Lista de obras -

A Systematic single nucleotide polymorphism screen to fine-map alcohol dependence genes on chromosome 7 identifies association with a novel susceptibility gene ACN9

artículo científico publicado en 2007

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease.

artículo científico publicado en 2017

A genome-wide association study of alcohol dependence

artículo científico publicado en 2010

A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks

scientific journal article

A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin

artículo científico publicado en 2015

A risk allele for nicotine dependence in CHRNA5 is a protective allele for cocaine dependence

artículo científico publicado en 2008

Alcohol dependence with comorbid drug dependence: genetic and phenotypic associations suggest a more severe form of the disorder with stronger genetic contribution to risk

artículo científico publicado en 2007

Analysis of whole genome-transcriptomic organization in brain to identify genes associated with alcoholism

article

Association and expression analyses with single-nucleotide polymorphisms in TOMM40 in Alzheimer disease

artículo científico publicado en 2011

Association of CHRM2 with IQ: converging evidence for a gene influencing intelligence

artículo científico publicado en 2006

Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels

artículo científico publicado en 2011

Association of substance dependence phenotypes in the COGA sample

artículo científico publicado en 2014

Association studies between common variants in prolyl isomerase Pin1 and the risk for late-onset Alzheimer's disease

artículo científico publicado en 2007

Association studies testing for risk for late-onset Alzheimer's disease with common variants in the beta-amyloid precursor protein (APP).

artículo científico publicado en 2007

CYP2A6 metabolism in the development of smoking behaviors in young adults

artículo científico publicado en 2016

Cerebrospinal fluid APOE levels: an endophenotype for genetic studies for Alzheimer's disease

artículo científico publicado en 2012

Chitinase-3-like 1 protein (CHI3L1) locus influences cerebrospinal fluid levels of YKL-40.

artículo científico publicado en 2016

Cis-regulatory variants affect CHRNA5 mRNA expression in populations of African and European ancestry

artículo científico publicado en 2013

Coding variants in TREM2 increase risk for Alzheimer's disease

artículo científico publicado en 2014

Evidence of common and specific genetic effects: association of the muscarinic acetylcholine receptor M2 (CHRM2) gene with alcohol dependence and major depressive syndrome

artículo científico publicado en 2004

Exome chip meta-analysis fine maps causal variants and elucidates the genetic architecture of rare coding variants in smoking and alcohol use

artículo científico publicado en 2018

Family-based association analyses of alcohol dependence phenotypes across DRD2 and neighboring gene ANKK1.

artículo científico publicado en 2007

Family-based association analysis of alcohol dependence criteria and severity

artículo científico publicado en 2013

Functional Variants in TAS2R38 and TAS2R16 Influence Alcohol Consumption in High-Risk Families of African-American Origin

article

Functional variant in a bitter-taste receptor (hTAS2R16) influences risk of alcohol dependence

artículo científico publicado en 2005

GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease

artículo científico publicado en 2013

Genetic Comparison of Symptomatic and Asymptomatic Persons With Alzheimer Disease Neuropathology

artículo científico publicado en 2016

Genetic studies of plasma analytes identify novel potential biomarkers for several complex traits.

artículo científico publicado en 2016

Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers

artículo científico publicado en 2017

Genome-wide association study of CSF levels of 59 alzheimer's disease candidate proteins: significant associations with proteins involved in amyloid processing and inflammation

artículo científico publicado en 2014

Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families

scientific journal article

Linkage analyses of IQ in the collaborative study on the genetics of alcoholism (COGA) sample

artículo científico publicado en 2005

Linkage scan for quantitative traits identifies new regions of interest for substance dependence in the Collaborative Study on the Genetics of Alcoholism (COGA) sample

artículo científico publicado en 2007

Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci

artículo científico publicado en 2019

Missense variant in TREML2 protects against Alzheimer's disease

scientific article published on 21 December 2013

Phosphorylated tau-Aβ42 ratio as a continuous trait for biomarker discovery for early-stage Alzheimer's disease in multiplex immunoassay panels of cerebrospinal fluid

artículo científico publicado en 2014

Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease

artículo científico publicado en 2014

Risk for nicotine dependence and lung cancer is conferred by mRNA expression levels and amino acid change in CHRNA5.

scientific article published on 14 May 2009

SNPs associated with cerebrospinal fluid phospho-tau levels influence rate of decline in Alzheimer's disease

