Որոնման արդյունքները - David Sexton
- Ցուցադրվում են 1 - 13 արդյունքները 13
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1
Novel rare variants in congenital cardiac arrhythmia genes are frequent in drug-induced torsades de pointes Andrea H. Ramirez, Christian M. Shaffer, Jessica Delaney, David Sexton, Shawn Levy, Mark J. Rieder, D A Nickerson, Alfred L. George, D M Roden
Հրապարակվել է 2012Artigo -
2
Acute Multiple Organ Failure in Adult Mice Deleted for the Developmental Regulator Wt1 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
Հրապարակվել է 2011Artigo -
3
Enzymatic Removal of Ribonucleotides from DNA Is Essential for Mammalian Genome Integrity and Development 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
Հրապարակվել է 2012Artigo -
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A Major Predisposition Locus for Severe Obesity, at 4p15-p14 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
Հրապարակվել է 2002Artigo -
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Rare genetic variants impact muscle strength 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
Հրապարակվել է 2023Artigo -
6
Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor 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
Հրապարակվել է 2009Artigo -
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Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice 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
Հրապարակվել է 2011Artigo -
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The expanding genetic overlap between multiple sclerosis and type I diabetes 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
Հրապարակվել է 2008Artigo -
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Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes 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
Հրապարակվել է 2022Artigo -
10
Refining genetic associations in multiple sclerosis 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
Հրապարակվել է 2008Carta -
11
Lithium in patients with amyotrophic lateral sclerosis (LiCALS): a phase 3 multicentre, randomised, double-blind, placebo-controlled trial 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
Հրապարակվել է 2013Artigo -
12
Meta-analysis of pharmacogenetic interactions in amyotrophic lateral sclerosis clinical trials 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
Հրապարակվել է 2017Revisão -
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Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank 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
Հրապարակվել է 2021Revisão
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Gene
Genetics
Medicine
Internal medicine
Genotype
Single-nucleotide polymorphism
Endocrinology
Exome sequencing
Genome-wide association study
Mutation
Phenotype
Disease
Exome
Genetic association
Immunology
Missense mutation
Amyotrophic lateral sclerosis
Biobank
Cell biology
Clinical trial
Ion
Ionic bonding
Lithium (medication)
Lithium carbonate
Multiple sclerosis
Randomized controlled trial
Alternative medicine
Anemia
Anophthalmia