William G. Newman
1966–2025 年に発表
- 別表記
- William G Newman
- 130
- 論文数
- 23,548
- 被引用数
- 65
- h 指数
- 120
- i10 指数
被引用数
引用元
国・地域
機関
- Harvard University1.2%
- Broad Institute0.7%
- Inserm0.7%
- University of Manchester0.7%
- Massachusetts General Hospital0.7%
- University of Cambridge0.6%
- その他95.4%
分野
- Biochemistry, Genetics and Molecular Biology55.9%
- Medicine26.5%
- Immunology and Microbiology10.1%
- Neuroscience2.2%
- Pharmacology, Toxicology and Pharmaceutics1.8%
- Computer Science0.5%
- その他3%
トピック
- Inflammatory Bowel Disease6.9%
- Gut microbiota and health3.9%
- Genetic Associations and Epidemiology3.6%
- Genomics and Rare Diseases1.9%
- Immune Cell Function and Interaction1.9%
- IL-33, ST2, and ILC Pathways1.7%
- その他80.1%
共著者
- D. Gareth Evans22
- John McDermott19
- Glenda M. Beaman15
- Jill Urquhart15
- Jamie M. Ellingford13
- Sanjeev S. Bhaskar13
- Anthony Howell12
- Graeme C. Black12
- James O’Sullivan12
- Miriam J. Smith12
- Raymond T. O’Keefe10
- Adrian S. Woolf9
- Katherine Payne9
- Siddharth Banka9
- Simon G. Williams9
- Elaine F. Harkness8
- Elke M. van Veen8
- Helen Byers8
- Helen M. Stuart8
- Huw B. Thomas8
- Leigh Demain8
- Andrew J. Wallace7
- Filipa M. Lopes7
- James Lee7
全論文
- Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations
著者: Jimmy Z. Liu, Suzanne van Sommeren, Hailiang Huang, Siew C. Ng, Rudi Alberts, Atsushi Takahashi, Stephan Ripke, James Lee, Luke Jostins-Dean, Tejas Shah, Shifteh Abedian, Jae Hee Cheon, Judy H. Cho, Naser Ebrahim Daryani, Lude Franke, Yuta Fuyuno, Ailsa Hart, Ramesh C. Juyal, Garima Juyal, Won Ho Kim, Andrew P. Morris, Hossein Poustchi, William G Newman, Vandana Midha, Timothy R. Orchard, Homayon Vahedi, Ajit Sood, Joseph J.�Y. Sung, Reza Malekzadeh, Harm-Jan Westra, Keiko Yamazaki, Suk-Kyun Yang, Jeffrey C. Barrett, Andre Franke, Behrooz Z Alizadeh, Miles Parkes, B.K. Thelma, Mark Daly, Michiaki Kubo, Carl A. Anderson, Rinse K. Weersma - Nature Genetics 2015 被引用: 2,749
- Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease
著者: Luke Jostins, Stephan Ripke, Rinse K. Weersma, Richard H. Duerr, Dermot McGovern, Ken Hui, James Lee, L. Philip Schumm, Yashoda Sharma, Carl A. Anderson, Jonah Essers, Mitja Mitrovič, Kaida Ning, Isabelle Cleynen, Emilie Théâtre, Sarah L. Spain, Soumya Raychaudhuri, Philippe Goyette, Zhi Wei, Clara Abraham, Jean–Paul Achkar, Tariq Ahmad, Leila Amininejad, Ashwin N. Ananthakrishnan, Vibeke Andersen, Jane M. Andrews, Leonard Baidoo, Tobias Balschun, Peter A. Bampton, Alain Bitton, Gabrielle Boucher, Stephan Brand, Carsten Büning, Ariella Cohain, Sven Cichon, Mauro D’Amato, Dirk de Jong, Kathy L. Devaney, Marla C. Dubinsky, Cathryn Edwards, David Ellinghaus, Lynnette Ferguson, Denis Franchimont, Karin Fransén, Richard B. Gearry, Michel Georges, Christian