Resultados da busca - David Sexton

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  1. 1
    Novel rare variants in congenital cardiac arrhythmia genes are frequent in drug-induced torsades de pointes

    Novel rare variants in congenital cardiac arrhythmia genes are frequent in drug-induced torsades de pointes por Andrea H. Ramirez, Christian M. Shaffer, Jessica Delaney, David Sexton, Shawn Levy, Mark J. Rieder, D A Nickerson, Alfred L. George, D M Roden

    Publicado em 2012
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  2. 2
    Acute Multiple Organ Failure in Adult Mice Deleted for the Developmental Regulator Wt1

    Acute Multiple Organ Failure in Adult Mice Deleted for the Developmental Regulator Wt1 por You-Ying Chau, David G. Brownstein, Heidi K. Mjoseng, Wen‐Chin Lee, Natalija Buza-Vidas, Claus Nerlov, Sten Eirik W. Jacobsen, Paul Perry, Rachel L. Berry, Anna Thornburn, David Sexton, Nik Morton, Peter Hohenstein, Elisabeth Freyer, Kay Samuel, Rob van’t Hof, Nicholas D. Hastie

    Publicado em 2011
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  3. 3
    Enzymatic Removal of Ribonucleotides from DNA Is Essential for Mammalian Genome Integrity and Development

    Enzymatic Removal of Ribonucleotides from DNA Is Essential for Mammalian Genome Integrity and Development por Martin A.M. Reijns, Björn Rabe, Rachel E. Rigby, Pleasantine Mill, Katy R. Astell, Laura A. Lettice, Shelagh Boyle, Andrea Leitch, Margaret Keighren, Fiona Kilanowski, Paul S. Devenney, David Sexton, Graeme R. Grimes, Ian Holt, Robert E. Hill, Martin S. Taylor, Kirstie A. Lawson, Julia R. Dorin, Andrew P. Jackson

    Publicado em 2012
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  4. 4
    A Major Predisposition Locus for Severe Obesity, at 4p15-p14

    A Major Predisposition Locus for Severe Obesity, at 4p15-p14 por Steven Stone, Victor Abkevich, Steven C. Hunt, Alexander Gutin, Deanna L. Russell, Chris Neff, Robyn Riley, Georges C. Frech, Charles H. Hensel, Srikanth Jammulapati, Jennifer Potter, David Sexton, Thanh V. Tran, Drew Gibbs, Diana Iliev, Richard E. Gress, Brian T. Bloomquist, John M. Amatruda, M.M. Peter Rae, D. Adams, H. Mark Skolnick, Donna Shattuck

    Publicado em 2002
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  5. 5
    Rare genetic variants impact muscle strength

    Rare genetic variants impact muscle strength por Yunfeng Huang, Dóra Bodnár, Chia‐Yen Chen, Gabriela Sánchez-Andrade, Mark Sanderson, Christopher D. Whelan, Paola G. Bronson, David Sexton, Sally John, Eric Marshall, Mehool Patel, Saranya Duraisamy, T. Swan, Denis Baird, Susan Eaton, Jake Gagnon, Feng Gao, Cynthia S. Gubbels, Varant Kupelian, Kejie Li, Dawei Liu, Stephanie Loomis, Helen McLaughlin, Adele A. Mitchell, Benjamin B. Sun, Jun Shi, Katherine G. Meilleur, Matthew E. Hurles, Sebastian S. Gerety, Ellen Tsai, Heiko Runz

    Publicado em 2023
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  6. 6
    Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor

    Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor por Maria Ban, An Goris, Åslaug Rudjord Lorentzen, Amie Baker, Tania Mihalova, Gillian Ingram, David R. Booth, Robert Heard, Graeme J. Stewart, Elke Bogaert, Bénédicte Dubois, Hanne F. Harbo, Elisabeth Gulowsen Celius, Anne Spurkland, Richard C. Strange, Clive Hawkins, Neil P. Robertson, Frank Dudbridge, James Wason, Philip L. De Jager, David A. Hafler, John D. Rioux, Adrian J. Ivinson, Jacob L. McCauley, Margaret A. Pericak‐Vance, Jorge R. Oksenberg, Stephen L. Hauser, David Sexton, Jonathan L. Haines, Stephen Sawcer

