Items where Author is "103145"

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Number of items: 153.

2016

Charoen, P; Nitsch, D; Engmann, J; Shah, T; White, J; Zabaneh, D; Jefferis, B; Wannamethee, G; Whincup, P; Mulick Cassidy, A; +31 more... (2016) Mendelian Randomisation study of the influence of eGFR on coronary heart disease. Sci Rep, 6. p. 28514. ISSN 2045-2322 DOI: 10.1038/srep28514
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Swerdlow, DI; Kuchenbaecker, KB; Shah, S; Sofat, R; Holmes, MV; White, J; Mindell, JS; Kivimaki, M; Brunner, EJ; Whittaker, JC; +2 more... (2016) Selecting instruments for Mendelian randomization in the wake of genome-wide association studies. International journal of epidemiology. ISSN 0300-5771 DOI: 10.1093/ije/dyw088 Full text not available from this repository.

2015

Moore, GE; Ishida, M; Demetriou, C; Al-Olabi, L; Leon, LJ; Thomas, AC; Abu-Amero, S; Frost, JM; Stafford, JL; Chaoqun, Y; +12 more... (2015) The role and interaction of imprinted genes in human fetal growth. Philosophical transactions of the Royal Society of London Series B, Biological sciences, 370 (1663). ISSN 0962-8436 DOI: 10.1098/rstb.2014.0074
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Nelson, MR; Tipney, H; Painter, JL; Shen, J; Nicoletti, P; Shen, Y; Floratos, A; Sham, PC; Li, MJ; Wang, J; +3 more... (2015) The support of human genetic evidence for approved drug indications. Nature genetics, 47 (8). pp. 856-60. ISSN 1061-4036 DOI: 10.1038/ng.3314 Full text not available from this repository.

Nüesch, E; Dale, C; Palmer, TM; White, J; Keating, BJ; van Iperen, EP; Goel, A; Padmanabhan, S; Asselbergs, FW; EPIC-Netherland Investigators, ; +71 more... (2015) Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis. International journal of epidemiology. ISSN 0300-5771 DOI: 10.1093/ije/dyv074 Full text not available from this repository.

Swerdlow, DI; Preiss, D; Kuchenbaecker, KB; Holmes, MV; Engmann, JE; Shah, T; Sofat, R; Stender, S; Johnson, PC; Scott, RA; +126 more... (2015) HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials. Lancet, 385 (9965). pp. 351-61. ISSN 0140-6736 DOI: 10.1016/S0140-6736(14)61183-1
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Xu, CF; Johnson, T; Garcia-Donas, J; Choueiri, TK; Sternberg, CN; Davis, ID; Bing, N; Deen, KC; Xue, Z; McCann, L; +6 more... (2015) IL8 polymorphisms and overall survival in pazopanib- or sunitinib-treated patients with renal cell carcinoma. British journal of cancer, 112 (7). pp. 1190-8. ISSN 0007-0920 DOI: 10.1038/bjc.2015.64
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2014

Futema, M; Shah, S; Cooper, JA; Li, K; Whittall, RA; Sharifi, M; Goldberg, O; Drogari, E; Mollaki, V; Wiegman, A; +16 more... (2014) Refinement of Variant Selection for the LDL Cholesterol Genetic Risk Score in the Diagnosis of the Polygenic Form of Clinical Familial Hypercholesterolemia and Replication in Samples from 6 Countries. Clinical chemistry. ISSN 0009-9147 DOI: 10.1373/clinchem.2014.231365 Full text not available from this repository.

Talmud, PJ; Cooper, JA; Morris, RW; Dudbridge, F; Shah, T; Engmann, J; Dale, C; White, J; McLachlan, S; Zabaneh, D; +21 more... (2014) Sixty-five common genetic variants and prediction of type 2 diabetes. Diabetes. ISSN 0012-1797 DOI: 10.2337/db14-1504
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Vimaleswaran, KS; Cavadino, A; Berry, DJ; LifeLines Cohort Study investigators, ; Jorde, R; Dieffenbach, AK; Lu, C; Alves, AC; Heerspink, HJ; Tikkanen, E; +98 more... (2014) Association of vitamin D status with arterial blood pressure and hypertension risk: a mendelian randomisation study. The lancet Diabetes & endocrinology. ISSN 2213-8587 DOI: 10.1016/S2213-8587(14)70113-5
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2013

Chan, K; Patel, RS; Newcombe, P; Nelson, CP; Qasim, A; Epstein, SE; Burnett, S; Vaccarino, VL; Zafari, AM; Shah, SH; +42 more... (2013) Association Between the Chromosome 9p21 Locus and Angiographic Coronary Artery Disease Burden A Collaborative Meta-Analysis. Journal of the American College of Cardiology, 61 (9). pp. 957-970. ISSN 0735-1097 DOI: 10.1016/j.jacc.2012.10.051 Full text not available from this repository.

Dixon, PH; Wadsworth, CA; Chambers, J; Donnelly, J; Cooley, S; Buckley, R; Mannino, R; Jarvis, S; Syngelaki, A; Geenes, V; +13 more... (2013) A Comprehensive Analysis of Common Genetic Variation Around Six Candidate Loci for Intrahepatic Cholestasis of Pregnancy. The American journal of gastroenterology, 109 (1). pp. 76-84. ISSN 0002-9270 DOI: 10.1038/ajg.2013.406
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Hu, Y; Li, L; Ehm, MG; Bing, N; Song, K; Nelson, MR; Talmud, PJ; Hingorani, AD; Kumari, M; Kivimäki, M; +6 more... (2013) The benefits of using genetic information to design prevention trials. American journal of human genetics, 92 (4). pp. 547-57. ISSN 0002-9297 DOI: 10.1016/j.ajhg.2013.03.003 Full text not available from this repository.

Khan, TA; Shah, T; Prieto, D; Zhang, W; Price, J; Fowkes, GR; Cooper, J; Talmud, PJ; Humphries, SE; Sundstrom, J; +39 more... (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. International journal of epidemiology, 42 (2). pp. 475-492. ISSN 0300-5771 DOI: 10.1093/ije/dyt034 Full text not available from this repository.

