Ida Maria Westin

发表

TCF4 trinucleotide repeat expansion in Swedish cases with Fuchs' endothelial corneal dystrophy

I. Golovleva, Berit Byström, A. Viberg, 2021, Acta ophthalmologica.

EYS mutations and implementation of minigene assay for variant classification in EYS-associated retinitis pigmentosa in northern Sweden

L. Österman, M. Holmberg, I. Golovleva, 2020, Scientific Reports.

Lower Fractions of TCF4 Transcripts Spanning over the CTG18.1 Trinucleotide Repeat in Human Corneal Endothelium

I. Golovleva, Berit Byström, A. Viberg, 2021, Genes.

DNA methylation changes and increased mRNA expression of coagulation proteins, factor V and thrombomodulin in Fuchs endothelial corneal dystrophy

M. Landfors, I. Golovleva, Berit Byström, 2023, Cellular and Molecular Life Sciences.

Genetic screening in sudden cardiac death in the young can save future lives

S. Mörner, J. Jonasson, K. Cederquist, 2015, International Journal of Legal Medicine.

Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis

S. Jensen, A. Rydberg, A. Winbo, 2017, BMC Medical Genetics.

ATP‐binding cassette subfamily A, member 4 intronic variants c.4773+3A>G and c.5461‐10T>C cause Stargardt disease due to defective splicing

L. Österman, O. Sandgren, M. Holmberg, 2018, Acta ophthalmologica.

DNA methylation changes and increased mRNA expression of coagulation proteins, factor V and thrombomodulin in Fuchs endothelial corneal dystrophy

M. Landfors, I. Golovleva, Berit Byström, 2023, Cellular and Molecular Life Sciences.

CTG18.1 expansion in transcription factor 4 (TCF4) in corneal graft failure: preliminary study

Berit Byström, A. Viberg, Ida Maria Westin, 2024, Cell and Tissue Banking.