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Novel C8orf37 mutations cause retinitis pigmentosa in consanguineous families of Pakistani origin.
Ravesh Z, El Asrag ME, Weisschuh N, McKibbin M, Reuter P, Watson CM, Baumann B, Poulter JA, Sajid S, Panagiotou ES, O'Sullivan J, Abdelhamed Z, Bonin M, Soltanifar M, Black GC, Amin-ud Din M, Toomes C, Ansar M, Inglehearn CF, Wissinger B, Ali M. Ravesh Z, et al. Among authors: sajid s. Mol Vis. 2015 Mar 7;21:236-43. eCollection 2015. Mol Vis. 2015. PMID: 25802487 Free PMC article.
Genetic analysis of consanguineous families presenting with congenital ocular defects.
Ullah E, Nadeem Saqib MA, Sajid S, Shah N, Zubair M, Khan MA, Ahmed I, Ali G, Dutta AK, Danda S, Lao R, Ling-Fung Tang P, Kwok PY, Ansar M, Slavotinek A. Ullah E, et al. Among authors: sajid s. Exp Eye Res. 2016 May;146:163-171. doi: 10.1016/j.exer.2016.03.014. Epub 2016 Mar 16. Exp Eye Res. 2016. PMID: 26995144
Mutation of ATF6 causes autosomal recessive achromatopsia.
Ansar M, Santos-Cortez RL, Saqib MA, Zulfiqar F, Lee K, Ashraf NM, Ullah E, Wang X, Sajid S, Khan FS, Amin-ud-Din M; University of Washington Center for Mendelian Genomics; Smith JD, Shendure J, Bamshad MJ, Nickerson DA, Hameed A, Riazuddin S, Ahmed ZM, Ahmad W, Leal SM. Ansar M, et al. Among authors: sajid s. Hum Genet. 2015 Sep;134(9):941-50. doi: 10.1007/s00439-015-1571-4. Epub 2015 Jun 11. Hum Genet. 2015. PMID: 26063662 Free PMC article.
Revitalizing tetanus vaccine literacy post road accidents: a comprehensive examination of knowledge and awareness initiative among non-medical university students in Lahore, Pakistan.
Ayub F, Saleem W, Shahid MA, Hussain Khan MA, Suleiman AK, Akram L, Sajid S, Bukhsh A, Baig MR, Khan TM. Ayub F, et al. Among authors: sajid s. Front Immunol. 2024 Dec 18;15:1468356. doi: 10.3389/fimmu.2024.1468356. eCollection 2024. Front Immunol. 2024. PMID: 39744642 Free PMC article.
170 results