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Sulem

Showing results (271-280 of 323) with videos related to

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The New England Journal of Medicine|June 20, 2024
Homozygosity for R47H in <i>TREM2</i> and the Risk of Alzheimer's DiseaseHreinn Stefansson, G Bragi Walters, Gardar Sveinbjornsson, et al.
Nature Communications|January 23, 2026
De novo variants in the splicing factor gene SF3B1 are associated with neurodevelopmental disordersKevin Uguen, Tiffany Bergot, Marie-Pier Scott-Boyer, et al.
Human Molecular Genetics|January 12, 2013
A genome-wide association study of early menopause and the combined impact of identified variantsJohn R B Perry, Tanguy Corre, Tõnu Esko, et al.
Communications Biology|December 6, 2024
Novel loci and biomedical consequences of iron homoeostasis variationElias Allara, Steven Bell, Rebecca Smith, et al.
Human Molecular Genetics|May 28, 2014
Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancerThorunn Rafnar, Patrick Sulem, Gudmar Thorleifsson, et al.
Nature Genetics|February 12, 2008
Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancerJulius Gudmundsson, Patrick Sulem, Thorunn Rafnar, et al.
Nature Communications|March 26, 2025
Missense variants in FRS3 affect body mass index in populations of diverse ancestriesAndrea B Jonsdottir, Gardar Sveinbjornsson, Rosa B Thorolfsdottir, et al.
Nature Communications|June 10, 2023
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethalityAsmundur Oddsson, Patrick Sulem, Gardar Sveinbjornsson, et al.
Nature Communications|July 3, 2023
Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethalityAsmundur Oddsson, Patrick Sulem, Gardar Sveinbjornsson, et al.
Nature Genetics|February 10, 2009
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarctionDaniel F Gudbjartsson, Unnur S Bjornsdottir, Eva Halapi, et al.
Pageof 33

Showing results (271-280 of 323) with videos related to

Sort By:
Pageof 33
The New England Journal of Medicine|June 20, 2024
Homozygosity for R47H in <i>TREM2</i> and the Risk of Alzheimer's DiseaseHreinn Stefansson, G Bragi Walters, Gardar Sveinbjornsson, et al.
Nature Communications|January 23, 2026
De novo variants in the splicing factor gene SF3B1 are associated with neurodevelopmental disordersKevin Uguen, Tiffany Bergot, Marie-Pier Scott-Boyer, et al.
Human Molecular Genetics|January 12, 2013
A genome-wide association study of early menopause and the combined impact of identified variantsJohn R B Perry, Tanguy Corre, Tõnu Esko, et al.
Communications Biology|December 6, 2024
Novel loci and biomedical consequences of iron homoeostasis variationElias Allara, Steven Bell, Rebecca Smith, et al.
Human Molecular Genetics|May 28, 2014
Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancerThorunn Rafnar, Patrick Sulem, Gudmar Thorleifsson, et al.
Nature Genetics|February 12, 2008
Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancerJulius Gudmundsson, Patrick Sulem, Thorunn Rafnar, et al.
Nature Communications|March 26, 2025
Missense variants in FRS3 affect body mass index in populations of diverse ancestriesAndrea B Jonsdottir, Gardar Sveinbjornsson, Rosa B Thorolfsdottir, et al.
Nature Communications|June 10, 2023
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethalityAsmundur Oddsson, Patrick Sulem, Gardar Sveinbjornsson, et al.
Nature Communications|July 3, 2023
Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethalityAsmundur Oddsson, Patrick Sulem, Gardar Sveinbjornsson, et al.
Nature Genetics|February 10, 2009
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarctionDaniel F Gudbjartsson, Unnur S Bjornsdottir, Eva Halapi, et al.
Pageof 33