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- 2024
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Mark
The HLA region in ANCA-associated vasculitis : characterisation of genetic associations in a Scandinavian patient population
(
- Contribution to journal › Article
- 2022
-
Mark
Identification and Functional Characterization of a Novel Susceptibility Locus for Small Vessel Vasculitis with MPO-ANCA
(
- Contribution to journal › Article
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Mark
Implementing precision medicine in a regionally organized healthcare system in Sweden
(
- Contribution to journal › Letter
- 2020
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Mark
ABCB1 single-nucleotide variants and survival in patients with glioblastoma treated with radiotherapy concomitant with temozolomide
(
- Contribution to journal › Article
- 2016
-
Mark
Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden
(
- Contribution to journal › Article
- 2013
-
Mark
NOTCH1 mutations influence survival in chronic lymphocytic leukemia patients
(
- Contribution to journal › Article
- 2012
-
Mark
Befolkningsstudier behövs--även LifeGene!
(
- Contribution to journal › Article
- 2011
-
Mark
Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice
(
- Contribution to journal › Article
- 2010
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Mark
MDM2 SNP309 promoter polymorphism, an independent prognostic factor in chronic lymphocytic leukemia
(
- Contribution to journal › Article
- 2008
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Mark
Notch1 is a frequent mutational target in chemically induced lymphoma in mouse
(
- Contribution to journal › Article
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Mark
Exploring the two-gene ratio in breast cancer-independent roles for HOXB13 and IL17BR in prediction of clinical outcome
(
- Contribution to journal › Article
- 2006
-
Mark
Pharmacogenetics during standardised initiation of thiopurine therapy in inflammatory bowel disease.
(
- Contribution to journal › Article
- 2004
-
Mark
Identification of two novel sequence variants affecting thiopurine methyltransferase enzyme activity.
(
- Contribution to journal › Article
- 2003
-
Mark
Urinary excretion of total cystine and the dibasic amino acids arginine, lysine and ornithine in relation to genetic findings in patients with cystinuria treated with sulfhydryl compounds.
(
- Contribution to journal › Article