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Association between genetically proxied PCSK9 inhibition and prostate cancer risk: A Mendelian randomisation study

PLoS medicine, 2023-01, Vol.20 (1), p.e1003988

2023

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Searching for the causal effects of body mass index in over 300 000 participants in UK Biobank, using Mendelian randomization

PLoS genetics, 2019-02, Vol.15 (2), p.e1007951

2019

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The variant call format provides efficient and robust storage of GWAS summary statistics

Genome Biology, 2021-01, Vol.22 (1), p.32-32, Article 32

2021

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Triangulating evidence in health sciences with Annotated Semantic Queries

Bioinformatics (Oxford, England), 2024-09, Vol.40 (9)

2024

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FATHMM-XF: accurate prediction of pathogenic point mutations via extended features

Bioinformatics, 2018-02, Vol.34 (3), p.511-513

2018

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Associations between high blood pressure and DNA methylation

PloS one, 2020-01, Vol.15 (1), p.e0227728

2020

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DrivR-Base: a feature extraction toolkit for variant effect prediction model construction

Bioinformatics (Oxford, England), 2024-03, Vol.40 (4)

2024

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An integrative approach to predicting the functional effects of non-coding and coding sequence variation

Bioinformatics, 2015-05, Vol.31 (10), p.1536-1543

2015

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MELODI Presto: a fast and agile tool to explore semantic triples derived from biomedical literature

Bioinformatics, 2021-05, Vol.37 (4), p.583-585

2021

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The MR-Base platform supports systematic causal inference across the human phenome

eLife, 2018-05, Vol.7

2018

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Systematic identification of genetic influences on methylation across the human life course

Genome Biology, 2016-03, Vol.17 (1), p.61-61, Article 61

2016

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The Effect of Circulating Zinc, Selenium, Copper and Vitamin K1 on COVID-19 Outcomes: A Mendelian Randomization Study

Nutrients, 2022-01, Vol.14 (2), p.233

2022

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Association of physical activity intensity and bout length with mortality: An observational study of 79,503 UK Biobank participants

PLoS medicine, 2021-09, Vol.18 (9), p.e1003757-e1003757

2021

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Diagnosis of Coronary Heart Diseases Using Gene Expression Profiling; Stable Coronary Artery Disease, Cardiac Ischemia with and without Myocardial Necrosis

PloS one, 2016-03, Vol.11 (3), p.e0149475-e0149475

2016

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Exploiting horizontal pleiotropy to search for causal pathways within a Mendelian randomization framework

Nature communications, 2020-02, Vol.11 (1), p.1010-1010, Article 1010

2020

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Cubic exact solutions for the estimation of pairwise haplotype frequencies: implications for linkage disequilibrium analyses and a web tool 'CubeX'

BMC bioinformatics, 2007-11, Vol.8 (1), p.428-428, Article 428

2007

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Predicting the Functional, Molecular, and Phenotypic Consequences of Amino Acid Substitutions using Hidden Markov Models

Human mutation, 2013-01, Vol.34 (1), p.57-65

2013

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Prenatal exposure to maternal smoking and offspring DNA methylation across the lifecourse: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC)

Human molecular genetics, 2015-04, Vol.24 (8), p.2201-2217

2015

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Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data

Nature genetics, 2019-02, Vol.51 (2), p.230-236

2019

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CScape-somatic: distinguishing driver and passenger point mutations in the cancer genome

Bioinformatics, 2020-06, Vol.36 (12), p.3637-3644

2020

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Liver Function and Risk of Type 2 Diabetes: Bidirectional Mendelian Randomization Study

Diabetes (New York, N.Y.), 2019-08, Vol.68 (8), p.1681-1691

2019

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Hardy-Weinberg Equilibrium Testing of Biological Ascertainment for Mendelian Randomization Studies

American journal of epidemiology, 2009-02, Vol.169 (4), p.505-514

2009

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Maternal pre-pregnancy BMI and gestational weight gain, offspring DNA methylation and later offspring adiposity: findings from the Avon Longitudinal Study of Parents and Children

International journal of epidemiology, 2015-08, Vol.44 (4), p.1288-1304

2015

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Drug target Mendelian randomisation: are we really instrumenting drug use? Reply to Anderson EL, Williams DM [letter]

Diabetologia, 2023-06, Vol.66 (6), p.1159-1161

2023

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Association between genetically proxied PCSK9 inhibition and prostate cancer risk: A Mendelian randomisation study

Searching for the causal effects of body mass index in over 300 000 participants in UK Biobank, using Mendelian randomization

The variant call format provides efficient and robust storage of GWAS summary statistics

Triangulating evidence in health sciences with Annotated Semantic Queries

FATHMM-XF: accurate prediction of pathogenic point mutations via extended features

Associations between high blood pressure and DNA methylation

DrivR-Base: a feature extraction toolkit for variant effect prediction model construction

An integrative approach to predicting the functional effects of non-coding and coding sequence variation

Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases

MELODI Presto: a fast and agile tool to explore semantic triples derived from biomedical literature

The MR-Base platform supports systematic causal inference across the human phenome

Systematic identification of genetic influences on methylation across the human life course

The Effect of Circulating Zinc, Selenium, Copper and Vitamin K1 on COVID-19 Outcomes: A Mendelian Randomization Study

Association of physical activity intensity and bout length with mortality: An observational study of 79,503 UK Biobank participants

Diagnosis of Coronary Heart Diseases Using Gene Expression Profiling; Stable Coronary Artery Disease, Cardiac Ischemia with and without Myocardial Necrosis

Exploiting horizontal pleiotropy to search for causal pathways within a Mendelian randomization framework

Cubic exact solutions for the estimation of pairwise haplotype frequencies: implications for linkage disequilibrium analyses and a web tool 'CubeX'

Predicting the Functional, Molecular, and Phenotypic Consequences of Amino Acid Substitutions using Hidden Markov Models

Prenatal exposure to maternal smoking and offspring DNA methylation across the lifecourse: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC)

Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data

CScape-somatic: distinguishing driver and passenger point mutations in the cancer genome

Liver Function and Risk of Type 2 Diabetes: Bidirectional Mendelian Randomization Study

Hardy-Weinberg Equilibrium Testing of Biological Ascertainment for Mendelian Randomization Studies

Maternal pre-pregnancy BMI and gestational weight gain, offspring DNA methylation and later offspring adiposity: findings from the Avon Longitudinal Study of Parents and Children

Drug target Mendelian randomisation: are we really instrumenting drug use? Reply to Anderson EL, Williams DM [letter]

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