Kết quả tìm kiếm - Daniele Merico
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How to visually interpret biological data using networks Bằng Daniele Merico, David Gfeller, Gary D. Bader
Được phát hành 2009Artigo -
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Enrichment Map – a Cytoscape app to visualize and explore OMICs pathway enrichment results Bằng Ruth Isserlin, Daniele Merico, Véronique Voisin, Gary D. Bader
Được phát hành 2014Pré-impressão -
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WordCloud: a Cytoscape plugin to create a visual semantic summary of networks Bằng Layla Oesper, Daniele Merico, Ruth Isserlin, Gary D. Bader
Được phát hành 2011Artigo -
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The Histone-Like NF-Y Is a Bifunctional Transcription Factor Bằng Michele Ceribelli, Diletta Dolfini, Daniele Merico, Raffaella Gatta, M Viganò, Giulio Pavesi, Roberto Mantovani
Được phát hành 2008Artigo -
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Pathway enrichment analysis and visualization of omics data using g:Profiler, GSEA, Cytoscape and EnrichmentMap Bằng Jüri Reimand, Ruth Isserlin, Véronique Voisin, Mike Kucera, Christian Tannus-Lopes, Asha Rostamianfar, Lina Wadi, Mona Meyer, J. D. Wong, Changjiang Xu, Daniele Merico, Gary D. Bader
Được phát hành 2019Artigo -
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Rare Copy Number Variations in Adults with Tetralogy of Fallot Implicate Novel Risk Gene Pathways Bằng Candice K. Silversides, Anath C. Lionel, Gregory Costain, Daniele Merico, Ohsuke Migita, Ben Liu, Tracy J. Yuen, Jessica Rickaby, Bhooma Thiruvahindrapuram, Christian R. Marshall, Stephen W. Scherer, Anne S. Bassett
Được phát hành 2012Artigo -
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A microcosting and cost–consequence analysis of clinical genomic testing strategies in autism spectrum disorder Bằng Kate Tsiplova, Richard M. Zur, Christian R. Marshall, Dimitri J. Stavropoulos, Sérgio L. Pereira, Daniele Merico, Edwin J. Young, Wilson W. L. Sung, Stephen W. Scherer, Wendy J. Ungar
Được phát hành 2017Artigo -
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Differential altered stability and transcriptional activity of ΔNp63 mutants in distinct ectodermal dysplasias Bằng Gareth J. Browne, Rita Cipollone, Anna Maria Lena, Valeria Serra, Huiqing Zhou, Hans van Bokhoven, Volker Dötsch, Daniele Merico, Roberto Mantovani, Alessandro Terrinoni, Richard A. Knight, Eleonora Candi, Gerry Melino
Được phát hành 2011Artigo -
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Combined immunodeficiency and atopy caused by a dominant negative mutation in caspase activation and recruitment domain family member 11 (CARD11) Bằng Harjit Dadi, Tyler A. Jones, Daniele Merico, Nigel Sharfe, Adi Ovadia, Yael Dinur Schejter, Brenda Reid, Mark Sun, Linda Vong, Adelle Atkinson, Sasson Lavi, Joel L. Pomerantz, Chaim M. Roifman
Được phát hành 2017Artigo -
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A Discovery Resource of Rare Copy Number Variations in Individuals with Autism Spectrum Disorder Bằng Aparna Prasad, Daniele Merico, Bhooma Thiruvahindrapuram, John Wei, Anath C. Lionel, Daisuke Sato, Jessica Rickaby, Chao Lu, Peter Szatmari, Wendy Roberts, Bridget A. Fernandez, Christian R. Marshall, Eli Hatchwell, Peggy S. Eis, Stephen W. Scherer
Được phát hành 2012Artigo -
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Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays Bằng Gregory Costain, A. C. Lionel, Daniele Merico, Patricia H. Forsythe, Kay Russell, Chelsea Lowther, Tracy J. Yuen, Janice Husted, Dimitrios J. Stavropoulos, Marsha Speevak, Eva W. C. Chow, C. R. Marshall, Stephen W. Scherer, A. S. Bassett
Được phát hành 2013Artigo -
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Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome Bằng Daniele Merico, Mehdi Zarrei, Gregory Costain, Lucas Ogura, Babak Alipanahi, Matthew J. Gazzellone, Nancy J. Butcher, Bhooma Thiruvahindrapuram, Thomas Nalpathamkalam, Eva W.C. Chow, Danielle M. Andrade, Brendan J. Frey, Christian R. Marshall, Stephen W. Scherer, Anne S. Bassett
Được phát hành 2015Artigo -
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The human splicing code reveals new insights into the genetic determinants of disease Bằng Hui Xiong, Babak Alipanahi, Leo J. Lee, Hannes Bretschneider, Daniele Merico, Ryan K. C. Yuen, Yimin Hua, Serge Gueroussov, Hamed S. Najafabadi, Timothy Hughes, Quaid Morris, Yoseph Barash, Adrian R. Krainer, Nebojša Jojić, Stephen W. Scherer, Benjamin J. Blencowe, Brendan J. Frey
Được phát hành 2014Artigo -
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A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence Data Bằng Brett Trost, Susan Walker, Zhuozhi Wang, Bhooma Thiruvahindrapuram, Jeffrey R. MacDonald, Wilson W. L. Sung, Sérgio L. Pereira, J. Andrew Whitney, Ada J. S. Chan, Giovanna Pellecchia, Miriam S. Reuter, Si Lok, Ryan K. C. Yuen, Christian R. Marshall, Daniele Merico, Stephen W. Scherer
Được phát hành 2018Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Biology
Gene
Genetics
Genome
Medicine
Copy-number variation
Psychiatry
Computational biology
Phenotype
Gene expression
Genotype
Single-nucleotide polymorphism
Autism
Autism spectrum disorder
Bioinformatics
Mutation
Schizophrenia (object-oriented programming)
Psychology
Genome-wide association study
Population
Computer science
Environmental health
Internal medicine
Candidate gene
Exome sequencing
Whole genome sequencing
RNA
Cancer research
Cell biology
DNA sequencing