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Joshua M Korn

Showing results (1-10 of 34) with videos related to

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Nature Genetics|February 15, 2011
Discovery and genotyping of genome structural polymorphism by sequencing on a population scaleRobert E Handsaker, Joshua M Korn, James Nemesh, et al.
BMC Cancer|June 20, 2022
Contribution and clinical relevance of germline variation to the cancer transcriptomeBernard Pereira, Emma Labrot, Eric Durand, et al.
Plos Genetics|September 15, 2010
Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain functionSoumya Raychaudhuri, Joshua M Korn, Steven A McCarroll, et al.
Plos Computational Biology|July 19, 2012
Efficiency and power as a function of sequence coverage, SNP array density, and imputationJason Flannick, Joshua M Korn, Pierre Fontanillas, et al.
Plos Computational Biology|July 20, 2018
Correction of copy number induced false positives in CRISPR screensAntoine de Weck, Javad Golji, Michael D Jones, et al.
Molecular Cancer Research : MCR|August 22, 2023
Generating a Murine PTEN Null Cell Line to Discover the Key Role of p110β-PAK1 in Castration-Resistant Prostate Cancer InvasionHaizhen Wang, Yu Zhou, Chen Chu, et al.
The Journal of Biological Chemistry|October 6, 2012
Isocitrate dehydrogenase (IDH) mutations promote a reversible ZEB1/microRNA (miR)-200-dependent epithelial-mesenchymal transition (EMT)Alexandra R Grassian, Fallon Lin, Rosemary Barrett, et al.
Oncotarget|February 18, 2020
Patient-derived glioblastoma cultures as a tool for small-molecule drug discoveryLing F Ye, Eduard Reznik, Joshua M Korn, et al.
Molecular Cancer Research : MCR|June 29, 2017
BRAF-inhibitor Associated MEK Mutations Increase RAF-Dependent and -Independent Enzymatic ActivityCaroline M Emery, Kelli-Ann Monaco, Ping Wang, et al.
Nature Genetics|September 9, 2008
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVsJoshua M Korn, Finny G Kuruvilla, Steven A McCarroll, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Nature Genetics|February 15, 2011
Discovery and genotyping of genome structural polymorphism by sequencing on a population scaleRobert E Handsaker, Joshua M Korn, James Nemesh, et al.
BMC Cancer|June 20, 2022
Contribution and clinical relevance of germline variation to the cancer transcriptomeBernard Pereira, Emma Labrot, Eric Durand, et al.
Plos Genetics|September 15, 2010
Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain functionSoumya Raychaudhuri, Joshua M Korn, Steven A McCarroll, et al.
Plos Computational Biology|July 19, 2012
Efficiency and power as a function of sequence coverage, SNP array density, and imputationJason Flannick, Joshua M Korn, Pierre Fontanillas, et al.
Plos Computational Biology|July 20, 2018
Correction of copy number induced false positives in CRISPR screensAntoine de Weck, Javad Golji, Michael D Jones, et al.
Molecular Cancer Research : MCR|August 22, 2023
Generating a Murine PTEN Null Cell Line to Discover the Key Role of p110β-PAK1 in Castration-Resistant Prostate Cancer InvasionHaizhen Wang, Yu Zhou, Chen Chu, et al.
The Journal of Biological Chemistry|October 6, 2012
Isocitrate dehydrogenase (IDH) mutations promote a reversible ZEB1/microRNA (miR)-200-dependent epithelial-mesenchymal transition (EMT)Alexandra R Grassian, Fallon Lin, Rosemary Barrett, et al.
Oncotarget|February 18, 2020
Patient-derived glioblastoma cultures as a tool for small-molecule drug discoveryLing F Ye, Eduard Reznik, Joshua M Korn, et al.
Molecular Cancer Research : MCR|June 29, 2017
BRAF-inhibitor Associated MEK Mutations Increase RAF-Dependent and -Independent Enzymatic ActivityCaroline M Emery, Kelli-Ann Monaco, Ping Wang, et al.
Nature Genetics|September 9, 2008
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVsJoshua M Korn, Finny G Kuruvilla, Steven A McCarroll, et al.
Pageof 4