Gieger, Jürgen Glas, Talin Haritunians, Ailsa Hart, Chris Hawkey, Matija Hedl, Xinli Hu, Tom H. Karlsen, Limas Kupčinskas, Subra Kugathasan, Anna Latiano, Debby Laukens, Ian C. Lawrance, Charlie W. Lees, Édouard Louis, Gillian Mahy, John Mansfield, Angharad R. Morgan, Craig Mowat, William G. Newman, Orazio Palmieri, Cyriel Y. Ponsioen, Uroš Potočnik, Natalie J. Prescott, Miguel Regueiro, Jerome I. Rotter, Richard K. Russell, Jeremy Sanderson, Miquel Sans, Jack Satsangi, Stefan Schreiber, Lisa A. Simms, Jurgita Šventoraitytė, Stephan R. Targan, Kent D. Taylor, Mark Tremelling, Hein W. Verspaget, Martine De Vos, Cisca Wijmenga, David C. Wilson, Juliane Winkelmann, Ramnik J. Xavier, Sebastian Zeißig, Bin Zhang, Hu Zhang, Hongyu Zhao, Mark S. Silverberg, Vito Annese, Håkon Håkonarson, Steven R. Brant, Graham Radford‐Smith, Christopher G. Mathew, John D. Rioux, Eric E. Schadt ほか 6 名 - Nature 2012 被引用: 4,917
- Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease
著者: 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 - Nature Genetics 2017 被引用: 1,543
- Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
著者: André Franke, Dermot McGovern, Jeffrey C. Barrett, Kai Wang, Graham Radford‐Smith, Tariq Ahmad, Charlie W. Lees, Tobias Balschun, James Lee, Rebecca Roberts, Carl A. Anderson, Joshua C Bis, Suzanne Bumpstead, David Ellinghaus, Eleonora M Festen, Michel Georges, Todd J. Green, Talin Haritunians, Luke Jostins, Anna Latiano, Christopher G. Mathew, Grant W. Montgomery, Natalie J. Prescott, Soumya Raychaudhuri, Jerome I. Rotter, L. Philip Schumm, Yashoda Sharma, Lisa A. Simms, Kent D. Taylor, David C. Whiteman, Cisca Wijmenga, Robert N. Baldassano, Murray L. Barclay, Theodore M. Bayless, Stephan Brand, Carsten Büning, Albert Cohen, J F. Colombel, Mario Cottone, Laura Stronati, Ted Denson, Martine De Vos, R. D’Incà, Marla C. Dubinsky, Cathryn Edwards, Tim Florin, Denis Franchimont, Richard B. Gearry, Jürgen Glas, A. Van Gossum, Stephen L. Guthery, Jonas Halfvarson, Hein W. Verspaget, Jean‐Pierre Hugot, Amir Karban, Debby Laukens, Ian C. Lawrance, Marc Lémann, Arie Levine, Cécile Libioulle, Édouard Louis, Craig Mowat, William G. Newman, Julián Panés, Anne Phillips, Deborah D. Proctor, Miguel Regueiro, Richard K. Russell, Paul Rutgeerts, Jeremy Sanderson, Miquel Sans, Frank Seibold, A. Hillary Steinhart, Pieter Stokkers, Leif Törkvist, Gerd A. Kullak‐Ublick, David C. Wilson, Thomas D. Walters, Stephan R. Targan, Steven R. Brant, John D. Rioux, Mauro D’Amato, Rinse K. Weersma, Subra Kugathasan, Anne M. Griffiths, John Mansfield, Séverine Vermeire, Richard H. Duerr, Mark S. Silverberg, Jack Satsangi, Stefan Schreiber, Judy H. Cho, Vito Annese, Håkon Håkonarson, Mark J. Daly, Miles Parkes - Nature Genetics 2010 被引用: 2,581