Shah, S; Casas, JP; Drenos, F; Whittaker, J; Deanfield, J; Swerdlow, DI; Holmes, MV; Kivimaki, M; Langenberg, C; Wareham, N; +13 more... (2013) Causal Relevance of Blood Lipid Fractions in the Development of Carotid Atherosclerosis Mendelian Randomization Analysis. Circulation Cardiovascular genetics, 6 (1). pp. 63-72. ISSN 1942-325X DOI: 10.1161/CIRCGENETICS.112.963140 Full text not available from this repository.

Shah, T; Engmann, J; Dale, C; Shah, S; White, J; Giambartolomei, C; McLachlan, S; Zabaneh, D; Cavadino, A; Finan, C; +35 more... (2013) Population Genomics of Cardiometabolic Traits: Design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) Consortium. PLoS One, 8 (8). e71345. ISSN 1932-6203 DOI: 10.1371/journal.pone.0071345
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Shah, T; Zabaneh, D; Gaunt, T; Swerdlow, DI; Shah, S; Talmud, PJ; Day, IN; Whittaker, J; Holmes, MV; Sofat, R; +5 more... (2013) Gene-Centric Analysis Identifies Variants Associated With Interleukin-6 Levels and Shared Pathways With Other Inflammation Markers. Circulation Cardiovascular genetics, 6 (2). 163-+. ISSN 1942-325X DOI: 10.1161/CIRCGENETICS.112.964254 Full text not available from this repository.

Talmud, PJ; Shah, S; Whittall, R; Futema, M; Howard, P; Cooper, JA; Harrison, SC; LI, K; Drenos, F; Karpe, F; +9 more... (2013) Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolaemia: a case-control study. Lancet, 381 (9874). pp. 1293-1301. ISSN 0140-6736 DOI: 10.1016/S0140-6736(12)62127-8 Full text not available from this repository.

Vimaleswaran, KS; Berry, DJ; Lu, C; Tikkanen, E; Pilz, S; Hiraki, LT; Cooper, JD; Dastani, Z; LI, R; Houston, DK; +49 more... (2013) Causal Relationship between Obesity and Vitamin D Status: Bi-Directional Mendelian Randomization Analysis of Multiple Cohorts. PLoS medicine, 10 (2). ISSN 1549-1277 DOI: 10.1371/journal.pmed.1001383
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Vimaleswaran, KS; Cavadino, A; Berry, DJ; Whittaker, JC; Power, C; Jaervelin, MR; Hyppoenen, E; Genetic Invest Anthropometric, Trai; (2013) Genetic association analysis of vitamin D pathway with obesity traits. International journal of obesity and related metabolic disorders , 37 (10). pp. 1399-1406. ISSN 0307-0565 DOI: 10.1038/ijo.2013.6 Full text not available from this repository.

Warren, H; Casas, JP; Hingorani, A; Dudbridge, F; Whittaker, J; (2013) Genetic Prediction of Quantitative Lipid Traits: Comparing Shrinkage Models to Gene Scores. Genetic epidemiology, 38 (1). pp. 72-83. ISSN 0741-0395 DOI: 10.1002/gepi.21777 Full text not available from this repository.

2012

Asselbergs, FW; Guo, Y; van Iperen, EP; Sivapalaratnam, S; Tragante, V; Lanktree, MB; Lange, LA; Almoguera, B; Appelman, YE; Barnard, J; +161 more... (2012) Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. American journal of human genetics, 91 (5). pp. 823-38. ISSN 0002-9297 DOI: 10.1016/j.ajhg.2012.08.032 Full text not available from this repository.

Gaunt, TR; Shah, S; Nelson, CP; Drenos, F; Braund, PS; Adeniran, I; Folkersen, L; Lawlor, DA; Casas, JP; Amuzu, A; +15 more... (2012) Integration of Genetics into a Systems Model of Electrocardiographic Traits Using HumanCVD BeadChip. Circulation Cardiovascular genetics, 5 (6). pp. 630-638. ISSN 1942-325X DOI: 10.1161/CIRCGENETICS.112.962852 Full text not available from this repository.

Ishida, M; Monk, D; Duncan, AJ; Abu-Amero, S; Chong, JH; Ring, SM; Pembrey, ME; Hindmarsh, PC; Whittaker, JC; Stanier, P; +1 more... (2012) Maternal Inheritance of a Promoter Variant in the Imprinted PHLDA2 Gene Significantly Increases Birth Weight. American journal of human genetics, 90 (4). pp. 715-719. ISSN 0002-9297 DOI: 10.1016/j.ajhg.2012.02.021 Full text not available from this repository.

McCarthy, LC; Newcombe, PJ; Whittaker, JC; Wurzelmann, JI; Fries, MA; Burnham, NR; Cai, G; Stinnett, SW; Trivedi, TM; Xu, CF; (2012) Predictive models of choroidal neovascularization and geographic atrophy incidence applied to clinical trial design. American journal of ophthalmology, 154 (3). 568-578.e12. ISSN 0002-9394 DOI: 10.1016/j.ajo.2012.03.021 Full text not available from this repository.

Mead, S; Uphill, J; Beck, J; Poulter, M; Campbell, T; Lowe, J; Adamson, G; Hummerich, H; Klopp, N; Ruckert, IM; +11 more... (2012) Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. Human molecular genetics, 21 (8). pp. 1897-1906. ISSN 0964-6906 DOI: 10.1093/hmg/ddr607 Full text not available from this repository.

Nelson, MR; Wegmann, D; Ehm, MG; Kessner, D; St Jean, P; Verzilli, C; Shen, J; Tang, Z; Bacanu, SA; Fraser, D; +21 more... (2012) An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people. Science (New York, NY), 337 (6090). pp. 100-4. ISSN 0036-8075 DOI: 10.1126/science.1217876 Full text not available from this repository.

Newcombe, PJ; Reck, BH; Sun, J; Platek, GT; Verzilli, C; Kader, AK; Kim, ST; Hsu, FC; Zhang, Z; Zheng, SL; +6 more... (2012) A comparison of Bayesian and frequentist approaches to incorporating external information for the prediction of prostate cancer risk. Genetic epidemiology, 36 (1). pp. 71-83. ISSN 0741-0395 DOI: 10.1002/gepi.21600 Full text not available from this repository.

Rubio, JP; Topp, S; Warren, L; St Jean, PL; Wegmann, D; Kessner, D; Novembre, J; Shen, J; Fraser, D; Aponte, J; +7 more... (2012) Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in Europe. Human mutation, 33 (7). pp. 1087-98. ISSN 1059-7794 DOI: 10.1002/humu.22075 Full text not available from this repository.

