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HGG Advances
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October 4, 2021
Genetic discovery and risk characterization in type 2 diabetes across diverse populations
Linda M Polfus, Burcu F Darst, Heather Highland, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 7, 2025
Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia
Runjia Li, Sarah A Gagliano Taliun, Kevin Liao, et al.
HGG Advances
|
August 31, 2025
Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia
Runjia Li, Sarah A Gagliano Taliun, Kevin Liao, et al.
The American Journal of Clinical Nutrition
|
December 21, 2014
Habitual sleep duration is associated with BMI and macronutrient intake and may be modified by CLOCK genetic variants
Hassan S Dashti, Jack L Follis, Caren E Smith, et al.
Human Genetics
|
January 24, 2019
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data
Karen Y He, Xiaoyin Li, Tanika N Kelly, et al.
Genome Biology
|
June 9, 2026
Publisher Correction: Whole genome sequence analysis of pulmonary function and COPD in 44,287 multi-ancestry participants
Wonji Kim, Xiaowei Hu, Kangjin Kim, et al.
Genome Biology
|
January 15, 2026
Whole genome sequence analysis of pulmonary function and COPD in 44,287 multi-ancestry participants
Wonji Kim, Xiaowei Hu, Kangjin Kim, et al.
American Journal of Respiratory Cell and Molecular Biology
|
October 28, 2017
Multiethnic Meta-Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea-related Quantitative Trait Locus in Men
Han Chen, Brian E Cade, Kevin J Gleason, et al.
Nature Methods
|
December 31, 2025
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions
Eric Van Buren, Yi Zhang, Xihao Li, et al.
Nature Genetics
|
December 23, 2022
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies
Xihao Li, Corbin Quick, Hufeng Zhou, et al.
Page
of 13
Search research articles
Search
Showing results (71-80 of 127) with videos related to
Sort By:
Page
of 13
HGG Advances
|
October 4, 2021
Genetic discovery and risk characterization in type 2 diabetes across diverse populations
Linda M Polfus, Burcu F Darst, Heather Highland, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 7, 2025
Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia
Runjia Li, Sarah A Gagliano Taliun, Kevin Liao, et al.
HGG Advances
|
August 31, 2025
Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia
Runjia Li, Sarah A Gagliano Taliun, Kevin Liao, et al.
The American Journal of Clinical Nutrition
|
December 21, 2014
Habitual sleep duration is associated with BMI and macronutrient intake and may be modified by CLOCK genetic variants
Hassan S Dashti, Jack L Follis, Caren E Smith, et al.
Human Genetics
|
January 24, 2019
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data
Karen Y He, Xiaoyin Li, Tanika N Kelly, et al.
Genome Biology
|
June 9, 2026
Publisher Correction: Whole genome sequence analysis of pulmonary function and COPD in 44,287 multi-ancestry participants
Wonji Kim, Xiaowei Hu, Kangjin Kim, et al.
Genome Biology
|
January 15, 2026
Whole genome sequence analysis of pulmonary function and COPD in 44,287 multi-ancestry participants
Wonji Kim, Xiaowei Hu, Kangjin Kim, et al.
American Journal of Respiratory Cell and Molecular Biology
|
October 28, 2017
Multiethnic Meta-Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea-related Quantitative Trait Locus in Men
Han Chen, Brian E Cade, Kevin J Gleason, et al.
Nature Methods
|
December 31, 2025
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions
Eric Van Buren, Yi Zhang, Xihao Li, et al.
Nature Genetics
|
December 23, 2022
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies
Xihao Li, Corbin Quick, Hufeng Zhou, et al.
Page
of 13