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Nature Communications
|
March 19, 2025
Diverse ancestral representation improves genetic intolerance metrics
Alexander L Han, Chloe F Sands, Dorota Matelska, et al.
American Journal of Human Genetics
|
February 22, 2023
Effects of protein-coding variants on blood metabolite measurements and clinical biomarkers in the UK Biobank
Abhishek Nag, Ryan S Dhindsa, Lawrence Middleton, et al.
Nature
|
November 8, 2005
Oncogenic pathway signatures in human cancers as a guide to targeted therapies
Andrea H Bild, Guang Yao, Jeffrey T Chang, et al.
Plos Genetics
|
February 3, 2026
Rare heterozygous missense variants in VSX2 are associated with retinal detachment
Daniel C Brock, Justin S Dhindsa, Yifan Chen, et al.
Nature Genetics
|
September 11, 2024
Disease prediction with multi-omics and biomarkers empowers case-control genetic discoveries in the UK Biobank
Manik Garg, Marcin Karpinski, Dorota Matelska, et al.
Plos Computational Biology
|
October 2, 2018
meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arrays
Sahar Gelfman, Quanli Wang, Yi-Fan Lu, et al.
Nature
|
August 10, 2021
Rare variant contribution to human disease in 281,104 UK Biobank exomes
Quanli Wang, Ryan S Dhindsa, Keren Carss, et al.
Biorxiv : the Preprint Server for Biology
|
August 12, 2025
Population-scale sequencing resolves correlates and determinants of latent Epstein-Barr Virus infection
Sherry S Nyeo, Erin M Cumming, Oliver S Burren, et al.
Lancet (London, England)
|
February 5, 2019
Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study
Slavé Petrovski, Vimla Aggarwal, Jessica L Giordano, et al.
ESC Heart Failure
|
June 23, 2022
Pharmacogenomic study of heart failure and candesartan response from the CHARM programme
Marie-Pierre Dubé, Olympe Chazara, Audrey Lemaçon, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 67) with videos related to
Sort By:
Page
of 7
Nature Communications
|
March 19, 2025
Diverse ancestral representation improves genetic intolerance metrics
Alexander L Han, Chloe F Sands, Dorota Matelska, et al.
American Journal of Human Genetics
|
February 22, 2023
Effects of protein-coding variants on blood metabolite measurements and clinical biomarkers in the UK Biobank
Abhishek Nag, Ryan S Dhindsa, Lawrence Middleton, et al.
Nature
|
November 8, 2005
Oncogenic pathway signatures in human cancers as a guide to targeted therapies
Andrea H Bild, Guang Yao, Jeffrey T Chang, et al.
Plos Genetics
|
February 3, 2026
Rare heterozygous missense variants in VSX2 are associated with retinal detachment
Daniel C Brock, Justin S Dhindsa, Yifan Chen, et al.
Nature Genetics
|
September 11, 2024
Disease prediction with multi-omics and biomarkers empowers case-control genetic discoveries in the UK Biobank
Manik Garg, Marcin Karpinski, Dorota Matelska, et al.
Plos Computational Biology
|
October 2, 2018
meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arrays
Sahar Gelfman, Quanli Wang, Yi-Fan Lu, et al.
Nature
|
August 10, 2021
Rare variant contribution to human disease in 281,104 UK Biobank exomes
Quanli Wang, Ryan S Dhindsa, Keren Carss, et al.
Biorxiv : the Preprint Server for Biology
|
August 12, 2025
Population-scale sequencing resolves correlates and determinants of latent Epstein-Barr Virus infection
Sherry S Nyeo, Erin M Cumming, Oliver S Burren, et al.
Lancet (London, England)
|
February 5, 2019
Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study
Slavé Petrovski, Vimla Aggarwal, Jessica L Giordano, et al.
ESC Heart Failure
|
June 23, 2022
Pharmacogenomic study of heart failure and candesartan response from the CHARM programme
Marie-Pierre Dubé, Olympe Chazara, Audrey Lemaçon, et al.
Page
of 7