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William G. Newman

University of Manchester

78H指数
630论文数
3.6W被引数
收录论文 201
发表时间
Identification of substrates of the human mitochondrial ClpXP protease and its implications for Perrault syndrome鉴定人线粒体ClpXP蛋白酶的底物及其对佩罗综合征的启示
err2026-09-24
err0
errOAAI
errMazen E. Aljghami; Trevor M. Morey; Mark F. Mabanglo; Jonathan J. Meyrick; Huw B. Thomas; Jiacheng Yu; Arveen Tahmasebi; King Lam Lai; Benjamin Bernard Armando Raymond; Matthias Trost; Robert W. Taylor; Raymond T. O’Keefe; William G. Newman; Uwe Richter; Walid A. Houry
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Connective tissue and genetics in the pathogenesis of rectal prolapse: A scoping review结缔组织和遗传在直肠脱垂发病机制中的作用:一项范围综述
err2026-09-22
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errOAAI
errMatthew Davenport; Alexander O'Connor; William G. Newman; Andrew P. Morris; Abhiram Sharma; Gemma Faulkner; Dipesh H. Vasant; John McLaughlin; Edward Kiff; Karen Telford
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MT-RNR1 genotype testing for preventing aminoglycoside-mediated ototoxicity: A guideline developed by the UK Centre of Excellence in Regulatory Science and Innovation in Pharmacogenomics (CERSI-PGx)MT-RNR1基因分型检测以预防氨基糖苷类药物介导的耳毒性:由英国药代遗传学监管科学与创新卓越中心(CERSI-PGx)制定指南
err2026-09-15
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errOAAI
errJohn H. McDermott; Sian Hilton; Cinzia Dello Russo; Nicola Booth; Simon Drysdale; Philip Howard; Stephen Hughes; Mallinath Chakraborty; Helen McDevitt; Charlotte Alston; Maya Desai; Mike Beadsworth; Adam Reynolds; Serim Min; Katherine Payne; Munir Pirmohamed; William G. Newman
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Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disorders对常染色体纯合拷贝数缺失的外显子进行系统分析提高了诊断效率并发现了超罕见隐性障碍
err2026-06-27
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PREAI
errAnkur Chaurasia; Anju Shukla; Shruti Pande; Greeshma Purushothama; Akhil Kanathay Ashokan; Purvi Majethia; Namanpreet Kaur; Priyanka Upadhyai; Neha Quadri; Gandham SriLakshmi Bhavani; Dhanya Lakshmi Narayanan; Shalini S. Nayak; Sheela Nampoothiri; Ataf H. Sabir; Alaa A. Mohammed; Sophie Shaw; Verity L. Hartill; Christopher M. Watson; Colin A. Johnson; Afrah Alshammari; Andrew E. Fry; James A. Poulter; William G. Newman; Paul R. Kasher; Siddharth Banka; Katta M. Girisha
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Cardiovascular prescriber attitudes to pharmacogenomics: a survey by the ESC working group on cardiovascular pharmacotherapy心血管处方者对药物基因组学的态度:欧洲心脏病学会心血管药物治疗工作组的一项调查
err2026-04-23
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errOAAI
errEmma F. Magavern; G.-Andrei Dan; Gianluigi Savarese; Claudio Borghi; Dobramir Dobrev; Juan Tamargo; Peter Ferdinandy; John H. McDermott; William G. Newman; Munir Pirmohamed; Mark J. Caulfield; Juan Carlos Kaski
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Expanding the genotypic spectrum of combined oxidative phosphorylation deficiency 54扩展线粒体复合体缺陷54型的基因型谱
err2026-03-03
err0
PREAI
errLai, King Lam; Smith, Thomas B.; Maroofian, Reza; Zaki, Maha S.; Ramadesikan, Swetha; Reynolds, Tamara; Koboldt, Daniel C.; Hunter, Jesse M.; Vidaurre, Jorge; Atanasova, Mihaela; Marsden, Brian D.; Yue, Wyatt W.; Houlden, Henry; Taylor, Robert W.; Newman, William G.; O'keefe, Raymond T.