- Recommendations for clinical interpretation of variants found in non-coding regions of the genome
著者: Jamie M. Ellingford, Joo Wook Ahn, Richard D. Bagnall, Diana Baralle, Stephanie Barton, C. Ryan Campbell, Kate Downes, Sian Ellard, Celia Duff‐Farrier, David Fitzpatrick, John M. Greally, Jodie Ingles, Neesha Krishnan, Jenny Lord, Hilary C. Martin, William G. Newman, Anne O’Donnell‐Luria, Simon Ramsden, Heidi L. Rehm, Ebony Richardson, Moriel Singer‐Berk, Jenny C. Taylor, Maggie Williams, Jordan C. Wood, Caroline F. Wright, Steven M. Harrison, Nicola Whiffin - Genome Medicine 2022 被引用: 256
- Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
著者: Carl A. Anderson, Gabrielle Boucher, Charlie W. Lees, André Franke, Mauro D’Amato, Kent D. Taylor, James Lee, Philippe Goyette, Marcin Imieliński, Anna Latiano, Caroline Lagacé, Regan Scott, Leila Amininejad, Suzannah Bumpstead, Leonard Baidoo, Robert N. Baldassano, Murray L. Barclay, Theodore M. Bayless, Stephan Brand, Carsten Büning, Jean‐Frédéric Colombel, Lee A. Denson, Martine De Vos, Marla C. Dubinsky, Cathryn Edwards, David Ellinghaus, Rudolf S.N. Fehrmann, James Floyd, Timothy H. Florin, Denis Franchimont, Lude Franke, Michel Georges, Jürgen Glas, Nicole L. Glazer, Stephen L. Guthery, Talin Haritunians, Nicholas K. Hayward, Jean‐Pierre Hugot, Gilles Jobin, Debby Laukens, Ian C. Lawrance, Marc Lémann, Arie Levine, Cécile Libioulle, Édouard Louis, Dermot McGovern, Mónica Milla, Grant W. Montgomery, Katherine I. Morley, Craig Mowat, Aylwin Ng, William G. Newman, Roel A. Ophoff, Laura Papi, Orazio Palmieri, Laurent Peyrin‐Biroulet, Julián Panés, Anne Phillips, Natalie J. Prescott, Deborah D. Proctor, Rebecca Roberts, Richard K. Russell, Paul Rutgeerts, Jeremy Sanderson, Miquel Sans, L. Philip Schumm, Frank Seibold, Yashoda Sharma, Lisa A. Simms, Mark Seielstad, A. Hillary Steinhart, Stephan R. Targan, Leonard H. van den Berg, Morten Vatn, Hein W. Verspaget, Thomas D. Walters, Cisca Wijmenga, David C. Wilson, Harm-Jan Westra, Ramnik J. Xavier, Zhen Zhao, Cyriel Y. Ponsioen, Vibeke Andersen, Leif Törkvist, Maria Gazouli, Nicholas P. Anagnou, Tom H. Karlsen, Limas Kupčinskas, Jurgita Šventoraitytė, John Mansfield, Subra Kugathasan, Mark S. Silverberg, Jonas Halfvarson, Jerome I. Rotter, Christopher G. Mathew, Anne M. Griffiths, Richard B. Gearry, Tariq Ahmad, Steven R. Brant, Mathias Chamaillard ほか 13 名 - Nature Genetics 2011 被引用: 1,353
- Germline selection shapes human mitochondrial DNA diversity
