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- 2023
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Mark
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
(
- Contribution to journal › Article
- 2022
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Mark
A relatively common hypomorphic variant in WARS2 causes monogenic disease
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- Contribution to journal › Debate/Note/Editorial
- 2017
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Mark
The functional effect of rare variants in complement genes on C3b degradation in patients with age-related macular degeneration
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- Contribution to journal › Article
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Mark
Genetic variation of the Toll-like receptors in a Swedish allergic rhinitis case population
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- Contribution to journal › Article
- 2011
-
Mark
Heredity in Parkinson's disease. From rare mutations to common genetic risk factors.
(
- Thesis › Doctoral thesis (compilation)