh AH, Bamukhayyar SS, Meyer BF, Al-Owain M. Imtiaz F, et al. Among authors: taibah k. BMC Med Genet. 2011 Jul 4;12:91. doi: 10.1186/1471-2350-12-91. BMC Med Genet. 2011. PMID: 21726435 Free PMC article.

5

USH1G with unique retinal findings caused by a novel truncating mutation identified by genome-wide linkage analysis.

Imtiaz F, Taibah K, Bin-Khamis G, Kennedy S, Hemidan A, Al-Qahtani F, Tabbara K, Al Mubarak B, Ramzan K, Meyer BF, Al-Owain M. Imtiaz F, et al. Among authors: taibah k. Mol Vis. 2012;18:1885-94. Epub 2012 Jul 12. Mol Vis. 2012. PMID: 22876113 Free PMC article.

6

Homozygosity mapping identifies a novel GIPC3 mutation causing congenital nonsyndromic hearing loss in a Saudi family.

Ramzan K, Al-Owain M, Allam R, Berhan A, Abuharb G, Taibah K, Imtiaz F. Ramzan K, et al. Among authors: taibah k. Gene. 2013 May 25;521(1):195-9. doi: 10.1016/j.gene.2013.03.042. Epub 2013 Mar 16. Gene. 2013. PMID: 23510777

7

Rearrangements of chromosome arm 3q in poorly differentiated nasopharyngeal carcinoma.

Waghray M, Parhar RS, Taibah K, al-Sedairy S. Waghray M, et al. Among authors: taibah k. Genes Chromosomes Cancer. 1992 Jun;4(4):326-30. doi: 10.1002/gcc.2870040409. Genes Chromosomes Cancer. 1992. PMID: 1377940

8

Osteogenic sarcoma metastasizing to the larynx.

Saleem M, Taibah K, Gangopadhyay K. Saleem M, et al. Among authors: taibah k. J Otolaryngol. 2002 Jun;31(3):189-92. doi: 10.2310/7070.2002.11022. J Otolaryngol. 2002. PMID: 12121029 No abstract available.

9

Solitary fibrous tumor of the parapharyngeal space: a case report and review of the literature.

Gangopadhyay K, Taibah K, Manohar MB, Kfoury H. Gangopadhyay K, et al. Among authors: taibah k. Ear Nose Throat J. 1996 Oct;75(10):681-4. Ear Nose Throat J. 1996. PMID: 8942090 Review.

10

Obstructive endotracheal lesions of thyroid cancer.

Ahmed M, Saleem M, Al-Arifi A, Almahfouz A, Mahasin Z, Al-Sobhi S, Ingemansson S, Taibah K. Ahmed M, et al. Among authors: taibah k. J Laryngol Otol. 2002 Aug;116(8):613-21. doi: 10.1258/00222150260171614. J Laryngol Otol. 2002. PMID: 12389690 Review.

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