著者: Wei Wei, Salih Tuna, Michael J. Keogh, Katherine R. Smith, Katherine R. Smith, Timothy J. Aitman, Phil L. Beales, David Bennett, Daniel P. Gale, Maria A. K. Bitner-Glindzicz, Graeme C. Black, Paul Brennan, Perry Elliott, Frances Flinter, R. Andrés Floto, Henry Houlden, Melita Irving, Ania Koziell, Eamonn R. Maher, Hugh S. Markus, Nicholas W. Morrell, William G. Newman, Irene Roberts, John A. Sayer, Kenneth G. C. Smith, Kenneth G. C. Smith, Jenny C. Taylor, Hugh Watkins, Andrew R. Webster, Andrew O.M. Wilkie, Catherine Williamson, NIHR BioResource–Rare Diseases, 100,000 Genomes Project–Rare Diseases Pilot, Sofie Ashford, Christopher J. Penkett, Kathleen Stirrups, Augusto Rendon, Willem H. Ouwehand, John R. Bradley, F. Lucy Raymond, Mark Caulfield, Ernest Turro, Patrick F. Chinnery, Aarnoud Huissoon, Abigail Crisp-Hihn, Adam Shaw, Adam J. Mead, Adam P. Levine, Adrian J. Thrasher, Agnieszka Bierżyńska, Ahamad Hassan, Ajith Kumar, Alba Sanchis‐Juan, Alex Richter, Allan Lawrie, Amy Frary, Andrea H. Németh, Andrea Olschewski, Andreas C. Themistocleous, Andrew C. Browning, Andrew Mumford, Andrew M. Schaefer, Andrew Marshall, Andrew O.M. Wilkie, Andrew Peacock, Andrew R. Harper, Andrew R. Webster, Andrew S.C. Rice, Angela Pyle, Ania Koziell, Anna M. Drazyk, Anne M. Kelly, Annette Wagner, Anthony Attwood, Anthony De Soyza, Anthony M. Vandersteen, Anthony T. Moore, Anton Vonk Noordegraaf, Anupama Rao, Archana Herwadkar, Arjan C. Houweling, Arjune Sen, Augusto Rendon, Austen Worth, Barbara Girerd, Bella Madan, Brian T. Wilson, Carmen Bugarin Diz, Carmen Treacy, Carole Brewer, Carolyn Campbell, Carolyn M. Millar, Catherine Roughley, Catherine Titterton, Catherine Williamson, Cecilia Compton, Cesare Danesino, Chantal Thys, Charaka Hadinnapola, Charu Deshpande ほか 305 名 - Science 2019 被引用: 251
- Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders
著者: Víctor Faùndes, William G. Newman, Laura Bernardini, Natalie Canham, Jill Clayton‐Smith, Bruno Dallapiccola, Sally Davies, Michelle Demos, Amy Goldman, Harinder Gill, Rachel Horton, Bronwyn Kerr, Dhavendra Kumar, Anna Lehman, Shane McKee, Jenny Morton, Michael Parker, Julia Rankin, Lisa Robertson, I. Karen Temple, Shelin Adam, Christèle du Souich, Alison M. Elliott, Anna Lehman, Jill Mwenifumbo, Tanya N. Nelson, Clara van Karnebeek, Jan M. Friedman, Jeremy F. McRae, Stephen Clayton, Tomas Fitzgerald, Joanna Kaplanis, Elena Prigmore, Diana Rajan, Alejandro Sifrim, Stuart Aitken, Nadia Akawi, Mohsan Alvi, Kirsty Ambridge, Daniel M. Barrett, Tanya Bayzetinova, Philip Jones, Wendy D. Jones, Daniel King, Netravathi Krishnappa, Laura E. Mason, Tarjinder Singh, Adrian R. Tivey, Munaza Ahmed, Uruj Anjum, Hayley Archer, Ruth Armstrong, Jana Awada, Meena Balasubramanian, Siddharth Banka, Diana Baralle, Angela Barnicoat, Paul Batstone, David Baty, Chris Bennett, Jonathan Berg, Birgitta Bernhard, A. Paul Bevan, Maria Bitner‐Glindzicz, Edward Blair, Moira Blyth, David Bohanna, Louise Bourdon, David Bourn, Lisa Bradley, Angela F. Brady, Simon Brent, Carole Brewer, Kate Brunstrom, David J. Bunyan, John Burn, Natalie Canham, Bruce Castle, Kate Chandler, Elena Chatzimichali, Deirdre Cilliers, Angus Clarke, Susan Clasper, Jill Clayton‐Smith, Virginia Clowes, Andrea Coates, Trevor Cole, Irina Colgiu, Amanda Collins, Morag N. Collinson, Fiona Connell, Nicola Cooper, Helen Cox, Lara Cresswell, Gareth Cross, Yanick J. Crow, Mariella D’Alessandro, Tabib Dabir, Rosemarie Davidson, Sally Davies ほか 231 名 - The American Journal of Human Genetics 2017 被引用: 278
