Lista de obras - Marie-Claude Babron - Dominio Público Uruguay

A New Correction for Multiple Testing in Gene-Gene Interaction Studies.

artículo científico publicado en 2015

A novel locus for autosomal dominant “uncomplicated” hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3

A second locus for Marfan syndrome maps to chromosome 3p24.2-p25.

artículo científico publicado en 1994

A systematic study of oligodendrocyte growth factors as candidates for genetic susceptibility to MS

artículo científico publicado en 1998

An ordered subset approach to including covariates in the transmission disequilibrium test

artículo científico publicado en 2007

Antiphospholipid antibodies in patients with childhood onset systemic lupus erythematosus and their relatives. A French cooperative study

article

Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sex

artículo científico publicado en 1997

Apolipoprotein E-epsilon 4 allele and Alzheimer's disease

artículo científico publicado en 1993

Assessing the effect of multiple linkage tests in complex diseases.

artículo científico publicado en 1990

Autosomal dominant Marfan-like connective-tissue disorder with aortic dilation and skeletal anomalies not linked to the fibrillin genes

artículo científico publicado en 1993

Can whole-exome sequencing data be used for linkage analysis?

artículo científico publicado en 2015

Caution in the interpretation of MLS

artículo científico publicado en 1997

Chromosome 17q22–q24 and multiple sclerosis genetic susceptibility

article

Clinical and demographic factors and outcome of amyotrophic lateral sclerosis in relation to population ancestral origin.

artículo científico

Comparative Power of Family-Based Association Strategies to Detect Disease-Causing Variants Under Two-Locus Models

artículo científico publicado en 2012

Comparing the power of linkage detection by the transmission disequilibrium test and the identity-by-descent test

article

Could inbred cases identified in GWAS data succeed in detecting rare recessive variants where affected sib-pairs have failed?

artículo científico publicado en 2012

Cytokines in genetic susceptibility to multiple sclerosis: a candidate gene approach. French Multiple Sclerosis Genetics Group.

artículo científico publicado en 2000

Detection of susceptibility loci by genome-wide linkage analysis

artículo científico publicado en 2005

Determination of the real effect of genes identified in GWAS: the example of IL2RA in multiple sclerosis

artículo científico publicado en 2011

Discrimination between genetic models for insulin dependent diabetes mellitus

artículo científico publicado en 1986

Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families

artículo científico publicado en 2001

FSuite: exploiting inbreeding in dense SNP chip and exome data

artículo científico publicado en 2014

Failure to replicate linkage between chromosome 5q11-q13 markers and schizophrenia in 28 families

artículo científico publicado en 1992

Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci

artículo científico publicado en 2007

Genetic analysis of multiple sclerosis in Europeans: French data

artículo científico publicado en 2003

Genetic association and gene-environment interaction: a new method for overcoming the lack of exposure information in controls.

artículo científico publicado en 2010

Genetic interaction of CTLA-4 with HLA-DR15 in multiple sclerosis patients

artículo científico publicado en 2003

Genetic variants in DNA repair pathways and risk of upper aerodigestive tract cancers: combined analysis of data from two genome-wide association studies in European populations

artículo científico publicado en 2014

Genome search in celiac disease.

artículo científico publicado en 1998

HLA-DQ relative risks for coeliac disease in European populations: a study of the European Genetics Cluster on Coeliac Disease.

artículo científico publicado en 2004

HLA-DRB1*15 allele influences the later course of relapsing remitting multiple sclerosis

article

HLA-associated diseases: a new method for performing linkage analysis with other markers than HLA.

artículo científico publicado en 1984

Hereditary retinoblastoma: can balanced insertion entirely explain the differences of expressivity among families?

artículo científico publicado en 1990

Heterogeneity of marker allele frequencies hinders interpretation of linkage analysis: Illustration on chromosome 18 markers ⬇️

artículo científico publicado el 1 de enero de 1997

High level of inbreeding in final phase of 1000 Genomes Project

artículo científico publicado en 2015

High risk genotypes for celiac disease

artículo científico publicado en 1994

Homogeneity of asthma genome scan results.

artículo científico publicado en 2001

Homozygous STIL mutation causes holoprosencephaly and microcephaly in two siblings

artículo científico publicado en 2015

IFIH1-GCA-KCNH7 locus is not associated with genetic susceptibility to multiple sclerosis in French patients

artículo científico publicado en 2009

IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations.

artículo científico publicado en 2008

Impact of the diagnosis definition on linkage detection

artículo científico publicado en 2005

Interactive effect of two candidate genes in a disease: extension of the marker-association-segregation chi(2) method.

