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Lars Feuk

Showing results (81-90 of 103) with videos related to

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Genome Research|July 1, 2006
Copy number variation: new insights in genome diversityJennifer L Freeman, George H Perry, Lars Feuk, et al.
BMC Research Notes|October 11, 2023
Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REHMariya Lysenkova Wiklander, Elin Övernäs, Johanna Lagensjö, et al.
Nature Genetics|November 23, 2006
Genome assembly comparison identifies structural variants in the human genomeRazi Khaja, Junjun Zhang, Jeffrey R MacDonald, et al.
Human Mutation|August 20, 2015
Diagnostic interpretation of array data using public databases and internet sourcesNicole de Leeuw, Trijnie Dijkhuizen, Jayne Y Hehir-Kwa, et al.
American Journal of Human Genetics|April 17, 2012
Genetic adaptation of fatty-acid metabolism: a human-specific haplotype increasing the biosynthesis of long-chain omega-3 and omega-6 fatty acidsAdam Ameur, Stefan Enroth, Asa Johansson, et al.
American Journal of Human Genetics|October 13, 2006
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxiaLars Feuk, Aino Kalervo, Marita Lipsanen-Nyman, et al.
Nature Biotechnology|May 10, 2011
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variantsDalila Pinto, Katayoon Darvishi, Xinghua Shi, et al.
Human Molecular Genetics|December 24, 2004
Elevated amyloid beta protein (Abeta42) and late onset Alzheimer's disease are associated with single nucleotide polymorphisms in the urokinase-type plasminogen activator geneNilüfer Ertekin-Taner, James Ronald, Lars Feuk, et al.
European Journal of Human Genetics : EJHG|August 24, 2017
SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish populationAdam Ameur, Johan Dahlberg, Pall Olason, et al.
Genome Research|November 24, 2006
Accurate and reliable high-throughput detection of copy number variation in the human genomeHeike Fiegler, Richard Redon, Dan Andrews, et al.
Pageof 11

Showing results (81-90 of 103) with videos related to

Sort By:
Pageof 11
Genome Research|July 1, 2006
Copy number variation: new insights in genome diversityJennifer L Freeman, George H Perry, Lars Feuk, et al.
BMC Research Notes|October 11, 2023
Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REHMariya Lysenkova Wiklander, Elin Övernäs, Johanna Lagensjö, et al.
Nature Genetics|November 23, 2006
Genome assembly comparison identifies structural variants in the human genomeRazi Khaja, Junjun Zhang, Jeffrey R MacDonald, et al.
Human Mutation|August 20, 2015
Diagnostic interpretation of array data using public databases and internet sourcesNicole de Leeuw, Trijnie Dijkhuizen, Jayne Y Hehir-Kwa, et al.
American Journal of Human Genetics|April 17, 2012
Genetic adaptation of fatty-acid metabolism: a human-specific haplotype increasing the biosynthesis of long-chain omega-3 and omega-6 fatty acidsAdam Ameur, Stefan Enroth, Asa Johansson, et al.
American Journal of Human Genetics|October 13, 2006
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxiaLars Feuk, Aino Kalervo, Marita Lipsanen-Nyman, et al.
Nature Biotechnology|May 10, 2011
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variantsDalila Pinto, Katayoon Darvishi, Xinghua Shi, et al.
Human Molecular Genetics|December 24, 2004
Elevated amyloid beta protein (Abeta42) and late onset Alzheimer's disease are associated with single nucleotide polymorphisms in the urokinase-type plasminogen activator geneNilüfer Ertekin-Taner, James Ronald, Lars Feuk, et al.
European Journal of Human Genetics : EJHG|August 24, 2017
SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish populationAdam Ameur, Johan Dahlberg, Pall Olason, et al.
Genome Research|November 24, 2006
Accurate and reliable high-throughput detection of copy number variation in the human genomeHeike Fiegler, Richard Redon, Dan Andrews, et al.
Pageof 11