- Population screening requires robust evidence—genomics is no exception
著者: Clare Turnbull, Helen V. Firth, Andrew O.M. Wilkie, William G. Newman, F. Lucy Raymond, Ian Tomlinson, Robin Lachmann, Caroline F. Wright, Sarah Wordsworth, Angela George, Margaret McCartney, Anneke Lucassen - The Lancet 2023 被引用: 55
- Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease
著者: Emma M. Jenkinson, Atteeq U. Rehman, Tom Walsh, Jill Clayton‐Smith, Kwanghyuk Lee, Robert J. Morell, Meghan C. Drummond, Shaheen N. Khan, Muhammad Asif Naeem, Bushra Rauf, Neil Billington, Julie M. Schultz, Jill Urquhart, Ming K. Lee, Andrew Berry, Neil A. Hanley, Sarju Mehta, Deirdre Cilliers, Peter Clayton, Helen Kingston, Miriam J. Smith, Thomas T. Warner, Graeme C. Black, Dorothy Trump, J.R. Davis, Wasim Ahmad, Suzanne M. Leal, Sheikh Riazuddin, Mary‐Claire King, Thomas B. Friedman, William G. Newman - The American Journal of Human Genetics 2013 被引用: 245
- Integrating polygenic risk scores in the prediction of type 2 diabetes risk and subtypes in British Pakistanis and Bangladeshis: A population-based cohort study
著者: Sam Hodgson, Qin Qin Huang, Neneh Sallah, Chris Griffiths, William G. Newman, Richard C. Trembath, John Wright, R Thomas Lumbers, Karoline Kuchenbaecker, David A. van Heel, Rohini Mathur, Hilary C. Martin, Sarah Finer - PLoS Medicine 2022 被引用: 71
- Rapid Point-of-Care Genotyping to Avoid Aminoglycoside-Induced Ototoxicity in Neonatal Intensive Care
著者: John McDermott, Ajit Mahaveer, Rachel James, Nicola Booth, M. Turner, Karen Harvey, Gino Miele, Glenda M. Beaman, Duncan Stoddard, Karen Tricker, Rachel Corry, Julia Garlick, Shaun Ainsworth, Thomas Beevers, Iain Bruce, Richard Body, Fiona Ulph, Rhona MacLeod, Peter Roberts, Paul Wilson, William G. Newman, PALOH Study Team, Imelda Mayor, C. Darrell Jennings, Karen Dockery, Jenna Hill, Joanne Windrow, Patrick O. McGowan, Amy Ingham, Sarah Rushton, Poly Kirkilli, Suzanne Parsons, Ruth Gottstein, Ngozi Edi-Osagie, Christine Ashworth, Maxine Brandall, Kath Eaton - JAMA Pediatrics 2022 被引用: 86
- Heterozygous Mutations in TREX1 Cause Familial Chilblain Lupus and Dominant Aicardi-Goutières Syndrome
著者: Gillian Rice, William G. Newman, John Dean, Teresa Patrick, Rekha Parmar, Kim Flintoff, Peter Robins, Scott Harvey, Thomas Hollis, Ann M. O’Hara, Ariane L. Herrick, A P Bowden, Fred W. Perrino, Tomas Lindahl, Deborah E. Barnes, Yanick J. Crow - The American Journal of Human Genetics 2007 被引用: 408
- Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot
著者: Donna J. Page, Matthieu J. Miossec, Simon G. Williams, Richard M. Monaghan, Elisavet Fotiou, Heather J. Cordell, Louise Sutcliffe, Ana Töpf, Mathieu Bourgey, Guillaume Bourque, Robert Eveleigh, Sally L. Dunwoodie, David S. Winlaw, Shoumo Bhattacharya, Jeroen Breckpot, Koenraad Devriendt, Marc Gewillig, J. David Brook, Kerry Setchfield, Frances Bu’Lock, John O’Sullivan, Graham Stuart, Connie R. Bezzina, Barbara J.M. Mulder, Alex V. Postma, James R. Bentham, Martín Baron, Sanjeev S. Bhaskar, Graeme C. Black, William G. Newman, Kathryn E. Hentges, G.M. Lathrop, Mauro Santibanez‐Koref, Bernard Keavney - Circulation Research 2019 被引用: 198
- Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases
著者: Bergithe E Oftedal, Alexander Hellesen, Martina M. Erichsen, Eirik Bratland, Ayelet Vardi, Jaakko Perheentupa, E. Helen Kemp, Torunn Fiskerstrand, Marte K. Viken, Anthony P. Weetman, Sarel J. Fleishman, Siddharth Banka, William G. Newman, William A. Sewell, Leila Sozaeva, Tetyana Zayats, Kristoffer Haugarvoll, Elizaveta Orlova, Jan Haavik, Stefan Johansson, Per M. Knappskog, Kristian Løvås, Anette S. B. Wolff, Jakub Abramson, Eystein S. Husebye - Immunity 2015 被引用: 283
- Epidermal Growth Factor Receptor in Pancreatic Cancer
著者: Melissa Oliveira‐Cunha, William G. Newman, Ajith K. Siriwardena - Cancers 2011 被引用: 165
- Bi-allelic variants in the mitochondrial RNase P subunit PRORP cause mitochondrial tRNA processing defects and pleiotropic multisystem presentations
著者: Irit Hochberg, Leigh Demain, Julie Richer, Kyle Thompson, Jill Urquhart, Alessandro Rea, Waheeda Pagarkar, Agustí Rodríguez‐Palmero, Agatha Schlüter, Edgard Verdura, Aurora Pujol, Pilar Quijada‐Fraile, Albert Amberger, Andrea Deutschmann, Sandra Demetz, Meredith Gillespie, Inna A. Belyantseva, Hugh J. McMillan, Melanie Barzik, Glenda M. Beaman, Reeya Motha, Kah Ying Ng, James O’Sullivan, Simon G. Williams, Sanjeev S. Bhaskar, Isabella Rachel Lawrence, Emma M. Jenkinson, Jessica L. Zambonin, Zeev Blumenfeld, Sergey Yalonetsky, Stephanie Oerum, Walter Rossmanith, Wyatt W. Yue, Johannes Zschocke, Kevin J. Munro, Brendan J. Battersby, Thomas B. Friedman, Robert W. Taylor, Raymond T. O’Keefe, William G. Newman - The American Journal of Human Genetics 2021 被引用: 57
- Breast cancer risks associated with missense variants in breast cancer susceptibility genes
