檢索結果 - Angela Matchan

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  1. 1
    Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits

    Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits 由 Lorraine Southam, Arthur Gilly, Dániel Süveges, Aliki‐Eleni Farmaki, Jeremy Schwartzentruber, Ioanna Tachmazidou, Angela Matchan, Nigel W. Rayner, Emmanouil Tsafantakis, Maria Karaleftheri, Yali Xue, George Dedoussis, Eleftheria Zeggini

    出版 2017
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    Artigo
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  2. 2
    Transcription Factor Activities Enhance Markers of Drug Sensitivity in Cancer

    Transcription Factor Activities Enhance Markers of Drug Sensitivity in Cancer 由 Luz García‐Alonso, Francesco Iorio, Angela Matchan, Nuno A. Fonseca, Patricia Jaaks, Gareth Peat, Miguel Pignatelli, Fiammetta Falcone, Cyril H. Benes, Ian Dunham, Graham R. Bignell, Simon S. McDade, Mathew J. Garnett, Julio Sáez-Rodríguez

    出版 2017
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    Artigo
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  3. 3
    Functional linkage of gene fusions to cancer cell fitness assessed by pharmacological and CRISPR-Cas9 screening

    Functional linkage of gene fusions to cancer cell fitness assessed by pharmacological and CRISPR-Cas9 screening 由 Gabriele Picco, Elisabeth Chen, Luz García‐Alonso, Fiona M. Behan, Emanuel Gonçalves, Graham R. Bignell, Angela Matchan, Beiyuan Fu, Ruby Banerjee, Elizabeth Anderson, Adam P. Butler, Cyril H. Benes, Ultan McDermott, David J. Dow, Francesco Iorio, Euan A. Stronach, Fengtang Yang, Kosuke Yusa, Julio Sáez-Rodríguez, Mathew J. Garnett

    出版 2019
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    Artigo
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  4. 4
    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 由 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

    出版 2013
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    Artigo
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  5. 5
    RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome

    RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome 由 Nina Bögershausen, I-Chun Tsai, Esther Pohl, Pelin Özlem Şimşek‐Kiper, Filippo Beleggia, E. Ferda Perçin, Katharina Keupp, Angela Matchan, Esther Milz, Yasemin Alanay, Hülya Kayserili, Yicheng Liu, Siddharth Banka, Andrea Kranz, Martin Zenker, Dagmar Wieczorek, Nursel Elçioğlu, Paolo Prontera, Stanislas Lyonnet, Thomas Meitinger, Aengus Stewart, Dian Donnai, Tim M. Strom, Koray Boduroğlu, Gökhan Yigit, Yun Li, Nicholas Katsanis, Bernd Wollnik

    出版 2015
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    Artigo
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  6. 6
    Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants

    Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants 由 Kalliope Panoutsopoulou, Konstantinos Hatzikotoulas, Dionysia K. Xifara, Vincenza Colonna, Aliki‐Eleni Farmaki, Graham R. S. Ritchie, Lorraine Southam, Arthur Gilly, Ioanna Tachmazidou, Segun Fatumo, Angela Matchan, Nigel W. Rayner, Ιωάννα Ντάλλα, Massimo Mezzavilla, Yuan Chen, Chrysoula Kiagiadaki, Eleni Zengini, Vasiliki Mamakou, Antonis Athanasiadis, Μαργαρίτα Γιαννακοπούλου, Vassiliki-Eirini Kariakli, Rebecca N. Nsubuga, Alex Karabarinde, Manjinder S. Sandhu, Gil McVean, Chris Tyler‐Smith, Emmanouil Tsafantakis, Maria Karaleftheri, Yali Xue, George Dedoussis, Eleftheria Zeggini

    出版 2014
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    Artigo
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  7. 7
    Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

    Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps 由 Valentina Iotchkova, Jie Huang, John Morris, Deepti Jain, Caterina Barbieri, Klaudia Walter, Josine L. Min, Lu Chen, William J. Astle, Massimiliano Cocca, Patrick Deelen, Heather Elding, Aliki‐Eleni Farmaki, Christopher S. Franklin, Mattias Frånberg, Tom R. Gaunt, Albert Hofman, Tao Jiang, Marcus E. Kleber, Geneviève Lachance, Jian’an Luan, Giovanni Malerba, Angela Matchan, Daniel G. Mead, Yasin Memari, Ιωάννα Ντάλλα, Kalliope Panoutsopoulou, Raha Pazoki, John R. B. Perry, Fernando Rivadeneira, Maria Sabater‐Lleal, Bengt Sennblad, So–Youn Shin, Lorraine Southam, Michela Traglia, Freerk van Dijk, Jin‐Moo Lee, Gianluigi Zaza, Weihua Zhang, Najaf Amin, Adam S. Butterworth, John C. Chambers, George Dedoussis, Abbas Dehghan, Oscar H. Franco, Lude Franke, Mattia Frontini, Giovanni Gambaro, Paolo Gasparini, Anders Hamsten, Aaron Issacs, Jaspal S. Kooner, Charles Kooperberg, Claudia Langenberg, Winfried März, Robert A. Scott, Morris A. Swertz, Daniela Toniolo, André G. Uitterlinden, Cornelia M. van Duijn, Hugh Watkins, Eleftheria Zeggini, Mathew T Maurano, Nicholas J. Timpson, Alexander P. Reiner, Paul L. Auer, Nicole Soranzo

    出版 2016
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  8. 8
    100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care — Preliminary Report

    100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care — Preliminary Report 由 Damian Smedley, Katherine R. Smith, A. Martı́n, Ellen A Thomas, Ellen M. McDonagh, Valentina Cipriani, Jamie M. Ellingford, Gavin Arno, Arianna Tucci, Jana Vandrovcová, G. C. Chan, Hywel Williams, Thiloka Ratnaike, Wei Wei, Kathleen Stirrups, Kristina Ibáñez, Loukas Moutsianas, Matthias Wielscher, Anna C. Need, Michael R. Barnes, Letizia Vestito, James Buchanan, Sarah Wordsworth, Sofie Ashford, Karola Rehmström, Emily Li, Gavin Fuller, Philip Twiss, Olivera Spasić-Bošković, Sally Halsall, R. Andres Floto, Kenneth Poole, Annette Wagner, Sarju Mehta, Mark Gurnell, Nigel Burrows, Roger James, Christopher J. Penkett, Eleanor Dewhurst, Stefan Gräf, Rutendo Mapeta, Mary Kasanicki, Andrea Haworth, Helen Savage, Melanie Babcock, Martin G. Reese, Mark Bale, Emma L. Baple, C. R. Boustred, Helen Brittain, Anna de Burca, Marta Bleda, A. Devereau, Dina Halai, Eik Haraldsdottir, Zerin Hyder, Dalia Kasperavičiūtė, Christine Patch, Dimitris Polychronopoulos, Angela Matchan, Răzvan Sultana, Mina Ryten, Ana Lisa Taylor Tavares, Carolyn Tregidgo, Clare Turnbull, M. J. Welland, S. M. Wood, Catherine Snow, Eleanor Williams, S. E. A. Leigh, Rebecca E. Foulger, Louise C. Daugherty, Olivia Niblock, Ivone Leong, Caroline F. Wright, Jim Davies, Charles Crichton, James Welch, Kerrie Woods, Lara Abulhoul, Paul Aurora, Detlef Böckenhauer, Alexander Broomfield, Maureen Cleary, Tanya Lam, Mehul Dattani, Emma Footitt, Vijeya Ganesan, Stephanie Grünewald, Sandrine Compeyrot‐Lacassagne, Francesco Muntoni, Clarissa Pilkington, Rosaline C. M. Quinlivan, Nikhil Thapar, Colin Wallis, Lucy R. Wedderburn, Austen Worth, Teofila Bueser, Cecilia Compton, Charu Deshpande

    出版 2021
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  9. 9
    Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

    Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension 由 Praveen Surendran, Fotios Drenos, Robin Young, Helen R. Warren, James P. Cook, Alisa K. Manning, Niels Grarup, Xueling Sim, Daniel R. Barnes, Kate Witkowska, James R Staley, Vinicius Tragante, Taru Tukiainen, Hanieh Yaghootkar, Nicholas G. D. Masca, Daniel F. Freitag, Teresa Ferreira, Olga Giannakopoulou, Andrew Tinker, Magdaléna Harakaľová, Evelin Mihailov, Chunyu Liu, Aldi T. Kraja, Yan V. Sun, Asif Rasheed, Maria Samuel, Wei Zhao, Lori L. Bonnycastle, Anne Jackson, Narisu Narisu, Amy J. Swift, Lorraine Southam, Jonathan Marten, Jeroen R. Huyghe, Alena Stančáková, Cristiano Fava, Therese Ohlsson, Angela Matchan, Kathleen Stirrups, Jette Bork‐Jensen, Anette P. Gjesing, Jukka Kontto, Markus Perola, Susan Shaw-Hawkins, Aki S. Havulinna, He Zhang, Louise A. Donnelly, Christopher J. Groves, Nigel W. Rayner, Matt J. Neville, Neil R. Robertson, Andrianos M. Yiorkas, Karl‐Heinz Herzig, Eero Kajantie, Weihua Zhang, Sara M. Willems, Lars Lannfelt, Giovanni Malerba, Nicole Soranzo, Elisabetta Trabetti, Niek Verweij, Εvangelos Εvangelou, Alireza Moayyeri, Anne‐Claire Vergnaud, Christopher P. Nelson, Alaitz Poveda, Tibor V. Varga, Muriel Caslake, Anton J. M. de Craen, Stella Trompet, Jian’an Luan, Robert A. Scott, Sarah E. Harris, David C. Liewald, Riccardo E. Marioni, Cristina Menni, Aliki-Eleni Farmaki, Göran Hallmans, Frida Renström, Jennifer E. Huffman, Maija Hassinen, Stephen Burgess, Ramachandran S. Vasan, Janine F. Felix, Maria Uria-Nickelsen, Anders Mälarstig, Dermot F. Reilly, Maarten Hoek, Thomas Vogt, Honghuang Lin, Wolfgang Lieb, Matthew Traylor, Hugh S. Markus, Heather M. Highland, Anne E. Justice, Eirini Marouli, Jaana Lindström, Matti Uusitupa, Pirjo Komulainen, Timo A. Lakka

    出版 2016
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    Revisão
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  10. 10
    Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits

    Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits 由 Ioanna Tachmazidou, Dániel Süveges, Josine L. Min, Graham R. S. Ritchie, Julia Steinberg, Klaudia Walter, Valentina Iotchkova, Jeremy Schwartzentruber, Jie Huang, Yasin Memari, Shane McCarthy, Andrew Crawford, Cristina Bombieri, Massimiliano Cocca, Aliki-Eleni Farmaki, Tom R. Gaunt, Jari Lahti, Marjolein N. Kooijman, Benjamin Lehne, Giovanni Malerba, Satu Männistö, Angela Matchan, Carolina Medina‐Gómez, Sarah Metrustry, Abhishek Nag, Ιωάννα Ντάλλα, Lavinia Paternoster, Nigel W. Rayner, Cinzia Sala, William R. Scott, Hashem A. Shihab, Lorraine Southam, Beaté St Pourcain, Michela Traglia, Katerina Trajanoska, Gianluigi Zaza, Weihua Zhang, María Soler Artigas, Narinder Bansal, Marianne Benn, Zhongsheng Chen, Petr Danecek, Wei‐Yu Lin, Adam E. Locke, Jian’an Luan, Alisa K. Manning, Antonella Mulas, Carlo Sidore, Anne Tybjærg‐Hansen, Anette Varbo, Magdalena Żołędziewska, Chris Finan, Konstantinos Hatzikotoulas, Audrey E. Hendricks, John P. Kemp, Alireza Moayyeri, Kalliope Panoutsopoulou, Michał Szpak, Scott G. Wilson, Michael Boehnke, Francesco Cucca, Emanuele Di Angelantonio, Claudia Langenberg, Cecilia M. Lindgren, Mark I. McCarthy, Andrew P. Morris, Børge G. Nordestgaard, Robert A. Scott, Martin D. Tobin, Nicholas J. Wareham, Paul R. Burton, John C. Chambers, George Davey Smith, George Dedoussis, Janine F. Felix, Oscar H. Franco, Giovanni Gambaro, Paolo Gasparini, Christopher J. Hammond, Albert Hofman, Vincent W. V. Jaddoe, Marcus E. Kleber, Jaspal S. Kooner, Markus Perola, Caroline L. Relton, Susan M. Ring, Fernando Rivadeneira, Veikko Salomaa, Timothy D. Spector, Oliver Stegle, Daniela Toniolo, André G. Uitterlinden, Inês Barroso, Celia M.T. Greenwood, John R. B. Perry, Brian R. Walker, Adam S. Butterworth, Yali Xue, Richard Durbin, Kerrin S. Small

    出版 2017
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