نتائج البحث - Felicity Payne

تنقيح النتائج
  1. 1
    Evaluating the discriminative power of multi-trait genetic risk scores for type 2 diabetes in a northern Swedish population

    Evaluating the discriminative power of multi-trait genetic risk scores for type 2 diabetes in a northern Swedish population حسب Bénédicte Fontaine‐Bisson, Frida Renström, Olov Rolandsson, Felicity Payne, Göran Hallmans, Inês Barroso, Paul W. Franks

    منشور في 2010
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    Artigo
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  2. 2
    Replication and extension of genome-wide association study results for obesity in 4923 adults from northern Sweden

    Replication and extension of genome-wide association study results for obesity in 4923 adults from northern Sweden حسب Frida Renström, Felicity Payne, Anna Nordström, Ema C. Brito, Olov Rolandsson, Göran Hallmans, Inês Barroso, Peter Nordström, Paul W. Franks

    منشور في 2009
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  3. 3
    Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations

    Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations حسب Paul W. Franks, Olov Rolandsson, S. L. Debenham, Katherine A. Fawcett, Felicity Payne, Christian Dina, Philippe Froguel, Karen L. Mohlke, Cristen J. Willer, Tommy Olsson, Nicholas J. Wareham, G. Hallmans, Inês Barroso, Manjinder S. Sandhu

    منشور في 2007
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    Artigo
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  4. 4
    Transcription and DNA Methylation Patterns of Blood-Derived CD8+ T Cells Are Associated With Age and Inflammatory Bowel Disease But Do Not Predict Prognosis

    Transcription and DNA Methylation Patterns of Blood-Derived CD8+ T Cells Are Associated With Age and Inflammatory Bowel Disease But Do Not Predict Prognosis حسب Marco Gasparetto, Felicity Payne, Komal Nayak, Judith Kraiczy, Claire Glemas, Yosef Philip-McKenzie, Alexander Ross, Rachel D. Edgar, Daniel R. Zerbino, Camilla Salvestrini, Franco Torrente, Nicholas T. Ventham, Rahul Kalla, Jack Satsangi, Peter Sarkies, Robert Heuschkel, Matthias Zilbauer

    منشور في 2020
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  5. 5
    Hypomorphism in human NSMCE2 linked to primordial dwarfism and insulin resistance

    Hypomorphism in human NSMCE2 linked to primordial dwarfism and insulin resistance حسب Felicity Payne, Rita Colnaghi, Nuno Rocha, Asha Seth, J. Ieuan Harris, Gillian Carpenter, William Bottomley, Eleanor Wheeler, Stephen Q. Wong, Vladimı́r Saudek, David B. Savage, Stephen O’Rahilly, Jean‐Claude Carel, Inês Barroso, Mark O’Driscoll, Robert K. Semple

    منشور في 2014
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  6. 6
    An Activating Mutation of <i>AKT2</i> and Human Hypoglycemia

    An Activating Mutation of <i>AKT2</i> and Human Hypoglycemia حسب Khalid Hussain, Benjamin Challis, Nuno Rocha, Felicity Payne, Marina Minic, Alastair Thompson, Allan Daly, Clare L. Scott, Jeffrey R. Harris, B. J. L. Smillie, David B. Savage, Uma Ramaswami, Pascale de Lonlay, Stephen O’Rahilly, Inês Barroso, Robert K. Semple

    منشور في 2011
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  7. 7
    Mutations disrupting the Kennedy phosphatidylcholine pathway in humans with congenital lipodystrophy and fatty liver disease

    Mutations disrupting the Kennedy phosphatidylcholine pathway in humans with congenital lipodystrophy and fatty liver disease حسب Felicity Payne, Koini Lim, Amandine Girousse, Rebecca J. Brown, Nora Kory, Ann L. Robbins, Yali Xue, Alison Sleigh, Elaine Cochran, Claire Adams, Arundhati Dev Borman, David L. Russel‐Jones, Phillip Görden, Robert K. Semple, Vladimı́r Saudek, Stephen O’Rahilly, Tobias C. Walther, Inês Barroso, David B. Savage

    منشور في 2014
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  8. 8
    Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription

    Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription حسب Gaëlle Marenne, Audrey E. Hendricks, Aliki Perdikari, Rebecca Bounds, Felicity Payne, Julia M. Keogh, Christopher J. Lelliott, Elana Henning, Saad Pathan, Sofie Ashford, Elena G. Bochukova, Vanisha Mistry, Allan Daly, Caroline Hayward, Nicholas J. Wareham, Stephen O’Rahilly, Claudia Langenberg, Eleanor Wheeler, Eleftheria Zeggini, I. Sadaf Farooqi, Inês Barroso

