His scientific interests lie mostly in Genetics, Disease, Cancer research, Exome sequencing and Exome. His research on Genetics frequently connects to adjacent areas such as Schizophrenia. His Disease study combines topics in areas such as Stage, Proportional hazards model and Oncology.
His biological study deals with issues like Head and neck squamous-cell carcinoma, which deal with fields such as Significance analysis of microarrays, Growth factor receptor and Epidermal growth factor receptor. His Exome sequencing research incorporates themes from Missense mutation and Diffuse large B-cell lymphoma. His study in Exome is interdisciplinary in nature, drawing from both ZNF423, Epigenetics of autism, Genetic model, Point mutation and Nonsense mutation.
Shawn Levy mainly focuses on Genetics, Gene, Cancer research, Genome-wide association study and Internal medicine. His study focuses on the intersection of Genetics and fields such as Bipolar disorder with connections in the field of Schizophrenia. His study looks at the relationship between Cancer research and fields such as Pathology, as well as how they intersect with chemical problems.
His Genome-wide association study study integrates concerns from other disciplines, such as Genetic association and Candidate gene. His research investigates the connection with Internal medicine and areas like Endocrinology which intersect with concerns in Cell biology. Shawn Levy works mostly in the field of Gene expression, limiting it down to concerns involving RNA and, occasionally, Molecular biology.
His primary areas of study are Mycobacterium tuberculosis, Genetics, Acid-fast, Gene and Virology. His research on Mycobacterium tuberculosis also deals with topics like
In his study, Gene expression is inextricably linked to Expression quantitative trait loci, which falls within the broad field of Bipolar disorder. His Genome-wide association study and Genetic variation study are his primary interests in Gene. His Genome-wide association study research includes themes of Schizophrenia, Phenotype, Quantitative trait locus, Exome and Heritability.
His primary areas of investigation include Virology, Genetic variation, Gene, Transcriptome and Genetics. Shawn Levy integrates many fields, such as Virology and engineering, in his works. His Genetic variation research incorporates elements of RNA, NSP1, Pathogen and Disease.
In the subject of general Gene, his work in Expression quantitative trait loci, Druggability and Genome-wide association study is often linked to Prefrontal cortex and Furin, thereby combining diverse domains of study. Shawn Levy interconnects Neurotypical, Autism, Autism spectrum disorder, Stem cell and Sperm in the investigation of issues within Transcriptome. Shawn Levy is interested in Gene expression, which is a branch of Genetics.
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An integrated encyclopedia of DNA elements in the human genome
Ian Dunham;Anshul Kundaje;Shelley F. Aldred;Patrick J. Collins.
The MicroArray Quality Control (MAQC) project shows inter- and intraplatform reproducibility of gene expression measurements
Leming Shi;Laura H. Reid;Wendell D. Jones;Richard Shippy.
Nature Biotechnology (2006)
Patterns and rates of exonic de novo mutations in autism spectrum disorders
Benjamin M. Neale;Yan Kou;Li Liu;Avi Ma'Ayan.
The ADP/ATP translocator is not essential for the mitochondrial permeability transition pore
Jason E. Kokoszka;Jason E. Kokoszka;Katrina G. Waymire;Katrina G. Waymire;Shawn E. Levy;Shawn E. Levy;James E. Sligh;James E. Sligh.
A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy;Sayantan Das;Warren Kretzschmar;Olivier Delaneau.
Nature Genetics (2016)
A comprehensive evaluation of multicategory classification methods for microarray gene expression cancer diagnosis
Alexander Statnikov;Constantin F. Aliferis;Ioannis Tsamardinos;Douglas Hardin.
Next-generation genotype imputation service and methods.
Sayantan Das;Lukas Forer;Sebastian Schönherr;Carlo Sidore;Carlo Sidore.
Nature Genetics (2016)
Strong association of de novo copy number mutations with sporadic schizophrenia.
Bin Xu;J Louw Roos;Shawn Levy;E J van Rensburg.
Nature Genetics (2008)
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
Elizabeth T. Cirulli;Brittany N Lasseigne;Slave Petrovski;Peter C Sapp.
A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium
Zhenqiang Su;Paweł P. Łabaj;Sheng Li;Jean Thierry-Mieg.
Nature Biotechnology (2014)
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