Irina Golovleva

Vetenskaplig meritering: Docent

Kontakt

irina.golovleva@umu.se

090-785 68 20

Verksam som

Adjungerad professor vid Institutionen för medicinsk biovetenskap Enhet: Medicinsk och klinisk genetik

By 6M, vån 1, Sjukhusområdet Umeå universitet, 901 85 Umeå

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.

Hearing impairment and vestibular function in patients with a pathogenic splice variant in the LHX3 gene

BMC Medical Genomics, BioMed Central (BMC) 2024, Vol. 17, (1)

Kjellgren, Åsa; Lundgren, Elenor; Golovleva, Irina; et al.

Hyperinsulinemia in Sotos syndrome with a de novo NSD1 deletion

Journal of clinical research in pediatric endocrinology

Lundberg, Elena; Burstedt, Magnus; Golovleva, Irina

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.

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.

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.

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.

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.

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.

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.

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

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.

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.

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.

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.

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.

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.

Molecular classification of malignat glioma

Neuro-Oncology, Oxford University Press 2017, Vol. 19, (S3) : 88-88

Johansson, Gunnar; Brännström, Thomas; Andersson, Ulrika; et al.

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.

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.

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

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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

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.

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.

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.

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.

Visa publikationer i DiVA

Forskargrupper

Forskningsledare

Irina Golovlevas labb