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- 2023
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Mark
A novel scatterplot-based method to detect copy number variation (CNV)
(
- Contribution to journal › Article
- 2021
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Mark
The copy number variation and stroke (CaNVAS) risk and outcome study
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- Contribution to journal › Article
- 2019
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Mark
Genetic Imbalance Is Associated With Functional Outcome After Ischemic Stroke
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- Contribution to journal › Article
- 2014
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Mark
Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3
(
- Contribution to journal › Article
- 2013
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Mark
Genome-wide investigation of gene-environment interactions in colorectal cancer
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- Contribution to journal › Article
- 2012
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Mark
The changing landscape of genetic testing and its impact on clinical and laboratory services and research in Europe
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- Contribution to journal › Article
- 2011
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Mark
Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities Background Document to the ESHG recommendations on genetic testing and common disorders
(
- Contribution to journal › Article
- 2010
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Mark
Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility
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- Contribution to journal › Article