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An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci

Nature genetics, 2021-11, Vol.53 (11), p.1527-1533

2021

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Atlas of plasma NMR biomarkers for health and disease in 118,461 individuals from the UK Biobank

Nature communications, 2023-02, Vol.14 (1), p.604-604, Article 604

2023

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Haploview: Visualization and analysis of SNP genotype data

Cold Spring Harbor protocols, 2009-10, Vol.2009 (10), p.pdb.ip71

Barrett, Jeffrey C

2009

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Common genetic variants contribute to risk of rare severe neurodevelopmental disorders

Nature (London), 2018-10, Vol.562 (7726), p.268-271

2018

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De novo mutations in regulatory elements in neurodevelopmental disorders

Nature (London), 2018-03, Vol.555 (7698), p.611-616

2018

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Evaluating coverage of genome-wide association studies

Nature genetics, 2006-06, Vol.38 (6), p.659-662

2006

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How next-generation sequencing is transforming complex disease genetics

Trends in genetics, 2013-01, Vol.29 (1), p.23-30

2013

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Synthetic associations are unlikely to account for many common disease genome-wide association signals

PLoS biology, 2011-01, Vol.9 (1), p.e1000580-e1000580

2011

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Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci

Nature genetics, 2008-12, Vol.40 (12), p.1399-1401

2008

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Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania

PloS one, 2014-11, Vol.9 (11), p.e111464-e111464

2014

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Variation at Spike position 142 in SARS-CoV-2 Delta genomes is a technical artifact caused by dropout of a sequencing amplicon

Wellcome open research, 2021, Vol.6, p.305-305

2021

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Common deletion polymorphisms in the human genome

Nature genetics, 2006-01, Vol.38 (1), p.86-92

2006

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Strategies for fine-mapping complex traits

Human molecular genetics, 2015-10, Vol.24 (R1), p.R111-R119

2015

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Genetic risk prediction in complex disease

Human molecular genetics, 2011-10, Vol.20 (2), p.R182-R188

2011

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Using genetic prediction from known complex disease Loci to guide the design of next-generation sequencing experiments

PloS one, 2013-10, Vol.8 (10), p.e76328-e76328

2013

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Understanding inflammatory bowel disease via immunogenetics

Journal of autoimmunity, 2015-11, Vol.64, p.91-100

2015

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Covid-19 Vaccine Effectiveness against the Omicron (B.1.1.529) Variant

The New England journal of medicine, 2022-04, Vol.386 (16), p.1532-1546

2022

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Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders

Genetics in medicine, 2018-10, Vol.20 (10), p.1216-1223

2018

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Evoker: a visualization tool for genotype intensity data

Bioinformatics, 2010-07, Vol.26 (14), p.1786-1787

2010

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The zebrafish reference genome sequence and its relationship to the human genome

Nature (London), 2013-04, Vol.496 (7446), p.498-503

2013

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The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability

Nature genetics, 2017-08, Vol.49 (8), p.1167-1173

2017

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An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci

Atlas of plasma NMR biomarkers for health and disease in 118,461 individuals from the UK Biobank

Haploview: Visualization and analysis of SNP genotype data

Common genetic variants contribute to risk of rare severe neurodevelopmental disorders

De novo mutations in regulatory elements in neurodevelopmental disorders

Evaluating coverage of genome-wide association studies

Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7

How next-generation sequencing is transforming complex disease genetics

Synthetic associations are unlikely to account for many common disease genome-wide association signals

Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci

Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania

Variation at Spike position 142 in SARS-CoV-2 Delta genomes is a technical artifact caused by dropout of a sequencing amplicon

Common deletion polymorphisms in the human genome

Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes

Strategies for fine-mapping complex traits

Genetic risk prediction in complex disease

Using genetic prediction from known complex disease Loci to guide the design of next-generation sequencing experiments

Understanding inflammatory bowel disease via immunogenetics

Covid-19 Vaccine Effectiveness against the Omicron (B.1.1.529) Variant

Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders

Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease

Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics

Evoker: a visualization tool for genotype intensity data

The zebrafish reference genome sequence and its relationship to the human genome

The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability

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