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Plos Genetics
|
June 12, 2013
Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets
Niels Grarup, Patrick Sulem, Camilla H Sandholt, et al.
Communications Biology
|
June 10, 2021
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis
Erna V Ivarsdottir, Hilma Holm, Stefania Benonisdottir, et al.
Nature
|
September 30, 2017
Parental influence on human germline de novo mutations in 1,548 trios from Iceland
Hákon Jónsson, Patrick Sulem, Birte Kehr, et al.
Nature Communications
|
August 29, 2018
MAP1B mutations cause intellectual disability and extensive white matter deficit
G 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 osteoarthritis
Unnur 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 database
Run 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 Naming
Rosa S Gisladottir, Erna V Ivarsdottir, Agnar Helgason, et al.
Brain Communications
|
November 23, 2022
Thirty novel sequence variants impacting human intracranial volume
Muhammad 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 recombination
Valgerdur 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 disorder
Thorgeir E Thorgeirsson, Vinicius Tragante, Gardar Sveinbjornsson, et al.
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of 28
Search research articles
Search
Showing results (81-90 of 280) with videos related to
Sort By:
Page
of 28
Plos Genetics
|
June 12, 2013
Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets
Niels Grarup, Patrick Sulem, Camilla H Sandholt, et al.
Communications Biology
|
June 10, 2021
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis
Erna V Ivarsdottir, Hilma Holm, Stefania Benonisdottir, et al.
Nature
|
September 30, 2017
Parental influence on human germline de novo mutations in 1,548 trios from Iceland
Hákon Jónsson, Patrick Sulem, Birte Kehr, et al.
Nature Communications
|
August 29, 2018
MAP1B mutations cause intellectual disability and extensive white matter deficit
G 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 osteoarthritis
Unnur 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 database
Run 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 Naming
Rosa S Gisladottir, Erna V Ivarsdottir, Agnar Helgason, et al.
Brain Communications
|
November 23, 2022
Thirty novel sequence variants impacting human intracranial volume
Muhammad 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 recombination
Valgerdur 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 disorder
Thorgeir E Thorgeirsson, Vinicius Tragante, Gardar Sveinbjornsson, et al.
Page
of 28