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- 2019
-
Mark
GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways
- Contribution to journal › Article
- 2017
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Mark
Application of whole-exome sequencing to direct the specific functional testing and diagnosis of rare inherited bleeding disorders in patients from the Öresund Region, Scandinavia
- Contribution to journal › Article
-
Mark
Metachronous and synchronous occurrence of 5 primary malignancies in a female patient between 1997 and 2013 : A case report with germline and somatic genetic analysis
- Contribution to journal › Article
- 2016
-
Mark
The genetic architecture of type 2 diabetes
- Contribution to journal › Article
-
Mark
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
- Contribution to journal › Article
- 2014
-
Mark
Neuroacanthocytosis - Clinical variability (a report on six cases)
(2014) Eighteenth International Congress of Parkinson's Disease and Movement Disorders In Movement Disorders 29(Suppl 1). p.194-194
- Contribution to journal › Published meeting abstract
- 2011
-
Mark
Thirty-years' experience of prenatal diagnosis of haemophilia in Sweden
(2011) XXIII Congress of the International Society on Thrombosis and Haemostasis In Journal of Thrombosis and Haemostasis 9. p.462-462
- Contribution to journal › Published meeting abstract
- 2010
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Mark
Benchmarks for Cystic Fibrosis carrier screening: A European consensus document
- Contribution to journal › Scientific review
- 2007
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Mark
Genetic and genomic analysis of arthritis regulating regions in human and mouse
(2007) In Lund University Faculty of Medicine Doctoral Dissertation Series
- Thesis › Doctoral thesis (compilation)
- 2003
-
Mark
A twin study of anxiety-related behaviours in pre-school children
- Contribution to journal › Article
