Cecil CAM; Walton E; Jaffee SR; O'Connor T; Maughan B; Relton CL; Smith RG; McArdle W; Gaunt TR; Ouellet-Morin I; Barker ED, 2018. Neonatal DNA methylation and early-onset conduct problems: A genome-wide, prospective study.  Dev Psychopathol 30(2):383-397

Ambatipudi S; Langdon R; Richmond RC; Suderman M; Koestler DC; Kelsey KT; Kazmi N; Penfold C; Ho KM; McArdle W; Ring SM; Pring M; Waterboer T; Pawlita M; Gaunt TR; Davey Smith G; Thomas S; Ness AR; Relton CL, 2018. DNA methylation derived systemic inflammation indices are associated with head and neck cancer development and survival.  Oral Oncol 85:87-94

Elsworth B; Dawe K; Vincent EE; Langdon R; Lynch BM; Martin RM; Relton C; Higgins JPT; Gaunt TR, 2018. MELODI: Mining Enriched Literature Objects to Derive Intermediates.  Int J Epidemiol.

Guyatt AL; Burrows K; Guthrie PAI; Ring S; McArdle W; Day INM; Ascione R; Lawlor DA; Gaunt TR; Rodriguez S, 2018. Cardiometabolic phenotypes and mitochondrial DNA copy number in two cohorts of UK women.  Mitochondrion 39:9-19

Felix JF; Joubert BR; Baccarelli AA; Sharp GC; Almqvist C; Annesi-Maesano I; Arshad H; Baïz N; Bakermans-Kranenburg MJ; Bakulski KM; Binder EB; Bouchard L; Breton CV; Brunekreef B; Brunst KJ; Burchard EG; Bustamante M; Chatzi L; Cheng Munthe-Kaas M; Corpeleijn E; Czamara D; Dabelea D; Davey Smith G; De Boever P; Duijts L; Dwyer T; Eng C; Eskenazi B; Everson TM; Falahi F; Fallin MD; Farchi S; Fernandez MF; Gao L; Gaunt TR; Ghantous A; Gillman MW; Gonseth S; Grote V; Gruzieva O; Håberg SE; Herceg Z; Hivert MF; Holland N; Holloway JW; Hoyo C; Hu D; Huang RC; Huen K; Järvelin MR; Jima DD; Just AC; Karagas MR; Karlsson R; Karmaus W; Kechris KJ; Kere J; Kogevinas M; Koletzko B; Koppelman GH; Küpers LK; Ladd-Acosta C; Lahti J; Lambrechts N; Langie SAS; Lie RT; Liu AH; Magnus MC; Magnus P; Maguire RL; Marsit CJ; McArdle W; Melén E; Melton P; Murphy SK; Nawrot TS; Nisticò L; Nohr EA; Nordlund B; Nystad W; Oh SS; Oken E; Page CM; Perron P; Pershagen G; Pizzi C; Plusquin M; Raikkonen K; Reese SE; Reischl E; Richiardi L; Ring S; Roy RP; Rzehak P; Schoeters G; Schwartz DA; Sebert S; Snieder H; Sørensen TIA; Starling AP; Sunyer J; Taylor JA; Tiemeier H; Ullemar V; Vafeiadi M; Van Ijzendoorn MH; Vonk JM; Vriens A; Vrijheid M; Wang P; Wiemels JL; Wilcox AJ; Wright RJ; Xu CJ; Xu Z; Yang IV; Yousefi P; Zhang H; Zhang W; Zhao S; Agha G; Relton CL; Jaddoe VWV; London SJ, 2018. Cohort Profile: Pregnancy And Childhood Epigenetics (PACE) Consortium.  Int J Epidemiol 47(1):22-23u

Rogers MF; Shihab HA; Mort M; Cooper DN; Gaunt TR; Campbell C, 2018. FATHMM-XF: accurate prediction of pathogenic point mutations via extended features.  Bioinformatics 34(3):511-513

Barker ED; Walton E; Cecil CAM; Rowe R; Jaffee SR; Maughan B; O'Connor TG; Stringaris A; Meehan AJ; McArdle W; Relton CL; Gaunt TR, 2018. A Methylome-Wide Association Study of Trajectories of Oppositional Defiant Behaviors and Biological Overlap With Attention Deficit Hyperactivity Disorder.  Child Dev 89(5):1839-1855

Staley JR; Suderman M; Simpkin AJ; Gaunt TR; Heron J; Relton CL; Tilling K, 2018. Longitudinal analysis strategies for modelling epigenetic trajectories.  Int J Epidemiol 47(2):516-525

Lawn RB; Anderson EL; Suderman M; Simpkin AJ; Gaunt TR; Teschendorff AE; Widschwendter M; Hardy R; Kuh D; Relton CL; Howe LD, 2018. Psychosocial adversity and socioeconomic position during childhood and epigenetic age: analysis of two prospective cohort studies.  Hum Mol Genet 27(7):1301-1308

Barker ED; Cecil CAM; Walton E; Houtepen LC; O'Connor TG; Danese A; Jaffee SR; Jensen SKG; Pariante C; McArdle W; Gaunt TR; Relton CL; Roberts S, 2018. Inflammation-related epigenetic risk and child and adolescent mental health: A prospective study from pregnancy to middle adolescence.  Dev Psychopathol 30(3):1145-1156

Cuellar Partida G; Laurin C; Ring SM; Gaunt TR; McRae AF; Visscher PM; Montgomery GW; Martin NG; Hemani G; Suderman M; Relton CL; Davey Smith G; Evans DM, 2018. Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans.  Hum Mol Genet 27(16):2927-2939

Slieker RC; Relton CL; Gaunt TR; Slagboom PE; Heijmans BT, 2018. Age-related DNA methylation changes are tissue-specific with ELOVL2 promoter methylation as exception.  Epigenetics Chromatin 11(1):25

Zheng J; Richardson TG; Millard LAC; Hemani G; Elsworth BL; Raistrick CA; Vilhjalmsson B; Neale BM; Haycock PC; Smith GD; Gaunt TR, 2018. PhenoSpD: an integrated toolkit for phenotypic correlation estimation and multiple testing correction using GWAS summary statistics.  Gigascience 7.

Guyatt AL; Stergiakouli E; Martin J; Walters J; O'Donovan M; Owen M; Thapar A; Kirov G; Rodriguez S; Rai D; Zammit S; Gaunt TR, 2018. Association of copy number variation across the genome with neuropsychiatric traits in the general population.  Am J Med Genet B Neuropsychiatr Genet 177(5):489-502

Hemani G; Zheng J; Elsworth B; Wade KH; Haberland V; Baird D; Laurin C; Burgess S; Bowden J; Langdon R; Tan VY; Yarmolinsky J; Shihab HA; Timpson NJ; Evans DM; Relton C; Martin RM; Davey Smith G; Gaunt TR; Haycock PC, 2018. The MR-Base platform supports systematic causal inference across the human phenome.  Elife 7.

Richardson TG; Haycock PC; Zheng J; Timpson NJ; Gaunt TR; Davey Smith G; Relton CL; Hemani G, 2018. Systematic Mendelian randomization framework elucidates hundreds of CpG sites which may mediate the influence of genetic variants on disease.  Hum Mol Genet 27(18):3293-3304

Rogers MF; Shihab HA; Ferlaino M; Gaunt TR; Campbell C, 2017. Predicting the Pathogenic Impact of Sequence Variation in the Human Genome.  Stud Health Technol Inform 235:91-95

Fairoozy RH; Cooper J; White J; Giambartolomei C; Folkersen L; Wannamethee SG; Jefferis BJ; Whincup P; Ben-Shlomo Y; Kumari M; Kivimaki M; Wong A; Hardy R; Kuh D; Gaunt TR; Casas JP; McLachlan S; Price JF; Hingorani A; Franco-Cereceda A; Grewal T; Kalea AZ; Humphries SE, 2017. Identifying low density lipoprotein cholesterol associated variants in the Annexin A2 (ANXA2) gene.  Atherosclerosis 261:60-68

Shihab HA; Rogers MF; Campbell C; Gaunt TR, 2017. HIPred: an integrative approach to predicting haploinsufficient genes.  Bioinformatics 33(12):1751-1757

Elliott HR; Shihab HA; Lockett GA; Holloway JW; McRae AF; Smith GD; Ring SM; Gaunt TR; Relton CL, 2017. Role of DNA Methylation in Type 2 Diabetes Etiology: Using Genotype as a Causal Anchor.  Diabetes 66(6):1713-1722

Rijlaarsdam J; Cecil CA; Walton E; Mesirow MS; Relton CL; Gaunt TR; McArdle W; Barker ED, 2017. Prenatal unhealthy diet, insulin-like growth factor 2 gene (IGF2) methylation, and attention deficit hyperactivity disorder symptoms in youth with early-onset conduct problems.  J Child Psychol Psychiatry 58(1):19-27

Beaney KE; Smith AJP; Folkersen L; Palmen J; Wannamethee SG; Jefferis BJ; Whincup P; Gaunt TR; Casas JP; Ben-Shlomo Y; Price JF; Kumari M; Wong A; Ong K; Hardy R; Kuh D; Wareham N; Kivimaki M; Eriksson P; Humphries SE; Consortium U, 2017. Functional Analysis of the Coronary Heart Disease Risk Locus on Chromosome 21q22.  Dis Markers 2017:1096916

Walton E; Pingault JB; Cecil CA; Gaunt TR; Relton CL; Mill J; Barker ED, 2017. Epigenetic profiling of ADHD symptoms trajectories: a prospective, methylome-wide study.  Mol Psychiatry 22(2):250-256

Zheng J; Rodriguez S; Laurin C; Baird D; Trela-Larsen L; Erzurumluoglu MA; Zheng Y; White J; Giambartolomei C; Zabaneh D; Morris R; Kumari M; Casas JP; Hingorani AD; Evans DM; Gaunt TR; Day IN, 2017. HAPRAP: a haplotype-based iterative method for statistical fine mapping using GWAS summary statistics.  Bioinformatics 33(1):79-86

Zheng J; Erzurumluoglu AM; Elsworth BL; Kemp JP; Howe L; Haycock PC; Hemani G; Tansey K; Laurin C; Pourcain BS; Warrington NM; Finucane HK; Price AL; Bulik-Sullivan BK; Anttila V; Paternoster L; Gaunt TR; Evans DM; Neale BM, 2017. LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis.  Bioinformatics 33(2):272-279

Shihab HA; Rogers MF; Ferlaino M; Campbell C; Gaunt TR, 2017. GTB - an online genome tolerance browser.  BMC Bioinformatics 18(1):20

