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Author Details

Ian N M Day
1982
224
57
PMIDPaper TitleJournal TitlePublished Year
28818596Cardiometabolic phenotypes and mitochondrial DNA copy number in two cohorts of UK women.Mitochondrion2018
27591082HAPRAP: a haplotype-based iterative method for statistical fine mapping using GWAS summary statistics.Bioinformatics2017
29032015Possible positive effect of the APOE ε2 allele on cognition in early to mid-adult life.Neurobiology of Learning and Memory2017
27555663Frequency of KLK3 gene deletions in the general population.Annals of Clinical Biochemistry2017
26781229Plasma urate concentration and risk of coronary heart disease: a Mendelian randomisation analysis.Lancet Diabetes Endocrinol2016
25920552Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array.Eur J Hum Genet2016
27338949Mendelian Randomisation study of the influence of eGFR on coronary heart disease.Scientific Reports2016
26831755A study of common Mendelian disease carriers across ageing British cohorts: meta-analyses reveal heterozygosity for alpha 1-antitrypsin deficiency increases respiratory capacity and height.Journal of Medical Genetics2016
27000383Importance of Genetic Studies in Consanguineous Populations for the Characterization of Novel Human Gene Functions.Annals of Human Genetics2016
26671949Effect of smoking on physical and cognitive capability in later life: a multicohort study using observational and genetic approaches.BMJ Open2015
25799584Proxy molecular diagnosis from whole-exome sequencing reveals Papillon-Lefevre syndrome caused by a missense mutation in CTSC.PLoS ONE2015
25583119An integrative approach to predicting the functional effects of non-coding and coding sequence variation.Bioinformatics2015
26287823Possible Association of APOE Genotype with Working Memory in Young Adults.PLoS ONE2015
26106619Identifying Highly Penetrant Disease Causal Mutations Using Next Generation Sequencing: Guide to Whole Process.Biomed Res Int2015
25224326Nonsense mutation in coiled-coil domain containing 151 gene (CCDC151) causes primary ciliary dyskinesia.Human Mutation2014
25329069Canonical correlation analysis for gene-based pleiotropy discovery.PLoS Comput Biol2014
25484485Influence of adiposity-related genetic markers in a population of saudi arabians where other variables influencing obesity may be reduced.Disease Markers2014
25525287Haptoglobin duplicon, hemoglobin, and vitamin C: analyses in the british women's heart and health study and Caerphilly prospective study.Dis Markers2014
24162466A pathway-based data integration framework for prediction of disease progression.Bioinformatics2014
25228436Evaluating the role of a galanin enhancer genotype on a range of metabolic, depressive and addictive phenotypes.Am J Med Genet B Neuropsychiatr Genet2014
24980617Ranking non-synonymous single nucleotide polymorphisms based on disease concepts.Hum Genomics2014
25170087FH4=STAP1. Another gene for familial hypercholesterolemia? Relevance to cascade testing and drug development?Circulation Research2014
25073452Associations between APOE and low-density lipoprotein cholesterol genotypes and cognitive and physical capability: the HALCyon programme.2014
23325016Dependence of deodorant usage on ABCC11 genotype: scope for personalized genetics in personal hygiene.2013
22721421Non-replication of an association of Apolipoprotein E2 with sinistrality.Laterality2013
22977227Influence of common genetic variation on blood lipid levels, cardiovascular risk, and coronary events in two British prospective cohort studies.Eur Heart J2013
23768161Cytokine gene polymorphisms and outcome after traumatic brain injury.Journal of Neurotrauma2013
23894584Associations between a polymorphism in the pleiotropic GCKR and Age-related phenotypes: the HALCyon programme.PLoS ONE2013
23977022Population genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) Consortium.PLoS One2013
24178511Gene-centric association signals for haemostasis and thrombosis traits identified with the HumanCVD BeadChip.Thromb Haemost2013
23916927Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization study.J Am Coll Cardiol2013
23278391Sequential sentinel SNP Regional Association Plots (SSS-RAP): an approach for testing independence of SNP association signals using meta-analysis data.Annals of Human Genetics2013
23188048A gene-centric analysis of activated partial thromboplastin time and activated protein C resistance using the HumanCVD focused genotyping array.Eur J Hum Genet2013
23468552Genetic variants influencing biomarkers of nutrition are not associated with cognitive capability in middle-aged and older adults.Journal of Nutrition2013
23667688Structural and population-based evaluations of TBC1D1 p.Arg125Trp.PLoS One2013
23033316Predicting the functional, molecular, and phenotypic consequences of amino acid substitutions using hidden Markov models.Hum Mutat2013
23620363Predicting the functional consequences of cancer-associated amino acid substitutions.Bioinformatics2013
23169475Very low PSA concentrations and deletions of the KLK3 gene.Clin Chem2013
23505291Gene-centric analysis identifies variants associated with interleukin-6 levels and shared pathways with other inflammation markers.Circ Cardiovasc Genet2013
23072920Genetic markers of bone and joint health and physical capability in older adults: the HALCyon programme.2013
23569189Apolipoprotein E genotype, cardiovascular biomarkers and risk of stroke: systematic review and meta-analysis of 14,015 stroke cases and pooled analysis of primary biomarker data from up to 60,883 individuals.Int J Epidemiol2013
22238593A genome-wide association search for type 2 diabetes genes in African Americans.PLoS One2012
22479202Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.PLoS Genet2012
22433445Complexity of a complex trait locus: HP, HPR, haemoglobin and cholesterol.Gene2012
22384920From a single whole exome read to notions of clinical screening: primary ciliary dyskinesia and RSPH9 p.Lys268del in the Arabian Peninsula.Ann Hum Genet2012
22679311Inflammation and not cardiovascular risk factors is associated with short leukocyte telomere length in 13- to 16-year-old adolescents.Arteriosclerosis, Thrombosis, and Vascular Biology2012
22607059Molecular and population analysis of natural selection on the human haptoglobin duplication.Ann Hum Genet2012
23063622Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.Am J Hum Genet2012
23139254Integration of genetics into a systems model of electrocardiographic traits using HumanCVD BeadChip.Circ Cardiovasc Genet2012
22253814A multi-cohort study of polymorphisms in the GH/IGF axis and physical capability: the HALCyon programme.PLoS ONE2012
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