Search Results - Weedon, Michael

A Comparative Safety Analysis of Medicines Based on the UK Pharmacovigilance and General Practice Prescribing Data in England by MOKBEL, KINAN, DANIELS, ROB, WEEDON, MICHAEL N., JACKSON, LEIGH

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Epigenetic regulation of mitochondrial function in neurodegenerative disease: new insights from advances in genomic technologies by Devall, Matthew, Roubroeks, Janou, Mill, Jonathan, Weedon, Michael, Lunnon, Katie

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Genotyping arrays are extremely unreliable for detecting very rare variants in human genetic studies: an example from a recent study of MC4R by Weedon, Michael N, Wright, Caroline F, Patel, Kashyap, Frayling, Timothy M

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Clinical and research uses of genetic risk scores in type 1 diabetes by Sharp, Seth A, Weedon, Michael N, Hagopian, William A, Oram, Richard A

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A cautionary tale: the non-causal association between type 2 diabetes risk SNP, rs7756992, and levels of non-coding RNA, CDKAL1-v1 by Locke, Jonathan M., Wei, Fan-Yan, Tomizawa, Kazuhito, Weedon, Michael N., Harries, Lorna W.

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Cohort profile for the MASTERMIND study: using the Clinical Practice Research Datalink (CPRD) to investigate stratification of response to treatment in patients with type 2 diabete... by Rodgers, Lauren R, Weedon, Michael N, Henley, William E, Hattersley, Andrew T, Shields, Beverley M

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Analysis of large scale sequencing cohorts does not support the role of variants in UCP2 as a cause of hyperinsulinaemic hypoglycaemia by Laver, Thomas W, Weedon, Michael N, Caswell, Richard, Hussain, Khalid, Ellard, Sian, Flanagan, Sarah E

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Events in Early Life are Associated with Female Reproductive Ageing: A UK Biobank Study by Ruth, Katherine S., Perry, John R. B., Henley, William E., Melzer, David, Weedon, Michael N., Murray, Anna

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Length of FMR1 repeat alleles within the normal range does not substantially affect the risk of early menopause by Ruth, Katherine S., Bennett, Claire E., Schoemaker, Minouk J., Weedon, Michael N., Swerdlow, Anthony J., Murray, Anna

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PLIN1 Haploinsufficiency Causes a Favorable Metabolic Profile by Patel, Kashyap A, Burman, Shivang, Laver, Thomas W, Hattersley, Andrew T, Frayling, Timothy M, Weedon, Michael N

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Frequency and phenotype of type 1 diabetes in the first six decades of life: a cross-sectional, genetically stratified survival analysis from UK Biobank by Thomas, Nicholas J, Jones, Samuel E, Weedon, Michael N, Shields, Beverley M, Oram, Richard A, Hattersley, Andrew T

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A study of association between common variation in the growth hormone-chorionic somatomammotropin hormone gene cluster and adult fasting insulin in a UK Caucasian population by Freathy, Rachel M, Mitchell, Simon MS, Knight, Beatrice, Shields, Beverley, Weedon, Michael N, Hattersley, Andrew T, Frayling, Timothy M

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Interrogating Type 2 Diabetes Genome-Wide Association Data Using a Biological Pathway-Based Approach by Perry, John R.B., McCarthy, Mark I., Hattersley, Andrew T., Zeggini, Eleftheria, Weedon, Michael N., Frayling, Timothy M.

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Zinc Transporter 8 autoantibodies (ZnT8A) and a Type 1 diabetes-genetic risk score can exclude individuals with type 1 diabetes from inappropriate genetic testing for monogenic dia... by Patel, Kashyap A, Weedon, Michael N, Shields, Beverley M., Pearson, Ewan R, Hattersley, Andrew T., McDonald, Timothy J.

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Rare genetic variants in genes and loci linked to dominant monogenic developmental disorders cause milder related phenotypes in the general population by Kingdom, Rebecca, Tuke, Marcus, Wood, Andrew, Beaumont, Robin N., Frayling, Timothy M., Weedon, Michael N., Wright, Caroline F.

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The clinical consequences of heterogeneity within and between different diabetes types by Redondo, Maria J., Hagopian, William A., Oram, Richard, Steck, Andrea K., Vehik, Kendra, Weedon, Michael, Balasubramanyam, Ashok, Dabelea, Dana

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Regional differences in mitochondrial DNA methylation in human post-mortem brain tissue by Devall, Matthew, Smith, Rebecca G., Jeffries, Aaron, Hannon, Eilis, Davies, Matthew N., Schalkwyk, Leonard, Mill, Jonathan, Weedon, Michael, Lunnon, Katie

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A Type 1 diabetes genetic risk score can aid discrimination between Type 1 and Type 2 diabetes in young adults by Oram, Richard A, Patel, Kashyap, Hill, Anita, Shields, Beverley, McDonald, Timothy J, Jones, Angus, Hattersley, Andrew T, Weedon, Michael N

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Next generation sequencing of chromosomal rearrangements in patients with split-hand/split-foot malformation provides evidence for DYNC1I1 exonic enhancers of DLX5/6 expression in... by Lango Allen, Hana, Caswell, Richard, Xie, Weijia, Xu, Xiao, Wragg, Christopher, Turnpenny, Peter D, Turner, Claire L S, Weedon, Michael N, Ellard, Sian

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Assessing the Combined Impact of 18 Common Genetic Variants of Modest Effect Sizes on Type 2 Diabetes Risk by Lango, Hana, Palmer, Colin N.A., Morris, Andrew D., Zeggini, Eleftheria, Hattersley, Andrew T., McCarthy, Mark I., Frayling, Timothy M., Weedon, Michael N.

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