Saleha S - Search Results

1

Novel mutations in ALDH1A3 associated with autosomal recessive anophthalmia/microphthalmia, and review of the literature.

Lin S, Harlalka GV, Hameed A, Reham HM, Yasin M, Muhammad N, Khan S, Baple EL, Crosby AH, Saleha S. Lin S, et al. Among authors: saleha s. BMC Med Genet. 2018 Sep 10;19(1):160. doi: 10.1186/s12881-018-0678-6. BMC Med Genet. 2018. PMID: 30200890 Free PMC article.

2

MC1R gene mutation and its association with oculocutaneous albinism type (OCA) phenotype in a consanguineous Pakistani family.

Saleha SB, Ajaml M, Jamil M, Nasir M, Hameed A. Saleha SB, et al. J Dermatol Sci. 2013 Apr;70(1):68-70. doi: 10.1016/j.jdermsci.2012.11.591. Epub 2012 Dec 7. J Dermatol Sci. 2013. PMID: 23312576 No abstract available.

3

In silico analysis of a disease-causing mutation in PCDH15 gene in a consanguineous Pakistani family with Usher phenotype.

Saleha S, Ajmal M, Jamil M, Nasir M, Hameed A. Saleha S, et al. Int J Ophthalmol. 2016 May 18;9(5):662-8. doi: 10.18240/ijo.2016.05.04. eCollection 2016. Int J Ophthalmol. 2016. PMID: 27275418 Free PMC article.

4

Gene mapping in an anophthalmic pedigree of a consanguineous Pakistani family opened new horizons for research.

Saleha S, Ajmal M, Zafar S, Hameed A. Saleha S, et al. Balkan J Med Genet. 2016 Aug 2;19(1):77-84. doi: 10.1515/bjmg-2016-0010. eCollection 2016 Jul 1. Balkan J Med Genet. 2016. PMID: 27785411 Free PMC article.

5

Baseline characteristics of infected foot ulcers in patients with diabetes at a tertiary care hospital in Pakistan.

Yasin M, Zafar S, Rahman H, Khan TA, Nazir S, Shah S, Dawood M, Ahmad S, Basit A, Khan SN, Saleha S. Yasin M, et al. Among authors: saleha s. J Wound Care. 2018 Oct 1;27(Sup10):S26-S32. doi: 10.12968/jowc.2018.27.Sup10.S26. J Wound Care. 2018. PMID: 30307815

6

USH2A gene variants cause Keratoconus and Usher syndrome phenotypes in Pakistani families.

Ahmed AN, Tahir R, Khan N, Ahmad M, Dawood M, Basit A, Yasin M, Nowshid M, Marwan M, Sultan K, Saleha S. Ahmed AN, et al. Among authors: saleha s. BMC Ophthalmol. 2021 Apr 29;21(1):191. doi: 10.1186/s12886-021-01957-9. BMC Ophthalmol. 2021. PMID: 33926394 Free PMC article.

7

Novel mutations in PDE6A and CDHR1 cause retinitis pigmentosa in Pakistani families.

Dawood M, Lin S, Din TU, Shah IU, Khan N, Jan A, Marwan M, Sultan K, Nowshid M, Tahir R, Ahmed AN, Yasin M, Baple EL, Crosby AH, Saleha S. Dawood M, et al. Among authors: saleha s. Int J Ophthalmol. 2021 Dec 18;14(12):1843-1851. doi: 10.18240/ijo.2021.12.06. eCollection 2021. Int J Ophthalmol. 2021. PMID: 34926197 Free PMC article.

8

Fragile X premutation carrier screening in Pakistani preconception women in primary care consultation.

Meraj N, Yasin M, Rehman ZU, Tahir H, Jadoon H, Khan N, Shahid R, Zubair M, Zulfiqar I, Jabeen M, Neelam S, Hameed A, Saleha S. Meraj N, et al. Among authors: saleha s. BMC Womens Health. 2022 Mar 4;22(1):57. doi: 10.1186/s12905-022-01632-1. BMC Womens Health. 2022. PMID: 35246105 Free PMC article.

9

Maternal FMR1 alleles expansion in newborns during transmission: a prospective cohort study.

Shahid R, Yasin M, Rehman ZU, Jadoon H, Tahir H, Meraj N, Khan N, Zubair M, Zulfiqar I, Nowshid M, Azeem A, Jabeen M, Hameed A, Saleha S. Shahid R, et al. Among authors: saleha s. Pediatr Res. 2023 Feb;93(3):720-724. doi: 10.1038/s41390-022-02128-2. Epub 2022 Jun 9. Pediatr Res. 2023. PMID: 35681093

10

Unravelling the genetic basis of retinal dystrophies in Pakistani consanguineous families.

Marwan M, Dawood M, Ullah M, Shah IU, Khan N, Hassan MT, Karam M, Rawlins LE, Baple EL, Crosby AH, Saleha S. Marwan M, et al. Among authors: saleha s. BMC Ophthalmol. 2023 May 10;23(1):205. doi: 10.1186/s12886-023-02948-8. BMC Ophthalmol. 2023. PMID: 37165311 Free PMC article.

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