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Showing results (931-940 of 1,201) with videos related to

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Nature Genetics|June 15, 2021
Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetesCatherine C Robertson, Jamie R J Inshaw, Suna Onengut-Gumuscu, et al.
Nature|May 24, 2013
Negligible impact of rare autoimmune-locus coding-region variants on missing heritabilityKaren A Hunt, Vanisha Mistry, Nicholas A Bockett, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 18, 2018
Human airway branch variation and chronic obstructive pulmonary diseaseBenjamin M Smith, Hussein Traboulsi, John H M Austin, et al.
Diabetologia|December 24, 2021
Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE StudyCarolina G Downie, Sofia F Dimos, Stephanie A Bien, et al.
Nature Communications|August 25, 2018
Deep-coverage whole genome sequences and blood lipids among 16,324 individualsPradeep Natarajan, Gina M Peloso, Seyedeh Maryam Zekavat, et al.
American Journal of Respiratory and Critical Care Medicine|August 22, 2025
Associations of High Attenuation Area-related Proteomic Biomarkers with Fibrotic or Subpleural Interstitial Lung AbnormalitiesJohn S Kim, Catherine L Debban, Daniel Guzman, et al.
Sleep|July 30, 2025
Genome-wide Gene by Sleepiness Interaction Analysis for Sleep ApneaPavithra Nagarajan, Nuzulul Kurniansyah, Jiwon Lee, et al.
Genes|August 6, 2021
Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino PopulationsJia Wen, Munan Xie, Bryce Rowland, et al.
Medrxiv : the Preprint Server for Health Sciences|December 9, 2024
Multi-ancestry genome-wide association study reveals novel genetic signals for lung function declineBonnie K Patchen, Jingwen Zhang, Nathan Gaddis, et al.
Cell Genomics|October 23, 2023
The functional impact of rare variation across the regulatory cascadeTaibo Li, Nicole Ferraro, Benjamin J Strober, et al.
Pageof 121

Showing results (931-940 of 1,201) with videos related to

Sort By:
Pageof 121
Nature Genetics|June 15, 2021
Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetesCatherine C Robertson, Jamie R J Inshaw, Suna Onengut-Gumuscu, et al.
Nature|May 24, 2013
Negligible impact of rare autoimmune-locus coding-region variants on missing heritabilityKaren A Hunt, Vanisha Mistry, Nicholas A Bockett, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 18, 2018
Human airway branch variation and chronic obstructive pulmonary diseaseBenjamin M Smith, Hussein Traboulsi, John H M Austin, et al.
Diabetologia|December 24, 2021
Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE StudyCarolina G Downie, Sofia F Dimos, Stephanie A Bien, et al.
Nature Communications|August 25, 2018
Deep-coverage whole genome sequences and blood lipids among 16,324 individualsPradeep Natarajan, Gina M Peloso, Seyedeh Maryam Zekavat, et al.
American Journal of Respiratory and Critical Care Medicine|August 22, 2025
Associations of High Attenuation Area-related Proteomic Biomarkers with Fibrotic or Subpleural Interstitial Lung AbnormalitiesJohn S Kim, Catherine L Debban, Daniel Guzman, et al.
Sleep|July 30, 2025
Genome-wide Gene by Sleepiness Interaction Analysis for Sleep ApneaPavithra Nagarajan, Nuzulul Kurniansyah, Jiwon Lee, et al.
Genes|August 6, 2021
Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino PopulationsJia Wen, Munan Xie, Bryce Rowland, et al.
Medrxiv : the Preprint Server for Health Sciences|December 9, 2024
Multi-ancestry genome-wide association study reveals novel genetic signals for lung function declineBonnie K Patchen, Jingwen Zhang, Nathan Gaddis, et al.
Cell Genomics|October 23, 2023
The functional impact of rare variation across the regulatory cascadeTaibo Li, Nicole Ferraro, Benjamin J Strober, et al.
Pageof 121