WordCloud: a Cytoscape plugin to create a visual semantic summary of networks

por Oesper, Layla, Merico, Daniele, Isserlin, Ruth, Bader, Gary D
Publicado 2011

Enrichment Map – a Cytoscape app to visualize and explore OMICs pathway enrichment results

por Isserlin, Ruth, Merico, Daniele, Voisin, Veronique, Bader, Gary D.
Publicado 2014

Genetic Analysis Workshop 18 single-nucleotide variant prioritization based on protein impact, sequence conservation, and gene annotation

por Nalpathamkalam, Thomas, Derkach, Andriy, Paterson, Andrew D, Merico, Daniele
Publicado 2014

A curated census of pathogenic and likely pathogenic UTR variants and evaluation of deep learning models for variant effect prediction

por Bohn, Emma, Lau, Tammy T. Y., Wagih, Omar, Masud, Tehmina, Merico, Daniele
Publicado 2023

Enrichment Map: A Network-Based Method for Gene-Set Enrichment Visualization and Interpretation

por Merico, Daniele, Isserlin, Ruth, Stueker, Oliver, Emili, Andrew, Bader, Gary D.
Publicado 2010

Evaluation of gene-based association tests for analyzing rare variants using Genetic Analysis Workshop 18 data

por Derkach, Andriy, Lawless , Jerry F, Merico, Daniele, Paterson, Andrew D, Sun, Lei
Publicado 2014

MicroRNA Expression during Bovine Oocyte Maturation and Fertilization

por Gilchrist, Graham C., Tscherner, Allison, Nalpathamkalam, Thomas, Merico, Daniele, LaMarre, Jonathan
Publicado 2016

Using Next-Generation Sequencing Transcriptomics To Determine Markers of Post-traumatic Symptoms: Preliminary Findings from a Post-deployment Cohort of Soldiers

por Boscarino, Cathy, Nalpathamkalam, Thomas, Pellecchia, Giovanna, Li, Weili, Thiruvahindrapuram, Bhooma, Merico, Daniele
Publicado 2019

A balance between NF-Y and p53 governs the pro- and anti-apoptotic transcriptional response

por Benatti, Paolo, Basile, Valentina, Merico, Daniele, Fantoni, Luca Isaia, Tagliafico, Enrico, Imbriano, Carol
Publicado 2008

Pathway analysis of dilated cardiomyopathy using global proteomic profiling and enrichment maps

por Isserlin, Ruth, Merico, Daniele, Alikhani-Koupaei, Rasoul, Gramolini, Anthony, Bader, Gary D, Emili, Andrew
Publicado 2010

Protein Kinase C Epsilon and Genetic Networks in Osteosarcoma Metastasis

por Goudarzi, Atta, Gokgoz, Nalan, Gill, Mona, Pinnaduwage, Dushanthi, Merico, Daniele, Wunder, Jay S., Andrulis, Irene L.
Publicado 2013

Performance of case-control rare copy number variation annotation in classification of autism

por Engchuan, Worrawat, Dhindsa, Kiret, Lionel, Anath C, Scherer, Stephen W, Chan, Jonathan H, Merico, Daniele
Publicado 2015

Transcriptional Network of p63 in Human Keratinocytes

por Pozzi, Silvia, Zambelli, Federico, Merico, Daniele, Pavesi, Giulio, Robert, Amélie, Maltère, Peggy, Gidrol, Xavier, Mantovani, Roberto, Vigano, M. Alessandra
Publicado 2009

MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion Syndrome

por Merico, Daniele, Costain, Gregory, Butcher, Nancy J., Warnica, William, Ogura, Lucas, Alfred, Simon E., Brzustowicz, Linda M., Bassett, Anne S.
Publicado 2014

A homozygous mutation in the stem II domain of RNU4ATAC causes typical Roifman syndrome

por Dinur Schejter, Yael, Ovadia, Adi, Alexandrova, Roumiana, Thiruvahindrapuram, Bhooma, Pereira, Sergio L., Manson, David E., Vincent, Ajoy, Merico, Daniele, Roifman, Chaim M.
Publicado 2017

Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson’s disease

por Butcher, Nancy J., Merico, Daniele, Zarrei, Mehdi, Ogura, Lucas, Marshall, Christian R., Chow, Eva W. C., Lang, Anthony E., Scherer, Stephen W., Bassett, Anne S.
Publicado 2017

Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia

por Mojarad, Bahareh A., Yin, Yue, Manshaei, Roozbeh, Backstrom, Ian, Costain, Gregory, Heung, Tracy, Merico, Daniele, Marshall, Christian R., Bassett, Anne S., Yuen, Ryan K. C.
Publicado 2021

Rare Copy Number Variations in Adults with Tetralogy of Fallot Implicate Novel Risk Gene Pathways

por Silversides, Candice K., Lionel, Anath C., Costain, Gregory, Merico, Daniele, Migita, Ohsuke, Liu, Ben, Yuen, Tracy, Rickaby, Jessica, Thiruvahindrapuram, Bhooma, Marshall, Christian R., Scherer, Stephen W., Bassett, Anne S.
Publicado 2012

Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia

por Lowther, Chelsea, Merico, Daniele, Costain, Gregory, Waserman, Jack, Boyd, Kerry, Noor, Abdul, Speevak, Marsha, Stavropoulos, Dimitri J., Wei, John, Lionel, Anath C., Marshall, Christian R., Scherer, Stephen W., Bassett, Anne S.
Publicado 2017

Transcriptome-wide characterization of the endogenous miR-34A-p53 tumor suppressor network

por Samuel, Nardin, Wilson, Gavin, Said, Badr Id, Pan, Anna, Deblois, Genevieve, Fischer, Nicholas W., Alexandrova, Roumiana, Casallo, Guillermo, Paton, Tara, Lupien, Mathieu, Gariepy, Jean, Merico, Daniele, Hudson, Thomas J., Malkin, David
Publicado 2016