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Genetic architecture: the shape of the genetic contribution to human traits and disease

Nature reviews. Genetics, 2018-02, Vol.19 (2), p.110-124

2018

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Vitamin D and Risk of Multiple Sclerosis: A Mendelian Randomization Study

PLoS medicine, 2015-08, Vol.12 (8), p.e1001866-e1001866

2015

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Germline and somatic FGFR1 abnormalities in dysembryoplastic neuroepithelial tumors

Acta neuropathologica, 2016-06, Vol.131 (6), p.847-863

2016

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A Review of the Epigenetic Clock: Emerging Biomarkers for Asthma and Allergic Disease

Genes, 2023-08, Vol.14 (9), p.1724

2023

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Improved prediction of fracture risk leveraging a genome-wide polygenic risk score

Genome medicine, 2021-02, Vol.13 (1), p.16-15, Article 16

2021

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The empirical power of rare variant association methods: results from sanger sequencing in 1,998 individuals

PLoS genetics, 2012-02, Vol.8 (2), p.e1002496-e1002496

2012

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Polygenic risk for coronary heart disease acts through atherosclerosis in type 2 diabetes

Cardiovascular diabetology, 2020-01, Vol.19 (1), p.12-12, Article 12

2020

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Identifying Differential Methylation in Cancer Epigenetics via a Bayesian Functional Regression Model

Biomolecules (Basel, Switzerland), 2024-06, Vol.14 (6), p.639

2024

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Estimating Genome-Wide Significance for Whole-Genome Sequencing Studies

Genetic epidemiology, 2014-05, Vol.38 (4), p.281-290

2014

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A region-based gene association study combined with a leave-one-out sensitivity analysis identifies SMG1 as a pancreatic cancer susceptibility gene

PLoS genetics, 2019-08, Vol.15 (8), p.e1008344-e1008344

2019

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PRS-on-Spark (PRSoS): a novel, efficient and flexible approach for generating polygenic risk scores

BMC bioinformatics, 2018-08, Vol.19 (1), p.295-295, Article 295

2018

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The performance of a new local false discovery rate method on tests of association between coronary artery disease (CAD) and genome-wide genetic variants

PloS one, 2017-09, Vol.12 (9), p.e0185174-e0185174

2017

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Novel insights into systemic sclerosis using a sensitive computational method to analyze whole-genome bisulfite sequencing data

Clinical epigenetics, 2023-06, Vol.15 (1), p.96-96, Article 96

2023

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Capturing additional genetic risk from family history for improved polygenic risk prediction

Communications biology, 2022-06, Vol.5 (1), p.595-11, Article 595

2022

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Functional normalization of 450k methylation array data improves replication in large cancer studies

Genome biology, 2014-12, Vol.15 (12), p.503-503, Article 503

2014

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Statistical power in COVID-19 case-control host genomic study design

Genome medicine, 2020-12, Vol.12 (1), p.115-8, Article 115

2020

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Individuals with common diseases but with a low polygenic risk score could be prioritized for rare variant screening

Genetics in medicine, 2021-03, Vol.23 (3), p.508-515

2021

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MDiNE: a model to estimate differential co-occurrence networks in microbiome studies

Bioinformatics, 2020-03, Vol.36 (6), p.1840-1847

2020

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An evaluation of methods correcting for cell-type heterogeneity in DNA methylation studies

Genome Biology, 2016-05, Vol.17 (1), p.84-84, Article 84

2016

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Chromosome-breakage genomic instability and chromothripsis in breast cancer

BMC genomics, 2014-07, Vol.15 (1), p.579-579

2014

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utility and predictive value of combinations of low penetrance genes for screening and risk prediction of colorectal cancer

Human genetics, 2010-07, Vol.128 (1), p.89-101

2010

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The genomic landscape of TP53 and p53 annotated high grade ovarian serous carcinomas from a defined founder population associated with patient outcome

PloS one, 2012-09, Vol.7 (9), p.e45484-e45484

2012

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Dementia with Lewy bodies post-mortem brains reveal differentially methylated CpG sites with biomarker potential

Communications biology, 2022-11, Vol.5 (1), p.1279-11, Article 1279

2022

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Genetic architecture: the shape of the genetic contribution to human traits and disease

Vitamin D and Risk of Multiple Sclerosis: A Mendelian Randomization Study

Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study

Germline and somatic FGFR1 abnormalities in dysembryoplastic neuroepithelial tumors

A Review of the Epigenetic Clock: Emerging Biomarkers for Asthma and Allergic Disease

Improved prediction of fracture risk leveraging a genome-wide polygenic risk score

The empirical power of rare variant association methods: results from sanger sequencing in 1,998 individuals

Polygenic risk for coronary heart disease acts through atherosclerosis in type 2 diabetes

Identifying Differential Methylation in Cancer Epigenetics via a Bayesian Functional Regression Model

Estimating Genome-Wide Significance for Whole-Genome Sequencing Studies

A region-based gene association study combined with a leave-one-out sensitivity analysis identifies SMG1 as a pancreatic cancer susceptibility gene

PRS-on-Spark (PRSoS): a novel, efficient and flexible approach for generating polygenic risk scores

A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene

The performance of a new local false discovery rate method on tests of association between coronary artery disease (CAD) and genome-wide genetic variants

Novel insights into systemic sclerosis using a sensitive computational method to analyze whole-genome bisulfite sequencing data

Capturing additional genetic risk from family history for improved polygenic risk prediction

Functional normalization of 450k methylation array data improves replication in large cancer studies

Statistical power in COVID-19 case-control host genomic study design

Individuals with common diseases but with a low polygenic risk score could be prioritized for rare variant screening

MDiNE: a model to estimate differential co-occurrence networks in microbiome studies

An evaluation of methods correcting for cell-type heterogeneity in DNA methylation studies

Chromosome-breakage genomic instability and chromothripsis in breast cancer

utility and predictive value of combinations of low penetrance genes for screening and risk prediction of colorectal cancer

The genomic landscape of TP53 and p53 annotated high grade ovarian serous carcinomas from a defined founder population associated with patient outcome

Dementia with Lewy bodies post-mortem brains reveal differentially methylated CpG sites with biomarker potential

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