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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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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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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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Apolipoprotein E4 and coronary heart disease in middle-aged men who smoke: a prospective study

The Lancet (British edition), 2001-07, Vol.358 (9276), p.115-119

2001

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A gene-centric analysis of activated partial thromboplastin time and activated protein C resistance using the HumanCVD focused genotyping array

European journal of human genetics : EJHG, 2013-07, Vol.21 (7), p.779-783

2013

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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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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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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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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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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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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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Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array

European journal of human genetics : EJHG, 2016-01, Vol.24 (1), p.106-112

2016

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C-reactive protein and its role in metabolic syndrome: mendelian randomisation study

The Lancet (British edition), 2005-12, Vol.366 (9501), p.1954-1959

2005

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Influence of common genetic variation on blood lipid levels, cardiovascular risk, and coronary events in two British prospective cohort studies

European heart journal, 2013-04, Vol.34 (13), p.972-981

2013

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Two British women studies replicated the association between the Val66Met polymorphism in the brain-derived neurotrophic factor ( ) and BMI

European journal of human genetics : EJHG, 2009-08, Vol.17 (8), p.1050-1055

2009

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Canonical Correlation Analysis for Gene-Based Pleiotropy Discovery: e1003876

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

2014

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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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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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Frequency of KLK3 gene deletions in the general population

Annals of clinical biochemistry, 2017-07, Vol.54 (4), p.472-480

2017

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Identifying Highly Penetrant Disease Causal Mutations Using Next Generation Sequencing: Guide to Whole Process

BioMed research international, 2015-01, Vol.2015 (2015), p.1-16

2015

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Variants in the human insulin gene that affect pre-mRNA splicing : Is -23HphI a functional single nucleotide polymorphism at IDDM2?

Diabetes (New York, N.Y.), 2006, Vol.55 (1), p.260-264

2006

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Sequential Sentinel SNP Regional Association Plots (SSS‐RAP): An Approach for Testing Independence of SNP Association Signals Using Meta‐Analysis Data

Annals of human genetics, 2013-01, Vol.77 (1), p.67-79

2013

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Molecular and Population Analysis of Natural Selection on the Human Haptoglobin Duplication

Annals of human genetics, 2012-09, Vol.76 (5), p.352-362

2012

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Associations between APOE and low-density lipoprotein cholesterol genotypes and cognitive and physical capability: the HALCyon programme

AGE, 2014-08, Vol.36 (4), p.9673-9673, Article 9673

2014

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From a Single Whole Exome Read to Notions of Clinical Screening: Primary Ciliary Dyskinesia and RSPH9 p.Lys268del in the Arabian Peninsula

Annals of human genetics, 2012-05, Vol.76 (3), p.211-220

2012

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

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

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

Apolipoprotein E4 and coronary heart disease in middle-aged men who smoke: a prospective study

A gene-centric analysis of activated partial thromboplastin time and activated protein C resistance using the HumanCVD focused genotyping array

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

Ranking non-synonymous single nucleotide polymorphisms based on disease concepts

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

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

dbSNP in the detail and copy number complexities

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

Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array

C-reactive protein and its role in metabolic syndrome: mendelian randomisation study

Influence of common genetic variation on blood lipid levels, cardiovascular risk, and coronary events in two British prospective cohort studies

Two British women studies replicated the association between the Val66Met polymorphism in the brain-derived neurotrophic factor ( ) and BMI

Canonical Correlation Analysis for Gene-Based Pleiotropy Discovery: e1003876

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

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

Frequency of KLK3 gene deletions in the general population

Identifying Highly Penetrant Disease Causal Mutations Using Next Generation Sequencing: Guide to Whole Process

Variants in the human insulin gene that affect pre-mRNA splicing : Is -23HphI a functional single nucleotide polymorphism at IDDM2?

Sequential Sentinel SNP Regional Association Plots (SSS‐RAP): An Approach for Testing Independence of SNP Association Signals Using Meta‐Analysis Data

Molecular and Population Analysis of Natural Selection on the Human Haptoglobin Duplication

Associations between APOE and low-density lipoprotein cholesterol genotypes and cognitive and physical capability: the HALCyon programme

From a Single Whole Exome Read to Notions of Clinical Screening: Primary Ciliary Dyskinesia and RSPH9 p.Lys268del in the Arabian Peninsula

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