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Irina Golovleva
Vetenskaplig meritering:
Docent
Kontakt
E-post
irina.golovleva@umu.se
Telefon
090-785 68 20
Verksam vid
Anknytning
Adjungerad professor vid
Institutionen för medicinsk biovetenskap
Enhet: Medicinsk och klinisk genetik
Plats
By 6M, vån 1, Sjukhusområdet
Umeå universitet, 901 85 Umeå
Publikationer
Publikationer
Forskning
Forskning
2024
CTG18.1 expansion in transcription factor 4 (TCF4) in corneal graft failure: preliminary study
Cell and Tissue Banking
, Springer Science+Business Media B.V. 2024, Vol. 25 : 613-618
Boström, Ida Maria; Viberg, Andreas; Golovleva, Irina; et al.
2023
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)
, Springer 2023, Vol. 80, (3)
Westin, Ida Maria; Landfors, Mattias; Giannopoulos, Antonios; et al.
2022
A Study Protocol for Validation and Implementation of Whole-Genome and -Transcriptome Sequencing as a Comprehensive Precision Diagnostic Test in Acute Leukemias
Frontiers in Medicine
, Frontiers Media S.A. 2022, Vol. 9
Berglund, Eva; Barbany, Gisela; Orsmark-Pietras, Christina; et al.
2022
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia
Human Mutation
, John Wiley & Sons 2022, Vol. 43, (7) : 832-858
Solaki, Maria; Baumann, Britta; Reuter, Peggy; et al.
2022
TCF4
trinucleotide repeat expansion in Swedish cases with Fuchs’ endothelial corneal dystrophy
Acta Ophthalmologica
, John Wiley & Sons 2022, Vol. 100, (5) : 541-548
Viberg, Andreas; Westin, Ida Maria; Golovleva, Irina; et al.
2021
EYS mutations and implementation of minigene assay for variant classification in EYS-associated retinitis pigmentosa in northern Sweden
Scientific Reports
, Nature Publishing Group 2021, Vol. 11, (1)
Westin, Ida Maria; Jonsson, Frida; Österman, Lennart; et al.
2021
Lower fractions of TCF4 transcripts spanning over the CTG18.1 trinucleotide repeat in human corneal endothelium
Genes
, MDPI 2021, Vol. 12, (12)
Westin, Ida Maria; Viberg, Andreas; Byström, Berit; et al.
2020
DNA methylation and copy number variation profiling of T-cell lymphoblastic leukemia and lymphoma
Blood Cancer Journal
, Nature Publishing Group 2020, Vol. 10, (4)
Haider, Zahra; Landfors, Mattias; Golovleva, Irina; et al.
2020
Differential tissue specific expression of Kif23 alternative transcripts in mice with the human mutation causing congenital dyserythropoietic anemia type III
Blood Cells, Molecules & Diseases
, Elsevier 2020, Vol. 85
Vikberg, Ann-Louise; Malla, Sandhya; Golovleva, Irina
2019
The Genetic Architecture of Gliomagenesis-Genetic Risk Variants Linked to Specific Molecular Subtypes
Cancers
, MDPI 2019, Vol. 11, (12)
Wu, Wendy Yi-Ying; Johansson, Gunnar; Wibom, Carl; et al.
2018
Phenotypic expression of EYS mutations in patients with autosomal recessive retinitis pigmentosa in northern Sweden
Investigative Ophthalmology and Visual Science
, The Association for Research in Vision and Ophthalmology, Inc. 2018, Vol. 59, (9)
Burstedt, Marie; Jonsson, Frida; Westin, Ida Maria; et al.
2018
Non-homologous recombination between Alu and LINE-1 repeats results in a 91 kb deletion in
MERTK
causing severe retinitis pigmentosa
Molecular Vision
, Vol. 24 : 667-678
Jonsson, Frida; Burstedt, Marie; Kellgren, Therese; et al.
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
Acta Ophthalmologica
, John Wiley & Sons 2018, Vol. 96, (7) : 737-743
Jonsson, Frida; Westin, Ida Maria; Österman, Lennart; et al.
2018
Mutations in the gene PDE6C encoding the catalytic subunit of the cone photoreceptor phosphodiesterase in patients with achromatopsia
Human Mutation
, John Wiley & Sons 2018, Vol. 39, (10) : 1366-1371
Weisschuh, Nicole; Stingl, Katarina; Audo, Isabelle; et al.
2017
High Levels of the AR-V7 Splice Variant and Co-Amplification of the Golgi Protein Coding YIPF6 in AR Amplified Prostate Cancer Bone Metastases
The Prostate
, Wiley-Blackwell Publishing Inc. 2017, Vol. 77, (6) : 625-638
Djusberg, Erik; Jernberg, Emma; Thysell, Elin; et al.
