L
Loukas Moutsianas
Researcher at Wellcome Trust Sanger Institute
Publications - 74
Citations - 16517
Loukas Moutsianas is an academic researcher from Wellcome Trust Sanger Institute. The author has contributed to research in topics: Genome-wide association study & Medicine. The author has an hindex of 28, co-authored 49 publications receiving 13675 citations. Previous affiliations of Loukas Moutsianas include University of Oxford & Wellcome Trust Centre for Human Genetics.
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Journal ArticleDOI
HLA*IMP—an integrated framework for imputing classical HLA alleles from SNP genotypes
TL;DR: The HLA*IMP as discussed by the authors algorithm combines local data preparation and QC with probabilistic imputation through a remote server, and achieves state-of-the-art performance.
Journal ArticleDOI
Whole-genome sequencing reveals host factors underlying critical COVID-19
Athanasios Kousathanas,Erola Pairo-Castineira,Konrad Rawlik,Alexander Stuckey,Christopher A. Odhams,S. Walker,Clark D Russell,Tomas Malinauskas,Yang Wu,Jonathan E Millar,Xia Shen,Katherine S. Elliott,Fiona Griffiths,Wilna Oosthuyzen,K.W. Morrice,Seán Keating,Bo Wang,Daniel R. Rhodes,Lucija Klaric,Marie Zechner,Nicholas J. Parkinson,Afshan Siddiq,Peter GoddardP. Goddard,Sally Donovan,David M. Maslove,Alistair Nichol,Malcolm G Semple,Tala Zainy,Fiona Maleady-Crowe,L. Todd,Shahla Karbalaei Salehi,Julian C. Knight,Greg Elgar,G. Chan,Prabhu Arumugam,Christine Patch,Augusto Rendon,David Bentley,Clarence D. Kingsley,Jack A. Kosmicki,Julie Horowitz,Aris Baras,Gonçalo R. Abecasis,Manuel A. R. Ferreira,Anne E. Justice,Tooraj Mirshahi,Matthew T. Oetjens,Daniel J. Rader,Marylyn D. Ritchie,Anurag Verma,Tom Fowler,Manu Shankar-Hari,Charlotte Summers,Charles J. Hinds,Peter Horby,Lowell Ling,D. McAuley,Hugh Montgomery,Peter J. M. Openshaw,Paul Elliott,Timothy S. Walsh,Albert Tenesa,Angie Fawkes,Lee Murphy,Kathryn M Rowan,Chris P. Ponting,Veronique Vitart,James F. Wilson,Andrew D. Bretherick,Richard T. Scott,Sara Clohisey Hendry,Loukas Moutsianas,Andy Law,Mark J. Caulfield,J Kenneth Baillie +74 more
TL;DR: The GenOMICC (Genetics of Mortality in Critical Care) study enables the comparison of genomes from individuals who are critically ill with those of population controls to find underlying disease mechanisms as mentioned in this paper .
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
Ashley Beecham,Nikolaos A. Patsopoulos,Nikolaos A. Patsopoulos,Dionysia K. Xifara,Mary F. Davis,Anu Kemppinen,Chris Cotsapas,Chris Cotsapas,Tejas S. Shah,Chris C. A. Spencer,David R. Booth,An Goris,Annette Bang Oturai,Janna Saarela,Bertrand Fontaine,Bernhard Hemmer,C. Martin,Frauke Zipp,Sandra D'Alfonso,Filippo Martinelli-Boneschi,Bruce V. Taylor,Hanne F. Harbo,Ingrid Kockum,Jan Hillert,Tomas Olsson,Maria Ban,Jorge R. Oksenberg,Rogier Q. Hintzen,Lisa F. Barcellos,Lisa F. Barcellos,Lisa F. Barcellos,Cristina Agliardi,Lars Alfredsson,Mehdi Alizadeh,Carl A. Anderson,Robert Andrews,Helle Bach Søndergaard,Amie Baker,Gavin Band,Sergio E. Baranzini,Nadia Barizzone,Jeffrey C. Barrett,Céline Bellenguez,Laura Bergamaschi,Luisa Bernardinelli,Achim Berthele,Viola Biberacher,Thomas M.C. Binder,Hannah Blackburn,Izaura Lima Bomfim,Paola Brambilla,Simon Broadley,Bruno Brochet,Lou Brundin,Dorothea Buck,Helmut Butzkueven,Helmut Butzkueven,Stacy J. Caillier,William Camu,Wassila Carpentier,Paola Cavalla,Elisabeth Gulowsen Celius,Irene Coman,Giancarlo Comi,Lucia Corrado,Leentje Cosemans,Isabelle Cournu-Rebeix,Bruce A.C. Cree,Daniele Cusi,Vincent Damotte,Gilles Defer,Silvia Delgado,Panos Deloukas,Alessia Di Sapio,Alexander T. Dilthey,Peter Donnelly,Bénédicte Dubois,Martin Duddy,Sarah Edkins,Irina Elovaara,Federica Esposito,Nikos Evangelou,Barnaby Fiddes,Judith Field,Andre Franke,Colin Freeman,Irene Y. Frohlich,Daniela Galimberti,Christian Gieger,Pierre-Antoine Gourraud,Christiane Graetz,Andrew Graham,Verena Grummel,Clara Guaschino,Athena Hadjixenofontos,Hakon Hakonarson,Christopher Halfpenny,Gillian L Hall,Per Hall,Anders Hamsten,James Harley,Timothy Harrower,Clive Hawkins,Garrett Hellenthal,Charles Hillier,Jeremy Hobart,M.