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Vincent Plagnol

2003–2025 年に発表

128
論文数
33,979
被引用数
90
h 指数
127
i10 指数

被引用数

Vincent Plagnol の年別被引用数1979 年: 被引用 2 件1980 年: 被引用 1 件1988 年: 被引用 1 件1990 年: 被引用 1 件1991 年: 被引用 3 件1993 年: 被引用 2 件1997 年: 被引用 1 件2002 年: 被引用 2 件2003 年: 被引用 2 件2004 年: 被引用 4 件2005 年: 被引用 23 件2006 年: 被引用 36 件2007 年: 被引用 66 件2008 年: 被引用 166 件2009 年: 被引用 268 件2010 年: 被引用 281 件2011 年: 被引用 358 件2012 年: 被引用 359 件2013 年: 被引用 410 件2014 年: 被引用 429 件2015 年: 被引用 494 件2016 年: 被引用 487 件2017 年: 被引用 528 件2018 年: 被引用 535 件2019 年: 被引用 1,413 件2020 年: 被引用 1,421 件2021 年: 被引用 1,380 件2022 年: 被引用 998 件2023 年: 被引用 729 件2024 年: 被引用 1,228 件2025 年: 被引用 570 件2026 年: 被引用 33 件1981〜1987 年は被引用が無いため表示していません1989 年は被引用が無いため表示していません1992 年は被引用が無いため表示していません1994〜1996 年は被引用が無いため表示していません1998〜2001 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 5,271 件、この内訳の 21.3%イギリス: 引用元論文 2,945 件、この内訳の 11.9%ドイツ: 引用元論文 1,578 件、この内訳の 6.4%中国: 引用元論文 1,471 件、この内訳の 5.9%カナダ: 引用元論文 996 件、この内訳の 4%オランダ: 引用元論文 984 件、この内訳の 4%フランス: 引用元論文 947 件、この内訳の 3.8%オーストラリア: 引用元論文 902 件、この内訳の 3.6%イタリア: 引用元論文 871 件、この内訳の 3.5%スペイン: 引用元論文 685 件、この内訳の 2.8%スウェーデン: 引用元論文 652 件、この内訳の 2.6%スイス: 引用元論文 534 件、この内訳の 2.2%
0%21.3%その他 28%

機関

分野

  • Biochemistry, Genetics and Molecular Biology48.4%
  • Medicine35%
  • Immunology and Microbiology6.2%
  • Neuroscience2.5%
  • Agricultural and Biological Sciences2.2%
  • Mathematics2%
  • その他3.7%

トピック

  • Genetic Associations and Epidemiology5.8%
  • Genomics and Rare Diseases2.2%
  • Parkinson's Disease Mechanisms and Treatments2.1%
  • Diabetes and associated disorders1.9%
  • Genetic Mapping and Diversity in Plants and Animals1.8%
  • Genomic variations and chromosomal abnormalities1.7%
  • その他84.5%

共著者

全論文

検索で開く
  1. Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics

    著者: Claudia Giambartolomei, Damjan Vukcevic, Eric E. Schadt, Lude Franke, Aroon D. Hingorani, Chris Wallace, Vincent Plagnol - PLoS Genetics 2014 被引用: 4,553

  2. UK Biobank release and systematic evaluation of optimised polygenic risk scores for 53 diseases and quantitative traits

    著者: Deborah J. Thompson, Daniel Wells, Saskia Selzam, Iliana Peneva, Rachel Moore, Kevin Sharp, William A. Tarran, Edward J. Beard, Fernando Riveros-Mckay, Carla Giner-Delgado, Duncan S. Palmer, Priyanka Seth, Jamie Harrison, Marta Futema, Gil McVean, Vincent Plagnol, Peter Donnelly, Michael E. Weale - medRxiv 2022 被引用: 268