Shah, S; Casas, JP; Gaunt, TR; Cooper, J; Drenos, F; Zabaneh, D; Swerdlow, DI; Shah, T; Sofat, R; Palmen, J; +10 more... (2012) Influence of common genetic variation on blood lipid levels, cardiovascular risk, and coronary events in two British prospective cohort studies. European heart journal. ISSN 0195-668X DOI: 10.1093/eurheartj/ehs243 Full text not available from this repository.

Sofat, R; Casas, JP; Webster, AR; Bird, AC; Mann, SS; Yates, JR; Moore, AT; Sepp, T; Cipriani, V; Bunce, C; +43 more... (2012) Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype. International journal of epidemiology, 41 (1). pp. 250-62. ISSN 0300-5771 DOI: 10.1093/ije/dyr204 Full text not available from this repository.

Song, K; Nelson, MR; Aponte, J; Manas, ES; Bacanu, SA; Yuan, X; Kong, X; Cardon, L; Mooser, VE; Whittaker, JC; +1 more... (2012) Sequencing of Lp-PLA2-encoding PLA2G7 gene in 2000 Europeans reveals several rare loss-of-function mutations. The pharmacogenomics journal, 12 (5). pp. 425-31. ISSN 1470-269X DOI: 10.1038/tpj.2011.20
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Walker, Jemma; (2012) Bayesian modelling in genetic association studies. PhD thesis, London School of Hygiene & Tropical Medicine.
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Warren, LL; Li, L; Nelson, MR; Ehm, MG; Shen, J; Fraser, DJ; Aponte, JL; Nangle, KL; Slater, AJ; Woollard, PM; +12 more... (2012) Deep resequencing unveils genetic architecture of ADIPOQ and identifies a novel low-frequency variant strongly associated with adiponectin variation. Diabetes, 61 (5). pp. 1297-301. ISSN 0012-1797 DOI: 10.2337/db11-0985
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2011

Balchin, I; Whittaker, JC; Lamont, RF; Steer, PJ; (2011) Maternal and Fetal Characteristics Associated With Meconium-Stained Amniotic Fluid. Obstetrics and gynecology, 117 (4). pp. 828-35. ISSN 0029-7844 DOI: 10.1097/AOG.0b013e3182117a26 Full text not available from this repository.

Brown, AA; Richardson, S; Whittaker, J; (2011) Application of the Lasso to Expression Quantitative Trait Loci Mapping. Statistical applications in genetics and molecular biology, 10 (1). ISSN 2194-6302 DOI: 10.2202/1544-6115.1606 Full text not available from this repository.

C Reactive Protein Coronary Heart Disease Genetics Collaboration, ; Wensley, F; Gao, P; Burgess, S; Kaptoge, S; Di Angelantonio, E; Shah, T; Engert, JC; Clarke, R; Davey-Smith, G; +12 more... (2011) Association between C reactive protein and coronary heart disease: mendelian randomisation analysis based on individual participant data. BMJ, 342. d548. ISSN 1468-5833 DOI: 10.1136/bmj.d548
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Dixon, PH; Wadsworth, CA; Chambers, J; Donnelly, JC; Cooley, SM; Kubitz, R; Lammert, F; Marschall, HU; Glantz, A; Khan, SA; +3 more... (2011) DOES COMMON GENETIC VARIATION AROUND THE PREGNANE-X RECEPTOR INFLUENCE SUSCEPTIBILITY TO INTRAHEPATIC CHOLESTASIS OF PREGNANCY? [Conference or Workshop Item] Full text not available from this repository.

Hyppönen, E; Fararouei, M; Sovio, U; Hartikainen, AL; Pouta, A; Robertson, C; Whittaker, JC; Jarvelin, MR; (2011) High-Dose Vitamin D Supplements Are Not Associated with Linear Growth in a Large Finnish Cohort. The Journal of nutrition, 141 (5). pp. 843-8. ISSN 0022-3166 DOI: 10.3945/jn.110.133009 Full text not available from this repository.

Li, L; Li, Y; Browning, SR; Browning, BL; Slater, AJ; Kong, X; Aponte, JL; Mooser, VE; Chissoe, SL; Whittaker, JC; +2 more... (2011) Performance of genotype imputation for rare variants identified in exons and flanking regions of genes. PLoS One, 6 (9). e24945. ISSN 1932-6203 DOI: 10.1371/journal.pone.0024945
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Shah, S; Nelson, CP; Gaunt, TR; van der Harst, P; Barnes, T; Braund, PS; Lawlor, DA; Casas, JP; Padmanabhan, S; Drenos, F; +30 more... (2011) Four Genetic Loci Influencing Electrocardiographic Indices of Left Ventricular Hypertrophy. Circulation Cardiovascular genetics, 4 (6). pp. 626-35. ISSN 1942-325X DOI: 10.1161/CIRCGENETICS.111.960203 Full text not available from this repository.

Spraggs, CF; Budde, LR; Briley, LP; Bing, N; Cox, CJ; King, KS; Whittaker, JC; Mooser, VE; Preston, AJ; Stein, SH; +1 more... (2011) HLA-DQA1*02:01 is a major risk factor for lapatinib-induced hepatotoxicity in women with advanced breast cancer. Journal of clinical oncology , 29 (6). pp. 667-73. ISSN 0732-183X DOI: 10.1200/JCO.2010.31.3197 Full text not available from this repository.

Talmud, PJ; Cooper, JA; Gaunt, T; Holmes, MV; Shah, S; Palmen, J; Drenos, F; Shah, T; Kumari, M; Kivimaki, M; +6 more... (2011) Variants of ADRA2A are associated with fasting glucose, blood pressure, body mass index and type 2 diabetes risk: meta-analysis of four prospective studies. Diabetologia, 54 (7). pp. 1710-1719. ISSN 0012-186X DOI: 10.1007/s00125-011-2108-6
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Wadsworth, CA; Dixon, PH; Wong, JH; Chapman, MH; McKay, SC; Sharif, A; Spalding, DR; Pereira, SP; Thomas, HC; Taylor-Robinson, SD; +3 more... (2011) Genetic Factors in the Pathogenesis of Cholangiocarcinoma. Digestive diseases (Basel, Switzerland), 29 (1). pp. 93-97. ISSN 0257-2753 DOI: 10.1159/000324688 Full text not available from this repository.

