Výsledky vyhledávání - Loukas Moutsianas

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  1. 1
    HLA*IMP—an integrated framework for imputing classical HLA alleles from SNP genotypes

    HLA*IMP—an integrated framework for imputing classical HLA alleles from SNP genotypes Autor Alexander Dilthey, Loukas Moutsianas, Stephen Leslie, Gil McVean

    Vydáno 2011
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  2. 2
    Multi-Population Classical HLA Type Imputation

    Multi-Population Classical HLA Type Imputation Autor Alexander Dilthey, Stephen Leslie, Loukas Moutsianas, Judong Shen, Charles Cox, Matthew R. Nelson, Gil McVean

    Vydáno 2013
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  3. 3
    Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging

    Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging Autor Ida Surakka, Kati Kristiansson, Verneri Anttila, Michael Inouye, C. Barnes, Loukas Moutsianas, Veikko Salomaa, Mark J. Daly, Aarno Palotie, Leena Peltonen, Samuli Ripatti

    Vydáno 2010
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  4. 4
    A Genomics England haplotype reference panel and imputation of UK Biobank

    A Genomics England haplotype reference panel and imputation of UK Biobank Autor Sinan Shi, Simone Rubinacci, Sile Hu, Loukas Moutsianas, Alexander Stuckey, Anna C. Need, Pier Francesco Palamara, Mark J. Caulfield, Jonathan Marchini, Simon Myers

    Vydáno 2024
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  5. 5
    Equity in cancer genomics in the UK: a cross-sectional analysis of a national cancer cohort

    Equity in cancer genomics in the UK: a cross-sectional analysis of a national cancer cohort Autor Nguyễn Thị Hoài Thu, Sam Tallman, Yoonsu Cho, Alona Sosinsky, John C. Ambrose, S. Thorn, Maxine Mackintosh, Matthew Brown, Loukas Moutsianas, Matt J. Silver, Karoline Kuchenbaecker

    Vydáno 2025
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  6. 6
    Revisiting the Thrifty Gene Hypothesis via 65 Loci Associated with Susceptibility to Type 2 Diabetes

    Revisiting the Thrifty Gene Hypothesis via 65 Loci Associated with Susceptibility to Type 2 Diabetes Autor Qasim Ayub, Loukas Moutsianas, Yuan Chen, Kalliope Panoutsopoulou, Vincenza Colonna, Luca Pagani, Inga Prokopenko, Graham R. S. Ritchie, Chris Tyler‐Smith, Mark I. McCarthy, Eleftheria Zeggini, Yali Xue

    Vydáno 2014
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  7. 7
    The Power of Gene-Based Rare Variant Methods to Detect Disease-Associated Variation and Test Hypotheses About Complex Disease

    The Power of Gene-Based Rare Variant Methods to Detect Disease-Associated Variation and Test Hypotheses About Complex Disease Autor Loukas Moutsianas, Vineeta Agarwala, Christian Fuchsberger, Jason Flannick, Manuel A. Rivas, Kyle J. Gaulton, Patrick K. Albers, Gil McVean, Michael Boehnke, David Altshuler, Mark I. McCarthy

    Vydáno 2015
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  8. 8
    Hypoxia induces a lipogenic cancer cell phenotype via HIF1α-dependent and -independent pathways

    Hypoxia induces a lipogenic cancer cell phenotype via HIF1α-dependent and -independent pathways Autor Alessandro Valli, Miguel Rodríguez, Loukas Moutsianas, Román Fischer, Vita Fedele, Hong-Lei Huang, Ruud van Stiphout, Dylan T. Jones, Michael McCarthy, Maria Vinaxia, Kaori Igarashi, Maya Sato, Tomoyoshi Soga, Francesca M. Buffa, James McCullagh, Óscar Yanes, Adrian L. Harris, Benedikt M. Kessler

    Vydáno 2014
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  9. 9
    Genetic and chemotherapeutic influences on germline hypermutation

    Genetic and chemotherapeutic influences on germline hypermutation Autor Joanna Kaplanis, Benjamin Ide, Rashesh Sanghvi, Matthew D. C. Neville, Petr Danecek, Tim H. H. Coorens, Elena Prigmore, Patrick Short, Giuseppe Gallone, Jeremy F. McRae, Loukas Moutsianas, Chris A. Odhams, Jenny Carmichael, Angela Barnicoat, Helen V. Firth, Patrick O’Brien, Raheleh Rahbari, Matthew E. Hurles

    Vydáno 2022
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  10. 10
    A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates

