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David N Cooper

Showing results (111-120 of 398) with videos related to

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Human Mutation|July 29, 2011
Prediction of functional regulatory SNPs in monogenic and complex diseaseYiqiang Zhao, Wyatt T Clark, Matthew Mort, et al.
Human Genetics|May 11, 2005
Molecular characterisation of the pericentric inversion that distinguishes human chromosome 5 from the homologous chimpanzee chromosomeJustyna M Szamalek, Violaine Goidts, Nadia Chuzhanova, et al.
Bioinformatics (Oxford, England)|April 27, 2013
Predicting the functional consequences of cancer-associated amino acid substitutionsHashem A Shihab, Julian Gough, David N Cooper, et al.
Neuroimage|August 14, 2023
Inferring the genetic relationship between brain imaging-derived phenotypes and risk of complex diseases by Mendelian randomization and genome-wide colocalizationSiying Lin, Haoyang Zhang, Mengling Qi, et al.
Human Genomics|August 3, 2011
Cross-comparison of the genome sequences from human, chimpanzee, Neanderthal and a Denisovan hominin identifies novel potentially compensated mutationsGuojie Zhang, Zhang Pei, Edward V Ball, et al.
Human Mutation|October 19, 2017
Quantitative mapping of genetic similarity in human heritable diseases by shared mutationsHuiying Zhao, Yuedong Yang, Yutong Lu, et al.
Neurogenetics|May 15, 2012
Dissecting the clinical phenotype associated with mosaic type-2 NF1 microdeletionsHildegard Kehrer-Sawatzki, Julia Vogt, Tanja Mußotter, et al.
Human Genetics|November 28, 2018
Ultra-deep amplicon sequencing indicates absence of low-grade mosaicism with normal cells in patients with type-1 NF1 deletionsAnna Summerer, Eleonora Schäfer, Victor-Felix Mautner, et al.
Human Mutation|September 2, 2017
Consideration of the haplotype diversity at nonallelic homologous recombination hotspots improves the precision of rearrangement breakpoint identificationMorten Hillmer, Anna Summerer, Victor-Felix Mautner, et al.
Genes|November 18, 2020
Role of the Common <i>PRSS1-PRSS2</i> Haplotype in Alcoholic and Non-Alcoholic Chronic Pancreatitis: Meta- and Re-AnalysesAnthony F Herzig, Emmanuelle Génin, David N Cooper, et al.
Pageof 40

Showing results (111-120 of 398) with videos related to

Sort By:
Pageof 40
Human Mutation|July 29, 2011
Prediction of functional regulatory SNPs in monogenic and complex diseaseYiqiang Zhao, Wyatt T Clark, Matthew Mort, et al.
Human Genetics|May 11, 2005
Molecular characterisation of the pericentric inversion that distinguishes human chromosome 5 from the homologous chimpanzee chromosomeJustyna M Szamalek, Violaine Goidts, Nadia Chuzhanova, et al.
Bioinformatics (Oxford, England)|April 27, 2013
Predicting the functional consequences of cancer-associated amino acid substitutionsHashem A Shihab, Julian Gough, David N Cooper, et al.
Neuroimage|August 14, 2023
Inferring the genetic relationship between brain imaging-derived phenotypes and risk of complex diseases by Mendelian randomization and genome-wide colocalizationSiying Lin, Haoyang Zhang, Mengling Qi, et al.
Human Genomics|August 3, 2011
Cross-comparison of the genome sequences from human, chimpanzee, Neanderthal and a Denisovan hominin identifies novel potentially compensated mutationsGuojie Zhang, Zhang Pei, Edward V Ball, et al.
Human Mutation|October 19, 2017
Quantitative mapping of genetic similarity in human heritable diseases by shared mutationsHuiying Zhao, Yuedong Yang, Yutong Lu, et al.
Neurogenetics|May 15, 2012
Dissecting the clinical phenotype associated with mosaic type-2 NF1 microdeletionsHildegard Kehrer-Sawatzki, Julia Vogt, Tanja Mußotter, et al.
Human Genetics|November 28, 2018
Ultra-deep amplicon sequencing indicates absence of low-grade mosaicism with normal cells in patients with type-1 NF1 deletionsAnna Summerer, Eleonora Schäfer, Victor-Felix Mautner, et al.
Human Mutation|September 2, 2017
Consideration of the haplotype diversity at nonallelic homologous recombination hotspots improves the precision of rearrangement breakpoint identificationMorten Hillmer, Anna Summerer, Victor-Felix Mautner, et al.
Genes|November 18, 2020
Role of the Common <i>PRSS1-PRSS2</i> Haplotype in Alcoholic and Non-Alcoholic Chronic Pancreatitis: Meta- and Re-AnalysesAnthony F Herzig, Emmanuelle Génin, David N Cooper, et al.
Pageof 40