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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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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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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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UCHL1 (PGP 9.5): neuronal biomarker and ubiquitin system protein

Progress in neurobiology, 2010-03, Vol.90 (3), p.327-362

2010

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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 consequences of cancer-associated amino acid substitutions

Bioinformatics, 2013-06, Vol.29 (12), p.1504-1510

2013

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Ranking non-synonymous single nucleotide polymorphisms based on disease concepts

Human genomics, 2014-06, Vol.8 (1), p.11-11, Article 11

2014

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Canonical correlation analysis for gene-based pleiotropy discovery

PLoS computational biology, 2014-10, Vol.10 (10), p.e1003876-e1003876

2014

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dbSNP in the detail and copy number complexities

Human mutation, 2010, Vol.31 (1), p.2-4

Day, Ian N.M

2010

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Possible Association of APOE Genotype with Working Memory in Young Adults

PloS one, 2015-08, Vol.10 (8), p.e0135894-e0135894

2015

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ACTN3 genotype, athletic status, and life course physical capability: meta-analysis of the published literature and findings from nine studies

Human mutation, 2011-09, Vol.32 (9), p.1008-1018

2011

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A pathway-based data integration framework for prediction of disease progression

Bioinformatics, 2014-03, Vol.30 (6), p.838-845

2014

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Importance of Genetic Studies in Consanguineous Populations for the Characterization of Novel Human Gene Functions

Annals of human genetics, 2016-05, Vol.80 (3), p.187-196

2016

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MIDAS: software for analysis and visualisation of interallelic disequilibrium between multiallelic markers

BMC bioinformatics, 2006-04, Vol.7 (1), p.227-227, Article 227

2006

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FH4=STAP1. Another Gene for Familial Hypercholesterolemia?: Relevance to Cascade Testing and Drug Development?

Circulation research, 2014-08, Vol.115 (6), p.534-536

Day, Ian N.M

2014

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Nonsense Mutation in Coiled-Coil Domain Containing 151 Gene (CCDC151) Causes Primary Ciliary Dyskinesia

Human mutation, 2014-12, Vol.35 (12), p.1446-1448

2014

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IQ, Educational Attainment, Memory and Plasma Lipids: Associations with Apolipoprotein E Genotype in 5995 Children

Biological psychiatry (1969), 2011-07, Vol.70 (2), p.152-158

2011

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Associations between a polymorphism in the pleiotropic GCKR and Age-related phenotypes: the HALCyon programme

PloS one, 2013-07, Vol.8 (7), p.e70045-e70045

2013

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Genetic markers of bone and joint health and physical capability in older adults: the HALCyon programme

Bone (New York, N.Y.), 2013-01, Vol.52 (1), p.278-285

2013

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Influences of matrix metalloproteinase-3 gene variation on extent of coronary atherosclerosis and risk of myocardial infarction

Journal of the American College of Cardiology, 2003-06, Vol.41 (12), p.2130-2137

2003

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Association of C-reactive protein with blood pressure and hypertension: life course confounding and mendelian randomization tests of causality

Arteriosclerosis, thrombosis, and vascular biology, 2005-05, Vol.25 (5), p.1051

2005

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Clustered environments and randomized genes: a fundamental distinction between conventional and genetic epidemiology

PLoS medicine, 2007-12, Vol.4 (12), p.e352

2007

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Inflammation and not cardiovascular risk factors is associated with short leukocyte telomere length in 13- to 16-year-old adolescents

Arteriosclerosis, thrombosis, and vascular biology, 2012-08, Vol.32 (8), p.2029

2012

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Genetic Variants in the Vitamin D Receptor Are Associated with Advanced Prostate Cancer at Diagnosis: Findings from the Prostate Testing for Cancer and Treatment Study and a Systematic Review

Cancer epidemiology, biomarkers & prevention, 2009-11, Vol.18 (11), p.2874-2881

2009

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

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

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

UCHL1 (PGP 9.5): neuronal biomarker and ubiquitin system protein

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

Predicting the functional consequences of cancer-associated amino acid substitutions

Ranking non-synonymous single nucleotide polymorphisms based on disease concepts

Canonical correlation analysis for gene-based pleiotropy discovery

dbSNP in the detail and copy number complexities

Possible Association of APOE Genotype with Working Memory in Young Adults

ACTN3 genotype, athletic status, and life course physical capability: meta-analysis of the published literature and findings from nine studies

A pathway-based data integration framework for prediction of disease progression

Importance of Genetic Studies in Consanguineous Populations for the Characterization of Novel Human Gene Functions

MIDAS: software for analysis and visualisation of interallelic disequilibrium between multiallelic markers

FH4=STAP1. Another Gene for Familial Hypercholesterolemia?: Relevance to Cascade Testing and Drug Development?

The association of C-reactive protein and CRP genotype with coronary heart disease: findings from five studies with 4,610 cases amongst 18,637 participants

Nonsense Mutation in Coiled-Coil Domain Containing 151 Gene (CCDC151) Causes Primary Ciliary Dyskinesia

IQ, Educational Attainment, Memory and Plasma Lipids: Associations with Apolipoprotein E Genotype in 5995 Children

Associations between a polymorphism in the pleiotropic GCKR and Age-related phenotypes: the HALCyon programme

Genetic markers of bone and joint health and physical capability in older adults: the HALCyon programme

Influences of matrix metalloproteinase-3 gene variation on extent of coronary atherosclerosis and risk of myocardial infarction

Association of C-reactive protein with blood pressure and hypertension: life course confounding and mendelian randomization tests of causality

Clustered environments and randomized genes: a fundamental distinction between conventional and genetic epidemiology

Inflammation and not cardiovascular risk factors is associated with short leukocyte telomere length in 13- to 16-year-old adolescents

Genetic Variants in the Vitamin D Receptor Are Associated with Advanced Prostate Cancer at Diagnosis: Findings from the Prostate Testing for Cancer and Treatment Study and a Systematic Review

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