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Lista de obras de Renato Polimanti

A genome-wide gene-by-trauma interaction study of alcohol misuse in two independent cohorts identifies PRKG1 as a risk locus

artículo científico

A large-scale genome-wide association study meta-analysis of cannabis use disorder

artículo científico publicado en 2020

A putative causal relationship between genetically determined female body shape and posttraumatic stress disorder

artículo científico publicado en 2017

ACE2 Netlas: In-silico functional characterization and drug-gene interactions of ACE2 gene network to understand its potential involvement in COVID-19 susceptibility

artículo científico publicado en 2020

ADH1B: From alcoholism, natural selection, and cancer to the human phenome

artículo científico publicado en 2017

ATP7B variants as modulators of copper dyshomeostasis in Alzheimer's disease

artículo científico publicado en 2013

Allergy-specific Phenome-Wide Association Study for Immunogenes in Turkish Children

artículo científico publicado en 2016

Ancestry-specific and sex-specific risk alleles identified in a genome-wide gene-by-alcohol dependence interaction study of risky sexual behaviors

artículo científico publicado en 2017

Antioxidant status and APOE genotype as susceptibility factors for neurodegeneration in Alzheimer's disease and vascular dementia

artículo científico publicado en 2013

Association between the c. 2495 A>G ATP7B Polymorphism and Sporadic Alzheimer's Disease

artículo científico publicado en 2011

Association of K832R and R952K SNPs of Wilson's Disease Gene with Alzheimer's Disease

article

Biological factors and age-dependence of primary motor cortex experimental plasticity

artículo científico publicado en 2015

Copper Hypothesis in the Missing Hereditability of Sporadic Alzheimer's Disease: ATP7B Gene as Potential Harbor of Rare Variants ⬇️

artículo científico publicado el 1 de enero de 2012

Copper status in Alzheimer's disease and other neurodegenerative disorders 2013.

artículo científico publicado en 2013

Cross-Phenotype Polygenic Risk Score Analysis of Persistent Post-Concussive Symptoms in U.S. Army Soldiers with Deployment-Acquired Traumatic Brain Injury

artículo científico

Deciphering the Biological Mechanisms Underlying the Genome-Wide Associations between Computerized Device Use and Psychiatric Disorders

scientific article published on 21 November 2019

Deletion polymorphism of GSTT1 gene as protective marker for allergic rhinitis.

artículo científico publicado en 2014

Dissecting ancestry genomic background in substance dependence genome-wide association studies

artículo científico publicado en 2015

Drinking and smoking polygenic risk is associated with childhood and early-adulthood psychiatric and behavioral traits independently of substance use and psychiatric genetic risk

artículo científico publicado en 2021

Duplication of FOXP2 binding sites within CNTNAP2 gene in a girl with neurodevelopmental delay

artículo científico publicado en 2016

Epigenetic profiling of Italian patients identified methylation sites associated with hereditary transthyretin amyloidosis

scientific article published on 17 November 2020

Evidence of Polygenic Adaptation in the Systems Genetics of Anthropometric Traits

artículo científico publicado en 2016

Evidence of causal effect of major depression on alcohol dependence: findings from the psychiatric genomics consortium

artículo científico publicado en 2019

Explorative genetic association study of GSTT2B copy number variant in complex disease risks

artículo científico publicado en 2015

Functional diversity of the glutathione peroxidase gene family among human populations: implications for genetic predisposition to disease and drug response.

artículo científico publicado en 2013

Functional polymorphisms of GSTA1 and GSTO2 genes associated with asthma in Italian children

article

Functional variability of glutathione S-transferases in Basque populations.

artículo científico publicado en 2014

Functional variation of the transthyretin gene among human populations and its correlation with amyloidosis phenotypes

artículo científico publicado en 2013

GPX1*Pro198Leu AND GPX3 rs2070593 as genetic risk markers for Italian asthmatic patients

artículo científico publicado en 2016

GSTA1 gene variation associated with gestational hypertension and its involvement in pregnancy-related pathogenic conditions

artículo científico publicado en 2015

GSTA1*-69C/T and GSTO2*N142D as asthma- and allergy-related risk factors in Italian adult patients

artículo científico publicado en 2014

GSTA1, GSTO1 and GSTO2 gene polymorphisms in Italian asthma patients

artículo científico publicado en 2010

GSTM1 null genotype as risk factor for late-onset Alzheimer's disease in Italian patients.