Xu, CF; Bing, NX; Ball, HA; Rajagopalan, D; Sternberg, CN; Hutson, TE; de Souza, P; Xue, ZG; McCann, L; King, KS; +6 more... (2011) Pazopanib efficacy in renal cell carcinoma: evidence for predictive genetic markers in angiogenesis-related and exposure-related genes. Journal of clinical oncology , 29 (18). pp. 2557-64. ISSN 0732-183X DOI: 10.1200/JCO.2010.32.9110 Full text not available from this repository.

Zabaneh, D; Gaunt, TR; Kumari, M; Drenos, F; Shah, S; Berry, D; Power, C; Hypponen, E; Shah, T; Palmen, J; +18 more... (2011) Genetic Variants Associated with von Willebrand Factor Levels in Healthy Men and Women Identified Using the HumanCVD BeadChip. Annals of human genetics. ISSN 0003-4800 DOI: 10.1111/j.1469-1809.2011.00654.x Full text not available from this repository.

Zabaneh, D; Kumari, M; Sandhu, M; Wareham, N; Wainwright, N; Papamarkou, T; Hopewell, J; Clarke, R; LI, K; Palmen, J; +16 more... (2011) Meta analysis of candidate gene variants outside the LPA locus with Lp(a) plasma levels in 14,500 participants of six White European cohorts. Atherosclerosis, 217 (2). pp. 447-451. ISSN 0021-9150 DOI: 10.1016/j.atherosclerosis.2011.04.015 Full text not available from this repository.

de Iorio, M; Newcombe, PJ; Tachmazidou, I; Verzilli, CJ; Whittaker, JC; (2011) Bayesian Semiparametric Meta-Analysis for Genetic Association Studies. Genetic epidemiology, 35 (5). pp. 333-340. ISSN 0741-0395 DOI: 10.1002/gepi.20581 Full text not available from this repository.

2010

Burgess, S; Thompson, SG; CRP CHD Genetics Collaboration, ; Burgess, S; Thompson, SG; Andrews, G; Samani, NJ; Hall, A; Whincup, P; Morris, R; +107 more... (2010) Bayesian methods for meta-analysis of causal relationships estimated using genetic instrumental variables. Statistics in medicine, 29 (12). pp. 1298-311. ISSN 0277-6715 DOI: 10.1002/sim.3843 Full text not available from this repository.

Dixon, PH; Wadsworth, CA; Chambers, J; Donnelly, J; Cooley, SM; Jarvis, S; Kubitz, R; Lammert, F; Marschall, HU; Glantz, A; +4 more... (2010) The Role of Common Genetic Variation around Six Candidate Loci for Susceptibility to Intrahepatic Cholestasis of Pregnancy. Hepatology (Baltimore, Md), 52 (4). 479A-479A. ISSN 0270-9139 Full text not available from this repository.

Fararouei, M; Robertson, C; Whittaker, J; Sovio, U; Ruokonen, A; Pouta, A; Hartikainen, AL; Jarvelin, MR; Hypponen, E; (2010) Maternal Hb during pregnancy and offspring's educational achievement: a prospective cohort study over 30 years. The British journal of nutrition. pp. 1-6. ISSN 0007-1145 DOI: 10.1017/S0007114510002175
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Morris, DL; Roberts, AL; Witherden, AS; Tarzi, R; Barros, P; Whittaker, JC; Cook, TH; Aitman, TJ; Vyse, TJ; (2010) Evidence for both copy number and allelic (NA1/NA2) risk at the FCGR3B locus in systemic lupus erythematosus. European journal of human genetics , 18 (9). pp. 1027-1031. ISSN 1018-4813 DOI: 10.1038/ejhg.2010.56 Full text not available from this repository.

Shah, S; Drenos, F; Shah, T; Palmen, J; Sofat, R; Kumari, M; Pallas, J; MacFarlane, P; Whittaker, J; Talmud, P; +2 more... (2010) Identification of Genes Associated with Qt Interval Using the 50k Cardio-Metabolic Snp Chip: Results from the Whitehall II Study. [Conference or Workshop Item] Full text not available from this repository.

Shah, T; Newcombe, P; Smeeth, L; Addo, J; Casas, JP; Whittaker, J; Miller, MA; Tinworth, L; Jeffery, S; Strazzullo, P; +2 more... (2010) Ancestry as a Determinant of Mean Population C-Reactive Protein Values: Implications for Cardiovascular Risk Prediction. Circulation Cardiovascular genetics, 3 (5). pp. 436-44. ISSN 1942-325X DOI: 10.1161/CIRCGENETICS.110.957431 Full text not available from this repository.

Sofat, R; Casas, JP; Kumari, M; Talmud, PJ; Ireland, H; Kivimaki, M; Marmot, M; Hughes, AD; Thom, S; Ebrahim, S; +5 more... (2010) Genetic variation in complement factor H and risk of coronary heart disease: Eight new studies and a meta-analysis of around 48,000 individuals. Atherosclerosis. ISSN 0021-9150 DOI: 10.1016/j.atherosclerosis.2010.07.021 Full text not available from this repository.

2009

Balchin, I; Whittaker, JC; Lamont, RF; Steer, PJ; (2009) The effect of exclusion of cases with unrecorded best estimate of gestational age on the estimates of preterm birth rate. BJOG , 116 (9). pp. 1218-1224. ISSN 1470-0328 DOI: 10.1111/j.1471-0528.2009.02184.x Full text not available from this repository.

Casas, Juan-Pablo; (2009) Mendelian randomisation and cardiovascular disease. PhD thesis, London School of Hygiene & Tropical Medicine.
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Chapman, JM; Onnie, CM; Prescott, NJ; Fisher, SA; Mansfield, JC; Mathew, CG; Lewis, CM; Verzilli, CJ; Whittaker, JC; (2009) Searching for Genotype-Phenotype Structure: Using Hierarchical Log-Linear Models in Crohn Disease. American journal of human genetics, 84 (2). pp. 178-87. ISSN 0002-9297 DOI: 10.1016/j.ajhg.2008.12.015 Full text not available from this repository.

