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

European journal of epidemiology, 2016-03, Vol.31 (3), p.229-245

2016

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Strategies for phasing and imputation in a population isolate

Genetic epidemiology, 2018-03, Vol.42 (2), p.201-213

2018

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Interactive effect between ATPase-related genes and early-life tobacco smoke exposure on bronchial hyper-responsiveness detected in asthma-ascertained families

Thorax, 2019-03, Vol.74 (3), p.254-260

2019

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High level of inbreeding in final phase of 1000 Genomes Project

Scientific reports, 2015-12, Vol.5 (1), p.17453-17453, Article 17453

2015

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Homozygous STIL mutation causes holoprosencephaly and microcephaly in two siblings

PloS one, 2015-02, Vol.10 (2), p.e0117418-e0117418

2015

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A New Correction for Multiple Testing in Gene–Gene Interaction Studies

Annals of human genetics, 2015-09, Vol.79 (5), p.380-384

2015

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

International journal of epidemiology, 2017-02, Vol.46 (1), p.57-74

2017

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

PloS one, 2012-10, Vol.7 (10), p.e46519-e46519

2012

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FSuite: exploiting inbreeding in dense SNP chip and exome data

Bioinformatics (Oxford, England), 2014-07, Vol.30 (13), p.1940-1941

2014

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

Genetic epidemiology, 2012-12, Vol.36 (8), p.848-855

2012

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Meta and pooled analysis of European coeliac disease data

European journal of human genetics : EJHG, 2003-11, Vol.11 (11), p.828-834

2003

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

European journal of human genetics : EJHG, 2016-04, Vol.24 (4), p.581-586

2016

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Genetic Association and Gene-Environment Interaction: A New Method for Overcoming the Lack of Exposure Information in Controls

American journal of epidemiology, 2011-01, Vol.173 (2), p.225-235

2011

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

Human genetics, 2007-11, Vol.122 (3-4), p.261-273

2007

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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

Carcinogenesis (New York), 2014-07, Vol.35 (7), p.1523-1527

2014

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The ordered transmission disequilibrium test: detection of modifier genes

Genetic epidemiology, 2009-01, Vol.33 (1), p.1-5

2009

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

Annals of neurology, 2003-07, Vol.54 (1), p.119-122

2003

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

Carcinogenesis (New York), 2012-05, Vol.33 (5), p.1059-1064

2012

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

Nature genetics, 1994-11, Vol.8 (3), p.264-268

1994

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

European journal of human genetics : EJHG, 2012-03, Vol.20 (3), p.321-325

2012

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

European journal of human genetics : EJHG, 2009-06, Vol.17 (6), p.844-847

2009

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Could Inbred Cases Identified in GWAS Data Succeed in Detecting Rare Recessive Variants Where Affected Sib-Pairs Have Failed?

Human heredity, 2012-01, Vol.74 (3/4), p.142-152

2012

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

Genetic epidemiology, 2007, Vol.31 (S1), p.S86-S95

2007

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Meta-Analysis of Genome-Wide Linkage Studies in Celiac Disease

Human heredity, 2009-01, Vol.68 (4), p.223-230

2009

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

Strategies for phasing and imputation in a population isolate

Interactive effect between ATPase-related genes and early-life tobacco smoke exposure on bronchial hyper-responsiveness detected in asthma-ascertained families

High level of inbreeding in final phase of 1000 Genomes Project

Pleiotropic Effects of CEP290 ( NPHP6) Mutations Extend to Meckel Syndrome

Homozygous STIL mutation causes holoprosencephaly and microcephaly in two siblings

A New Correction for Multiple Testing in Gene–Gene Interaction Studies

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

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

FSuite: exploiting inbreeding in dense SNP chip and exome data

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

Meta and pooled analysis of European coeliac disease data

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

Genetic Association and Gene-Environment Interaction: A New Method for Overcoming the Lack of Exposure Information in Controls

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

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

The ordered transmission disequilibrium test: detection of modifier genes

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

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

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

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

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

Could Inbred Cases Identified in GWAS Data Succeed in Detecting Rare Recessive Variants Where Affected Sib-Pairs Have Failed?

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

Meta-Analysis of Genome-Wide Linkage Studies in Celiac Disease

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