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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2011 3
2014 3
2015 5
2017 2
2018 3
2019 2
2020 7
2021 8
2022 5
2023 5
2024 1

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41 results

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Page 1
Delineation of a Human Mendelian Disorder of the DNA Demethylation Machinery: TET3 Deficiency.
Beck DB, Petracovici A, He C, Moore HW, Louie RJ, Ansar M, Douzgou S, Sithambaram S, Cottrell T, Santos-Cortez RLP, Prijoles EJ, Bend R, Keren B, Mignot C, Nougues MC, Õunap K, Reimand T, Pajusalu S, Zahid M, Saqib MAN, Buratti J, Seaby EG, McWalter K, Telegrafi A, Baldridge D, Shinawi M, Leal SM, Schaefer GB, Stevenson RE, Banka S, Bonasio R, Fahrner JA. Beck DB, et al. Among authors: saqib man. Am J Hum Genet. 2020 Feb 6;106(2):234-245. doi: 10.1016/j.ajhg.2019.12.007. Epub 2020 Jan 9. Am J Hum Genet. 2020. PMID: 31928709 Free PMC article.
Health research funding and its output in Pakistan.
Saqib MAN, Rafique I. Saqib MAN, et al. East Mediterr Health J. 2021 Sep 21;27(9):906-910. doi: 10.26719/emhj.21.038. East Mediterr Health J. 2021. PMID: 34569046 Free article.
Neurological disorders and disability in Pakistan: A cross-sectional multicenter study.
Wasay M, Awan S, Shahbaz N, Khan S, Sher K, Malik A, Mustafa S, Siddiqi AI, Barech S, Farooq A, Hameed S, Siddiqui M, Ahmad A, Asif A, Sherin A, Majid H, Nauman A, Soomro B, Subhan M, Rafique I, Saqib MAN. Wasay M, et al. Among authors: saqib man. J Neurol Sci. 2023 Sep 15;452:120754. doi: 10.1016/j.jns.2023.120754. Epub 2023 Jul 30. J Neurol Sci. 2023. PMID: 37562167
Effect of COVID-19 lockdown on patients with chronic diseases.
Saqib MAN, Siddiqui S, Qasim M, Jamil MA, Rafique I, Awan UA, Ahmad H, Afzal MS. Saqib MAN, et al. Diabetes Metab Syndr. 2020 Nov-Dec;14(6):1621-1623. doi: 10.1016/j.dsx.2020.08.028. Epub 2020 Aug 27. Diabetes Metab Syndr. 2020. PMID: 32889403 Free PMC article.
COVID-19, economic impact and child mortality: A global concern.
Kabir M, Saqib MAN, Zaid M, Ahmed H, Afzal MS. Kabir M, et al. Among authors: saqib man. Clin Nutr. 2020 Jul;39(7):2322-2323. doi: 10.1016/j.clnu.2020.05.027. Epub 2020 May 30. Clin Nutr. 2020. PMID: 32499056 Free PMC article. No abstract available.
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: saqib ma. 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.
41 results