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Jonathan Pevsner

Showing results (21-30 of 76) with videos related to

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The Journal of Pediatrics|October 8, 2019
Sturge-Weber Syndrome Patient Registry: Delayed Diagnosis and Poor Seizure ControlSoonweng Cho, Biswajit Maharathi, Karen L Ball, et al.
BMC Bioinformatics|January 20, 2006
Analysis and visualization of chromosomal abnormalities in SNP data with SNPscanJason C Ting, Ying Ye, George H Thomas, et al.
BMC Medical Genetics|September 19, 2009
Locations and patterns of meiotic recombination in two-generation pedigreesJason C Ting, Elisha D O Roberson, Duane G Currier, et al.
Annual Review of Genetics|September 11, 2020
Mosaicism in Human Health and DiseaseJeremy Thorpe, Ikeoluwa A Osei-Owusu, Bracha Erlanger Avigdor, et al.
Plos One|May 15, 2008
Efficient array-based identification of novel cardiac genes through differentiation of mouse ESCsRonald A Miller, Nicolas Christoforou, Jonathan Pevsner, et al.
Plos One|November 28, 2012
Unexpected relationships and inbreeding in HapMap phase III populationsEric L Stevens, Joseph D Baugher, Matthew D Shirley, et al.
BMC Research Notes|August 5, 2018
Genetic and genomic stability across lymphoblastoid cell line expansionsLaura B Scheinfeldt, Kelly Hodges, Jonathan Pevsner, et al.
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|August 19, 2008
Estimating genome-wide copy number using allele-specific mixture modelsWenyi Wang, Benilton Carvalho, Nathaniel D Miller, et al.
Experimental Cell Research|February 15, 2005
mVps24p functions in EGF receptor sorting/trafficking from the early endosomeQing Yan, Piper Reid Hunt, Laurence Frelin, et al.
American Journal of Medical Genetics. Part A|August 16, 2014
A novel variant in GABRB2 associated with intellectual disability and epilepsySiddharth Srivastava, Julie Cohen, Jonathan Pevsner, et al.
Pageof 8

Showing results (21-30 of 76) with videos related to

Sort By:
Pageof 8
The Journal of Pediatrics|October 8, 2019
Sturge-Weber Syndrome Patient Registry: Delayed Diagnosis and Poor Seizure ControlSoonweng Cho, Biswajit Maharathi, Karen L Ball, et al.
BMC Bioinformatics|January 20, 2006
Analysis and visualization of chromosomal abnormalities in SNP data with SNPscanJason C Ting, Ying Ye, George H Thomas, et al.
BMC Medical Genetics|September 19, 2009
Locations and patterns of meiotic recombination in two-generation pedigreesJason C Ting, Elisha D O Roberson, Duane G Currier, et al.
Annual Review of Genetics|September 11, 2020
Mosaicism in Human Health and DiseaseJeremy Thorpe, Ikeoluwa A Osei-Owusu, Bracha Erlanger Avigdor, et al.
Plos One|May 15, 2008
Efficient array-based identification of novel cardiac genes through differentiation of mouse ESCsRonald A Miller, Nicolas Christoforou, Jonathan Pevsner, et al.
Plos One|November 28, 2012
Unexpected relationships and inbreeding in HapMap phase III populationsEric L Stevens, Joseph D Baugher, Matthew D Shirley, et al.
BMC Research Notes|August 5, 2018
Genetic and genomic stability across lymphoblastoid cell line expansionsLaura B Scheinfeldt, Kelly Hodges, Jonathan Pevsner, et al.
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|August 19, 2008
Estimating genome-wide copy number using allele-specific mixture modelsWenyi Wang, Benilton Carvalho, Nathaniel D Miller, et al.
Experimental Cell Research|February 15, 2005
mVps24p functions in EGF receptor sorting/trafficking from the early endosomeQing Yan, Piper Reid Hunt, Laurence Frelin, et al.
American Journal of Medical Genetics. Part A|August 16, 2014
A novel variant in GABRB2 associated with intellectual disability and epilepsySiddharth Srivastava, Julie Cohen, Jonathan Pevsner, et al.
Pageof 8