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- 2014
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Mark
GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma.
- Contribution to journal › Article
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Mark
Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease.
- Contribution to journal › Article
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Mark
Defining the role of common variation in the genomic and biological architecture of adult human height.
- Contribution to journal › Article
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Mark
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.
- Contribution to journal › Article
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Mark
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
- Contribution to journal › Article
- 2013
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Mark
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk
- Contribution to journal › Article
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Mark
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
- Contribution to journal › Article
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Mark
A functional variant in the CFI gene confers a high risk of age-related macular degeneration
- Contribution to journal › Article
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Mark
The CCND1 c.870G > A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma
- Contribution to journal › Article
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Mark
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
- Contribution to journal › Article
