Linda Köhn

Forskningsingenjör, förste vid Institutionen för strålningsvetenskaper Enhet: Onkologi

linda.kohn@umu.se

090-785 85 22

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

Senaste publikationer

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.

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.

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

Evelönn, Emma Andersson; 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.

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Linda Köhn

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