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Patrick Sulem

Showing results (161-170 of 260) with videos related to

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European Heart Journal|July 24, 2020
Genetic variability in the absorption of dietary sterols affects the risk of coronary artery diseaseAnna Helgadottir, Gudmar Thorleifsson, Kristjan F Alexandersson, et al.
Obstetrical & Gynecological Survey|January 20, 2026
Sequence Diversity Lost in Early PregnancyGudny A Arnadottir, Hakon Johnsson, Tanja Schlaikjær Hartwig, et al.
Nature Communications|February 15, 2017
A genome-wide association study yields five novel thyroid cancer risk lociJulius Gudmundsson, Gudmar Thorleifsson, Jon K Sigurdsson, et al.
Nature Genetics|October 14, 2008
Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traitsSimon N Stacey, Daniel F Gudbjartsson, Patrick Sulem, et al.
Nature|June 26, 2020
FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid diseaseSaedis Saevarsdottir, Thorunn A Olafsdottir, Erna V Ivarsdottir, et al.
European Heart Journal|October 25, 2022
Genetic insight into sick sinus syndromeRosa B Thorolfsdottir, Gardar Sveinbjornsson, Hildur M Aegisdottir, et al.
Nature Genetics|September 22, 2009
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibilityJulius Gudmundsson, Patrick Sulem, Daniel F Gudbjartsson, et al.
Nature Communications|June 16, 2021
Molecular benchmarks of a SARS-CoV-2 epidemicHakon Jonsson, Olafur T Magnusson, Pall Melsted, et al.
The Journal of Allergy and Clinical Immunology|October 18, 2024
A partial loss-of-function variant in STAT6 protects against type 2 asthmaKatla Kristjansdottir, Gudmundur L Norddahl, Erna V Ivarsdottir, et al.
European Heart Journal|February 7, 2023
Genetic variants associated with syncope implicate neural and autonomic processesHildur M Aegisdottir, Rosa B Thorolfsdottir, Gardar Sveinbjornsson, et al.
Pageof 26

Showing results (161-170 of 260) with videos related to

Sort By:
Pageof 26
European Heart Journal|July 24, 2020
Genetic variability in the absorption of dietary sterols affects the risk of coronary artery diseaseAnna Helgadottir, Gudmar Thorleifsson, Kristjan F Alexandersson, et al.
Obstetrical & Gynecological Survey|January 20, 2026
Sequence Diversity Lost in Early PregnancyGudny A Arnadottir, Hakon Johnsson, Tanja Schlaikjær Hartwig, et al.
Nature Communications|February 15, 2017
A genome-wide association study yields five novel thyroid cancer risk lociJulius Gudmundsson, Gudmar Thorleifsson, Jon K Sigurdsson, et al.
Nature Genetics|October 14, 2008
Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traitsSimon N Stacey, Daniel F Gudbjartsson, Patrick Sulem, et al.
Nature|June 26, 2020
FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid diseaseSaedis Saevarsdottir, Thorunn A Olafsdottir, Erna V Ivarsdottir, et al.
European Heart Journal|October 25, 2022
Genetic insight into sick sinus syndromeRosa B Thorolfsdottir, Gardar Sveinbjornsson, Hildur M Aegisdottir, et al.
Nature Genetics|September 22, 2009
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibilityJulius Gudmundsson, Patrick Sulem, Daniel F Gudbjartsson, et al.
Nature Communications|June 16, 2021
Molecular benchmarks of a SARS-CoV-2 epidemicHakon Jonsson, Olafur T Magnusson, Pall Melsted, et al.
The Journal of Allergy and Clinical Immunology|October 18, 2024
A partial loss-of-function variant in STAT6 protects against type 2 asthmaKatla Kristjansdottir, Gudmundur L Norddahl, Erna V Ivarsdottir, et al.
European Heart Journal|February 7, 2023
Genetic variants associated with syncope implicate neural and autonomic processesHildur M Aegisdottir, Rosa B Thorolfsdottir, Gardar Sveinbjornsson, et al.
Pageof 26