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Genetic Epidemiology 1 : Key concepts in genetic epidemiologyBURTON, Paul R; TOBIN, Martin D; HOPPER, John L et al.Lancet (British edition). 2005, Vol 366, Num 9489, pp 941-951, issn 0140-6736, 11 p.Article

Understanding the impact of pre-analytic variation in haematological and clinical chemistry analytes on the power of association studiesGAYE, Amadou; PEAKMAN, Tim; TOBIN, Martin D et al.International journal of epidemiology. 2014, Vol 43, Num 5, pp 1633-1644, issn 0300-5771, 12 p.Article

Genomic copy number variation, human health, and diseaseWAIN, Louise V; ARMOUR, John A. L; TOBIN, Martin D et al.Lancet (British edition). 2009, Vol 374, Num 9686, pp 340-350, issn 0140-6736, 11 p.Article

Blood Pressure Loci Identified with a Gene-Centric ArrayJOHNSON, Toby; GAUNT, Tom R; SEVER, Peter et al.American journal of human genetics. 2011, Vol 89, Num 6, pp 688-700, issn 0002-9297, 13 p.Article

Common variants near TERC are associated with mean telomere lengthCODD, Veryan; MANGINO, Massimo; GUANGJU ZHAI et al.Nature genetics. 2010, Vol 42, Num 3, pp 197-199, issn 1061-4036, 3 p.Article

Four Genetic Loci Influencing Electrocardiographic Indices of Left Ventricular HypertrophySHAH, Sonia; NELSON, Christopher P; KIVIMAKI, Mika et al.Circulation. Cardiovascular genetics (Print). 2011, Vol 4, Num 6, pp 626-635, issn 1942-325X, 10 p.Article

Genetic Architecture of Ambulatory Blood Pressure in the General Population: Insights From Cardiovascular Gene-Centric ArrayTOMASZEWSKI, Maciej; DEBIEC, Radoslaw; WATERWORTH, Dawn et al.Hypertension (Dallas, Tex. 1979). 2010, Vol 56, Num 6, pp 1069-1076, issn 0194-911X, 8 p.Article

Common Variation in the WNK1 Gene and Blood Pressure in Childhood : The Avon Longitudinal Study of Parents and ChildrenTOBIN, Martin D; TIMPSON, Nicholas J; BURTON, Paul R et al.Hypertension (Dallas, Tex. 1979). 2008, Vol 52, Num 5, pp 974-979, issn 0194-911X, 6 p.Article

APOM and high-density lipoprotein cholesterol are associated with lung function and per cent emphysemaBURKART, Kristin M; MANICHAIKUL, Ani; KAUFMAN, Joel D et al.The European respiratory journal. 2014, Vol 43, Num 4, pp 1003-1017, issn 0903-1936, 15 p.Article

Genome-wide association study identifies eight loci associated with blood pressureNEWTON-CHEH, Christopher; JOHNSON, Toby; PAPADAKIS, Konstantinos et al.Nature genetics. 2009, Vol 41, Num 6, pp 666-676, issn 1061-4036, 11 p.Article

Association of WNK1 gene polymorphisms and haplotypes with ambulatory blood pressure in the general populationTOBIN, Martin D; RALEIGH, Stuart M; RIDGE, Cathy et al.Circulation (New York, N.Y.). 2005, Vol 112, Num 22, pp 3423-3429, issn 0009-7322, 7 p.Article

Allelic variant of NOSIAP effects on cardiac alternans of repolarization during exercise testingKOSKELA, Jenni; KAHONEN, Mika; TURJANMAA, Väinö et al.Scandinavian journal of clinical & laboratory investigation. 2012, Vol 72, Num 2, pp 100-107, issn 0036-5513, 8 p.Article

Common Variants in Genes Underlying Monogenic Hypertension and Hypotension and Blood Pressure in the General PopulationTOBIN, Martin D; TOMASZEWSKI, Maciej; BRAUND, Peter S et al.Hypertension (Dallas, Tex. 1979). 2008, Vol 51, Num 6, pp 1658-1664, issn 0194-911X, 7 p.Article

Covariance components models for longitudinal family data. CommentaryBURTON, Paul R; SCURRAH, Katrina J; TOBIN, Martin D et al.International journal of epidemiology. 2005, Vol 34, Num 5, pp 1063-1079, issn 0300-5771, 17 p.Article

Apolipoprotein E isoforms, serum cholesterol, and cancer. CommentariesKATAN, M. B; KEAVNEY, Bernard; THOMPSON, John R et al.International journal of epidemiology. 2004, Vol 33, Num 1, pp 9-42, issn 0300-5771, 34 p.Article

Integration of Genetics into a Systems Model of Electrocardiographic Traits Using HumanCVD BeadChipGAUNT, Tom R; SHAH, Sonia; KIVIMAKI, Mika et al.Circulation. Cardiovascular genetics (Print). 2012, Vol 5, Num 6, pp 630-638, issn 1942-325X, 9 p.Article

Dense Genotyping of Candidate Gene Loci Identifies Variants Associated With High-Density Lipoprotein CholesterolEDMONDSON, Andrew C; BRAUND, Peter S; TOBIN, Martin D et al.Circulation. Cardiovascular genetics (Print). 2011, Vol 4, Num 2, pp 145-155, issn 1942-325X, 11 p.Article

Genomewide association analysis of coronary artery diseaseSAMANI, Nilesh J; ERDMANN, Jeanette; BARRETT, Jennifer H et al.The New England journal of medicine. 2007, Vol 357, Num 5, pp 443-453, issn 0028-4793, 11 p.Article

An integrated approach to the meta-analysis of genetic association studies using Mendelian randomizationMINELLI, Cosetta; THOMPSON, John R; TOBIN, Martin D et al.American journal of epidemiology. 2004, Vol 160, Num 5, pp 445-452, issn 0002-9262, 8 p.Article

Effect of Five Genetic Variants Associated with Lung Function on the Risk of Chronic Obstructive Lung Disease, and Their Joint Effects on Lung FunctionARTIGAS, Maria Soler; WAIN, Louise V; KERR, Shona M et al.American journal of respiratory and critical care medicine. 2011, Vol 184, Num 7, pp 786-795, issn 1073-449X, 10 p.Article

A large genome scan for rare CNVs in amyotrophic lateral sclerosisBLAUW, Hylke M; AL-CHALABI, Ammar; VAN'T SLOT, Ruben et al.Human molecular genetics (Print). 2010, Vol 19, Num 20, pp 4091-4099, issn 0964-6906, 9 p.Article

DataSHIELD: resolving a conflict in contemporary bioscience—performing a pooled analysis of individual-level data without sharing the dataWOLFSON, Michael; WALLACE, Susan E; FORTIER, Isabel et al.International journal of epidemiology. 2010, Vol 39, Num 5, pp 1372-1382, issn 0300-5771, 11 p.Article

Adjusting for bias and unmeasured confounding in Mendelian randomization studies with binary responsesPALMER, Tom M; THOMPSON, John R; TOBIN, Martin D et al.International journal of epidemiology. 2008, Vol 37, Num 5, pp 1161-1168, issn 0300-5771, 8 p.Article

Coronary Artery Disease-Associated Locus on Chromosome 9p21 and Early Markers of AtherosclerosisSAMANI, Nilesh J; RAITAKARI, Olli T; TAITTONEN, Leena et al.Arteriosclerosis, thrombosis, and vascular biology. 2008, Vol 28, Num 9, pp 1679-1683, issn 1079-5642, 5 p.Article