artículo científico publicado en 1994

Introduction: Heterogeneity

artículo científico publicado en 2001

Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study

artículo científico publicado en 2003

Investigation of the HLA component involved in rheumatoid arthritis (RA) by using the marker association-segregation chi-square (MASC) method: rejection of the unifying-shared-epitope hypothesis ⬇️

artículo científico publicado el 1 de septiembre de 1993

Is a single mutation at the same locus responsible for all affected cases in a large Alzheimer pedigree (FAD4)?

artículo científico publicado en 1993

Lack of Correlation Between Genotype and Phenotype in Celiac Disease ⬇️

artículo científico publicado el 1 de marzo de 1998

Letter to the Editor: No evidence for association between the EIF2B5 gene and multiple sclerosis in French families

article

Linkage analyses of rheumatoid arthritis and related quantitative phenotypes: the GAW15 experience

artículo científico publicado en 2007

Linkage and association study of the CTLA-4 region in coeliac disease for Italian and Tunisian populations.

artículo científico publicado en 1999

Linkage detection by the Affected-Pedigree-Member method: what is really tested?

artículo científico publicado en 1993

Lung cancer and DNA repair genes: multilevel association analysis from the International Lung Cancer Consortium

artículo científico publicado en 2012

Manic depressive illness is linked to factor IX in a French pedigree.

artículo científico publicado en 1992

Meta and pooled analysis of European coeliac disease data

artículo científico publicado en 2003

Meta-analysis of genome-wide linkage studies in celiac disease

artículo científico publicado en 2009

Modeling the effect of a genetic factor for a complex trait in a simulated population

artículo científico publicado en 2005

Modeling the role of two susceptibility loci by the MASC method

scientific article published on 01 January 1995

No effect of the alpha1-antichymotrypsin A allele in Alzheimer's disease

artículo científico publicado en 1997

On the choice of linkage statistics

artículo científico publicado en 2007

Pleiotropic effects of CEP290 (NPHP6) mutations extend to Meckel syndrome

artículo científico publicado en 2007

Rare and low frequency variant stratification in the UK population: description and impact on association tests.

artículo científico publicado en 2012

Saturation of the 5q31-q33 Candidate Region for Coeliac Disease

artículo científico publicado en 2003

Segregation analysis of Alzheimer pedigrees: rare Mendelian dominant mutation(s) explain a minority of early-onset cases. French Alzheimer Collaborative Group.

artículo científico publicado en 1996

Strategies for phasing and imputation in a population isolate.

artículo científico publicado en 2018

Study of two ectopeptidases in the susceptibility to celiac disease: two newly identified polymorphisms of dipeptidylpeptidase IV.

artículo científico publicado en 2000

Susceptibility to coeliac disease in Tunisian children and GM immunoglobulin allotypes.

artículo científico publicado en 1999

Synergistic effect of two HLA heterodimers in the susceptibility to celiac disease in Tunisia ⬇️

artículo científico publicado el 1 de enero de 1997

Systematic search of susceptibility loci with methods using gametic disequilibrium

scientific article published on 01 January 1995

The COL5A3 and MMP9 genes interact in eczema susceptibility.

artículo científico publicado en 2017

The Gm-Pi linkage in 843 French families: effect of the alleles Pi Z and Pi S

article

The ordered transmission disequilibrium test: detection of modifier genes

article

Triangle Test Statistic in Discordant Sib Pairs: Test of Genetic Heterogeneity of Asthma and Atopy in CSGA Families

artículo científico publicado en 2001

Variation in worldwide incidence of amyotrophic lateral sclerosis: a meta-analysis

artículo científico publicado en 2016

[Unfavorable outcomes in disseminated lupus erythematosus in children. Cooperative study in the Paris region]

artículo científico publicado en 1991

Lista de obras de Marie-Claude Babron

A New Correction for Multiple Testing in Gene-Gene Interaction Studies.

A novel locus for autosomal dominant “uncomplicated” hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3

A second locus for Marfan syndrome maps to chromosome 3p24.2-p25.

A systematic study of oligodendrocyte growth factors as candidates for genetic susceptibility to MS

An ordered subset approach to including covariates in the transmission disequilibrium test

Antiphospholipid antibodies in patients with childhood onset systemic lupus erythematosus and their relatives. A French cooperative study

Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sex

Apolipoprotein E-epsilon 4 allele and Alzheimer's disease

Assessing the effect of multiple linkage tests in complex diseases.

Autosomal dominant Marfan-like connective-tissue disorder with aortic dilation and skeletal anomalies not linked to the fibrillin genes

Can whole-exome sequencing data be used for linkage analysis?

Caution in the interpretation of MLS

Chromosome 17q22–q24 and multiple sclerosis genetic susceptibility

Clinical and demographic factors and outcome of amyotrophic lateral sclerosis in relation to population ancestral origin.

