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Lars Feuk

Showing results (71-80 of 103) with videos related to

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Journal of Medical Genetics|June 24, 2016
Mutations in HECW2 are associated with intellectual disability and epilepsyJonatan Halvardson, Jin J Zhao, Ammar Zaghlool, et al.
The Journal of Clinical Investigation|October 21, 2014
Abolished InsP3R2 function inhibits sweat secretion in both humans and miceJoakim Klar, Chihiro Hisatsune, Shahid M Baig, et al.
Genome Biology|December 2, 2020
Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activityIda Höijer, Josefin Johansson, Sanna Gudmundsson, et al.
Nature Genetics|September 30, 2010
Public data archives for genomic structural variationDeanna M Church, Ilkka Lappalainen, Tam P Sneddon, et al.
Bioinformatics (Oxford, England)|February 19, 2026
Nallo: a Nextflow pipeline for comprehensive human long-read genome analysisFelix Lenner, Anders Jemt, Lucia Peña Pérez, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 10, 2017
Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disabilityJin J Zhao, Jonatan Halvardson, Cecilia S Zander, et al.
Human Molecular Genetics|April 2, 2003
Haplotypes extending across ACE are associated with Alzheimer's diseasePatrick G Kehoe, Hagit Katzov, Lars Feuk, et al.
Neurobiology of Aging|February 19, 2005
Sequence variants of IDE are associated with the extent of beta-amyloid deposition in the Alzheimer's disease brainMia E-L Blomqvist, Katy Chalmers, Niels Andreasen, et al.
Nature Communications|August 24, 2023
Long-read whole-genome analysis of human single cellsJoanna Hård, Jeff E Mold, Jesper Eisfeldt, et al.
Genome Biology|May 21, 2010
Towards a comprehensive structural variation map of an individual human genomeAndy W Pang, Jeffrey R MacDonald, Dalila Pinto, et al.
Pageof 11

Showing results (71-80 of 103) with videos related to

Sort By:
Pageof 11
Journal of Medical Genetics|June 24, 2016
Mutations in HECW2 are associated with intellectual disability and epilepsyJonatan Halvardson, Jin J Zhao, Ammar Zaghlool, et al.
The Journal of Clinical Investigation|October 21, 2014
Abolished InsP3R2 function inhibits sweat secretion in both humans and miceJoakim Klar, Chihiro Hisatsune, Shahid M Baig, et al.
Genome Biology|December 2, 2020
Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activityIda Höijer, Josefin Johansson, Sanna Gudmundsson, et al.
Nature Genetics|September 30, 2010
Public data archives for genomic structural variationDeanna M Church, Ilkka Lappalainen, Tam P Sneddon, et al.
Bioinformatics (Oxford, England)|February 19, 2026
Nallo: a Nextflow pipeline for comprehensive human long-read genome analysisFelix Lenner, Anders Jemt, Lucia Peña Pérez, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 10, 2017
Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disabilityJin J Zhao, Jonatan Halvardson, Cecilia S Zander, et al.
Human Molecular Genetics|April 2, 2003
Haplotypes extending across ACE are associated with Alzheimer's diseasePatrick G Kehoe, Hagit Katzov, Lars Feuk, et al.
Neurobiology of Aging|February 19, 2005
Sequence variants of IDE are associated with the extent of beta-amyloid deposition in the Alzheimer's disease brainMia E-L Blomqvist, Katy Chalmers, Niels Andreasen, et al.
Nature Communications|August 24, 2023
Long-read whole-genome analysis of human single cellsJoanna Hård, Jeff E Mold, Jesper Eisfeldt, et al.
Genome Biology|May 21, 2010
Towards a comprehensive structural variation map of an individual human genomeAndy W Pang, Jeffrey R MacDonald, Dalila Pinto, et al.
Pageof 11