Lista de obras -

A MULTIVARIATE FINITE MIXTURE LATENT TRAJECTORY MODEL WITH APPLICATION TO DEMENTIA STUDIES

artículo científico publicado en 2016

A genome-wide association study of interhemispheric theta EEG coherence: implications for neural connectivity and alcohol use behavior

artículo científico publicado en 2020

Alcohol use disorder, psychiatric comorbidities, marriage and divorce in a high-risk sample.

artículo científico publicado en 2022

Alcohol-preferring rats show decreased corticotropin-releasing hormone-2 receptor expression and differences in HPA activation compared to alcohol-nonpreferring rats

artículo científico publicado en 2014

Allele-Specific Expression and High-Throughput Reporter Assay Reveal Functional Variants in Human Brains with Alcohol Use Disorders

Allele-specific expression and high-throughput reporter assay reveal functional genetic variants associated with alcohol use disorders

scientific article published on 02 September 2019

Analysis of variation in expression of autosomal dominant osteopetrosis type 2: searching for modifier genes

artículo científico publicado en 2005

Association of adenylate cyclase 10 (ADCY10) polymorphisms and bone mineral density in healthy adults

artículo científico publicado en 2008

Association of adiposity genetic variants with menarche timing in 92,105 women of European descent

artículo científico publicado en 2013

Bone mineral density variation in men is influenced by sex-specific and non sex-specific quantitative trait loci

artículo científico publicado en 2009

CLCN7 polymorphisms and bone mineral density in healthy premenopausal white women and in white men.

artículo científico publicado en 2008

Calcium-Sensing Receptor Genotype and Response to Cinacalcet in Patients Undergoing Hemodialysis

artículo científico publicado en 2017

Charcot-Marie-Tooth gene, SBF2, associated with taxane-induced peripheral neuropathy in African Americans

artículo científico publicado en 2016

Contribution of the LRP5 gene to normal variation in peak BMD in women

artículo científico publicado en 2004

Exome Sequencing Identifies Candidate Genetic Modifiers of Syndromic and Familial Thoracic Aortic Aneurysm Severity.

artículo científico publicado en 2017

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

False positive rates in association studies as a function of degree of stratification

artículo científico publicado en 2004

Fine mapping and expression of candidate genes within the chromosome 10 QTL region of the high and low alcohol-drinking rats

artículo científico publicado en 2010

Genetic Influences on Plasma Homocysteine Levels in African Americans and Yoruba Nigerians

artículo científico publicado en 2015

Genetic Variants Associated with Circulating Fibroblast Growth Factor 23

Genetic Variants Associated with Circulating Parathyroid Hormone

artículo científico publicado en 2016

Genome screen in familial intracranial aneurysm

Genome screen to detect linkage to common susceptibility genes for intracranial and aortic aneurysms

artículo científico publicado en 2008

Genome screen to detect linkage to intracranial aneurysm susceptibility genes: the Familial Intracranial Aneurysm (FIA) study

artículo científico publicado en 2008

Genome-Wide Association Studies for Taxane-Induced Peripheral Neuropathy in ECOG-5103 and ECOG-1199.

artículo científico publicado en 2015

Genome-Wide Association Study for Anthracycline-Induced Congestive Heart Failure

artículo científico publicado en 2016

Genome-wide admixture mapping of DSM-IV alcohol dependence, criterion count, and the self-rating of the effects of ethanol in African American populations

scientific article published on 11 July 2020

Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population

artículo científico publicado en 2018

Genome-wide association studies of alcohol dependence, DSM-IV criterion count and individual criteria

artículo científico publicado en 2019

Genome-wide association studies of the self-rating of effects of ethanol (SRE)

scientific article published on 03 July 2019

Genome-wide association study identifies loci associated with liability to alcohol and drug dependence that is associated with variability in reward-related ventral striatum activity in African- and European-Americans

artículo científico publicado en 2019

Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American women

artículo científico publicado en 2010

Genome-wide association study of intracranial aneurysm identifies a new association on chromosome 7.

artículo científico publicado en 2014

Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk

artículo científico publicado en 2012

Genome-wide association study of serum iron phenotypes in premenopausal women of European descent

artículo científico publicado en 2015

Genomewide SNP screen to detect quantitative trait loci for alcohol preference in the high alcohol preferring and low alcohol preferring mice

artículo científico publicado en 2008

Human ALOX12, but Not ALOX15, Is Associated With BMD in White Men and Women

article

Identification of Functional Genetic Variants Associated with Alcohol Dependence and Related Phenotypes Using a High-Throughput Assay

artículo científico publicado en 2020

Identification of a linkage disequilibrium block in chromosome 1q associated with BMD in premenopausal white women

artículo científico publicado en 2008

Impact of Genetic Ancestry on Outcomes in ECOG-ACRIN-E5103

artículo científico publicado en 2017

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

artículo científico publicado en 2021

Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm

artículo científico publicado en 2015

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

Meta-Analysis of Genetic Influences on Initial Alcohol Sensitivity

artículo científico publicado en 2018

Meta-analysis of genome-wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women

artículo científico publicado en 2013

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

artículo científico publicado en 2019

Multi-omics integration analysis identifies novel genes for alcoholism with potential overlap with neurodegenerative diseases

artículo científico publicado en 2021

Polymorphisms in the estrogen receptor beta (ESR2) gene are associated with bone mineral density in Caucasian men and women

artículo científico publicado en 2005

Quantitative trait locus for body weight identified on rat chromosome 4 in inbred alcohol-preferring and -nonpreferring rats: potential implications for neuropeptide Y and corticotrophin releasing hormone 2

artículo científico publicado en 2013

Replication of previous genome-wide association studies of bone mineral density in premenopausal American women