著者: Leila Dorling, Sara Carvalho, Jamie Allen, Michael T. Parsons, Cristina Fortuño, Anna González‐Neira, Stephan Heijl, Muriel A. Adank, Thomas U. Ahearn, Irene L. Andrulis, Päivi Auvinen, Heiko Becher, Matthias W. Beckmann, Sabine Behrens, Marina Bermisheva, Natalia Bogdanova, Stig E. Bojesen, Manjeet K. Bolla, Michael Bremer, Ignacio Briceño, Nicola J. Camp, Archie Campbell, Jose E. Castelao, Jenny Chang-Claude, Stephen J. Chanock, Georgia Chenevix‐Trench, NBCS Collaborators, J. Margriet Collée, Kamila Czene, Joe Dennis, Thilo Dörk, Mikael Eriksson, D. Gareth Evans, Peter A. Fasching, Jonine D. Figueroa, Henrik L. Flyger, Marike Gabrielson, Manuela Gago-Domínguez, Montserrat García‐Closas, Graham G. Giles, Gord Glendon, Pascal Guénel, Melanie Gündert, Andreas Hadjisavvas, Eric Hahnen, Per Hall, Ute Hamann, Elaine F. Harkness, Mikael Hartman, Frans B.L. Hogervorst, Antoinette Hollestelle, Reiner Hoppe, Anthony Howell, kConFab Investigators, SGBCC Investigators, Anna Jakubowska, Audrey Jung, Elza Khusnutdinova, Sung-Won Kim, Yon‐Dschun Ko, Vessela N. Kristensen, Inge M. M. Lakeman, Jingmei Li, Annika Lindblom, Maria A. Loizidou, Artitaya Lophatananon, Jan Lubiński, Craig Luccarini, Michael J. Madsen, Arto Mannermaa, Mehdi Manoochehri, Sara Margolin, Dimitrios Mavroudis, Roger L. Milne, Nur Aishah Mohd Taib, Kenneth Muir, Heli Nevanlinna, William G. Newman, Jan C. Oosterwijk, Sue K. Park, Paolo Peterlongo, Paolo Radice, Emmanouil Saloustros, Elinor J. Sawyer, Rita K. Schmutzler, Mitul Shah, Xueling Sim, Melissa C. Southey, Harald Surowy, Maija Suvanto, Ian Tomlinson, Diana Torres, Thérèse Truong, Christi J. van Asperen, Regina Waltes, Qin Wang, Xiaohong R. Yang, Paul D.P. Pharoah, Marjanka K. Schmidt, Javier Benı́tez ほか 9 名 - Genome Medicine 2022 被引用: 55
- Germline Mutations in SUFU Cause Gorlin Syndrome–Associated Childhood Medulloblastoma and Redefine the Risk Associated With PTCH1 Mutations
著者: Miriam J. Smith, Christian Beetz, Simon G. Williams, Sanjeev S. Bhaskar, James O’Sullivan, Beverley Anderson, Sarah B. Daly, Jill Urquhart, Zaynab Bholah, Deemesh Oudit, Edmund Cheesman, Anna Kelsey, Martin G. McCabe, William G. Newman, D. Gareth Evans - Journal of Clinical Oncology 2014 被引用: 296
- Identification of Patients With Variants in TPMT and Dose Reduction Reduces Hematologic Events During Thiopurine Treatment of Inflammatory Bowel Disease
著者: Marieke J. H. Coenen, Dirk J. de Jong, Corine J. van Marrewijk, Luc J. J. Derijks, Sita H. Vermeulen, Dennis R. Wong, Olaf H. Klungel, André L. M. Verbeek, P. M. Hooymans, Wilbert H.M. Peters, René H. M. te Morsche, William G. Newman, Hans Scheffer, Henk‐Jan Guchelaar, Barbara Franke, A.A.M. Masclee, Marieke Pierik, Wout Mares, Wim Hameeteman, Peter J. Wahab, H Seinen, M. C. M. Rijk, Ivar M Harkema, Marc de Bièvre, Liekele E. Oostenbrug, C. M. Bakker, Michèl Aquarius, C. van Deursen, A.B. van Nunen, Jelle G. Goedhard, Michael Hamacher, Ingrid Gisbertz, B.J. Brenninkmeijer, Adriaan C.I.T.L. Tan, M. N. Aparicio-Pagés, Ellen M. Witteman, Sebastiaan A.C. van Tuyl, Ronald Breumelhof, Arnold