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Xihong Lin

Showing results (331-340 of 340) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|July 10, 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.
Genome Biology|September 9, 2025
Whole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individualsMargaret Sunitha Selvaraj, Xihao Li, Zilin Li, et al.
Research Square|January 14, 2021
Federated Learning used for predicting outcomes in SARS-COV-2 patientsMona Flores, Ittai Dayan, Holger Roth, et al.
Nature Computational Science|February 7, 2025
A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.
Nature Communications|October 11, 2022
Whole genome sequence analysis of blood lipid levels in >66,000 individualsMargaret Sunitha Selvaraj, Xihao Li, Zilin Li, et al.
Communications Biology|July 28, 2022
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed programDaniel DiCorpo, Sheila M Gaynor, Emily M Russell, et al.
Nature Medicine|September 16, 2021
Federated learning for predicting clinical outcomes in patients with COVID-19Ittai Dayan, Holger R Roth, Aoxiao Zhong, et al.
Nature Communications|April 11, 2025
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk alleleXinruo Zhang, Jennifer A Brody, Mariaelisa Graff, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2023
WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELEXinruo Zhang, Jennifer A Brody, Mariaelisa Graff, et al.
Nature|February 11, 2021
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed ProgramDaniel Taliun, Daniel N Harris, Michael D Kessler, et al.
Pageof 34

Showing results (331-340 of 340) with videos related to

Sort By:
Pageof 34
You have reached the last page of results.This site can display upto 340 results.
Medrxiv : the Preprint Server for Health Sciences|July 10, 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.
Genome Biology|September 9, 2025
Whole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individualsMargaret Sunitha Selvaraj, Xihao Li, Zilin Li, et al.
Research Square|January 14, 2021
Federated Learning used for predicting outcomes in SARS-COV-2 patientsMona Flores, Ittai Dayan, Holger Roth, et al.
Nature Computational Science|February 7, 2025
A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.
Nature Communications|October 11, 2022
Whole genome sequence analysis of blood lipid levels in >66,000 individualsMargaret Sunitha Selvaraj, Xihao Li, Zilin Li, et al.
Communications Biology|July 28, 2022
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed programDaniel DiCorpo, Sheila M Gaynor, Emily M Russell, et al.
Nature Medicine|September 16, 2021
Federated learning for predicting clinical outcomes in patients with COVID-19Ittai Dayan, Holger R Roth, Aoxiao Zhong, et al.
Nature Communications|April 11, 2025
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk alleleXinruo Zhang, Jennifer A Brody, Mariaelisa Graff, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2023
WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELEXinruo Zhang, Jennifer A Brody, Mariaelisa Graff, et al.
Nature|February 11, 2021
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed ProgramDaniel Taliun, Daniel N Harris, Michael D Kessler, et al.
Pageof 34