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Showing results (151-160 of 218) with videos related to

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The New England Journal of Medicine|April 11, 2019
Molecular Genetic Anatomy and Risk Profile of Hirschsprung's DiseaseJoseph M Tilghman, Albee Y Ling, Tychele N Turner, et al.
Plos Genetics|March 28, 2019
Genomic inversions and GOLGA core duplicons underlie disease instability at the 15q25 locusFlavia A M Maggiolini, Stuart Cantsilieris, Pietro D'Addabbo, et al.
BMC Medical Genomics|March 29, 2011
Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardationTracy Tucker, Alexandre Montpetit, David Chai, et al.
Plos Genetics|November 22, 2011
Relative burden of large CNVs on a range of neurodevelopmental phenotypesSanthosh Girirajan, Zoran Brkanac, Bradley P Coe, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 4, 2018
Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypesHui Guo, Michael H Duyzend, Bradley P Coe, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|December 23, 2018
Integrative Genomic Analyses Identifies GGA2 as a Cooperative Driver of EGFR-Mediated Lung TumorigenesisHannah O'Farrell, Bryant Harbourne, Zimple Kurlawala, et al.
Genome Research|November 3, 2016
Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23.1 regionKiana Mohajeri, Stuart Cantsilieris, John Huddleston, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 24, 2017
Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorderDaniel Seung Kim, Amber A Burt, Jane E Ranchalis, et al.
Nature Genetics|July 27, 2021
Recent ultra-rare inherited variants implicate new autism candidate risk genesAmy B Wilfert, Tychele N Turner, Shwetha C Murali, et al.
Plos Medicine|July 30, 2010
Integrative genomic analyses identify BRF2 as a novel lineage-specific oncogene in lung squamous cell carcinomaWilliam W Lockwood, Raj Chari, Bradley P Coe, et al.
Pageof 22

Showing results (151-160 of 218) with videos related to

Sort By:
Pageof 22
The New England Journal of Medicine|April 11, 2019
Molecular Genetic Anatomy and Risk Profile of Hirschsprung's DiseaseJoseph M Tilghman, Albee Y Ling, Tychele N Turner, et al.
Plos Genetics|March 28, 2019
Genomic inversions and GOLGA core duplicons underlie disease instability at the 15q25 locusFlavia A M Maggiolini, Stuart Cantsilieris, Pietro D'Addabbo, et al.
BMC Medical Genomics|March 29, 2011
Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardationTracy Tucker, Alexandre Montpetit, David Chai, et al.
Plos Genetics|November 22, 2011
Relative burden of large CNVs on a range of neurodevelopmental phenotypesSanthosh Girirajan, Zoran Brkanac, Bradley P Coe, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 4, 2018
Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypesHui Guo, Michael H Duyzend, Bradley P Coe, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|December 23, 2018
Integrative Genomic Analyses Identifies GGA2 as a Cooperative Driver of EGFR-Mediated Lung TumorigenesisHannah O'Farrell, Bryant Harbourne, Zimple Kurlawala, et al.
Genome Research|November 3, 2016
Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23.1 regionKiana Mohajeri, Stuart Cantsilieris, John Huddleston, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 24, 2017
Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorderDaniel Seung Kim, Amber A Burt, Jane E Ranchalis, et al.
Nature Genetics|July 27, 2021
Recent ultra-rare inherited variants implicate new autism candidate risk genesAmy B Wilfert, Tychele N Turner, Shwetha C Murali, et al.
Plos Medicine|July 30, 2010
Integrative genomic analyses identify BRF2 as a novel lineage-specific oncogene in lung squamous cell carcinomaWilliam W Lockwood, Raj Chari, Bradley P Coe, et al.
Pageof 22