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Bioinformatics (Oxford, England)
|
June 21, 2011
Epistasis detection on quantitative phenotypes by exhaustive enumeration using GPUs
Tony Kam-Thong, Benno Pütz, Nazanin Karbalai, et al.
Journal of Psychiatric Research
|
June 1, 2012
ANK3 and CACNA1C--missing genetic link for bipolar disorder and major depressive disorder in two German case-control samples
Stefan Kloiber, Darina Czamara, Nazanin Karbalai, et al.
Human Heredity
|
September 12, 2012
GLIDE: GPU-based linear regression for detection of epistasis
Tony Kam-Thong, Chloé-Agathe Azencott, Lawrence Cayton, et al.
Plos One
|
March 30, 2012
PTPN2 gene variants are associated with susceptibility to both Crohn's disease and ulcerative colitis supporting a common genetic disease background
Jürgen Glas, Johanna Wagner, Julia Seiderer, et al.
Carcinogenesis
|
December 4, 2013
Integrating gene expression and epidemiological data for the discovery of genetic interactions associated with cancer risk
Núria Bonifaci, Eva Colas, Jordi Serra-Musach, et al.
Plos One
|
August 20, 2015
Solid Organ Transplantation in Patients with Inflammatory Bowel Diseases (IBD): Analysis of Transplantation Outcome and IBD Activity in a Large Single Center Cohort
Fabian Schnitzler, Matthias Friedrich, Johannes Stallhofer, et al.
Plos One
|
June 28, 2013
A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype
Johanna Hass, Esther Walton, Holger Kirsten, et al.
Neuron
|
June 8, 2015
Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders
Janine Arloth, Ryan Bogdan, Peter Weber, et al.
Plos One
|
October 21, 2014
The challenges of genome-wide interaction studies: lessons to learn from the analysis of HDL blood levels
Elisabeth M van Leeuwen, Françoise A S Smouter, Tony Kam-Thong, et al.
Genome Research
|
March 20, 2014
Restless legs syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon
Derek Spieler, Maria Kaffe, Franziska Knauf, et al.
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of 2
Search research articles
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Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Bioinformatics (Oxford, England)
|
June 21, 2011
Epistasis detection on quantitative phenotypes by exhaustive enumeration using GPUs
Tony Kam-Thong, Benno Pütz, Nazanin Karbalai, et al.
Journal of Psychiatric Research
|
June 1, 2012
ANK3 and CACNA1C--missing genetic link for bipolar disorder and major depressive disorder in two German case-control samples
Stefan Kloiber, Darina Czamara, Nazanin Karbalai, et al.
Human Heredity
|
September 12, 2012
GLIDE: GPU-based linear regression for detection of epistasis
Tony Kam-Thong, Chloé-Agathe Azencott, Lawrence Cayton, et al.
Plos One
|
March 30, 2012
PTPN2 gene variants are associated with susceptibility to both Crohn's disease and ulcerative colitis supporting a common genetic disease background
Jürgen Glas, Johanna Wagner, Julia Seiderer, et al.
Carcinogenesis
|
December 4, 2013
Integrating gene expression and epidemiological data for the discovery of genetic interactions associated with cancer risk
Núria Bonifaci, Eva Colas, Jordi Serra-Musach, et al.
Plos One
|
August 20, 2015
Solid Organ Transplantation in Patients with Inflammatory Bowel Diseases (IBD): Analysis of Transplantation Outcome and IBD Activity in a Large Single Center Cohort
Fabian Schnitzler, Matthias Friedrich, Johannes Stallhofer, et al.
Plos One
|
June 28, 2013
A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype
Johanna Hass, Esther Walton, Holger Kirsten, et al.
Neuron
|
June 8, 2015
Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders
Janine Arloth, Ryan Bogdan, Peter Weber, et al.
Plos One
|
October 21, 2014
The challenges of genome-wide interaction studies: lessons to learn from the analysis of HDL blood levels
Elisabeth M van Leeuwen, Françoise A S Smouter, Tony Kam-Thong, et al.
Genome Research
|
March 20, 2014
Restless legs syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon
Derek Spieler, Maria Kaffe, Franziska Knauf, et al.
Page
of 2