Daniele Merico mainly focuses on Genetics, Whole genome sequencing, Copy-number variation, Genome-wide association study and Autism spectrum disorder. Genetics is a component of her Gene, Mutation, Fragile X syndrome, Mutation rate and DNA repair studies. Her Whole genome sequencing study combines topics in areas such as Genetic variation and DNA sequencing.
Daniele Merico interconnects Gene duplication, Autism and Intellectual disability in the investigation of issues within Genome-wide association study. Her work carried out in the field of Autism brings together such families of science as SYNGAP1 and CHD2. Her Autism spectrum disorder study integrates concerns from other disciplines, such as Genetic heterogeneity and Proband.
Daniele Merico mostly deals with Genetics, Gene, Copy-number variation, Genome and Whole genome sequencing. Her Genetics study frequently draws connections to other fields, such as Autism. Her Gene study combines topics from a wide range of disciplines, such as Molecular biology, Computational biology and Immunodeficiency.
Her Copy-number variation research is multidisciplinary, incorporating elements of Schizophrenia, Human genome, Autism spectrum disorder, Genetic variation and Etiology. Her study in Whole genome sequencing is interdisciplinary in nature, drawing from both Allele and Genotype. While the research belongs to areas of Genome-wide association study, Daniele Merico spends her time largely on the problem of Bioinformatics, intersecting her research to questions surrounding Visualization.
Her scientific interests lie mostly in Genetics, Copy-number variation, Gene, Genetic variation and Genome. Her works in CRISPR, Compound heterozygosity, Exon and RNA splicing are all subjects of inquiry into Genetics. Her research integrates issues of Schizophrenia, Endophenotype, Proband, Genotype and Etiology in her study of Copy-number variation.
The various areas that she examines in her Gene study include Cancer research and Pancreatic cancer. Her Genetic variation research is multidisciplinary, relying on both Binding site, Whole genome sequencing and DNA sequencing. Her Genome research incorporates elements of Multiple comparisons problem, Missense mutation, Visualization and Candidate gene.
Her main research concerns Exome sequencing, Genetics, Proband, Copy-number variation and Whole genome sequencing. Her work deals with themes such as Genetic disorder, Cerebral palsy, Genotype and Etiology, which intersect with Exome sequencing. Her work on CRISPR, Phenotype and Gene Knockout Techniques as part of her general Genetics study is frequently connected to Neurogenin-2 and Induced pluripotent stem cell, thereby bridging the divide between different branches of science.
Her Proband research focuses on DNA microarray and how it connects with Computational biology. Daniele Merico has included themes like Sequence analysis, Bioinformatics, Exome, Genetic variation and DNA sequencing in her Whole genome sequencing study. The study incorporates disciplines such as Cancer research and Pancreatic cancer in addition to Gene.
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Functional impact of global rare copy number variation in autism spectrum disorders
Dalila Pinto;Alistair T. Pagnamenta;Lambertus Klei;Richard Anney.
Enrichment Map: A Network-Based Method for Gene-Set Enrichment Visualization and Interpretation
Daniele Merico;Ruth Isserlin;Oliver Stueker;Andrew Emili.
PLOS ONE (2010)
The human splicing code reveals new insights into the genetic determinants of disease
Hui Y. Xiong;Babak Alipanahi;Babak Alipanahi;Leo J. Lee;Leo J. Lee;Hannes Bretschneider.
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
Dalila Pinto;Elsa Delaby;Elsa Delaby;Elsa Delaby;Daniele Merico;Mafalda Barbosa.
American Journal of Human Genetics (2014)
Pathway enrichment analysis and visualization of omics data using g:Profiler, GSEA, Cytoscape and EnrichmentMap
Jüri Reimand;Jüri Reimand;Ruth Isserlin;Veronique Voisin;Mike Kucera.
Nature Protocols (2019)
A copy number variation map of the human genome
Mehdi Zarrei;Jeffrey R. MacDonald;Daniele Merico;Stephen W. Scherer.
Nature Reviews Genetics (2015)
Immune Checkpoint Inhibition for Hypermutant Glioblastoma Multiforme Resulting From Germline Biallelic Mismatch Repair Deficiency
Eric Bouffet;Valérie Larouche;Brittany B. Campbell;Daniele Merico.
Journal of Clinical Oncology (2016)
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
Christian R Marshall;Daniel P Howrigan;Daniel P Howrigan;Daniele Merico;Bhooma Thiruvahindrapuram.
Nature Genetics (2017)
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
Ryan K C Yuen;Daniele Merico;Matt Bookman;Jennifer L. Howe.
Whole-genome sequencing of quartet families with autism spectrum disorder
Ryan K C Yuen;Bhooma Thiruvahindrapuram;Daniele Merico;Susan Walker.
Nature Medicine (2015)
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