List of works - Pierre Zalloua

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

scientific article (publication date: 25 May 2016)

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

scientific article

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

scientific article published on 8 May 2013

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

scientific article

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

scientific article

Anhidrotic ectodermal dysplasia. Report of a rare mutation in EDA1

scientific article published on 31 July 2008

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 04 December 2020

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

scientific article published in February 2003

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

scientific article published on 11 October 2013

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

scientific article published on 21 November 2015

Characterization of a large Lebanese family segregating IgA nephropathy

scientific article published on 15 December 2006

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

scientific article published on 11 January 2016

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

scientific article published on 01 January 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

scientific article

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

scientific article published on 29 May 2007

Effective treatment of hypereosinophilic syndrome with imatinib mesylate

scientific article published in January 2003

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

scientific article

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

scientific article

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

scientific article published in January 2005

Genetically determined height and coronary artery disease

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 20 February 2019

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

scientific article

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

scientific article

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

scientific article (publication date: 2011)

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

scientific article published on 02 December 2012

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

scientific article published on 22 April 2020

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

scientific article published on May 2017

Molecular basis of oculocutaneous albinism type 1 in Lebanese patients

scientific article published on 04 June 2005

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

scientific article

Nicotine metabolism in healthy smokers and patients with cardiovascular diseases.

scientific article published in December 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

scientific article

Parallel evolution of genes and languages in the Caucasus region

scientific article

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

scientific article

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.

scientific article published in April 2005

Predictors of coronary artery disease in the Lebanese population.

scientific article published on 27 June 2005

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

scientific article published on March 2010

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

scientific article

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

scientific article

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

scientific article published in September 2011

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

scientific article

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

scientific article published on 13 March 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

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

scientific article published on 08 December 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

scientific article published on 01 May 2006

To the Editor

scientific article published on 01 September 2006

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

scientific article published on 01 July 2002

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

scientific article published on 02 February 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

scientific article

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

scientific article published in 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.

scientific article published in February 2007

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

scientific article published on 2 April 2015

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

scientific article

List of works by Pierre 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

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