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Sulem

Showing results (131-140 of 322) with videos related to

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Nature|September 30, 2017
Parental influence on human germline de novo mutations in 1,548 trios from IcelandHákon Jónsson, Patrick Sulem, Birte Kehr, et al.
Nature Communications|August 29, 2018
MAP1B mutations cause intellectual disability and extensive white matter deficitG Bragi Walters, Omar Gustafsson, Gardar Sveinbjornsson, et al.
Nature Genetics|October 31, 2018
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritisUnnur Styrkarsdottir, Sigrun H Lund, Gudmar Thorleifsson, et al.
European Journal of Human Genetics : EJHG|August 31, 2021
Sequence variants in malignant hyperthermia genes in Iceland: classification and actionable findings in a population databaseRun Fridriksdottir, Arnar J Jonsson, Brynjar O Jensson, et al.
Current Biology : CB|October 9, 2020
Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and NamingRosa S Gisladottir, Erna V Ivarsdottir, Agnar Helgason, et al.
Brain Communications|November 23, 2022
Thirty novel sequence variants impacting human intracranial volumeMuhammad Sulaman Nawaz, Gudmundur Einarsson, Mariana Bustamante, et al.
Nature Structural & Molecular Biology|January 29, 2024
Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombinationValgerdur Steinthorsdottir, Bjarni V Halldorsson, Hakon Jonsson, et al.
Nature Genetics|March 26, 2025
Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorderThorgeir E Thorgeirsson, Vinicius Tragante, Gardar Sveinbjornsson, et al.
Nature Communications|November 14, 2013
A common variant at 8q24.21 is associated with renal cell cancerJulius Gudmundsson, Patrick Sulem, Daniel F Gudbjartsson, et al.
Circulation. Genomic and Precision Medicine|December 14, 2020
Lifelong Reduction in LDL (Low-Density Lipoprotein) Cholesterol due to a Gain-of-Function Mutation in <i>LDLR</i>Eythor Bjornsson, Kristbjorg Gunnarsdottir, Gisli H Halldorsson, et al.
Pageof 33

Showing results (131-140 of 322) with videos related to

Sort By:
Pageof 33
Nature|September 30, 2017
Parental influence on human germline de novo mutations in 1,548 trios from IcelandHákon Jónsson, Patrick Sulem, Birte Kehr, et al.
Nature Communications|August 29, 2018
MAP1B mutations cause intellectual disability and extensive white matter deficitG Bragi Walters, Omar Gustafsson, Gardar Sveinbjornsson, et al.
Nature Genetics|October 31, 2018
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritisUnnur Styrkarsdottir, Sigrun H Lund, Gudmar Thorleifsson, et al.
European Journal of Human Genetics : EJHG|August 31, 2021
Sequence variants in malignant hyperthermia genes in Iceland: classification and actionable findings in a population databaseRun Fridriksdottir, Arnar J Jonsson, Brynjar O Jensson, et al.
Current Biology : CB|October 9, 2020
Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and NamingRosa S Gisladottir, Erna V Ivarsdottir, Agnar Helgason, et al.
Brain Communications|November 23, 2022
Thirty novel sequence variants impacting human intracranial volumeMuhammad Sulaman Nawaz, Gudmundur Einarsson, Mariana Bustamante, et al.
Nature Structural & Molecular Biology|January 29, 2024
Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombinationValgerdur Steinthorsdottir, Bjarni V Halldorsson, Hakon Jonsson, et al.
Nature Genetics|March 26, 2025
Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorderThorgeir E Thorgeirsson, Vinicius Tragante, Gardar Sveinbjornsson, et al.
Nature Communications|November 14, 2013
A common variant at 8q24.21 is associated with renal cell cancerJulius Gudmundsson, Patrick Sulem, Daniel F Gudbjartsson, et al.
Circulation. Genomic and Precision Medicine|December 14, 2020
Lifelong Reduction in LDL (Low-Density Lipoprotein) Cholesterol due to a Gain-of-Function Mutation in <i>LDLR</i>Eythor Bjornsson, Kristbjorg Gunnarsdottir, Gisli H Halldorsson, et al.
Pageof 33