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Susan Redline

Showing results (851-860 of 959) with videos related to

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Frontiers in Endocrinology|May 20, 2022
The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry PopulationsZhe Wang, Shing Wan Choi, Nathalie Chami, et al.
Research Square|September 15, 2025
Wearable-derived Sleep Measurements are Associated with Long-COVID in the RECOVER Adult CohortSairam Parthasarathy, Shari Brosnahan, Solveig Sieberts, et al.
Nature Communications|May 7, 2024
Determinants of mosaic chromosomal alteration fitnessYash Pershad, Taralynn Mack, Hannah Poisner, et al.
Plos Genetics|April 17, 2019
Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleepBrian E Cade, Han Chen, Adrienne M Stilp, et al.
American Journal of Human Genetics|January 15, 2019
Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing StudiesHan Chen, Jennifer E Huffman, Jennifer A Brody, et al.
Frontiers in Genetics|January 1, 2024
Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine programNicole D Armstrong, Vinodh Srinivasasainagendra, Farah Ammous, et al.
Cancer Causes & Control : CCC|February 5, 2013
The 2011-2016 Transdisciplinary Research on Energetics and Cancer (TREC) initiative: rationale and designRuth E Patterson, Graham A Colditz, Frank B Hu, et al.
Nature Communications|August 30, 2022
Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genesJennifer L Halford, Valerie N Morrill, Seung Hoan Choi, et al.
Circulation. Genomic and Precision Medicine|July 28, 2021
Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry AnalysisSeung Hoan Choi, Sean J Jurgens, Christopher M Haggerty, et al.
Nature Genetics|October 31, 2023
Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencingYasminka A Jakubek, Ying Zhou, Adrienne Stilp, et al.
Pageof 96

Showing results (851-860 of 959) with videos related to

Sort By:
Pageof 96
Frontiers in Endocrinology|May 20, 2022
The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry PopulationsZhe Wang, Shing Wan Choi, Nathalie Chami, et al.
Research Square|September 15, 2025
Wearable-derived Sleep Measurements are Associated with Long-COVID in the RECOVER Adult CohortSairam Parthasarathy, Shari Brosnahan, Solveig Sieberts, et al.
Nature Communications|May 7, 2024
Determinants of mosaic chromosomal alteration fitnessYash Pershad, Taralynn Mack, Hannah Poisner, et al.
Plos Genetics|April 17, 2019
Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleepBrian E Cade, Han Chen, Adrienne M Stilp, et al.
American Journal of Human Genetics|January 15, 2019
Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing StudiesHan Chen, Jennifer E Huffman, Jennifer A Brody, et al.
Frontiers in Genetics|January 1, 2024
Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine programNicole D Armstrong, Vinodh Srinivasasainagendra, Farah Ammous, et al.
Cancer Causes & Control : CCC|February 5, 2013
The 2011-2016 Transdisciplinary Research on Energetics and Cancer (TREC) initiative: rationale and designRuth E Patterson, Graham A Colditz, Frank B Hu, et al.
Nature Communications|August 30, 2022
Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genesJennifer L Halford, Valerie N Morrill, Seung Hoan Choi, et al.
Circulation. Genomic and Precision Medicine|July 28, 2021
Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry AnalysisSeung Hoan Choi, Sean J Jurgens, Christopher M Haggerty, et al.
Nature Genetics|October 31, 2023
Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencingYasminka A Jakubek, Ying Zhou, Adrienne Stilp, et al.
Pageof 96