  3. The UK10K project identifies rare variants in health and disease

    著者: Writing group, Klaudia Walter, Josine L. Min, Jie Huang, Lucy Crooks, Yasin Memari, Shane McCarthy, John R. B. Perry, Changjiang Xu, Marta Futema, Daniel Lawson, Valentina Iotchkova, Stephan Schiffels, Audrey E. Hendricks, Petr Danecek, Rui Li, James S. Floyd, Louise V. Wain, Inês Barroso, Steve E. Humphries, Matthew E. Hurles, Eleftheria Zeggini, Jeffrey C. Barrett, Vincent Plagnol, J. Brent Richards, Celia M. T. Greenwood, Nicholas J. Timpson, Richard Durbin, Nicole Soranzo, Production group, Senduran Bala, Peter Clapham, Guy Coates, Tony Cox, Allan Daly, Petr Danecek, Yuanping Du, Richard Durbin, Sarah Edkins, Peter Ellis, Paul Flicek, Xiaosen Guo, Xueqin Guo, Liren Huang, David K. Jackson, Christopher Joyce, Thomas Keane, Anja Kolb-Kokocinski, Cordelia Langford, Rui Li, Jieqin Liang, Hong Lin, Ryan Liu, John Maslen, Shane McCarthy, Dawn Muddyman, Michael A. Quail, Jim Stalker, Jianping Sun, Jing Tian, Guangbiao Wang, Jun Wang, Yu Wang, Kim Wong, Pingbo Zhang, Cohorts group, Inês Barroso, Ewan Birney, Chris Boustred, Lu Chen, Gail Clement, Massimiliano Cocca, Petr Danecek, George Davey Smith, Ian N.M. Day, Aaron Day-Williams, Thomas A. Down, Ian Dunham, Richard Durbin, David M. Evans, Tom R. Gaunt, Matthias Geihs, Celia M. T. Greenwood, Deborah Hart, Audrey E. Hendricks, Bryan Howie, Jie Huang, Tim Hubbard, Pirro G. Hysi, Valentina Iotchkova, Yalda Jamshidi, Konrad J. Karczewski, John P. Kemp, Geneviève Lachance, Daniel Lawson, Monkol Lek, Margarida Lopes, Daniel G. MacArthur, Jonathan Marchini, Massimo Mangino ほか 249 名 - Nature 2015 被引用: 1,195

  4. Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

    著者: Jeffrey C. Barrett, David Clayton, Patrick Concannon, Beena Akolkar, Jason D. Cooper, Henry A Erlich, Cécile Julier, Grant Morahan, Jørn Nerup, Concepcion R. Nierras, Vincent Plagnol, Flemming Pociot, Helen Schuilenburg, Deborah J. Smyth, Helen Stevens, John A. Todd, Neil Walker, Stephen S. Rich - Nature Genetics 2009 被引用: 1,773

  5. Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease

    著者: Laurie Robak, Iris E. Jansen, Jeroen van Rooij, André G. Uitterlinden, Robert Kraaij, Joseph Jankovic, Peter Heutink, Joshua Shulman, Mike A. Nalls, Vincent Plagnol, Dena G Hernandez, Manu Sharma, Una‐Marie Sheerin, Mohamad Saad, Javier Simón‐Sánchez, Claudia Schulte, Suzanne Lesage, Sigurlaug Sveinbjörnsdóttir, Sampath Arepalli, Roger A. Barker, Yoav Ben-, Henk W. Berendse, Daniela Berg, Kailash P. Bhatia, Rob M.A. de Bie, Alessandro Biffi, Bas Bloem, Zoltán Bochdanovits, Michael von Bonin, José Brás, Kathrin Brockmann, Janet Brooks, David J. Burn, Elisa Majounie, Gavin Charlesworth, Codrin Lungu, Honglei Chen, Patrick F. Chinnery, Sean Chong, Carl E Clarke, Mark Cookson, Jonathan M. Cooper, Jean‐Christophe Corvol, Carl Counsell, Philippe Damier, Jean‐François Dartigues, Panos Deloukas, Günther Deuschl, David T. Dexter, Karin D. van Dijk, Allissa Dillman, F. Durif, Alexandra Dürr, Sarah Edkins, Jonathan Evans, Thomas Foltynie, Jing Dong, Michelle Gardner, J. Raphael Gibbs, Alison Goate, Emma Gray, Rita Guerreiro, Clare Harris, Jacobus J. van Hilten, Albert Hofman, Albert R. Hollenbeck, Janice L. Holton, Michele Hu, Xuemei Huang, Isabel Wurster, Walter Mätzler, Gavin Hudson, Sarah Hunt, Johanna Huttenlocher, Thomas Illig, Pálmi V. Jónsson, Jean‐Charles Lambert, Cordelia Langford, Andrew J. Lees, Peter Lichtner, Patricia Limousin, Grisel Lopez, Delia Lorenz, Codrin Lungu, Alisdair McNeill, Catriona Moorby, Matthew Moore, Huw R. Morris, Karen Morrison, Valentina Escott‐Price, Ese Mudanohwo, Sean S. O’Sullivan, Justin Pearson, Joel S. Perlmutter, Hjörvar Pétursson, Pierre Pollak, Bart Post, Simon Potter, Bernard Ravina, Tamás Révész ほか 40 名 - Brain 2017 被引用: 451

