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Showing results (411-420 of 488) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|August 30, 2023
Rare damaging <i>CCR2</i> variants are associated with lower lifetime cardiovascular riskMarios K Georgakis, Rainer Malik, Omar El Bounkari, et al.
Nature Genetics|August 26, 2020
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scaleXihao Li, Zilin Li, Hufeng Zhou, et al.
Journal of the American Heart Association|February 14, 2025
Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural VariantsKruthika R Iyer, Shoa L Clarke, Rodrigo Guarischi-Sousa, et al.
Circulation. Genomic and Precision Medicine|November 28, 2023
Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical AtherosclerosisNatalie R Hasbani, Kenneth E Westerman, Soo Heon Kwak, et al.
Genome Medicine|March 22, 2025
Rare damaging CCR2 variants are associated with lower lifetime cardiovascular riskMarios K Georgakis, Rainer Malik, Omar El Bounkari, et al.
Nature Genetics|March 4, 2014
Loss-of-function mutations in SLC30A8 protect against type 2 diabetesJason Flannick, Gudmar Thorleifsson, Nicola L Beer, et al.
Nature Methods|October 27, 2022
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studiesZilin Li, Xihao Li, Hufeng Zhou, et al.
Medrxiv : the Preprint Server for Health Sciences|May 5, 2025
Genome-wide association study and multi-ancestry meta-analysis identify common variants associated with carotid artery intima-media thicknessDevendra Meena, Jian Huang, Marjan Zare, et al.
American Journal of Human Genetics|October 6, 2023
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing studyYuxuan Wang, Margaret Sunitha Selvaraj, Xihao Li, et al.
Stroke|July 14, 2018
Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance ImagingXueqiu Jian, Claudia L Satizabal, Albert V Smith, et al.
Pageof 49

Showing results (411-420 of 488) with videos related to

Sort By:
Pageof 49
Medrxiv : the Preprint Server for Health Sciences|August 30, 2023
Rare damaging <i>CCR2</i> variants are associated with lower lifetime cardiovascular riskMarios K Georgakis, Rainer Malik, Omar El Bounkari, et al.
Nature Genetics|August 26, 2020
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scaleXihao Li, Zilin Li, Hufeng Zhou, et al.
Journal of the American Heart Association|February 14, 2025
Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural VariantsKruthika R Iyer, Shoa L Clarke, Rodrigo Guarischi-Sousa, et al.
Circulation. Genomic and Precision Medicine|November 28, 2023
Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical AtherosclerosisNatalie R Hasbani, Kenneth E Westerman, Soo Heon Kwak, et al.
Genome Medicine|March 22, 2025
Rare damaging CCR2 variants are associated with lower lifetime cardiovascular riskMarios K Georgakis, Rainer Malik, Omar El Bounkari, et al.
Nature Genetics|March 4, 2014
Loss-of-function mutations in SLC30A8 protect against type 2 diabetesJason Flannick, Gudmar Thorleifsson, Nicola L Beer, et al.
Nature Methods|October 27, 2022
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studiesZilin Li, Xihao Li, Hufeng Zhou, et al.
Medrxiv : the Preprint Server for Health Sciences|May 5, 2025
Genome-wide association study and multi-ancestry meta-analysis identify common variants associated with carotid artery intima-media thicknessDevendra Meena, Jian Huang, Marjan Zare, et al.
American Journal of Human Genetics|October 6, 2023
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing studyYuxuan Wang, Margaret Sunitha Selvaraj, Xihao Li, et al.
Stroke|July 14, 2018
Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance ImagingXueqiu Jian, Claudia L Satizabal, Albert V Smith, et al.
Pageof 49