Wahl S; Drong A; Lehne B; Loh M; Scott WR; Kunze S; Tsai PC; Ried JS; Zhang W; Yang Y; Tan S; Fiorito G; Franke L; Guarrera S; Kasela S; Kriebel J; Richmond RC; Adamo M; Afzal U; Ala-Korpela M; Albetti B; Ammerpohl O; Apperley JF; Beekman M; Bertazzi PA; Black SL; Blancher C; Bonder MJ; Brosch M; Carstensen-Kirberg M; de Craen AJ; de Lusignan S; Dehghan A; Elkalaawy M; Fischer K; Franco OH; Gaunt TR; Hampe J; Hashemi M; Isaacs A; Jenkinson A; Jha S; Kato N; Krogh V; Laffan M; Meisinger C; Meitinger T; Mok ZY; Motta V; Ng HK; Nikolakopoulou Z; Nteliopoulos G; Panico S; Pervjakova N; Prokisch H; Rathmann W; Roden M; Rota F; Rozario MA; Sandling JK; Schafmayer C; Schramm K; Siebert R; Slagboom PE; Soininen P; Stolk L; Strauch K; Tai ES; Tarantini L; Thorand B; Tigchelaar EF; Tumino R; Uitterlinden AG; van Duijn C; van Meurs JB; Vineis P; Wickremasinghe AR; Wijmenga C; Yang TP; Yuan W; Zhernakova A; Batterham RL; Smith GD; Deloukas P; Heijmans BT; Herder C; Hofman A; Lindgren CM; Milani L; van der Harst P; Peters A; Illig T; Relton CL; Waldenberger M; Järvelin MR; Bollati V; Soong R; Spector TD; Scott J; McCarthy MI; Elliott P; Bell JT; Matullo G; Gieger C; Kooner JS; Grallert H; Chambers JC, 2017. Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity.  Nature 541(7635):81-86

Simpkin AJ; Howe LD; Tilling K; Gaunt TR; Lyttleton O; McArdle WL; Ring SM; Horvath S; Smith GD; Relton CL, 2017. The epigenetic clock and physical development during childhood and adolescence: longitudinal analysis from a UK birth cohort.  Int J Epidemiol 46(2):549-558

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Arathimos R; Suderman M; Sharp GC; Burrows K; Granell R; Tilling K; Gaunt TR; Henderson J; Ring S; Richmond RC; Relton CL, 2017. Epigenome-wide association study of asthma and wheeze in childhood and adolescence.  Clin Epigenetics 9:112

Millard LAC; Davies NM; Gaunt TR; Davey Smith G; Tilling K, 2017. Software Application Profile: PHESANT: a tool for performing automated phenome scans in UK Biobank.  Int J Epidemiol.

Kazmi N; Gaunt TR; Relton C; Micali N, 2017. Maternal eating disorders affect offspring cord blood DNA methylation: a prospective study.  Clin Epigenetics 9:120

Millard LAC; Tilling K; Lawlor DA; Flach PA; Gaunt TR, 2017. Physical activity phenotyping with activity bigrams, and their association with BMI.  Int J Epidemiol 46(6):1857-1870

Dale CE; Fatemifar G; Palmer TM; White J; Prieto-Merino D; Zabaneh D; Engmann JEL; Shah T; Wong A; Warren HR; McLachlan S; Trompet S; Moldovan M; Morris RW; Sofat R; Kumari M; Hyppönen E; Jefferis BJ; Gaunt TR; Ben-Shlomo Y; Zhou A; Gentry-Maharaj A; Ryan A; Mutsert R; Noordam R; Caulfield MJ; Jukema JW; Worrall BB; Munroe PB; Menon U; Power C; Kuh D; Lawlor DA; Humphries SE; Mook-Kanamori DO; Sattar N; Kivimaki M; Price JF; Davey Smith G; Dudbridge F; Hingorani AD; Holmes MV; Casas JP, 2017. Causal Associations of Adiposity and Body Fat Distribution With Coronary Heart Disease, Stroke Subtypes, and Type 2 Diabetes Mellitus: A Mendelian Randomization Analysis.  Circulation 135(24):2373-2388

Milaniak I; Cecil CAM; Barker ED; Relton CL; Gaunt TR; McArdle W; Jaffee SR, 2017. Variation in DNA methylation of the oxytocin receptor gene predicts children's resilience to prenatal stress.  Dev Psychopathol 29(5):1663-1674

Ferlaino M; Rogers MF; Shihab HA; Mort M; Cooper DN; Gaunt TR; Campbell C, 2017. An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome.  BMC Bioinformatics 18(1):442

Borges MC; Barros AJD; Ferreira DLS; Casas JP; Horta BL; Kivimaki M; Kumari M; Menon U; Gaunt TR; Ben-Shlomo Y; Freitas DF; Oliveira IO; Gentry-Maharaj A; Fourkala E; Lawlor DA; Hingorani AD, 2017. Metabolic Profiling of Adiponectin Levels in Adults: Mendelian Randomization Analysis.  Circ Cardiovasc Genet 10.

Holzinger ER; Verma SS; Moore CB; Hall M; De R; Gilbert-Diamond D; Lanktree MB; Pankratz N; Amuzu A; Burt A; Dale C; Dudek S; Furlong CE; Gaunt TR; Kim DS; Riess H; Sivapalaratnam S; Tragante V; van Iperen EPA; Brautbar A; Carrell DS; Crosslin DR; Jarvik GP; Kuivaniemi H; Kullo IJ; Larson EB; Rasmussen-Torvik LJ; Tromp G; Baumert J; Cruickshanks KJ; Farrall M; Hingorani AD; Hovingh GK; Kleber ME; Klein BE; Klein R; Koenig W; Lange LA; Mӓrz W; North KE; Charlotte Onland-Moret N; Reiner AP; Talmud PJ; van der Schouw YT; Wilson JG; Kivimaki M; Kumari M; Moore JH; Drenos F; Asselbergs FW; Keating BJ; Ritchie MD, 2017. Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.  BioData Min 10:25

Tachmazidou I; Süveges D; Min JL; Ritchie GRS; Steinberg J; Walter K; Iotchkova V; Schwartzentruber J; Huang J; Memari Y; McCarthy S; Crawford AA; Bombieri C; Cocca M; Farmaki AE; Gaunt TR; Jousilahti P; Kooijman MN; Lehne B; Malerba G; Männistö S; Matchan A; Medina-Gomez C; Metrustry SJ; Nag A; Ntalla I; Paternoster L; Rayner NW; Sala C; Scott WR; Shihab HA; Southam L; St Pourcain B; Traglia M; Trajanoska K; Zaza G; Zhang W; Artigas MS; Bansal N; Benn M; Chen Z; Danecek P; Lin WY; Locke A; Luan J; Manning AK; Mulas A; Sidore C; Tybjaerg-Hansen A; Varbo A; Zoledziewska M; Finan C; Hatzikotoulas K; Hendricks AE; Kemp JP; Moayyeri A; Panoutsopoulou K; Szpak M; Wilson SG; Boehnke M; Cucca F; Di Angelantonio E; Langenberg C; Lindgren C; McCarthy MI; Morris AP; Nordestgaard BG; Scott RA; Tobin MD; Wareham NJ; Burton P; Chambers JC; Smith GD; Dedoussis G; Felix JF; Franco OH; Gambaro G; Gasparini P; Hammond CJ; Hofman A; Jaddoe VWV; Kleber M; Kooner JS; Perola M; Relton C; Ring SM; Rivadeneira F; Salomaa V; Spector TD; Stegle O; Toniolo D; Uitterlinden AG; Barroso I; Greenwood CMT; Perry JRB; Walker BR; Butterworth AS; Xue Y; Durbin R; Small KS; Soranzo N; Timpson NJ; Zeggini E, 2017. Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.  Am J Hum Genet 100(6):865-884

Richardson TG; Zheng J; Davey Smith G; Timpson NJ; Gaunt TR; Relton CL; Hemani G, 2017. Mendelian Randomization Analysis Identifies CpG Sites as Putative Mediators for Genetic Influences on Cardiovascular Disease Risk.  Am J Hum Genet 101(4):590-602

Rogers MF; Shihab HA; Gaunt TR; Campbell C, 2017. CScape: a tool for predicting oncogenic single-point mutations in the cancer genome.  Sci Rep 7(1):11597

Lewis SJ; Gardner M; Higgins J; Holly JMP; Gaunt TR; Perks CM; Turner SD; Rinaldi S; Thomas S; Harrison S; Lennon RJ; Tan V; Borwick C; Emmett P; Jeffreys M; Northstone K; Mitrou G; Wiseman M; Thompson R; Martin RM, 2017. Developing the WCRF International/University of Bristol Methodology for Identifying and Carrying Out Systematic Reviews of Mechanisms of Exposure-Cancer Associations.  Cancer Epidemiol Biomarkers Prev 26(11):1667-1675

Nüesch E; Dale C; Palmer TM; White J; Keating BJ; van Iperen EP; Goel A; Padmanabhan S; Asselbergs FW; Verschuren WM; Wijmenga C; Van der Schouw YT; Onland-Moret NC; Lange LA; Hovingh GK; Sivapalaratnam S; Morris RW; Whincup PH; Wannamethe GS; Gaunt TR; Ebrahim S; Steel L; Nair N; Reiner AP; Kooperberg C; Wilson JF; Bolton JL; McLachlan S; Price JF; Strachan MW; Robertson CM; Kleber ME; Delgado G; März W; Melander O; Dominiczak AF; Farrall M; Watkins H; Leusink M; Maitland-van der Zee AH; de Groot MC; Dudbridge F; Hingorani A; Ben-Shlomo Y; Lawlor DA; Amuzu A; Caufield M; Cavadino A; Cooper J; Davies TL; Drenos F; Engmann J; Finan C; Giambartolomei C; Hardy R; Humphries SE; Hypponen E; Kivimaki M; Kuh D; Kumari M; Ong K; Plagnol V; Power C; Richards M; Shah S; Shah T; Sofat R; Talmud PJ; Wareham N; Warren H; Whittaker JC; Wong A; Zabaneh D; Davey Smith G; Wells JC; Leon DA; Holmes MV; Casas JP, 2016. Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis.  Int J Epidemiol 45(6):1927-1937

Rijlaarsdam J; Pappa I; Walton E; Bakermans-Kranenburg MJ; Mileva-Seitz VR; Rippe RC; Roza SJ; Jaddoe VW; Verhulst FC; Felix JF; Cecil CA; Relton CL; Gaunt TR; McArdle W; Mill J; Barker ED; Tiemeier H; van IJzendoorn MH, 2016. An epigenome-wide association meta-analysis of prenatal maternal stress in neonates: A model approach for replication.  Epigenetics 11(2):140-9

Kazmi N; Gaunt TR, 2016. Diagnosis of Coronary Heart Diseases Using Gene Expression Profiling; Stable Coronary Artery Disease, Cardiac Ischemia with and without Myocardial Necrosis.  PLoS One 11(3):e0149475

Erzurumluoglu AM; Shihab HA; Rodriguez S; Gaunt TR; Day IN, 2016. Importance of Genetic Studies in Consanguineous Populations for the Characterization of Novel Human Gene Functions.  Ann Hum Genet 80(3):187-96

Richmond RC; Sharp GC; Ward ME; Fraser A; Lyttleton O; McArdle WL; Ring SM; Gaunt TR; Lawlor DA; Davey Smith G; Relton CL, 2016. DNA Methylation and BMI: Investigating Identified Methylation Sites at HIF3A in a Causal Framework.  Diabetes 65(5):1231-44