  6. A robust model for read count data in exome sequencing experiments and implications for copy number variant calling

    著者: Vincent Plagnol, James Curtis, Michael Epstein, Kin Y. Mok, Emma Stebbings, Sofia Grigoriadou, Nicholas W. Wood, Sophie Hambleton, Siobhan O. Burns, Adrian J. Thrasher, Dinakantha Kumararatne, Rainer Doffinger, Sergey Nejentsev - Bioinformatics, Bioinform. 2012 被引用: 753

  7. Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

    著者: Keren Carss, Gavin Arno, Marie Erwood, Jonathan Stephens, Alba Sanchis-Juan, Sarah Hull, Karyn Mégy, Detelina Grozeva, Eleanor Dewhurst, Samantha Malka, Vincent Plagnol, Christopher J. Penkett, Kathleen Stirrups, Roberta Rizzo, Genevieve Wright, Dragana Josifova, Maria Bitner‐Glindzicz, Richard H. Scott, Emma Clement, Louise Allen, Ruth Armstrong, Angela F. Brady, Jenny Carmichael, Manali Chitre, Robert Henderson, Jane A. Hurst, Robert E. MacLaren, Elaine Murphy, Joan Paterson, Elisabeth Rosser, Dorothy Thompson, Emma Wakeling, Willem H. Ouwehand, Michel Michaelides, Anthony T. Moore, Andrew R. Webster, F. Lucy Raymond, Timothy J. Aitman, Hana Alachkar, Sonia Ali, Louise Allen, David Allsup, Gautum Ambegaonkar, Julie Anderson, Richard Antrobus, Ruth Armstrong, Gavin Arno, Gururaj Arumugakani, Sofie Ashford, William F. Astle, Antony Attwood, Steve Austin, Chiara Bacchelli, Tamam Bakchoul, Tadbir K. Bariana, Helen Baxendale, David Bennett, Claire Bethune, Shahnaz Bibi, Maria Bitner‐Glindzicz, Marta Bleda, Harm Boggard, Paula Bolton‐Maggs, Claire Booth, John R. Bradley, Angie Brady, Matthew A. Brown, Michael J. Browning, Christine Bryson, Siobhan O. Burns, Paul Calleja, Natalie Canham, Jenny Carmichael, Keren Carss, Mark J. Caulfield, Elizabeth Chalmers, Anita Chandra, Patrick F. Chinnery, Manali Chitre, Colin Church, Emma Clement, Emma Clement, Virginia Clowes, Gerry Coghlan, Peter Collins, Nichola Cooper, Amanda Creaser-Myers, Rosa DaCosta, Louise C. Daugherty, Sophie Davies, John S. Davis, Minka De Vries, Patrick Deegan, Sri V. V. Deevi, Charu Deshpande, Lisa Devlin, Eleanor Dewhurst, Rainer Döffinger, Natalie Dormand, Elizabeth Drewe ほか 211 名 - The American Journal of Human Genetics 2016 被引用: 484

  8. Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

    著者: Gosia Trynka, PreventCD Study Group, Karen A. Hunt, Nicholas Bockett, Jihane Romanos, Vanisha Mistry, Agata Szperl, Sjoerd F. Bakker, Maria Teresa Bardella, Leena Bhaw, Gemma Castillejo, Emilio G. de la Concha, Rodrigo Coutinho de Almeida, Kerith‐Rae Dias, Cleo C. van Diemen, P Dubois, Richard H. Duerr, Sarah Edkins, Lude Franke, Karin Fransén, Javier Cuesta, Graham Heap, Barbara Hrdličková, Sarah Hunt, Leticia Plaza Izurieta, Valentina Izzo, Leo A. B. Joosten, Cordelia Langford, Maria Cristina Mazzilli, Charles A. Mein, Vandana Midah, Mitja Mitrovič, Barbara Mora, Marinita Morelli, Sarah Nutland, Concepción Núñez, Suna Önengüt-Gümüşcü, Kerra Pearce, Mathieu Platteel, Isabel Polanco, Simon Potter, Carmen Ribes‐Koninckx, Isis Ricaño-Ponce, Stephen S. Rich, Anna Rybak, José Luis Santiago, Sabyasachi Senapati, Ajit Sood, Hania Szajewska, Riccardo Troncone, Jezabel Varadé, Chris Wallace, Victorien M. Wolters, Alexandra Zhernakova, B.K. Thelma, Božena Cukrowská, Elena Urcelay, José Ramón Bilbao, M. L. Mearin, Donatella Barisani, Jeffrey C. Barrett, Vincent Plagnol, Panos Deloukas, Cisca Wijmenga, David A. van Heel - Nature Genetics 2011 被引用: 864