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Threshold-Based Overlap of Breast Cancer High-Risk Classification Using Family History, Polygenic Risk Scores, and Traditional Risk Models in 180,398 Women基于家族史、多基因风险评分和传统风险模型的乳腺癌高风险分类阈值重叠:一项针对180,398名女性的研究
err2025-11-03
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errOAAI
errPeh Joo Ho; Christine Kim Yan Loo; Ryan Jak Yang Lim; Meng Huang Goh; Mustapha Abubakar; Thomas U. Ahearn; Irene L. Andrulis; Natalia N. Antonenkova; Kristan J. Aronson; Annelie Augustinsson; Sabine Behrens; Clara Bodelon; Natalia V. Bogdanova; Manjeet K. Bolla; Kristen D. Brantley; Hermann Brenner; Helen Byers; Nicola J. Camp; Jose E. Castelao; Melissa H. Cessna; Jenny Chang-Claude; Stephen J. Chanock; Georgia Chenevix-Trench; Ji-Yeob Choi; Sarah V. Colonna; Kamila Czene; Mary B. Daly; Francoise Derouane; Thilo Dörk; A. Heather Eliassen; Christoph Engel; Mikael Eriksson; D. Gareth Evans; Olivia Fletcher; Lin Fritschi; Manuela Gago-Dominguez; Jeanine M. Genkinger; Willemina R. R. Geurts-Giele; Gord Glendon; Per Hall; Ute Hamann; Cecilia Y. S. Ho; Weang-Kee Ho; Maartje J. Hooning; Reiner Hoppe; Anthony Howell; Keith Humphreys; Hidemi Ito; Motoki Iwasaki; Anna Jakubowska; Helena Jernström; Esther M. John; Nichola Johnson; Daehee Kang; Sung-Won Kim; Cari M. Kitahara; Yon-Dschun Ko; Peter Kraft; Ava Kwong; Diether Lambrechts; Susanna Larsson; Shuai Li; Annika Lindblom; Martha Linet; Jolanta Lissowska; Artitaya Lophatananon; Robert J. MacInnis; Arto Mannermaa; Siranoush Manoukian; Sara Margolin; Keitaro Matsuo; Kyriaki Michailidou; Roger L. Milne; Nur Aishah Mohd Taib; Kenneth R. Muir; Rachel A. Murphy; William G. Newman; Katie M. O’Brien; Nadia Obi; Olufunmilayo I. Olopade; Mihalis I. Panayiotidis; Sue K. Park; Tjoung-Won Park-Simon; Alpa V. Patel; Paolo Peterlongo; Dijana Plaseska-Karanfilska; Katri Pylkäs; Muhammad U. Rashid; Gad Rennert; Juan Rodriguez; Emmanouil Saloustros; Dale P. Sandler; Elinor J. Sawyer; Christopher G. Scott; Shamim Shahi; Xiao-Ou Shu; Katerina Shulman; Jacques Simard; Melissa C. Southey; Jennifer Stone; Jack A. Taylor; Soo-Hwang Teo; Lauren R. Teras; Mary Beth Terry; Diana Torres; Celine M. Vachon; Maxime Van Houdt; Jelle Verhoeven; Clarice R. Weinberg; Alicja Wolk; Taiki Yamaji; Cheng Har Yip; Wei Zheng; Mikael Hartman; Jingmei Li; on behalf of the ABCTB Investigators; kConFab Investigators; MyBrCa Investigators; SGBCC Investigators
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Large-scale meta-analysis and precision functional assays identify FANCM regions in which PTVs confer different risks for ER-negative and triple-negative breast cancer大规模元分析和精确功能测定识别出FANCM区域,其中致病性体细胞突变(PTVs)对ER阴性和三阴性乳腺癌产生不同的风险。
err2025-10-30
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errOAAI
errAmandine Billaud; Gisella Figlioli; Clémence Mooser; Irene Casamassima; Violette Azzoni; Jahnavi Srivatsa; Mara Colombo; Laura Caleca; Thomas U. Ahearn; Irene L. Andrulis; Antonis C. Antoniou; Matthias W. Beckmann; Sabine Behrens; Marina Bermisheva; Natalia V. Bogdanova; Manjeet K. Bolla; Bernardo Bonanni; Thomas Brüning; Nicola J. Camp; Archie Campbell; Jose E. Castelao; Melissa H. Cessna; Jenny Chang-Claude; Kamila Czene; Joe Dennis; Peter Devilee; Thilo Dörk; Alison M. Dunning; Mikael Eriksson; D.Gareth Evans; Peter A. Fasching; Jonine D. Figueroa; Marike Gabrielson; Manuela Gago-Dominguez; Anna González-Neira; Pascal Guénel; Andreas Hadjisavvas; Eric Hahnen; Ute Hamann; Peter Hillemanns; Antoinette Hollestelle; Maartje J. Hooning; Reiner Hoppe; Anthony Howell; Anna Jakubowska; Vessela N. Kristensen; Jan Lubiński; Michael Lush; Siranoush Manoukian; Dimitrios Mavroudis; Roger L. Milne; Anna Marie Mulligan; William G. Newman; Nadia Obi; Mihalis I. Panayiotidis; Guillermo Pita; Muhammad U. Rashid; Valerie Rhenius; Emmanouil Saloustros; Elinor J. Sawyer; Rita K. Schmutzler; Mitul Shah; Melissa C. Southey; Amanda B. Spurdle; Ian Tomlinson; Thérèse Truong; Qin Wang; Camilla Wendt; Paul L. Auer; Nicholas