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Showing results (11-20 of 29) with videos related to

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Briefings in Bioinformatics|December 9, 2021
eSCAN: scan regulatory regions for aggregate association testing using whole-genome sequencing dataYingxi Yang, Quan Sun, Le Huang, et al.
Nature Genetics|January 26, 2026
Reply to: a quantitative trait locus for reduced microglial APOE expression associates with reduced cerebral amyloid angiopathyLincoln M P Shade, Qi Qiao, Yuriko Katsumata, et al.
Current Oncology (Toronto, Ont.)|February 24, 2022
Real-World Treatment Patterns and Clinical Effectiveness of Palbociclib Plus an Aromatase Inhibitor as First-Line Therapy in Advanced/Metastatic Breast Cancer: Analysis from the US Syapse Learning Health NetworkJeanna Wallenta Law, Debanjali Mitra, Henry G Kaplan, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|March 28, 2025
HSR25-178: Initial Clinical Presentation (ICP) and Pre-Diagnostic Journey During 18 Months Before a First Non-Small Cell Lung Cancer (NSCLC) Diagnosis: US Retrospective Cohort StudyMelissa L Santorelli, Molly Scannell Bryan, Ashwini Arunachalam, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2024
The Genetic Determinants and Genomic Consequences of Non-Leukemogenic Somatic Point MutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
Nature Communications|October 16, 2025
Genetic determinants and genomic consequences of non-leukemogenic somatic point mutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
HGG Advances|December 26, 2022
Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variantsKristin L Young, Virginia Fisher, Xuan Deng, et al.
Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, 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.
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.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Briefings in Bioinformatics|December 9, 2021
eSCAN: scan regulatory regions for aggregate association testing using whole-genome sequencing dataYingxi Yang, Quan Sun, Le Huang, et al.
Nature Genetics|January 26, 2026
Reply to: a quantitative trait locus for reduced microglial APOE expression associates with reduced cerebral amyloid angiopathyLincoln M P Shade, Qi Qiao, Yuriko Katsumata, et al.
Current Oncology (Toronto, Ont.)|February 24, 2022
Real-World Treatment Patterns and Clinical Effectiveness of Palbociclib Plus an Aromatase Inhibitor as First-Line Therapy in Advanced/Metastatic Breast Cancer: Analysis from the US Syapse Learning Health NetworkJeanna Wallenta Law, Debanjali Mitra, Henry G Kaplan, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|March 28, 2025
HSR25-178: Initial Clinical Presentation (ICP) and Pre-Diagnostic Journey During 18 Months Before a First Non-Small Cell Lung Cancer (NSCLC) Diagnosis: US Retrospective Cohort StudyMelissa L Santorelli, Molly Scannell Bryan, Ashwini Arunachalam, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2024
The Genetic Determinants and Genomic Consequences of Non-Leukemogenic Somatic Point MutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
Nature Communications|October 16, 2025
Genetic determinants and genomic consequences of non-leukemogenic somatic point mutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
HGG Advances|December 26, 2022
Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variantsKristin L Young, Virginia Fisher, Xuan Deng, et al.
Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, 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.
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.
Pageof 3