    A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates Autor Ioanna Tachmazidou, George Dedoussis, Lorraine Southam, Aliki‐Eleni Farmaki, Graham R. S. Ritchie, Dionysia K. Xifara, Angela Matchan, Konstantinos Hatzikotoulas, Nigel W. Rayner, Yuan Chen, Toni I. Pollin, Jeffrey R. O’Connell, Laura M. Yerges-Armstrong, Chrysoula Kiagiadaki, Kalliope Panoutsopoulou, Jeremy Schwartzentruber, Loukas Moutsianas, Emmanouil Tsafantakis, Chris Tyler‐Smith, Gil McVean, Yali Xue, Eleftheria Zeggini

    Vydáno 2013
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  11. 11
    Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7

    Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7 Autor Yang Luo, Katrina M. de Lange, Luke Jostins, Loukas Moutsianas, Joshua C. Randall, Nicholas A. Kennedy, Christopher A Lamb, Shane McCarthy, Tariq Ahmad, Cathryn Edwards, Eva Serra, Ailsa Hart, C J Hawkey, John Mansfield, Craig Mowat, William G. Newman, Sam Nichols, Martin Pollard, Jack Satsangi, Alison Simmons, Mark Tremelling, Holm H. Uhlig, David C. Wilson, James Lee, Natalie J. Prescott, Charlie W. Lees, Christopher G. Mathew, Miles Parkes, Jeffrey C. Barrett, Carl A. Anderson

    Vydáno 2017
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  12. 12
    Increased frequency of repeat expansion mutations across different populations

    Increased frequency of repeat expansion mutations across different populations Autor Kristina Ibáñez, Bharati Jadhav, Matteo Zanovello, Delia Gagliardi, Christopher Clarkson, Stefano Facchini, Paras Garg, Alejandro Martin-Trujillo, Scott J Gies, Valentina Galassi Deforie, Anupriya Dalmia, Davina J. Hensman Moss, Jana Vandrovcová, Clarissa Rocca, Loukas Moutsianas, Chiara Marini‐Bettolo, Helen Walker, Chris Turner, Maryam Shoai, Jeffrey D. Long, Pietro Fratta, Douglas R. Langbehn, Sarah J. Tabrizi, Mark J. Caulfield, Andrea Cortese, Valentina Escott‐Price, John Hardy, Henry Houlden, Andrew J. Sharp, Arianna Tucci

    Vydáno 2024
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  13. 13
    Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease

    Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease Autor Katrina M. de Lange, Loukas Moutsianas, James Lee, Christopher A Lamb, Yang Luo, Nicholas A. Kennedy, Luke Jostins, Daniel L Rice, Javier Gutierrez‐Achury, Sun‐Gou Ji, Graham Heap, Elaine R. Nimmo, Cathryn Edwards, Paul Henderson, Craig Mowat, Jeremy Sanderson, Jack Satsangi, Alison Simmons, David C. Wilson, Mark Tremelling, Ailsa Hart, Christopher G. Mathew, William G. Newman, Miles Parkes, Charlie W. Lees, Holm H. Uhlig, C J Hawkey, Natalie J. Prescott, Tariq Ahmad, John Mansfield, Carl A. Anderson, Jeffrey C. Barrett

    Vydáno 2017
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  14. 14
    GWAS and meta-analysis identifies multiple new genetic mechanisms underlying severe Covid-19

    GWAS and meta-analysis identifies multiple new genetic mechanisms underlying severe Covid-19 Autor Erola Pairo‐Castineira, Konrad Rawlik, Lucija Klarić, Athanasios Kousathanas, Anne Richmond, Jonathan Millar, Clark D Russell, Tomas Malinauskas, Ryan S. Thwaites, A. Stuckey, Christopher A. Odhams, Susan Walker, Fiona Griffiths, Wilna Oosthuyzen, Kirstie Morrice, Seán Keating, Alistair Nichol, Malcolm G. Semple, Julian C. Knight, Manu Shankar‐Hari, Charlotte Summers, Charles Hinds, Peter Horby, Lowell Ling, Daniel F. McAuley, Hugh Montgomery, Peter Openshaw, Timothy Walsh, Albert Tenesa, Richard H. Scott, Mark J. Caulfield, Loukas Moutsianas, Chris P. Ponting, James F. Wilson, Véronique Vitart, Alexandre C. Pereira, André Ducati Luchessi, Esteban J. Parra, Raquel Cruz, Ángel Carracedo, Angie Fawkes, Lee Murphy, Kathy Rowan, Andy Law, Sara Clohisey, J. Kenneth Baillie

    Vydáno 2022
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  15. 15
    Genetic mechanisms of critical illness in Covid-19