  9. CHiCAGO: robust detection of DNA looping interactions in Capture Hi-C data

    著者: Jonathan Cairns, Paula Freire-Pritchett, Steven Wingett, Csilla Várnai, Andrew Dimond, Vincent Plagnol, Daniel R. Zerbino, Stefan Schoenfelder, Biola M. Javierre, Cameron S. Osborne, Peter Fraser, Mikhail Spivakov - Genome biology 2016 被引用: 464

  10. Markov chain Monte Carlo without likelihoods

    著者: Paul Marjoram, John Molitor, Vincent Plagnol, Simon Tavaré - National Academy of Sciences, Proceedings of the National Academy of Sciences 2003 被引用: 1,250

  11. Phosphoinositide 3-Kinase δ Gene Mutation Predisposes to Respiratory Infection and Airway Damage

    著者: Ivan L. Ângulo, Oscar Vadas, Fabien Garçon, Edward Banham-Hall, Vincent Plagnol, Timothy Ronan Leahy, Helen Baxendale, Tanya Coulter, James Curtis, Changxin Wu, Katherine G. Blake-Palmer, Olga Perišić, Deborah J. Smyth, Mailis Maes, Christine Fiddler, Jatinder K. Juss, Deirdre Cilliers, Gašper Markelj, Anita Chandra, George E. Farmer, Anna Kielkowska, Jonathan Clark, Sven Kracker, Marianne Debré, Capucine Pïcard, Isabelle Pellier, Nada Jabado, James Morris, Gabriela Barcenas‐Morales, Alain Fischer, Len Stephens, Phillip T. Hawkins, Jeffrey C. Barrett, Mario Abinun, Menna R. Clatworthy, Anne Durandy, Rainer Döffinger, Edwin R. Chilvers, Andrew J. Cant, Dinakantha Kumararatne, Klaus Okkenhaug, Roger Williams, Alison M. Condliffe, Sergey Nejentsev - Science 2013 被引用: 631

  12. Integrated Polygenic Tool Substantially Enhances Coronary Artery Disease Prediction

    著者: Fernando Riveros-Mckay, Michael E. Weale, Rachel Moore, Saskia Selzam, Eva Krapohl, R. Michael Sivley, William A. Tarran, Peter Sørensen, Alexander S. Lachapelle, Jonathan A. Griffiths, Ayden Saffari, John Deanfield, Chris C. A. Spencer, Julia Hippisley‐Cox, David J. Hunter, Jack W. O’Sullivan, Euan A. Ashley, Vincent Plagnol, Peter Donnelly - Circulation Genomic and Precision Medicine 2021 被引用: 177

  13. Atlas of the clinical genetics of human dilated cardiomyopathy

    著者: Jan Haas, Karen Frese, Barbara Peil, Wanda Kloos, Andreas Keller, Rouven Nietsch, Zhu Feng, Sabine Müller, Elham Kayvanpour, Britta Vogel, Farbod Sedaghat‐Hamedani, Wei-Keat Lim, Xiaohong Zhao, Dmitriy Fradkin, Doreen Köhler, Simon Fischer, Jennifer Franke, Sabine Marquart, Ioana Barb, Daniel Tian Li, Ali Amr, Philipp Ehlermann, Derliz Mereles, Tanja Weis, Sarah Hassel, Andreas Kremer, Vanessa King, Emil Wirsz, Richard Isnard, Michel Komajda, Alessandra Serio, Maurizia Grasso, Petros Syrris, Eleanor Wicks, Vincent Plagnol, Luís R. Lopes, Tenna Gadgaard, Hans Eiskjær, Mads Emil Jørgensen, Diego García-Giustiniani, Martín Ortiz-Genga, María G. Crespo‐Leiro, Rondal H. Lekanne Dit Deprez, Imke Christiaans, Ingrid A van Rijsingen, Arthur A. Wilde, Anders Waldenström, Martino Bolognesi, Riccardo Bellazzi, Stellan Mörner, Justo Lorenzo Bermejo, Lorenzo Monserrat, Eric Villard, Jens Mogensen, Yigal M. Pinto, Philippe Charron, Perry Elliott, Eloisa Arbustini, Hugo A. Katus, Benjamin Meder - European Heart Journal 2014 被引用: 568

