Ohcanbohtosat - Quanli Wang
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TLR4 plays a crucial role in MSC-induced inhibition of NK cell function Dahkki Ying Lu, Jin Liu, Yang Liu, Ya-Ru Qin, Qun Luo, Quanli Wang, Haifeng Duan
Almmustuhtton 2015Artigo -
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Orion: Detecting regions of the human non-coding genome that are intolerant to variation using population genetics Dahkki Ayal B. Gussow, Brett Copeland, Ryan S. Dhindsa, Quanli Wang, Slavé Petrovski, William H. Majoros, Andrew S. Allen, David B. Goldstein
Almmustuhtton 2017Artigo -
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Optimizing genomic medicine in epilepsy through a gene-customized approach to missense variant interpretation Dahkki Joshua L. Traynelis, Michael Silk, Quanli Wang, Samuel F. Berkovic, Liping Liu, David B. Ascher, David J. Balding, Slavé Petrovski
Almmustuhtton 2017Artigo -
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Cancer-driving mutations are enriched in genic regions intolerant to germline variation Dahkki Dimitrios Vitsios, Ryan S. Dhindsa, Dorota Matelska, Jonathan Mitchell, Xuequing Zou, Joshua Armenia, Fengyuan Hu, Quanli Wang, Ben S. Sidders, Andrew R. Harper, Slavé Petrovski
Almmustuhtton 2022Artigo -
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Maternal iron intake during pregnancy and birth outcomes: a cross-sectional study in Northwest China Dahkki Jiaomei Yang, Yue Cheng, Leilei Pei, Yufen Jiang, Fangliang Lei, Lingxia Zeng, Quanli Wang, Qiang Li, Yijun Kang, Yuan Li Shen, Shaonong Dang, Hong Yan
Almmustuhtton 2017Artigo -
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Inhibition of microRNA 128 promotes excitability of cultured cortical neuronal networks Dahkki K. Melodi McSweeney, Ayal B. Gussow, Shelton S. Bradrick, Sarah A. Dugger, Sahar Gelfman, Quanli Wang, Slavé Petrovski, Wayne N. Frankel, Michael J. Boland, David B. Goldstein
Almmustuhtton 2016Artigo -
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Dietary intakes and dietary patterns among pregnant women in Northwest China Dahkki Jiaomei Yang, Shaonong Dang, Yue Cheng, Huizhen Qiu, Baibing Mi, Yufen Jiang, Pengfei Qu, Lingxia Zeng, Quanli Wang, Qiang Li, Yijun Kang, Yuan Li Shen, Hong Yan
Almmustuhtton 2016Artigo -
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A Genomic Strategy to Elucidate Modules of Oncogenic Pathway Signaling Networks Dahkki Jeffrey T. Chang, Carlos M. Carvalho, Seiichi Mori, Andrea H. Bild, Michael L. Gatza, Quanli Wang, Joseph E. Lucas, Anil Potti, Phillip G. Febbo, Mike West, Joseph R. Nevins
Almmustuhtton 2009Artigo -
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Assessing the Role of Rare Genetic Variation in Patients With Heart Failure Dahkki Gundula Povysil, Olympe Chazara, Keren Carss, Sri V. V. Deevi, Quanli Wang, Javier Armisen, Dirk S. Paul, Christopher B. Granger, John Kjekshus, Vimla S. Aggarwal, Carolina Haefliger, David B. Goldstein
Almmustuhtton 2020Artigo -
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Annotating pathogenic non-coding variants in genic regions Dahkki Sahar Gelfman, Quanli Wang, K. Melodi McSweeney, Zhong Ren, Francesca La Carpia, Matthew Halvorsen, Kelly Schoch, Fanni Ratzon, Erin L. Heinzen, Michael J. Boland, Slavé Petrovski, David B. Goldstein
Almmustuhtton 2017Artigo -
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Diverse ancestral representation improves genetic intolerance metrics Dahkki Alexander Han, Chloe F. Sands, Dorota Matelska, Jessica C. Butts, Vida Ravanmehr, Fengyuan Hu, Esmeralda Villavicencio Gonzalez, Nicholas Katsanis, Carlos D. Bustamante, Quanli Wang, Slavé Petrovski, Dimitrios Vitsios, Ryan S. Dhindsa
Almmustuhtton 2024Pré-impressão -
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Effects of protein-coding variants on blood metabolite measurements and clinical biomarkers in the UK Biobank Dahkki Abhishek Nag, Ryan S. Dhindsa, Lawrence Middleton, Xiao Jiang, Dimitrios Vitsios, Eleanor M. Wigmore, Erik L. Allman, Anna Reznichenko, Keren Carss, Katherine R. Smith, Quanli Wang, Benjamin Challis, Dirk S. Paul, Andrew R. Harper, Slavé Petrovski
Almmustuhtton 2023Artigo -
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Disease prediction with multi-omics and biomarkers empowers case–control genetic discoveries in the UK Biobank Dahkki Manik Garg, Marcin Karpiński, Dorota Matelska, Lawrence Middleton, Oliver S. Burren, Fengyuan Hu, Eleanor Wheeler, Katherine R. Smith, Margarete A. Fabre, Jonathan Mitchell, Amanda O’Neill, Euan A. Ashley, Andrew R. Harper, Quanli Wang, Ryan S. Dhindsa, Slavé Petrovski, Dimitrios Vitsios
Almmustuhtton 2024Artigo
Ohcanreaiddut:
Laktáseaddji fáttát
Biology
Genetics
Gene
Medicine
Computational biology
Exome sequencing
Mutation
Exome
Internal medicine
Genome
Bioinformatics
Disease
Phenotype
Genetic variation
Genotype
Single-nucleotide polymorphism
Biobank
Genetic association
Genome-wide association study
Pathology
Computer science
Evolutionary biology
Population
Cancer
Environmental health
Astrophysics
Coding region
Endocrinology
Genomics
Germline