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Stuart Macgregor

Showing results (191-200 of 337) with videos related to

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Human Molecular Genetics|January 7, 2021
Germline variants are associated with increased primary melanoma tumor thickness at diagnosisErnest Mangantig, Stuart MacGregor, Mark M Iles, et al.
JAMA Ophthalmology|September 30, 2018
Myocilin Gene Gln368Ter Variant Penetrance and Association With Glaucoma in Population-Based and Registry-Based StudiesXikun Han, Emmanuelle Souzeau, Jue-Sheng Ong, et al.
Medrxiv : the Preprint Server for Health Sciences|November 26, 2025
Genome-wide analysis in over 1.6 million participants uncovers 147 loci associated with obstructive sleep apnoeaLuis M García-Marín, Zuriel Ceja, Abishna Parasuraman, et al.
Scientific Reports|November 29, 2016
GWAS study using DNA pooling strategy identifies association of variant rs4910623 in OR52B4 gene with anti-VEGF treatment response in age-related macular degenerationMoeen Riaz, Laura Lorés-Motta, Andrea J Richardson, et al.
Scientific Reports|January 26, 2018
Genome-wide association study of paclitaxel and carboplatin disposition in women with epithelial ovarian cancerBo Gao, Yi Lu, Annemieke J M Nieuweboer, et al.
Nature Communications|August 23, 2025
Large-scale GWAS of strabismus identifies risk loci and provides support for a link with maternal smokingWeixiong He, Peter J van der Most, Jue-Sheng Ong, et al.
Journal of Translational Medicine|September 5, 2022
Higher polygenic risk for melanoma is associated with improved survival in a high ultraviolet radiation settingMathias Seviiri, Richard A Scolyer, D Timothy Bishop, et al.
Plos One|September 26, 2015
Polymorphisms in Genes of Relevance for Oestrogen and Oxytocin Pathways and Risk of Barrett's Oesophagus and Oesophageal Adenocarcinoma: A Pooled Analysis from the BEACON ConsortiumKatarina Lagergren, Weronica E Ek, David Levine, et al.
Human Mutation|May 12, 2017
Haplotype reference consortium panel: Practical implications of imputations with large reference panelsAdriana I Iglesias, Sven J van der Lee, Pieter W M Bonnemaijer, et al.
Pigment Cell & Melanoma Research|January 31, 2013
Association between putative functional variants in the PSMB9 gene and risk of melanoma--re-analysis of published melanoma genome-wide association studiesJi Qian, Hongliang Liu, Sheng Wei, et al.
Pageof 34

Showing results (191-200 of 337) with videos related to

Sort By:
Pageof 34
Human Molecular Genetics|January 7, 2021
Germline variants are associated with increased primary melanoma tumor thickness at diagnosisErnest Mangantig, Stuart MacGregor, Mark M Iles, et al.
JAMA Ophthalmology|September 30, 2018
Myocilin Gene Gln368Ter Variant Penetrance and Association With Glaucoma in Population-Based and Registry-Based StudiesXikun Han, Emmanuelle Souzeau, Jue-Sheng Ong, et al.
Medrxiv : the Preprint Server for Health Sciences|November 26, 2025
Genome-wide analysis in over 1.6 million participants uncovers 147 loci associated with obstructive sleep apnoeaLuis M García-Marín, Zuriel Ceja, Abishna Parasuraman, et al.
Scientific Reports|November 29, 2016
GWAS study using DNA pooling strategy identifies association of variant rs4910623 in OR52B4 gene with anti-VEGF treatment response in age-related macular degenerationMoeen Riaz, Laura Lorés-Motta, Andrea J Richardson, et al.
Scientific Reports|January 26, 2018
Genome-wide association study of paclitaxel and carboplatin disposition in women with epithelial ovarian cancerBo Gao, Yi Lu, Annemieke J M Nieuweboer, et al.
Nature Communications|August 23, 2025
Large-scale GWAS of strabismus identifies risk loci and provides support for a link with maternal smokingWeixiong He, Peter J van der Most, Jue-Sheng Ong, et al.
Journal of Translational Medicine|September 5, 2022
Higher polygenic risk for melanoma is associated with improved survival in a high ultraviolet radiation settingMathias Seviiri, Richard A Scolyer, D Timothy Bishop, et al.
Plos One|September 26, 2015
Polymorphisms in Genes of Relevance for Oestrogen and Oxytocin Pathways and Risk of Barrett's Oesophagus and Oesophageal Adenocarcinoma: A Pooled Analysis from the BEACON ConsortiumKatarina Lagergren, Weronica E Ek, David Levine, et al.
Human Mutation|May 12, 2017
Haplotype reference consortium panel: Practical implications of imputations with large reference panelsAdriana I Iglesias, Sven J van der Lee, Pieter W M Bonnemaijer, et al.
Pigment Cell & Melanoma Research|January 31, 2013
Association between putative functional variants in the PSMB9 gene and risk of melanoma--re-analysis of published melanoma genome-wide association studiesJi Qian, Hongliang Liu, Sheng Wei, et al.
Pageof 34