Clarke, MC; Tanskanen, A; Huttunen, M; Whittaker, JC; Cannon, M; (2009) Evidence for an interaction between familial liability and prenatal exposure to infection in the causation of schizophrenia. The American journal of psychiatry, 166 (9). pp. 1025-30. ISSN 0002-953X DOI: 10.1176/appi.ajp.2009.08010031 Full text not available from this repository.

Doudney, K; Grinham, J; Whittaker, J; Lynch, SA; Thompson, D; Moore, GE; Copp, AJ; Greene, NDE; Stanier, P; (2009) Evaluation of Folate Metabolism Gene Polymorphisms as Risk Factors for Open and Closed Neural Tube Defects. American journal of medical genetics Part A, 149A (7). pp. 1585-1589. ISSN 1552-4825 DOI: 10.1002/ajmg.a.32937 Full text not available from this repository.

Khalique, L; Ayhan, A; Whittaker, JC; Singh, N; Jocobs, IJ; Gayther, SA; Ramus, SJ; (2009) The clonal evolution of metastases from primary serous epithelial ovarian cancers. International journal of cancer Journal international du cancer, 124 (7). pp. 1579-1586. ISSN 0020-7136 DOI: 10.1002/ijc.24148 Full text not available from this repository.

Lunn, DJ; Best, N; Whittaker, JC; (2009) Generic reversible jump MCMC using graphical models. Statistics and computing, 19 (4). pp. 395-408. ISSN 0960-3174 DOI: 10.1007/s11222-008-9100-0 Full text not available from this repository.

Mead, S; Poulter, M; Uphill, J; Beck, J; Whitfield, J; Webb, TEF; Campbell, T; Adamson, G; Deriziotis, P; Tabrizi, SJ; +5 more... (2009) Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. Lancet neurology, 8 (1). pp. 57-66. ISSN 1474-4422 DOI: 10.1016/S1474-4422(08)70265-5
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Mead, S; Whitfield, J; Poulter, M; Shah, P; Uphill, J; Campbell, T; Al-Dujaily, H; Hummerich, H; Beck, J; Mein, CA; +4 more... (2009) A Novel Protective Prion Protein Variant that Colocalizes with Kuru Exposure. The New England journal of medicine, 361 (21). pp. 2056-65. ISSN 0028-4793 DOI: 10.1056/NEJMoa0809716
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Newcombe, PJ; Verzilli, C; Casas, JP; Hingorani, AD; Smeeth, L; Whittaker, JC; (2009) Multilocus Bayesian Meta-Analysis of Gene-Disease Associations. American journal of human genetics, 84 (5). pp. 567-80. ISSN 0002-9297 DOI: 10.1016/j.ajhg.2009.04.001 Full text not available from this repository.

Rao, R; Tah, V; Casas, JP; Hingorani, A; Whittaker, J; Smeeth, L; Sharma, P; (2009) Ischaemic Stroke Subtypes and Their Genetic Basis: A Comprehensive Meta-Analysis of Small and Large Vessel Stroke. European neurology, 61 (2). pp. 76-86. ISSN 0014-3022 DOI: 10.1159/000177939 Full text not available from this repository.

Rhodes, B; Hunnangkul, S; Morris, DL; Hsaio, LC; Graham, DSC; Nitsch, D; Whittaker, JC; Vyse, TJ; (2009) The heritability and genetics of complement C3 expression in UK SLE families. Genes and immunity, 10 (5). pp. 525-530. ISSN 1466-4879 DOI: 10.1038/gene.2009.23 Full text not available from this repository.

Shah, S; Drenos, F; Shah, T; Palmen, J; Verzilli, C; Sofat, R; Kumari, M; Kivamaki, M; Pallas, J; MacFarlane, P; +4 more... (2009) IDENTIFICATION OF GENES ASSOCIATED WITH QT INTERVAL USING THE 50K CARDIO-METABOLIC SNP CHIP: RESULTS FROM THE WHITEHALL II STUDY. [Conference or Workshop Item] Full text not available from this repository.

Sovio, U; Bennett, AJ; Millwood, IY; Molitor, J; O'Reilly, PF; Timpson, NJ; Kaakinen, M; Laitinen, J; Haukka, J; Pillas, D; +13 more... (2009) Genetic Determinants of Height Growth Assessed Longitudinally from Infancy to Adulthood in the Northern Finland Birth Cohort 1966. PLoS genetics, 5 (3). e1000409. ISSN 1553-7390 DOI: 10.1371/journal.pgen.1000409
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Talmud, PJ; Drenos, F; Shah, S; Shah, T; Palmen, J; Verzilli, C; Gaunt, TR; Pallas, J; Lovering, R; LI, K; +27 more... (2009) Gene-centric Association Signals for Lipids and Apolipoproteins Identified via the HumanCVD BeadChip. American journal of human genetics, 85 (5). pp. 628-642. ISSN 0002-9297 DOI: 10.1016/j.ajhg.2009.10.014 Full text not available from this repository.

Webb, TEF; Whittaker, J; Collinge, J; Mead, S; (2009) Age of Onset and Death in Inherited Prion Disease Are Heritable. American journal of medical genetics Part B, Neuropsychiatric genetics , 150B (4). pp. 496-501. ISSN 1552-4841 DOI: 10.1002/ajmg.b.30844 Full text not available from this repository.

2008

Balchin, I; Whittaker, JC; Lamont, RF; Steer, PJ; (2008) Timing of Planned Cesarean Delivery by Racial Group. Obstetrics and gynecology, 111 (3). pp. 659-666. ISSN 0029-7844 DOI: 10.1097/AOG.0b013e318163cd55 Full text not available from this repository.

Chadeau-Hyam, M; Hoggart, CJ; O'Reilly, PF; Whittaker, JC; De Iorio, M; Balding, DJ; (2008) Fregene: Simulation of realistic sequence-level data in populations and ascertained samples. BMC Bioinformatics, 9 (1). p. 364. ISSN 1471-2105 DOI: 10.1186/1471-2105-9-364
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Chapman, J; Whittaker, J; (2008) Analysis of multiple SNPs in a candidate gene or region. Genetic epidemiology, 32 (6). pp. 560-6. ISSN 0741-0395 DOI: 10.1002/gepi.20330 Full text not available from this repository.