2017
Molecular classification of malignat glioma
Neuro-Oncology
, Oxford University Press 2017, Vol. 19, (S3) : 88-88
Johansson, Gunnar; Brännström, Thomas; Andersson, Ulrika; et al.
2017
Mutation analysis and copy number alterations of KIF23 in non-small-cell lung cancer exhibiting KIF23 over-expression
OncoTargets and Therapy
, DOVE MEDICAL PRESS LTD 2017, Vol. 10 : 4969-4979
Vikberg, Ann-Louise; Vooder, Tonu; Lokk, Kaie; et al.
2016
Genetic risk variants in the CDKN2A/B, RTEL1 and EGFR genes are associated with somatic biomarkers in glioma
Journal of Neuro-Oncology
, Vol. 127, (3) : 483-492
Ghasimi, Soma; Wibom, Carl; Dahlin, Anna M.; et al.
2016
Heterogeneity and complexity of EYS mutations in autosomal recessive retinitis pigmentosa in northern Sweden
Investigative Ophthalmology and Visual Science
, ASSOC RESEARCH VISION OPHTHALMOLOGY INC 2016, Vol. 57, (12)
Golovleva, Irina; Jonsson, Frida; Burstedt, Marie
2016
Congenital Dyserythropoietic Anemia Type III and Primary Hemochromatosis; Coexistence of Mutations in
KIF23
and
HFE.
Journal of Hematology and Blood Disorders
, Annex Publishers 2016, Vol. 1, (2)
Liljeholm, Maria; Vikberg, Ann-Louise; Golovleva, Irina; et al.
2015
Mutations in Collagen, Type XVII, Alpha 1 (
COL17A1
) Cause Epithelial Recurrent Erosion Dystrophy (ERED)
Human Mutation
, John Wiley & Sons 2015, Vol. 36, (4) : 463-473
Jonsson, Frida; Byström, Berit; Davidson, Alice E.; et al.
2015
Congenital dyserythropoietic anemia type III and primary hemochromatosis; coexistence of mutations in KIF23 and HFE
Haematologica
, Vol. 100 : 594-594
Liljeholm, Maria; Vikberg, Ann-Louise; Golovleva, Irina; et al.
2015
The clinical impact of IKZF1 deletions in paediatric B-cell precursor acute lymphoblastic leukaemia is independent of minimal residual disease stratification in Nordic Society for Paediatric Haematology and Oncology treatment protocols used between 1992 and 2013
British Journal of Haematology
, Vol. 170, (6) : 847-858
Olsson, Linda; Oefverholm, Ingegerd Ivanov; Norén-Nyström, Ulrika; et al.
2014
Microbiology of folliculitis: a histological study of 39 cases
Acta Pathologica, Microbiologica et Immunologica Scandinavica (APMIS)
, Wiley-Blackwell 2014, Vol. 122, (1) : 25-32
Jahns, Anika C.; Lundskog, Bertil; Berg, Johanna; et al.
2014
Genetic heterogeneity and clinical outcome in a Swedish family with retinal degeneration caused by mutations in CRB1 and ABCA4 genes
Retinal Degenerative Diseases: Mechanisms and Experimental Therapy
, Springer Berlin/Heidelberg 2014 : 177-183
Jonsson, Frida; Burstedt, Marie S; Sandgren, Ola; et al.
2014
Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countries
Journal of Hematology & Oncology
, Vol. 7 : 32-
Lundin, Catarina; Forestier, Erik; Andersen, Mette Klarskov; et al.
2014
PROGNOSTIC IMPACT OF IKZF1 DELETIONS IN PEDIATRIC B-CELL PRECURSOR ACUTE LYMPHOBLASTIC LEUKEMIA TREATED ACCORDING TO NOPHO PROTOCOLS - THE SWEDISH EXPERIENCE
Haematologica
, Vol. 99, (Suppl 1) : 9-9
Ofverholm, I. Ivanov; Olsson, L.; Norén-Nyström, Ulrika; 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
Spatial distribution of bacterial-fungal communities in facial skin
Journal of dermatological science (Amsterdam)
, Vol. 70, (1) : 71-73
Jahns, Anika C; Golovleva, Irina; Palmer, Ruth H; et al.
2013
Simultaneous visualization of Propionibacterium acnes and Propionibacterium granulosum with immunofluorescence and fluorescence in situ hybridization
Anaerobe
, Elsevier 2013, Vol. 23 : 48-54
Jahns, Anika C; Oprica, Cristina; Vassilaki, Ismini; et al.
2013
Novel mutations in CRB1 and ABCA4 genes cause Leber congenital amaurosis and Stargardt disease in a Swedish family
European Journal of Human Genetics
, Nature Publishing Group 2013, Vol. 21, (11) : 1266-1271
Jonsson, Frida; Burstedt, Marie S; Sandgren, Ola; et al.
