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- 2023
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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
2023) In Kidney International Reports(
- Contribution to journal › Article
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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 › Letter
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Mark
The etiology of Parkinson's disease. Genetic and non-genetic risk factors for a multifactorial disease
2023) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
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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
Rare-variant collapsing analyses reveal novel risk genes for arterial and venous cardiovascular diseases in the UK biobank
(
- Contribution to journal › Letter
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Mark
Birth Weight Is Associated With Clonal Hematopoiesis of Indeterminate Potential and Cardiovascular Outcomes in Adulthood
(
- Contribution to journal › Article
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Mark
Oxidative stress-related genetic variation and antioxidant vitamin intake in intact and ruptured abdominal aortic aneurysm : a Swedish population-based retrospective cohort study
2023) In European Journal of Preventive Cardiology(
- Contribution to journal › Article
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Mark
Cerebellar and subcortical atrophy contribute to psychiatric symptoms in frontotemporal dementia
(
- Contribution to journal › Article