Chapman, JM; Onnie, C; Prescott, N; Fisher, S; Lewis, C; Mathew, C; Verzilli, CJ; Whittaker, JC; (2008) Searching for genotype-phenotype structure: Trying to understand Crohn's disease. Annals of human genetics, 72. p. 688. ISSN 0003-4800 Full text not available from this repository.

Elmasry, K; Ramus, S; Whittaker, J; Luo, Z; Gammerman, A; Lu, K; Ayhan, A; Singh, N; McGluggage, G; Jacobs, I; +1 more... (2008) Genetic diagnosis and clinical outcome in patients with synchronous ovarian and endometrial cancer. [Conference or Workshop Item] Full text not available from this repository.

Graham, DS; Graham, RR; Manku, H; Wong, AK; Whittaker, JC; Gaffney, PM; Moser, KL; Rioux, JD; Altshuler, D; Behrens, TW; +1 more... (2008) Polymorphism at the TNF superfamily gene TNFSF4 confers susceptibility to systemic lupus erythematosus. Nature genetics, 40 (1). pp. 83-9. ISSN 1061-4036 DOI: 10.1038/ng.2007.47 Full text not available from this repository.

Hoggart, CJ; Clark, TG; de Lorio, M; Whittaker, JC; Balding, DJ; (2008) Genome-wide significance for dense SNP and resequencing data. Genetic epidemiology, 32 (2). pp. 179-185. ISSN 0741-0395 DOI: 10.1002/gepi.20292 Full text not available from this repository.

Hunnangkul, S; Nitsch, D; Rhodes, B; Chadha, S; Roberton, CA; Pessôa-Lopes, P; Norsworthy, PJ; Fernando, MM; Charles, P; Mackworth-Young, C; +3 more... (2008) Familial clustering of non-nuclear autoantibodies and C3 and C4 complement components in systemic lupus erythematosus. Arthritis and rheumatism, 58 (4). pp. 1116-1124. ISSN 0004-3591 DOI: 10.1002/art.23400 Full text not available from this repository.

Newcombe, PJ; Verzilli, C; Pablo-Casas, J; Whittaker, J; (2008) Meta-analysis of gene/disease association studies. Annals of human genetics, 72. p. 689. ISSN 0003-4800 Full text not available from this repository.

Ramus, SJ; Elmasry, K; Luo, Z; Gammerman, A; Lu, K; Ayhan, A; Singh, N; McCluggage, WG; Jacobs, IJ; Whittaker, JC; +1 more... (2008) Predicting clinical outcome in patients diagnosed with synchronous ovarian and endometrial cancer. Clinical cancer research , 14 (18). pp. 5840-8. ISSN 1078-0432 DOI: 10.1158/1078-0432.CCR-08-0373 Full text not available from this repository.

Rhodes, B; Meek, J; Whittaker, JC; Vyse, TJ; (2008) Quantification of the genetic component of basal C-reactive protein expression in SLE nuclear families. Annals of human genetics, 72. pp. 611-620. ISSN 0003-4800 Full text not available from this repository.

Rhodes, B; Meek, J; Whittaker, JC; Vyse, TJ; (2008) Quantification of the Genetic Component of Basal C-Reactive Protein Expression in SLE Nuclear Families. Annals of human genetics, 72 (Pt 5). pp. 611-20. ISSN 0003-4800 DOI: 10.1111/j.1469-1809.2008.00444.x Full text not available from this repository.

Rhodes, B; Morris, DL; Subrahmanyan, L; Aubin, C; de Leon, CFM; Kelly, JF; Evans, DA; Whittaker, JC; Oksenberg, JR; de Jager, PL; +1 more... (2008) Fine-mapping the genetic basis of CRP regulation in African Americans: a Bayesian approach. Human genetics, 123 (6). pp. 633-642. ISSN 0340-6717 DOI: 10.1007/s00439-008-0517-5 Full text not available from this repository.

Verzilli, C; Shah, T; Casas, JP; Chapman, J; Sandhu, M; Debenham, SL; Boekholdt, MS; Khaw, KT; Wareham, NJ; Judson, R; +10 more... (2008) Bayesian meta-analysis of genetic association studies with different sets of markers. American journal of human genetics, 82 (4). pp. 859-72. ISSN 0002-9297 DOI: 10.1016/j.ajhg.2008.01.016 Full text not available from this repository.

Webb, TE; Whittaker, J; Collinge, J; Mead, S; (2008) Age of onset and death in inherited prion disease are heritable. American journal of medical genetics Part B, Neuropsychiatric genetics , 150B (4). pp. 496-501. ISSN 1552-4841 DOI: 10.1002/ajmg.b.30844 Full text not available from this repository.

2007

Apostolidou, S; Abu-Amero, S; O'Donoghue, K; Frost, J; Olafsdottir, O; Chavele, KM; Whittaker, JC; Loughna, P; Stanier, P; Moore, GF; (2007) Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight. Journal of molecular medicine (Berlin, Germany), 85 (4). pp. 379-387. ISSN 0946-2716 DOI: 10.1007/s00109-006-0131-8 Full text not available from this repository.

Baksh, MF; Balding, DJ; Vyse, TJ; Whittaker, JC; (2007) Family-based association analysis with ordered categorical phenotypes, covariates and interactions. Genetic epidemiology, 31 (1). pp. 1-8. ISSN 0741-0395 DOI: 10.1002/gepi.20183 Full text not available from this repository.

Barton, SJ; Richardson, S; Perkins, DN; Bellahn, I; Bryant, TN; Whittaker, JC; (2007) Using Statistical Models To Identify Factors That Have a Role in Defining the Abundance of Ions Produced by Tandem MS. Analytical chemistry, 79 (15). pp. 5601-5607. ISSN 0003-2700 DOI: 10.1021/ac0700272 Full text not available from this repository.

Chapman, J; Verzilli, C; Whittaker, J; (2007) Large scale association studies: Implications for FDRs and a simple Bayesian alternative. [Conference or Workshop Item] Full text not available from this repository.

Drenos, F; Whittaker, JC; Humphries, SE; (2007) The use of meta-analysis risk estimates for candidate genes in combination to predict coronary heart disease risk. Annals of human genetics, 71 (Pt 5). pp. 611-9. ISSN 0003-4800 DOI: 10.1111/j.1469-1809.2007.00359.x Full text not available from this repository.

