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Renato Polimanti

Name	Renato Polimanti
Ort	Italien
Geschlecht	männlich
Akademischer Grad bzw. Titel	PhD
Beziehung	Yale University. School of Medicine
Quelle	Homepage: https://medicine.yale.edu/profile/renato_polimanti/ (Stand: 28.11.2015)
Datensatztyp	Person
GND-Nummer	1200596366
Datensatz-ID	1200596366
Beteiligt an alle anzeigen Association patterns of antisocial personality disorder across substance use disorders Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder Effects of genetically predicted posttraumatic stress disorder on autoimmune phenotypes Clinical spectrum of Transthyretin amyloidogenic mutations among diverse population origins Estimating the direct effects of the genetic liabilities to bipolar disorder, schizophrenia, and behavioral traits on suicide attempt using a multivariable Mendelian randomization approach The impact of assortative mating, participation bias and socioeconomic status on the polygenic risk of behavioural and psychiatric traits Pleiotropy and genetically inferred causality linking multisite chronic pain to substance use disorders Correction: Psychosocial moderators of polygenic risk scores of inflammatory biomarkers in relation to GrimAge Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications Genome-wide association studies and cross-population meta-analyses investigating short and long sleep duration Characterizing the polygenic architecture of complex traits in populations of East Asian and European descent Sex differences in the polygenic architecture of hearing problems in adults Enrichment of self-domestication and neural crest function loci in the heritability of neurodevelopmental disorders Phenome-wide genetic-correlation analysis and genetically informed causal inference of amyotrophic lateral sclerosis Phenome-wide association study of loci harboring de novo tandem repeat mutations in UK Biobank exomes Denisovan and Neanderthal archaic introgression differentially impacted the genetics of complex traits in modern populations Genetic variants associated with psychiatric disorders are enriched at epigenetically active sites in lymphoid cells 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 Multivariate genome-wide analysis of education, socioeconomic status and brain phenome Epigenetic profiling of Italian patients identified methylation sites associated with hereditary transthyretin amyloidosis Investigating Causality Between Blood Metabolites and Emotional and Behavioral Responses to Traumatic Stress: a Mendelian Randomization Study 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

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Renato Polimanti

Association patterns of antisocial personality disorder across substance use disorders

Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder

Effects of genetically predicted posttraumatic stress disorder on autoimmune phenotypes

Clinical spectrum of Transthyretin amyloidogenic mutations among diverse population origins

Estimating the direct effects of the genetic liabilities to bipolar disorder, schizophrenia, and behavioral traits on suicide attempt using a multivariable Mendelian randomization approach

The impact of assortative mating, participation bias and socioeconomic status on the polygenic risk of behavioural and psychiatric traits

Pleiotropy and genetically inferred causality linking multisite chronic pain to substance use disorders

Correction: Psychosocial moderators of polygenic risk scores of inflammatory biomarkers in relation to GrimAge

Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference

Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications

Genome-wide association studies and cross-population meta-analyses investigating short and long sleep duration

Characterizing the polygenic architecture of complex traits in populations of East Asian and European descent

Sex differences in the polygenic architecture of hearing problems in adults

Enrichment of self-domestication and neural crest function loci in the heritability of neurodevelopmental disorders

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

Phenome-wide association study of loci harboring de novo tandem repeat mutations in UK Biobank exomes

Denisovan and Neanderthal archaic introgression differentially impacted the genetics of complex traits in modern populations

Genetic variants associated with psychiatric disorders are enriched at epigenetically active sites in lymphoid cells

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

Multivariate genome-wide analysis of education, socioeconomic status and brain phenome

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

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

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