This page shows the publications Pierre Zalloua has written about Phenotype.
J-Resolved 1H NMR 1D-Projections for Large-Scale Metabolic Phenotyping Studies: Application to Blood Plasma Analysis. Anal Chem. 2017 11 07; 89(21):11405-11412.
Characterizing redescriptions using persistent homology to isolate genetic pathways contributing to pathogenesis. BMC Syst Biol. 2016 Jan 11; 10 Suppl 1:10.
The I allele of the angiotensin converting enzyme I/D polymorphism confers protection against coronary artery disease. Coron Artery Dis. 2010 May; 21(3):151-6.
Molecular basis of oculocutaneous albinism type 1 in Lebanese patients. J Hum Genet. 2005; 50(6):317-319.
Beta-globin gene cluster haplotypes and HbF levels are not the only modulators of sickle cell disease in Lebanon. Eur J Haematol. 2003 Feb; 70(2):79-83.
The codons 8/9 (+G) mutation found for the first time in the Lebanese population. Hemoglobin. 2003 Feb; 27(1):1-5.
Association analyses based on false discovery rate implicate new loci for coronary artery disease. Nat Genet. 2017 Sep; 49(9):1385-1391.
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease. Nat Genet. 2015 Oct; 47(10):1121-1130.
Large scale association analysis identifies three susceptibility loci for coronary artery disease. PLoS One. 2011; 6(12):e29427.
Characterization of a large Lebanese family segregating IgA nephropathy. Nephrol Dial Transplant. 2007 Mar; 22(3):772-7.
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