Simpkin AJ; Hemani G; Suderman M; Gaunt TR; Lyttleton O; Mcardle WL; Ring SM; Sharp GC; Tilling K; Horvath S; Kunze S; Peters A; Waldenberger M; Ward-Caviness C; Nohr EA; Sørensen TI; Relton CL; Smith GD, 2016. Prenatal and early life influences on epigenetic age in children: a study of mother-offspring pairs from two cohort studies.  Hum Mol Genet 25(1):191-201

Fernandez-Lozano C; Seoane JA; Gestal M; Gaunt TR; Dorado J; Pazos A; Campbell C, 2016. Texture analysis in gel electrophoresis images using an integrative kernel-based approach.  Sci Rep 6:19256

Gaunt TR; Shihab HA; Hemani G; Min JL; Woodward G; Lyttleton O; Zheng J; Duggirala A; McArdle WL; Ho K; Ring SM; Evans DM; Davey Smith G; Relton CL, 2016. Systematic identification of genetic influences on methylation across the human life course.  Genome Biol 17:61

White J; Sofat R; Hemani G; Shah T; Engmann J; Dale C; Shah S; Kruger FA; Giambartolomei C; Swerdlow DI; Palmer T; McLachlan S; Langenberg C; Zabaneh D; Lovering R; Cavadino A; Jefferis B; Finan C; Wong A; Amuzu A; Ong K; Gaunt TR; Warren H; Davies TL; Drenos F; Cooper J; Ebrahim S; Lawlor DA; Talmud PJ; Humphries SE; Power C; Hypponen E; Richards M; Hardy R; Kuh D; Wareham N; Ben-Shlomo Y; Day IN; Whincup P; Morris R; Strachan MW; Price J; Kumari M; Kivimaki M; Plagnol V; Whittaker JC; Smith GD; Dudbridge F; Casas JP; Holmes MV; Hingorani AD, 2016. Plasma urate concentration and risk of coronary heart disease: a Mendelian randomisation analysis.  Lancet Diabetes Endocrinol 4(4):327-36

Rodriguez S; Gaunt TR; Guo Y; Zheng J; Barnes MR; Tang W; Danish F; Johnson A; Castillo BA; Li YR; Hakonarson H; Buxbaum SG; Palmer T; Tsai MY; Lange LA; Ebrahim S; Davey Smith G; Lawlor DA; Folsom AR; Hoogeveen R; Reiner A; Keating B; Day IN, 2016. Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array.  Eur J Hum Genet 24(1):106-12

Richardson TG; Campbell C; Timpson NJ; Gaunt TR, 2016. Incorporating Non-Coding Annotations into Rare Variant Analysis.  PLoS One 11(4):e0154181

Joubert BR; Felix JF; Yousefi P; Bakulski KM; Just AC; Breton C; Reese SE; Markunas CA; Richmond RC; Xu CJ; Küpers LK; Oh SS; Hoyo C; Gruzieva O; Söderhäll C; Salas LA; Baïz N; Zhang H; Lepeule J; Ruiz C; Ligthart S; Wang T; Taylor JA; Duijts L; Sharp GC; Jankipersadsing SA; Nilsen RM; Vaez A; Fallin MD; Hu D; Litonjua AA; Fuemmeler BF; Huen K; Kere J; Kull I; Munthe-Kaas MC; Gehring U; Bustamante M; Saurel-Coubizolles MJ; Quraishi BM; Ren J; Tost J; Gonzalez JR; Peters MJ; Håberg SE; Xu Z; van Meurs JB; Gaunt TR; Kerkhof M; Corpeleijn E; Feinberg AP; Eng C; Baccarelli AA; Benjamin Neelon SE; Bradman A; Merid SK; Bergström A; Herceg Z; Hernandez-Vargas H; Brunekreef B; Pinart M; Heude B; Ewart S; Yao J; Lemonnier N; Franco OH; Wu MC; Hofman A; McArdle W; Van der Vlies P; Falahi F; Gillman MW; Barcellos LF; Kumar A; Wickman M; Guerra S; Charles MA; Holloway J; Auffray C; Tiemeier HW; Smith GD; Postma D; Hivert MF; Eskenazi B; Vrijheid M; Arshad H; Antó JM; Dehghan A; Karmaus W; Annesi-Maesano I; Sunyer J; Ghantous A; Pershagen G; Holland N; Murphy SK; DeMeo DL; Burchard EG; Ladd-Acosta C; Snieder H; Nystad W; Koppelman GH; Relton CL; Jaddoe VW; Wilcox A; Melén E; London SJ, 2016. DNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysis.  Am J Hum Genet 98(4):680-96

Iotchkova V; Huang J; Morris JA; Jain D; Barbieri C; Walter K; Min JL; Chen L; Astle W; Cocca M; Deelen P; Elding H; Farmaki AE; Franklin CS; Franberg M; Gaunt TR; Hofman A; Jiang T; Kleber ME; Lachance G; Luan J; Malerba G; Matchan A; Mead D; Memari Y; Ntalla I; Panoutsopoulou K; Pazoki R; Perry JRB; Rivadeneira F; Sabater-Lleal M; Sennblad B; Shin SY; Southam L; Traglia M; van Dijk F; van Leeuwen EM; Zaza G; Zhang W; Amin N; Butterworth A; Chambers JC; Dedoussis G; Dehghan A; Franco OH; Franke L; Frontini M; Gambaro G; Gasparini P; Hamsten A; Issacs A; Kooner JS; Kooperberg C; Langenberg C; Marz W; Scott RA; Swertz MA; Toniolo D; Uitterlinden AG; van Duijn CM; Watkins H; Zeggini E; Maurano MT; Timpson NJ; Reiner AP; Auer PL; Soranzo N, 2016. Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.  Nat Genet 48(11):1303-1312

Cecil CA; Walton E; Smith RG; Viding E; McCrory EJ; Relton CL; Suderman M; Pingault JB; McArdle W; Gaunt TR; Mill J; Barker ED, 2016. DNA methylation and substance-use risk: a prospective, genome-wide study spanning gestation to adolescence.  Transl Psychiatry 6(12):e976

Richardson TG; Timpson NJ; Campbell C; Gaunt TR, 2016. A pathway-centric approach to rare variant association analysis.  Eur J Hum Genet 25(1):123-129

Richardson TG; Shihab HA; Hemani G; Zheng J; Hannon E; Mill J; Carnero-Montoro E; Bell JT; Lyttleton O; McArdle WL; Ring SM; Rodriguez S; Campbell C; Smith GD; Relton CL; Timpson NJ; Gaunt TR, 2016. Collapsed methylation quantitative trait loci analysis for low frequency and rare variants.  Hum Mol Genet 25(19):4339-4349

Drenos F; Davey Smith G; Ala-Korpela M; Kettunen J; Würtz P; Soininen P; Kangas AJ; Dale C; Lawlor DA; Gaunt TR; Casas JP; Timpson NJ, 2016. Metabolic Characterization of a Rare Genetic Variation Within APOC3 and Its Lipoprotein Lipase-Independent Effects.  Circ Cardiovasc Genet 9(3):231-9

Bonilla C; Lewis SJ; Rowlands MA; Gaunt TR; Davey Smith G; Gunnell D; Palmer T; Donovan JL; Hamdy FC; Neal DE; Eeles R; Easton D; Kote-Jarai Z; Al Olama AA; Benlloch S; Muir K; Giles GG; Wiklund F; Grönberg H; Haiman CA; Schleutker J; Nordestgaard BG; Travis RC; Pashayan N; Khaw KT; Stanford JL; Blot WJ; Thibodeau S; Maier C; Kibel AS; Cybulski C; Cannon-Albright L; Brenner H; Park J; Kaneva R; Batra J; Teixeira MR; Pandha H; Lathrop M; Martin RM; Holly JM, 2016. Assessing the role of insulin-like growth factors and binding proteins in prostate cancer using Mendelian randomization: Genetic variants as instruments for circulating levels.  Int J Cancer 139(7):1520-33

McLachlan S; Giambartolomei C; White J; Charoen P; Wong A; Finan C; Engmann J; Shah T; Hersch M; Podmore C; Cavadino A; Jefferis BJ; Dale CE; Hypponen E; Morris RW; Casas JP; Kumari M; Ben-Shlomo Y; Gaunt TR; Drenos F; Langenberg C; Kuh D; Kivimaki M; Rueedi R; Waeber G; Hingorani AD; Price JF; Walker AP, 2016. Replication and Characterization of Association between ABO SNPs and Red Blood Cell Traits by Meta-Analysis in Europeans.  PLoS One 11(6):e0156914

Richardson TG; Shihab HA; Rivas MA; McCarthy MI; Campbell C; Timpson NJ; Gaunt TR, 2016. A Protein Domain and Family Based Approach to Rare Variant Association Analysis.  PLoS One 11(4):e0153803

Shihab HA; Rogers MF; Gough J; Mort M; Cooper DN; Day IN; Gaunt TR; Campbell C, 2015. An integrative approach to predicting the functional effects of non-coding and coding sequence variation.  Bioinformatics 31(10):1536-43

King DA; Jones WD; Crow YJ; Dominiczak AF; Foster NA; Gaunt TR; Harris J; Hellens SW; Homfray T; Innes J; Jones EA; Joss S; Kulkarni A; Mansour S; Morris AD; Parker MJ; Porteous DJ; Shihab HA; Smith BH; Tatton-Brown K; Tolmie JL; Trzaskowski M; Vasudevan PC; Wakeling E; Wright M; Plomin R; Timpson NJ; Hurles ME, 2015. Mosaic structural variation in children with developmental disorders.  Hum Mol Genet 24(10):2733-45

Würtz P; Havulinna AS; Soininen P; Tynkkynen T; Prieto-Merino D; Tillin T; Ghorbani A; Artati A; Wang Q; Tiainen M; Kangas AJ; Kettunen J; Kaikkonen J; Mikkilä V; Jula A; Kähönen M; Lehtimäki T; Lawlor DA; Gaunt TR; Hughes AD; Sattar N; Illig T; Adamski J; Wang TJ; Perola M; Ripatti S; Vasan RS; Raitakari OT; Gerszten RE; Casas JP; Chaturvedi N; Ala-Korpela M; Salomaa V, 2015. Metabolite profiling and cardiovascular event risk: a prospective study of 3 population-based cohorts.  Circulation 131(9):774-85

Holmes MV; Asselbergs FW; Palmer TM; Drenos F; Lanktree MB; Nelson CP; Dale CE; Padmanabhan S; Finan C; Swerdlow DI; Tragante V; van Iperen EP; Sivapalaratnam S; Shah S; Elbers CC; Shah T; Engmann J; Giambartolomei C; White J; Zabaneh D; Sofat R; McLachlan S; Doevendans PA; Balmforth AJ; Hall AS; North KE; Almoguera B; Hoogeveen RC; Cushman M; Fornage M; Patel SR; Redline S; Siscovick DS; Tsai MY; Karczewski KJ; Hofker MH; Verschuren WM; Bots ML; van der Schouw YT; Melander O; Dominiczak AF; Morris R; Ben-Shlomo Y; Price J; Kumari M; Baumert J; Peters A; Thorand B; Koenig W; Gaunt TR; Humphries SE; Clarke R; Watkins H; Farrall M; Wilson JG; Rich SS; de Bakker PI; Lange LA; Davey Smith G; Reiner AP; Talmud PJ; Kivimäki M; Lawlor DA; Dudbridge F; Samani NJ; Keating BJ; Hingorani AD; Casas JP, 2015. Mendelian randomization of blood lipids for coronary heart disease.  Eur Heart J 36(9):539-50

