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R Gaunt

Showing results (121-130 of 287) with videos related to

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Bioinformatics (Oxford, England)|March 11, 2021
Erratum to: EpiGraphDB: a database and data mining platform for health data scienceYi Liu, Benjamin Elsworth, Pau Erola, et al.
Annals of Human Genetics|October 19, 2006
Refined association mapping for a quantitative trait: weight in the H19-IGF2-INS-TH regionW Zhang, N Maniatis, S Rodriguez, et al.
Plos Medicine|January 3, 2023
Association between genetically proxied PCSK9 inhibition and prostate cancer risk: A Mendelian randomisation studySi Fang, James Yarmolinsky, Dipender Gill, et al.
Journal of Medical Genetics|May 3, 2005
Angiotensin II type I receptor gene polymorphism: anthropometric and metabolic syndrome traitsM R Abdollahi, T R Gaunt, H E Syddall, et al.
Bioinformatics (Oxford, England)|November 9, 2020
EpiGraphDB: a database and data mining platform for health data scienceYi Liu, Benjamin Elsworth, Pau Erola, et al.
Nucleic Acids Research|February 9, 2011
Amplification ratio control system for copy number variation genotypingPhilip A I Guthrie, Tom R Gaunt, Mohammed R Abdollahi, et al.
Journal of Neuroinflammation|November 18, 2023
Cytokine enrichment in deep cerebellar nuclei is contributed by multiple glial populations and linked to reduced amyloid plaque pathologyJessica R Gaunt, Norliyana Zainolabidin, Alaric K K Yip, et al.
Wellcome Open Research|November 20, 2019
Using the MR-Base platform to investigate risk factors and drug targets for thousands of phenotypesVenexia M Walker, Neil M Davies, Gibran Hemani, et al.
Bioinformatics (Oxford, England)|January 14, 2015
An integrative approach to predicting the functional effects of non-coding and coding sequence variationHashem A Shihab, Mark F Rogers, Julian Gough, et al.
Human Molecular Genetics|June 13, 2018
Systematic Mendelian randomization framework elucidates hundreds of CpG sites which may mediate the influence of genetic variants on diseaseTom G Richardson, Philip C Haycock, Jie Zheng, et al.
Pageof 29

Showing results (121-130 of 287) with videos related to

Sort By:
Pageof 29
Bioinformatics (Oxford, England)|March 11, 2021
Erratum to: EpiGraphDB: a database and data mining platform for health data scienceYi Liu, Benjamin Elsworth, Pau Erola, et al.
Annals of Human Genetics|October 19, 2006
Refined association mapping for a quantitative trait: weight in the H19-IGF2-INS-TH regionW Zhang, N Maniatis, S Rodriguez, et al.
Plos Medicine|January 3, 2023
Association between genetically proxied PCSK9 inhibition and prostate cancer risk: A Mendelian randomisation studySi Fang, James Yarmolinsky, Dipender Gill, et al.
Journal of Medical Genetics|May 3, 2005
Angiotensin II type I receptor gene polymorphism: anthropometric and metabolic syndrome traitsM R Abdollahi, T R Gaunt, H E Syddall, et al.
Bioinformatics (Oxford, England)|November 9, 2020
EpiGraphDB: a database and data mining platform for health data scienceYi Liu, Benjamin Elsworth, Pau Erola, et al.
Nucleic Acids Research|February 9, 2011
Amplification ratio control system for copy number variation genotypingPhilip A I Guthrie, Tom R Gaunt, Mohammed R Abdollahi, et al.
Journal of Neuroinflammation|November 18, 2023
Cytokine enrichment in deep cerebellar nuclei is contributed by multiple glial populations and linked to reduced amyloid plaque pathologyJessica R Gaunt, Norliyana Zainolabidin, Alaric K K Yip, et al.
Wellcome Open Research|November 20, 2019
Using the MR-Base platform to investigate risk factors and drug targets for thousands of phenotypesVenexia M Walker, Neil M Davies, Gibran Hemani, et al.
Bioinformatics (Oxford, England)|January 14, 2015
An integrative approach to predicting the functional effects of non-coding and coding sequence variationHashem A Shihab, Mark F Rogers, Julian Gough, et al.
Human Molecular Genetics|June 13, 2018
Systematic Mendelian randomization framework elucidates hundreds of CpG sites which may mediate the influence of genetic variants on diseaseTom G Richardson, Philip C Haycock, Jie Zheng, et al.
Pageof 29