Mujtaba G - Search Results

1

Bi-allelic Pro291Leu variant in KCNQ4 leads to early onset non-syndromic hearing loss.

Ramzan M, Idrees H, Mujtaba G, Sobreira N, Witmer PD, Naz S. Ramzan M, et al. Among authors: mujtaba g. Gene. 2019 Jul 15;705:109-112. doi: 10.1016/j.gene.2019.04.064. Epub 2019 Apr 24. Gene. 2019. PMID: 31028865 Free PMC article.

2

A p.C343S missense mutation in PJVK causes progressive hearing loss.

Mujtaba G, Bukhari I, Fatima A, Naz S. Mujtaba G, et al. Gene. 2012 Aug 1;504(1):98-101. doi: 10.1016/j.gene.2012.05.013. Epub 2012 May 14. Gene. 2012. PMID: 22617256 Free PMC article.

3

Spectrum of genetic variants in moderate to severe sporadic hearing loss in Pakistan.

Ramzan M, Bashir R, Salman M, Mujtaba G, Sobreira N, Witmer PD; Baylor-Hopkins Center for Mendelian Genomics; Naz S. Ramzan M, et al. Among authors: mujtaba g. Sci Rep. 2020 Jul 17;10(1):11902. doi: 10.1038/s41598-020-68779-5. Sci Rep. 2020. PMID: 32681043 Free PMC article.

4

Contribution of GJB2 mutations to hearing loss in the Hazara Division of Pakistan.

Bukhari I, Mujtaba G, Naz S. Bukhari I, et al. Among authors: mujtaba g. Biochem Genet. 2013 Aug;51(7-8):524-9. doi: 10.1007/s10528-013-9583-z. Epub 2013 Mar 17. Biochem Genet. 2013. PMID: 23504403 Free PMC article.

5

Mutations of GJB2 encoding connexin 26 contribute to non-syndromic moderate and severe hearing loss in Pakistan.

Salman M, Bashir R, Imtiaz A, Maqsood A, Mujtaba G, Iqbal M, Naz S. Salman M, et al. Among authors: mujtaba g. Eur Arch Otorhinolaryngol. 2015 Aug;272(8):2071-5. doi: 10.1007/s00405-015-3523-y. Epub 2015 Jan 31. Eur Arch Otorhinolaryngol. 2015. PMID: 25636251 Free PMC article.

6

A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss.

Mujtaba G, Schultz JM, Imtiaz A, Morell RJ, Friedman TB, Naz S. Mujtaba G, et al. J Med Genet. 2015 Aug;52(8):548-52. doi: 10.1136/jmedgenet-2015-103023. Epub 2015 May 4. J Med Genet. 2015. PMID: 25941349 Free PMC article.

7

Genetic causes of moderate to severe hearing loss point to modifiers.

Naz S, Imtiaz A, Mujtaba G, Maqsood A, Bashir R, Bukhari I, Khan MR, Ramzan M, Fatima A, Rehman AU, Iqbal M, Chaudhry T, Lund M, Brewer CC, Morell RJ, Friedman TB. Naz S, et al. Among authors: mujtaba g. Clin Genet. 2017 Apr;91(4):589-598. doi: 10.1111/cge.12856. Epub 2016 Oct 6. Clin Genet. 2017. PMID: 27573290 Free PMC article.

8

Exome sequencing identifies a novel frameshift variant causing hypomagnesemia with secondary hypocalcemia.

Azim MK, Mehnaz A, Ahmed JZ, Mujtaba G. Azim MK, et al. Among authors: mujtaba g. CEN Case Rep. 2019 Feb;8(1):42-47. doi: 10.1007/s13730-018-0362-x. Epub 2018 Aug 24. CEN Case Rep. 2019. PMID: 30144020 Free PMC article.

9

Molecular detection and genetic characterization of human metapneumovirus strains circulating in Islamabad, Pakistan.

Arshad Y, Rana MS, Ikram A, Salman M, Aamir UB, Zaidi SSZ, Alam MM, Sharif S, Shaukat S, Khurshid A, Hakim R, Mujtaba G, Umair M, Sattar S, Bostan N. Arshad Y, et al. Among authors: mujtaba g. Sci Rep. 2022 Feb 18;12(1):2790. doi: 10.1038/s41598-022-06537-5. Sci Rep. 2022. PMID: 35181674 Free PMC article.

10

Molecular analysis of group A rotaviruses detected in hospitalized children from Rawalpindi, Pakistan during 2014.

Umair M, Abbasi BH, Nisar N, Alam MM, Sharif S, Shaukat S, Rana MS, Khurshid A, Mujtaba G, Aamir UB, Zaidi SSZ. Umair M, et al. Among authors: mujtaba g. Infect Genet Evol. 2017 Sep;53:160-166. doi: 10.1016/j.meegid.2017.05.009. Epub 2017 May 17. Infect Genet Evol. 2017. PMID: 28527973

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

63 results

Search Page

Filters