Swerdlow DI; Preiss D; Kuchenbaecker KB; Holmes MV; Engmann JE; Shah T; Sofat R; Stender S; Johnson PC; Scott RA; Leusink M; Verweij N; Sharp SJ; Guo Y; Giambartolomei C; Chung C; Peasey A; Amuzu A; Li K; Palmen J; Howard P; Cooper JA; Drenos F; Li YR; Lowe G; Gallacher J; Stewart MC; Tzoulaki I; Buxbaum SG; van der A DL; Forouhi NG; Onland-Moret NC; van der Schouw YT; Schnabel RB; Hubacek JA; Kubinova R; Baceviciene M; Tamosiunas A; Pajak A; Topor-Madry R; Stepaniak U; Malyutina S; Baldassarre D; Sennblad B; Tremoli E; de Faire U; Veglia F; Ford I; Jukema JW; Westendorp RG; de Borst GJ; de Jong PA; Algra A; Spiering W; Maitland-van der Zee AH; Klungel OH; de Boer A; Doevendans PA; Eaton CB; Robinson JG; Duggan D; Kjekshus J; Downs JR; Gotto AM; Keech AC; Marchioli R; Tognoni G; Sever PS; Poulter NR; Waters DD; Pedersen TR; Amarenco P; Nakamura H; McMurray JJ; Lewsey JD; Chasman DI; Ridker PM; Maggioni AP; Tavazzi L; Ray KK; Seshasai SR; Manson JE; Price JF; Whincup PH; Morris RW; Lawlor DA; Smith GD; Ben-Shlomo Y; Schreiner PJ; Fornage M; Siscovick DS; Cushman M; Kumari M; Wareham NJ; Verschuren WM; Redline S; Patel SR; Whittaker JC; Hamsten A; Delaney JA; Dale C; Gaunt TR; Wong A; Kuh D; Hardy R; Kathiresan S; Castillo BA; van der Harst P; Brunner EJ; Tybjaerg-Hansen A; Marmot MG; Krauss RM; Tsai M; Coresh J; Hoogeveen RC; Psaty BM; Lange LA; Hakonarson H; Dudbridge F; Humphries SE; Talmud PJ; Kivimäki M; Timpson NJ; Langenberg C; Asselbergs FW; Voevoda M; Bobak M; Pikhart H; Wilson JG; Reiner AP; Keating BJ; Hingorani AD; Sattar N, 2015. HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials.  Lancet 385(9965):351-61

Gaunt TR; Davey Smith G, 2015. eNOS and coronary artery disease: publication bias and the eclipse of hypothesis-driven meta-analysis in genetic association studies.  Gene 556(2):257-8

Richmond RC; Simpkin AJ; Woodward G; Gaunt TR; Lyttleton O; McArdle WL; Ring SM; Smith AD; Timpson NJ; Tilling K; Davey Smith G; Relton CL, 2015. Prenatal exposure to maternal smoking and offspring DNA methylation across the lifecourse: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC).  Hum Mol Genet 24(8):2201-17

Chambers JC; Loh M; Lehne B; Drong A; Kriebel J; Motta V; Wahl S; Elliott HR; Rota F; Scott WR; Zhang W; Tan ST; Campanella G; Chadeau-Hyam M; Yengo L; Richmond RC; Adamowicz-Brice M; Afzal U; Bozaoglu K; Mok ZY; Ng HK; Pattou F; Prokisch H; Rozario MA; Tarantini L; Abbott J; Ala-Korpela M; Albetti B; Ammerpohl O; Bertazzi PA; Blancher C; Caiazzo R; Danesh J; Gaunt TR; de Lusignan S; Gieger C; Illig T; Jha S; Jones S; Jowett J; Kangas AJ; Kasturiratne A; Kato N; Kotea N; Kowlessur S; Pitkäniemi J; Punjabi P; Saleheen D; Schafmayer C; Soininen P; Tai ES; Thorand B; Tuomilehto J; Wickremasinghe AR; Kyrtopoulos SA; Aitman TJ; Herder C; Hampe J; Cauchi S; Relton CL; Froguel P; Soong R; Vineis P; Jarvelin MR; Scott J; Grallert H; Bollati V; Elliott P; McCarthy MI; Kooner JS, 2015. Epigenome-wide association of DNA methylation markers in peripheral blood from Indian Asians and Europeans with incident type 2 diabetes: a nested case-control study.  Lancet Diabetes Endocrinol 3(7):526-534

Erzurumluoglu AM; Alsaadi MM; Rodriguez S; Alotaibi TS; Guthrie PA; Lewis S; Ginwalla A; Gaunt TR; Alharbi KK; Alsaif FM; Alsaadi BM; Day IN, 2015. Proxy molecular diagnosis from whole-exome sequencing reveals Papillon-Lefevre syndrome caused by a missense mutation in CTSC.  PLoS One 10(3):e0121351

Erzurumluoglu AM; Rodriguez S; Shihab HA; Baird D; Richardson TG; Day IN; Gaunt TR, 2015. Identifying Highly Penetrant Disease Causal Mutations Using Next Generation Sequencing: Guide to Whole Process.  Biomed Res Int 2015:923491

Davies NM; Gaunt TR; Lewis SJ; Holly J; Donovan JL; Hamdy FC; Kemp JP; Eeles R; Easton D; Kote-Jarai Z; Al Olama AA; Benlloch S; Muir K; Giles GG; Wiklund F; Gronberg H; Haiman CA; Schleutker J; Nordestgaard BG; Travis RC; Neal D; Pashayan N; Khaw KT; Stanford JL; Blot WJ; Thibodeau S; Maier C; Kibel AS; Cybulski C; Cannon-Albright L; Brenner H; Park J; Kaneva R; Batra J; Teixeira MR; Pandha H; Lathrop M; Smith GD; Martin RM, 2015. The effects of height and BMI on prostate cancer incidence and mortality: a Mendelian randomization study in 20,848 cases and 20,214 controls from the PRACTICAL consortium.  Cancer Causes Control 26(11):1603-16

Männik K; Mägi R; Macé A; Cole B; Guyatt AL; Shihab HA; Maillard AM; Alavere H; Kolk A; Reigo A; Mihailov E; Leitsalu L; Ferreira AM; Nõukas M; Teumer A; Salvi E; Cusi D; McGue M; Iacono WG; Gaunt TR; Beckmann JS; Jacquemont S; Kutalik Z; Pankratz N; Timpson N; Metspalu A; Reymond A, 2015. Copy number variations and cognitive phenotypes in unselected populations.  JAMA 313(20):2044-54

Sharp GC; Lawlor DA; Richmond RC; Fraser A; Simpkin A; Suderman M; Shihab HA; Lyttleton O; McArdle W; Ring SM; Gaunt TR; Davey Smith G; Relton CL, 2015. 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.  Int J Epidemiol 44(4):1288-304

Simpkin AJ; Suderman M; Gaunt TR; Lyttleton O; McArdle WL; Ring SM; Tilling K; Davey Smith G; Relton CL, 2015. Longitudinal analysis of DNA methylation associated with birth weight and gestational age.  Hum Mol Genet 24(13):3752-63

Yoneyama S; Guo Y; Lanktree MB; Barnes MR; Elbers CC; Karczewski KJ; Padmanabhan S; Bauer F; Baumert J; Beitelshees A; Berenson GS; Boer JM; Burke G; Cade B; Chen W; Cooper-Dehoff RM; Gaunt TR; Gieger C; Gong Y; Gorski M; Heard-Costa N; Johnson T; Lamonte MJ; McDonough C; Monda KL; Onland-Moret NC; Nelson CP; O'Connell JR; Ordovas J; Peter I; Peters A; Shaffer J; Shen H; Smith E; Speilotes L; Thomas F; Thorand B; Monique Verschuren WM; Anand SS; Dominiczak A; Davidson KW; Hegele RA; Heid I; Hofker MH; Huggins GS; Illig T; Johnson JA; Kirkland S; König W; Langaee TY; McCaffery J; Melander O; Mitchell BD; Munroe P; Murray SS; Papanicolaou G; Redline S; Reilly M; Samani NJ; Schork NJ; Van Der Schouw YT; Shimbo D; Shuldiner AR; Tobin MD; Wijmenga C; Yusuf S; Hakonarson H; Lange LA; Demerath EW; Fox CS; North KE; Reiner AP; Keating B; Taylor KC, 2014. Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations.  Hum Mol Genet 23(9):2498-510

Seoane JA; Day IN; Gaunt TR; Campbell C, 2014. A pathway-based data integration framework for prediction of disease progression.  Bioinformatics 30(6):838-45

Tragante V; Barnes MR; Ganesh SK; Lanktree MB; Guo W; Franceschini N; Smith EN; Johnson T; Holmes MV; Padmanabhan S; Karczewski KJ; Almoguera B; Barnard J; Baumert J; Chang YP; Elbers CC; Farrall M; Fischer ME; Gaunt TR; Gho JM; Gieger C; Goel A; Gong Y; Isaacs A; Kleber ME; Mateo Leach I; McDonough CW; Meijs MF; Melander O; Nelson CP; Nolte IM; Pankratz N; Price TS; Shaffer J; Shah S; Tomaszewski M; van der Most PJ; Van Iperen EP; Vonk JM; Witkowska K; Wong CO; Zhang L; Beitelshees AL; Berenson GS; Bhatt DL; Brown M; Burt A; Cooper-DeHoff RM; Connell JM; Cruickshanks KJ; Curtis SP; Davey-Smith G; Delles C; Gansevoort RT; Guo X; Haiqing S; Hastie CE; Hofker MH; Hovingh GK; Kim DS; Kirkland SA; Klein BE; Klein R; Li YR; Maiwald S; Newton-Cheh C; O'Brien ET; Onland-Moret NC; Palmas W; Parsa A; Penninx BW; Pettinger M; Vasan RS; Ranchalis JE; M Ridker P; Rose LM; Sever P; Shimbo D; Steele L; Stolk RP; Thorand B; Trip MD; van Duijn CM; Verschuren WM; Wijmenga C; Wyatt S; Young JH; Zwinderman AH; Bezzina CR; Boerwinkle E; Casas JP; Caulfield MJ; Chakravarti A; Chasman DI; Davidson KW; Doevendans PA; Dominiczak AF; FitzGerald GA; Gums JG; Fornage M; Hakonarson H; Halder I; Hillege HL; Illig T; Jarvik GP; Johnson JA; Kastelein JJ; Koenig W; Kumari M; März W; Murray SS; O'Connell JR; Oldehinkel AJ; Pankow JS; Rader DJ; Redline S; Reilly MP; Schadt EE; Kottke-Marchant K; Snieder H; Snyder M; Stanton AV; Tobin MD; Uitterlinden AG; van der Harst P; van der Schouw YT; Samani NJ; Watkins H; Johnson AD; Reiner AP; Zhu X; de Bakker PI; Levy D; Asselbergs FW; Munroe PB; Keating BJ, 2014. Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci.  Am J Hum Genet 94(3):349-60

