检索结果 - Weedon, Michael

A Comparative Safety Analysis of Medicines Based on the UK Pharmacovigilance and General Practice Prescribing Data in England 由 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 由 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 由 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 由 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 由 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... 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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... 由 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 由 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 由 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 由 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 由 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... 由 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 由 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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