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Kari Stefansson

Showing results (31-40 of 687) with videos related to

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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.
Arthritis and Rheumatism|February 7, 2003
The inheritance of hand osteoarthritis in IcelandHelgi Jonsson, Ileana Manolescu, Stefan Einar Stefansson, et al.
Clinical Journal of the American Society of Nephrology : CJASN|April 27, 2022
GWAS of HematuriaSarah A Gagliano Taliun, Patrick Sulem, Gardar Sveinbjornsson, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|September 9, 2004
A genetic contribution to inflammatory bowel disease in Iceland: a genealogic approachInga Reynisdottir, Daniel F Gudbjartsson, Johann Heidar Johannsson, et al.
International Journal of Data Mining and Bioinformatics|October 23, 2015
The effect of SNPs on expression levels in Nimblegen RNA expression microarraysSigrun Helga Lund, Asgeir Sigurdsson, Sigurjon Axel Gudjonsson, et al.
Plos One|June 18, 2014
A method for detecting long non-coding RNAs with tiled RNA expression microarraysSigrun Helga Lund, Daniel Fannar Gudbjartsson, Thorunn Rafnar, et al.
Plos Genetics|June 21, 2008
A drastic reduction in the life span of cystatin C L68Q carriers due to life-style changes during the last two centuriesAstridur Palsdottir, Agnar Helgason, Snaebjorn Palsson, et al.
Nucleic Acids Research|December 5, 2003
A novel MALDI-TOF based methodology for genotyping single nucleotide polymorphismsThorarinn Blondal, Benedikt G Waage, Sigurdur V Smarason, et al.
Gene|November 6, 2004
Multiple novel transcription initiation sites for NRG1Valgerdur Steinthorsdottir, Hreinn Stefansson, Shyamali Ghosh, et al.
Molecular Psychiatry|September 23, 2022
Working memory and reaction time variability mediate the relationship between polygenic risk and ADHD traits in a general population sampleMia Moses, Jeggan Tiego, Ditte Demontis, et al.
Pageof 69

Showing results (31-40 of 687) with videos related to

Sort By:
Pageof 69
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.
Arthritis and Rheumatism|February 7, 2003
The inheritance of hand osteoarthritis in IcelandHelgi Jonsson, Ileana Manolescu, Stefan Einar Stefansson, et al.
Clinical Journal of the American Society of Nephrology : CJASN|April 27, 2022
GWAS of HematuriaSarah A Gagliano Taliun, Patrick Sulem, Gardar Sveinbjornsson, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|September 9, 2004
A genetic contribution to inflammatory bowel disease in Iceland: a genealogic approachInga Reynisdottir, Daniel F Gudbjartsson, Johann Heidar Johannsson, et al.
International Journal of Data Mining and Bioinformatics|October 23, 2015
The effect of SNPs on expression levels in Nimblegen RNA expression microarraysSigrun Helga Lund, Asgeir Sigurdsson, Sigurjon Axel Gudjonsson, et al.
Plos One|June 18, 2014
A method for detecting long non-coding RNAs with tiled RNA expression microarraysSigrun Helga Lund, Daniel Fannar Gudbjartsson, Thorunn Rafnar, et al.
Plos Genetics|June 21, 2008
A drastic reduction in the life span of cystatin C L68Q carriers due to life-style changes during the last two centuriesAstridur Palsdottir, Agnar Helgason, Snaebjorn Palsson, et al.
Nucleic Acids Research|December 5, 2003
A novel MALDI-TOF based methodology for genotyping single nucleotide polymorphismsThorarinn Blondal, Benedikt G Waage, Sigurdur V Smarason, et al.
Gene|November 6, 2004
Multiple novel transcription initiation sites for NRG1Valgerdur Steinthorsdottir, Hreinn Stefansson, Shyamali Ghosh, et al.
Molecular Psychiatry|September 23, 2022
Working memory and reaction time variability mediate the relationship between polygenic risk and ADHD traits in a general population sampleMia Moses, Jeggan Tiego, Ditte Demontis, et al.
Pageof 69