Holmes MV; Dale CE; Zuccolo L; Silverwood RJ; Guo Y; Ye Z; Prieto-Merino D; Dehghan A; Trompet S; Wong A; Cavadino A; Drogan D; Padmanabhan S; Li S; Yesupriya A; Leusink M; Sundstrom J; Hubacek JA; Pikhart H; Swerdlow DI; Panayiotou AG; Borinskaya SA; Finan C; Shah S; Kuchenbaecker KB; Shah T; Engmann J; Folkersen L; Eriksson P; Ricceri F; Melander O; Sacerdote C; Gamble DM; Rayaprolu S; Ross OA; McLachlan S; Vikhireva O; Sluijs I; Scott RA; Adamkova V; Flicker L; Bockxmeer FM; Power C; Marques-Vidal P; Meade T; Marmot MG; Ferro JM; Paulos-Pinheiro S; Humphries SE; Talmud PJ; Mateo Leach I; Verweij N; Linneberg A; Skaaby T; Doevendans PA; Cramer MJ; van der Harst P; Klungel OH; Dowling NF; Dominiczak AF; Kumari M; Nicolaides AN; Weikert C; Boeing H; Ebrahim S; Gaunt TR; Price JF; Lannfelt L; Peasey A; Kubinova R; Pajak A; Malyutina S; Voevoda MI; Tamosiunas A; Maitland-van der Zee AH; Norman PE; Hankey GJ; Bergmann MM; Hofman A; Franco OH; Cooper J; Palmen J; Spiering W; de Jong PA; Kuh D; Hardy R; Uitterlinden AG; Ikram MA; Ford I; Hyppönen E; Almeida OP; Wareham NJ; Khaw KT; Hamsten A; Husemoen LL; Tjønneland A; Tolstrup JS; Rimm E; Beulens JW; Verschuren WM; Onland-Moret NC; Hofker MH; Wannamethee SG; Whincup PH; Morris R; Vicente AM; Watkins H; Farrall M; Jukema JW; Meschia J; Cupples LA; Sharp SJ; Fornage M; Kooperberg C; LaCroix AZ; Dai JY; Lanktree MB; Siscovick DS; Jorgenson E; Spring B; Coresh J; Li YR; Buxbaum SG; Schreiner PJ; Ellison RC; Tsai MY; Patel SR; Redline S; Johnson AD; Hoogeveen RC; Hakonarson H; Rotter JI; Boerwinkle E; de Bakker PI; Kivimaki M; Asselbergs FW; Sattar N; Lawlor DA; Whittaker J; Davey Smith G; Mukamal K; Psaty BM; Wilson JG; Lange LA; Hamidovic A; Hingorani AD; Nordestgaard BG; Bobak M; Leon DA; Langenberg C; Palmer TM; Reiner AP; Keating BJ; Dudbridge F; Casas JP, 2014. Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data.  BMJ 349:g4164

Alharbi KK; Richardson TG; Khan IA; Syed R; Mohammed AK; Boustred CR; Gaunt TR; Tamimi W; Al-Daghri NM; Day IN, 2014. Influence of adiposity-related genetic markers in a population of saudi arabians where other variables influencing obesity may be reduced.  Dis Markers 2014:758232

Shihab HA; Gough J; Mort M; Cooper DN; Day IN; Gaunt TR, 2014. Ranking non-synonymous single nucleotide polymorphisms based on disease concepts.  Hum Genomics 8:11

Seoane JA; Campbell C; Day IN; Casas JP; Gaunt TR, 2014. Canonical correlation analysis for gene-based pleiotropy discovery.  PLoS Comput Biol 10(10):e1003876

Alsaadi MM; Erzurumluoglu AM; Rodriguez S; Guthrie PA; Gaunt TR; Omar HZ; Mubarak M; Alharbi KK; Al-Rikabi AC; Day IN, 2014. Nonsense mutation in coiled-coil domain containing 151 gene (CCDC151) causes primary ciliary dyskinesia.  Hum Mutat 35(12):1446-8

Gaunt TR; Lowe GD; Lawlor DA; Casas JP; Day IN, 2013. A gene-centric analysis of activated partial thromboplastin time and activated protein C resistance using the HumanCVD focused genotyping array.  Eur J Hum Genet 21(7):779-83

Shihab HA; Gough J; Cooper DN; Stenson PD; Barker GL; Edwards KJ; Day IN; Gaunt TR, 2013. Predicting the functional, molecular, and phenotypic consequences of amino acid substitutions using hidden Markov models.  Hum Mutat 34(1):57-65

Shah S; Casas JP; Gaunt TR; Cooper J; Drenos F; Zabaneh D; Swerdlow DI; Shah T; Sofat R; Palmen J; Kumari M; Kivimaki M; Ebrahim S; Smith GD; Lawlor DA; Talmud PJ; Whittaker J; Day IN; Hingorani AD; Humphries SE, 2013. Influence of common genetic variation on blood lipid levels, cardiovascular risk, and coronary events in two British prospective cohort studies.  Eur Heart J 34(13):972-81

Zheng J; Gaunt TR; Day IN, 2013. Sequential sentinel SNP Regional Association Plots (SSS-RAP): an approach for testing independence of SNP association signals using meta-analysis data.  Ann Hum Genet 77(1):67-79

Shihab HA; Gough J; Cooper DN; Day IN; Gaunt TR, 2013. Predicting the functional consequences of cancer-associated amino acid substitutions.  Bioinformatics 29(12):1504-10

Ganesh SK; Tragante V; Guo W; Guo Y; Lanktree MB; Smith EN; Johnson T; Castillo BA; Barnard J; Baumert J; Chang YP; Elbers CC; Farrall M; Fischer ME; Franceschini N; Gaunt TR; Gho JM; Gieger C; Gong Y; Isaacs A; Kleber ME; Mateo Leach I; McDonough CW; Meijs MF; Mellander O; Molony CM; Nolte IM; Padmanabhan S; Price TS; Rajagopalan R; Shaffer J; Shah S; Shen H; Soranzo N; van der Most PJ; Van Iperen EP; Van Setten J; Vonk JM; Zhang L; Beitelshees AL; Berenson GS; Bhatt DL; Boer JM; Boerwinkle E; Burkley B; Burt A; Chakravarti A; Chen W; Cooper-Dehoff RM; Curtis SP; Dreisbach A; Duggan D; Ehret GB; Fabsitz RR; Fornage M; Fox E; Furlong CE; Gansevoort RT; Hofker MH; Hovingh GK; Kirkland SA; Kottke-Marchant K; Kutlar A; Lacroix AZ; Langaee TY; Li YR; Lin H; Liu K; Maiwald S; Malik R; Murugesan G; Newton-Cheh C; O'Connell JR; Onland-Moret NC; Ouwehand WH; Palmas W; Penninx BW; Pepine CJ; Pettinger M; Polak JF; Ramachandran VS; Ranchalis J; Redline S; Ridker PM; Rose LM; Scharnag H; Schork NJ; Shimbo D; Shuldiner AR; Srinivasan SR; Stolk RP; Taylor HA; Thorand B; Trip MD; van Duijn CM; Verschuren WM; Wijmenga C; Winkelmann BR; Wyatt S; Young JH; Boehm BO; Caulfield MJ; Chasman DI; Davidson KW; Doevendans PA; Fitzgerald GA; Gums JG; Hakonarson H; Hillege HL; Illig T; Jarvik GP; Johnson JA; Kastelein JJ; Koenig W; März W; Mitchell BD; Murray SS; Oldehinkel AJ; Rader DJ; Reilly MP; Reiner AP; Schadt EE; Silverstein RL; Snieder H; Stanton AV; Uitterlinden AG; van der Harst P; van der Schouw YT; Samani NJ; Johnson AD; Munroe PB; de Bakker PI; Zhu X; Levy D; Keating BJ; Asselbergs FW, 2013. Loci influencing blood pressure identified using a cardiovascular gene-centric array.  Hum Mol Genet 22(8):1663-78

Holmes MV; Simon T; Exeter HJ; Folkersen L; Asselbergs FW; Guardiola M; Cooper JA; Palmen J; Hubacek JA; Carruthers KF; Horne BD; Brunisholz KD; Mega JL; van Iperen EPA; Li M; Leusink M; Trompet S; Verschuren JJW; Hovingh GK; Dehghan A; Nelson CP; Kotti S; Danchin N; Scholz M; Haase CL; Rothenbacher D; Swerdlow DI; Kuchenbaecker KB; Staines-Urias E; Goel A; van 't Hooft F; Gertow K; de Faire U; Panayiotou AG; Tremoli E; Baldassarre D; Veglia F; Holdt LM; Beutner F; Gansevoort RT; Navis GJ; Mateo Leach I; Breitling LP; Brenner H; Thiery J; Dallmeier D; Franco-Cereceda A; Boer JMA; Stephens JW; Hofker MH; Tedgui A; Hofman A; Uitterlinden AG; Adamkova V; Pitha J; Onland-Moret NC; Cramer MJ; Nathoe HM; Spiering W; Klungel OH; Kumari M; Whincup PH; Morrow DA; Braund PS; Hall AS; Olsson AG; Doevendans PA; Trip MD; Tobin MD; Hamsten A; Watkins H; Koenig W; Nicolaides AN; Teupser D; Day INM; Carlquist JF; Gaunt TR; Ford I; Sattar N; Tsimikas S; Schwartz GG; Lawlor DA; Morris RW; Sandhu MS; Poledne R; Maitland-van der Zee AH; Khaw KT; Keating BJ; van der Harst P; Price JF; Mehta SR; Yusuf S; Witteman JCM; Franco OH; Jukema JW; de Knijff P; Tybjaerg-Hansen A; Rader DJ; Farrall M; Samani NJ; Kivimaki M; Fox KAA; Humphries SE; Anderson JL; Boekholdt SM; Palmer TM; Eriksson P; Paré G; Hingorani AD; Sabatine MS; Mallat Z; Casas JP; Talmud PJ, 2013. Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization study.  J Am Coll Cardiol 62(21):1966-1976

Gaunt TR; Zabaneh D; Shah S; Guyatt A; Ladroue C; Kumari M; Drenos F; Shah T; Talmud PJ; Casas JP; Lowe G; Rumley A; Lawlor DA; Kivimaki M; Whittaker J; Hingorani AD; Humphries SE; Day IN, 2013. Gene-centric association signals for haemostasis and thrombosis traits identified with the HumanCVD BeadChip.  Thromb Haemost 110(5):995-1003

