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Daniele Merico

Showing results (31-40 of 94) with videos related to

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NPJ Genomic Medicine|December 22, 2017
A homozygous mutation in the stem II domain of <i>RNU4ATAC</i> causes typical Roifman syndromeYael Dinur Schejter, Adi Ovadia, Roumiana Alexandrova, et al.
The EMBO Journal|October 13, 2006
New p63 targets in keratinocytes identified by a genome-wide approachM Alessandra Viganò, Jérôme Lamartine, Barbara Testoni, et al.
Journal of Biomedical Informatics|January 16, 2010
An ontological modeling approach to cerebrovascular disease studies: the NEUROWEB caseGianluca Colombo, Daniele Merico, Giorgio Boncoraglio, et al.
Plos One|April 22, 2017
Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's diseaseNancy J Butcher, Daniele Merico, Mehdi Zarrei, et al.
Translational Psychiatry|February 2, 2021
Genome sequencing broadens the range of contributing variants with clinical implications in schizophreniaBahareh A Mojarad, Yue Yin, Roozbeh Manshaei, et al.
American Journal of Medical Genetics. Part A|April 4, 2017
A de novo deletion in a boy with cerebral palsy suggests a refined critical region for the 4q21.22 microdeletion syndromeMehdi Zarrei, Daniele Merico, Barbara Kellam, et al.
Nature Protocols|January 22, 2019
Pathway enrichment analysis and visualization of omics data using g:Profiler, GSEA, Cytoscape and EnrichmentMapJüri Reimand, Ruth Isserlin, Veronique Voisin, et al.
Gene Expression Patterns : GEP|April 1, 2004
Analysis of the gene expression profile of mouse male meiotic germ cellsPellegrino Rossi, Susanna Dolci, Claudio Sette, et al.
The Journal of Allergy and Clinical Immunology|August 6, 2025
Autosomal-dominant Roquin-1 immunodeficiency and hyperinflammationAmit Nahum, Nigel Sharfe, Daniele Merico, et al.
NPJ Genomic Medicine|January 13, 2025
Pre-T cell receptor-α immunodeficiency detected exclusively using whole genome sequencingDaniele Merico, Nigel Sharfe, Harjit Dadi, et al.
Pageof 10

Showing results (31-40 of 94) with videos related to

Sort By:
Pageof 10
NPJ Genomic Medicine|December 22, 2017
A homozygous mutation in the stem II domain of <i>RNU4ATAC</i> causes typical Roifman syndromeYael Dinur Schejter, Adi Ovadia, Roumiana Alexandrova, et al.
The EMBO Journal|October 13, 2006
New p63 targets in keratinocytes identified by a genome-wide approachM Alessandra Viganò, Jérôme Lamartine, Barbara Testoni, et al.
Journal of Biomedical Informatics|January 16, 2010
An ontological modeling approach to cerebrovascular disease studies: the NEUROWEB caseGianluca Colombo, Daniele Merico, Giorgio Boncoraglio, et al.
Plos One|April 22, 2017
Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's diseaseNancy J Butcher, Daniele Merico, Mehdi Zarrei, et al.
Translational Psychiatry|February 2, 2021
Genome sequencing broadens the range of contributing variants with clinical implications in schizophreniaBahareh A Mojarad, Yue Yin, Roozbeh Manshaei, et al.
American Journal of Medical Genetics. Part A|April 4, 2017
A de novo deletion in a boy with cerebral palsy suggests a refined critical region for the 4q21.22 microdeletion syndromeMehdi Zarrei, Daniele Merico, Barbara Kellam, et al.
Nature Protocols|January 22, 2019
Pathway enrichment analysis and visualization of omics data using g:Profiler, GSEA, Cytoscape and EnrichmentMapJüri Reimand, Ruth Isserlin, Veronique Voisin, et al.
Gene Expression Patterns : GEP|April 1, 2004
Analysis of the gene expression profile of mouse male meiotic germ cellsPellegrino Rossi, Susanna Dolci, Claudio Sette, et al.
The Journal of Allergy and Clinical Immunology|August 6, 2025
Autosomal-dominant Roquin-1 immunodeficiency and hyperinflammationAmit Nahum, Nigel Sharfe, Daniele Merico, et al.
NPJ Genomic Medicine|January 13, 2025
Pre-T cell receptor-α immunodeficiency detected exclusively using whole genome sequencingDaniele Merico, Nigel Sharfe, Harjit Dadi, et al.
Pageof 10