  14. Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

    著者: Genetics of Type 1 Diabetes in Finland, 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 - Nature Genetics 2007 被引用: 1,457

  15. Biallelic RIPK1 mutations in humans cause severe immunodeficiency, arthritis, and intestinal inflammation

    著者: Delphine Cuchet-Lourenço, Davide Eletto, Changxin Wu, Vincent Plagnol, Olivier Papapietro, James Curtis, Lourdes Ceron‐Gutierrez, Chris M. Bacon, Scott Hackett, Badr Alsaleem, Mailis Maes, Miguel Gaspar, Ali Alisaac, Emma Goss, Eman AlIdrissi, Daniela Siegmund, Harald Wajant, Dinakantha Kumararatne, Mofareh AlZahrani, Peter D. Arkwright, Mario Abinun, Rainer Döffinger, Sergey Nejentsev - Science 2018 被引用: 240

  16. A systematic evaluation of the performance and properties of the UK Biobank Polygenic Risk Score (PRS) Release

    著者: Deborah J. Thompson, Daniel Wells, Saskia Selzam, Iliana Peneva, Rachel Moore, Kevin Sharp, William A. Tarran, Edward J. Beard, Fernando Riveros-Mckay, Carla Giner-Delgado, Duncan S. Palmer, Priyanka Seth, Jamie Harrison, Marta Futema, Gil McVean, Vincent Plagnol, Peter Donnelly, Michael E. Weale - PLoS ONE 2024 被引用: 135

  17. Quantitative analysis of cryptic splicing associated with TDP-43 depletion

    著者: Jack Humphrey, Warren Emmett, Pietro Fratta, Adrian M. Isaacs, Vincent Plagnol - BMC Medical Genomics 2017 被引用: 125

  18. Development of a highly sensitive liquid biopsy platform to detect clinically-relevant cancer mutations at low allele fractions in cell-free DNA

    著者: Davina Gale, Andrew Lawson, Karen Howarth, Mikidache Madi, Bradley Durham, Sarah Smalley, John D. Calaway, Shannon Blais, Greg Jones, James J. Clark, Peter Dimitrov, Michelle Pugh, Samuel Woodhouse, Michael Epstein, Ana Fernández-González, Alexandra S. Whale, Jim F. Huggett, Carole A. Foy, Gerwyn M. Jones, Hadas Raveh-Amit, Karin Schmitt, Alison S. Devonshire, Emma Green, Tim Forshew, Vincent Plagnol, Nitzan Rosenfeld - PLoS ONE 2018 被引用: 171

  19. FUS ALS-causative mutations impair FUS autoregulation and splicing factor networks through intron retention

    著者: Jack Humphrey, Nicol Birsa, Carmelo Milioto, Martha McLaughlin, Agnieszka M Ule, David Robaldo, Andrea Eberle, Rahel Kräuchi, Matthew P. Bentham, Anna‐Leigh Brown, Seth Jarvis, Cristian Bodo, Maria Giovanna Garone, Anny Devoy, Gianni Sorarú, Alessandro Rosa, Irene Bozzoni, Elizabeth Fisher, Oliver Mühlemann, Giampietro Schiavo, Marc‐David Ruepp, Adrian M. Isaacs, Vincent Plagnol, Pietro Fratta - Nucleic Acids Research 2020 被引用: 113

  20. The Effect of Inhaled IFN-β on Worsening of Asthma Symptoms Caused by Viral Infections. A Randomized Trial

    著者: Ratko Djukanović, Tim Harrison, Sebastian L. Johnston, Flic Gabbay, Peter Wark, Neil C. Thomson, Robert Niven, Dave Singh, Helen K. Reddel, Donna E. Davies, Richard Marsden, Christine B. Boxall, Sarah Dudley, Vincent Plagnol, Stephen T. Holgate, Phillip Monk - American Journal of Respiratory and Critical Care Medicine 2014 被引用: 269

