Torthaí cuardaigh - Quanli Wang
- 1 - 20 toradh as 35 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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1
Image segmentation and dynamic lineage analysis in single‐cell fluorescence microscopy de réir Quanli Wang, Jarad Niemi, Cheemeng Tan, Lingchong You, Mike West
Foilsithe / Cruthaithe 2009Artigo -
2
Genic Intolerance to Functional Variation and the Interpretation of Personal Genomes de réir Slavé Petrovski, Quanli Wang, Erin L. Heinzen, Andrew S. Allen, David B. Goldstein
Foilsithe / Cruthaithe 2013Artigo -
3
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4
Correction: Genic Intolerance to Functional Variation and the Interpretation of Personal Genomes de réir Slavé Petrovski, Quanli Wang, Erin L. Heinzen, Andrew S. Allen, David B. Goldstein
Foilsithe / Cruthaithe 2013Artigo -
5
TLR4 plays a crucial role in MSC-induced inhibition of NK cell function de réir Ying Lu, Jin Liu, Yang Liu, Ya-Ru Qin, Qun Luo, Quanli Wang, Haifeng Duan
Foilsithe / Cruthaithe 2015Artigo -
6
High-Dimensional Sparse Factor Modeling: Applications in Gene Expression Genomics de réir Carlos M. Carvalho, Jeffrey T. Chang, Joseph E. Lucas, Joseph R. Nevins, Quanli Wang, Mike West
Foilsithe / Cruthaithe 2008Artigo -
7
The Intolerance of Regulatory Sequence to Genetic Variation Predicts Gene Dosage Sensitivity de réir Slavé Petrovski, Ayal B. Gussow, Quanli Wang, Matthew Halvorsen, Yujun Han, William H. Weir, Andrew S. Allen, David B. Goldstein
Foilsithe / Cruthaithe 2015Artigo -
8
Orion: Detecting regions of the human non-coding genome that are intolerant to variation using population genetics de réir Ayal B. Gussow, Brett Copeland, Ryan S. Dhindsa, Quanli Wang, Slavé Petrovski, William H. Majoros, Andrew S. Allen, David B. Goldstein
Foilsithe / Cruthaithe 2017Artigo -
9
Optimizing genomic medicine in epilepsy through a gene-customized approach to missense variant interpretation de réir Joshua L. Traynelis, Michael Silk, Quanli Wang, Samuel F. Berkovic, Liping Liu, David B. Ascher, David J. Balding, Slavé Petrovski
Foilsithe / Cruthaithe 2017Artigo -
10
Cancer-driving mutations are enriched in genic regions intolerant to germline variation de réir 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
Foilsithe / Cruthaithe 2022Artigo -
11
Maternal iron intake during pregnancy and birth outcomes: a cross-sectional study in Northwest China de réir 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
Foilsithe / Cruthaithe 2017Artigo -
12
Inhibition of microRNA 128 promotes excitability of cultured cortical neuronal networks de réir 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
Foilsithe / Cruthaithe 2016Artigo -
13
Dietary intakes and dietary patterns among pregnant women in Northwest China de réir 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
Foilsithe / Cruthaithe 2016Artigo -
14
A Genomic Strategy to Elucidate Modules of Oncogenic Pathway Signaling Networks de réir 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
Foilsithe / Cruthaithe 2009Artigo -
15
Assessing the Role of Rare Genetic Variation in Patients With Heart Failure de réir 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
Foilsithe / Cruthaithe 2020Artigo -
16
A pathway-based classification of human breast cancer de réir Michael L. Gatza, Joseph E. Lucas, William T. Barry, Jong Wook Kim, Quanli Wang, Matthew D. Crawford, Michael Datto, Michael J. Kelley, Bernard Mathey-Prévôt, Anil Potti, Joseph R. Nevins
Foilsithe / Cruthaithe 2010Artigo -
17
Annotating pathogenic non-coding variants in genic regions de réir 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
Foilsithe / Cruthaithe 2017Artigo -
18
Diverse ancestral representation improves genetic intolerance metrics de réir 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
Foilsithe / Cruthaithe 2024Pré-impressão -
19
Effects of protein-coding variants on blood metabolite measurements and clinical biomarkers in the UK Biobank de réir 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
Foilsithe / Cruthaithe 2023Artigo -
20
Disease prediction with multi-omics and biomarkers empowers case–control genetic discoveries in the UK Biobank de réir 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
Foilsithe / Cruthaithe 2024Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
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