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Publication of 2016:
101. Sheikh IA, Ahmad E, Jamal MS, Rehan M, Assidi M, Tayubi IA, AlBasri SF, Bajouh OS, Turki RF, Abuzenadah AM, Damanhouri GA, Beg MA, Al-Qahtani M. Spontaneous preterm birth and single nucleotide gene polymorphisms: a recent update. BMC Genomics. 2016 Oct 17;17(Suppl 9):759. Review.
102. Rasool M, Malik A, Jabbar U, Begum I, Qazi MH, Asif M, Naseer MI, Ansari SA, Jarullah J, Haque A, Jamal MS. Effect of iron overload on renal functions and oxidative stress in beta thalassemia patients. Saudi Med J. 2016 Nov;37(11):1239-1242. doi: 10.15537/smj.2016.11.16242.
103. Pannkuk EL, Laiakis EC, Mak TD, Astarita G, Authier S, Wong K, Fornace AJ Jr. A Lipidomic and Metabolomic Serum Signature from Nonhuman Primates Exposed to Ionizing Radiation. Metabolomics. 2016 May;12(5). pii: 80. doi: 10.1007/s11306-016-1010-0. Epub 2016 Mar 15. PubMed PMID: 28220056; PubMed Central PMCID: PMC5314995.
104. Novroski NM, King JL, Churchill JD, Seah LH, Budowle B. Characterization of genetic sequence variation of 58 STR loci in four major population groups. Forensic Sci Int Genet. 2016 Nov;25:214-226. doi: 10.1016/j.fsigen.2016.09.007. Epub 2016 Sep 28
105. Naseer MI, Sogaty S, Rasool M, Chaudhary AG, Abutalib YA, Walker S, Marshall CR, Merico D, Carter MT, Scherer SW, Al-Qahtani MH, Zarrei M. Microcephaly-capillary malformation syndrome: Brothers with a homozygous STAMBP mutation, uncovered by exome sequencing. Am J Med Genet A. 2016 Nov;170(11):3018-3022. doi: 10.1002/ajmg.a.37845.
106. Algahtani H, Naseer MI, Al-Qahtani M, Abdulrahman SA, Boker F, Shirah B. Congenital insensitivity to pain with anhidrosis: A report of two siblings with a novel mutation in (TrkA) NTRK1 gene in a Saudi family. J Neurol Sci. 2016 Nov 15;370:35-38. doi: 10.1016/j.jns.2016.09.016.
107. Mohamed AB, Hindawi SI, Al-Harthi S, Alam Q, Alam MZ, Haque A, Ahmad W, Damanhouri GA. Allelic variance among ABO blood group genotypes in a population from the western region of Saudi Arabia. Blood Res. 2016 Dec;51(4):274-278. doi: 10.5045/br.2016.51.4.274. Epub 2016 Dec 23.
108. Naseer MI, Rasool M, Jan MM, Chaudhary AG, Pushparaj PN, Abuzenadah AM, Al-Qahtani MH. A novel mutation in PGAP2 gene causes developmental delay, intellectual disability, epilepsy and microcephaly in consanguineous Saudi family. J Neurol Sci. 2016 Dec 15;371:121-125. doi: 10.1016/j.jns.2016.10.027.
109. Arooj M, Malik A, Basit A, Husain Qazi M, Asif M, Sarwar Jamal M, Mostafa Mahmoud M, Choudhry H, Natesan Pushparaj P, Rasool M. Implications of prognostic variables in the assessment of autoimmunity in hepatitis C patients receiving interferon therapy. Bioinformation. 2016 Jun 15;12(3):131-134. doi: 10.6026/97320630012131. eCollection 2016. PubMed PMID: 28149047; PubMed Central PMCID: PMC5267956.



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