Lista de obras - Pierre A Zalloua - Dominio Público Uruguay

A European Mitochondrial Haplotype Identified in Ancient Phoenician Remains from Carthage, North Africa

artículo científico publicado en 2016

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

artículo científico publicado en 2015

A novel ALMS1 splice mutation in a non-obese juvenile-onset insulin-dependent syndromic diabetic patient.

artículo científico publicado en 2013

ALOX5AP gene variants show differential association with coronary artery disease in different populations.

artículo científico publicado en 2010

Accurate and rapid prenatal diagnosis of the most frequent East Mediterranean beta-thalassemia mutations.

artículo científico publicado en 2004

Anhidrotic ectodermal dysplasia. Report of a rare mutation in EDA1

artículo científico publicado en 2008

Arsenic/interferon specifically reverses 2 distinct gene networks critical for the survival of HTLV-1-infected leukemic cells

artículo científico publicado en 2003

Association of hypertension with coronary artery disease onset in the Lebanese population

artículo científico publicado en 2014

Association of waterpipe smoking with myocardial infarction and determinants of metabolic syndrome among catheterized patients.

artículo científico publicado en 2017

Autosomal genetics and Y-chromosome haplogroup L1b-M317 reveal Mount Lebanon Maronites as a persistently non-emigrating population

artículo científico publicado en 2020

Beta-globin gene cluster haplotypes and HbF levels are not the only modulators of sickle cell disease in Lebanon.

artículo científico publicado en 2003

Boston type I keratoprosthesis for treatment of gelatinous drop-like corneal dystrophy after repeated graft failure

artículo científico publicado en 2013

Caffeine Impact on Metabolic Syndrome Components Is Modulated by a CYP1A2 Variant

artículo científico publicado en 2015

Characterization of a large Lebanese family segregating IgA nephropathy

artículo científico publicado en 2006

Characterizing redescriptions using persistent homology to isolate genetic pathways contributing to pathogenesis.

artículo científico publicado en 2016

Circulating lipid levels and risk of coronary artery disease in a large group of patients undergoing coronary angiography

artículo científico publicado en 2015

Deep phylogenetic analysis of haplogroup G1 provides estimates of SNP and STR mutation rates on the human Y-chromosome and reveals migrations of Iranic speakers

artículo científico publicado en 2015

Development and evaluation of real-time polymerase chain reaction assays on whole blood and paraffin-embedded tissues for rapid diagnosis of human brucellosis

artículo científico publicado en 2007

Effective treatment of hypereosinophilic syndrome with imatinib mesylate

artículo científico publicado en 2003

Fertility drugs and the risk of breast cancer: a meta-analysis and review.

artículo científico publicado en 2010

Genetic evidence for an origin of the Armenians from Bronze Age mixing of multiple populations

artículo científico publicado en 2015

Genetic heterogeneity of Beta thalassemia in Lebanon reflects historic and recent population migration.

artículo científico publicado en 2005

Genetically determined height and coronary artery disease

artículo científico publicado en 2015

Genetics of the peloponnesean populations and the theory of extinction of the medieval peloponnesean Greeks

artículo científico publicado en 2017

Genome-wide and paternal diversity reveal a recent origin of human populations in North Africa

artículo científico publicado en 2013

Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis

artículo científico publicado en 2012

Genome-wide diversity in the levant reveals recent structuring by culture

artículo científico publicado en 2013

Genomic ancestry of North Africans supports back-to-Africa migrations

artículo científico publicado en 2012

Geographic population structure analysis of worldwide human populations infers their biogeographical origins

artículo científico publicado en 2014

Geographical structure of the Y-chromosomal genetic landscape of the Levant: a coastal-inland contrast

artículo científico publicado en 2009

Gestational diabetes mellitus and macrosomia predispose to diabetes in the Lebanese population

artículo científico publicado en 2019

Identifying genetic traces of historical expansions: Phoenician footprints in the Mediterranean

artículo científico publicado en 2008

Impact of inflammation, gene variants, and cigarette smoking on coronary artery disease risk

article

Influences of history, geography, and religion on genetic structure: the Maronites in Lebanon

artículo científico publicado en 2011

Large scale association analysis identifies three susceptibility loci for coronary artery disease

artículo científico publicado en 2011

Large-scale association analysis identifies new risk loci for coronary artery disease

artículo científico publicado en 2012

Lies, Gosh Darn Lies, and Not Enough Good Statistics: Why Epidemic Model Parameter Estimation Fails

artículo científico publicado en 2020

Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions

artículo científico publicado en 2017

Molecular basis of oculocutaneous albinism type 1 in Lebanese patients

artículo científico publicado en 2005

Multivariate epidemiologic analysis of type 2 diabetes mellitus risks in the Lebanese population

artículo científico publicado en 2014

Nicotine metabolism in healthy smokers and patients with cardiovascular diseases.

