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Vincent Plagnol

Active 2003–2025

128
Papers
33,979
Citations
90
h-index
127
i10-index

Citations

Citations per year for Vincent Plagnol1979: 2 citations1980: 1 citations1988: 1 citations1990: 1 citations1991: 3 citations1993: 2 citations1997: 1 citations2002: 2 citations2003: 2 citations2004: 4 citations2005: 23 citations2006: 36 citations2007: 66 citations2008: 166 citations2009: 268 citations2010: 281 citations2011: 358 citations2012: 359 citations2013: 410 citations2014: 429 citations2015: 494 citations2016: 487 citations2017: 528 citations2018: 535 citations2019: 1,413 citations2020: 1,421 citations2021: 1,380 citations2022: 998 citations2023: 729 citations2024: 1,228 citations2025: 570 citations2026: 33 citations1981–1987: no citations, so these years are not shown1989: no citations, so this year is not shown1992: no citations, so this year is not shown1994–1996: no citations, so these years are not shown1998–2001: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 5,271 citing papers, 21.3% of this breakdownUnited Kingdom: 2,945 citing papers, 11.9% of this breakdownGermany: 1,578 citing papers, 6.4% of this breakdownChina: 1,471 citing papers, 5.9% of this breakdownCanada: 996 citing papers, 4% of this breakdownNetherlands: 984 citing papers, 4% of this breakdownFrance: 947 citing papers, 3.8% of this breakdownAustralia: 902 citing papers, 3.6% of this breakdownItaly: 871 citing papers, 3.5% of this breakdownSpain: 685 citing papers, 2.8% of this breakdownSweden: 652 citing papers, 2.6% of this breakdownSwitzerland: 534 citing papers, 2.2% of this breakdown
0%21.3%Other 28%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology48.4%
  • Medicine35%
  • Immunology and Microbiology6.2%
  • Neuroscience2.5%
  • Agricultural and Biological Sciences2.2%
  • Mathematics2%
  • Other3.7%

Topics

  • 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%
  • Other84.5%

Coauthors

All papers

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  1. Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics

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

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

    Authors: 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 cited by 268

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

    Authors: 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 and 249 more - Nature 2015 cited by 1,195

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

    Authors: 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 cited by 1,773

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

    Authors: 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 and 40 more - Brain 2017 cited by 451

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

    Authors: 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 cited by 753

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

    Authors: 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 and 211 more - The American Journal of Human Genetics 2016 cited by 484

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

    Authors: 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 cited by 864

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

    Authors: 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 cited by 464

  10. Markov chain Monte Carlo without likelihoods

    Authors: Paul Marjoram, John Molitor, Vincent Plagnol, Simon Tavaré - National Academy of Sciences, Proceedings of the National Academy of Sciences 2003 cited by 1,250

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

    Authors: 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 cited by 631

  12. Integrated Polygenic Tool Substantially Enhances Coronary Artery Disease Prediction

    Authors: 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 cited by 177

  13. Atlas of the clinical genetics of human dilated cardiomyopathy

    Authors: 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 cited by 568

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

    Authors: 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 cited by 1,457

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

    Authors: 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 cited by 240

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

    Authors: 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 cited by 135

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

    Authors: Jack Humphrey, Warren Emmett, Pietro Fratta, Adrian M. Isaacs, Vincent Plagnol - BMC Medical Genomics 2017 cited by 125

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

    Authors: 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 cited by 171

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

    Authors: 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 cited by 113

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

    Authors: 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 cited by 269

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

    Authors: 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 cited by 97

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

    Authors: 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 cited by 919

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

    Authors: 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 and 117 more - Nature 2010 cited by 818

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

    Authors: 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 cited by 220