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Sulem

Showing results (201-210 of 323) with videos related to

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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.
Nature Genetics|August 27, 2024
Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiencyAsmundur Oddsson, Valgerdur Steinthorsdottir, Gudjon R Oskarsson, et al.
The New England Journal of Medicine|November 8, 2023
Actionable Genotypes and Their Association with Life Span in IcelandBrynjar O Jensson, Gudny A Arnadottir, Hildigunnur Katrinardottir, et al.
Nature|May 21, 2025
Sequence diversity lost in early pregnancyGudny A Arnadottir, Hakon Jonsson, Tanja Schlaikjær Hartwig, et al.
Plos One|June 8, 2010
Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studiesKatherine S Elliott, Eleftheria Zeggini, Mark I McCarthy, et al.
Nature Communications|April 10, 2015
New basal cell carcinoma susceptibility lociSimon N Stacey, Hannes Helgason, Sigurjon A Gudjonsson, et al.
Pageof 33

Showing results (201-210 of 323) with videos related to

Sort By:
Pageof 33
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.
Nature Genetics|August 27, 2024
Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiencyAsmundur Oddsson, Valgerdur Steinthorsdottir, Gudjon R Oskarsson, et al.
The New England Journal of Medicine|November 8, 2023
Actionable Genotypes and Their Association with Life Span in IcelandBrynjar O Jensson, Gudny A Arnadottir, Hildigunnur Katrinardottir, et al.
Nature|May 21, 2025
Sequence diversity lost in early pregnancyGudny A Arnadottir, Hakon Jonsson, Tanja Schlaikjær Hartwig, et al.
Plos One|June 8, 2010
Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studiesKatherine S Elliott, Eleftheria Zeggini, Mark I McCarthy, et al.
Nature Communications|April 10, 2015
New basal cell carcinoma susceptibility lociSimon N Stacey, Hannes Helgason, Sigurjon A Gudjonsson, et al.
Pageof 33