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Sarah Hunt

Showing results (71-80 of 83) with videos related to

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Nucleic Acids Research|December 4, 2012
Ensembl 2013Paul Flicek, Ikhlak Ahmed, M Ridwan Amode, et al.
Nucleic Acids Research|December 10, 2013
Ensembl 2014Paul Flicek, M Ridwan Amode, Daniel Barrell, et al.
Human Molecular Genetics|November 4, 2010
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21, , Chris C A Spencer, et al.
Nature Communications|July 9, 2014
The correlation between reading and mathematics ability at age twelve has a substantial genetic componentOliver S P Davis, Gavin Band, Matti Pirinen, et al.
Nature Genetics|November 8, 2011
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac diseaseGosia Trynka, Karen A Hunt, Nicholas A Bockett, et al.
Nature Genetics|December 28, 2011
Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestryKaren A Hunt, Deborah J Smyth, Tobias Balschun, et al.
Biological Psychiatry|July 23, 2013
A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation, , Elvira Bramon, et al.
Nature Genetics|February 7, 2012
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke, , Céline Bellenguez, et al.
Nature|September 3, 2010
Integrating common and rare genetic variation in diverse human populations, David M Altshuler, Richard A Gibbs, et al.
Nature Genetics|December 9, 2008
Variants in MTNR1B influence fasting glucose levelsInga Prokopenko, Claudia Langenberg, Jose C Florez, et al.
Pageof 9

Showing results (71-80 of 83) with videos related to

Sort By:
Pageof 9
Nucleic Acids Research|December 4, 2012
Ensembl 2013Paul Flicek, Ikhlak Ahmed, M Ridwan Amode, et al.
Nucleic Acids Research|December 10, 2013
Ensembl 2014Paul Flicek, M Ridwan Amode, Daniel Barrell, et al.
Human Molecular Genetics|November 4, 2010
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21, , Chris C A Spencer, et al.
Nature Communications|July 9, 2014
The correlation between reading and mathematics ability at age twelve has a substantial genetic componentOliver S P Davis, Gavin Band, Matti Pirinen, et al.
Nature Genetics|November 8, 2011
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac diseaseGosia Trynka, Karen A Hunt, Nicholas A Bockett, et al.
Nature Genetics|December 28, 2011
Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestryKaren A Hunt, Deborah J Smyth, Tobias Balschun, et al.
Biological Psychiatry|July 23, 2013
A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation, , Elvira Bramon, et al.
Nature Genetics|February 7, 2012
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke, , Céline Bellenguez, et al.
Nature|September 3, 2010
Integrating common and rare genetic variation in diverse human populations, David M Altshuler, Richard A Gibbs, et al.
Nature Genetics|December 9, 2008
Variants in MTNR1B influence fasting glucose levelsInga Prokopenko, Claudia Langenberg, Jose C Florez, et al.
Pageof 9