Stronkhorst, L.P.L. Gilissen, E Schoon, J.W.M. Tjhie-Wensing, Andy Temmerman, J. J. Nicolaï, Jeroen D. van Bergeijk, D. J. Bac, Ben Witteman, Nofel Mahmmod, J J Uil, H. Akol, Rob J. Ouwendijk, I P van Munster, Marieke Pennings, A. M. P. De Schryver, T. J. M. van Ditzhuijsen, Robert C.H. Scheffer, Tessa E H Römkens, D.L. Schipper, Paul Bus, J.W.A. Straathof, M. L. Verhulst, Paul J. Boekema, Johannes T. Kamphuis, H.J. van Wijk, Jan Salemans, J Vermeijden, S. D. J. Van Der Werf, Robert J. Verburg, P. Spoelstra, J. Marleen L. de Vree, K Linde, H. J. A. Jebbink, Marnix Jansen, H. Holwerda, N. van Bentem, Jeroen J. Kolkman, M.G.V.M. Russel, G. H. Van Olffen, Marjo J. Kerbert-Dreteler, Marloes Bargeman, J.M. Götz, R Schröder, Jeroen M. Jansen, L.P. Bos, L.G.J.B. Engels, Mariëlle Romberg‐Camps, Eric T.P. Keulen, Aura A. J. van Esch, Joost P.H. Drenth, Mariëtte C.A. van Kouwen, Geert Wanten, T.J. Bisseling, Tessa E H Römkens, M.W.J. van Vugt, Paul C. van de Meeberg, Susan Hazel, W.N.H.M. Stuifbergen, M.J.A.L. Grubben, Ulrike de Wit, G.A.H. Dodemont ほか 15 名 - Gastroenterology 2015 被引用: 197
- Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7
著者: 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 - Nature Genetics 2017 被引用: 179
- Pharmacogenomic Testing to Support Prescribing in Primary Care: a Structured Review of Implementation Models
著者: Judith Hayward, John McDermott, Nadeem Qureshi, William G. Newman - Pharmacogenomics 2021 被引用: 36
- Human SNP Links Differential Outcomes in Inflammatory and Infectious Disease to a FOXO3-Regulated Pathway
著者: James Lee, Marion Espéli, Carl A. Anderson, Michelle A. Linterman, Joanna Pocock, Naomi Williams, Rebecca L Roberts, Sébastien Viatte, Bo Fu, Norbert Peshu, Tran Tinh Hien, Nguyen Hoan Phu, Emma Wesley, Cathryn Edwards, Tariq Ahmad, John Mansfield, Richard B. Gearry, Sarah J. Dunstan, Thomas N. Williams, Anne Barton, Carola G. Vinuesa, Anne Phillips, Craig Mowat, Hazel E. Drummond, Nick Kennedy, Charlie W. Lees, Jack Satsangi, Kirstin M. Taylor, Natalie J. Prescott, Christopher G. Mathew, Peter T. Simpson, Alison Simmons, Mohammed Imran Khan, William G. Newman, C J Hawkey, Ailsa Hart, David C. Wilson, Paul Henderson, Jeffrey C. Barrett, Miles Parkes, Paul Lyons, Kenneth G. C. Smith - Cell 2013 被引用: 230
- ORAI1 Mutations with Distinct Channel Gating Defects in Tubular Aggregate Myopathy
著者: Johann Böhm, Monica Bulla, Jill Urquhart, Edoardo Malfatti, Simon G. Williams, James O’Sullivan, Anastazja Szlauer‐Stefańska, Catherine Koch, Giovanni Baranello, Marina Mora, Michela Ripolone, Raffaella Violano, Maurizio Moggio, Helen Kingston, Timothy Dawson, Christian DeGoede, John Nixon, Anne Boland, Jean‐François Deleuze, Norma B. Romero, William G. Newman, Nicolas Demaurex, Jocelyn Laporte - Human Mutation 2017 被引用: 100