    Publicado em 2009
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  7. 7
    Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice

    Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice por Joe Rainger, Ellen van Beusekom, Jacqueline Ramsay, Lisa McKie, Lihadh Al‐Gazali, R Pallotta, Anita Saponari, Peter Branney, Malcolm E Fisher, Harris Morrison, Louise S. Bicknell, Philippe Gautier, Paul Perry, Kishan Sokhi, David Sexton, Tanya Bardakjian, Adele Schneider, Nursel Elcioğlu, Ferda Özkınay, Rainer Koenig, André Mégarbané, C. Nur Semerci, Ayesha Khan, Saemah Nuzhat Zafar, Raoul C. M. Hennekam, Sérgio B. Sousa, Lina Ramos, Livia Garavelli, Andrea Superti Furga, Anita Wischmeijer, Ian J. Jackson, Gabriele Gillessen‐Kaesbach, Han G. Brunner, Dagmar Wieczorek, Hans van Bokhoven, David Fitzpatrick

    Publicado em 2011
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  8. 8
    The expanding genetic overlap between multiple sclerosis and type I diabetes

    The expanding genetic overlap between multiple sclerosis and type I diabetes por David R. Booth, Robert Heard, Graeme J. Stewart, An Goris, Rita Dobosi, Bénédicte Dubois, Åslaug Rudjord Lorentzen, Elisabeth Gulowsen Celius, Hanne F. Harbo, Anne Spurkland, Tomas Olsson, Ingrid Kockum, Jenny Link, Jan Hillert, Maria Ban, Amie Baker, Stephen Sawcer, Alastair Compston, Tania Mihalova, Richard C. Strange, Clive Hawkins, Gillian Ingram, Neil P. Robertson, Philip L. De Jager, David A. Hafler, Lisa F. Barcellos, Adrian J. Ivinson, Margaret A. Pericak‐Vance, Jorge R. Oksenberg, Stephen L. Hauser, Jacob L. McCauley, David Sexton, Jonathan L. Haines

    Publicado em 2008
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  9. 9
    Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes

    Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes por Konrad J. Karczewski, Matthew Solomonson, Katherine R. Chao, Julia K. Goodrich, Grace Tiao, Wenhan Lu, Bridget Riley‐Gillis, Ellen Tsai, Hye In Kim, Xiuwen Zheng, Fedik Rahimov, Sahar Esmaeeli, A. Jason Grundstad, Mark Reppell, Jeff Waring, Howard Jacob, David Sexton, Paola G. Bronson, Xing Chen, Xinli Hu, Jacqueline I. Goldstein, Daniel King, Christopher Vittal, Timothy Poterba, Duncan S. Palmer, Claire Churchhouse, Daniel P. Howrigan, Wei Zhou, Nicholas A. Watts, Kevin Nguyen, Huy Nguyen, Cara Mason, Christopher Farnham, Charlotte Tolonen, Laura D. Gauthier, Namrata Gupta, Daniel G. MacArthur, Heidi L. Rehm, Cotton Seed, Anthony Philippakis, Mark J. Daly, J. Wade Davis, Heiko Runz, Melissa Miller, Benjamin M. Neale

    Publicado em 2022
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  10. 10
    Refining genetic associations in multiple sclerosis

