Hasil Pencarian - Michael N. Weedon

Perbaiki Hasil
  1. 1
    SavvyCNV: Genome-wide CNV calling from off-target reads.

    SavvyCNV: Genome-wide CNV calling from off-target reads. oleh Thomas W Laver, Elisa De Franco, Matthew B Johnson, Kashyap A Patel, Sian Ellard, Michael N Weedon, Sarah E Flanagan, Matthew N Wakeling

    Diterbitkan 2022-03-01
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  2. 2
    A genome-wide association study identifies 5 loci associated with frozen shoulder and implicates diabetes as a causal risk factor.

    A genome-wide association study identifies 5 loci associated with frozen shoulder and implicates diabetes as a causal risk factor. oleh Harry D Green, Alistair Jones, Jonathan P Evans, Andrew R Wood, Robin N Beaumont, Jessica Tyrrell, Timothy M Frayling, Christopher Smith, Michael N Weedon

    Diterbitkan 2021-06-01
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  3. 3
    A genome-wide association study identifies 5 loci associated with frozen shoulder and implicates diabetes as a causal risk factor

    A genome-wide association study identifies 5 loci associated with frozen shoulder and implicates diabetes as a causal risk factor oleh Harry D. Green, Alistair Jones, Jonathan P. Evans, Andrew R. Wood, Robin N. Beaumont, Jessica Tyrrell, Timothy M. Frayling, Christopher Smith, Michael N. Weedon

    Diterbitkan 2021-06-01
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  4. 4
    Identification and analysis of individuals who deviate from their genetically-predicted phenotype.

    Identification and analysis of individuals who deviate from their genetically-predicted phenotype. oleh Gareth Hawkes, Loic Yengo, Sailaja Vedantam, Eirini Marouli, Robin N Beaumont, GIANT Consortium, Jessica Tyrrell, Michael N Weedon, Joel Hirschhorn, Timothy M Frayling, Andrew R Wood

    Diterbitkan 2023-09-01
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  5. 5
    Estimating disease prevalence in large datasets using genetic risk scores

    Estimating disease prevalence in large datasets using genetic risk scores oleh Benjamin D. Evans, Piotr Słowiński, Andrew T. Hattersley, Samuel E. Jones, Seth Sharp, Robert A. Kimmitt, Michael N. Weedon, Richard A. Oram, Krasimira Tsaneva-Atanasova, Nicholas J. Thomas

    Diterbitkan 2021-11-01
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  6. 6
    Combining information from common type 2 diabetes risk polymorphisms improves disease prediction.

    Combining information from common type 2 diabetes risk polymorphisms improves disease prediction. oleh Michael N Weedon, Mark I McCarthy, Graham Hitman, Mark Walker, Christopher J Groves, Eleftheria Zeggini, N William Rayner, Beverley Shields, Katharine R Owen, Andrew T Hattersley, Timothy M Frayling

    Diterbitkan 2006-10-01
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  7. 7
    IgA Nephropathy Genetic Risk Score to Estimate the Prevalence of IgA Nephropathy in UK Biobank

    IgA Nephropathy Genetic Risk Score to Estimate the Prevalence of IgA Nephropathy in UK Biobank oleh Kittiya Sukcharoen, Seth A. Sharp, Nicholas J. Thomas, Robert A. Kimmitt, Jamie Harrison, Coralie Bingham, Monika Mozere, Michael N. Weedon, Jessica Tyrrell, Jonathan Barratt, Daniel P. Gale, Richard A. Oram

    Diterbitkan 2020-10-01
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  8. 8
    Insights into the genetics of menopausal vasomotor symptoms: genome-wide analyses of routinely-collected primary care health records

    Insights into the genetics of menopausal vasomotor symptoms: genome-wide analyses of routinely-collected primary care health records oleh Katherine S. Ruth, Robin N. Beaumont, Jonathan M. Locke, Jessica Tyrrell, Carolyn J. Crandall, Gareth Hawkes, Timothy M. Frayling, Julia K. Prague, Kashyap A. Patel, Andrew R. Wood, Michael N. Weedon, Anna Murray