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

The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-ε4 carriers

artículo científico publicado en 2013

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

Using dimensional models of externalizing psychopathology to aid in gene identification

artículo científico publicado en 2008

Validating predicted biological effects of Alzheimer's disease associated SNPs using CSF biomarker levels

artículo científico publicado en 2010

Variants in nicotinic receptors and risk for nicotine dependence

artículo científico publicado en 2008

Variants located upstream of CHRNB4 on chromosome 15q25.1 are associated with age at onset of daily smoking and habitual smoking

artículo científico publicado en 2012

Variation in MAPT is associated with cerebrospinal fluid tau levels in the presence of amyloid-beta deposition

artículo científico publicado en 2008

Lista de obras de

A Systematic single nucleotide polymorphism screen to fine-map alcohol dependence genes on chromosome 7 identifies association with a novel susceptibility gene ACN9

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease.

A genome-wide association study of alcohol dependence

A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks

A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin

A risk allele for nicotine dependence in CHRNA5 is a protective allele for cocaine dependence

Alcohol dependence with comorbid drug dependence: genetic and phenotypic associations suggest a more severe form of the disorder with stronger genetic contribution to risk

Analysis of whole genome-transcriptomic organization in brain to identify genes associated with alcoholism

Association and expression analyses with single-nucleotide polymorphisms in TOMM40 in Alzheimer disease

Association of CHRM2 with IQ: converging evidence for a gene influencing intelligence

Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels

Association of substance dependence phenotypes in the COGA sample

Association studies between common variants in prolyl isomerase Pin1 and the risk for late-onset Alzheimer's disease

Association studies testing for risk for late-onset Alzheimer's disease with common variants in the beta-amyloid precursor protein (APP).

CYP2A6 metabolism in the development of smoking behaviors in young adults

Cerebrospinal fluid APOE levels: an endophenotype for genetic studies for Alzheimer's disease

Chitinase-3-like 1 protein (CHI3L1) locus influences cerebrospinal fluid levels of YKL-40.

Cis-regulatory variants affect CHRNA5 mRNA expression in populations of African and European ancestry

Coding variants in TREM2 increase risk for Alzheimer's disease

Evidence of common and specific genetic effects: association of the muscarinic acetylcholine receptor M2 (CHRM2) gene with alcohol dependence and major depressive syndrome

Exome chip meta-analysis fine maps causal variants and elucidates the genetic architecture of rare coding variants in smoking and alcohol use

Family-based association analyses of alcohol dependence phenotypes across DRD2 and neighboring gene ANKK1.

Family-based association analysis of alcohol dependence criteria and severity

Functional Variants in TAS2R38 and TAS2R16 Influence Alcohol Consumption in High-Risk Families of African-American Origin

Functional variant in a bitter-taste receptor (hTAS2R16) influences risk of alcohol dependence

GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease

Genetic Comparison of Symptomatic and Asymptomatic Persons With Alzheimer Disease Neuropathology

Genetic studies of plasma analytes identify novel potential biomarkers for several complex traits.

Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers

Genome-wide association study of CSF levels of 59 alzheimer's disease candidate proteins: significant associations with proteins involved in amyloid processing and inflammation

Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families

Linkage analyses of IQ in the collaborative study on the genetics of alcoholism (COGA) sample

Linkage scan for quantitative traits identifies new regions of interest for substance dependence in the Collaborative Study on the Genetics of Alcoholism (COGA) sample

Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci

Missense variant in TREML2 protects against Alzheimer's disease

Phosphorylated tau-Aβ42 ratio as a continuous trait for biomarker discovery for early-stage Alzheimer's disease in multiplex immunoassay panels of cerebrospinal fluid

Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease

Risk for nicotine dependence and lung cancer is conferred by mRNA expression levels and amino acid change in CHRNA5.

SNPs associated with cerebrospinal fluid phospho-tau levels influence rate of decline in Alzheimer's disease

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

The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-ε4 carriers

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

Using dimensional models of externalizing psychopathology to aid in gene identification

Validating predicted biological effects of Alzheimer's disease associated SNPs using CSF biomarker levels

Variants in nicotinic receptors and risk for nicotine dependence

Variants located upstream of CHRNB4 on chromosome 15q25.1 are associated with age at onset of daily smoking and habitual smoking

Variation in MAPT is associated with cerebrospinal fluid tau levels in the presence of amyloid-beta deposition