Hoggart, C; de Iorio, M; Whittaker, J; Balding, D; (2007) Bayesian shrinkage priors for detecting multiple causal variants from genome-wide association studies. Annals of human genetics, 71. p. 557. ISSN 0003-4800 Full text not available from this repository.

Hoggart, CJ; Chadeau-Hyam, M; Clark, TG; Lampariello, R; Whittaker, JC; De Iorio, M; Balding, DJ; (2007) Sequence-level population simulations over large genomic regions. Genetics, 177 (3). pp. 1725-31. ISSN 0016-6731 DOI: 10.1534/genetics.106.069088 Full text not available from this repository.

Hoggart, CJ; de Iorio, M; Whittaker, JC; Balding, DJ; (2007) Simultaneous analysis of genome-wide SNP data. Genetic epidemiology, 31 (6). p. 609. ISSN 0741-0395 Full text not available from this repository.

Sharma, P; Whittaker, J; Casas, JP; Hingorani, AD; Ariyaratnam, R; (2007) Genetics of ischaemic stroke in ethnic minorities. [Conference or Workshop Item] Full text not available from this repository.

Van Mil, SW; Milona, A; Dixon, PH; Mullenbach, R; Geenes, VL; Chambers, J; Shevchuk, V; Moore, GE; Lammert, F; Glantz, AG; +5 more... (2007) Functional variants of the central bile acid sensor FXR identified in intrahepatic cholestasis of pregnancy. Gastroenterology, 133 (2). pp. 507-16. ISSN 0016-5085 DOI: 10.1053/j.gastro.2007.05.015 Full text not available from this repository.

Verzilli, C; Chapman, J; Hingorani, A; Pablo-Casas, J; Shah, T; Smeeth, L; Whittaker, J; (2007) Bayesian meta analysis of genetic association studies with different sets of markers. Annals of human genetics, 71. pp. 552-553. ISSN 0003-4800 Full text not available from this repository.

Whittaker, JC; Chapman, J; (2007) Analysis of multiple SNPs in a candidate gene or region. Genetic epidemiology, 31 (6). p. 650. ISSN 0741-0395 Full text not available from this repository.

2006

Apostolidou, S; Abu-Amero, S; O'Donoghue, K; Olafsdottir, O; Chavele, KM; Frost, J; Whittaker, JC; Loughna, P; Stanier, P; Moore, GE; (2006) Elevated maternal expression of the imprinted PHLDA2 gene is associated with low birth weight. [Conference or Workshop Item] Full text not available from this repository.

Baksh, MF; Balding, DJ; Vyse, TJ; Whittaker, JC; (2006) A likelihood ratio approach to family-based association studies with covariates. Annals of human genetics, 70 (Pt 1). pp. 131-9. ISSN 0003-4800 DOI: 10.1111/j.1529-8817.2005.00189.x Full text not available from this repository.

Graham, DS; Wong, AK; McHugh, NJ; Whittaker, JC; Vyse, TJ; (2006) Evidence for unique association signals in SLE at the CD28-CTLA4-ICOS locus in a family-based study. Human molecular genetics, 15 (21). pp. 3195-205. ISSN 0964-6906 DOI: 10.1093/hmg/ddl395 Full text not available from this repository.

Lunn, DJ; Whittaker, JC; Best, N; (2006) A Bayesian toolkit for genetic association studies. Genetic epidemiology, 30 (3). pp. 231-47. ISSN 0741-0395 DOI: 10.1002/gepi.20140 Full text not available from this repository.

Rohrmann, S; Linseisen, J; Boshuizen, HC; Whittaker, J; Agudo, A; Vineis, P; Boffetta, P; Jensen, MK; Olsen, A; Overvad, K; +34 more... (2006) Ethanol intake and risk of lung cancer in the European prospective investigation into cancer and nutrition (EPIC). American journal of epidemiology, 164 (11). pp. 1103-1114. ISSN 0002-9262 DOI: 10.1093/aje/kwj326 Full text not available from this repository.

Underwood, SL; Christoforou, A; Thomson, PA; Wray, NR; Tenesa, A; Whittaker, J; Adams, RA; le Hellard, S; Morris, SW; Blackwood, DHR; +3 more... (2006) Association analysis of the chromosome 4p-located G protein-coupled receptor 78 (GPR78) gene in bipolar affective disorder and schizophrenia. Molecular psychiatry, 11 (4). pp. 384-394. ISSN 1359-4184 DOI: 10.1038/sj.mp.4001786 Full text not available from this repository.

Verzilli, CJ; Stallard, N; Whittaker, JC; (2006) Bayesian graphical models for genomewide association studies. American journal of human genetics, 79 (1). pp. 100-112. ISSN 0002-9297 DOI: 10.1086/505313 Full text not available from this repository.

Waldron, ER; Whittaker, JC; Balding, DJ; (2006) Fine mapping of disease genes via haplotype clustering. Genetic epidemiology, 30 (2). pp. 170-9. ISSN 0741-0395 DOI: 10.1002/gepi.20134 Full text not available from this repository.

2005

Christoforou, A; Underwood, SL; Hellard, SL; Wray, NR; Morris, SW; Tenesa, A; Thomson, PA; Whittaker, J; Blackwood, DH; Muir, WJ; +2 more... (2005) Association analysis of the chromosome 4p-located G protein-coupled receptor 78 (GPR78) gene in bipolar affective disorder and schizophrenia. American journal of medical genetics Part B, Neuropsychiatric genetics , 138B (1). p. 47. ISSN 1552-4841 Full text not available from this repository.

Hubner, N; Wallace, CA; Zimdahl, H; Petretto, E; Schulz, H; Maciver, F; Mueller, M; Hummel, O; Monti, J; Zidek, V; +12 more... (2005) Integrated transcriptional profiling and linkage analysis for identification of genes underlying disease. Nature genetics, 37 (3). pp. 243-53. ISSN 1061-4036 DOI: 10.1038/ng1522 Full text not available from this repository.

Kelly, PJ; Stallard, N; Whittaker, JC; (2005) Statistical design and analysis of pharmacogenetic trials. Statistics in medicine, 24 (10). pp. 1495-508. ISSN 0277-6715 DOI: 10.1002/sim.2052 Full text not available from this repository.