2013
Erythrocyte Flow Cytometric Analysis in Congenital Dyserythropoietic Anemia Type III-Evaluation of Eosin-5´-Maleimide, CD55, and CD59
Journal of Blood Disorders & Transfusion
, OMICS International 2013, Vol. 121, (23) : 4791-4799
Liljeholm, Maria; Grönlund, Elisabeth; Golovleva, Irina; et al.
2013
Congenital dyserythropoietic anemia type III (CDA III) is caused by a mutation in kinesin family member, KIF23
Blood
, Washington: American Society of Hematology 2013, Vol. 121, (23) : 4791-4799
Liljeholm, Maria; Irvine, Andrew F; Vikberg, Ann-Louise; et al.
2013
Screening of a Large Cohort of Leber Congenital Amaurosis and Retinitis Pigmentosa Patients Identifies Novel LCA5 Mutations and New Genotype-Phenotype Correlations
Human Mutation
, John Wiley & Sons 2013, Vol. 34, (11) : 1537-1546
Mackay, Donna S; Borman, Arundhati Dev; Sui, Ruifang; et al.
2013
High modal number and triple trisomies are highly correlated favorable factors in childhood B-cell precursor high hyperdiploid acute lymphoblastic leukemia treated according to the NOPHO ALL 1992/2000 protocols
Haematologica
, Fondazione Ferrata Storti 2013, Vol. 98, (9) : 1424-1432
Paulsson, Kajsa; Forestier, Erik; Andersen, Mette K; 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.
2013
Loss of chromosomes is the primary event in near-haploid and low-hypodiploid acute lymphoblastic leukemia
Leukemia
, Vol. 27, (1) : 248-250
Safavi, S.; Forestier, Erik; Golovleva, Irina; et al.
2012
Pattern of tissue invasion by Propionibacterium acnes in acne vulgaris
Journal of dermatological science (Amsterdam)
, Vol. 67, (1) : 63-66
Alexeyev, Oleg A; Lundskog, Bertil; Ganceviciene, Ruta; et al.
2012
Reduction in WT1 Gene Expression During Early Treatment Predicts the Outcome in Patients With Acute Myeloid Leukemia
Diagnostic molecular pathology (Print)
, Lippincott Williams & Wilkins 2012, Vol. 21, (4) : 225-233
Andersson, Charlotta; Li, Xingru; Lorenz, Fryderyk; et al.
2012
Additional aberrations of the ETV6 and RUNX1 genes have no prognostic impact in 229 t(12;21)(p13;q22)-positive B-cell precursor acute lymphoblastic leukaemias treated according to the NOPHO-ALL-2000 protocol
Leukemia Research
, Vol. 36, (7) : 936-938
Barbany, Gisela; Andersen, Mette K; Autio, Kirsti; et al.
2012
An increased incidence of Propionibacterium acnes biofilms in acne vulgaris: a case-control study
British Journal of Dermatology
, Vol. 167, (1) : 50-58
Jahns, Anika C; Lundskog, Bertil; Ganceviciene, R; et al.
2011
Paediatric B-cell precursor acute lymphoblastic leukaemia with t(1;19)(q23;p13): clinical and cytogenetic characteristics of 47 cases from the Nordic countries treated according to NOPHO protocols
British Journal of Haematology
, Oxford: Blackwell Scientific 2011, Vol. 155, (2) : 235-243
Andersen, Mette K.; Autio, Kirsi; Barbany, Gisela; et al.
2011
The frequency and prognostic impact of dic(9;20)(p13.2;q11.2) in childhood B-cell precursor acute lymphoblastic leukemia: results from the NOPHO ALL-2000 trial
Leukemia
, London: Nature Publishing Group 2011, Vol. 25, (4) : 622-628
Zachariadis, V; Gauffin, F; Kuchinskaya, E; et al.
2010
Central Retinal Findings in Bothnia Dystrophy Caused by RLBP1 Sequence Variation
Archives of ophthalmology (1960)
, American Medical Association 2010, Vol. 128, (8) : 989-995
Burstedt, Marie; Golovleva, Irina
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.
2010
Molecular and clinical characterization of patients with overlapping 10p deletions
American Journal of Medical Genetics. Part A
, Vol. 152A, (5) : 1233-1243
Lindstrand, Anna; Malmgren, Helena; Verri, Annapia; et al.
2009
A chromosome 10 variant with a 12 Mb inversion [inv(10)(q11.22q21.1)] identical by descent and frequent in the Swedish population
American Journal of Medical Genetics
, Vol. 149A, (3) : 380-386
Entesarian, Miriam; Carlsson, Birgit; Mansouri, Mahmoud Reza; et al.
2009
Clinical and cytogenetic features of a population-based consecutive series of 285 pediatric T-cell acute lymphoblastic leukemias: rare T-cell receptor gene rearrangements are associated with poor outcome
Genes, Chromosomes and Cancer
, Vol. 48, (9) : 795-805
Karrman, Kristina; Forestier, Erik; Heyman, Mats; 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.
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