    منشور في 2020
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  9. 9
    Insulin resistance uncoupled from dyslipidemia due to C-terminal PIK3R1 mutations

    Insulin resistance uncoupled from dyslipidemia due to C-terminal PIK3R1 mutations حسب Isabel Huang‐Doran, Patsy R Tomlinson, Felicity Payne, Alexandra T. Gast, Alison Sleigh, William Bottomley, J. Ieuan Harris, Allan Daly, Nuno Rocha, Simon A. Rudge, Jonathan Clark, Albert Kwok, Stefano Romeo, Emma McCann, Barbara Müksch, Mehul Dattani, Stefano Zucchini, Michael J.O. Wakelam, Lazaros C. Foukas, David B. Savage, Rinki Murphy, Stephen O’Rahilly, Inês Barroso, Robert K. Semple

    منشور في 2016
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  10. 10
    Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes

    Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes حسب Amélie Bonnefond, Nathalie Clément, Katherine A. Fawcett, Loïc Yengo, Emmanuel Vaillant, Jean‐Luc Guillaume, Aurélie Dechaume, Felicity Payne, Ronan Roussel, Sébastien Czernichow, Serge Herçberg, Samy Hadjadj, Beverley Balkau, Michel Marre, Olivier Lantieri, Claudia Langenberg, Nabila Bouatia‐Naji, G. Charpentier, Martine Vaxillaire, Ghislain Rocheleau, Nicholas J. Wareham, Robert Sladek, Mark I. McCarthy, Christian Dina, Inês Barroso, Ralf Jockers, Philippe Froguel

    منشور في 2012
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  11. 11
    Mosaic overgrowth with fibroadipose hyperplasia is caused by somatic activating mutations in PIK3CA

    Mosaic overgrowth with fibroadipose hyperplasia is caused by somatic activating mutations in PIK3CA حسب Marjorie J. Lindhurst, Victoria E R Parker, Felicity Payne, Julie C. Sapp, Simon A. Rudge, Julie Harris, Alison M. Witkowski, Zuo‐Feng Zhang, Matthijs Groeneveld, Clare L. Scott, Allan Daly, Susan Huson, Laura L. Tosi, Michael L. Cunningham, Thomas N. Darling, Joseph S. Geer, Zoran Gucev, V. Reid Sutton, Christos Tziotzios, Adrian K. Dixon, Timothy R. Helliwell, Stephen O’Rahilly, David B. Savage, Michael J.O. Wakelam, Inês Barroso, Leslie G. Biesecker, Robert K. Semple

    منشور في 2012
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  12. 12
    Underlying Genetic Models of Inheritance in Established Type 2 Diabetes Associations

    Underlying Genetic Models of Inheritance in Established Type 2 Diabetes Associations حسب Georgia Salanti, Lorraine Southam, David Altshuler, Kristin Ardlie, Inês Barroso, Michael Boehnke, Marilyn C. Cornelis, Timothy M. Frayling, Harald Grallert, Niels Grarup, Leif Groop, Torben Hansen, Andrew T. Hattersley, Frank B. Hu, Kristian Hveem, Thomas Illig, Johanna Kuusisto, Markku Laakso, Claudia Langenberg, Valeriya Lyssenko, Mark I. McCarthy, Andrew P. Morris, Andrew D. Morris, Colin N. A. Palmer, Felicity Payne, Carl Platou, Laura J. Scott, Benjamin F. Voight, Nicholas J. Wareham, Eleftheria Zeggini, John P. A. Ioannidis

    منشور في 2009
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    Revisão
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  13. 13
    Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression

    Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression حسب Nuno Rocha, David A. Bulger, Andrea Frontini, Hannah Titheradge, Sigrid Bjerge Gribsholt, Rachel Knox, Matthew Page, Julie Harris, Felicity Payne, Claire Adams, Alison Sleigh, John R. Crawford, Anette P. Gjesing, Jette Bork‐Jensen, Oluf Pedersen, Inês Barroso, Torben Hansen, Helen Cox, Mary M. Reilly, Alexander M. Rossor, Rebecca J. Brown, Simeon I. Taylor, Duncan McHale, Martin Armstrong, Elif A Oral, Vladimı́r Saudek, Stephen O’Rahilly, Eamonn R. Maher, Bjørn Richelsen, David B. Savage, Robert K. Semple

    منشور في 2017
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  14. 14
    Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance

    Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance حسب Luca A. Lotta, Pawan Gulati, Felix R. Day, Felicity Payne, Halit Ongen, Martijn van de Bunt, Kyle J. Gaulton, John D. Eicher, Stephen J. Sharp, Jian’an Luan, Emanuella De Lucia Rolfe, Isobel D. Stewart, Eleanor Wheeler, Sara M. Willems, Claire Adams, Hanieh Yaghootkar, Nita G. Forouhi, Kay‐Tee Khaw, Andrew D. Johnson, Robert K. Semple, Timothy M. Frayling, John R. B. Perry, Emmanouil V. Dermitzakis, Mark I. McCarthy, Inês Barroso, Nicholas J. Wareham, David B. Savage, Claudia Langenberg, Stephen O’Rahilly, Robert A. Scott

