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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
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Mark
Contribution of rare and common coding variants to haematological malignancies in the UK biobank
- Contribution to journal › Article
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Mark
Gene Therapy with Etranacogene Dezaparvovec for Hemophilia B
- Contribution to journal › Article
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Mark
Factor B Mutation in Monozygotic Twins Discordant for Atypical Hemolytic Uremic Syndrome
- Contribution to journal › Article
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Mark
HNF1B variant without hyperglycaemia as a cause of isolated profound hypomagnesaemia
- Contribution to journal › Article
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Mark
Oxidative stress-related factors in abdominal aortic aneurysm: potential clinical implications
(2023) In Lund University, Faculty of Medicine Doctoral Dissertation Series
- Thesis › Doctoral thesis (compilation)
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Mark
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk
- Contribution to journal › Article
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Mark
Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson’s Disease Project
- Contribution to journal › Article
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Mark
Revisiting Diagnosis and Treatment of Hypertrophic Cardiomyopathy : Current Practice and Novel Perspectives
- Contribution to journal › Scientific review
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Mark
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
- Contribution to journal › Article