artículo científico publicado en 2012

GSTM1, GSTP1, and GSTT1 genetic variability in Turkish and worldwide populations.

artículo científico publicado en 2014

GSTO1 uncommon genetic variants are associated with recurrent miscarriage risk.

artículo científico publicado en 2014

GSTO1*E155del polymorphism associated with increased risk for late-onset Alzheimer's disease: association hypothesis for an uncommon genetic variant.

artículo científico publicado en 2011

GSTO2*N142D gene polymorphism associated with hypothyroidism in Italian patients

artículo científico publicado en 2012

GSTT1 and GSTM1 gene polymorphisms in European and African populations

article

Genetic Risk Variants Associated With Comorbid Alcohol Dependence and Major Depression.

artículo científico publicado en 2017

Genetic diversity of disease-associated loci in Turkish population.

artículo científico publicado en 2015

Genetic factor common to schizophrenia and HIV infection is associated with risky sexual behavior: antagonistic vs. synergistic pleiotropic SNPs enriched for distinctly different biological functions

artículo científico publicado en 2016

Genetic variability of glutathione S-transferase enzymes in human populations: functional inter-ethnic differences in detoxification systems.

artículo científico publicado en 2012

Genetically regulated multi-omics study for symptom clusters of posttraumatic stress disorder highlights pleiotropy with hematologic and cardio-metabolic traits

artículo científico publicado en 2022

Genome-wide Association Studies of Posttraumatic Stress Disorder in 2 Cohorts of US Army Soldiers

artículo científico publicado en 2016

Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk loci

artículo científico publicado en 2022

Genome-wide association study of body mass index in subjects with alcohol dependence

artículo científico publicado en 2015

Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits

artículo científico publicado en 2020

Glutaredoxin 1 is a major player in copper metabolism in neuroblastoma cells.

artículo científico publicado en 2013

Glutathione S-transferase gene polymorphisms and air pollution as interactive risk factors for asthma in a multicentre Italian field study: A preliminary study

artículo científico publicado en 2010

Glutathione S-transferase genes and the risk of recurrent miscarriage in Italian women

artículo científico publicado en 2012

Glutathione S-transferase polymorphisms, asthma susceptibility and confounding variables: a meta-analysis ⬇️

artículo científico publicado el 10 de enero de 2013

Glutathione S-transferase variants as risk factor for essential hypertension in Italian patients.

artículo científico publicado en 2011

Glutathione S-transferase ω class (GSTO) polymorphisms in a sample from Rome (Central Italy).

artículo científico publicado en 2010

HapMap-based study of human soluble glutathione S-transferase enzymes: the role of natural selection in shaping the single nucleotide polymorphism diversity of xenobiotic-metabolizing genes

artículo científico publicado en 2011

Haplotype analysis of non-HLA immunogenetic loci in Turkish and worldwide populations

artículo científico publicado en 2016

Haplotype differences for copy number variants in the 22q11.23 region among human populations: a pigmentation-based model for selective pressure

artículo científico publicado en 2014

Heterogeneity and Polygenicity in Psychiatric Disorders: A Genome-Wide Perspective

artículo científico publicado en 2020

Host genetic liability for severe COVID-19 overlaps with alcohol drinking behavior and diabetic outcomes and in over 1 million participants

artículo científico publicado en 2020

Human GST loci as markers of evolutionary forces: GSTO1*E155del and GSTO1*E208K polymorphisms may be under natural selection induced by environmental arsenic

artículo científico publicado en 2011

Human genetic variation of CYP450 superfamily: analysis of functional diversity in worldwide populations.

artículo científico publicado en 2012

Human pharmacogenomic variation of antihypertensive drugs: from population genetics to personalized medicine

scientific article published on 01 February 2014

In silico analysis of TTR gene (coding and non-coding regions, and interactive network) and its implications in transthyretin-related amyloidosis

artículo científico publicado en 2014

In silico investigation of the ATP7B gene: insights from functional prediction of non-synonymous substitution to protein structure.

