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Replicability and Prediction: Lessons and Challenges from GWAS

Trends in genetics, 2018-07, Vol.34 (7), p.504-517

2018

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High trans-ethnic replicability of GWAS results implies common causal variants

PLoS genetics, 2013-06, Vol.9 (6), p.e1003566-e1003566

2013

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The European Genome-phenome Archive of human data consented for biomedical research

Nature genetics, 2015-07, Vol.47 (7), p.692-695

2015

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Genetic and Clinical Factors Associated with Chronic Postsurgical Pain after Hernia Repair, Hysterectomy, and Thoracotomy: A Two-year Multicenter Cohort Study

Anesthesiology (Philadelphia), 2015-05, Vol.122 (5), p.1123-1141

2015

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Properties of human disease genes and the role of genes linked to Mendelian disorders in complex disease aetiology

Human molecular genetics, 2017-02, Vol.26 (3), p.489-500

2017

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Chimpanzee genomic diversity reveals ancient admixture with bonobos

Science (American Association for the Advancement of Science), 2016-10, Vol.354 (6311), p.477-481

2016

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Whole genome diversity of inherited chromosomally integrated HHV-6 derived from healthy individuals of diverse geographic origin

Scientific reports, 2018-02, Vol.8 (1), p.3472-13, Article 3472

2018

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Biological Processes Modulating Longevity across Primates: A Phylogenetic Genome-Phenome Analysis

Molecular biology and evolution, 2018-08, Vol.35 (8), p.1990-2004

2018

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Natural Selection in the Great Apes

Molecular biology and evolution, 2016-12, Vol.33 (12), p.3268-3283

2016

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Dynamics of DNA methylation in recent human and great ape evolution

PLoS genetics, 2013-09, Vol.9 (9), p.e1003763-e1003763

2013

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Combining Multiple Hypothesis Testing with Machine Learning Increases the Statistical Power of Genome-wide Association Studies

Scientific reports, 2016-11, Vol.6 (1), p.36671-36671, Article 36671

2016

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Transcriptional network analysis in frontal cortex in Lewy body diseases with focus on dementia with Lewy bodies

Brain pathology (Zurich, Switzerland), 2018-05, Vol.28 (3), p.315-333

2018

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267 Spanish Exomes Reveal Population-Specific Differences in Disease-Related Genetic Variation

Molecular biology and evolution, 2016-05, Vol.33 (5), p.1205-1218

2016

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A burst of segmental duplications in the genome of the African great ape ancestor

Nature, 2009-02, Vol.457 (7231), p.877-881

2009

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The impact of endogenous content, replicates and pooling on genome capture from faecal samples

Molecular ecology resources, 2018-03, Vol.18 (2), p.319-333

2018

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Genetic factors affecting EBV copy number in lymphoblastoid cell lines derived from the 1000 Genome Project samples

PloS one, 2017-06, Vol.12 (6), p.e0179446-e0179446

2017

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Genome-Wide Analysis of Wild-Type Epstein–Barr Virus Genomes Derived from Healthy Individuals of the 1000 Genomes Project

Genome biology and evolution, 2014-01, Vol.6 (4), p.846-860

2014

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Mendelian genes for Parkinson's disease contribute to the sporadic forms of the disease

Human molecular genetics, 2015-04, Vol.24 (7), p.2023-2034

2015

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Similar genomic proportions of copy number variation within gray wolves and modern dog breeds inferred from whole genome sequencing

BMC genomics, 2017-12, Vol.18 (1), p.977-977, Article 977

2017

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Transcriptional network analysis in frontal cortex in Lewy body diseases with focus on dementia with Lewy bodies

Brain pathology (Zurich, Switzerland), 2018-05

2018

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Copy number variation analysis in the great apes reveals species-specific patterns of structural variation

Genome research, 2011-10, Vol.21 (10), p.1626-1639

2011

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Differences in molecular evolutionary rates among microRNAs in the human and chimpanzee genomes

BMC genomics, 2016-07, Vol.17 (1), p.528-528, Article 528

2016

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New subtype of spinocerebellar ataxia with altered vertical eye movements mapping to chromosome 1p32

JAMA neurology, 2013-06, Vol.70 (6), p.764

2013

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Gorilla genome structural variation reveals evolutionary parallelisms with chimpanzee

Genome research, 2011-10, Vol.21 (10), p.1640-1649

2011

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Replicability and Prediction: Lessons and Challenges from GWAS

High trans-ethnic replicability of GWAS results implies common causal variants

The European Genome-phenome Archive of human data consented for biomedical research

Genetic and Clinical Factors Associated with Chronic Postsurgical Pain after Hernia Repair, Hysterectomy, and Thoracotomy: A Two-year Multicenter Cohort Study

Properties of human disease genes and the role of genes linked to Mendelian disorders in complex disease aetiology

Derived immune and ancestral pigmentation alleles in a 7,000-year-old Mesolithic European

Chimpanzee genomic diversity reveals ancient admixture with bonobos

Whole genome diversity of inherited chromosomally integrated HHV-6 derived from healthy individuals of diverse geographic origin

Biological Processes Modulating Longevity across Primates: A Phylogenetic Genome-Phenome Analysis

Natural Selection in the Great Apes

Dynamics of DNA methylation in recent human and great ape evolution

Combining Multiple Hypothesis Testing with Machine Learning Increases the Statistical Power of Genome-wide Association Studies

Transcriptional network analysis in frontal cortex in Lewy body diseases with focus on dementia with Lewy bodies

267 Spanish Exomes Reveal Population-Specific Differences in Disease-Related Genetic Variation

A burst of segmental duplications in the genome of the African great ape ancestor

The impact of endogenous content, replicates and pooling on genome capture from faecal samples

Genetic factors affecting EBV copy number in lymphoblastoid cell lines derived from the 1000 Genome Project samples

Genome-Wide Analysis of Wild-Type Epstein–Barr Virus Genomes Derived from Healthy Individuals of the 1000 Genomes Project

Mendelian genes for Parkinson's disease contribute to the sporadic forms of the disease

Similar genomic proportions of copy number variation within gray wolves and modern dog breeds inferred from whole genome sequencing

Transcriptional network analysis in frontal cortex in Lewy body diseases with focus on dementia with Lewy bodies

Copy number variation analysis in the great apes reveals species-specific patterns of structural variation

Differences in molecular evolutionary rates among microRNAs in the human and chimpanzee genomes

New subtype of spinocerebellar ataxia with altered vertical eye movements mapping to chromosome 1p32

Gorilla genome structural variation reveals evolutionary parallelisms with chimpanzee

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