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Caroline Hayward

Showing results (201-210 of 527) with videos related to

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The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|December 12, 2013
Glycans are a novel biomarker of chronological and biological agesJasminka Krištić, Frano Vučković, Cristina Menni, et al.
Cell Genomics|May 1, 2024
Blood-based epigenome-wide analyses of chronic low-grade inflammation across diverse population cohortsRobert F Hillary, Hong Kiat Ng, Daniel L McCartney, et al.
BMC Genetics|August 13, 2016
Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacityNick Shrine, Martin D Tobin, Claudia Schurmann, et al.
Human Molecular Genetics|January 2, 2017
Quantifying the extent to which index event biases influence large genetic association studiesHanieh Yaghootkar, Michael P Bancks, Sam E Jones, et al.
Kidney International|April 24, 2009
Genome-wide linkage analysis of serum creatinine in three isolated European populationsCristian Pattaro, Yurii S Aulchenko, Aaron Isaacs, et al.
Molecular & Cellular Proteomics : MCP|April 11, 2014
Comparative performance of four methods for high-throughput glycosylation analysis of immunoglobulin G in genetic and epidemiological researchJennifer E Huffman, Maja Pučić-Baković, Lucija Klarić, et al.
Human Molecular Genetics|April 16, 2013
Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachmentMirna Kirin, Aman Chandra, David G Charteris, et al.
Medrxiv : the Preprint Server for Health Sciences|December 11, 2023
Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive abilityZoe Schmilovich, Vincent-Raphaël Bourque, Elise Douard, et al.
Frontiers in Psychiatry|May 16, 2024
Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive abilityZoe Schmilovich, Vincent-Raphaël Bourque, Elise Douard, et al.
Human Molecular Genetics|December 15, 2010
Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levelsKonrad Oexle, Janina S Ried, Andrew A Hicks, et al.
Pageof 53

Showing results (201-210 of 527) with videos related to

Sort By:
Pageof 53
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|December 12, 2013
Glycans are a novel biomarker of chronological and biological agesJasminka Krištić, Frano Vučković, Cristina Menni, et al.
Cell Genomics|May 1, 2024
Blood-based epigenome-wide analyses of chronic low-grade inflammation across diverse population cohortsRobert F Hillary, Hong Kiat Ng, Daniel L McCartney, et al.
BMC Genetics|August 13, 2016
Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacityNick Shrine, Martin D Tobin, Claudia Schurmann, et al.
Human Molecular Genetics|January 2, 2017
Quantifying the extent to which index event biases influence large genetic association studiesHanieh Yaghootkar, Michael P Bancks, Sam E Jones, et al.
Kidney International|April 24, 2009
Genome-wide linkage analysis of serum creatinine in three isolated European populationsCristian Pattaro, Yurii S Aulchenko, Aaron Isaacs, et al.
Molecular & Cellular Proteomics : MCP|April 11, 2014
Comparative performance of four methods for high-throughput glycosylation analysis of immunoglobulin G in genetic and epidemiological researchJennifer E Huffman, Maja Pučić-Baković, Lucija Klarić, et al.
Human Molecular Genetics|April 16, 2013
Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachmentMirna Kirin, Aman Chandra, David G Charteris, et al.
Medrxiv : the Preprint Server for Health Sciences|December 11, 2023
Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive abilityZoe Schmilovich, Vincent-Raphaël Bourque, Elise Douard, et al.
Frontiers in Psychiatry|May 16, 2024
Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive abilityZoe Schmilovich, Vincent-Raphaël Bourque, Elise Douard, et al.
Human Molecular Genetics|December 15, 2010
Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levelsKonrad Oexle, Janina S Ried, Andrew A Hicks, et al.
Pageof 53