artículo científico publicado en 2013

Increased Risk of Multiple Outpatient Surgeries in African-American Carriers of Transthyretin Val122Ile Mutation Is Modulated by Non-Coding Variants

Integration of evidence across human and model organism studies: A meeting report

artículo científico publicado en 2021

Integrative analyses identify susceptibility genes underlying COVID-19 hospitalization

artículo científico publicado en 2020

International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci

scientific article published on 08 October 2019

International warfarin genotype-guided dosing algorithms in the Turkish population and their preventive effects on major and life-threatening hemorrhagic events.

artículo científico publicado en 2015

Intronic rs2147363 variant in ATP7B transcription factor-binding site associated with Alzheimer's disease

artículo científico publicado en 2013

Investigating Causality Between Blood Metabolites and Emotional and Behavioral Responses to Traumatic Stress: a Mendelian Randomization Study

scientific article published on 30 November 2019

Lack of association between essential hypertension and GSTO1 uncommon genetic variants in Italian patients.

artículo científico publicado en 2012

Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium

artículo científico publicado en 2020

Linkage disequilibrium and haplotype analysis of the ATP7B gene in Alzheimer's disease

artículo científico publicado en 2013

Low-copper diet as a preventive strategy for Alzheimer's disease.

artículo científico publicado en 2014

Metal-score as a potential non-invasive diagnostic test for Alzheimer's disease

artículo científico publicado en 2013

Most recent common ancestor ofTTRVal30Met mutation in Italian population and its potential role in genotype-phenotype correlation

article

Nutritional habits, lifestyle, and genetic predisposition in cardiovascular and metabolic traits in Turkish population.

artículo científico publicado en 2015

Phenome-Wide Association Study for Alcohol and Nicotine Risk Alleles in 26394 Women

artículo científico publicado en 2016

Phenome-wide association study for CYP2A6 alleles: rs113288603 is associated with hearing loss symptoms in elderly smokers

artículo científico publicado en 2017

Phenome-wide association study of TTR and RBP4 genes in 361,194 individuals reveals novel insights in the genetics of hereditary and wildtype transthyretin amyloidoses

artículo científico publicado en 2019

Phenome-wide genetic-correlation analysis and genetically informed causal inference of amyotrophic lateral sclerosis

artículo científico publicado en 2023

Phenomic Impact of Genetically-Determined Euthyroid Function and Molecular Differences between Thyroid Disorders

artículo científico publicado en 2018

Phenotype versus genotype methods for copy number variant analysis of glutathione S-transferases M1.

artículo científico publicado en 2013

Phenotypic and Molecular Characterization of Risk Loci Associated With Asthma and Lung Function

artículo científico publicado en 2020

Polygenic risk for autism spectrum disorder associates with anger recognition in a neurodevelopment-focused phenome-wide scan of unaffected youths from a population-based cohort

scientific article published on 17 September 2020

S100A10 identified in a genome-wide gene × cannabis dependence interaction analysis of risky sexual behaviours

artículo científico publicado en 2017

Schizophrenia and substance use comorbidity: a genome-wide perspective

artículo científico publicado en 2017

Serum proteins and work habits in a group of farm-workers exposed to EBDCs.

artículo científico publicado en 2010

Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

artículo científico publicado en 2020

Summaries of plenary and selected symposia sessions at the XXIV World Congress of Psychiatric Genetics; Jerusalem, Israel; 30 October 2016-3 November 2016.

artículo científico publicado en 2017

The Interplay Between Risky Sexual Behaviors and Alcohol Dependence: Genome-Wide Association and Neuroimaging Support for LHPP as a Risk Gene

artículo científico publicado en 2016

The association of obesity-related traits on COVID-19 severity and hospitalization is affected by socio-economic status: a multivariable Mendelian randomization study

scientific article published in 2022

Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

scholarly article published 10 March 2018

Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

artículo científico publicado en 2018

Trauma exposure interacts with the genetic risk of bipolar disorder in alcohol misuse of US soldiers.

artículo científico publicado en 2017

Widespread signatures of positive selection in common risk alleles associated to autism spectrum disorder

artículo científico publicado en 2017

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