    Diterbitkan 2023-10-01
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  9. 9
    Correlations in sleeping patterns and circadian preference between spouses

    Correlations in sleeping patterns and circadian preference between spouses oleh Rebecca C. Richmond, Laurence J. Howe, Karl Heilbron, Samuel Jones, Junxi Liu, 23andMe Research Team, Xin Wang, Michael N. Weedon, Martin K. Rutter, Deborah A. Lawlor, George Davey Smith, Céline Vetter

    Diterbitkan 2023-11-01
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  10. 10
    Sleep classification from wrist-worn accelerometer data using random forests

    Sleep classification from wrist-worn accelerometer data using random forests oleh Kalaivani Sundararajan, Sonja Georgievska, Bart H. W. te Lindert, Philip R. Gehrman, Jennifer Ramautar, Diego R. Mazzotti, Séverine Sabia, Michael N. Weedon, Eus J. W. van Someren, Lars Ridder, Jian Wang, Vincent T. van Hees

    Diterbitkan 2021-01-01
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  11. 11
    Genetic determinants of daytime napping and effects on cardiometabolic health

    Genetic determinants of daytime napping and effects on cardiometabolic health oleh Hassan S. Dashti, Iyas Daghlas, Jacqueline M. Lane, Yunru Huang, Miriam S. Udler, Heming Wang, Hanna M. Ollila, Samuel E. Jones, Jaegil Kim, Andrew R. Wood, 23andMe Research Team, Michael N. Weedon, Stella Aslibekyan, Marta Garaulet, Richa Saxena

    Diterbitkan 2021-02-01
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  12. 12
    Common variants show predicted polygenic effects on height in the tails of the distribution, except in extremely short individuals.

    Common variants show predicted polygenic effects on height in the tails of the distribution, except in extremely short individuals. oleh Yingleong Chan, Oddgeir L Holmen, Andrew Dauber, Lars Vatten, Aki S Havulinna, Frank Skorpen, Kirsti Kvaløy, Kaisa Silander, Thutrang T Nguyen, Cristen Willer, Michael Boehnke, Markus Perola, Aarno Palotie, Veikko Salomaa, Kristian Hveem, Timothy M Frayling, Joel N Hirschhorn, Michael N Weedon

    Diterbitkan 2011-12-01
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  13. 13
    Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.

    Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based i... oleh Andrew R Wood, John R B Perry, Toshiko Tanaka, Dena G Hernandez, Hou-Feng Zheng, David Melzer, J Raphael Gibbs, Michael A Nalls, Michael N Weedon, Tim D Spector, J Brent Richards, Stefania Bandinelli, Luigi Ferrucci, Andrew B Singleton, Timothy M Frayling

    Diterbitkan 2013-01-01
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  14. 14
    Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance

    Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance oleh Kashyap A. Patel, Jarno Kettunen, Markku Laakso, Alena Stančáková, Thomas W. Laver, Kevin Colclough, Matthew B. Johnson, Marc Abramowicz, Leif Groop, Päivi J. Miettinen, Maggie H. Shepherd, Sarah E. Flanagan, Sian Ellard, Nobuya Inagaki, Andrew T. Hattersley, Tiinamaija Tuomi, Miriam Cnop, Michael N. Weedon

    Diterbitkan 2017-10-01
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  15. 15
    The impact of Mendelian sleep and circadian genetic variants in a population setting.

