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Patrick Sulem

Showing results (211-220 of 260) with videos related to

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Nature Genetics|September 17, 2008
Sequence variant on 8q24 confers susceptibility to urinary bladder cancerLambertus A Kiemeney, Steinunn Thorlacius, Patrick Sulem, et al.
Nature Genetics|October 26, 2023
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without auraGyda Bjornsdottir, Mona A Chalmer, Lilja Stefansdottir, et al.
American Journal of Human Genetics|October 20, 2009
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinomaMaria Teresa Landi, Nilanjan Chatterjee, Kai Yu, et al.
Plos Genetics|July 28, 2010
Ancestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locusSimon N Stacey, Patrick Sulem, Carlo Zanon, 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.
Pageof 26

Showing results (211-220 of 260) with videos related to

Sort By:
Pageof 26
Nature Genetics|September 17, 2008
Sequence variant on 8q24 confers susceptibility to urinary bladder cancerLambertus A Kiemeney, Steinunn Thorlacius, Patrick Sulem, et al.
Nature Genetics|October 26, 2023
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without auraGyda Bjornsdottir, Mona A Chalmer, Lilja Stefansdottir, et al.
American Journal of Human Genetics|October 20, 2009
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinomaMaria Teresa Landi, Nilanjan Chatterjee, Kai Yu, et al.
Plos Genetics|July 28, 2010
Ancestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locusSimon N Stacey, Patrick Sulem, Carlo Zanon, 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.
Pageof 26