Pardi, F; Lewis, CM; Whittaker, JC; (2005) SNP selection for association studies: Maximizing power across SNP choice and study size. Annals of human genetics, 69. pp. 733-746. ISSN 0003-4800 DOI: 10.1111/j.1529-8817.2005.00202.x Full text not available from this repository.

Pardi, F; Sibly, RM; Wilkinson, MJ; Whittaker, JC; (2005) On the structural differences between markers and genomic AC microsatellites. Journal of molecular evolution, 60 (5). pp. 688-93. ISSN 0022-2844 DOI: 10.1007/s00239-004-0274-6 Full text not available from this repository.

Russell, AI; Graham, DS; Chadha, S; Roberton, C; Fernandez-Hart, T; Griffiths, B; D'Cruz, D; Nitsch, D; Whittaker, JC; Vyse, TJ; (2005) No association between E- and L-selectin genes and SLE: soluble L-selectin levels do correlate with genotype and a subset in SLE. Genes and immunity, 6 (5). pp. 422-9. ISSN 1466-4879 DOI: 10.1038/sj.gene.6364222 Full text not available from this repository.

Verzilli, CJ; Stallard, N; Whittaker, JC; (2005) Bayesian modelling of multivariate quantitative traits using seemingly unrelated regressions. Genetic epidemiology, 28 (4). pp. 313-25. ISSN 0741-0395 DOI: 10.1002/gepi.20072 Full text not available from this repository.

Verzilli, CJ; Whittaker, JC; Stallard, N; Chasman, D; (2005) A hierarchical Bayesian model for predicting the functional consequences of amino acid polymorphisms. Applied statistics, 54. pp. 191-207. ISSN 0035-9254 DOI: 10.1111/j.1467-9876.2005.00478.x Full text not available from this repository.

Waldron, ERB; Whittaker, JC; Balding, DJ; (2005) A spatial clustering approach to fine-mapping of disease genes. [Conference or Workshop Item] Full text not available from this repository.

2004

Russell, AI; Cunninghame Graham, DS; Shepherd, C; Roberton, CA; Whittaker, J; Meeks, J; Powell, RJ; Isenberg, DA; Walport, MJ; Vyse, TJ; (2004) Polymorphism at the C-reactive protein locus influences gene expression and predisposes to systemic lupus erythematosus. Human molecular genetics, 13 (1). pp. 137-47. ISSN 0964-6906 DOI: 10.1093/hmg/ddh021 Full text not available from this repository.

2003

Byng, MC; Whittaker, JC; Cuthbert, AP; Mathew, CG; Lewis, CM; (2003) SNP subset selection for genetic association studies. Annals of human genetics, 67 (Pt 6). pp. 543-56. ISSN 0003-4800 DOI: 10.1046/j.1529-8817.2003.00055.x Full text not available from this repository.

Denham, MC; Whittaker, JC; (2003) A Bayesian approach to disease gene location using allelic association. Biostatistics (Oxford, England), 4 (3). pp. 399-409. ISSN 1465-4644 DOI: 10.1093/biostatistics/4.3.399 Full text not available from this repository.

Morris, AP; Whittaker, JC; Xu, CF; Hosking, LK; Balding, DJ; (2003) Multipoint linkage-disequilibrium mapping narrows location interval and identifies mutation heterogeneity. Proceedings of the National Academy of Sciences of the United States of America, 100 (23). pp. 13442-6. ISSN 0027-8424 DOI: 10.1073/pnas.2235031100 Full text not available from this repository.

Sibly, RM; Meade, A; Boxall, N; Wilkinson, MJ; Corne, DW; Whittaker, JC; (2003) The structure of interrupted human AC microsatellites. Molecular biology and evolution, 20 (3). pp. 453-9. ISSN 0737-4038 DOI: 10.1093/molbev/msg056 Full text not available from this repository.

Whittaker, JC; Gharani, N; Hindmarsh, P; McCarthy, MI; (2003) Estimation and testing of parent-of-origin effects for quantitative traits. American journal of human genetics, 72 (4). pp. 1035-9. ISSN 0002-9297 DOI: 10.1086/374382 Full text not available from this repository.

Whittaker, JC; Harbord, RM; Boxall, N; Mackay, I; Dawson, G; Sibly, RM; (2003) Likelihood-based estimation of microsatellite mutation rates. Genetics, 164 (2). pp. 781-7. ISSN 0016-6731 Full text not available from this repository.

2002

Lange, C; Whittaker, JC; (2002) Generalised estimating equations: a hybrid approach for mean parameters in multivariate regression models. Statistical Modelling, 2. pp. 163-181. ISSN 1477-0342 Full text not available from this repository.

Lange, C; Whittaker, JC; (2002) Model selection for quasi-likelihood: a new approach. In: Gregori, D; Cameci, G; Friedl, H; Ferligoi, A; Wedlin, A, (eds.) Correlated Data Modeling. Economia/Ricerche, Collana. Full text not available from this repository.

Morris, AP; Whittaker, JC; Balding, DJ; (2002) Fine-scale mapping of disease loci via shattered coalescent modeling of genealogies. American journal of human genetics, 70 (3). pp. 686-707. ISSN 0002-9297 DOI: 10.1086/339271 Full text not available from this repository.

2001

Lange, C; Whittaker, JC; (2001) Mapping quantitative trait Loci using generalized estimating equations. Genetics, 159 (3). pp. 1325-37. ISSN 0016-6731 Full text not available from this repository.

Lange, C; Whittaker, JC; (2001) On prediction of genetic values in marker-assisted selection. Genetics, 159 (3). pp. 1375-81. ISSN 0016-6731 Full text not available from this repository.

Sibly, RM; Whittaker, JC; Talbot, M; (2001) A maximum-likelihood approach to fitting equilibrium models of microsatellite evolution. Molecular biology and evolution, 18 (3). pp. 413-7. ISSN 0737-4038 Full text not available from this repository.

Whittaker, JC; (2001) Marker assisted selection and introgression. In: Balding, DJ; Bishop, M; Cannings, C, (eds.) Handbook of Statistical Genetics. Wiley. Full text not available from this repository.

Whittaker, JC; Morris, AP; (2001) Family-based tests of association and/or linkage. Annals of human genetics, 65 (Pt 5). pp. 407-19. ISSN 0003-4800 DOI: 10.1017/S0003480001008818 Full text not available from this repository.

This list was generated on Wed Nov 8 17:24:02 2017 GMT.