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J Hocking

Showing results (141-150 of 163) with videos related to

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Annals of the Rheumatic Diseases|September 8, 2012
Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 regionMarjolein J Peters, Linda Broer, Hanneke L D M Willemen, et al.
Journal of Medical Genetics|December 18, 2013
A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locusLing Oei, Yi-Hsiang Hsu, Unnur Styrkarsdottir, et al.
Nature Genetics|November 10, 2009
Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis riskSoumya Raychaudhuri, Brian P Thomson, Elaine F Remmers, et al.
Biological Psychiatry|August 14, 2016
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics ConsortiumRobert A Power, Katherine E Tansey, Henriette Nørmølle Buttenschøn, et al.
Lancet (London, England)|June 15, 2010
Common genetic determinants of vitamin D insufficiency: a genome-wide association studyThomas J Wang, Feng Zhang, J Brent Richards, et al.
Nature Genetics|May 11, 2010
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk lociEli A Stahl, Soumya Raychaudhuri, Elaine F Remmers, et al.
Nature Communications|December 18, 2015
Corrigendum: Rare coding variants and X-linked loci associated with age at menarcheKathryn L Lunetta, Felix R Day, Patrick Sulem, et al.
Nature Communications|August 5, 2015
Rare coding variants and X-linked loci associated with age at menarcheKathryn L Lunetta, Felix R Day, Patrick Sulem, et al.
Nature Communications|March 10, 2015
Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levelsElisabeth M van Leeuwen, Lennart C Karssen, Joris Deelen, et al.
Journal of Medical Genetics|April 3, 2016
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levelsElisabeth M van Leeuwen, Aniko Sabo, Joshua C Bis, et al.
Pageof 17

Showing results (141-150 of 163) with videos related to

Sort By:
Pageof 17
Annals of the Rheumatic Diseases|September 8, 2012
Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 regionMarjolein J Peters, Linda Broer, Hanneke L D M Willemen, et al.
Journal of Medical Genetics|December 18, 2013
A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locusLing Oei, Yi-Hsiang Hsu, Unnur Styrkarsdottir, et al.
Nature Genetics|November 10, 2009
Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis riskSoumya Raychaudhuri, Brian P Thomson, Elaine F Remmers, et al.
Biological Psychiatry|August 14, 2016
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics ConsortiumRobert A Power, Katherine E Tansey, Henriette Nørmølle Buttenschøn, et al.
Lancet (London, England)|June 15, 2010
Common genetic determinants of vitamin D insufficiency: a genome-wide association studyThomas J Wang, Feng Zhang, J Brent Richards, et al.
Nature Genetics|May 11, 2010
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk lociEli A Stahl, Soumya Raychaudhuri, Elaine F Remmers, et al.
Nature Communications|December 18, 2015
Corrigendum: Rare coding variants and X-linked loci associated with age at menarcheKathryn L Lunetta, Felix R Day, Patrick Sulem, et al.
Nature Communications|August 5, 2015
Rare coding variants and X-linked loci associated with age at menarcheKathryn L Lunetta, Felix R Day, Patrick Sulem, et al.
Nature Communications|March 10, 2015
Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levelsElisabeth M van Leeuwen, Lennart C Karssen, Joris Deelen, et al.
Journal of Medical Genetics|April 3, 2016
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levelsElisabeth M van Leeuwen, Aniko Sabo, Joshua C Bis, et al.
Pageof 17