Khan TA; Shah T; Prieto D; Zhang W; Price J; Fowkes GR; Cooper J; Talmud PJ; Humphries SE; Sundstrom J; Hubacek JA; Ebrahim S; Lawlor DA; Ben-Shlomo Y; Abdollahi MR; Slooter AJ; Szolnoki Z; Sandhu M; Wareham N; Frikke-Schmidt R; Tybjærg-Hansen A; Fillenbaum G; Heijmans BT; Katsuya T; Gromadzka G; Singleton A; Ferrucci L; Hardy J; Worrall B; Rich SS; Matarin M; Whittaker J; Gaunt TR; Whincup P; Morris R; Deanfield J; Donald A; Davey Smith G; Kivimaki M; Kumari M; Smeeth L; Khaw KT; Nalls M; Meschia J; Sun K; Hui R; Day I; Hingorani AD; Casas JP, 2013. Apolipoprotein 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 Epidemiol 42(2):475-92

Alsaadi MM; Gaunt TR; Boustred CR; Guthrie PA; Liu X; Lenzi L; Rainbow L; Hall N; Alharbi KK; Day IN, 2012. From a single whole exome read to notions of clinical screening: primary ciliary dyskinesia and RSPH9 p.Lys268del in the Arabian Peninsula.  Ann Hum Genet 76(3):211-20

Alfred T; Ben-Shlomo Y; Cooper R; Hardy R; Cooper C; Deary IJ; Gaunt TR; Gunnell D; Harris SE; Kumari M; Martin RM; Sayer AA; Starr JM; Kuh D; Day IN, 2012. A multi-cohort study of polymorphisms in the GH/IGF axis and physical capability: the HALCyon programme.  PLoS One 7(1):e29883

Saxena R; Elbers CC; Guo Y; Peter I; Gaunt TR; Mega JL; Lanktree MB; Tare A; Castillo BA; Li YR; Johnson T; Bruinenberg M; Gilbert-Diamond D; Rajagopalan R; Voight BF; Balasubramanyam A; Barnard J; Bauer F; Baumert J; Bhangale T; Böhm BO; Braund PS; Burton PR; Chandrupatla HR; Clarke R; Cooper-DeHoff RM; Crook ED; Davey-Smith G; Day IN; de Boer A; de Groot MC; Drenos F; Ferguson J; Fox CS; Furlong CE; Gibson Q; Gieger C; Gilhuijs-Pederson LA; Glessner JT; Goel A; Gong Y; Grant SF; Grobbee DE; Hastie C; Humphries SE; Kim CE; Kivimaki M; Kleber M; Meisinger C; Kumari M; Langaee TY; Lawlor DA; Li M; Lobmeyer MT; Maitland-van der Zee AH; Meijs MF; Molony CM; Morrow DA; Murugesan G; Musani SK; Nelson CP; Newhouse SJ; O'Connell JR; Padmanabhan S; Palmen J; Patel SR; Pepine CJ; Pettinger M; Price TS; Rafelt S; Ranchalis J; Rasheed A; Rosenthal E; Ruczinski I; Shah S; Shen H; Silbernagel G; Smith EN; Spijkerman AW; Stanton A; Steffes MW; Thorand B; Trip M; van der Harst P; van der A DL; van Iperen EP; van Setten J; van Vliet-Ostaptchouk JV; Verweij N; Wolffenbuttel BH; Young T; Zafarmand MH; Zmuda JM; Boehnke M; Altshuler D; McCarthy M; Kao WH; Pankow JS; Cappola TP; Sever P; Poulter N; Caulfield M; Dominiczak A; Shields DC; Bhatt DL; Zhang L; Curtis SP; Danesh J; Casas JP; van der Schouw YT; Onland-Moret NC; Doevendans PA; Dorn GW 2nd; Farrall M; FitzGerald GA; Hamsten A; Hegele R; Hingorani AD; Hofker MH; Huggins GS; Illig T; Jarvik GP; Johnson JA; Klungel OH; Knowler WC; Koenig W; März W; Meigs JB; Melander O; Munroe PB; Mitchell BD; Bielinski SJ; Rader DJ; Reilly MP; Rich SS; Rotter JI; Saleheen D; Samani NJ; Schadt EE; Shuldiner AR; Silverstein R; Kottke-Marchant K; Talmud PJ; Watkins H; Asselbergs FW; de Bakker PI; McCaffery J; Wijmenga C; Sabatine MS; Wilson JG; Reiner A; Bowden DW; Hakonarson H; Siscovick DS; Keating BJ, 2012. Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci.  Am J Hum Genet 90(3):410-25

Guthrie PA; Rodriguez S; Gaunt TR; Lawlor DA; Smith GD; Day IN, 2012. Complexity of a complex trait locus: HP, HPR, haemoglobin and cholesterol.  Gene 499(1):8-13

Asselbergs FW; Guo Y; van Iperen EP; Sivapalaratnam S; Tragante V; Lanktree MB; Lange LA; Almoguera B; Appelman YE; Barnard J; Baumert J; Beitelshees AL; Bhangale TR; Chen YD; Gaunt TR; Gong Y; Hopewell JC; Johnson T; Kleber ME; Langaee TY; Li M; Li YR; Liu K; McDonough CW; Meijs MF; Middelberg RP; Musunuru K; Nelson CP; O'Connell JR; Padmanabhan S; Pankow JS; Pankratz N; Rafelt S; Rajagopalan R; Romaine SP; Schork NJ; Shaffer J; Shen H; Smith EN; Tischfield SE; van der Most PJ; van Vliet-Ostaptchouk JV; Verweij N; Volcik KA; Zhang L; Bailey KR; Bailey KM; Bauer F; Boer JM; Braund PS; Burt A; Burton PR; Buxbaum SG; Chen W; Cooper-Dehoff RM; Cupples LA; deJong JS; Delles C; Duggan D; Fornage M; Furlong CE; Glazer N; Gums JG; Hastie C; Holmes MV; Illig T; Kirkland SA; Kivimaki M; Klein R; Klein BE; Kooperberg C; Kottke-Marchant K; Kumari M; LaCroix AZ; Mallela L; Murugesan G; Ordovas J; Ouwehand WH; Post WS; Saxena R; Scharnagl H; Schreiner PJ; Shah T; Shields DC; Shimbo D; Srinivasan SR; Stolk RP; Swerdlow DI; Taylor HA Jr; Topol EJ; Toskala E; van Pelt JL; van Setten J; Yusuf S; Whittaker JC; Zwinderman AH; Anand SS; Balmforth AJ; Berenson GS; Bezzina CR; Boehm BO; Boerwinkle E; Casas JP; Caulfield MJ; Clarke R; Connell JM; Cruickshanks KJ; Davidson KW; Day IN; de Bakker PI; Doevendans PA; Dominiczak AF; Hall AS; Hartman CA; Hengstenberg C; Hillege HL; Hofker MH; Humphries SE; Jarvik GP; Johnson JA; Kaess BM; Kathiresan S; Koenig W; Lawlor DA; März W; Melander O; Mitchell BD; Montgomery GW; Munroe PB; Murray SS; Newhouse SJ; Onland-Moret NC; Poulter N; Psaty B; Redline S; Rich SS; Rotter JI; Schunkert H; Sever P; Shuldiner AR; Silverstein RL; Stanton A; Thorand B; Trip MD; Tsai MY; van der Harst P; van der Schoot E; van der Schouw YT; Verschuren WM; Watkins H; Wilde AA; Wolffenbuttel BH; Whitfield JB; Hovingh GK; Ballantyne CM; Wijmenga C; Reilly MP; Martin NG; Wilson JG; Rader DJ; Samani NJ; Reiner AP; Hegele RA; Kastelein JJ; Hingorani AD; Talmud PJ; Hakonarson H; Elbers CC; Keating BJ; Drenos F, 2012. Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.  Am J Hum Genet 91(5):823-38

Gaunt TR; Shah S; Nelson CP; Drenos F; Braund PS; Adeniran I; Folkersen L; Lawlor DA; Casas JP; Amuzu A; Kivimaki M; Whittaker J; Eriksson P; Zhang H; Hancox JC; Tomaszewski M; Burton PR; Tobin MD; Humphries SE; Talmud PJ; Macfarlane PW; Hingorani AD; Samani NJ; Kumari M; Day IN, 2012. Integration of genetics into a systems model of electrocardiographic traits using HumanCVD BeadChip.  Circ Cardiovasc Genet 5(6):630-8

Rodriguez S; Williams DM; Guthrie PA; McArdle WL; Smith GD; Evans DM; Gaunt TR; Day IN, 2012. Molecular and population analysis of natural selection on the human haptoglobin duplication.  Ann Hum Genet 76(5):352-62

Alharbi KK; Hou G; Chen XH; Gaunt TR; Syddall HE; Sayer AA; Dennison EM; Phillips DI; Cooper C; Day IN, 2011. Population mutation scanning of human GHR by meltMADGE and identification of a paucimorphic variant.  Genet Test Mol Biomarkers 15(12):855-60

Lanktree MB; Guo Y; Murtaza M; Glessner JT; Bailey SD; Onland-Moret NC; Lettre G; Ongen H; Rajagopalan R; Johnson T; Shen H; Nelson CP; Klopp N; Baumert J; Padmanabhan S; Pankratz N; Pankow JS; Shah S; Taylor K; Barnard J; Peters BJ; Maloney CM; Lobmeyer MT; Stanton A; Zafarmand MH; Romaine SP; Mehta A; van Iperen EP; Gong Y; Price TS; Smith EN; Kim CE; Li YR; Asselbergs FW; Atwood LD; Bailey KM; Bhatt D; Bauer F; Behr ER; Bhangale T; Boer JM; Boehm BO; Bradfield JP; Brown M; Braund PS; Burton PR; Carty C; Chandrupatla HR; Chen W; Connell J; Dalgeorgou C; Boer Ad; Drenos F; Elbers CC; Fang JC; Fox CS; Frackelton EC; Fuchs B; Furlong CE; Gibson Q; Gieger C; Goel A; Grobbee DE; Hastie C; Howard PJ; Huang GH; Johnson WC; Li Q; Kleber ME; Klein BE; Klein R; Kooperberg C; Ky B; Lacroix A; Lanken P; Lathrop M; Li M; Marshall V; Melander O; Mentch FD; Meyer NJ; Monda KL; Montpetit A; Murugesan G; Nakayama K; Nondahl D; Onipinla A; Rafelt S; Newhouse SJ; Otieno FG; Patel SR; Putt ME; Rodriguez S; Safa RN; Sawyer DB; Schreiner PJ; Simpson C; Sivapalaratnam S; Srinivasan SR; Suver C; Swergold G; Sweitzer NK; Thomas KA; Thorand B; Timpson NJ; Tischfield S; Tobin M; Tomaszewski M; Verschuren WM; Wallace C; Winkelmann B; Zhang H; Zheng D; Zhang L; Zmuda JM; Clarke R; Balmforth AJ; Danesh J; Day IN; Schork NJ; de Bakker PI; Delles C; Duggan D; Hingorani AD; Hirschhorn JN; Hofker MH; Humphries SE; Kivimaki M; Lawlor DA; Kottke-Marchant K; Mega JL; Mitchell BD; Morrow DA; Palmen J; Redline S; Shields DC; Shuldiner AR; Sleiman PM; Smith GD; Farrall M; Jamshidi Y; Christiani DC; Casas JP; Hall AS; Doevendans PA; Christie JD; Berenson GS; Murray SS; Illig T; Dorn GW 2nd; Cappola TP; Boerwinkle E; Sever P; Rader DJ; Reilly MP; Caulfield M; Talmud PJ; Topol E; Engert JC; Wang K; Dominiczak A; Hamsten A; Curtis SP; Silverstein RL; Lange LA; Sabatine MS; Trip M; Saleheen D; Peden JF; Cruickshanks KJ; März W; O'Connell JR; Klungel OH; Wijmenga C; Maitland-van der Zee AH; Schadt EE; Johnson JA; Jarvik GP; Papanicolaou GJ; Grant SF; Munroe PB; North KE; Samani NJ; Koenig W; Gaunt TR; Anand SS; van der Schouw YT; Soranzo N; Fitzgerald GA; Reiner A; Hegele RA; Hakonarson H; Keating BJ, 2011. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height.  Am J Hum Genet 88(1):6-18

