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Umeå universitet
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Huvudmenyn dold.
Personalbild Therese Kellgren

Therese Kellgren

Kontakt

E-post
therese.kellgren@umu.se
Telefon
090-786 63 06

Verksam vid

Anknytning
Universitetslektor vid Institutionen för matematik och matematisk statistik
Plats
MIT-huset, plan 3, Matematik och matematisk statistik, MIT.B.371 Umeå universitet, 901 87 Umeå
Anknytning
Anknuten som forskare till Umeå forskningscentrum för matematikdidaktik (UFM)
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
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