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Up, Periscope.
- Published in:
- Journalism & Mass Communication Quarterly, 2016, v. 93, n. 2, p. 312, doi. 10.1177/1077699016637106
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- Article
When Retweets Attack: Are Twitter Users Liable for Republishing the Defamatory Tweets of Others?
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- Journalism & Mass Communication Quarterly, 2013, v. 90, n. 2, p. 233, doi. 10.1177/1077699013482913
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- Article
Sequence Analysis and Characterization of Active Human Alu Subfamilies Based on the 1000 Genomes Pilot Project.
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- Genome Biology & Evolution, 2015, v. 7, n. 9, p. 2608, doi. 10.1093/gbe/evv167
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RUNNING HEAD: To Laugh or Not to Laugh.
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- Southwestern Mass Communication Journal, 2013, v. 28, n. 2, p. 1
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- Article
To Laugh or Not to Laugh.
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- Southwestern Mass Communication Journal, 2012, v. 27, n. 3, p. 1
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- Article
Mutations driving CLL and their evolution in progression and relapse.
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- Nature, 2015, v. 526, n. 7574, p. 525, doi. 10.1038/nature15395
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- Article
Discovery and characterization of artifactual mutations in deep coverage targeted capture sequencing data due to oxidative DNA damage during sample preparation.
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- Nucleic Acids Research, 2013, v. 41, n. 6, p. e67, doi. 10.1093/nar/gks1443
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- Article
The PROMISE Study: A Nationwide Project for Predicting the Progression of Developing Myeloma in a High-Risk Screened Population.
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- Clinical Lymphoma, Myeloma & Leukemia, 2019, v. 19, p. e310, doi. 10.1016/j.clml.2019.09.509
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- Article
Genomic profiling of smoldering multiple myeloma identifies patients at a high risk of disease progression.
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- Clinical Lymphoma, Myeloma & Leukemia, 2019, v. 19, p. e5, doi. 10.1016/j.clml.2019.09.007
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- Article
Sporadic hemangioblastomas are characterized by cryptic VHL inactivation.
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- Acta Neuropathologica Communications, 2014, v. 2, n. 1, p. 1, doi. 10.1186/s40478-014-0167-x
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- Article
Genetic subtypes of smoldering multiple myeloma are associated with distinct pathogenic phenotypes and clinical outcomes.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30694-w
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- Article
Mutational heterogeneity in cancer and the search for new cancer-associated genes.
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- Nature, 2013, v. 499, n. 7457, p. 214, doi. 10.1038/nature12213
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Mapping copy number variation by population-scale genome sequencing.
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- Nature, 2011, v. 470, n. 7332, p. 59, doi. 10.1038/nature09708
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- Article
Scotty: a web tool for designing RNA-Seq experiments to measure differential gene expression.
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- Bioinformatics, 2013, v. 29, n. 5, p. 656, doi. 10.1093/bioinformatics/btt015
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- Article
CAN I USE THIS PHOTO I FOUND ON FACEBOOK? APPLYING COPYRIGHT LAW AND FAIR USE ANALYSIS TO PHOTOGRAPHS ON SOCIAL NETWORKING SITES REPUBLISHED FOR NEWS REPORTING PURPOSES.
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- Journal on Telecommunications & High Technology Law, 2012, v. 10, n. 1, p. 93
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- Article
Copy Number Variation detection from 1000 Genomes project exon capture sequencing data.
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- BMC Bioinformatics, 2012, v. 13, n. 1, p. 1, doi. 10.1186/1471-2105-13-305
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- Article
Scalable whole-exome sequencing of cell-free DNA reveals high concordance with metastatic tumors.
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- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00965-y
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- Article
Clonal evolution in patients with chronic lymphocytic leukaemia developing resistance to BTK inhibition.
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- Nature Communications, 2016, v. 7, n. 5, p. 11589, doi. 10.1038/ncomms11589
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- Article
MOSAIK: A Hash-Based Algorithm for Accurate Next-Generation Sequencing Short-Read Mapping.
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- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0090581
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- Article
PRACTICAL TRANSPARENCY: HOW JOURNALISTS SHOULD APPROACH DIGITAL SHAMING AND THE "STREISAND EFFECT".
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- Journal of Media Law & Ethics, 2016, v. 5, n. 3/4, p. 4
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- Article
A Comprehensive Map of Mobile Element Insertion Polymorphisms in Humans.
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- PLoS Genetics, 2011, v. 7, n. 8, p. 1, doi. 10.1371/journal.pgen.1002236
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Genomic signatures of past and present chromosomal instability in Barrett's esophagus and early esophageal adenocarcinoma.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-41805-6
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Paired exome analysis of Barrett's esophagus and adenocarcinoma.
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- Nature Genetics, 2015, v. 47, n. 9, p. 1047, doi. 10.1038/ng.3343
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Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity.
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- Nature Genetics, 2013, v. 45, n. 5, p. 478, doi. 10.1038/ng.2591
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The genetic landscape of high-risk neuroblastoma.
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- Nature Genetics, 2013, v. 45, n. 3, p. 279, doi. 10.1038/ng.2529
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Genomic characterization of cervical lymph node metastases in papillary thyroid carcinoma following the Chornobyl accident.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-49292-z
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A (fire)cloud-based DNA methylation data preprocessing and quality control platform.
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- BMC Bioinformatics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12859-019-2750-4
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- Article
A remarkably simple genome underlies highly malignant pediatric rhabdoid cancers.
- Published in:
- Journal of Clinical Investigation, 2012, v. 122, n. 8, p. 2983, doi. 10.1172/JCI64400
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- Article