Linda Köhn

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090-785 85 22

Verksam vid

Första forskningsingenjör vid Institutionen för strålningsvetenskaper Enhet: Onkologi

6M, plan 3, Norrlands universitetssjukhus Umeå universitet, 901 87 Umeå

Tumor-educated platelets for early prostate cancer diagnosis, and therapy stratification in patients with metastasized castration resistant prostate cancer

Clinical Cancer Research, American Association for Cancer Research 2020, Vol. 26, (11) : 73-74

Tjon-Kon-Fat, Lee-Ann; Köhn, Linda; Best, Myron; et al.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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