artículo científico publicado en 2005

No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis ⬇️

scientific article published on 12 October 2016

Novel mutation causing partial biotinidase deficiency in a Syrian boy with infantile spasms and retardation

artículo científico publicado en 2006

Parallel evolution of genes and languages in the Caucasus region

artículo científico publicado en 2011

Patients with early onset of type 1 diabetes have significantly higher GG genotype at position 49 of the CTLA4 gene.

artículo científico publicado en 2004

People from Ibiza: an unexpected isolate in the Western Mediterranean

scientific article published on 14 February 2019

Phylogenetic assessment of heterotrophic bacteria from a water distribution system using 16S rDNA sequencing.

artículo científico publicado en 2005

Predictors of coronary artery disease in the Lebanese population.

artículo científico publicado en 2005

Prenatal and neonatal Group B Streptococcus screening and serotyping in Lebanon: incidence and implications.

artículo científico publicado en 2010

Prevalence of asthmatic symptoms in Lebanese patients with type 1 diabetes and their unaffected siblings compared to age-matched controls

artículo científico publicado en 2009

Pulmonary thromboembolism in beta-thalassemia intermedia: are we aware of this complication?

artículo científico publicado en 2002

Recombination gives a new insight in the effective population size and the history of the old world human populations

artículo científico publicado en 2011

Recombination networks as genetic markers in a human variation study of the Old World

artículo científico publicado en 2011

Screening for antiretroviral drug resistance among treatment-naive human immunodeficiency virus type 1-infected individuals in Lebanon.

artículo científico publicado en 2014

Shared genetic variants between serum levels of high-density lipoprotein cholesterol and wheezing in a cohort of children from Cyprus

scientific article published on 13 July 2016

Suicidal gene therapy in an NF-κB-controlled tumor environment as monitored by a secreted blood reporter ⬇️

artículo científico publicado el 9 de diciembre de 2010

T2DM GWAS in the Lebanese population confirms the role of TCF7L2 and CDKAL1 in disease susceptibility

artículo científico publicado en 2014

The Codons 8/9 (+G) Mutation Found for the First Time in the Lebanese Population

scientific article published on 01 February 2003

The DD genotype of the ACE gene polymorphism is associated with diabetic nephropathy in the type-1 diabetics

scientific article published on 01 February 2001

The consanguinity effect on QF-PCR diagnosis of autosomal anomalies

artículo científico publicado en 2006

To the Editor

artículo científico publicado en 2006

Type-2 diabetes family history delays the onset of type-1 diabetes

artículo científico publicado en 2002

Untargeted Mass Spectrometry Lipidomics identifies correlation between serum sphingomyelins and plasma cholesterol

artículo científico publicado en 2019

WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon

scientific article published on 20 September 2008

Y-chromosomal diversity in Lebanon is structured by recent historical events

artículo científico publicado en 2008

Y-chromosome and mtDNA genetics reveal significant contrasts in affinities of modern Middle Eastern populations with European and African populations

artículo científico publicado en 2013

Zidovudine and interferon-alpha treatment induces a high response rate and reduces HTLV-1 proviral load and VEGF plasma levels in patients with adult T-cell leukemia from North East Iran.

artículo científico publicado en 2007

mQTL.NMR: an integrated suite for genetic mapping of quantitative variations of (1)H NMR-based metabolic profiles

artículo científico publicado en 2015

mtDNA lineages reveal coronary artery disease-associated structures in the Lebanese population

artículo científico publicado en 2011

Lista de obras de Pierre A Zalloua

A European Mitochondrial Haplotype Identified in Ancient Phoenician Remains from Carthage, North Africa

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

A novel ALMS1 splice mutation in a non-obese juvenile-onset insulin-dependent syndromic diabetic patient.

ALOX5AP gene variants show differential association with coronary artery disease in different populations.

Accurate and rapid prenatal diagnosis of the most frequent East Mediterranean beta-thalassemia mutations.

Anhidrotic ectodermal dysplasia. Report of a rare mutation in EDA1

Arsenic/interferon specifically reverses 2 distinct gene networks critical for the survival of HTLV-1-infected leukemic cells

Association of hypertension with coronary artery disease onset in the Lebanese population

Association of waterpipe smoking with myocardial infarction and determinants of metabolic syndrome among catheterized patients.

Autosomal genetics and Y-chromosome haplogroup L1b-M317 reveal Mount Lebanon Maronites as a persistently non-emigrating population

Beta-globin gene cluster haplotypes and HbF levels are not the only modulators of sickle cell disease in Lebanon.

