Clinical Genomics Linköping

Publications

7 publications

Year 2020

PubMed DOI Crossref

Association between inflammasome-related polymorphisms and psoriatic arthritis.

Juneblad K, Kastbom A, Johansson L, ..., Söderkvist P, Alenius GM

Scand. J. Rheumatol. - (-) 1-7 [2020-12-10; online 2020-12-10]

Clinical Genomics Linköping

PubMed DOI Crossref

Activation of RAS Signalling is Associated with Altered Cell Adhesion in Phaeochromocytoma.

Rossitti HM, Dutta RK, Larsson C, ..., Söderkvist P, Gimm O

pii: ijms21218072 pmc: PMC7663737

Int J Mol Sci 21 (21) 8072 [2020-10-29; online 2020-10-29]

Bioinformatics Compute and Storage [Service] Clinical Genomics Linköping

PubMed DOI Crossref

ABCB1 single-nucleotide variants and survival in patients with glioblastoma treated with radiotherapy concomitant with temozolomide.

Malmström A, Łysiak M, Åkesson L, ..., Green H, Söderkvist P

pii: 10.1038/s41397-019-0107-z

Pharmacogenomics J. 20 (2) 213-219 [2020-04-00; online 2019-10-17]

Bioinformatics Compute and Storage [Service] Clinical Genomics Linköping

PubMed DOI Crossref

Do we really know who has an MGMT methylated glioma? Results of an international survey regarding use of MGMT analyses for glioma.

Malmström A, Łysiak M, Kristensen BW, ..., Henriksson R, Söderkvist P

pii: npz039 pmc: PMC6993038

Neurooncol Pract 7 (1) 68-76 [2020-01-00; online 2019-09-24]

Clinical Genomics Linköping

Year 2019

PubMed DOI Crossref

Novel BEST1 gene mutations associated with two different forms of macular dystrophy in Tunisian families.

Chibani Z, Abid IZ, Molbaek A, ..., Feki J, Hmani-Aifa M

Clin Exp Ophthalmol 47 (8) 1063-1073 [2019-11-00; online 2019-07-24]

Clinical Genomics Linköping

PubMed DOI Crossref

Assessment of genetic and non-genetic risk factors for venous thromboembolism in glioblastoma - The predictive significance of B blood group.

Heenkenda MK, Malmström A, Lysiak M, ..., Uppugunduri S, Osman A

pii: S0049-3848(19)30454-2

Thromb. Res. 183 (-) 136-142 [2019-11-00; online 2019-10-22]

Clinical Genomics Linköping

PubMed DOI Crossref

A somatic mutation in CLCN2 identified in a sporadic aldosterone-producing adenoma.

Dutta RK, Arnesen T, Heie A, ..., Söderkvist P, Gimm O

pii: EJE-19-0377

Eur. J. Endocrinol. 181 (5) K37-K41 [2019-11-00; online 2019-09-07]

Clinical Genomics Linköping

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