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

Genetic epidemiology, 1993, Vol.10 (6), p.389-394

1993

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Strategies for phasing and imputation in a population isolate

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

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

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

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

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

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

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

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