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Lincoln Nadauld

Showing results (11-20 of 19) with videos related to

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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.
European Journal of Preventive Cardiology|September 20, 2022
Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles: a Mendelian randomization analysisAnna Helgadottir, Gudmar Thorleifsson, Audunn Snaebjarnarson, et al.
Nature Genetics|January 19, 2023
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolismJonas Ghouse, Vinicius Tragante, Gustav Ahlberg, et al.
Journal of Cancer Research and Clinical Oncology|August 8, 2023
Multidimensional biomarker predicts disease control in response to immunotherapy in recurrent or metastatic head and neck squamous-cell carcinomaKevin C Flanagan, Jon Earls, Ian Schillebeeckx, et al.
Nature Genetics|October 25, 2022
Multiomics study of nonalcoholic fatty liver diseaseGardar Sveinbjornsson, Magnus O Ulfarsson, Rosa B Thorolfsdottir, et al.
Nature Genetics|April 17, 2024
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosisJonas Ghouse, Gardar Sveinbjörnsson, Marijana Vujkovic, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Biallelic variants in <i>POPDC2</i> cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
American Journal of Human Genetics|May 23, 2025
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
Nature Genetics|December 19, 2025
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease predictionAeron M Small, Ta-Yu Yang, Shinsuke Itoh, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
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.
European Journal of Preventive Cardiology|September 20, 2022
Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles: a Mendelian randomization analysisAnna Helgadottir, Gudmar Thorleifsson, Audunn Snaebjarnarson, et al.
Nature Genetics|January 19, 2023
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolismJonas Ghouse, Vinicius Tragante, Gustav Ahlberg, et al.
Journal of Cancer Research and Clinical Oncology|August 8, 2023
Multidimensional biomarker predicts disease control in response to immunotherapy in recurrent or metastatic head and neck squamous-cell carcinomaKevin C Flanagan, Jon Earls, Ian Schillebeeckx, et al.
Nature Genetics|October 25, 2022
Multiomics study of nonalcoholic fatty liver diseaseGardar Sveinbjornsson, Magnus O Ulfarsson, Rosa B Thorolfsdottir, et al.
Nature Genetics|April 17, 2024
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosisJonas Ghouse, Gardar Sveinbjörnsson, Marijana Vujkovic, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Biallelic variants in <i>POPDC2</i> cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
American Journal of Human Genetics|May 23, 2025
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
Nature Genetics|December 19, 2025
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease predictionAeron M Small, Ta-Yu Yang, Shinsuke Itoh, et al.
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