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Cell Genomics
|
September 19, 2025
Streamlining large-scale genomic data management: Insights from the UK Biobank whole-genome sequencing data
Xihao Li, Andrew R Wood, Yuxin Yuan, et al.
Briefings in Bioinformatics
|
January 15, 2026
CoxMDS: multiple data splitting for high-dimensional mediation analysis with survival outcomes in epigenome-wide studies
Minhao Yao, Peixin Tian, Xihao Li, et al.
HGG Advances
|
June 21, 2024
Additional impact of genetic ancestry over race/ethnicity to prevalence of KRAS mutations and allele-specific subtypes in non-small cell lung cancer
Xinan Wang, Kangcheng Hou, Biagio Ricciuti, et al.
HGG Advances
|
January 21, 2026
Application of the STAAR Framework in Detecting Rare Variant Associations with Alzheimer's Disease and Related Dementias: Insights and Implications
Dongyu Wang, Sabrina Abbruzzese, Nancy Heard-Costa, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 2, 2025
A novel two-sample Mendelian randomization framework integrating common and rare variants: application to assess the effect of HDL-C on preeclampsia risk
Yu Zhang, Ming Li, David M Haas, et al.
Respiratory Research
|
April 4, 2019
Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis
Zhaozhong Zhu, Xiaofang Wang, Xihao Li, et al.
American Journal of Human Genetics
|
September 13, 2024
Semi-supervised machine learning method for predicting homogeneous ancestry groups to assess Hardy-Weinberg equilibrium in diverse whole-genome sequencing studies
Derek Shyr, Rounak Dey, Xihao Li, et al.
Briefings in Bioinformatics
|
January 7, 2026
A novel two-sample Mendelian randomization framework integrating common and rare variants: application to assess the effect of HDL-C on preeclampsia risk
Yu Zhang, Ming Li, David M Haas, et al.
Nucleic Acids Research
|
December 3, 2025
FAVOR 2.0: A reengineered functional annotation of variants online resource for interpreting genomic variation
Hufeng Zhou, Vineet Verma, Xihao Li, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
March 12, 2026
APOE and plasma AD biomarkers: The role of genetic ancestry in Hispanics/Latinos
Caitlin Cheung, Natasha Z Anita, Paola Filigrana, et al.
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Search research articles
Search
Showing results (31-40 of 64) with videos related to
Sort By:
Page
of 7
Cell Genomics
|
September 19, 2025
Streamlining large-scale genomic data management: Insights from the UK Biobank whole-genome sequencing data
Xihao Li, Andrew R Wood, Yuxin Yuan, et al.
Briefings in Bioinformatics
|
January 15, 2026
CoxMDS: multiple data splitting for high-dimensional mediation analysis with survival outcomes in epigenome-wide studies
Minhao Yao, Peixin Tian, Xihao Li, et al.
HGG Advances
|
June 21, 2024
Additional impact of genetic ancestry over race/ethnicity to prevalence of KRAS mutations and allele-specific subtypes in non-small cell lung cancer
Xinan Wang, Kangcheng Hou, Biagio Ricciuti, et al.
HGG Advances
|
January 21, 2026
Application of the STAAR Framework in Detecting Rare Variant Associations with Alzheimer's Disease and Related Dementias: Insights and Implications
Dongyu Wang, Sabrina Abbruzzese, Nancy Heard-Costa, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 2, 2025
A novel two-sample Mendelian randomization framework integrating common and rare variants: application to assess the effect of HDL-C on preeclampsia risk
Yu Zhang, Ming Li, David M Haas, et al.
Respiratory Research
|
April 4, 2019
Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis
Zhaozhong Zhu, Xiaofang Wang, Xihao Li, et al.
American Journal of Human Genetics
|
September 13, 2024
Semi-supervised machine learning method for predicting homogeneous ancestry groups to assess Hardy-Weinberg equilibrium in diverse whole-genome sequencing studies
Derek Shyr, Rounak Dey, Xihao Li, et al.
Briefings in Bioinformatics
|
January 7, 2026
A novel two-sample Mendelian randomization framework integrating common and rare variants: application to assess the effect of HDL-C on preeclampsia risk
Yu Zhang, Ming Li, David M Haas, et al.
Nucleic Acids Research
|
December 3, 2025
FAVOR 2.0: A reengineered functional annotation of variants online resource for interpreting genomic variation
Hufeng Zhou, Vineet Verma, Xihao Li, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
March 12, 2026
APOE and plasma AD biomarkers: The role of genetic ancestry in Hispanics/Latinos
Caitlin Cheung, Natasha Z Anita, Paola Filigrana, et al.
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of 7