J. Boddicker; Clara Bodelon; Elizabeth S. Burnside; Fei Chen; Fergus J. Couch; Susan M. Domchek; Heather A. Eliassen; Christopher Haiman; James M. Hodge; Chunling Hu; Hongyan Huang; Sara Lindstrom; Maria Elena Martinez; Katherine L. Nathanson; Susan L. Neuhausen; Katie M. O’Brien; Janet E. Olson; Julie R. Palmer; Alpa V. Patel; Kathryn J. Ruddy; Dale P. Sandler; Lauren R. Teras; Clarice R. Weinberg; Jeffrey N. Weitzel; Stacey J. Winham; Siddhartha Yadav; Song Yao; Gary Zirpoli; Marketa Janatova; Zdenek Kleibl; Petra Kleiblova; Jana Soukupova; Qihong Zhao; Lisa Devereux; Paul A. James; Ian G. Campbell; Tu Nguyen-Dumont; James G. Dowty; Nadine Andrieu; Fabienne Lesueur; Dominique Stoppa-Lyonnet; Miguel de la Hoya; Paolo Radice; Claus Storgaard Sørensen; Paolo Peterlongo
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How to implement pre-emptive pharmacogenetic testing in the acute hospital setting如何在急性医院环境中实施预防性药物遗传学检测
err2025-09-01
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PREAI
errMcDermott, John Henry; Shoaib, Ali; Keen, Jessica; Skitterall, Charlotte; Sharma, Videha; Newman, William Gerard
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Acute-onset axonal neuropathy following infection in children with biallelic RCC1 variants: a case series儿童中biallelic RCC1变异者在感染后出现的急性起病轴索神经病:一个病例系列
err2025-07-16
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errOAAI
errJ Robert Harkness; John H McDermott; Shea Marsden; Peter Jamieson; Kay A Metcalfe; Naz Khan; William L Macken; Robert D S Pitceathly; Christopher J Record; Reza Maroofian; Kleopas Kleopa; Kyproula Christodoulou; Ataf Sabir; Lily Islam; Saikat Santra; Enise Avci Durmusalioglu; Tahir Atik; Esra Isik; Ozgur Cogulu; Jill E Urquhart; Glenda M Beaman; Leigh A Demain; Adam Jackson; Alexander J M Blakes; Helen J Byers; Hayley Bennett; Wei-Hsiang Lin; Antony Adamson; Sanjai Patel; Wyatt W Yue; Robert W Taylor; Janine Reunert; Thorsten Marquardt; Rebecca Buchert; Tobias Haack; Heike Losch; Lukas Ryba; Petra Lassuthova; Radka Valkovičová; Jana Haberlová; Barbora Lauerová; Eva Trúsiková; Kiran Polavarapu; Ozge Aksel Kilicarslan; Hanns Lochmüller; Mina Zamani; Niloofar Chamanrou; Gholamreza Shariati; Saeid Sadeghian; Reza Azizimalamiri; Sateesh Maddirevula; Muhammad AlMuhaizea; Fowzan S Alkuraya; Rita Horvath; Serdal Gungor; Adnan Manzur; Pinki Munot; Rachael Matthews; Siddharth Banka; Mary M Reilly; Daimark Bennett; Raymond T O’Keefe; William G Newman
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Bi-allelic variants in MRPL49 cause variable clinical presentations, including sensorineural hearing loss, leukodystrophy, and ovarian insufficiency
err2025-04-01
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errOAAI
errThomas, Huw B.; Demain, Leigh A. M.; Cabrera-Orefice, Alfredo; Schrauwen, Isabelle; Shamseldin, Hanan E.; Rea, Alessandro; Bharadwaj, Thashi; Smith, Thomas B.; Olahova, Monika; Thompson, Kyle; He, Langping; Kaur, Namanpreet; Shukla, Anju; Abukhalid, Musaad; Ansar, Muhammad; Rehman, Sakina; Riazuddin, Saima; Abdulwahab, Firdous; Smith, Janine M.; Stark, Zornitza; Mancilar, Hanifenur; Tumer, Sait; Esen, Fatma N.; Uctepe, Eyyup; Topcu, Vehap; Yesilyurt, Ahmet; Afzal, Erum; Salari, Mehri; Carroll, Christopher; Zifarelli, Giovanni; Bauer, Peter; Kor, Deniz; Bulut, Fatma D.; Houlden, Henry; Maroofian, Reza; Carrera, Samantha; Yue, Wyatt W.; Munro, Kevin J.; Alkuraya, Fowzan S.; Jamieson, Peter; Ahmed, Zubair M.; Leal, Suzanne M.; Taylor, Robert W.; Wittig, Ilka; O'Keefe, Raymond T.; Newman, William G.
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Development and Validation of a Rapid Point-of-Care [italic]CYP2C19 [/italic]Genotyping Platform
err2025-03-01
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errOAAI
errBurke, Kerry A.; Sullivan, James O '; Godfrey, Nicola; Sharma, Videha; Hilton, Sian; Wright, Stuart J.; Greaves, Nicholas S.; Newman, William G.; Mcdermott, John H.
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