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Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
February 16, 2020
A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes
Heike Kollmus, Helmut Fuchs, Christoph Lengger, et al.
Current Pharmaceutical Design
|
March 20, 2014
A systems medicine clinical platform for understanding and managing non- communicable diseases
Alfredo Cesario, Charles Auffray, Alvar Agusti, et al.
Science Translational Medicine
|
June 5, 2015
Global implementation of genomic medicine: We are not alone
Teri A Manolio, Marc Abramowicz, Fahd Al-Mulla, et al.
Nature Genetics
|
November 3, 2014
Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes
Julian Schubert, Aleksandra Siekierska, Mélanie Langlois, et al.
Genome Medicine
|
June 25, 2016
Making sense of big data in health research: Towards an EU action plan
Charles Auffray, Rudi Balling, Inês Barroso, et al.
Genome Medicine
|
November 9, 2016
Erratum to: Making sense of big data in health research: towards an EU action plan
Charles Auffray, Rudi Balling, Inês Barroso, et al.
Current Pharmaceutical Design
|
March 20, 2014
Systems medicine approaches for the definition of complex phenotypes in chronic diseases and ageing. From concept to implementation and policies
Jean Bousquet, Christian Jorgensen, Michel Dauzat, et al.
Genome Medicine
|
July 13, 2011
Systems medicine and integrated care to combat chronic noncommunicable diseases
Jean Bousquet, Josep M Anto, Peter J Sterk, et al.
Frontiers in Immunology
|
February 28, 2024
Drug-target identification in COVID-19 disease mechanisms using computational systems biology approaches
Anna Niarakis, Marek Ostaszewski, Alexander Mazein, et al.
The Lancet. Neurology
|
July 24, 2018
Rare coding variants in genes encoding GABA<sub>A</sub> receptors in genetic generalised epilepsies: an exome-based case-control study
Patrick May, Simon Girard, Merle Harrer, et al.
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of 12
Search research articles
Search
Showing results (101-110 of 112) with videos related to
Sort By:
Page
of 12
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
February 16, 2020
A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes
Heike Kollmus, Helmut Fuchs, Christoph Lengger, et al.
Current Pharmaceutical Design
|
March 20, 2014
A systems medicine clinical platform for understanding and managing non- communicable diseases
Alfredo Cesario, Charles Auffray, Alvar Agusti, et al.
Science Translational Medicine
|
June 5, 2015
Global implementation of genomic medicine: We are not alone
Teri A Manolio, Marc Abramowicz, Fahd Al-Mulla, et al.
Nature Genetics
|
November 3, 2014
Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes
Julian Schubert, Aleksandra Siekierska, Mélanie Langlois, et al.
Genome Medicine
|
June 25, 2016
Making sense of big data in health research: Towards an EU action plan
Charles Auffray, Rudi Balling, Inês Barroso, et al.
Genome Medicine
|
November 9, 2016
Erratum to: Making sense of big data in health research: towards an EU action plan
Charles Auffray, Rudi Balling, Inês Barroso, et al.
Current Pharmaceutical Design
|
March 20, 2014
Systems medicine approaches for the definition of complex phenotypes in chronic diseases and ageing. From concept to implementation and policies
Jean Bousquet, Christian Jorgensen, Michel Dauzat, et al.
Genome Medicine
|
July 13, 2011
Systems medicine and integrated care to combat chronic noncommunicable diseases
Jean Bousquet, Josep M Anto, Peter J Sterk, et al.
Frontiers in Immunology
|
February 28, 2024
Drug-target identification in COVID-19 disease mechanisms using computational systems biology approaches
Anna Niarakis, Marek Ostaszewski, Alexander Mazein, et al.
The Lancet. Neurology
|
July 24, 2018
Rare coding variants in genes encoding GABA<sub>A</sub> receptors in genetic generalised epilepsies: an exome-based case-control study
Patrick May, Simon Girard, Merle Harrer, et al.
Page
of 12