Comparative Power of Family-Based Association Strategies to Detect Disease-Causing Variants Under Two-Locus Models

Comparing the power of linkage detection by the transmission disequilibrium test and the identity-by-descent test

Could inbred cases identified in GWAS data succeed in detecting rare recessive variants where affected sib-pairs have failed?

Cytokines in genetic susceptibility to multiple sclerosis: a candidate gene approach. French Multiple Sclerosis Genetics Group.

Detection of susceptibility loci by genome-wide linkage analysis

Determination of the real effect of genes identified in GWAS: the example of IL2RA in multiple sclerosis

Discrimination between genetic models for insulin dependent diabetes mellitus

Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families

FSuite: exploiting inbreeding in dense SNP chip and exome data

Failure to replicate linkage between chromosome 5q11-q13 markers and schizophrenia in 28 families

Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci

Genetic analysis of multiple sclerosis in Europeans: French data

Genetic association and gene-environment interaction: a new method for overcoming the lack of exposure information in controls.

Genetic interaction of CTLA-4 with HLA-DR15 in multiple sclerosis patients

Genetic variants in DNA repair pathways and risk of upper aerodigestive tract cancers: combined analysis of data from two genome-wide association studies in European populations

Genome search in celiac disease.

HLA-DQ relative risks for coeliac disease in European populations: a study of the European Genetics Cluster on Coeliac Disease.

HLA-DRB1*15 allele influences the later course of relapsing remitting multiple sclerosis

HLA-associated diseases: a new method for performing linkage analysis with other markers than HLA.

Hereditary retinoblastoma: can balanced insertion entirely explain the differences of expressivity among families?

Heterogeneity of marker allele frequencies hinders interpretation of linkage analysis: Illustration on chromosome 18 markers ⬇️

High level of inbreeding in final phase of 1000 Genomes Project

High risk genotypes for celiac disease

Homogeneity of asthma genome scan results.

Homozygous STIL mutation causes holoprosencephaly and microcephaly in two siblings

IFIH1-GCA-KCNH7 locus is not associated with genetic susceptibility to multiple sclerosis in French patients

IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations.

Impact of the diagnosis definition on linkage detection

Interactive effect of two candidate genes in a disease: extension of the marker-association-segregation chi(2) method.

Introduction: Heterogeneity

Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study

Investigation of the HLA component involved in rheumatoid arthritis (RA) by using the marker association-segregation chi-square (MASC) method: rejection of the unifying-shared-epitope hypothesis ⬇️

Is a single mutation at the same locus responsible for all affected cases in a large Alzheimer pedigree (FAD4)?

Lack of Correlation Between Genotype and Phenotype in Celiac Disease ⬇️

Letter to the Editor: No evidence for association between the EIF2B5 gene and multiple sclerosis in French families

Linkage analyses of rheumatoid arthritis and related quantitative phenotypes: the GAW15 experience

Linkage and association study of the CTLA-4 region in coeliac disease for Italian and Tunisian populations.

Linkage detection by the Affected-Pedigree-Member method: what is really tested?

Lung cancer and DNA repair genes: multilevel association analysis from the International Lung Cancer Consortium

Manic depressive illness is linked to factor IX in a French pedigree.

Meta and pooled analysis of European coeliac disease data

Meta-analysis of genome-wide linkage studies in celiac disease

Modeling the effect of a genetic factor for a complex trait in a simulated population

Modeling the role of two susceptibility loci by the MASC method

No effect of the alpha1-antichymotrypsin A allele in Alzheimer's disease

On the choice of linkage statistics

Pleiotropic effects of CEP290 (NPHP6) mutations extend to Meckel syndrome

Rare and low frequency variant stratification in the UK population: description and impact on association tests.

Saturation of the 5q31-q33 Candidate Region for Coeliac Disease

Segregation analysis of Alzheimer pedigrees: rare Mendelian dominant mutation(s) explain a minority of early-onset cases. French Alzheimer Collaborative Group.

Strategies for phasing and imputation in a population isolate.

Study of two ectopeptidases in the susceptibility to celiac disease: two newly identified polymorphisms of dipeptidylpeptidase IV.

Susceptibility to coeliac disease in Tunisian children and GM immunoglobulin allotypes.

Synergistic effect of two HLA heterodimers in the susceptibility to celiac disease in Tunisia ⬇️

Systematic search of susceptibility loci with methods using gametic disequilibrium

The COL5A3 and MMP9 genes interact in eczema susceptibility.

The Gm-Pi linkage in 843 French families: effect of the alleles Pi Z and Pi S

The ordered transmission disequilibrium test: detection of modifier genes

Triangle Test Statistic in Discordant Sib Pairs: Test of Genetic Heterogeneity of Asthma and Atopy in CSGA Families

Variation in worldwide incidence of amyotrophic lateral sclerosis: a meta-analysis

[Unfavorable outcomes in disseminated lupus erythematosus in children. Cooperative study in the Paris region]