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Items: 1 to 20 of 83

1.

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.

Heart Rhythm. 2017 Apr 22. pii: S1547-5271(17)30494-0. doi: 10.1016/j.hrthm.2017.04.028. [Epub ahead of print]

PMID:
28438721
2.

Correction: A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics.

Mizzi C, Dalabira E, Kumuthini J, Dzimiri N, Balogh I, Başak N, Böhm R, Borg J, Borgiani P, Bozina N, Bruckmueller H, Burzynska B, Carracedo A, Cascorbi I, Deltas C, Dolzan V, Fenech A, Grech G, Kasiulevicius V, Kádaši Ľ, Kučinskas V, Khusnutdinova E, Loukas YL, Macek M Jr, Makukh H, Mathijssen R, Mitropoulos K, Mitropoulou C, Novelli G, Papantoni I, Pavlovic S, Saglio G, Sertić J, Stojiljkovic M, Stubbs AP, Squassina A, Torres M, Turnovec M, van Schaik RH, Voskarides K, Wakil SM, Werk A, Del Zompo M, Zukic B, Katsila T, Lee MT, Motsinger-Rief A, Mc Leod HL, van der Spek PJ, Patrinos GP.

PLoS One. 2017 Feb 16;12(2):e0172595. doi: 10.1371/journal.pone.0172595. eCollection 2017.

3.

Data on common variants associated with coronary artery disease/myocardial infarction in ethnic Arabs.

Wakil SM, Ram R, Muiya NP, Mehta M, Andres E, Mazhar N, Baz B, Hagos S, Alshahid M, Meyer BF, Morahan G, Dzimiri N.

Data Brief. 2016 Feb 9;7:172-176. eCollection 2016 Jun.

4.

Integrated Left Ventricular Global Transcriptome and Proteome Profiling in Human End-Stage Dilated Cardiomyopathy.

Colak D, Alaiya AA, Kaya N, Muiya NP, AlHarazi O, Shinwari Z, Andres E, Dzimiri N.

PLoS One. 2016 Oct 6;11(10):e0162669. doi: 10.1371/journal.pone.0162669. eCollection 2016.

5.

A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics.

Mizzi C, Dalabira E, Kumuthini J, Dzimiri N, Balogh I, Başak N, Böhm R, Borg J, Borgiani P, Bozina N, Bruckmueller H, Burzynska B, Carracedo A, Cascorbi I, Deltas C, Dolzan V, Fenech A, Grech G, Kasiulevicius V, Kádaši Ľ, Kučinskas V, Khusnutdinova E, Loukas YL, Macek M Jr, Makukh H, Mathijssen R, Mitropoulos K, Mitropoulou C, Novelli G, Papantoni I, Pavlovic S, Saglio G, Setric J, Stojiljkovic M, Stubbs AP, Squassina A, Torres M, Turnovec M, van Schaik RH, Voskarides K, Wakil SM, Werk A, Del Zompo M, Zukic B, Katsila T, Lee MT, Motsinger-Rief A, Mc Leod HL, van der Spek PJ, Patrinos GP.

PLoS One. 2016 Sep 16;11(9):e0162866. doi: 10.1371/journal.pone.0162866. eCollection 2016. Erratum in: PLoS One. 2017 Feb 16;12 (2):e0172595.

6.

A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia.

Ram R, Wakil SM, Muiya NP, Andres E, Mazhar N, Hagos S, Alshahid M, Meyer BF, Morahan G, Dzimiri N.

Clin Genet. 2017 Mar;91(3):371-378. doi: 10.1111/cge.12859. Epub 2017 Jan 30.

PMID:
27599772
7.

Integrated Genomic and Network-Based Analyses of Complex Diseases and Human Disease Network.

Al-Harazi O, Al Insaif S, Al-Ajlan MA, Kaya N, Dzimiri N, Colak D.

J Genet Genomics. 2016 Jun 20;43(6):349-67. doi: 10.1016/j.jgg.2015.11.002. Epub 2015 Dec 15. Review.

PMID:
27318646
8.

A common variant association study reveals novel susceptibility loci for low HDL-cholesterol levels in ethnic Arabs.

Wakil SM, Ram R, Muiya NP, Andres E, Mazhar N, Hagos S, Alshahid M, Meyer BF, Morahan G, Dzimiri N.

Clin Genet. 2016 Dec;90(6):518-525. doi: 10.1111/cge.12761. Epub 2016 Mar 8.

PMID:
26879886
9.

FBXO32, encoding a member of the SCF complex, is mutated in dilated cardiomyopathy.

Al-Yacoub N, Shaheen R, Awad SM, Kunhi M, Dzimiri N, Nguyen HC, Xiong Y, Al-Buraiki J, Al-Habeeb W, Alkuraya FS, Poizat C.