    Genetic mechanisms of critical illness in Covid-19 Autor Erola Pairo‐Castineira, Sara Clohisey, Lucija Klarić, Andrew D. Bretherick, Konrad Rawlik, Nick Parkinson, Dorota Pasko, Susan Walker, Anne Richmond, Max Head Fourman, Clark D Russell, Andrew Law, James Furniss, Viktoria‐Eleni Gountouna, Nicola Wrobel, Loukas Moutsianas, Bo Wang, Alison Meynert, Zhijian Yang, Ranran Zhai, Chenqing Zheng, Fiona Griffiths, Wilna Oosthuyzen, Graeme R. Grimes, Barbara Shih, Seán Keating, Marie Zechner, Chris Haley, David J. Porteous, Caroline Hayward, Julian C. Knight, Charlotte Summers, Manu Shankar‐Hari, Paul Klenerman, Lance Turtle, Antonia Ho, Charles Hinds, Peter Horby, Alistair Nichol, David M. Maslove, Lowell Ling, Daniel F. McAuley, Hugh Montgomery, Timothy Walsh, Xia Shen, Kathy Rowan, Angie Fawkes, Lee Murphy, Chris P. Ponting, Albert Tenesa, Mark J. Caulfield, Richard H. Scott, Peter Openshaw, Malcolm G. Semple, Véronique Vitart, James F. Wilson, J. Kenneth Baillie

    Vydáno 2020
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  16. 16
    Class II HLA interactions modulate genetic risk for multiple sclerosis

    Class II HLA interactions modulate genetic risk for multiple sclerosis Autor Loukas Moutsianas, Luke Jostins-Dean, Ashley Beecham, Alexander Dilthey, Dionysia K Xifara, Maria Ban, Tejas Shah, Nikolaos A. Patsopoulos, Lars Alfredsson, Carl A. Anderson, Kathrine E. Attfield, Sergio E. Baranzini, Jeffrey C. Barrett, Thomas M.C. Binder, David R. Booth, Dorothea Buck, Elisabeth Gulowsen Celius, Chris Cotsapas, Sandra D’Alfonso, Calliope A. Dendrou, Peter Donnelly, Bénédicte Dubois, Bertrand Fontaine, Lars Fugger, An Goris, Pierre‐Antoine Gourraud, Christiane Graetz, Bernhard Hemmer, Jan Hillert, Ingrid Kockum, Stephen Leslie, Christina M. Lill, Filippo Martinelli Boneschi, Jorge R. Oksenberg, Tomas Olsson, Annette Oturai, Janna Saarela, Helle Bach Søndergaard, Anne Spurkland, Bruce Taylor, Juliane Winkelmann, Frauke Zipp, Jonathan L. Haines, Margaret A. Pericak‐Vance, Chris C. A. Spencer, Graeme J. Stewart, David A. Hafler, Adrian J. Ivinson, Hanne F. Harbo, Stephen L. Hauser, Philip L. De Jager, Alastair Compston, Jacob L. McCauley, Stephen Sawcer, Gil McVean

    Vydáno 2015
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  17. 17
    Age and Sex Differences in the Genetics of Cardiomyopathy

    Age and Sex Differences in the Genetics of Cardiomyopathy Autor Oyediran Akinrinade, Robert Lesurf, J. C. Ambrose, Prabhu Arumugam, Marta Bleda, F. Boardman-Pretty, C. R. Boustred, Helen Brittain, M. J. Caulfield, G. C. Chan, Tom Fowler, Adam Giess, A. Hamblin, Shirley Henderson, Tim Hubbard, R. Jackson, L. J. Jones, Dalia Kasperavičiūtė, Melis Kayikci, Athanasios Kousathanas, L. Lahnstein, S. E. A. Leigh, I. U. S. Leong, Fabrice Lopez, F. Maleady-Crowe, Loukas Moutsianas, Michael Mueller, Nirupa Murugaesu, Anna C. Need, Peter O’Donovan, Chris A. Odhams, Christine Patch, D. Perez-Gil, Mariana Buongermino Pereira, J. Pullinger, T. Rahim, A. Rendon, T. Rogers, K. Savage, K. Sawant, Richard H. Scott, Afshan Siddiq, A. Sieghart, S. C. Smith, A. Sosinsky, Alexander Stuckey, M. Tanguy, Elaine Thomas, Simon R. Thompson, Arianna Tucci, Edward E. Walsh, M. J. Welland, Eleanor Williams, Katarzyna Witkowska, S. M. Wood, Jane Lougheed, Tapas Mondal, John Smythe, Luis Altamirano‐Diaz, Erwin Oechslin, Seema Mital

    Vydáno 2023
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  18. 18
    Multilocus Inherited Neoplasia Allele Syndrome (MINAS): an update

