"False"
Umeå universitet
printicon
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 Institutionen för folkhälsa och klinisk medicin
Plats
Registercentrum Norr, Norrlands universitetssjukhus Umeå universitet, by1a, B41, NUS, 901 85 Umeå
Anknytning
Anknuten som forskare till Umeå forskningscentrum för matematikdidaktik (UFM)
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
Visa publikationer i DiVA