Lista de obras - Richard Sherva - Dominio Público Uruguay

A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression

artículo científico publicado en 2011

A whole genome scan for pulse pressure/stroke volume ratio in African Americans: the HyperGEN study

artículo científico publicado en 2007

A whole-genome scan for stroke or myocardial infarction in family blood pressure program families

artículo científico publicado en 2008

ACSL6 is associated with the number of cigarettes smoked and its expression is altered by chronic nicotine exposure

artículo científico publicado en 2011

Association of granulomatosis with polyangiitis (Wegener's) with HLA-DPB1*04 and SEMA6A gene variants: evidence from genome-wide analysis

artículo científico publicado en 2013

Association of maternal and infant variants in PNOC and COMT genes with neonatal abstinence syndrome severity

artículo científico publicado en 2016

Calibrating longitudinal cognition in Alzheimer's disease across diverse test batteries and datasets

artículo científico publicado en 2014

Common CD36 SNPs reduce protein expression and may contribute to a protective atherogenic profile

artículo científico publicado en 2010

Common variants in WFS1 confer risk of type 2 diabetes

artículo científico publicado en 2007

Erratum: Genetic risk prediction and neurobiological understanding of alcoholism

scholarly article published in Translational Psychiatry

Evidence for a quantitative trait locus affecting low levels of apolipoprotein B and low density lipoprotein on chromosome 10 in Caucasian families.

artículo científico publicado en 2007

Evidence of CNIH3 involvement in opioid dependence.

artículo científico publicado en 2015

Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits

artículo científico publicado en 2020

Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster

artículo científico publicado en 2009

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

artículo científico publicado en 2017

Genetic modifiers of Hb E/beta0 thalassemia identified by a two-stage genome-wide association study

artículo científico publicado en 2010

Genetic risk prediction and neurobiological understanding of alcoholism

artículo científico publicado en 2014

Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes

artículo científico publicado en 2019

Genome-wide Association Study Identifies a Regulatory Variant of RGMA Associated With Opioid Dependence in European Americans.

artículo científico publicado en 2018

Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks

artículo científico publicado en 2016

Genome-wide association meta-analysis of age at first cannabis use

artículo científico publicado en 2018

Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence

artículo científico publicado en 2017

Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.

artículo científico publicado en 2017

Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci

artículo científico publicado en 2013

Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene

scientific article published on 20 August 2013

Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium

artículo científico publicado en 2016

Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans.

artículo científico publicado en 2014

Genome-wide association study of opioid dependence: multiple associations mapped to calcium and potassium pathways

artículo científico publicado en 2013

Genome-wide association study of the rate of cognitive decline in Alzheimer's disease

artículo científico publicado en 2013

Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence

artículo científico publicado en 2015

Genomewide Association Study for Maximum Number of Alcoholic Drinks in European Americans and African Americans

artículo científico publicado en 2015

Genomewide Association Study of Alcohol Dependence Identifies Risk Loci Altering Ethanol-Response Behaviors in Model Organisms

artículo científico publicado en 2017

Meta-analysis of genetic polymorphisms in granulomatosis with polyangiitis (Wegener's) reveals shared susceptibility loci with rheumatoid arthritis

artículo científico publicado en 2012

Multiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD.

artículo científico publicado en 2010

Nf1 regulates alcohol dependence-associated excessive drinking and gamma-aminobutyric acid release in the central amygdala in mice and is associated with alcohol dependence in humans

artículo científico publicado en 2014

No evidence for multiple loci affecting rheumatoid arthritis risk on chromosome 6p21.

artículo científico publicado en 2007

Oxytocin receptor gene polymorphisms, attachment, and PTSD: Results from the National Health and Resilience in Veterans Study

artículo científico

Population-specific risk of type 2 diabetes conferred by HNF4A P2 promoter variants: a lesson for replication studies

artículo científico publicado en 2008

Power and Pitfalls of the Genome-Wide Association Study Approach to Identify Genes for Alzheimer’s Disease ⬇️

artículo científico publicado el 1 de abril de 2011

Reply

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

artículo científico publicado en 2017

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

artículo científico publicado en 2020

Single Nucleotide Polymorphism Facilitated Down-Regulation of the Cohesin Stromal Antigen-1: Implications for Colorectal Cancer Racial Disparities.

