about
Whole-exome sequencing identifies KIZ as a ciliary gene associated with autosomal-recessive rod-cone dystrophyLrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB)A genome-wide association study identifies rs2000999 as a strong genetic determinant of circulating haptoglobin levelsTargeted next generation sequencing identifies novel mutations in RP1 as a relatively common cause of autosomal recessive rod-cone dystrophyNext-generation sequencing applied to a large French cone and cone-rod dystrophy cohort: mutation spectrum and new genotype-phenotype correlation.Pro- and anti-angiogenic VEGF mRNAs in autoimmune thyroid diseases.The rs3957357C>T SNP in GSTA1 Is Associated with a Higher Risk of Occurrence of Hepatocellular Carcinoma in European IndividualsGenome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans.A common variant highly associated with plasma VEGFA levels also contributes to the variation of both LDL-C and HDL-C.Cardiovascular diseases and genome-wide association studies.The familial dementia gene revisited: a missense mutation revealed by whole-exome sequencing identifies ITM2B as a candidate gene underlying a novel autosomal dominant retinal dystrophy in a large family.Cone dystrophy in patient with homozygous RP1L1 mutation.Further Insights into the Ciliary Gene and Protein KIZ and Its Murine Ortholog PLK1S1 Mutated in Rod-Cone Dystrophy.Relationship between catalase haplotype and arterial aging.A novel nonsense variant in REEP6 is involved in a sporadic rod-cone dystrophy case.Effect of SLCO1B1 gene polymorphisms and vitamin D on statin-induced myopathy.Newly identified synergy between clopidogrel and calcium-channel blockers for blood pressure regulation possibly involves CYP2C19 rs4244285.MERTK mutations update in inherited retinal diseases.ARL2BP mutations account for 0.1% of autosomal recessive rod-cone dystrophies with the report of a novel splice variant.Klotho KL-VS genotype is involved in blood pressure regulationDataset on significant role of Candesartan on cognitive functions in rats having memory impairment induced by electromagnetic wavesNovel Missense Mutations in Are Associated with Bestrophinopathies in Lebanese PatientsAssociation of TLR4 Polymorphisms, Expression, and Vitamin D with Helicobacter pylori InfectionNext generation sequencing and immuno-histochemistry profiling identify numerous biomarkers for personalized therapy of endometrioid endometrial carcinomaRICTOR gene amplification is correlated with metastasis and therapeutic resistance in triple-negative breast cancerPhenotype Analysis of Retinal Dystrophies in Light of the Underlying Genetic Defects: Application to Cone and Cone-Rod DystrophiesDetection of PIK3R1 (L449S) Mutation in a Patient with Ovarian Cancer: A Case ReportObesity status modifies the association between rs7556897T>C in the intergenic region SLC19A3-CCL20 and blood pressure in French childrenrs3851179G>A in PICALM is protective against Alzheimer's disease in five different countries surrounding the Mediterraneanrs2569190A>G in CD14 is Independently Associated with Hypercholesterolemia: A Brief ReportWhole exome sequencing resolves complex phenotype and identifies CC2D2A mutations underlying non-syndromic rod-cone dystrophyNext Generation Sequencing Identifies Five Novel Mutations in Lebanese Patients with Bardet-Biedl and Usher SyndromesNext-generation sequencing reveals mutations in RB1, CDK4 and TP53 that may promote chemo-resistance to palbociclib in ovarian cancerAssociation between SNPs of Circulating Vascular Endothelial Growth Factor Levels, Hypercholesterolemia and Metabolic SyndromePeripheral blood mononuclear cells extracts VEGF protein levels and VEGF mRNA: Associations with inflammatory molecules in a healthy populationrs622342A>C in SLC22A1 is associated with metformin pharmacokinetics and glycemic responseAPOE genotypes in Lebanon: distribution and association with hypercholesterolemia and Alzheimer's disease
P50
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P50
description
onderzoeker
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researcher ORCID ID = 0000-0002-8522-0445
@en
name
Said El Shamieh
@ast
Said El Shamieh
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Said El Shamieh
@es
Said El Shamieh
@nl
type
label
Said El Shamieh
@ast
Said El Shamieh
@en
Said El Shamieh
@es
Said El Shamieh
@nl
prefLabel
Said El Shamieh
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Said El Shamieh
@en
Said El Shamieh
@es
Said El Shamieh
@nl
P106
P1153
36682267500
P31
P496
0000-0002-8522-0445