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- 2023
-
Mark
Copy number variants suggest different molecular pathways for the pathogenesis of bladder exstrophy
(
- Contribution to journal › Article
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Mark
Parkinsonism in Genetic Neurodevelopmental Disorders : A Systematic Review
(
- Contribution to journal › Scientific review
- 2022
-
Mark
Early vascular aging and supernormal vascular aging : genetics, epigenetics, and the environment
2022) p.421-428(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Mer-tyrosine kinase : a novel susceptibility gene for SLE related end-stage renal disease
(
- Contribution to journal › Article
-
Mark
Editorial : Genotype–phenotype correlations in neurodegenerative diseases: From clinical features to neuroimaging signatures
(
- Contribution to journal › Debate/Note/Editorial
- 2021
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Mark
Molecular pathways in patients with systemic lupus erythematosus revealed by gene-centred DNA sequencing
(
- Contribution to journal › Article
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Mark
Toll-like receptors revisited; A possible role for TLR1 in lupus nephritis
(
- Contribution to journal › Letter
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Mark
Interaction between the STAT4 rs11889341(T) risk allele and smoking confers increased risk of myocardial infarction and nephritis in patients with systemic lupus erythematosus
(
- Contribution to journal › Article
- 2020
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Mark
Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk
(
- Contribution to journal › Article
-
Mark
The Role of Melanocyte Lineage Genes in Melanoma
2020) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
-
Mark
Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke
(
- Contribution to journal › Article
-
Mark
Developing a methodology to balance benefit-sharing : application in the context of biodiversity beyond national jurisdiction
(
- Contribution to journal › Article
- 2019
-
Mark
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
(
- Contribution to journal › Article
- 2018
-
Mark
Germline mutations in BRCA1 and BRCA2 incidentally revealed in a biobank research study : experiences from re-contacting mutation carriers and relatives
(
- Contribution to journal › Article
- 2017
-
Mark
New Genes Causing Hereditary Parkinson’s Disease or Parkinsonism
(
- Contribution to journal › Scientific review