Rodriguez S; Cook DG; Gaunt TR; Nightingale CM; Whincup PH; Day IN, 2011. Combined analysis of CHRNA5, CHRNA3 and CYP2A6 in relation to adolescent smoking behaviour.  J Psychopharmacol 25(7):915-23

Guthrie PA; Gaunt TR; Abdollahi MR; Rodriguez S; Lawlor DA; Smith GD; Day IN, 2011. Amplification ratio control system for copy number variation genotyping.  Nucleic Acids Res 39(8):e54

Zabaneh D; Gaunt TR; Kumari M; Drenos F; Shah S; Berry D; Power C; Hypponen E; Shah T; Palmen J; Pallas J; Talmud PJ; Casas JP; Sofat R; Lowe G; Rumley A; Morris RW; Whincup PH; Rodriguez S; Ebrahim S; Marmot MG; Smith GD; Lawlor DA; Kivimaki M; Whittaker J; Hingorani AD; Day IN; Humphries SE, 2011. Genetic variants associated with Von Willebrand factor levels in healthy men and women identified using the HumanCVD BeadChip.  Ann Hum Genet 75(4):456-67

Ehret GB; Munroe PB; Rice KM; Bochud M; Johnson AD; Chasman DI; Smith AV; Tobin MD; Verwoert GC; Hwang SJ; Pihur V; Vollenweider P; O'Reilly PF; Amin N; Bragg-Gresham JL; Teumer A; Glazer NL; Launer L; Zhao JH; Aulchenko Y; Heath S; Sõber S; Parsa A; Luan J; Arora P; Dehghan A; Zhang F; Lucas G; Hicks AA; Jackson AU; Peden JF; Tanaka T; Wild SH; Rudan I; Igl W; Milaneschi Y; Parker AN; Fava C; Chambers JC; Fox ER; Kumari M; Go MJ; van der Harst P; Kao WH; Sjögren M; Vinay DG; Alexander M; Tabara Y; Shaw-Hawkins S; Whincup PH; Liu Y; Shi G; Kuusisto J; Tayo B; Seielstad M; Sim X; Nguyen KD; Lehtimäki T; Matullo G; Wu Y; Gaunt TR; Onland-Moret NC; Cooper MN; Platou CG; Org E; Hardy R; Dahgam S; Palmen J; Vitart V; Braund PS; Kuznetsova T; Uiterwaal CS; Adeyemo A; Palmas W; Campbell H; Ludwig B; Tomaszewski M; Tzoulaki I; Palmer ND; Aspelund T; Garcia M; Chang YP; O'Connell JR; Steinle NI; Grobbee DE; Arking DE; Kardia SL; Morrison AC; Hernandez D; Najjar S; McArdle WL; Hadley D; Brown MJ; Connell JM; Hingorani AD; Day IN; Lawlor DA; Beilby JP; Lawrence RW; Clarke R; Hopewell JC; Ongen H; Dreisbach AW; Li Y; Young JH; Bis JC; Kähönen M; Viikari J; Adair LS; Lee NR; Chen MH; Olden M; Pattaro C; Bolton JA; Köttgen A; Bergmann S; Mooser V; Chaturvedi N; Frayling TM; Islam M; Jafar TH; Erdmann J; Kulkarni SR; Bornstein SR; Grässler J; Groop L; Voight BF; Kettunen J; Howard P; Taylor A; Guarrera S; Ricceri F; Emilsson V; Plump A; Barroso I; Khaw KT; Weder AB; Hunt SC; Sun YV; Bergman RN; Collins FS; Bonnycastle LL; Scott LJ; Stringham HM; Peltonen L; Perola M; Vartiainen E; Brand SM; Staessen JA; Wang TJ; Burton PR; Soler Artigas M; Dong Y; Snieder H; Wang X; Zhu H; Lohman KK; Rudock ME; Heckbert SR; Smith NL; Wiggins KL; Doumatey A; Shriner D; Veldre G; Viigimaa M; Kinra S; Prabhakaran D; Tripathy V; Langefeld CD; Rosengren A; Thelle DS; Corsi AM; Singleton A; Forrester T; Hilton G; McKenzie CA; Salako T; Iwai N; Kita Y; Ogihara T; Ohkubo T; Okamura T; Ueshima H; Umemura S; Eyheramendy S; Meitinger T; Wichmann HE; Cho YS; Kim HL; Lee JY; Scott J; Sehmi JS; Zhang W; Hedblad B; Nilsson P; Smith GD; Wong A; Narisu N; Stančáková A; Raffel LJ; Yao J; Kathiresan S; O'Donnell CJ; Schwartz SM; Ikram MA; Longstreth WT Jr; Mosley TH; Seshadri S; Shrine NR; Wain LV; Morken MA; Swift AJ; Laitinen J; Prokopenko I; Zitting P; Cooper JA; Humphries SE; Danesh J; Rasheed A; Goel A; Hamsten A; Watkins H; Bakker SJ; van Gilst WH; Janipalli CS; Mani KR; Yajnik CS; Hofman A; Mattace-Raso FU; Oostra BA; Demirkan A; Isaacs A; Rivadeneira F; Lakatta EG; Orru M; Scuteri A; Ala-Korpela M; Kangas AJ; Lyytikäinen LP; Soininen P; Tukiainen T; Würtz P; Ong RT; Dörr M; Kroemer HK; Völker U; Völzke H; Galan P; Hercberg S; Lathrop M; Zelenika D; Deloukas P; Mangino M; Spector TD; Zhai G; Meschia JF; Nalls MA; Sharma P; Terzic J; Kumar MV; Denniff M; Zukowska-Szczechowska E; Wagenknecht LE; Fowkes FG; Charchar FJ; Schwarz PE; Hayward C; Guo X; Rotimi C; Bots ML; Brand E; Samani NJ; Polasek O; Talmud PJ; Nyberg F; Kuh D; Laan M; Hveem K; Palmer LJ; van der Schouw YT; Casas JP; Mohlke KL; Vineis P; Raitakari O; Ganesh SK; Wong TY; Tai ES; Cooper RS; Laakso M; Rao DC; Harris TB; Morris RW; Dominiczak AF; Kivimaki M; Marmot MG; Miki T; Saleheen D; Chandak GR; Coresh J; Navis G; Salomaa V; Han BG; Zhu X; Kooner JS; Melander O; Ridker PM; Bandinelli S; Gyllensten UB; Wright AF; Wilson JF; Ferrucci L; Farrall M; Tuomilehto J; Pramstaller PP; Elosua R; Soranzo N; Sijbrands EJ; Altshuler D; Loos RJ; Shuldiner AR; Gieger C; Meneton P; Uitterlinden AG; Wareham NJ; Gudnason V; Rotter JI; Rettig R; Uda M; Strachan DP; Witteman JC; Hartikainen AL; Beckmann JS; Boerwinkle E; Vasan RS; Boehnke M; Larson MG; Järvelin MR; Psaty BM; Abecasis GR; Chakravarti A; Elliott P; van Duijn CM; Newton-Cheh C; Levy D; Caulfield MJ; Johnson T, 2011. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.  Nature 478(7367):103-9

Johnson T; Gaunt TR; Newhouse SJ; Padmanabhan S; Tomaszewski M; Kumari M; Morris RW; Tzoulaki I; O'Brien ET; Poulter NR; Sever P; Shields DC; Thom S; Wannamethee SG; Whincup PH; Brown MJ; Connell JM; Dobson RJ; Howard PJ; Mein CA; Onipinla A; Shaw-Hawkins S; Zhang Y; Davey Smith G; Day IN; Lawlor DA; Goodall AH; Fowkes FG; Abecasis GR; Elliott P; Gateva V; Braund PS; Burton PR; Nelson CP; Tobin MD; van der Harst P; Glorioso N; Neuvrith H; Salvi E; Staessen JA; Stucchi A; Devos N; Jeunemaitre X; Plouin PF; Tichet J; Juhanson P; Org E; Putku M; Sõber S; Veldre G; Viigimaa M; Levinsson A; Rosengren A; Thelle DS; Hastie CE; Hedner T; Lee WK; Melander O; Wahlstrand B; Hardy R; Wong A; Cooper JA; Palmen J; Chen L; Stewart AF; Wells GA; Westra HJ; Wolfs MG; Clarke R; Franzosi MG; Goel A; Hamsten A; Lathrop M; Peden JF; Seedorf U; Watkins H; Ouwehand WH; Sambrook J; Stephens J; Casas JP; Drenos F; Holmes MV; Kivimaki M; Shah S; Shah T; Talmud PJ; Whittaker J; Wallace C; Delles C; Laan M; Kuh D; Humphries SE; Nyberg F; Cusi D; Roberts R; Newton-Cheh C; Franke L; Stanton AV; Dominiczak AF; Farrall M; Hingorani AD; Samani NJ; Caulfield MJ; Munroe PB, 2011. Blood pressure loci identified with a gene-centric array.  Am J Hum Genet 89(6):688-700

Raistrick CA; Alharbi KK; Day IN; Gaunt TR, 2011. Analysis of potential genomic confounding in genetic association studies and an online genomic confounding browser (GCB).  Ann Hum Genet 75(6):723-31

Shah S; Nelson CP; Gaunt TR; van der Harst P; Barnes T; Braund PS; Lawlor DA; Casas JP; Padmanabhan S; Drenos F; Kivimaki M; Talmud PJ; Humphries SE; Whittaker J; Morris RW; Whincup PH; Dominiczak A; Munroe PB; Johnson T; Goodall AH; Cambien F; Diemert P; Hengstenberg C; Ouwehand WH; Felix JF; Glazer NL; Tomaszewski M; Burton PR; Tobin MD; van Veldhuisen DJ; de Boer RA; Navis G; van Gilst WH; Mayosi BM; Thompson JR; Kumari M; MacFarlane PW; Day IN; Hingorani AD; Samani NJ, 2011. Four genetic loci influencing electrocardiographic indices of left ventricular hypertrophy.  Circ Cardiovasc Genet 4(6):626-35

Rodriguez S; Eiriksdottir G; Gaunt TR; Harris TB; Launer LJ; Gudnason V; Day IN, 2010. IGF2BP1, IGF2BP2 and IGF2BP3 genotype, haplotype and genetic model studies in metabolic syndrome traits and diabetes.  Growth Horm IGF Res 20(4):310-8