    منشور في 2016
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  15. 15
    Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

    Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes حسب John A. Todd, Neil Walker, Jason D. Cooper, Deborah J. Smyth, Kate Downes, Vincent Plagnol, Rebecca Bailey, Sergey Nejentsev, Sarah F. Field, Felicity Payne, Christopher E. Lowe, Jeffrey S. Szeszko, Jason P. Hafler, Lauren R Zeitels, Jennie H. M. Yang, Adrian Vella, Sarah Nutland, Helen E. Stevens, Helen Schuilenburg, Gillian Coleman, M Maisuria, William Meadows, Luc J Smink, Barry Healy, Oliver S. Burren, Alex A C Lam, Nigel Ovington, James E. Allen, Ellen Adlem, Hin-Tak Leung, Chris Wallace, Joanna M. M. Howson, Cristian Guja, C Ionescu-Tîrgovişte, Matthew J. Simmonds, J. M. Heward, Stephen Gough, David B. Dunger, Linda S. Wicker, David Clayton

    منشور في 2007
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  16. 16
    Patient-derived organoid biobank identifies epigenetic dysregulation of intestinal epithelial MHC-I as a novel mechanism in severe Crohn’s Disease

    Patient-derived organoid biobank identifies epigenetic dysregulation of intestinal epithelial MHC-I as a novel mechanism in severe Crohn’s Disease حسب Thomas W. Dennison, Rachel D. Edgar, Felicity Payne, Komal Nayak, Alexander Ross, Aurélie Cenier, Claire Glemas, Federica Giachero, April Foster, Rebecca Harris, Judith Kraiczy, Camilla Salvestrini, Georgia Stavrou, Franco Torrente, Kimberley Brook, Claire Trayers, Rasa Elmentaite, Gehad Youssef, Bálint Tél, Douglas J. Winton, Nefeli Skoufou-Papoutsaki, Sam Adler, Philip Bufler, Aline Azabdaftari, Andreas Jenke, G Natasha, Natasha Thomas, Erasmo Miele, Abdulrahman Al-Mohammad, Greta Guarda, Subra Kugathasan, Suresh Venkateswaran, Menna R. Clatworthy, Tomas Castro‐Dopico, Ondřej Suchánek, Caterina Strisciuglio, Marco Gasparetto, Seokjun Lee, Xingze Xu, Erica Bello, Namshik Han, Daniel R. Zerbino, Sarah A. Teichmann, Josquin Nys, Robert Heuschkel, Francesca Perrone, Matthias Zilbauer

    منشور في 2024
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  17. 17
    Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

    Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease حسب Hironori Ueda, Joanna M. M. Howson, Laura Esposito, J. M. Heward, Snook, Giselle Chamberlain, Daniel B. Rainbow, Kara Hunter, Annabel N. Smith, Gianfranco Di Genova, Mathias Herr, Ingrid Dahlman, Felicity Payne, Deborah J. Smyth, Christopher Lowe, Rebecca C.J. Twells, Sarah Howlett, Barry Healy, Sarah Nutland, Helen Rance, Vin Everett, Luc J Smink, Alexander Lam, Heather J. Cordell, Neil Walker, Cristina Bordin, John S. Hulme, Costantino Motzo, Francesco Cucca, J. Fred Hess, Michael L. Metzker, Jane Rogers, Simon G. Gregory, Amit Allahabadia, Ratnasingam Nithiyananthan, Eva Tuomilehto‐Wolf, Jaakko Tuomilehto, Polly J. Bingley, Kathleen M. Gillespie, Dag E. Undlien, Kjersti S. Rønningen, Cristian Guja, C Ionescu-Tîrgovişte, David A. Savage, Alexander P. Maxwell, D. J. Carson, C. C. Patterson, Jayne A. Franklyn, David Clayton, Laurence B. Peterson, Linda S. Wicker, John A. Todd, Stephen Gough

    منشور في 2003
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  18. 18
    Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes

    Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes حسب John R. B. Perry, Michael N. Weedon, Claudia Langenberg, Anne Jackson, Valeriya Lyssenko, Thomas Sparsø, Guðmar Þorleifsson, Harald Grallert, Luigi Ferrucci, Marcello Maggio, Giuseppe Paolisso, Mark Walker, Colin N. A. Palmer, Felicity Payne, Elizabeth Young, Christian Herder, Narisu Narisu, Mario A. Morken, Lori L. Bonnycastle, Katharine R. Owen, Beverley M. Shields, Beatrice Knight, Amanda J. Bennett, Christopher J. Groves, Aimo Ruokonen, Marjo‐Riitta Järvelin, Ewan R. Pearson, Laura Pascoe, Ele Ferrannini, Stefan R. Bornstein, Heather M. Stringham, Laura J. Scott, Johanna Kuusisto, Peter M. Nilsson, Malin Neptin, Anette P. Gjesing, Charlotta Pisinger, Torsten Lauritzen, Annelli Sandbæk, Mike Sampson, Eleftheria Zeggini, Cecilia M. Lindgren, Valgerður Steinthórsdóttir, Unnur Þorsteinsdóttir, Torben Hansen, Peter Schwarz, Thomas Illig, Markku Laakso, Hreinn Stefánsson, Andrew D. Morris, Leif Groop, Oluf Pedersen, Michael Boehnke, Inês Barroso, Nicholas J. Wareham, Andrew T. Hattersley, Mark I. McCarthy, Timothy M. Frayling

    منشور في 2009
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  19. 19
    Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity

    Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity حسب Antigone S. Dimas, Vasiliki Lagou, Adam Barker, Joshua W. Knowles, Reedik Mägi, Marie‐France Hivert, Andrea Benazzo, Denis Rybin, Anne Jackson, Heather M. Stringham, Ci Song, Antje Fischer-Rosinský, Trine Welløv Boesgaard, Niels Grarup, Fahim Abbasi, Themistocles L. Assimes, Ke Hao, Xia Yang, Cécile Lecœur, Inês Barroso, Lori L. Bonnycastle, Yvonne Böttcher, Suzannah Bumpstead, Peter S. Chines, Michael R. Erdos, J. Graessler, Péter Kovács, Mario A. Morken, Narisu Narisu, Felicity Payne, Alena Stančáková, Amy J. Swift, Anke Tönjes, Stefan R. Bornstein, Stéphane Cauchi, Philippe Froguel, David Meyre, Peter E. H. Schwarz, Hans‐Ulrich Häring, Ulf Smith, Michael Boehnke, Richard N. Bergman, Francis S. Collins, Karen L. Mohlke, Jaakko Tuomilehto, Thomas Quertemous, Lars Lind, Torben Hansen, Oluf Pedersen, Mark Walker, A. Pfeiffer, Joachim Spranger, Michael Stümvoll, James B. Meigs, Nicholas J. Wareham, Johanna Kuusisto, Markku Laakso, Claudia Langenberg, Josée Dupuis, Richard M. Watanabe, José C. Florez, Erik Ingelsson, Mark I. McCarthy, Inga Prokopenko

    منشور في 2013
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  20. 20
    Monoallelic and Biallelic Mutations in MAB21L2 Cause a Spectrum of Major Eye Malformations

    Monoallelic and Biallelic Mutations in MAB21L2 Cause a Spectrum of Major Eye Malformations حسب Joe Rainger, Davut Pehli̇van, Stefan Johansson, Hemant Bengani, Luis Sánchez‐Pulido, Kathleen A. Williamson, Mehmet Türe, Heather Barker, Karen Rosendahl, Jürgen W. Spranger, Denise Horn, Alison Meynert, James Floyd, Trine Prescott, Carl A. Anderson, Jacqueline K. Rainger, Ender Karaca, Claudia Gonzaga‐Jauregui, Shalini N. Jhangiani, Donna M. Muzny, Anne Seawright, Dinesh C. Soares, Mira Kharbanda, Victoria Murday, Andrew J. Finch, Richard A. Gibbs, Veronica van Heyningen, Martin S. Taylor, Tahsin Yakut, Per M. Knappskog, Matthew E. Hurles, Chris P. Ponting, James R. Lupski, Gunnar Houge, David Fitzpatrick, Matthew E. Hurles, David Fitzpatrick, Saeed Al-Turki, Carl A. Anderson, Inês Barroso, Philip L. Beales, Jamie Bentham, Shoumo Bhattacharya, Keren Carss, Krishna Chatterjee, Sebhattin Cirak, Catherine Cosgrove, Allan Daly, Jamie Floyd, Chris Franklin, Marta Futema, Steve E. Humphries, Shane McCarthy, Hannah M. Mitchison, Francesco Muntoni, Alexandros Onoufriadis, Victoria Parker, Felicity Payne, Vincent Plagnol, Lucy Raymond, David B. Savage, Peter Scambler, Miriam Schmidts, Robert K. Semple, Eva Serra, Jim Stalker, Margriet van Kogelenberg, Parthiban Vijayarangakannan, Klaudia Walter, G Black Wood

    منشور في 2014
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