-M. Hoshi,Sarah E. Hunt,Maja Jagodic,Ilijas Jelcic,Ilijas Jelcic,Angela Jochim,B. E. Kendall,Allan G. Kermode,Allan G. Kermode,Trevor J. Kilpatrick,Keijo Koivisto,Ioanna Konidari,Thomas Korn,Helena C. Kronsbein,Cordelia Langford,Malin Larsson,Mark Lathrop,Mark Lathrop,Christine Lebrun-Frenay,Jeannette Lechner-Scott,Michelle Lee,Maurizio Leone,Virpi Leppa,Giuseppe Liberatore,Benedicte A. Lie,Christina M. Lill,Christina M. Lill,Magdalena Lindén,Jenny Link,Felix Luessi,Jan Lycke,Fabio Macciardi,Fabio Macciardi,Satu Männistö,Clara P. Manrique,Roland Martin,Roland Martin,Vittorio Martinelli,Deborah F. Mason,Gordon Mazibrada,Cristin McCabe,Inger Lise Mero,Julia Y Mescheriakova,Loukas Moutsianas,Kjell-Morten Myhr,Guy Nagels,Richard Nicholas,Petra Nilsson,Fredrik Piehl,Matti Pirinen,Siân Price,Hong Quach,Mauri Reunanen,Wim Robberecht,Neil Robertson,Mariaemma Rodegher,David Rog,Marco Salvetti,Nathalie Schnetz-Boutaud,Finn Sellebjerg,Rebecca C. Selter,Catherine Schaefer,Sandip Shaunak,Ling Shen,Simon Shields,Volker Siffrin,Mark Slee,Per Soelberg Sørensen,Melissa Sorosina,Mireia Sospedra,Mireia Sospedra,Anne Spurkland,Amy Strange,Emilie Sundqvist,Vincent Thijs,J W Thorpe,Anna Ticca,Pentti J. Tienari,Cornelia M. van Duijn,Elizabeth Visser,Steve Vucic,Helga Westerlind,James S. Wiley,Alastair Wilkins,James F. Wilson,Juliane Winkelmann,John Zajicek,Eva Zindler,Jonathan L. Haines,Margaret A. Pericak-Vance,Adrian J. Ivinson,Graeme J. Stewart,David A. Hafler,David A. Hafler,Stephen L. Hauser,Alastair Compston,Gil McVean,Philip L. De Jager,Philip L. De Jager,Stephen Sawcer,Jacob L. McCauley +206 more
TL;DR: Using the ImmunoChip custom genotyping array, this article analyzed 14,498 subjects with multiple sclerosis and 24,091 healthy controls for 161,311 autosomal variants and identified 135 potentially associated regions (P < 1.0 × 10(-4)).
Journal ArticleDOI
Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7
Yang Luo,Yang Luo,Yang Luo,Katrina M. de Lange,Luke Jostins,Luke Jostins,Loukas Moutsianas,Joshua C. Randall,Nicholas A. Kennedy,Christopher A. Lamb,Shane A. McCarthy,Tariq Ahmad,Cathryn Edwards,Eva Goncalves Serra,Ailsa Hart,Christopher J. Hawkey,John C. Mansfield,Craig Mowat,William G. Newman,Sam Nichols,Martin O. Pollard,Jack Satsangi,Alison Simmons,Alison Simmons,Mark Tremelling,Holm H. Uhlig,David C Wilson,David C Wilson,James Lee,Natalie J. Prescott,Charlie W. Lees,Christopher G. Mathew,Miles Parkes,Jeffrey C. Barrett,Carl A. Anderson +34 more
TL;DR: A burden of very rare, damaging missense variants in known Crohn's disease risk genes is detected, suggesting that more comprehensive sequencing studies will continue to improve understanding of the biology of complex diseases.
Journal ArticleDOI
The Power of Gene-Based Rare Variant Methods to Detect Disease-Associated Variation and Test Hypotheses About Complex Disease
Loukas Moutsianas,Vineeta Agarwala,Vineeta Agarwala,Christian Fuchsberger,Jason Flannick,Jason Flannick,Manuel A. Rivas,Kyle J. Gaulton,Patrick K. Albers,Gil McVean,Michael Boehnke,David Altshuler,Mark I. McCarthy +12 more
TL;DR: The results imply that tens of thousands of individuals, extensive functional annotation, or highly targeted hypothesis testing will be required to confidently detect or exclude rare variant signals at complex disease loci.