Irina Golovleva
6PUBLICATIONS
34CO-AUTHORS
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Publications (6)
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|Feb 11, 2023
DNA methylation changes and increased mRNA expression of coagulation proteins, factor V and thrombomodulin in Fuchs endothelial corneal dystrophy.Ida Maria Westin, Mattias Landfors, Antonios Giannopoulos
|Mar 25, 2022
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia.Maria Solaki, Britta Baumann, Peggy Reuter
|Dec 24, 2021
Lower Fractions of TCF4 Transcripts Spanning over the CTG18.1 Trinucleotide Repeat in Human Corneal Endothelium.Ida Maria Westin, Andreas Viberg, Berit Byström
|Oct 13, 2021
TCF4 trinucleotide repeat expansion in Swedish cases with Fuchs' endothelial corneal dystrophy.Andreas Viberg, Ida Maria Westin, Irina Golovleva
|Apr 30, 2020
DNA methylation and copy number variation profiling of T-cell lymphoblastic leukemia and lymphoma.Zahra Haider, Mattias Landfors, Irina Golovleva
|Feb 21, 2018
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.Frida Jonsson, Ida Maria Westin, Lennart Österman
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Frequent Collaborators
1 joint publications
Zahra Haider
1 joint publications
Sofie Degerman
1 joint publications
Berit Byström
1 joint publications
Maria Solaki
1 joint publications
Peggy Reuter
1 joint publications
Isabelle Audo
1 joint publications
Ghassan Balousha
1 joint publications
Francesco Benedicenti
1 joint publications
David Birch
1 joint publications
Pierre Bitoun
