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SARS-CoV-2 spike gene Sanger sequencing methodology to identify variants of concern.
Biotechniques. 2023 Feb;74(2):69-75. doi: 10.2144/btn-2021-0114. Epub 2023 Feb 16.
Biotechniques. 2023.
PMID: 36794696
Free PMC article.
Genetic Variability in the E6, E7, and L1 Genes of Human Papillomavirus Types 16 and 18 among Women in Saudi Arabia.
Alsanea M, Alsaleh A, Obeid D, Alhadeq F, Alahideb B, Alhamlan F.
Alsanea M, et al.
Viruses. 2022 Dec 30;15(1):109. doi: 10.3390/v15010109.
Viruses. 2022.
PMID: 36680149
Free PMC article.
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Variable phenotype of a null PPP1R13L allele in children with dilated cardiomyopathy.
Tulbah S, Alruwaili N, Alhashem A, Aljohany A, Alhadeq F, Brotons DCA, Alwadai A, Al-Hassnan ZN.
Tulbah S, et al.
Am J Med Genet A. 2024 Jan;194(1):59-63. doi: 10.1002/ajmg.a.63402. Epub 2023 Sep 12.
Am J Med Genet A. 2024.
PMID: 37698259
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Categorized Genetic Analysis in Childhood-Onset Cardiomyopathy.
Al-Hassnan ZN, Almesned A, Tulbah S, Alakhfash A, Alhadeq F, Alruwaili N, Alkorashy M, Alhashem A, Alrashdan A, Faqeih E, Alkhalifi SM, Al Humaidi Z, Sogaty S, Azhari N, Bakhaider AM, Al Asmari A, Awaji A, Albash B, Alhabdan M, Alghamdi MA, Alshuaibi W, Al-Hassnan RZ, Alshenqiti A, Alqahtani A, Shinwari Z, Rbabeh M, Takroni S, Alomrani A, Albert Brotons DC, AlQwaee AM, Almanea W, Alfadley FA, Alfayyadh M, Alwadai A.
Al-Hassnan ZN, et al.
Circ Genom Precis Med. 2020 Oct;13(5):504-514. doi: 10.1161/CIRCGEN.120.002969. Epub 2020 Sep 1.
Circ Genom Precis Med. 2020.
PMID: 32870709
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A novel homozygous SCN5A variant detected in sick sinus syndrome.
Alkorashy M, Al-Ghamdi B, Tulbah S, Al-Numair NS, Alhadeq F, A Takroni S, Al-Hassnan ZN.
Alkorashy M, et al.
Pacing Clin Electrophysiol. 2021 Feb;44(2):380-384. doi: 10.1111/pace.14077. Epub 2020 Oct 1.
Pacing Clin Electrophysiol. 2021.
PMID: 32965045
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The Effect of Poly(ADP-ribose) Polymerase-1 Gene 3'Untranslated Region Polymorphism in Colorectal Cancer Risk among Saudi Cohort.
Alhadheq AM, Purusottapatnam Shaik J, Alamri A, Aljebreen AM, Alharbi O, Almadi MA, Alhadeq F, Azzam NA, Semlali A, Alanazi M, Bazzi MD, Reddy Parine N.
Alhadheq AM, et al.
Dis Markers. 2016;2016:8289293. doi: 10.1155/2016/8289293. Epub 2016 Sep 25.
Dis Markers. 2016.
PMID: 27746584
Free PMC article.
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ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder.
Al-Hassnan ZN, Al-Dosary M, Alfadhel M, Faqeih EA, Alsagob M, Kenana R, Almass R, Al-Harazi OS, Al-Hindi H, Malibari OI, Almutari FB, Tulbah S, Alhadeq F, Al-Sheddi T, Alamro R, AlAsmari A, Almuntashri M, Alshaalan H, Al-Mohanna FA, Colak D, Kaya N.
Al-Hassnan ZN, et al.
J Med Genet. 2015 Mar;52(3):186-94. doi: 10.1136/jmedgenet-2014-102592. Epub 2014 Dec 24.
J Med Genet. 2015.
PMID: 25539947
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Clinical profile and mutation spectrum of long QT syndrome in Saudi Arabia: The impact of consanguinity.
Al-Hassnan ZN, Al-Fayyadh M, Al-Ghamdi B, Shafquat A, Mallawi Y, Al-Hadeq F, Tulbah S, Shinwari ZMA, Almesned A, Alakhfash A, Al Fadly F, Hersi AS, Alhayani A, Al-Hashem A, Arafah D, Dzimiri N, Meyer B, Rababh M, Al-Manea W.
Al-Hassnan ZN, et al.
Heart Rhythm. 2017 Aug;14(8):1191-1199. doi: 10.1016/j.hrthm.2017.04.028. Epub 2017 Apr 22.
Heart Rhythm. 2017.
PMID: 28438721
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