    Refining genetic associations in multiple sclerosis por David R. Booth, Robert Heard, Graeme J. Stewart, An Goris, Rita Dobosi, Bénédicte Dubois, Annette Oturai, Helle Bach Søndergaard, Finn Sellebjerg, Janna Saarela, Virpi Leppä, Aarno Palotie, L. Peltonen, B. Fontaine, Isabelle Cournu‐Rebeix, Françoise Clerget‐Darpoux, Marie‐Claude Babron, Frank Weber, Herta Flor, Bertram Müller‐Myhsok, Peter Rieckmann, Antje Kroner, Colin A. Graham, Koen Vandenbroeck, Stanley Hawkins, Sandra D’Alfonso, Laura Bergamaschi, Paola Naldi, Franca Rosa Guerini, Marco Salvetti, Daniela Galimberti, Rogier Q. Hintzen, Cornelia M. van Duijn, Åslaug Rudjord Lorentzen, Elisabeth Gulowsen Celius, Hanne F. Harbo, Anne Spurkland, Francesco Cucca, Maria Giovanna Marrosu, Manuel Comabella, Xavier Montalbán, Pablo Villoslada, Tomas Olsson, Ingrid Kockum, Jan Hillert, Maria Ban, Andrew Walton, S. Sawcer, Alastair Compston, Clive Hawkins, Tania Mihalova, Neil P. Robertson, Gillian Ingram, Philip L. De Jager, David A. Hafler, John D. Rioux, Mark J. Daly, Lisa F. Barcellos, Adrian J. Ivinson, Margaret A. Pericak‐Vance, J. Hoksenberg, Stephen L. Hauser, Jacob L. McCauley, David Sexton, Jonathan L. Haines

    Publicado em 2008
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  11. 11
    Lithium in patients with amyotrophic lateral sclerosis (LiCALS): a phase 3 multicentre, randomised, double-blind, placebo-controlled trial

    Lithium in patients with amyotrophic lateral sclerosis (LiCALS): a phase 3 multicentre, randomised, double-blind, placebo-controlled trial por Karen Morrison, Somendra Kumar Dhariwal, R. W. Hornabrook, L. Savage, David J. Burn, Tien K. Khoo, Joanna Kelly, Caroline Murphy, Ammar Al‐Chalabi, Anne H. Dougherty, P. Nigel Leigh, Lokesh Wijesekera, M Thornhill, Cathy Ellis, Kathleen O’Hanlon, JN Panicker, L Pate, Priscilla Ray, Lynne Wyatt, Carolyn Young, Larry J. Copeland, J. Ealing, Hisham Hamdalla, Iracema Leroi, Caroline Murphy, Fiadhnait O’Keeffe, E Oughton, Lillian Partington, Phyllis G. Paterson, Dennis J. Rog, A Sathish, David Sexton, Jeff Smith, H Vanek, Steve Hatfield Dodds, Timothy L. Williams, I Nick Steen, Janine Clarke, Chinea Eziefula, Robert Howard, Richard W. Orrell, Katie Sidle, Robin N. Sylvester, Whitney Barrett, Charlotte Merritt, Kevin Talbot, Martin R. Turner, C Whatley, Courtney Williams, John E. Williams, C Cosby, C. Oliver Hanemann, Iklil Iman, Ceib Philips, L Timings, Skye Crawford, Channa Hewamadduma, Rachel Hibberd, Hannah Hollinger, Christopher McDermott, G. Р. Mils, Muhammad Rafiq, Pamela J. Shaw, Albert A. Taylor, E Waines, Tamara Walsh, Robert Addison–Jones, Julie Birt, M Hare, Tabassum Majid

    Publicado em 2013
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  12. 12
    Meta-analysis of pharmacogenetic interactions in amyotrophic lateral sclerosis clinical trials