    Multilocus Inherited Neoplasia Allele Syndrome (MINAS): an update Autor Anthony McGuigan, James Whitworth, Avgi Andreou, Timothy J. Hearn, John C. Ambrose, Prabhu Arumugam, R. Bevers, Marta Bleda, F. Boardman-Pretty, C. R. Boustred, Helen Brittain, Mark J. Caulfield, G. C. Chan, Tom Fowler, Adam Giess, Angela Hamblin, S. A. Henderson, Tim Hubbard, Rachel Jackson, Lesley Jones, Dalia Kasperavičiūtė, Melis Kayikci, Athanasios Kousathanas, L. Lahnstein, S. E. A. Leigh, Ivone Leong, F. J. Lopez, F. Maleady-Crowe, Meriel McEntagart, Federico Minneci, Loukas Moutsianas, M. Mueller, Nirupa Murugaesu, Anna C. Need, Peter O’Donovan, Christopher A. Odhams, Christine Patch, D. Perez-Gil, Mariana Buongermino Pereira, J. Pullinger, T. Rahim, Augusto Rendon, T. Rogers, K. Savage, K. Sawant, Richard H. Scott, Afshan Siddiq, A. Sieghart, Sophie Smith, Alona Sosinsky, Alexander Stuckey, M. Tanguy, Ana Lisa Taylor Tavares, Ellen Thomas, Simon R. Thompson, Arianna Tucci, M. J. Welland, Eleanor Williams, Katarzyna Witkowska, Scott Wood, Marc Tischkowitz, Eamonn R. Maher

    Vydáno 2022
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  19. 19
    Rare variants in the sodium-dependent phosphate transporter gene SLC34A3 explain missing heritability of urinary stone disease

    Rare variants in the sodium-dependent phosphate transporter gene SLC34A3 explain missing heritability of urinary stone disease Autor Omid Sadeghi‐Alavijeh, Melanie Chan, Shabbir H. Moochhala, Sarah Howles, Daniel P. Gale, Detlef Böckenhauer, John C. Ambrose, Prabhu Arumugam, R. Bevers, Marta Bleda, F. Boardman-Pretty, C. R. Boustred, Helen Brittain, Mark J. Caulfield, G. C. Chan, Greg Elgar, Tom Fowler, Adam Giess, Angela Hamblin, Bingyang Shi, Tim Hubbard, R. Jackson, J. Louise Jones, Dalia Kasperavičiūtė, Melis Kayikci, Athanasios Kousathanas, L. Lahnstein, S. E. A. Leigh, I. U. S. Leong, Javier F. Lopez, F. Maleady-Crowe, Meriel McEntagart, Federico Minneci, Loukas Moutsianas, Michael Mueller, Nirupa Murugaesu, Anna C. Need, Peter O’Donovan, Chris A. Odhams, Christine Patch, Mariana Buongermino Pereira, D. Perez-Gil, J. Pullinger, T. Rahim, Augusto Rendon, Tim Rogers, K. Savage, Kushmita Sawant, Richard H. Scott, Afshan Siddiq, A. Sieghart, Samuel C. Smith, Alona Sosinsky, Alexander Stuckey, M. Tanguy, Ana Lisa Taylor Tavares, Ellen Thomas, Simon R. Thompson, Arianna Tucci, M. J. Welland, Eleanor Williams, Katarzyna Witkowska, S. M. Wood

    Vydáno 2023
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  20. 20
    The relationship between the gastric cancer microbiome and clinicopathological factors: a metagenomic investigation from the 100,000 genomes project and The Cancer Genome Atlas

    The relationship between the gastric cancer microbiome and clinicopathological factors: a metagenomic investigation from the 100,000 genomes project and The Cancer Genome Atlas Autor Mary E. Booth, Henry M. Wood, Mark A. Travis, J. C. Ambrose, P. Arumugam, R. Bevers, M. Bleda, F. Boardman-Pretty, C. R. Boustred, H. Brittain, Melissa A. Brown, M. J. Caulfield, Gcf Chan, A. Giess, John N. Griffin, Angela Hamblin, Shirley Henderson, Tim Hubbard, Rachel Jackson, Lesley Jones, Dalia Kasperavičiūtė, Melis Kayikci, Athanasios Kousathanas, L. Lahnstein, A. Lakey, S. E. A. Leigh, Ivone Leong, F. J. Lopez, F. Maleady-Crowe, Meriel McEntagart, Federico Minneci, Jonathan Mitchell, Loukas Moutsianas, Michael Mueller, Nirupa Murugaesu, A. C. Need, Peter O’Donovan, Christopher A. Odhams, Christine Patch, D. Perez-Gil, Mariana Buongermino Pereira, J. Pullinger, T. Rahim, Augusto Rendon, T. Rogers, K. Savage, K. Sawant, Richard H. Scott, A. Siddiq, A. Sieghart, Sean Smith, Alona Sosinsky, Alexander Stuckey, M. Tanguy, Ana Lisa Taylor Tavares, Elaine Thomas, S. R. Thompson, Arianna Tucci, M. J. Welland, E. Williams, Katarzyna Witkowska, Scott Wood, Magdalena Zarowiecki, Philip Quirke, Heike I. Grabsch

    Vydáno 2025
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