List of works - Alexandre Bureau

A genome-wide association study of suicidal behavior

scientific article published on 16 June 2015

A genome-wide copy number variant study of suicidal behavior

scientific article published on 26 May 2015

A multimodal attempt to follow-up linkage regions using RNA expression, SNPs and CpG methylation in schizophrenia and bipolar disorder kindreds

scientific article published on 06 November 2019

A new strategy for linkage analysis under epistasis taking into account genetic heterogeneity

scientific article published on 22 July 2009

An Assessment of Gene-by-Environment Interactions in Developmental Dyslexia-Related Phenotypes

article

An S-Plus Implementation of Hidden Markov Models in Continuous Time

An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypes

scientific article published on 24 November 2012

Application of microarray outlier detection methodology to psychiatric research

scientific article

Applications of continuous time hidden Markov models to the study of misclassified disease outcomes

scientific article

Association of polyaminergic loci with anxiety, mood disorders, and attempted suicide

scientific article

Association with replication between estrogen-related receptor gamma (ESRRgamma) polymorphisms and bone phenotypes in women of European ancestry

scientific article published in April 2010

Chromosome 13q13-q14 locus overlaps mood and psychotic disorders: the relevance for redefining phenotype

scientific article published on 28 January 2009

Considerations for the development of a reference method for sequencing of haploid DNA – an opinion paper on behalf of the IFCC Committee on Molecular Diagnostics. International Federation of Clinical Chemistry and Laboratory Medicine

article

Detection of Phenotype Modifier Genes Using Two-Locus Linkage Analysis in Complex Disorders Such as Major Psychosis

article

Differences and similarities in the serotonergic diathesis for suicide attempts and mood disorders: a 22-year longitudinal gene-environment study

scientific article published on 21 April 2009

Differential RNA expression between schizophrenic patients and controls of the dystrobrevin binding protein 1 and neuregulin 1 genes in immortalized lymphocytes

scientific article published on 30 January 2008

Estimating Interaction Between Genetic and Environmental Risk Factors

article

Estimating genetic effect sizes under joint disease-endophenotype models in presence of gene-environment interactions

scientific article published on 28 July 2015

Evidence for a novel glaucoma locus at chromosome 3p21-22

article

Extension of the generalized disequilibrium test to polytomous phenotypes and two-locus models

scientific article published on 8 August 2014

Follow-up of a major psychosis linkage site in 13q13-q14 reveals significant association in both case-control and family samples

scientific article

Genome-wide epigenetic regulation by early-life trauma.

scientific article published on July 2012

Global gene expression profiling of the polyamine system in suicide completers

scientific article published on 6 January 2011

High-density polymorphisms analysis of 23 candidate genes for association with bone mineral density

scientific article

Homozygous deletion of the very low density lipoprotein receptor gene causes autosomal recessive cerebellar hypoplasia with cerebral gyral simplification

scientific article

Identifying SNPs predictive of phenotype using random forests

scientific article published on 01 February 2005

Impulsive-aggressive behaviours and completed suicide across the life cycle: a predisposition for younger age of suicide.

scientific article published on 6 September 2007

Inferring Disease Risk Genes from Sequencing Data in Multiplex Pedigrees Through Sharing of Rare Variants

article

Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants

article

Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives

scientific article

Integration of Genetic Familial Dependence Structure in Latent Class Models

Latent class model with familial dependence to address heterogeneity in complex diseases: adapting the approach to family-based association studies

scientific article published on 09 February 2011

Mapping complex traits using Random Forests

scientific article

Pedigree selection and tests of linkage in a Hutterite asthma pedigree.

scientific article published on January 2001

Plasma polychlorinated biphenyl and organochlorine pesticide concentrations in dementia: the Canadian Study of Health and Aging

scientific article published on 20 May 2014

Polychlorinated biphenyls and organochlorine pesticides in plasma of older Canadians.

scientific article published on 14 October 2011

Polygenic risk scores distinguish patients from non-affected adult relatives and from normal controls in schizophrenia and bipolar disorder multi-affected kindreds

scientific article published on 28 November 2017

Profiling brain expression of the spermidine/spermine N1-acetyltransferase 1 (SAT1) gene in suicide

scientific article published in October 2009

Replication of linkage with bipolar disorder on chromosome 16p in the eastern Quebec population

scientific article published on 01 September 2008

Solving genetic heterogeneity in extended families by identifying sub-types of complex diseases

