Does Obesity Cause Thyroid Cancer? A Mendelian Randomization Study

由 Fussey, Jonathan Mark, Beaumont, Robin N, Wood, Andrew R, Vaidya, Bijay, Smith, Joel, Tyrrell, Jessica
發表在 J Clin Endocrinol Metab (2020)

Mendelian randomization supports a causative effect of TSH on thyroid carcinoma

由 Fussey, Jonathan M, Beaumont, Robin N, Wood, Andrew R, Vaidya, Bijay, Smith, Joel, Tyrrell, Jessica
發表在 Endocr Relat Cancer (2020)

Influence of cell distribution and diabetes status on the association between mitochondrial DNA copy number and aging phenotypes in the InCHIANTI study

由 Moore, Ann Zenobia, Ding, Jun, Tuke, Marcus A., Wood, Andrew R., Bandinelli, Stefania, Frayling, Timothy M., Ferrucci, Luigi
發表在 Aging Cell (2017)

The splice site variant rs11078928 may be associated with a genotype-dependent alteration in expression of GSDMB transcripts

由 Morrison, Faer S, Locke, Jonathan M, Wood, Andrew R, Tuke, Marcus, Pasko, Dorota, Murray, Anna, Frayling, Tim, Harries, Lorna W
出版 2013

Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank

由 Pilling, Luke C, Tamosauskaite, Jone, Jones, Garan, Wood, Andrew R, Jones, Lindsay, Kuo, Chai-Ling, Kuchel, George A, Ferrucci, Luigi, Melzer, David
發表在 BMJ (2019)

Quantification of the overall contribution of gene-environment interaction for obesity-related traits

由 Sulc, Jonathan, Mounier, Ninon, Günther, Felix, Winkler, Thomas, Wood, Andrew R., Frayling, Timothy M., Heid, Iris M., Robinson, Matthew R., Kutalik, Zoltán
發表在 Nat Commun (2020)

Genetic predictors of participation in optional components of UK Biobank

由 Tyrrell, Jessica, Zheng, Jie, Beaumont, Robin, Hinton, Kathryn, Richardson, Tom G., Wood, Andrew R., Davey Smith, George, Frayling, Timothy M., Tilling, Kate
發表在 Nat Commun (2021)

Large Copy-Number Variants in UK Biobank Caused by Clonal Hematopoiesis May Confound Penetrance Estimates

由 Tuke, Marcus, Tyrrell, Jessica, Ruth, Katherine S., Beaumont, Robin N., Wood, Andrew R., Murray, Anna, Frayling, Timothy M., Weedon, Michael N., Wright, Caroline F.
發表在 Am J Hum Genet (2020)

A 3D Renal Proximal Tubule on Chip Model Phenocopies Lowe Syndrome and Dent II Disease Tubulopathy

由 Naik, Sindhu, Wood, Andrew R., Ongenaert, Maté, Saidiyan, Paniz, Elstak, Edo D., Lanz, Henriëtte L., Stallen, Jan, Janssen, Richard, Smythe, Elizabeth, Erdmann, Kai S.
發表在 Int J Mol Sci (2021)

A genome-wide association study identifies 5 loci associated with frozen shoulder and implicates diabetes as a causal risk factor

由 Green, Harry D., Jones, Alistair, Evans, Jonathan P., Wood, Andrew R., Beaumont, Robin N., Tyrrell, Jessica, Frayling, Timothy M., Smith, Christopher, Weedon, Michael N.
發表在 PLoS Genet (2021)

Meta-analysis of genome-wide association studies for height and body mass index in ∼700000 individuals of European ancestry

由 Yengo, Loic, Sidorenko, Julia, Kemper, Kathryn E, Zheng, Zhili, Wood, Andrew R, Weedon, Michael N, Frayling, Timothy M, Hirschhorn, Joel, Yang, Jian, Visscher, Peter M
發表在 Hum Mol Genet (2018)

Another explanation for apparent epistasis

由 Wood, Andrew R., Tuke, Marcus A., Nalls, Mike A., Hernandez, Dena G., Bandinelli, Stefania, Singleton, Andrew B., Melzer, David, Ferrucci, Luigi, Frayling, Timothy M., Weedon, Michael N.
發表在 Nature (2014)

Variants in the FTO and CDKAL1 loci have recessive effects on risk of obesity and type 2 diabetes, respectively

由 Wood, Andrew R., Tyrrell, Jessica, Beaumont, Robin, Jones, Samuel E., Tuke, Marcus A., Ruth, Katherine S., Yaghootkar, Hanieh, Freathy, Rachel M., Murray, Anna, Frayling, Timothy M., Weedon, Michael N.
發表在 Diabetologia (2016)

Association of maternal circulating 25(OH)D and calcium with birth weight: A mendelian randomisation analysis

由 Thompson, William D., Tyrrell, Jessica, Borges, Maria-Carolina, Beaumont, Robin N., Knight, Bridget A., Wood, Andrew R., Ring, Susan M., Hattersley, Andrew T., Freathy, Rachel M., Lawlor, Debbie A.
發表在 PLoS Med (2019)

Assessment of MTNR1B Type 2 Diabetes Genetic Risk Modification by Shift Work and Morningness-Eveningness Preference in the UK Biobank

由 Dashti, Hassan S., Vetter, Céline, Lane, Jacqueline M., Smith, Matt C., Wood, Andrew R., Weedon, Michael N., Rutter, Martin K., Garaulet, Marta, Scheer, Frank A.J.L., Saxena, Richa
發表在 Diabetes (2020)

A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin–creatinine ratio

由 Casanova, Francesco, Tyrrell, Jessica, Beaumont, Robin N, Ji, Yingjie, Jones, Samuel E, Hattersley, Andrew T, Weedon, Michael N, Murray, Anna, Shore, Angela C, Frayling, Timothy M, Wood, Andrew R
發表在 Hum Mol Genet (2019)

A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin-creatinine ratio

由 Casanova, Francesco, Tyrrell, Jess, Beaumont, Robin N., Ji, Yingjie, Jones, Samuel E., Hattersley, Andrew T., Weedon, Michael N., Murray, Anna, Shore, Angela C., Frayling, Timothy M., Wood, Andrew R.
發表在 Diabetes (2020)

Genetic evidence that lower circulating FSH levels lengthen menstrual cycle, increase age at menopause and impact female reproductive health

由 Ruth, Katherine S., Beaumont, Robin N., Tyrrell, Jessica, Jones, Samuel E., Tuke, Marcus A., Yaghootkar, Hanieh, Wood, Andrew R., Freathy, Rachel M., Weedon, Michael N., Frayling, Timothy M., Murray, Anna
發表在 Hum Reprod (2016)

The common HNF1A variant I27L is a modifier of age at diabetes diagnosis in HNF1A-MODY individuals

由 Locke, Jonathan M, Saint-Martin, Cécile, Laver, Thomas W, Patel, Kashyap A, Wood, Andrew R, Sharp, Seth A, Ellard, Sian, Bellanné-Chantelot, Christine, Hattersley, Andrew T, Harries, Lorna W, Weedon, Michael N
發表在 Diabetes (2018)

Assessing the Pathogenicity, Penetrance, and Expressivity of Putative Disease-Causing Variants in a Population Setting

由 Wright, Caroline F., West, Ben, Tuke, Marcus, Jones, Samuel E., Patel, Kashyap, Laver, Thomas W., Beaumont, Robin N., Tyrrell, Jessica, Wood, Andrew R., Frayling, Timothy M., Hattersley, Andrew T., Weedon, Michael N.
發表在 Am J Hum Genet (2019)