Smart-Halajko MC; Robciuc MR; Cooper JA; Jauhiainen M; Kumari M; Kivimaki M; Khaw KT; Boekholdt SM; Wareham NJ; Gaunt TR; Day IN; Braund PS; Nelson CP; Hall AS; Samani NJ; Humphries SE; Ehnholm C; Talmud PJ, 2010. The relationship between plasma angiopoietin-like protein 4 levels, angiopoietin-like protein 4 genotype, and coronary heart disease risk.  Arterioscler Thromb Vasc Biol 30(11):2277-82

Gaunt TR; Rodriguez S; Guthrie PA; Day IN, 2010. An expectation-maximization program for determining allelic spectrum from CNV data (CoNVEM): insights into population allelic architecture and its mutational history.  Hum Mutat 31(4):414-20

Raistrick CA; Day IN; Gaunt TR, 2010. Genome-wide data-mining of candidate human splice translational efficiency polymorphisms (STEPs) and an online database.  PLoS One 5(10):e13340

Alharbi KK; Aldahmesh MA; Gaunt TR; Rassoulian H; Ai Guthrie P; Rodriguez S; Boustred CR; Spanakis E; Day IN, 2010. MeltMADGE for mutation scanning of specific genes in population studies.  Nat Protoc 5(11):1800-12

Dennison EM; Syddall HE; Jameson KA; Sayer AA; Gaunt TR; Rodriguez S; Day IN; Cooper C; Lips MA, 2009. A study of relationships between single nucleotide polymorphisms from the growth hormone-insulin-like growth factor axis and bone mass: the Hertfordshire cohort study.  J Rheumatol 36(7):1520-6

Rodriguez S; Gaunt TR; Day IN, 2009. Hardy-Weinberg equilibrium testing of biological ascertainment for Mendelian randomization studies.  Am J Epidemiol 169(4):505-14

Talmud PJ; Drenos F; Shah S; Shah T; Palmen J; Verzilli C; Gaunt TR; Pallas J; Lovering R; Li K; Casas JP; Sofat R; Kumari M; Rodriguez S; Johnson T; Newhouse SJ; Dominiczak A; Samani NJ; Caulfield M; Sever P; Stanton A; Shields DC; Padmanabhan S; Melander O; Hastie C; Delles C; Ebrahim S; Marmot MG; Smith GD; Lawlor DA; Munroe PB; Day IN; Kivimaki M; Whittaker J; Humphries SE; Hingorani AD, 2009. Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.  Am J Hum Genet 85(5):628-42

Abdollahi MR; Huang S; Rodriguez S; Guthrie PA; Smith GD; Ebrahim S; Lawlor DA; Day IN; Gaunt TR, 2008. Homogeneous assay of rs4343, an ACE I/D proxy, and an analysis in the British Women's Heart and Health Study (BWHHS).  Dis Markers 24(1):11-7

Lawlor DA; Harbord RM; Timpson NJ; Lowe GD; Rumley A; Gaunt TR; Baker I; Yarnell JW; Kivimäki M; Kumari M; Norman PE; Jamrozik K; Hankey GJ; Almeida OP; Flicker L; Warrington N; Marmot MG; Ben-Shlomo Y; Palmer LJ; Day IN; Ebrahim S; Smith GD, 2008. 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.  PLoS One 3(8):e3011

Lips MA; Syddall HE; Gaunt TR; Rodriguez S; Day IN; Cooper C; Dennison EM, 2007. Interaction between birthweight and polymorphism in the calcium-sensing receptor gene in determination of adult bone mass: the Hertfordshire cohort study.  J Rheumatol 34(4):769-75

Lawlor DA; Day IN; Gaunt TR; Hinks LJ; Timpson N; Ebrahim S; Davey Smith G, 2007. The association of the paraoxonase (PON1) Q192R polymorphism with depression in older women: findings from the British Women's Heart and Health Study.  J Epidemiol Community Health 61(1):85-7

Huang S; Chen XH; Payne JR; Pennell DJ; Gohlke P; Smith MJ; Day IN; Montgomery HE; Gaunt TR, 2007. Haplotype of growth hormone and angiotensin I-converting enzyme genes, serum angiotensin I-converting enzyme and ventricular growth: pathway inference in pharmacogenetics.  Pharmacogenet Genomics 17(4):291-4

Abdollahi MR; Lewis RM; Gaunt TR; Cumming DV; Rodriguez S; Rose-Zerilli M; Collins AR; Syddall HE; Howell WM; Cooper C; Godfrey KM; Cameron IT; Day IN, 2007. Quantitated transcript haplotypes (QTH) of AGTR1, reduced abundance of mRNA haplotypes containing 1166C (rs5186:A>C), and relevance to metabolic syndrome traits.  Hum Mutat 28(4):365-73

Rodriguez S; Gaunt TR; Day IN, 2007. Molecular genetics of human growth hormone, insulin-like growth factors and their pathways in common disease.  Hum Genet 122(1):1-21

Gaunt TR; Rodríguez S; Day IN, 2007. Cubic exact solutions for the estimation of pairwise haplotype frequencies: implications for linkage disequilibrium analyses and a web tool 'CubeX'.  BMC Bioinformatics 8:428

Rodriguez S; Gaunt TR; Vorechovsky I; Kralovicová J; Wood PJ; Day IN, 2007. Comment on: Marchand and Polychronakos (2007) Evaluation of polymorphic splicing in the mechanism of the association of the insulin gene with diabetes: Diabetes 56:709-713.  Diabetes 56(9):e16; author reply e17

Královicová J; Gaunt TR; Rodriguez S; Wood PJ; Day IN; Vorechovsky I, 2006. Variants in the human insulin gene that affect pre-mRNA splicing: is -23HphI a functional single nucleotide polymorphism at IDDM2?  Diabetes 55(1):260-4

Rodríguez S; Huang S; Chen XH; Gaunt TR; Syddall HE; Gilg JA; Miller GJ; Cooper CC; Cook DG; Whincup PH; Day IN, 2006. A study of TH01 and IGF2-INS-TH haplotypes in relation to smoking initiation in three independent surveys.  Pharmacogenet Genomics 16(1):15-23

Rodríguez S; Gaunt TR; Dennison E; Chen XH; Syddall HE; Phillips DI; Cooper C; Day IN, 2006. Replication of IGF2-INS-TH*5 haplotype effect on obesity in older men and study of related phenotypes.  Eur J Hum Genet 14(1):109-16

Christensen MB; Lawlor DA; Gaunt TR; Howell WM; Davey Smith G; Ebrahim S; Day IN, 2006. Genotype of galectin 2 (LGALS2) is associated with insulin-glucose profile in the British Women's Heart and Health Study.  Diabetologia 49(4):673-7

Gaunt TR; Rodriguez S; Zapata C; Day IN, 2006. MIDAS: software for analysis and visualisation of interallelic disequilibrium between multiallelic markers.  BMC Bioinformatics 7:227

Day IN; Rodriguez S; Královicová J; Wood PJ; Vorechovsky I; Gaunt TR, 2006. Questioning INS VNTR role in obesity and diabetes: subclasses tag IGF2-INS-TH haplotypes; and -23HphI as a STEP (splicing and translational efficiency polymorphism).  Physiol Genomics 28(1):113

Lawlor DA; Gaunt TR; Hinks LJ; Davey Smith G; Timpson N; Day IN; Ebrahim S, 2006. The association of the PON1 Q192R polymorphism with complications and outcomes of pregnancy: findings from the British Women's Heart and Health cohort study.  Paediatr Perinat Epidemiol 20(3):244-50

Zhang W; Maniatis N; Rodriguez S; Miller GJ; Day IN; Gaunt TR; Collins A; Morton NE, 2006. Refined association mapping for a quantitative trait: weight in the H19-IGF2-INS-TH region.  Ann Hum Genet 70(Pt 6):848-56

Abdollahi MR; Gaunt TR; Syddall HE; Cooper C; Phillips DI; Ye S; Day IN, 2005. Angiotensin II type I receptor gene polymorphism: anthropometric and metabolic syndrome traits.  J Med Genet 42(5):396-401

Timpson NJ; Lawlor DA; Harbord RM; Gaunt TR; Day IN; Palmer LJ; Hattersley AT; Ebrahim S; Lowe GD; Rumley A; Davey Smith G, 2005. C-reactive protein and its role in metabolic syndrome: mendelian randomisation study.  Lancet 366(9501):1954-9

Timpson NJ; Christensen M; Lawlor DA; Gaunt TR; Day IN; Ebrahim S; Davey Smith G, 2005. TAS2R38 (phenylthiocarbamide) haplotypes, coronary heart disease traits, and eating behavior in the British Women's Heart and Health Study.  Am J Clin Nutr 81(5):1005-11

Rodríguez S; Gaunt TR; O'Dell SD; Chen XH; Gu D; Hawe E; Miller GJ; Humphries SE; Day IN, 2004. Haplotypic analyses of the IGF2-INS-TH gene cluster in relation to cardiovascular risk traits.  Hum Mol Genet 13(7):715-25

Day IN; Chen XH; Gaunt TR; King TH; Voropanov A; Ye S; Rodriguez S; Syddall HE; Sayer AA; Dennison EM; Tabassum F; Barker DJ; Cooper C; Phillips DI, 2004. Late life metabolic syndrome, early growth, and common polymorphism in the growth hormone and placental lactogen gene cluster.  J Clin Endocrinol Metab 89(11):5569-76

Lawlor DA; Day IN; Gaunt TR; Hinks LJ; Briggs PJ; Kiessling M; Timpson N; Smith GD; Ebrahim S, 2004. The association of the PON1 Q192R polymorphism with coronary heart disease: findings from the British Women's Heart and Health cohort study and a meta-analysis.  BMC Genet 5:17

Gaunt TR; Hinks LJ; Rassoulian H; Day IN, 2003. Manual 768 or 384 well microplate gel 'dry' electrophoresis for PCR checking and SNP genotyping.  Nucleic Acids Res 31(9):e48

O'Dell SD; Syddall HE; Sayer AA; Cooper C; Fall CH; Dennison EM; Phillips DI; Gaunt TR; Briggs PJ; Day IN, 2002. Null mutation in human ciliary neurotrophic factor gene confers higher body mass index in males.  Eur J Hum Genet 10(11):749-52

Holloway JW; Lonjou C; Beghé B; Peng Q; Gaunt TR; Gomes I; Hall IP; Dewar JC; Wilkinson J; Thomas NS; Holgate ST; Morton NE, 2001. Linkage analysis of the 5q31-33 candidate region for asthma in 240 UK families.  Genes Immun 2(1):20-4

Gaunt TR; Cooper JA; Miller GJ; Day IN; O'Dell SD, 2001. Positive associations between single nucleotide polymorphisms in the IGF2 gene region and body mass index in adult males.  Hum Mol Genet 10(14):1491-501

O'Dell SD; Gaunt TR; Day IN, 2000. SNP genotyping by combination of 192-well MADGE, ARMS and computerized gel image analysis.  Biotechniques 29(3):500-4, 505-6

Publication list retrieved from NCBI using ImpactPubs

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