  21. Validation of an Integrated Risk Tool, Including Polygenic Risk Score, for Atherosclerotic Cardiovascular Disease in Multiple Ethnicities and Ancestries

    著者: Michael E. Weale, Fernando Riveros-Mckay, Saskia Selzam, Priyanka Seth, Rachel Moore, William A. Tarran, Eva Gradovich, Carla Giner-Delgado, Duncan S. Palmer, Daniel Wells, Ayden Saffari, R. Michael Sivley, Alexander S. Lachapelle, Hannah Wand, Shoa L. Clarke, Joshua W. Knowles, Jack W. O’Sullivan, Euan A. Ashley, Gil McVean, Vincent Plagnol, Peter Donnelly - The American Journal of Cardiology 2021 被引用: 97

  22. Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

    著者: Michael A Nalls, Michael A. Nalls, Vincent Plagnol, Dena G Hernandez, Manu Sharma, Una‐Marie Sheerin, Mohamad Saad, Javier Simón‐Sánchez, Claudia Schulte, Suzanne Lesage, Sigurlaug Sveinbjörnsdóttir, Maria Martinez, María Martínez, John Hardy, Peter Heutink, Alexis Brice, Thomas Gasser, Andrew B. Singleton - The Lancet 2011 被引用: 919

  23. Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

    著者: Elaine Green, Liz Forty, Ian Jones, Michael O‘Donovan, Michael J. Owen, Detelina Grozeva, George Kirov, Liz Forty, Nick Craddock, Ellie Russell, Matthew E. Hurles, Panos Deloukas, Richard Redon, Chris Tyler‐Smith, Kathy Stirrups, Hazel Arbury, C. Barnes, Armand Valsesia, Willem H. Ouwehand, Matthew E. Hurles, Eleanor Howard, Andrew Dunham, Anthony Attwood, Michael L. Mimmack, Dominic Kwiatkowski, Nigel P. Carter, Jan Aerts, Michael A. Quail, Sanjeev S. Bhaskar, Kevin Lewis, Naomi Hammond, Elilan Somaskantharajah, Donald F. Conrad, T. Daniel Andrews, Ifejinelo Onyiah, Chris M. Clee, Husam Hebaishi, Jeffrey C. Barrett, Cordelia F. Langford, John H. Burton, Samuel C. Robson, Sarah Hunt, Rhian Gwilliam, Emma Gray, Kirsten McLay, Carol Scott, Aarno Palotie, Kimmo Palin, Alison J. Coffey, Michael R. Stratton, Inês Barroso, Sarah Edkins, Tomas Fitzgerald, Christopher Yau, Zhan Su, Gil McVean, Niall J. Cardin, Christopher Holmes, Eleni Giannoulatou, Jonathan Marchini, Adam Auton, Simon Myers, Peter Donnelly, Julian Maller, Inga Prokopenko, Jake Byrnes, Richard D. Pearson, Andrew P. Morris, Mahim Jain, Adrian V. S. Hill, Dominic Kwiatkowski, Jake Byrnes, Neil Robertson, Damjan Vukcevic, Mark I. McCarthy, Vincent Plagnol, Oliver S. Burren, Mark I. McCarthy, Vincent Plagnol, Nigel Ovington, Meeta Maisuria-Armer, Joanna M. M. Howson, Jason D. Cooper, Oliver S. Burren, Debbie J. Smyth, Kate Downes, Matthew Woodburn, Neil Walker, John A. Todd, Helen E. Stevens, Chris Wallace, Matt Hardy, Helen Schuilenburg, J. Thompson, Louise V. Wain, Paul R. Burton, Martin D. Tobin, Tariq Ahmad, Nicholas A. Watkins, Jennifer D. Jolley ほか 117 名 - Nature 2010 被引用: 818

  24. Astrovirus VA1/HMO-C: An Increasingly Recognized Neurotropic Pathogen in Immunocompromised Patients

    著者: Julianne R. Brown, Sofia Morfopoulou, Jonathan Hubb, Warren Emmett, Winnie Ip, Divya Shah, Tony Brooks, Simon Paine, Glenn Anderson, Alex Virasami, C. Y. William Tong, Duncan A. Clark, Vincent Plagnol, Thomas S. Jacques, Waseem Qasim, Michael Hubank, Judith Breuer - Clinical Infectious Diseases 2015 被引用: 220