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David P Strachan

Showing results (121-130 of 237) with videos related to

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Lancet (London, England)|February 12, 2008
LDL-cholesterol concentrations: a genome-wide association studyManjinder S Sandhu, Dawn M Waterworth, Sally L Debenham, et al.
American Journal of Human Genetics|May 12, 2009
Genome-wide association analysis identifies PDE4D as an asthma-susceptibility geneBlanca E Himes, Gary M Hunninghake, James W Baurley, et al.
Nature Genetics|May 19, 2009
Genetic variation in LIN28B is associated with the timing of pubertyKen K Ong, Cathy E Elks, Shengxu Li, et al.
Human Genetics|February 23, 2016
Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain AtlasElse Eising, Sjoerd M H Huisman, Ahmed Mahfouz, et al.
The Journal of Allergy and Clinical Immunology|March 20, 2012
Genome-wide association study of lung function decline in adults with and without asthmaMedea Imboden, Emmanuelle Bouzigon, Ivan Curjuric, et al.
Cephalalgia : an International Journal of Headache|September 3, 2014
Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studiesDale R Nyholt, , Verneri Anttila, et al.
The Lancet. Respiratory Medicine|October 2, 2015
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK BiobankLouise V Wain, Nick Shrine, Suzanne Miller, et al.
Nature Genetics|June 16, 2009
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility lociPhilip L De Jager, Xiaoming Jia, Joanne Wang, et al.
Nature Genetics|March 4, 2008
Newly identified genetic risk variants for celiac disease related to the immune responseKaren A Hunt, Alexandra Zhernakova, Graham Turner, et al.
Thorax|February 27, 2016
Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12Victoria E Jackson, Ioanna Ntalla, Ian Sayers, et al.
Pageof 24

Showing results (121-130 of 237) with videos related to

Sort By:
Pageof 24
Lancet (London, England)|February 12, 2008
LDL-cholesterol concentrations: a genome-wide association studyManjinder S Sandhu, Dawn M Waterworth, Sally L Debenham, et al.
American Journal of Human Genetics|May 12, 2009
Genome-wide association analysis identifies PDE4D as an asthma-susceptibility geneBlanca E Himes, Gary M Hunninghake, James W Baurley, et al.
Nature Genetics|May 19, 2009
Genetic variation in LIN28B is associated with the timing of pubertyKen K Ong, Cathy E Elks, Shengxu Li, et al.
Human Genetics|February 23, 2016
Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain AtlasElse Eising, Sjoerd M H Huisman, Ahmed Mahfouz, et al.
The Journal of Allergy and Clinical Immunology|March 20, 2012
Genome-wide association study of lung function decline in adults with and without asthmaMedea Imboden, Emmanuelle Bouzigon, Ivan Curjuric, et al.
Cephalalgia : an International Journal of Headache|September 3, 2014
Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studiesDale R Nyholt, , Verneri Anttila, et al.
The Lancet. Respiratory Medicine|October 2, 2015
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK BiobankLouise V Wain, Nick Shrine, Suzanne Miller, et al.
Nature Genetics|June 16, 2009
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility lociPhilip L De Jager, Xiaoming Jia, Joanne Wang, et al.
Nature Genetics|March 4, 2008
Newly identified genetic risk variants for celiac disease related to the immune responseKaren A Hunt, Alexandra Zhernakova, Graham Turner, et al.
Thorax|February 27, 2016
Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12Victoria E Jackson, Ioanna Ntalla, Ian Sayers, et al.
Pageof 24