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Lars Feuk

Showing results (51-60 of 103) with videos related to

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Nature Genetics|September 5, 2007
Challenges and standards in integrating surveys of structural variationStephen W Scherer, Charles Lee, Ewan Birney, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|February 23, 2016
One CNV Discordance in NRXN1 Observed Upon Genome-wide Screening in 38 Pairs of Adult Healthy Monozygotic TwinsPatrik K E Magnusson, Donghwan Lee, Xu Chen, et al.
Frontiers in Genetics|October 15, 2019
Novel Y-Chromosome Long Non-Coding RNAs Expressed in Human Male CNS During Early DevelopmentMartin M Johansson, Philipp Pottmeier, Pascalina Suciu, et al.
Nature Genetics|August 3, 2004
Detection of large-scale variation in the human genomeA John Iafrate, Lars Feuk, Miguel N Rivera, et al.
Human Mutation|June 23, 2016
A Role for the Chromatin-Remodeling Factor BAZ1A in NeurodevelopmentAmmar Zaghlool, Jonatan Halvardson, Jin J Zhao, et al.
Nature Communications|February 3, 2022
CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generationsIda Höijer, Anastasia Emmanouilidou, Rebecka Östlund, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 8, 2008
Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndromeAdam Shlien, Uri Tabori, Christian R Marshall, et al.
Human Genetics|December 13, 2005
Towards compendia of negative genetic association studies: an example for Alzheimer diseaseMia E-L Blomqvist, Chandra Reynolds, Hagit Katzov, et al.
Clinical Genetics|December 8, 2018
Whole genome sequencing of consanguineous families reveals novel pathogenic variants in intellectual disabilityAnn-Charlotte Thuresson, Cecilia Soussi Zander, Jin J Zhao, et al.
European Journal of Human Genetics : EJHG|November 28, 2013
Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathyRonen Spiegel, Ann Saada, Jonatan Halvardson, et al.
Pageof 11

Showing results (51-60 of 103) with videos related to

Sort By:
Pageof 11
Nature Genetics|September 5, 2007
Challenges and standards in integrating surveys of structural variationStephen W Scherer, Charles Lee, Ewan Birney, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|February 23, 2016
One CNV Discordance in NRXN1 Observed Upon Genome-wide Screening in 38 Pairs of Adult Healthy Monozygotic TwinsPatrik K E Magnusson, Donghwan Lee, Xu Chen, et al.
Frontiers in Genetics|October 15, 2019
Novel Y-Chromosome Long Non-Coding RNAs Expressed in Human Male CNS During Early DevelopmentMartin M Johansson, Philipp Pottmeier, Pascalina Suciu, et al.
Nature Genetics|August 3, 2004
Detection of large-scale variation in the human genomeA John Iafrate, Lars Feuk, Miguel N Rivera, et al.
Human Mutation|June 23, 2016
A Role for the Chromatin-Remodeling Factor BAZ1A in NeurodevelopmentAmmar Zaghlool, Jonatan Halvardson, Jin J Zhao, et al.
Nature Communications|February 3, 2022
CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generationsIda Höijer, Anastasia Emmanouilidou, Rebecka Östlund, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 8, 2008
Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndromeAdam Shlien, Uri Tabori, Christian R Marshall, et al.
Human Genetics|December 13, 2005
Towards compendia of negative genetic association studies: an example for Alzheimer diseaseMia E-L Blomqvist, Chandra Reynolds, Hagit Katzov, et al.
Clinical Genetics|December 8, 2018
Whole genome sequencing of consanguineous families reveals novel pathogenic variants in intellectual disabilityAnn-Charlotte Thuresson, Cecilia Soussi Zander, Jin J Zhao, et al.
European Journal of Human Genetics : EJHG|November 28, 2013
Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathyRonen Spiegel, Ann Saada, Jonatan Halvardson, et al.
Pageof 11