artículo científico publicado en 2018

The executive prominent/memory prominent spectrum in Alzheimer's disease is highly heritable

artículo científico publicado en 2016

The genetics of alcohol dependence: Twin and SNP-based heritability, and genome-wide association study based on AUDIT scores

artículo científico publicado en 2015

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

Transethnic genome-wide scan identifies novel Alzheimer's disease loci

artículo científico publicado en 2017

Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans

artículo científico publicado en 2016

Using linkage and association to identify and model genetic effects: summary of GAW15 Group 4

article

Variants in the CD36 gene associate with the metabolic syndrome and high-density lipoprotein cholesterol

scientific article published on 27 February 2008

Variation in nicotinic acetylcholine receptor genes is associated with multiple substance dependence phenotypes

artículo científico publicado en 2010

Variations in opioid receptor genes in neonatal abstinence syndrome

artículo científico publicado en 2015

Lista de obras de Richard Sherva

A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression

A whole genome scan for pulse pressure/stroke volume ratio in African Americans: the HyperGEN study

A whole-genome scan for stroke or myocardial infarction in family blood pressure program families

ACSL6 is associated with the number of cigarettes smoked and its expression is altered by chronic nicotine exposure

Association of granulomatosis with polyangiitis (Wegener's) with HLA-DPB1*04 and SEMA6A gene variants: evidence from genome-wide analysis

Association of maternal and infant variants in PNOC and COMT genes with neonatal abstinence syndrome severity

Calibrating longitudinal cognition in Alzheimer's disease across diverse test batteries and datasets

Common CD36 SNPs reduce protein expression and may contribute to a protective atherogenic profile

Common variants in WFS1 confer risk of type 2 diabetes

Erratum: Genetic risk prediction and neurobiological understanding of alcoholism

Evidence for a quantitative trait locus affecting low levels of apolipoprotein B and low density lipoprotein on chromosome 10 in Caucasian families.

Evidence of CNIH3 involvement in opioid dependence.

Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits

Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster

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

Genetic modifiers of Hb E/beta0 thalassemia identified by a two-stage genome-wide association study

Genetic risk prediction and neurobiological understanding of alcoholism

Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes

Genome-wide Association Study Identifies a Regulatory Variant of RGMA Associated With Opioid Dependence in European Americans.

Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks

Genome-wide association meta-analysis of age at first cannabis use

Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence

Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.

Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci

Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene

Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium

Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans.

Genome-wide association study of opioid dependence: multiple associations mapped to calcium and potassium pathways

Genome-wide association study of the rate of cognitive decline in Alzheimer's disease

Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence

Genomewide Association Study for Maximum Number of Alcoholic Drinks in European Americans and African Americans

Genomewide Association Study of Alcohol Dependence Identifies Risk Loci Altering Ethanol-Response Behaviors in Model Organisms

Meta-analysis of genetic polymorphisms in granulomatosis with polyangiitis (Wegener's) reveals shared susceptibility loci with rheumatoid arthritis

Multiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD.

Nf1 regulates alcohol dependence-associated excessive drinking and gamma-aminobutyric acid release in the central amygdala in mice and is associated with alcohol dependence in humans

No evidence for multiple loci affecting rheumatoid arthritis risk on chromosome 6p21.

Oxytocin receptor gene polymorphisms, attachment, and PTSD: Results from the National Health and Resilience in Veterans Study

Population-specific risk of type 2 diabetes conferred by HNF4A P2 promoter variants: a lesson for replication studies

Power and Pitfalls of the Genome-Wide Association Study Approach to Identify Genes for Alzheimer’s Disease ⬇️

Reply

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

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

Single Nucleotide Polymorphism Facilitated Down-Regulation of the Cohesin Stromal Antigen-1: Implications for Colorectal Cancer Racial Disparities.

The executive prominent/memory prominent spectrum in Alzheimer's disease is highly heritable

The genetics of alcohol dependence: Twin and SNP-based heritability, and genome-wide association study based on AUDIT scores

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

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

Transethnic genome-wide scan identifies novel Alzheimer's disease loci

Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans

Using linkage and association to identify and model genetic effects: summary of GAW15 Group 4

Variants in the CD36 gene associate with the metabolic syndrome and high-density lipoprotein cholesterol

Variation in nicotinic acetylcholine receptor genes is associated with multiple substance dependence phenotypes

Variations in opioid receptor genes in neonatal abstinence syndrome