    Meta-analysis of pharmacogenetic interactions in amyotrophic lateral sclerosis clinical trials por Ruben P.A. van Eijk, Ashley Jones, William Sproviero, Aleksey Shatunov, Pamela J. Shaw, P. Nigel Leigh, Carolyn Young, Christopher E. Shaw, Gabriele Mora, Jessica Mandrioli, Giuseppe Borghero, Paolo Volanti, Frank P. Diekstra, Wouter van Rheenen, Esther Verstraete, Marinus J.C. Eijkemans, Jan H. Veldink, Adriano Chió, Ammar Al‐Chalabi, Leonard H. van den Berg, Michael A. van Es, Christopher Allen, Carl Counsell, Amanda Farrin, Ammar Al‐Chalabi, Brian Dickie, Joanna Kelly, P. Nigel Leigh, Caroline Murphy, C. Payán, Gemma Reynolds, Pamela J. Shaw, I Nick Steen, M Thornhill, Justin S. Waters, John Zajicek, P. Nigel Leigh, Ammar Al‐Chalabi, Pamela J. Shaw, Carolyn Young, M Thornhill, I Nick Steen, Caroline Murphy, Karen Morrison, Somendra Kumar Dhariwal, R. W. Hornabrook, L. Savage, David J. Burn, Tien K. Khoo, Joanna Kelly, Caroline Murphy, Ammar Al‐Chalabi, Anne H. Dougherty, P. Nigel Leigh, Lokesh Wijesekera, M Thornhill, Cathy Ellis, Azman Ali Raymond, Kathleen O’Hanlon, JN Panicker, L Pate, Priscilla Ray, Lynne Wyatt, Carolyn Young, Larry J. Copeland, J. Ealing, Hisham Hamdalla, Iracema Leroi, Caroline Murphy, Fiadhnait O’Keeffe, E Oughton, Lillian Partington, Phyllis G. Paterson, Dennis J. Rog, A Sathish, David Sexton, Jeff Smith, H Vanek, Steve Hatfield Dodds, Timothy L. Williams, I Nick Steen, Janine Clarke, Chinea Eziefula, Robert Howard, Richard W. Orrell, Katie Sidle, Robin N. Sylvester, Whitney Barrett, Charlotte Merritt, Kevin Talbot, Martin R. Turner, C Whatley, Courtney Williams, John E. Williams, C Cosby, C. Oliver Hanemann, I Imam, Ceri Phillips, L Timings, Skye Crawford

    Publicado em 2017
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  13. 13
    Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank

    Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank por Joseph D. Szustakowski, Suganthi Balasubramanian, Erika Kvikstad, Shareef Khalid, Paola G. Bronson, Ariella Sasson, Emily H. M. Wong, Daren Liu, J. Wade Davis, Carolina Haefliger, A. Katrina Loomis, Rajesh Mikkilineni, Hyun Ji Noh, Samir Wadhawan, Xiaodong Bai, Alicia Hawes, Olga Krasheninina, Ricardo H. Ulloa, Alex E. Lopez, Erin N. Smith, Jeffrey F. Waring, Christopher D. Whelan, Ellen Tsai, John D. Overton, William Salerno, Howard J. Jacob, Sándor Szalma, Heiko Runz, Gregory Hinkle, Paul Nioi, Slavé Petrovski, Melissa Miller, Aris Baras, Lyndon J. Mitnaul, Jeffrey G. Reid, Oleg Moiseyenko, Carlos Garcia Rios, Saurabh Saha, Gonçalo R. Abecasis, Nilanjana Banerjee, Christina Beechert, Boris Boutkov, Michael Cantor, Giovanni Coppola, Aris N. Economides, Gisu Eom, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Lukas Habegger, Marcus B. Jones, Rouel Lanche, Michael Lattari, Michelle G. LeBlanc, Dadong Li, Luca A. Lotta, Kia Manoochehri, Adam J. Mansfield, Evan K. Maxwell, Jason Mighty, Mrunali Nafde, Sean O’Keeffe, Max Orelus, Maria Sotiropoulos Padilla, Razvan Panea, Tommy Polanco, Manasi Pradhan, Ayesha Rasool, Thomas D. Schleicher, Deepika Sharma, Alan R. Shuldiner, Jeffrey Staples, Cristopher V. Van Hout, Louis Widom, Sarah E. Wolf, Sally John, Chia‐Yen Chen, David Sexton, Varant Kupelian, Eric Marshall, T. Swan, Susan Eaton, Jimmy Z. Liu, Stephanie Loomis, Megan E. Jensen, Saranya Duraisamy, Jason Tetrault, David Merberg, Sunita Badola, Mark Reppell, Jason Grundstad, Xiuwen Zheng, Aimée M. Deaton, Margaret M. Parker, Lucas D. Ward, Alexander O. Flynn-Carroll, Caroline A. Austin, Ruth March, Menelas N. Pangalos, Adam Platt

    Publicado em 2021
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