Linda Köhn

Senior research engineer at Department of Radiation Sciences
Oncology

Publications

Author

Title

Year sorteringsordning

Fulltext

Evelönn, Emma Andersson
Degerman, Sofie
Köhn, Linda; et al.

DNA methylation status defines clinicopathological parameters including survival for patients with clear cell renal cell carcinoma (ccRCC)
Tumor Biology, 37(8): 10219-10228

2016

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Köhn, Linda
Svenson, Ulrika
Ljungberg, Börje; 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), 23(5): 334-342

2015

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Reinis, Ainars
Golovleva, Irina
Köhn, Linda; et al.

Ocular phenotype of CORD5, an autosomal dominant retinal dystrophy associated with PITPNM3 p.Q626H mutation
Acta Ophthalmologica, 91(3): 259-266

2013

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Burstedt, Marie
Jonsson, Frida
Köhn, Linda; et al.

Genotype-phenotype correlations in Bothnia dystrophy caused by RLBP1 gene sequence variations
Acta Ophthalmologica, 91(5): 437-444

2013

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Golovleva, Irina
Köhn, Linda
Burstedt, Marie; et al.

Mutation spectra in autosomal dominant and recessive retinitis pigmentosa in northern sweden.
Advances in Experimental Medicine and Biology, 664: 255-262

2010

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Köhn, Linda
Kohl, Susanne
Bowne, Sara J; et al.

PITPNM3 is an uncommon cause of cone and cone-rod dystrophies.
Ophthalmic Genetics, 31(3): 139-140

2010

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Köhn, Linda
Bowne, Sara J
S Sullivan, Lori; 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, 17(5): 651-655

2009

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Köhn, Linda
Bowne, Sara J
Daiger, Stephen P; 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, 17(5): 651-655

2009

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Köhn, Linda
Burstedt, Marie SI
Jonsson, Frida; 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, 49(7): 3172-3177

2008

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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.
Recent Advances in Retinal Degeneration: 229-234

2008

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