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GWAS Central: a comprehensive resource for the comparison and interrogation of genome-wide association studies

European journal of human genetics : EJHG, 2013-12, Vol.22 (7), p.949-952

2013

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VariantValidator: Accurate validation, mapping, and formatting of sequence variation descriptions

Human mutation, 2018-01, Vol.39 (1), p.61-68

2018

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Blood and sputum eosinophils in COPD; relationship with bacterial load

Respiratory research, 2017-05, Vol.18 (1), p.88-88, Article 88

2017

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The sputum microbiome is distinct between COPD and health, independent of smoking history

Respiratory research, 2020-07, Vol.21 (1), p.183-183, Article 183

2020

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Consent Codes: Upholding Standard Data Use Conditions

PLoS genetics, 2016-01, Vol.12 (1), p.e1005772-e1005772

2016

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Data and sample sharing as an enabler for large-scale biomarker research and development: The EPND perspective

Frontiers in neurology, 2022-11, Vol.13, p.1031091-1031091

2022

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GWAS Central: a comprehensive resource for the discovery and comparison of genotype and phenotype data from genome-wide association studies

Nucleic acids research, 2020-01, Vol.48 (D1), p.D933

2020

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The Data Use Ontology to streamline responsible access to human biomedical datasets

Cell genomics, 2021-11, Vol.1 (2), p.None-None, Article 100028

2021

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Data sharing in neurodegenerative disease research: challenges and learnings from the innovative medicines initiative public-private partnership model

Frontiers in neurology, 2023-07, Vol.14, p.1187095-1187095

2023

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GWAS Central: an expanding resource for finding and visualising genotype and phenotype data from genome-wide association studies

Nucleic acids research, 2023-01, Vol.51 (D1), p.D986-D993

2023

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Common conditions of use elements. Atomic concepts for consistent and effective information governance

Scientific data, 2024-05, Vol.11 (1), p.465-465, Article 465

2024

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Defensins and the dynamic genome: what we can learn from structural variation at human chromosome band 8p23.1

Genome research, 2008-11, Vol.18 (11), p.1686-1697

2008

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Prescreening for European Prevention of Alzheimer Dementia (EPAD) trial-ready cohort: impact of AD risk factors and recruitment settings

Alzheimer's research & therapy, 2020-01, Vol.12 (1), p.8-8, Article 8

2020

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Responsible sharing of biomedical data and biospecimens via the "Automatable Discovery and Access Matrix" (ADA-M)

Npj genomic medicine, 2018-07, Vol.3 (1), p.17-6, Article 17

2018

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Operation Moonshot proposals are scientifically unsound

BMJ (Online), 2020-09, Vol.370, p.m3699

2020

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Single Nucleotide Polymorphisms in the Proximal Promoter Region of the Adiponectin (APM1) Gene Are Associated With Type 2 Diabetes in Swedish Caucasians

Diabetes (New York, N.Y.), 2004-02, Vol.53 (suppl 1), p.S31-S35

2004

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GWAS Central: a comprehensive resource for the comparison and interrogation of genome-wide association studies

European journal of human genetics : EJHG, 2014-07, Vol.22 (7), p.949-952

2014

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The FAIR Guiding Principles for scientific data management and stewardship

Scientific data, 2016-03, Vol.3 (1), p.160018-160018, Article 160018

2016

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MegaPlex PCR: a strategy for multiplex amplification

Nature methods, 2007-10, Vol.4 (10), p.835-837

2007

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Federated discovery and sharing of genomic data using Beacons

Nature biotechnology, 2019-03, Vol.37 (3), p.220-224

2019

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Array-based dynamic allele specific hybridization (Array-DASH): Optimization-free microarray processing for multiple simultaneous genomic assays

Analytical biochemistry, 2021-08, Vol.626, p.114124-114124, Article 114124

2021

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iFRET: an improved fluorescence system for DNA-melting analysis

Genome research, 2002-09, Vol.12 (9), p.1401-1407

2002

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GWAS Central: a comprehensive resource for the comparison and interrogation of genome-wide association studies

VariantValidator: Accurate validation, mapping, and formatting of sequence variation descriptions

International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases

Blood and sputum eosinophils in COPD; relationship with bacterial load

The sputum microbiome is distinct between COPD and health, independent of smoking history

Consent Codes: Upholding Standard Data Use Conditions

Data and sample sharing as an enabler for large-scale biomarker research and development: The EPND perspective

GWAS Central: a comprehensive resource for the discovery and comparison of genotype and phenotype data from genome-wide association studies

The Data Use Ontology to streamline responsible access to human biomedical datasets

Data sharing in neurodegenerative disease research: challenges and learnings from the innovative medicines initiative public-private partnership model

GWAS Central: an expanding resource for finding and visualising genotype and phenotype data from genome-wide association studies

Protocol for the development of the Wales Multimorbidity e-Cohort (WMC): data sources and methods to construct a population-based research platform to investigate multimorbidity

Common conditions of use elements. Atomic concepts for consistent and effective information governance

Defensins and the dynamic genome: what we can learn from structural variation at human chromosome band 8p23.1

Prescreening for European Prevention of Alzheimer Dementia (EPAD) trial-ready cohort: impact of AD risk factors and recruitment settings

Responsible sharing of biomedical data and biospecimens via the "Automatable Discovery and Access Matrix" (ADA-M)

Operation Moonshot proposals are scientifically unsound

Single Nucleotide Polymorphisms in the Proximal Promoter Region of the Adiponectin (APM1) Gene Are Associated With Type 2 Diabetes in Swedish Caucasians

GWAS Central: a comprehensive resource for the comparison and interrogation of genome-wide association studies

The FAIR Guiding Principles for scientific data management and stewardship

Sputum microbiome temporal variability and dysbiosis in chronic obstructive pulmonary disease exacerbations: an analysis of the COPDMAP study

MegaPlex PCR: a strategy for multiplex amplification

Federated discovery and sharing of genomic data using Beacons

Array-based dynamic allele specific hybridization (Array-DASH): Optimization-free microarray processing for multiple simultaneous genomic assays

iFRET: an improved fluorescence system for DNA-melting analysis

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