Boston type I keratoprosthesis for treatment of gelatinous drop-like corneal dystrophy after repeated graft failure

Caffeine Impact on Metabolic Syndrome Components Is Modulated by a CYP1A2 Variant

Characterization of a large Lebanese family segregating IgA nephropathy

Characterizing redescriptions using persistent homology to isolate genetic pathways contributing to pathogenesis.

Circulating lipid levels and risk of coronary artery disease in a large group of patients undergoing coronary angiography

Deep phylogenetic analysis of haplogroup G1 provides estimates of SNP and STR mutation rates on the human Y-chromosome and reveals migrations of Iranic speakers

Development and evaluation of real-time polymerase chain reaction assays on whole blood and paraffin-embedded tissues for rapid diagnosis of human brucellosis

Effective treatment of hypereosinophilic syndrome with imatinib mesylate

Fertility drugs and the risk of breast cancer: a meta-analysis and review.

Genetic evidence for an origin of the Armenians from Bronze Age mixing of multiple populations

Genetic heterogeneity of Beta thalassemia in Lebanon reflects historic and recent population migration.

Genetically determined height and coronary artery disease

Genetics of the peloponnesean populations and the theory of extinction of the medieval peloponnesean Greeks

Genome-wide and paternal diversity reveal a recent origin of human populations in North Africa

Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis

Genome-wide diversity in the levant reveals recent structuring by culture

Genomic ancestry of North Africans supports back-to-Africa migrations

Geographic population structure analysis of worldwide human populations infers their biogeographical origins

Geographical structure of the Y-chromosomal genetic landscape of the Levant: a coastal-inland contrast

Gestational diabetes mellitus and macrosomia predispose to diabetes in the Lebanese population

Identifying genetic traces of historical expansions: Phoenician footprints in the Mediterranean

Impact of inflammation, gene variants, and cigarette smoking on coronary artery disease risk

Influences of history, geography, and religion on genetic structure: the Maronites in Lebanon

Large scale association analysis identifies three susceptibility loci for coronary artery disease

Large-scale association analysis identifies new risk loci for coronary artery disease

Lies, Gosh Darn Lies, and Not Enough Good Statistics: Why Epidemic Model Parameter Estimation Fails

Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions

Molecular basis of oculocutaneous albinism type 1 in Lebanese patients

Multivariate epidemiologic analysis of type 2 diabetes mellitus risks in the Lebanese population

Nicotine metabolism in healthy smokers and patients with cardiovascular diseases.

No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis ⬇️

Novel mutation causing partial biotinidase deficiency in a Syrian boy with infantile spasms and retardation

Parallel evolution of genes and languages in the Caucasus region

Patients with early onset of type 1 diabetes have significantly higher GG genotype at position 49 of the CTLA4 gene.

People from Ibiza: an unexpected isolate in the Western Mediterranean

Phylogenetic assessment of heterotrophic bacteria from a water distribution system using 16S rDNA sequencing.

Predictors of coronary artery disease in the Lebanese population.

Prenatal and neonatal Group B Streptococcus screening and serotyping in Lebanon: incidence and implications.

Prevalence of asthmatic symptoms in Lebanese patients with type 1 diabetes and their unaffected siblings compared to age-matched controls

Pulmonary thromboembolism in beta-thalassemia intermedia: are we aware of this complication?

Recombination gives a new insight in the effective population size and the history of the old world human populations

Recombination networks as genetic markers in a human variation study of the Old World

Screening for antiretroviral drug resistance among treatment-naive human immunodeficiency virus type 1-infected individuals in Lebanon.

Shared genetic variants between serum levels of high-density lipoprotein cholesterol and wheezing in a cohort of children from Cyprus

Suicidal gene therapy in an NF-κB-controlled tumor environment as monitored by a secreted blood reporter ⬇️

T2DM GWAS in the Lebanese population confirms the role of TCF7L2 and CDKAL1 in disease susceptibility

The Codons 8/9 (+G) Mutation Found for the First Time in the Lebanese Population

The DD genotype of the ACE gene polymorphism is associated with diabetic nephropathy in the type-1 diabetics

The consanguinity effect on QF-PCR diagnosis of autosomal anomalies

To the Editor

Type-2 diabetes family history delays the onset of type-1 diabetes

Untargeted Mass Spectrometry Lipidomics identifies correlation between serum sphingomyelins and plasma cholesterol

WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon

Y-chromosomal diversity in Lebanon is structured by recent historical events

Y-chromosome and mtDNA genetics reveal significant contrasts in affinities of modern Middle Eastern populations with European and African populations

Zidovudine and interferon-alpha treatment induces a high response rate and reduces HTLV-1 proviral load and VEGF plasma levels in patients with adult T-cell leukemia from North East Iran.

mQTL.NMR: an integrated suite for genetic mapping of quantitative variations of (1)H NMR-based metabolic profiles

mtDNA lineages reveal coronary artery disease-associated structures in the Lebanese population