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Umeå University
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Staff photo Therese Kellgren

Therese Kellgren

Contact

E-mail
therese.kellgren@umu.se
Phone
+46 90 786 63 06

Works at

Affiliation
Associate professor at Department of Mathematics and Mathematical Statistics
Location
MIT-huset, plan 3, Matematik och matematisk statistik, MIT.B.371 Umeå universitet, 901 87 Umeå
Affiliation
Affiliated as research fellow at Umeå Mathematics Education Research Centre (UMERC)
Completed genome and emergence scenario of the multidrug-resistant nosocomial pathogen Staphylococcus epidermidis ST215
BMC Microbiology, BioMed Central (BMC) 2024, Vol. 24, (1)
Kellgren, Therese; Dwibedi, Chinmay Kumar; Widerström, Micael; et al.
VNTR polymorphism in the SLC6A3 gene does not influence dopamine transporter availability measured by [18F]FE-PE2I PET or [123I]FP-Cit SPECT
Nuclear medicine communications, Wolters Kluwer 2022, Vol. 43, (3) : 247-255
Jakobson Mo, Susanna; Axelsson, Jan; J. Stiernman, Lars; et al.
Parvimonas micra is associated with tumour immune profiles in molecular subtypes of colorectal cancer
Cancer Immunology and Immunotherapy, Springer 2022, Vol. 71 : 2565-2575
Löwenmark, Thyra; Li, Xingru; Löfgren Burström, Anna; et al.
Hidden patterns that matter: statistical methods for analysis of DNA and RNA data
Research report in mathematical statistics, 71/20
Kellgren, Therese
Centralization Within Sub-Experiments Enhances the Biological Relevance of Gene Co-expression Networks: A Plant Mitochondrial Case Study
Frontiers in Plant Science, Frontiers Media S.A. 2020, Vol. 11
Law, Simon R; Kellgren, Therese; Björk, Rafael; et al.
A Detailed Flow Cytometric Analysis of Immune Activity Profiles in Molecular Subtypes of Colorectal Cancer
Cancers, MDPI 2020, Vol. 12, (11)
Li, Xingru; Ling, Agnes; Kellgren, Therese G.; et al.
Non-homologous recombination between Alu and LINE-1 repeats results in a 91 kb deletion in MERTK causing severe retinitis pigmentosa
Molecular Vision, Vol. 24 : 667-678
Jonsson, Frida; Burstedt, Marie; Kellgren, Therese; et al.
SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts
Scientific Reports, Nature Publishing Group 2017, Vol. 7
Stattin, Eva-Lena; Henning, Petra; Klar, Joakim; et al.
Mutations in Collagen, Type XVII, Alpha 1 (COL17A1) Cause Epithelial Recurrent Erosion Dystrophy (ERED)
Human Mutation, John Wiley & Sons 2015, Vol. 36, (4) : 463-473
Jonsson, Frida; Byström, Berit; Davidson, Alice E.; et al.
The emergence of an antimicrobial resistant Staphylococcus epidermidis clone in Northern Europe
Kellgren, Therese; Dwibedi, Chinmay Kumar; Widerström, Micael; et al.
Experimental designs for finding disease-causing mutations in rare diseases
Kellgren, Therese; Rydén, Patrik
View publications in DiVA