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Pau Navarro

Showing results (31-40 of 98) with videos related to

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Nature Communications|March 25, 2022
Genetic regulation of post-translational modification of two distinct proteinsArianna Landini, Irena Trbojević-Akmačić, Pau Navarro, et al.
Human Molecular Genetics|April 29, 2015
Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-modelsAthina Spiliopoulou, Reka Nagy, Mairead L Bermingham, et al.
Nature Communications|December 3, 2021
Mapping the serum proteome to neurological diseases using whole genome sequencingGrace Png, Andrei Barysenka, Linda Repetto, et al.
Plos One|July 23, 2013
Local exome sequences facilitate imputation of less common variants and increase power of genome wide association studiesPeter K Joshi, James Prendergast, Ross M Fraser, et al.
Genome Biology|May 15, 2023
Phenome-wide analyses identify an association between the parent-of-origin effects dependent methylome and the rate of aging in humansChenhao Gao, Carmen Amador, Rosie M Walker, et al.
Frontiers in Nutrition|June 18, 2024
Dietary supplementation with plant extracts for amelioration of persistent myofascial discomfort in the cervical and back regions: a randomized double-blind controlled studySilvia Pérez-Piñero, Juan Carlos Muñoz-Carrillo, Jon Echepare-Taberna, et al.
Biorxiv : the Preprint Server for Biology|January 30, 2023
Phenome-wide analysis identifies parent-of-origin effects on the human methylome associated with changes in the rate of agingChenhao Gao, Carmen Amador, Rosie M Walker, et al.
Biological Psychiatry|July 17, 2016
A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive DisorderYanni Zeng, Pau Navarro, Ana M Fernandez-Pujals, et al.
Plos One|September 3, 2011
Characterisation of genome-wide association epistasis signals for serum uric acid in human population isolatesWenhua Wei, Gibran Hemani, Andrew A Hicks, et al.
Human Molecular Genetics|August 20, 2010
New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8Veronique Vitart, Goran Bencić, Caroline Hayward, et al.
Pageof 10

Showing results (31-40 of 98) with videos related to

Sort By:
Pageof 10
Nature Communications|March 25, 2022
Genetic regulation of post-translational modification of two distinct proteinsArianna Landini, Irena Trbojević-Akmačić, Pau Navarro, et al.
Human Molecular Genetics|April 29, 2015
Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-modelsAthina Spiliopoulou, Reka Nagy, Mairead L Bermingham, et al.
Nature Communications|December 3, 2021
Mapping the serum proteome to neurological diseases using whole genome sequencingGrace Png, Andrei Barysenka, Linda Repetto, et al.
Plos One|July 23, 2013
Local exome sequences facilitate imputation of less common variants and increase power of genome wide association studiesPeter K Joshi, James Prendergast, Ross M Fraser, et al.
Genome Biology|May 15, 2023
Phenome-wide analyses identify an association between the parent-of-origin effects dependent methylome and the rate of aging in humansChenhao Gao, Carmen Amador, Rosie M Walker, et al.
Frontiers in Nutrition|June 18, 2024
Dietary supplementation with plant extracts for amelioration of persistent myofascial discomfort in the cervical and back regions: a randomized double-blind controlled studySilvia Pérez-Piñero, Juan Carlos Muñoz-Carrillo, Jon Echepare-Taberna, et al.
Biorxiv : the Preprint Server for Biology|January 30, 2023
Phenome-wide analysis identifies parent-of-origin effects on the human methylome associated with changes in the rate of agingChenhao Gao, Carmen Amador, Rosie M Walker, et al.
Biological Psychiatry|July 17, 2016
A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive DisorderYanni Zeng, Pau Navarro, Ana M Fernandez-Pujals, et al.
Plos One|September 3, 2011
Characterisation of genome-wide association epistasis signals for serum uric acid in human population isolatesWenhua Wei, Gibran Hemani, Andrew A Hicks, et al.
Human Molecular Genetics|August 20, 2010
New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8Veronique Vitart, Goran Bencić, Caroline Hayward, et al.
Pageof 10