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Bing Ge

McGill University

39H指数
167论文数
8.7K被引数
收录论文 60
发表时间
Functional assessment of a convergent gene network underlying allergic diseases and IgE过敏性疾病和IgE的汇聚基因网络功能评估
err2026-02-20
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errOAAI
errPradeep Eranti; Raphaël Vernet; Christophe Linhard; Bing Ge; Laura Beaumier; Anne-Marie Madore; Sébastien Chanoine; Bénédicte L. Tremblay; Xiaojian Shao; Isabelle Pin; Mark Lathrop; Elin Grundberg; Valérie Siroux; Tomi Pastinen; Catherine Laprise; Emmanuelle Bouzigon; Florence Demenais
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CpG methylation changes associated with hyperglycemia in type 1 diabetes occur at angiogenic glomerular and retinal gene loci与1型糖尿病高血糖相关的CpG甲基化变化发生在血管生成性肾小球和视网膜基因位点。
err2025-05-08
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errShao, Xiaojian; Le Fur, Sophie; Cheung, Warren; Belot, Marie-Pierre; Perge, Kevin; Bouhours-Nouet, Natacha; Bensignor, Candace; Levaillant, Lucie; Ge, Bing; Kwan, Tony; Lathrop, Mark; Pastinen, Tomi; Bougneres, Pierre
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Complex trait associations in rare diseases and impacts on Mendelian variant interpretation
err2024-09-18
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errSmail, Craig; Ge, Bing; Keever-Keigher, Marissa R.; Schwendinger-Schreck, Carl; Cheung, Warren A.; Johnston, Jeffrey J.; Barrett, Cassandra; Feldman, Keith; Cohen, Ana S. A.; Farrow, Emily G.; Thiffault, Isabelle; Grundberg, Elin; Pastinen, Tomi
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Short-term lifestyle education on obesity reduction in adolescents
err2024-03-25
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errNing, Feng; Sun, Xiaohui; Ge, Bing; Li, Shunping; Hou, Binghui; Wang, Yumei; Zhang, Dong
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Association of seafood consumption with cardiovascular disease among adults in Qingdao, China
err2024-03-01
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PREAI
errYan, Hongxuan; Sun, Xiaohui; Wu, Yili; Ge, Bing; Wang, Weijing; Liu, Xiao; Pan, Chi; Ning, Feng; Pang, Zengchang; Zhang, Dongfeng
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Subtraction Improves the Accuracy of Coronary CT Angiography in Patients with Severe Calcifications in Identifying Moderate and Severe Stenosis: A Multicenter Study
err2023-12-01
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PREAI
errQiao, Jinhan; Li, Sheng; Yang, Hongzhi; Chen, Xiaolong; Zhu, Tingting; Li, Qian; Wan, Weijia; Xu, Yinghao; Ge, Bing; Zhao, Yun; Tang, Yuanyuan; Li, Fang; He, Yi; Xia, Liming
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Comparison of Three Algorithms for Predicting Infarct Volume in Patients with Acute Ischemic Stroke by CT Perfusion Software: Bayesian, CSVD, and OSVD
err2023-05-20
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errYao, Yunzhuo; Gu, Sirun; Liu, Jiayang; Li, Jing; Wu, Jiajing; Luo, Tianyou; Li, Yongmei; Ge, Bing; Wang, Jingjie
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Asthma-associated polymorphisms in 17q12-21 locus modulate methylation and gene expression of GSDMA in naive CD4+ T cells
err2020-03-01
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PREAI
errMadore, Anne-Marie; Pain, Lucile; Boucher-Lafleur, Anne-Marie; Morin, Andreanne; Meloche, Jolyane; Simon, Marie-Michelle; Ge, Bing; Kwan, Tony; Cheung, Warren A.; Pastinen, Tomi; Laprise, Catherine
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Allelic imbalance in KMT2A-rearranged infant acute lymphoblastic leukemia
err2019-07-01
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PREAI
errYoo, Byunggil; Farooqi, Midhat S.; Kostadinov, Rumen; Cheung, Warren; Farrow, Emily; Kelley, Shannon; Miller, Neil; Ge, Bing; Gibson, Margaret; Brown, Patrick; Guest, Erin M.; Pastinen, Tomi
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Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome (vol 18, 50, 2017)等位基因甲基化的功能变异强调了强大的遗传贡献,并揭示了人类表观基因组中新的表观遗传改变 (卷18,50,2017)
err2019-05-07
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errCheung, Warren A.; Shao, Xiaojian; Morin, Andreanne; Siroux, Valerie; Kwan, Tony; Ge, Bing; Aissi, Dylan; Chen, Lu; Vasquez, Louella; Allum, Fiona; Guenard, Frederic; Bouzigon, Emmanuelle; Simon, Marie-Michelle; Boulier, Elodie; Redensek, Adriana; Watt, Stephen; Datta, Avik; Clarke, Laura; Flicek, Paul; Mead, Daniel; Paul, Dirk S.; Beck, Stephan; Bourque, Guillaume; Lathrop, Mark; Tchernof, Andre; Vohl, Marie-Claude; Demenais, Florence; Pin, Isabelle; Downes, Kate; Stunnenberg, Hendrick G.; Soranzo, Nicole; Pastinen, Tomi; Grundberg, Elin
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Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements
err2019-03-14
err18
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errAllum, Fiona; Hedman, Asa K.; Shaol, Xiaojian; Cheung, Warren A.; Vijay, Jinchu; Guenard, Frederic; Kwan, Tony; Simon, Marie-Michelle; Ge, Bing; Moura, Cristiano; Boulier, Elodie; Ronnblom, Lars; Bernatsky, Sasha; Lathropl, Mark; McCarthy, Mark, I; Deloukas, Panos; Tchernof, Andre; Pastinen, Tomi; Vohl, Marie-Claude; Grundberg, Elin
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Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes
errBONE
IF3.6
err2018-09-01
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errGregson, Celia L.; Newell, Felicity; Leo, Paul J.; Clark, Graeme R.; Paternoster, Lavinia; Marshall, Mhairi; Forgetta, Vincenzo; Morris, John A.; Ge, Bing; Bao, Xiao; Bassett, J. H. Duncan; Williams, Graham R.; Youlten, Scott E.; Croucher, Peter I.; Smith, George Davey; Evans, David M.; Kemp, John P.; Brown, Matthew A.; Tobias, Jon H.; Duncan, Emma L.
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Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome
err2017-03-10
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errOAAI
errCheung, Warren A.; Shao, Xiaojian; Morin, Andreanne; Siroux, Valerie; Kwan, Tony; Ge, Bing; Aissi, Dylan; Chen, Lu; Vasquez, Louella; Allum, Fiona; Guenard, Frederic; Bouzigon, Emmanuelle; Simon, Marie-Michelle; Boulier, Elodie; Redensek, Adriana; Watt, Stephen; Datta, Avik; Clarke, Laura; Flicek, Paul; Mead, Daniel; Paul, Dirk S.; Beck, Stephan; Bourque, Guillaume; Lathrop, Mark; Tchernof, Andre; Vohl, Marie-Claude; Demenais, Florence; Pin, Isabelle; Downes, Kate; Stunnenberg, Hendrick G.; Soranzo, Nicole; Pastinen, Tomi; Grundberg, Elin
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