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English
Umeå universitet
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Linda Köhn

Kontakt

E-post
linda.kohn@umu.se
Telefon
090-785 85 22

Verksam vid

Anknytning
Första forskningsingenjör vid Institutionen för strålningsvetenskaper Enhet: Onkologi
Plats
6M, plan 3, Norrlands universitetssjukhus Umeå universitet, 901 87 Umeå
2019
DNA methylation associates with survival in non-metastatic clear cell renal cell carcinoma
BMC Cancer, BioMed Central 2019, Vol. 19
Andersson Evelönn, Emma; Landfors, Mattias; Haider, Zahra; et al.
2019
An integrated transcriptome analysis in T-cell acute lymphoblastic leukemia links DNA methylation subgroups to dysregulated TAL1 and ANTP homeobox gene expression
Cancer Medicine, John Wiley & Sons 2019, Vol. 8, (1) : 311-324
Haider, Zahra; Larsson, Pär; Landfors, Mattias; et al.
2017
Liquid biopsies in lung cancer: time to implement research technologies in routine care?
Annals of Translational Medicine, AME Publishing Company 2017, Vol. 5, (13)
Köhn, Linda; Johansson, Mikael; Grankvist, Kjell; et al.
2016
DNA methylation status defines clinicopathological parameters including survival for patients with clear cell renal cell carcinoma (ccRCC)
Tumor Biology, Vol. 37, (8) : 10219-10228
Andersson Evelönn, Emma; Degerman, Sofie; Köhn, Linda; et al.
2015
Specific Genomic Aberrations Predict Survival, But Low Mutation Rate in Cancer Hot Spots, in Clear Cell Renal Cell Carcinoma
Applied immunohistochemistry & molecular morphology (Print), Vol. 23, (5) : 334-342
Köhn, Linda; Svenson, Ulrika; Ljungberg, Börje; et al.
2013
Genotype-phenotype correlations in Bothnia dystrophy caused by RLBP1 gene sequence variations
Acta Ophthalmologica, Vol. 91, (5) : 437-444
Burstedt, Marie; Jonsson, Frida; Köhn, Linda; et al.
2013
Ocular phenotype of CORD5, an autosomal dominant retinal dystrophy associated with PITPNM3 p.Q626H mutation
Acta Ophthalmologica, Vol. 91, (3) : 259-266
Reinis, Ainars; Golovleva, Irina; Köhn, Linda; et al.
2010
Mutation spectra in autosomal dominant and recessive retinitis pigmentosa in northern sweden.
Advances in Experimental Medicine and Biology, Vol. 664 : 255-262
Golovleva, Irina; Köhn, Linda; Burstedt, Marie; et al.
2010
PITPNM3 is an uncommon cause of cone and cone-rod dystrophies.
Ophthalmic Genetics, Informa Healthcare 2010, Vol. 31, (3) : 139-140
Köhn, Linda; Kohl, Susanne; Bowne, Sara J; et al.
2009
Breakpoint characterization of a novel ~59 kb genomic deletion on 19q13.42 in autosomal dominant retinitis pigmentosa with reduced penetrance
European Journal of Human Genetics, Nature publishing group 2009, Vol. 17, (5) : 651-655
Köhn, Linda; Bowne, Sara J; Daiger, Stephen P; et al.
2009
Breakpoint characterization of a novel approximately 59 kb genomic deletion on 19q13.42 in autosomal-dominant retinitis pigmentosa with incomplete penetrance.
European Journal of Human Genetics, Vol. 17, (5) : 651-655
Köhn, Linda; Bowne, Sara J; S Sullivan, Lori; et al.
2008
Carrier of R14W in carbonic anhydrase IV presents Bothnia dystrophy phenotype caused by two allelic mutations in RLBP1
Investigative Ophthalmology and Visual Science, Association for Research in Vision and Ophthalmology 2008, Vol. 49, (7) : 3172-3177
Köhn, Linda; Burstedt, Marie SI; Jonsson, Frida; et al.
2008
Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families.
Recent Advances in Retinal Degeneration, Springer 2008 : 229-234
Köhn, Linda; Kadzhaev, Konstantin; Burstedt, Marie S I; et al.
2007
Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families
European Journal of Human Genetics, Nature publishing group 2007, Vol. 15, (6) : 664-671
Köhn, Linda; Kadzhaev, Konstantin; Burstedt, Marie SI; et al.
Visa publikationer i DiVA