artículo científico publicado en 2010

SIBLING family genes and bone mineral density: association and allele-specific expression in humans

artículo científico publicado en 2014

Sex-specific quantitative trait loci contribute to normal variation in bone structure at the proximal femur in men

artículo científico publicado en 2005

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

artículo científico publicado en 2016

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

artículo científico publicado en 2020

Steroid Pathway Genes and Neonatal Respiratory Distress After Betamethasone Use in Anticipated Preterm Birth

artículo científico publicado en 2015

The Genetic Relationship Between Alcohol Consumption and Aspects of Problem Drinking in an Ascertained Sample

scientific article published on 21 May 2019

The relationship between smoking and replicated sequence variants on chromosomes 8 and 9 with familial intracranial aneurysm

artículo científico publicado en 2010

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

artículo científico publicado en 2018

Whole-Exome Sequencing in Familial Parkinson Disease

artículo científico publicado en 2015

Lista de obras de

A MULTIVARIATE FINITE MIXTURE LATENT TRAJECTORY MODEL WITH APPLICATION TO DEMENTIA STUDIES

A genome-wide association study of interhemispheric theta EEG coherence: implications for neural connectivity and alcohol use behavior

Alcohol use disorder, psychiatric comorbidities, marriage and divorce in a high-risk sample.

Alcohol-preferring rats show decreased corticotropin-releasing hormone-2 receptor expression and differences in HPA activation compared to alcohol-nonpreferring rats

Allele-Specific Expression and High-Throughput Reporter Assay Reveal Functional Variants in Human Brains with Alcohol Use Disorders

Allele-specific expression and high-throughput reporter assay reveal functional genetic variants associated with alcohol use disorders

Analysis of variation in expression of autosomal dominant osteopetrosis type 2: searching for modifier genes

Association of adenylate cyclase 10 (ADCY10) polymorphisms and bone mineral density in healthy adults

Association of adiposity genetic variants with menarche timing in 92,105 women of European descent

Bone mineral density variation in men is influenced by sex-specific and non sex-specific quantitative trait loci

CLCN7 polymorphisms and bone mineral density in healthy premenopausal white women and in white men.

Calcium-Sensing Receptor Genotype and Response to Cinacalcet in Patients Undergoing Hemodialysis

Charcot-Marie-Tooth gene, SBF2, associated with taxane-induced peripheral neuropathy in African Americans

Contribution of the LRP5 gene to normal variation in peak BMD in women

Exome Sequencing Identifies Candidate Genetic Modifiers of Syndromic and Familial Thoracic Aortic Aneurysm Severity.

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

False positive rates in association studies as a function of degree of stratification

Fine mapping and expression of candidate genes within the chromosome 10 QTL region of the high and low alcohol-drinking rats

Genetic Influences on Plasma Homocysteine Levels in African Americans and Yoruba Nigerians

Genetic Variants Associated with Circulating Fibroblast Growth Factor 23

Genetic Variants Associated with Circulating Parathyroid Hormone

Genome screen in familial intracranial aneurysm

Genome screen to detect linkage to common susceptibility genes for intracranial and aortic aneurysms

Genome screen to detect linkage to intracranial aneurysm susceptibility genes: the Familial Intracranial Aneurysm (FIA) study

Genome-Wide Association Studies for Taxane-Induced Peripheral Neuropathy in ECOG-5103 and ECOG-1199.

Genome-Wide Association Study for Anthracycline-Induced Congestive Heart Failure

Genome-wide admixture mapping of DSM-IV alcohol dependence, criterion count, and the self-rating of the effects of ethanol in African American populations

Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population

Genome-wide association studies of alcohol dependence, DSM-IV criterion count and individual criteria

Genome-wide association studies of the self-rating of effects of ethanol (SRE)

Genome-wide association study identifies loci associated with liability to alcohol and drug dependence that is associated with variability in reward-related ventral striatum activity in African- and European-Americans

Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American women

Genome-wide association study of intracranial aneurysm identifies a new association on chromosome 7.

Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk

Genome-wide association study of serum iron phenotypes in premenopausal women of European descent

Genomewide SNP screen to detect quantitative trait loci for alcohol preference in the high alcohol preferring and low alcohol preferring mice

Human ALOX12, but Not ALOX15, Is Associated With BMD in White Men and Women

Identification of Functional Genetic Variants Associated with Alcohol Dependence and Related Phenotypes Using a High-Throughput Assay

Identification of a linkage disequilibrium block in chromosome 1q associated with BMD in premenopausal white women

Impact of Genetic Ancestry on Outcomes in ECOG-ACRIN-E5103

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

Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm

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

Meta-Analysis of Genetic Influences on Initial Alcohol Sensitivity

Meta-analysis of genome-wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women

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

Multi-omics integration analysis identifies novel genes for alcoholism with potential overlap with neurodegenerative diseases

Polymorphisms in the estrogen receptor beta (ESR2) gene are associated with bone mineral density in Caucasian men and women

Quantitative trait locus for body weight identified on rat chromosome 4 in inbred alcohol-preferring and -nonpreferring rats: potential implications for neuropeptide Y and corticotrophin releasing hormone 2

Replication of previous genome-wide association studies of bone mineral density in premenopausal American women

SIBLING family genes and bone mineral density: association and allele-specific expression in humans

Sex-specific quantitative trait loci contribute to normal variation in bone structure at the proximal femur in men

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

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

Steroid Pathway Genes and Neonatal Respiratory Distress After Betamethasone Use in Anticipated Preterm Birth

The Genetic Relationship Between Alcohol Consumption and Aspects of Problem Drinking in an Ascertained Sample

The relationship between smoking and replicated sequence variants on chromosomes 8 and 9 with familial intracranial aneurysm

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

Whole-Exome Sequencing in Familial Parkinson Disease