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Nature Genetics
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August 29, 2024
Rare coding variant analysis for human diseases across biobanks and ancestries
Sean J Jurgens, Xin Wang, Seung Hoan Choi, et al.
Plos Genetics
|
September 3, 2016
Whole Exome Sequencing in Atrial Fibrillation
Steven A Lubitz, Jennifer A Brody, Nathan A Bihlmeyer, et al.
Nature Genetics
|
June 13, 2022
Genetic analysis of right heart structure and function in 40,000 people
James P Pirruccello, Paolo Di Achille, Victor Nauffal, et al.
Journal of the American College of Cardiology
|
June 6, 2020
Limitations of Contemporary Guidelines for Managing Patients at High Genetic Risk of Coronary Artery Disease
Krishna G Aragam, Amanda Dobbyn, Renae Judy, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 20, 2024
Rare genetic variation in VE-PTP is associated with central serous chorioretinopathy, venous dysfunction and glaucoma
Joel T Rämö, Bryan Gorman, Lu-Chen Weng, et al.
Circulation
|
November 13, 2020
Clinical Application of a Novel Genetic Risk Score for Ischemic Stroke in Patients With Cardiometabolic Disease
Nicholas A Marston, Parth N Patel, Frederick K Kamanu, et al.
Nature Genetics
|
November 27, 2021
Deep learning enables genetic analysis of the human thoracic aorta
James P Pirruccello, Mark D Chaffin, Elizabeth L Chou, et al.
Journal of Lipid Research
|
November 8, 2014
Genetic loci associated with circulating levels of very long-chain saturated fatty acids
Rozenn N Lemaitre, Irena B King, Edmond K Kabagambe, et al.
Nature Communications
|
May 3, 2025
Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucoma
Joel T Rämö, Bryan R Gorman, Lu-Chen Weng, et al.
Plos Genetics
|
August 11, 2011
Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium
Rozenn N Lemaitre, Toshiko Tanaka, Weihong Tang, et al.
Page
of 16
Search research articles
Search
Showing results (121-130 of 160) with videos related to
Sort By:
Page
of 16
Nature Genetics
|
August 29, 2024
Rare coding variant analysis for human diseases across biobanks and ancestries
Sean J Jurgens, Xin Wang, Seung Hoan Choi, et al.
Plos Genetics
|
September 3, 2016
Whole Exome Sequencing in Atrial Fibrillation
Steven A Lubitz, Jennifer A Brody, Nathan A Bihlmeyer, et al.
Nature Genetics
|
June 13, 2022
Genetic analysis of right heart structure and function in 40,000 people
James P Pirruccello, Paolo Di Achille, Victor Nauffal, et al.
Journal of the American College of Cardiology
|
June 6, 2020
Limitations of Contemporary Guidelines for Managing Patients at High Genetic Risk of Coronary Artery Disease
Krishna G Aragam, Amanda Dobbyn, Renae Judy, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 20, 2024
Rare genetic variation in VE-PTP is associated with central serous chorioretinopathy, venous dysfunction and glaucoma
Joel T Rämö, Bryan Gorman, Lu-Chen Weng, et al.
Circulation
|
November 13, 2020
Clinical Application of a Novel Genetic Risk Score for Ischemic Stroke in Patients With Cardiometabolic Disease
Nicholas A Marston, Parth N Patel, Frederick K Kamanu, et al.
Nature Genetics
|
November 27, 2021
Deep learning enables genetic analysis of the human thoracic aorta
James P Pirruccello, Mark D Chaffin, Elizabeth L Chou, et al.
Journal of Lipid Research
|
November 8, 2014
Genetic loci associated with circulating levels of very long-chain saturated fatty acids
Rozenn N Lemaitre, Irena B King, Edmond K Kabagambe, et al.
Nature Communications
|
May 3, 2025
Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucoma
Joel T Rämö, Bryan R Gorman, Lu-Chen Weng, et al.
Plos Genetics
|
August 11, 2011
Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium
Rozenn N Lemaitre, Toshiko Tanaka, Weihong Tang, et al.
Page
of 16