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Showing results (51-60 of 62) with videos related to

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Nature Genetics|November 14, 2025
Genome-wide association study and polygenic risk prediction of hypothyroidismSøren A Rand, Gustav Ahlberg, Vinicius Tragante, et al.
International Journal of Epidemiology|October 4, 2022
Cohort Profile: The Danish Blood Donor StudyChristian Erikstrup, Erik Sørensen, Kaspar R Nielsen, et al.
Cell|September 15, 2023
Complex effects of sequence variants on lipid levels and coronary artery diseaseAudunn S Snaebjarnarson, Anna Helgadottir, Gudny A Arnadottir, et al.
Circulation Research|October 7, 2022
Genetic Variants Close to <i>TTN</i>, <i>NKX2-5</i>, and <i>MYH6</i> Associate With AVNRTLaura Andreasen, Gustav Ahlberg, Hildur M Ægisdottir, 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.
JHEP Reports : Innovation in Hepatology|August 18, 2025
Genome-wide meta-analysis identifies nine loci associated with higher risk of hepatocellular carcinoma developmentJonas Ghouse, Helene Gellert-Kristensen, Colm J O'Rourke, et al.
Medrxiv : the Preprint Server for Health Sciences|September 26, 2025
The genetic architecture of fibromyalgia across 2.5 million individualsIsabel Kerrebijn, Gyda Bjornsdottir, Keon Arbabi, et al.
Nature Genetics|April 14, 2025
Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrumSamvida S Venkatesh, Laura B L Wittemans, Duncan S Palmer, et al.
Medrxiv : the Preprint Server for Health Sciences|April 2, 2024
Genome-wide analyses identify 21 infertility loci and over 400 reproductive hormone loci across the allele frequency spectrumSamvida S Venkatesh, Laura B L Wittemans, Duncan S Palmer, et al.
Nature Genetics|October 26, 2023
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without auraGyda Bjornsdottir, Mona A Chalmer, Lilja Stefansdottir, et al.
Pageof 7

Showing results (51-60 of 62) with videos related to

Sort By:
Pageof 7
Nature Genetics|November 14, 2025
Genome-wide association study and polygenic risk prediction of hypothyroidismSøren A Rand, Gustav Ahlberg, Vinicius Tragante, et al.
International Journal of Epidemiology|October 4, 2022
Cohort Profile: The Danish Blood Donor StudyChristian Erikstrup, Erik Sørensen, Kaspar R Nielsen, et al.
Cell|September 15, 2023
Complex effects of sequence variants on lipid levels and coronary artery diseaseAudunn S Snaebjarnarson, Anna Helgadottir, Gudny A Arnadottir, et al.
Circulation Research|October 7, 2022
Genetic Variants Close to <i>TTN</i>, <i>NKX2-5</i>, and <i>MYH6</i> Associate With AVNRTLaura Andreasen, Gustav Ahlberg, Hildur M Ægisdottir, 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.
JHEP Reports : Innovation in Hepatology|August 18, 2025
Genome-wide meta-analysis identifies nine loci associated with higher risk of hepatocellular carcinoma developmentJonas Ghouse, Helene Gellert-Kristensen, Colm J O'Rourke, et al.
Medrxiv : the Preprint Server for Health Sciences|September 26, 2025
The genetic architecture of fibromyalgia across 2.5 million individualsIsabel Kerrebijn, Gyda Bjornsdottir, Keon Arbabi, et al.
Nature Genetics|April 14, 2025
Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrumSamvida S Venkatesh, Laura B L Wittemans, Duncan S Palmer, et al.
Medrxiv : the Preprint Server for Health Sciences|April 2, 2024
Genome-wide analyses identify 21 infertility loci and over 400 reproductive hormone loci across the allele frequency spectrumSamvida S Venkatesh, Laura B L Wittemans, Duncan S Palmer, et al.
Nature Genetics|October 26, 2023
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without auraGyda Bjornsdottir, Mona A Chalmer, Lilja Stefansdottir, et al.
Pageof 7