खोज परिणाम - Weedon, Michael

परिणाम को परिष्कृत करें
  1. 1
    A Comparative Safety Analysis of Medicines Based on the UK Pharmacovigilance and General Practice Prescribing Data in England

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

    प्रकाशित 2022
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  2. 2
    Epigenetic regulation of mitochondrial function in neurodegenerative disease: new insights from advances in genomic technologies

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

    प्रकाशित 2016
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  3. 3
    Genotyping arrays are extremely unreliable for detecting very rare variants in human genetic studies: an example from a recent study of MC4R

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

    प्रकाशित 2021
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  4. 4
    Clinical and research uses of genetic risk scores in type 1 diabetes

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

    प्रकाशित 2018
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  5. 5
    A cautionary tale: the non-causal association between type 2 diabetes risk SNP, rs7756992, and levels of non-coding RNA, CDKAL1-v1

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

    प्रकाशित 2015
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  6. 6
    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 diabetes

    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... द्वारा Rodgers, Lauren R, Weedon, Michael N, Henley, William E, Hattersley, Andrew T, Shields, Beverley M

    प्रकाशित 2017
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  7. 7
    Analysis of large scale sequencing cohorts does not support the role of variants in UCP2 as a cause of hyperinsulinaemic hypoglycaemia

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

    प्रकाशित 2017
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  8. 8
    Events in Early Life are Associated with Female Reproductive Ageing: A UK Biobank Study

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

    प्रकाशित 2016
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  9. 9
    Length of FMR1 repeat alleles within the normal range does not substantially affect the risk of early menopause

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

    प्रकाशित 2016
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  10. 10
    PLIN1 Haploinsufficiency Causes a Favorable Metabolic Profile

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

    प्रकाशित 2022
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  11. 11
    Frequency and phenotype of type 1 diabetes in the first six decades of life: a cross-sectional, genetically stratified survival analysis from UK Biobank

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

    प्रकाशित 2018
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  12. 12
    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

    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 द्वारा Freathy, Rachel M, Mitchell, Simon MS, Knight, Beatrice, Shields, Beverley, Weedon, Michael N, Hattersley, Andrew T, Frayling, Timothy M

    प्रकाशित 2006
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  13. 13
    Interrogating Type 2 Diabetes Genome-Wide Association Data Using a Biological Pathway-Based Approach

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

    प्रकाशित 2009
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  14. 14
    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 diabetes

    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... द्वारा Patel, Kashyap A, Weedon, Michael N, Shields, Beverley M., Pearson, Ewan R, Hattersley, Andrew T., McDonald, Timothy J.

    प्रकाशित 2019
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  15. 15
    Rare genetic variants in genes and loci linked to dominant monogenic developmental disorders cause milder related phenotypes in the general population

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

    प्रकाशित 2022
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  16. 16
    The clinical consequences of heterogeneity within and between different diabetes types

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

    प्रकाशित 2020
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  17. 17
    Regional differences in mitochondrial DNA methylation in human post-mortem brain tissue

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

    प्रकाशित 2017
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  18. 18
    A Type 1 diabetes genetic risk score can aid discrimination between Type 1 and Type 2 diabetes in young adults

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

    प्रकाशित 2015
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  19. 19
    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 humans

    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... द्वारा Lango Allen, Hana, Caswell, Richard, Xie, Weijia, Xu, Xiao, Wragg, Christopher, Turnpenny, Peter D, Turner, Claire L S, Weedon, Michael N, Ellard, Sian

    प्रकाशित 2014
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  20. 20
    Assessing the Combined Impact of 18 Common Genetic Variants of Modest Effect Sizes on Type 2 Diabetes Risk

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

    प्रकाशित 2008
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