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Lars Feuk

Showing results (11-20 of 103) with videos related to

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Human Molecular Genetics|October 4, 2007
Copy-number variation in control population cohortsDalila Pinto, Christian Marshall, Lars Feuk, et al.
Human Mutation|December 24, 2002
Further evidence for role of a promoter variant in the TNFRSF6 gene in Alzheimer diseaseLars Feuk, Jonathan A Prince, Kaj Blennow, et al.
Genes|December 3, 2020
Evaluation of Single-Molecule Sequencing Technologies for Structural Variant Detection in Two Swedish Human GenomesNazeefa Fatima, Anna Petri, Ulf Gyllensten, et al.
Genome Biology|July 27, 2010
Identification of novel exons and transcribed regions by chimpanzee transcriptome sequencingAnna Wetterbom, Adam Ameur, Lars Feuk, et al.
Human Genomics|July 20, 2006
Strategies for the detection of copy number and other structural variants in the human genomeAndrew R Carson, Lars Feuk, Mansoor Mohammed, et al.
Human Molecular Genetics|May 3, 2006
Structural variants: changing the landscape of chromosomes and design of disease studiesLars Feuk, Christian R Marshall, Richard F Wintle, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 29, 2005
Mutation screening of a haplotype block around the insulin degrading enzyme gene and association with Alzheimer's diseaseLars Feuk, Shane McCarthy, Björn Andersson, et al.
Genomics|August 8, 2006
Frequent appearance of novel protein-coding sequences by frameshift translationKohji Okamura, Lars Feuk, Tomàs Marquès-Bonet, et al.
Human Genetics|December 14, 2020
Hybrid sequencing resolves two germline ultra-complex chromosomal rearrangements consisting of 137 breakpoint junctions in a single carrierJesper Eisfeldt, Maria Pettersson, Anna Petri, et al.
BMC Medical Genomics|June 27, 2020
Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variantsJoakim Klar, Helene Engstrand-Lilja, Khurram Maqbool, et al.
Pageof 11

Showing results (11-20 of 103) with videos related to

Sort By:
Pageof 11
Human Molecular Genetics|October 4, 2007
Copy-number variation in control population cohortsDalila Pinto, Christian Marshall, Lars Feuk, et al.
Human Mutation|December 24, 2002
Further evidence for role of a promoter variant in the TNFRSF6 gene in Alzheimer diseaseLars Feuk, Jonathan A Prince, Kaj Blennow, et al.
Genes|December 3, 2020
Evaluation of Single-Molecule Sequencing Technologies for Structural Variant Detection in Two Swedish Human GenomesNazeefa Fatima, Anna Petri, Ulf Gyllensten, et al.
Genome Biology|July 27, 2010
Identification of novel exons and transcribed regions by chimpanzee transcriptome sequencingAnna Wetterbom, Adam Ameur, Lars Feuk, et al.
Human Genomics|July 20, 2006
Strategies for the detection of copy number and other structural variants in the human genomeAndrew R Carson, Lars Feuk, Mansoor Mohammed, et al.
Human Molecular Genetics|May 3, 2006
Structural variants: changing the landscape of chromosomes and design of disease studiesLars Feuk, Christian R Marshall, Richard F Wintle, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 29, 2005
Mutation screening of a haplotype block around the insulin degrading enzyme gene and association with Alzheimer's diseaseLars Feuk, Shane McCarthy, Björn Andersson, et al.
Genomics|August 8, 2006
Frequent appearance of novel protein-coding sequences by frameshift translationKohji Okamura, Lars Feuk, Tomàs Marquès-Bonet, et al.
Human Genetics|December 14, 2020
Hybrid sequencing resolves two germline ultra-complex chromosomal rearrangements consisting of 137 breakpoint junctions in a single carrierJesper Eisfeldt, Maria Pettersson, Anna Petri, et al.
BMC Medical Genomics|June 27, 2020
Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variantsJoakim Klar, Helene Engstrand-Lilja, Khurram Maqbool, et al.
Pageof 11