Symptom dimensions as alternative phenotypes to address genetic heterogeneity in schizophrenia and bipolar disorder

scientific article published on 25 April 2012

UGT2B17 gene deletion associated with an increase in bone mineral density similar to the effect of hormone replacement in postmenopausal women

article

Using disease symptoms to improve detection of linkage under genetic heterogeneity

scientific article

Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts

scientific article

List of works by Alexandre Bureau

A genome-wide association study of suicidal behavior

A genome-wide copy number variant study of suicidal behavior

A multimodal attempt to follow-up linkage regions using RNA expression, SNPs and CpG methylation in schizophrenia and bipolar disorder kindreds

A new strategy for linkage analysis under epistasis taking into account genetic heterogeneity

An Assessment of Gene-by-Environment Interactions in Developmental Dyslexia-Related Phenotypes

An S-Plus Implementation of Hidden Markov Models in Continuous Time

An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypes

Application of microarray outlier detection methodology to psychiatric research

Applications of continuous time hidden Markov models to the study of misclassified disease outcomes

Association of polyaminergic loci with anxiety, mood disorders, and attempted suicide

Association with replication between estrogen-related receptor gamma (ESRRgamma) polymorphisms and bone phenotypes in women of European ancestry

Chromosome 13q13-q14 locus overlaps mood and psychotic disorders: the relevance for redefining phenotype

Considerations for the development of a reference method for sequencing of haploid DNA – an opinion paper on behalf of the IFCC Committee on Molecular Diagnostics. International Federation of Clinical Chemistry and Laboratory Medicine

Detection of Phenotype Modifier Genes Using Two-Locus Linkage Analysis in Complex Disorders Such as Major Psychosis

Differences and similarities in the serotonergic diathesis for suicide attempts and mood disorders: a 22-year longitudinal gene-environment study

Differential RNA expression between schizophrenic patients and controls of the dystrobrevin binding protein 1 and neuregulin 1 genes in immortalized lymphocytes

Estimating Interaction Between Genetic and Environmental Risk Factors

Estimating genetic effect sizes under joint disease-endophenotype models in presence of gene-environment interactions

Evidence for a novel glaucoma locus at chromosome 3p21-22

Extension of the generalized disequilibrium test to polytomous phenotypes and two-locus models

Follow-up of a major psychosis linkage site in 13q13-q14 reveals significant association in both case-control and family samples

Genome-wide epigenetic regulation by early-life trauma.

Global gene expression profiling of the polyamine system in suicide completers

High-density polymorphisms analysis of 23 candidate genes for association with bone mineral density

Homozygous deletion of the very low density lipoprotein receptor gene causes autosomal recessive cerebellar hypoplasia with cerebral gyral simplification

Identifying SNPs predictive of phenotype using random forests

Impulsive-aggressive behaviours and completed suicide across the life cycle: a predisposition for younger age of suicide.

Inferring Disease Risk Genes from Sequencing Data in Multiplex Pedigrees Through Sharing of Rare Variants

Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants

Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives

Integration of Genetic Familial Dependence Structure in Latent Class Models

Latent class model with familial dependence to address heterogeneity in complex diseases: adapting the approach to family-based association studies

Mapping complex traits using Random Forests

Pedigree selection and tests of linkage in a Hutterite asthma pedigree.

Plasma polychlorinated biphenyl and organochlorine pesticide concentrations in dementia: the Canadian Study of Health and Aging

Polychlorinated biphenyls and organochlorine pesticides in plasma of older Canadians.

Polygenic risk scores distinguish patients from non-affected adult relatives and from normal controls in schizophrenia and bipolar disorder multi-affected kindreds

Profiling brain expression of the spermidine/spermine N1-acetyltransferase 1 (SAT1) gene in suicide

Replication of linkage with bipolar disorder on chromosome 16p in the eastern Quebec population

Solving genetic heterogeneity in extended families by identifying sub-types of complex diseases

Symptom dimensions as alternative phenotypes to address genetic heterogeneity in schizophrenia and bipolar disorder

UGT2B17 gene deletion associated with an increase in bone mineral density similar to the effect of hormone replacement in postmenopausal women

Using disease symptoms to improve detection of linkage under genetic heterogeneity

Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts