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Showing results (691-700 of 716) with videos related to

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Human Mutation|December 25, 2007
Recommendations for locus-specific databases and their curationR G H Cotton, A D Auerbach, J S Beckmann, et al.
European Journal of Human Genetics : EJHG|June 21, 2012
Toward a roadmap in global biobanking for healthJennifer R Harris, Paul Burton, Bartha Maria Knoppers, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 1, 2008
Parent of origin effects in attention/deficit hyperactivity disorder (ADHD): analysis of data from the international multicenter ADHD genetics (IMAGE) programRichard J L Anney, Ziarih Hawi, Karen Sheehan, et al.
Database : the Journal of Biological Databases and Curation|July 15, 2010
Finding and sharing: new approaches to registries of databases and services for the biomedical sciencesDamian Smedley, Paul Schofield, Chao-Kung Chen, et al.
BMJ Open|January 20, 2021
Protocol for the development of the Wales Multimorbidity e-Cohort (WMC): data sources and methods to construct a population-based research platform to investigate multimorbidityJane Lyons, Ashley Akbari, Utkarsh Agrawal, et al.
European Journal of Human Genetics : EJHG|June 2, 2021
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseasesBirte Zurek, Kornelia Ellwanger, Lisenka E L M Vissers, et al.
Science (New York, N.Y.)|November 8, 2008
GENETICS. The Human Variome ProjectRichard G H Cotton, Arleen D Auerbach, Myles Axton, et al.
Nature Reviews. Drug Discovery|October 14, 2017
Legacy data sharing to improve drug safety assessment: the eTOX projectFerran Sanz, François Pognan, Thomas Steger-Hartmann, et al.
Gigascience|September 20, 2024
An interconnected data infrastructure to support large-scale rare disease researchLennart F Johansson, Steve Laurie, Dylan Spalding, et al.
American Journal of Human Genetics|May 6, 2017
International Cooperation to Enable the Diagnosis of All Rare Genetic DiseasesKym M Boycott, Ana Rath, Jessica X Chong, et al.
Pageof 72

Showing results (691-700 of 716) with videos related to

Sort By:
Pageof 72
Human Mutation|December 25, 2007
Recommendations for locus-specific databases and their curationR G H Cotton, A D Auerbach, J S Beckmann, et al.
European Journal of Human Genetics : EJHG|June 21, 2012
Toward a roadmap in global biobanking for healthJennifer R Harris, Paul Burton, Bartha Maria Knoppers, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 1, 2008
Parent of origin effects in attention/deficit hyperactivity disorder (ADHD): analysis of data from the international multicenter ADHD genetics (IMAGE) programRichard J L Anney, Ziarih Hawi, Karen Sheehan, et al.
Database : the Journal of Biological Databases and Curation|July 15, 2010
Finding and sharing: new approaches to registries of databases and services for the biomedical sciencesDamian Smedley, Paul Schofield, Chao-Kung Chen, et al.
BMJ Open|January 20, 2021
Protocol for the development of the Wales Multimorbidity e-Cohort (WMC): data sources and methods to construct a population-based research platform to investigate multimorbidityJane Lyons, Ashley Akbari, Utkarsh Agrawal, et al.
European Journal of Human Genetics : EJHG|June 2, 2021
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseasesBirte Zurek, Kornelia Ellwanger, Lisenka E L M Vissers, et al.
Science (New York, N.Y.)|November 8, 2008
GENETICS. The Human Variome ProjectRichard G H Cotton, Arleen D Auerbach, Myles Axton, et al.
Nature Reviews. Drug Discovery|October 14, 2017
Legacy data sharing to improve drug safety assessment: the eTOX projectFerran Sanz, François Pognan, Thomas Steger-Hartmann, et al.
Gigascience|September 20, 2024
An interconnected data infrastructure to support large-scale rare disease researchLennart F Johansson, Steve Laurie, Dylan Spalding, et al.
American Journal of Human Genetics|May 6, 2017
International Cooperation to Enable the Diagnosis of All Rare Genetic DiseasesKym M Boycott, Ana Rath, Jessica X Chong, et al.
Pageof 72