Genome Biol. 2016 Jan 11;17:2. doi: 10.1186/s13059-015-0861-4.

10.

A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs.

Wakil SM, Ram R, Muiya NP, Mehta M, Andres E, Mazhar N, Baz B, Hagos S, Alshahid M, Meyer BF, Morahan G, Dzimiri N.

Atherosclerosis. 2016 Feb;245:62-70. doi: 10.1016/j.atherosclerosis.2015.11.019. Epub 2015 Nov 22.

PMID:
26708285
11.

Possible involvement of the JAK/STAT signaling pathway in N-acetylcysteine-mediated antidepressant-like effects.

Al-Samhari MM, Al-Rasheed NM, Al-Rejaie S, Al-Rasheed NM, Hasan IH, Mahmoud AM, Dzimiri N.

Exp Biol Med (Maywood). 2016 Mar;241(5):509-18. doi: 10.1177/1535370215619707. Epub 2015 Dec 6.

12.

The potential role of the sodium iodide symporter gene polymorphism in the development of differentiated thyroid cancer.

Al-Rasheed MM, Alzahrani AS, Macadam A, Overall A, Gard P, Dzimiri N.

Gene. 2015 Nov 10;572(2):163-8. doi: 10.1016/j.gene.2015.07.009. Epub 2015 Jul 6.

PMID:
26160439
13.

The Affymetrix DMET Plus platform reveals unique distribution of ADME-related variants in ethnic Arabs.

Wakil SM, Nguyen C, Muiya NP, Andres E, Lykowska-Tarnowska A, Baz B, Tahir AI, Meyer BF, Morahan G, Dzimiri N.

Dis Markers. 2015;2015:542543. doi: 10.1155/2015/542543. Epub 2015 Feb 22.

14.

Genotyping of CYP2C19 polymorphisms and its clinical validation in the ethnic Arab population.

Tayeb HT, Bakheet DH, Zaza K, Wakil SM, Dzimiri N.

J Pharm Pharmacol. 2015 Jul;67(7):972-9. doi: 10.1111/jphp.12391. Epub 2015 Feb 14. Retraction in: J Pharm Pharmacol. 2016 Mar;68(3):421.

PMID:
25684066
15.

A new susceptibility locus for myocardial infarction, hypertension, type 2 diabetes mellitus, and dyslipidemia on chromosome 12q24.

Wakil SM, Muiya NP, Tahir AI, Al-Najai M, Baz B, Andres E, Mazhar N, Al Tassan N, Alshahid M, Meyer BF, Dzimiri N.

Dis Markers. 2014;2014:291419. doi: 10.1155/2014/291419. Epub 2014 Jun 26.

16.

A study of the role of GATA2 gene polymorphism in coronary artery disease risk traits.

Muiya NP, Wakil S, Al-Najai M, Tahir AI, Baz B, Andres E, Al-Boudari O, Al-Tassan N, Al-Shahid M, Meyer BF, Dzimiri N.

Gene. 2014 Jul 10;544(2):152-8. doi: 10.1016/j.gene.2014.04.064. Epub 2014 Apr 28.

PMID:
24786211
17.

The 3'-UTR of the adiponectin Q gene harbours susceptibility loci for atherosclerosis and its metabolic risk traits.

Muiya N, Al-Najai M, Tahir AI, Elhawari S, Gueco D, Andres E, Mazhar N, Altassan N, Meyer BF, Alshahid M, Dzimiri N.

BMC Med Genet. 2013 Dec 13;14:127. doi: 10.1186/1471-2350-14-127.

18.

A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders.

Muiya NP, Wakil SM, Tahir AI, Hagos S, Najai M, Gueco D, Al-Tassan N, Andres E, Mazher N, Meyer BF, Dzimiri N.

Hum Genomics. 2013 Dec 12;7:25. doi: 10.1186/1479-7364-7-25.

19.

New susceptibility locus for obesity and dyslipidaemia on chromosome 3q22.3.

Alshahid M, Wakil SM, Al-Najai M, Muiya NP, Elhawari S, Gueco D, Andres E, Hagos S, Mazhar N, Meyer BF, Dzimiri N.

Hum Genomics. 2013 Jun 5;7:15. doi: 10.1186/1479-7364-7-15.

20.

Association of the angiotensinogen gene polymorphism with atherosclerosis and its risk traits in the Saudi population.

Al-Najai M, Muiya P, Tahir AI, Elhawari S, Gueco D, Andres E, Mazhar N, Altassan N, Alshahid M, Dzimiri N.

BMC Cardiovasc Disord. 2013 Mar 11;13:17. doi: 10.1186/1471-2261-13-17.

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