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Patrick Sulem

Showing results (141-150 of 260) with videos related to

Pageof 26
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Nature|September 11, 2024
Genetic links between ovarian ageing, cancer risk and de novo mutation ratesStasa Stankovic, Saleh Shekari, Qin Qin Huang, et al.
Plos Genetics|June 14, 2012
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseasesRui Li, Felix F Brockschmidt, Amy K Kiefer, et al.
Human Molecular Genetics|December 1, 2025
Observational and Mendelian randomization studies of plasma sclerostin levels do not provide evidence of cardiovascular adverse effects of sclerostin inhibitionRosa B Thorolfsdottir, Gardar Sveinbjornsson, Grimur Hjorleifsson Eldjarn, et al.
Plos Genetics|March 9, 2017
A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthmaDirk Smith, Hannes Helgason, Patrick Sulem, et al.
Nature Genetics|April 9, 2008
Many sequence variants affecting diversity of adult human heightDaniel F Gudbjartsson, G Bragi Walters, Gudmar Thorleifsson, et al.
Nature Genetics|February 10, 2009
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populationsJulius Gudmundsson, Patrick Sulem, Daniel F Gudbjartsson, et al.
Nature Communications|September 14, 2024
Sequence variants influencing the regulation of serum IgG subclass levelsThorunn A Olafsdottir, Gudmar Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, et al.
Communications Biology|July 10, 2023
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticariaRagnar P Kristjansson, Gudjon R Oskarsson, Astros Skuladottir, et al.
Nature|July 3, 2007
Variants conferring risk of atrial fibrillation on chromosome 4q25Daniel F Gudbjartsson, David O Arnar, Anna Helgadottir, et al.
Nature Genetics|December 3, 2021
Large-scale integration of the plasma proteome with genetics and diseaseEgil Ferkingstad, Patrick Sulem, Bjarni A Atlason, et al.
Pageof 26

Showing results (141-150 of 260) with videos related to

Sort By:
Pageof 26
Nature|September 11, 2024
Genetic links between ovarian ageing, cancer risk and de novo mutation ratesStasa Stankovic, Saleh Shekari, Qin Qin Huang, et al.
Plos Genetics|June 14, 2012
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseasesRui Li, Felix F Brockschmidt, Amy K Kiefer, et al.
Human Molecular Genetics|December 1, 2025
Observational and Mendelian randomization studies of plasma sclerostin levels do not provide evidence of cardiovascular adverse effects of sclerostin inhibitionRosa B Thorolfsdottir, Gardar Sveinbjornsson, Grimur Hjorleifsson Eldjarn, et al.
Plos Genetics|March 9, 2017
A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthmaDirk Smith, Hannes Helgason, Patrick Sulem, et al.
Nature Genetics|April 9, 2008
Many sequence variants affecting diversity of adult human heightDaniel F Gudbjartsson, G Bragi Walters, Gudmar Thorleifsson, et al.
Nature Genetics|February 10, 2009
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populationsJulius Gudmundsson, Patrick Sulem, Daniel F Gudbjartsson, et al.
Nature Communications|September 14, 2024
Sequence variants influencing the regulation of serum IgG subclass levelsThorunn A Olafsdottir, Gudmar Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, et al.
Communications Biology|July 10, 2023
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticariaRagnar P Kristjansson, Gudjon R Oskarsson, Astros Skuladottir, et al.
Nature|July 3, 2007
Variants conferring risk of atrial fibrillation on chromosome 4q25Daniel F Gudbjartsson, David O Arnar, Anna Helgadottir, et al.
Nature Genetics|December 3, 2021
Large-scale integration of the plasma proteome with genetics and diseaseEgil Ferkingstad, Patrick Sulem, Bjarni A Atlason, et al.
Pageof 26