    The impact of Mendelian sleep and circadian genetic variants in a population setting. oleh Michael N Weedon, Samuel E Jones, Jacqueline M Lane, Jiwon Lee, Hanna M Ollila, Amy Dawes, Jess Tyrrell, Robin N Beaumont, Timo Partonen, Ilona Merikanto, Stephen S Rich, Jerome I Rotter, Timothy M Frayling, Martin K Rutter, Susan Redline, Tamar Sofer, Richa Saxena, Andrew R Wood

    Diterbitkan 2022-09-01
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  16. 16
    Applying a genetic risk score model to enhance prediction of future multiple sclerosis diagnosis at first presentation with optic neuritis

    Applying a genetic risk score model to enhance prediction of future multiple sclerosis diagnosis at first presentation with optic neuritis oleh Pavel Loginovic, Feiyi Wang, Jiang Li, Lauric Ferrat, Uyenlinh L. Mirshahi, H. Shanker Rao, Axel Petzold, Jessica Tyrrell, Harry D. Green, Michael N. Weedon, Andrea Ganna, Tiinamaija Tuomi, David J. Carey, UKBB Eye & Vision Consortium, FinnGen, Geisinger-Regeneron DiscovEHR Collaboration, Richard A. Oram, Tasanee Braithwaite

    Diterbitkan 2024-02-01
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  17. 17
    Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers.

    Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers. oleh Luke C Pilling, Janice L Atkins, Michael O Duff, Robin N Beaumont, Samuel E Jones, Jessica Tyrrell, Chia-Ling Kuo, Katherine S Ruth, Marcus A Tuke, Hanieh Yaghootkar, Andrew R Wood, Anna Murray, Michael N Weedon, Lorna W Harries, George A Kuchel, Luigi Ferrucci, Timothy M Frayling, David Melzer

    Diterbitkan 2017-01-01
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  18. 18
    Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome [version 2; peer review: 2 approved, 1 approved with reservations]

    Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome [version 2; peer review: 2 approved, 1 approved with reservations] oleh Indraneel Banerjee, Senthil Senniappan, Thomas W. Laver, Richard Caswell, Martin Zenker, Klaus Mohnike, Tim Cheetham, Matthew N. Wakeling, Dunia Ismail, Belinda Lennerz, Miranda Splitt, Merih Berberoğlu, Susann Empting, Martin Wabitsch, Simone Pötzsch, Pratik Shah, Zeynep Siklar, Charles F. Verge, Michael N. Weedon, Sian Ellard, Khalid Hussain, Sarah E. Flanagan

    Diterbitkan 2020-08-01
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  19. 19
    Genetic scores to stratify risk of developing multiple islet autoantibodies and type 1 diabetes: A prospective study in children.

    Genetic scores to stratify risk of developing multiple islet autoantibodies and type 1 diabetes: A prospective study in children. oleh Ezio Bonifacio, Andreas Beyerlein, Markus Hippich, Christiane Winkler, Kendra Vehik, Michael N Weedon, Michael Laimighofer, Andrew T Hattersley, Jan Krumsiek, Brigitte I Frohnert, Andrea K Steck, William A Hagopian, Jeffrey P Krischer, Åke Lernmark, Marian J Rewers, Jin-Xiong She, Jorma Toppari, Beena Akolkar, Richard A Oram, Stephen S Rich, Anette-G Ziegler, TEDDY Study Group

    Diterbitkan 2018-04-01
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  20. 20
    The role of accelerometer-derived sleep traits on glycated haemoglobin and glucose levels: a Mendelian randomization study

    The role of accelerometer-derived sleep traits on glycated haemoglobin and glucose levels: a Mendelian randomization study oleh Junxi Liu, Rebecca C. Richmond, Emma L. Anderson, Jack Bowden, Ciarrah-Jane S. Barry, Hassan S. Dashti, Iyas S. Daghlas, Jacqueline M. Lane, Simon D. Kyle, Céline Vetter, Claire L. Morrison, Samuel E. Jones, Andrew R. Wood, Timothy M. Frayling, Alison K. Wright, Matthew J. Carr, Simon G. Anderson, Richard A. Emsley, David W. Ray, Michael N. Weedon, Richa Saxena, Martin K. Rutter, Deborah A. Lawlor

    Diterbitkan 2024-06-01
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