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

William G. Newman の年別被引用数1967 年: 被引用 1 件1969 年: 被引用 1 件1970 年: 被引用 1 件1973 年: 被引用 1 件1974 年: 被引用 2 件1975 年: 被引用 4 件1977 年: 被引用 2 件1979 年: 被引用 1 件1980 年: 被引用 1 件1982 年: 被引用 1 件1983 年: 被引用 1 件1985 年: 被引用 1 件1991 年: 被引用 1 件1994 年: 被引用 1 件1995 年: 被引用 1 件1996 年: 被引用 1 件1997 年: 被引用 4 件1998 年: 被引用 3 件1999 年: 被引用 4 件2000 年: 被引用 2 件2001 年: 被引用 3 件2002 年: 被引用 3 件2003 年: 被引用 6 件2004 年: 被引用 3 件2005 年: 被引用 6 件2006 年: 被引用 5 件2007 年: 被引用 9 件2008 年: 被引用 19 件2009 年: 被引用 26 件2010 年: 被引用 26 件2011 年: 被引用 143 件2012 年: 被引用 206 件2013 年: 被引用 287 件2014 年: 被引用 333 件2015 年: 被引用 346 件2016 年: 被引用 366 件2017 年: 被引用 368 件2018 年: 被引用 356 件2019 年: 被引用 975 件2020 年: 被引用 938 件2021 年: 被引用 940 件2022 年: 被引用 836 件2023 年: 被引用 658 件2024 年: 被引用 1,012 件2025 年: 被引用 373 件2026 年: 被引用 11 件1968 年は被引用が無いため表示していません1971〜1972 年は被引用が無いため表示していません1976 年は被引用が無いため表示していません1978 年は被引用が無いため表示していません1981 年は被引用が無いため表示していません1984 年は被引用が無いため表示していません1986〜1990 年は被引用が無いため表示していません1992〜1993 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 2,960 件、この内訳の 21.5%イギリス: 引用元論文 1,481 件、この内訳の 10.8%中国: 引用元論文 979 件、この内訳の 7.1%ドイツ: 引用元論文 813 件、この内訳の 5.9%カナダ: 引用元論文 606 件、この内訳の 4.4%イタリア: 引用元論文 572 件、この内訳の 4.1%フランス: 引用元論文 548 件、この内訳の 4%オランダ: 引用元論文 547 件、この内訳の 4%オーストラリア: 引用元論文 489 件、この内訳の 3.5%スウェーデン: 引用元論文 341 件、この内訳の 2.5%日本: 引用元論文 330 件、この内訳の 2.4%スペイン: 引用元論文 312 件、この内訳の 2.3%
0%21.5%その他 27.5%

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

全論文

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  1. Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  2. Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Carl A. Anderson, Jeffrey C. Barrett - Nature Genetics 2017 被引用: 1,543

  4. Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  5. Recommendations for clinical interpretation of variants found in non-coding regions of the genome

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , - Genome Medicine 2022 被引用: 256

  6. Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  7. Germline selection shapes human mitochondrial DNA diversity

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  8. Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  9. Population screening requires robust evidence—genomics is no exception

    著者: , , , , , , , , , , , - The Lancet 2023 被引用: 55

  10. Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , William G. Newman - The American Journal of Human Genetics 2013 被引用: 245

  11. 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: , , , , , , , , , , , , - PLoS Medicine 2022 被引用: 71

  12. Rapid Point-of-Care Genotyping to Avoid Aminoglycoside-Induced Ototoxicity in Neonatal Intensive Care

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Poly Kirkilli, Suzanne Parsons, Ruth Gottstein, Ngozi Edi-Osagie, Christine Ashworth, Maxine Brandall, Kath Eaton - JAMA Pediatrics 2022 被引用: 86

  13. Heterozygous Mutations in TREX1 Cause Familial Chilblain Lupus and Dominant Aicardi-Goutières Syndrome

    著者: , , , , , , , , , , , , , , , - The American Journal of Human Genetics 2007 被引用: 408

  14. Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kathryn E. Hentges, G.M. Lathrop, Mauro Santibanez‐Koref, Bernard Keavney - Circulation Research 2019 被引用: 198

  15. Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases

    著者: , , , , , , , , , , , , , , , , , , , , , , , , - Immunity 2015 被引用: 283

  16. Epidermal Growth Factor Receptor in Pancreatic Cancer

    著者: , , - Cancers 2011 被引用: 165

  17. Bi-allelic variants in the mitochondrial RNase P subunit PRORP cause mitochondrial tRNA processing defects and pleiotropic multisystem presentations

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  18. Breast cancer risks associated with missense variants in breast cancer susceptibility genes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  19. Germline Mutations in SUFU Cause Gorlin Syndrome–Associated Childhood Medulloblastoma and Redefine the Risk Associated With PTCH1 Mutations

    著者: , , , , , , , , , , , , , , - Journal of Clinical Oncology 2014 被引用: 296

  20. Identification of Patients With Variants in TPMT and Dose Reduction Reduces Hematologic Events During Thiopurine Treatment of Inflammatory Bowel Disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2017 被引用: 179

  22. Pharmacogenomic Testing to Support Prescribing in Primary Care: a Structured Review of Implementation Models

    著者: , , , - Pharmacogenomics 2021 被引用: 36

  23. Human SNP Links Differential Outcomes in Inflammatory and Infectious Disease to a FOXO3-Regulated Pathway

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  24. ORAI1 Mutations with Distinct Channel Gating Defects in Tubular Aggregate Myopathy

    著者: , , , , , , , , , , , , , , , , , , , , , , - Human Mutation 2017 被引用: 100