Irina Golovleva

ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 9

Top Venues

Cellular and molecular life sciences : CMLS

Acta ophthalmologica

Human mutation

Blood cancer journal

Umeå Universitet Medicinska fakulteten

Institute of Virus Preparations (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Umeå Universitet Medicinska fakulteten Jan 02 1998

Sweden

clinical scientist, adj lecturer, Associate Professor :: Medical and Clinical Genetics

Umeå Universitet Medicinska fakulteten Oct 01 1997 - Dec 31 1997

Sweden

researcher :: Medical Genetics

Great Ormond Street Hospital For Children NHS Trust Oct 01 1996 - Oct 01 1997

United Kingdom

postdoc :: Cancer Biology, Molecular Haematology

Umeå Universitet Medicinska fakulteten Feb 15 1993 - Mar 01 1996

Sweden

postdoc :: Cell and Molecular Biology

Institut Pasteur Aug 01 1994 - Jan 15 1996

France

research fellow :: Immunogenetics

Education History

Institute of Virus Preparations Sep 01 1985 - Nov 23 1989

Russia

PHD :: Immunology

Russian State Medical University Sep 01 1976 - Jun 25 1982

Russia

MSC :: Medical-Biological Faculty

Publications

Ida Maria Westin, Mattias Landfors, Antonios Giannopoulos, Andreas Viberg, Pia Osterman, Berit Byström, Sofie Degerman, Irina Golovleva
DNA methylation changes and increased mRNA expression of coagulation proteins, factor V and thrombomodulin in Fuchs endothelial corneal dystrophy. Cellular and molecular life sciences : CMLS 80 (3) (2023)
Ida Maria Westin, Mattias Landfors, Antonios Giannopoulos, Andreas Viberg, Pia Osterman, Berit Byström, Sofie Degerman, Irina Golovleva
DNA methylation changes and increased mRNA expression of coagulation proteins, factor V and thrombomodulin in Fuchs endothelial corneal dystrophy. Cellular and molecular life sciences : CMLS 80 (3) (2023)
Ida Maria Westin, Mattias Landfors, Antonios Giannopoulos, Andreas Viberg, Pia Osterman, Berit Byström, Sofie Degerman, Irina Golovleva
DNA methylation changes and increased mRNA expression of coagulation proteins, factor V and thrombomodulin in Fuchs endothelial corneal dystrophy. Cellular and molecular life sciences : CMLS 80 (3) (2023)
Ida Maria Westin, Mattias Landfors, Antonios Giannopoulos, Andreas Viberg, Pia Osterman, Berit Byström, Sofie Degerman, Irina Golovleva
DNA methylation changes and increased mRNA expression of coagulation proteins, factor V and thrombomodulin in Fuchs endothelial corneal dystrophy. Cellular and molecular life sciences : CMLS 80 (3) (2023)
Maria Solaki, Britta Baumann, Peggy Reuter, Sten Andreasson, Isabelle Audo, Carmen Ayuso, Ghassan Balousha, Francesco Benedicenti, David Geoffrey Birch, Pierre Bitoun, Delphine Blain, Beatrice Bocquet, Kari Branham, Jaume Catala, Elfride De Baere, Helene Dollfus, Mohammed Falana, Roberto Giorda, Irina Golovleva, Irene Gottlob, John R Heckenlively, Samuel G Jacobson, Kaylie D Jones, Herbert Jägle, Andreas R Janecke, Ulrich Kellner, Petra Liskova, Birgit Lorenz, Loreto Martorell, André M Vieira Messias, Isabelle Meunier, Fernanda Belga Ottoni Porto, Eleni Papageorgiou, Astrid S Plomp, Thomy J L de Ravel, Charlotte M Reiff, Agnes B Renner, Thomas Rosenberg, Günther Rudolph, Roberto Salati, E Cumhur Sener, Paul A Sieving, Franco Stanzial, Elias I Traboulsi, Stephen H Tsang, Balázs Varsanyi, Richard G Weleber, Ditta Zobor, Katarina Stingl, Bernd Wissinger, Susanne Kohl
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia. Human mutation 43 (7) (2022)
Andreas Viberg, Ida Maria Westin, Irina Golovleva, Berit Byström
TCF4 trinucleotide repeat expansion in Swedish cases with Fuchs' endothelial corneal dystrophy. Acta ophthalmologica (2021)
Ida Maria Westin, Andreas Viberg, Berit Byström, Irina Golovleva
Lower Fractions of TCF4 Transcripts Spanning over the CTG18.1 Trinucleotide Repeat in Human Corneal Endothelium. Genes 12 (12) (2021)
Zahra Haider, Mattias Landfors, Irina Golovleva, Martin Erlanson, Kjeld Schmiegelow, Trond Flægstad, Jukka Kanerva, Ulrika Norén-Nyström, Magnus Hultdin, Sofie Degerman
DNA methylation and copy number variation profiling of T-cell lymphoblastic leukemia and lymphoma. Blood cancer journal 10 (4) (2020)
Frida Jonsson, Ida Maria Westin, Lennart Österman, Ola Sandgren, Marie Burstedt, Monica Holmberg, Irina Golovleva
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. Acta ophthalmologica 96 (7) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Irina Golovleva