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Human Genomics
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April 12, 2025
Genomics and athletic performance: an emerging discipline that is not yet ready for society
Aikaterini Psatha, Christina Mitropoulou, George P Patrinos
Human Genomics
|
June 16, 2023
The impact of ACE2 polymorphisms (rs1978124, rs2285666, and rs2074192) and ACE1 rs1799752 in the mortality rate of COVID-19 in different SARS-CoV-2 variants
Farzaneh Sheikhian, Sahar Sadeghi Mofrad, Samira Tarashi, et al.
Human Genomics
|
June 2, 2023
Modeling the longitudinal changes of ancestry diversity in the Million Veteran Program
Frank R Wendt, Gita A Pathak, Jacqueline Vahey, et al.
Human Genomics
|
March 5, 2026
Epigenetic corepressor BCORL1 predominates as a driver of clonal hematopoiesis of indeterminate potential in patients undergoing chronic hemodialysis: a multicenter cohort study
Kuan-Chieh Wang, Wei Wang, Chiung-Ying Huang, et al.
Human Genomics
|
June 3, 2023
Genomic approaches to identify and investigate genes associated with atrial fibrillation and heart failure susceptibility
Kush Ketan Patel, Cynthia Venkatesan, Habiba Abdelhalim, et al.
Human Genomics
|
June 5, 2023
Distribution of alpha1 antitrypsin rare alleles in six countries: Results from the Progenika diagnostic network
José Luis Lopez-Campos, Noelia Rapun, Karen Czischke, et al.
Human Genomics
|
February 6, 2024
A broad wastewater screening and clinical data surveillance for virus-related diseases in the metropolitan Detroit area in Michigan
Yabing Li, Brijen Miyani, Russell A Faust, et al.
Human Genomics
|
February 4, 2024
Causal associations of COVID-19 on neurosurgical diseases risk: a Mendelian randomization study
Lirui Dai, Liang Lyu, Peizhi Zhou, et al.
Human Genomics
|
March 25, 2024
Large-scale next generation sequencing based analysis of SLCO1B1 pharmacogenetics variants in the Saudi population
Ewa Goljan, Mohammed Abouelhoda, Asma Tahir, et al.
Human Genomics
|
February 23, 2024
Meta-analysis of 46,000 germline de novo mutations linked to human inherited disease
Mónica Lopes-Marques, Matthew Mort, João Carneiro, et al.
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Search research articles
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Showing results (491-500 of 1,110) with videos related to
Sort By:
Page
of 111
Human Genomics
|
April 12, 2025
Genomics and athletic performance: an emerging discipline that is not yet ready for society
Aikaterini Psatha, Christina Mitropoulou, George P Patrinos
Human Genomics
|
June 16, 2023
The impact of ACE2 polymorphisms (rs1978124, rs2285666, and rs2074192) and ACE1 rs1799752 in the mortality rate of COVID-19 in different SARS-CoV-2 variants
Farzaneh Sheikhian, Sahar Sadeghi Mofrad, Samira Tarashi, et al.
Human Genomics
|
June 2, 2023
Modeling the longitudinal changes of ancestry diversity in the Million Veteran Program
Frank R Wendt, Gita A Pathak, Jacqueline Vahey, et al.
Human Genomics
|
March 5, 2026
Epigenetic corepressor BCORL1 predominates as a driver of clonal hematopoiesis of indeterminate potential in patients undergoing chronic hemodialysis: a multicenter cohort study
Kuan-Chieh Wang, Wei Wang, Chiung-Ying Huang, et al.
Human Genomics
|
June 3, 2023
Genomic approaches to identify and investigate genes associated with atrial fibrillation and heart failure susceptibility
Kush Ketan Patel, Cynthia Venkatesan, Habiba Abdelhalim, et al.
Human Genomics
|
June 5, 2023
Distribution of alpha1 antitrypsin rare alleles in six countries: Results from the Progenika diagnostic network
José Luis Lopez-Campos, Noelia Rapun, Karen Czischke, et al.
Human Genomics
|
February 6, 2024
A broad wastewater screening and clinical data surveillance for virus-related diseases in the metropolitan Detroit area in Michigan
Yabing Li, Brijen Miyani, Russell A Faust, et al.
Human Genomics
|
February 4, 2024
Causal associations of COVID-19 on neurosurgical diseases risk: a Mendelian randomization study
Lirui Dai, Liang Lyu, Peizhi Zhou, et al.
Human Genomics
|
March 25, 2024
Large-scale next generation sequencing based analysis of SLCO1B1 pharmacogenetics variants in the Saudi population
Ewa Goljan, Mohammed Abouelhoda, Asma Tahir, et al.
Human Genomics
|
February 23, 2024
Meta-analysis of 46,000 germline de novo mutations linked to human inherited disease
Mónica Lopes-Marques, Matthew Mort, João Carneiro, et al.
Page
of 111