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Daniele Merico

Showing results (71-80 of 94) with videos related to

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Scientific Reports|July 2, 2016
Indexing Effects of Copy Number Variation on Genes Involved in Developmental DelayMohammed Uddin, Giovanna Pellecchia, Bhooma Thiruvahindrapuram, et al.
Human Molecular Genetics|May 8, 2023
Gene copy number variation and pediatric mental health/neurodevelopment in a general populationMehdi Zarrei, Christie L Burton, Worrawat Engchuan, et al.
Human Molecular Genetics|February 9, 2013
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizuresAnath C Lionel, Andrea K Vaags, Daisuke Sato, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 11, 2015
BRAF mutation and CDKN2A deletion define a clinically distinct subgroup of childhood secondary high-grade gliomaMatthew Mistry, Nataliya Zhukova, Daniele Merico, et al.
JAMA|September 2, 2015
Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum DisorderKristiina Tammimies, Christian R Marshall, Susan Walker, et al.
American Journal of Human Genetics|July 16, 2013
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencingYong-hui Jiang, Ryan K C Yuen, Xin Jin, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 23, 2016
Immune Checkpoint Inhibition for Hypermutant Glioblastoma Multiforme Resulting From Germline Biallelic Mismatch Repair DeficiencyEric Bouffet, Valérie Larouche, Brittany B Campbell, et al.
NPJ Genomic Medicine|August 16, 2016
Genome-wide characteristics of <i>de novo</i> mutations in autismRyan K C Yuen, Daniele Merico, Hongzhi Cao, et al.
American Journal of Medical Genetics. Part A|February 5, 2016
Clinical delineation of the PACS1-related syndrome--Report on 19 patientsJanneke H M Schuurs-Hoeijmakers, Megan L Landsverk, Nicola Foulds, et al.
Cancer Cell|January 29, 2019
Integration of Genomic and Transcriptional Features in Pancreatic Cancer Reveals Increased Cell Cycle Progression in MetastasesAshton A Connor, Robert E Denroche, Gun Ho Jang, et al.
Pageof 10

Showing results (71-80 of 94) with videos related to

Sort By:
Pageof 10
Scientific Reports|July 2, 2016
Indexing Effects of Copy Number Variation on Genes Involved in Developmental DelayMohammed Uddin, Giovanna Pellecchia, Bhooma Thiruvahindrapuram, et al.
Human Molecular Genetics|May 8, 2023
Gene copy number variation and pediatric mental health/neurodevelopment in a general populationMehdi Zarrei, Christie L Burton, Worrawat Engchuan, et al.
Human Molecular Genetics|February 9, 2013
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizuresAnath C Lionel, Andrea K Vaags, Daisuke Sato, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 11, 2015
BRAF mutation and CDKN2A deletion define a clinically distinct subgroup of childhood secondary high-grade gliomaMatthew Mistry, Nataliya Zhukova, Daniele Merico, et al.
JAMA|September 2, 2015
Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum DisorderKristiina Tammimies, Christian R Marshall, Susan Walker, et al.
American Journal of Human Genetics|July 16, 2013
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencingYong-hui Jiang, Ryan K C Yuen, Xin Jin, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 23, 2016
Immune Checkpoint Inhibition for Hypermutant Glioblastoma Multiforme Resulting From Germline Biallelic Mismatch Repair DeficiencyEric Bouffet, Valérie Larouche, Brittany B Campbell, et al.
NPJ Genomic Medicine|August 16, 2016
Genome-wide characteristics of <i>de novo</i> mutations in autismRyan K C Yuen, Daniele Merico, Hongzhi Cao, et al.
American Journal of Medical Genetics. Part A|February 5, 2016
Clinical delineation of the PACS1-related syndrome--Report on 19 patientsJanneke H M Schuurs-Hoeijmakers, Megan L Landsverk, Nicola Foulds, et al.
Cancer Cell|January 29, 2019
Integration of Genomic and Transcriptional Features in Pancreatic Cancer Reveals Increased Cell Cycle Progression in MetastasesAshton A Connor, Robert E Denroche, Gun Ho Jang, et al.
Pageof 10