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Paul Iw de Bakker

Showing results (1-10 of 8) with videos related to

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BMC Structural Biology|February 2, 2008
Comparative modelling by restraint-based conformational samplingNicholas Furnham, Paul Iw de Bakker, Swanand Gore, et al.
European Journal of Human Genetics : EJHG|November 24, 2016
A framework for the detection of de novo mutations in family-based sequencing dataLaurent C Francioli, Mircea Cretu-Stancu, Kiran V Garimella, et al.
Genome Medicine|January 20, 2011
Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association dataJoanne H Wang, Derek Pappas, Philip L De Jager, et al.
European Journal of Human Genetics : EJHG|April 6, 2017
Genetic variants associated with type 2 diabetes and adiposity and risk of intracranial and abdominal aortic aneurysmsFemke Ng van 't Hof, Julien Vaucher, Michael V Holmes, et al.
European Journal of Human Genetics : EJHG|April 13, 2017
Missing heritability: is the gap closing? An analysis of 32 complex traits in the Lifelines Cohort StudyIlja M Nolte, Peter J van der Most, Behrooz Z Alizadeh, et al.
Pharmacogenomics|April 6, 2016
A genetic risk score is associated with statin-induced low-density lipoprotein cholesterol loweringMaarten Leusink, Anke H Maitland-van der Zee, Bo Ding, et al.
European Journal of Human Genetics : EJHG|January 7, 2016
The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north-south gradient among EuropeansJessica Becker, Stephan L Haas, Anna Mokrowiecka, et al.
Nature Genetics|September 13, 2016
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertensionPraveen Surendran, Fotios Drenos, Robin Young, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
BMC Structural Biology|February 2, 2008
Comparative modelling by restraint-based conformational samplingNicholas Furnham, Paul Iw de Bakker, Swanand Gore, et al.
European Journal of Human Genetics : EJHG|November 24, 2016
A framework for the detection of de novo mutations in family-based sequencing dataLaurent C Francioli, Mircea Cretu-Stancu, Kiran V Garimella, et al.
Genome Medicine|January 20, 2011
Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association dataJoanne H Wang, Derek Pappas, Philip L De Jager, et al.
European Journal of Human Genetics : EJHG|April 6, 2017
Genetic variants associated with type 2 diabetes and adiposity and risk of intracranial and abdominal aortic aneurysmsFemke Ng van 't Hof, Julien Vaucher, Michael V Holmes, et al.
European Journal of Human Genetics : EJHG|April 13, 2017
Missing heritability: is the gap closing? An analysis of 32 complex traits in the Lifelines Cohort StudyIlja M Nolte, Peter J van der Most, Behrooz Z Alizadeh, et al.
Pharmacogenomics|April 6, 2016
A genetic risk score is associated with statin-induced low-density lipoprotein cholesterol loweringMaarten Leusink, Anke H Maitland-van der Zee, Bo Ding, et al.
European Journal of Human Genetics : EJHG|January 7, 2016
The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north-south gradient among EuropeansJessica Becker, Stephan L Haas, Anna Mokrowiecka, et al.
Nature Genetics|September 13, 2016
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertensionPraveen Surendran, Fotios Drenos, Robin Young, et al.
Pageof 1