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Hreinn Stefansson

Showing results (1-10 of 183) with videos related to

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Biological Psychiatry|June 18, 2021
Cognition in SchizophreniaHreinn Stefansson, Kari Stefansson
Annals of Medicine|March 6, 2004
Neuregulin 1 and schizophreniaHreinn Stefansson, Valgerdur Steinthorsdottir, Thorgeir E Thorgeirsson, et al.
Journal of Learning Disabilities|March 5, 2013
The Adult Reading History Questionnaire (ARHQ) in Icelandic: Psychometric Properties and Factor StructureGyda Bjornsdottir, Jonas G Halldorsson, Stacy Steinberg, et al.
Human Molecular Genetics|July 19, 2015
Heterozygote carriers for CNVs in PARK2 are at increased risk of Parkinson's diseaseJohanna Huttenlocher, Hreinn Stefansson, Stacy Steinberg, et al.
Human Molecular Genetics|March 16, 2004
A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration)Ragnheidur Fossdal, Fridbert Jonasson, Gudlaug T Kristjansdottir, et al.
Biological Psychiatry|April 15, 2011
Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patientsJacobine E Buizer-Voskamp, Jan-Willem Muntjewerff, , et al.
BMC Bioinformatics|January 23, 2026
CNValidatron: accurate and efficient validation of PennCNV calls using computer visionSimone Montalbano, G Bragi Walters, Gudbjorn F Jonsson, et al.
Gene|November 6, 2004
Multiple novel transcription initiation sites for NRG1Valgerdur Steinthorsdottir, Hreinn Stefansson, Shyamali Ghosh, et al.
American Journal of Medical Genetics. Part A|February 13, 2009
A chromosome 10 variant with a 12 Mb inversion [inv(10)(q11.22q21.1)] identical by descent and frequent in the Swedish populationMiriam Entesarian, Birgit Carlsson, Mahmoud Reza Mansouri, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
CNValidatron: Accurate And Efficient Validation of PennCNV Calls Using Computer VisionSimone Montalbano, G Bragi Walters, Gudbjorn F Jonsson, et al.
Pageof 19

Showing results (1-10 of 183) with videos related to

Sort By:
Pageof 19
Biological Psychiatry|June 18, 2021
Cognition in SchizophreniaHreinn Stefansson, Kari Stefansson
Annals of Medicine|March 6, 2004
Neuregulin 1 and schizophreniaHreinn Stefansson, Valgerdur Steinthorsdottir, Thorgeir E Thorgeirsson, et al.
Journal of Learning Disabilities|March 5, 2013
The Adult Reading History Questionnaire (ARHQ) in Icelandic: Psychometric Properties and Factor StructureGyda Bjornsdottir, Jonas G Halldorsson, Stacy Steinberg, et al.
Human Molecular Genetics|July 19, 2015
Heterozygote carriers for CNVs in PARK2 are at increased risk of Parkinson's diseaseJohanna Huttenlocher, Hreinn Stefansson, Stacy Steinberg, et al.
Human Molecular Genetics|March 16, 2004
A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration)Ragnheidur Fossdal, Fridbert Jonasson, Gudlaug T Kristjansdottir, et al.
Biological Psychiatry|April 15, 2011
Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patientsJacobine E Buizer-Voskamp, Jan-Willem Muntjewerff, , et al.
BMC Bioinformatics|January 23, 2026
CNValidatron: accurate and efficient validation of PennCNV calls using computer visionSimone Montalbano, G Bragi Walters, Gudbjorn F Jonsson, et al.
Gene|November 6, 2004
Multiple novel transcription initiation sites for NRG1Valgerdur Steinthorsdottir, Hreinn Stefansson, Shyamali Ghosh, et al.
American Journal of Medical Genetics. Part A|February 13, 2009
A chromosome 10 variant with a 12 Mb inversion [inv(10)(q11.22q21.1)] identical by descent and frequent in the Swedish populationMiriam Entesarian, Birgit Carlsson, Mahmoud Reza Mansouri, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
CNValidatron: Accurate And Efficient Validation of PennCNV Calls Using Computer VisionSimone Montalbano, G Bragi Walters, Gudbjorn F Jonsson, et al.
Pageof 19