Author

Irina Golovleva

Observed names: Golovleva I, Golovleva, I, Golovleva, Irina, I GOLOVLEVA, I Golovleva, I. Golovleva, IRINA GOLOVLEVA

Observed institutions: Massachusetts Eye and Ear Infirmary, Harvard University, University of Cape Town, National University of Singapore, Vilnius University, McGill University Health Centre, Blood Cancer UK, University Hospital of Umeå, Eastern Finland Laboratory Center, University College London, Umeå University

ORCID: 0000-0001-8741-0616

Observed ORCID: 0000-0001-8741-0616

OpenAlex ID: A5009390244

An increased incidence of Propionibacterium acnes biofilms in acne vulgaris: a case-control study

2012 · A.C. Jahns, B. Lundskog, et al. · British Journal of Dermatology · 237

Cloning, Characterization, and Expression of Human LIG1

2001 · Jonas Nilsson, Christina Vallbo, et al. · Biochemical and Biophysical Research Communications · 140

Alterations in the expression, structure and function of progesterone receptor membrane component-1 (PGRMC1) in premature ovarian failure

2008 · Mahmoud Reza Mansouri, Jens Schuster, et al. · Human Molecular Genetics · 137

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Congenital dyserythropoietic anemia type III (CDA III) is caused by a mutation in kinesin family member, KIF23

2013 · Maria Liljeholm, Andrew F. Irvine, et al. · Blood · 111

Outcome of ETV6/RUNX1‐positive childhood acute lymphoblastic leukaemia in the NOPHO‐ALL‐1992 protocol: frequent late relapses but good overall survival

2008 · Erik Forestier, Mats Heyman, et al. · British Journal of Haematology · 106

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Molecular and clinical characterization of patients with overlapping 10p deletions

2010 · Anna Lindstrand, Helena Malmgren, et al. · American Journal of Medical Genetics Part A · 102

Direct Visualization ofPropionibacterium acnesin Prostate Tissue by Multicolor Fluorescent In Situ Hybridization Assay

2007 · Oleg A. Alexeyev, Ingrid Marklund, et al. · Journal of Clinical Microbiology · 93

Prognostic significance of risk group stratification in elderly patients with acute myeloid leukaemia

2001 · Anders Wahlin, Berit Markevärn, et al. · British Journal of Haematology · 87

Characterization and tissue-specific expression of human LRIG2

2004 · Camilla Holmlund, Jonas Nilsson, et al. · Gene · 74

Ocular phenotype of bothnia dystrophy, an autosomal recessive retinitis pigmentosa associated with an R234W mutation in the RLBP1 gene.

2001 · M S Burstedt, K Forsman-Semb, et al. · PubMed · 74

Disease-causing Mutations in the Cellular Retinaldehyde Binding Protein Tighten and Abolish Ligand Interactions

2003 · Irina Golovleva, Sanjoy Bhattacharya, et al. · Journal of Biological Chemistry · 71

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Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families

2007 · Linda Köhn, Konstantin Kadzhaev, et al. · European Journal of Human Genetics · 64

Loss of chromosomes is the primary event in near-haploid and low-hypodiploid acute lymphoblastic leukemia

2012 · S Safavi, E Forestier, et al. · Leukemia · 60

Mutations in Collagen, Type XVII, Alpha 1 ( COL17A1 ) Cause Epithelial Recurrent Erosion Dystrophy (ERED)

2015 · Frida Jonsson, Berit Byström, et al. · Human Mutation · 55

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Characterisation of dic(9;20)(p11–13;q11) in childhood B‐cell precursor acute lymphoblastic leukaemia by tiling resolution array‐based comparative genomic hybridisation reveals clustered breakpoints at 9p13.2 and 20q11.2

2006 · Jacqueline Schoumans, Bertil Johansson, et al. · British Journal of Haematology · 55

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

2013 · K. Paulsson, E. Forestier, et al. · Haematologica · 54

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The clinical impact of IKZF 1 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

2015 · Linda Olsson, Ingegerd Ivanov Öfverholm, et al. · British Journal of Haematology · 46

Cytogenetic patterns in ETV6/RUNX1‐positive pediatric B‐cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature

2007 · Erik Forestier, Mette K. Andersen, et al. · Genes Chromosomes and Cancer · 46

Two Swedish founder MSH6 mutations, one nonsense and one missense, conferring high cumulative risk of Lynch syndrome

2005 · K Cederquist, M Emanuelsson, et al. · Clinical Genetics · 45

Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: A population‐based study in northern Sweden

2004 · Kristina Cederquist, Monica Emanuelsson, et al. · International Journal of Cancer · 41

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Pattern of tissue invasion by Propionibacterium acnes in acne vulgaris

2012 · Oleg A. Alexeyev, Bertil Lundskog, et al. · Journal of Dermatological Science · 40

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

2009 · Kristina Karrman, Erik Forestier, et al. · Genes Chromosomes and Cancer · 39

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

2011 · Mette K. Andersen, Kirsi Autio, et al. · British Journal of Haematology · 38

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Screening of a Large Cohort of Leber Congenital Amaurosis and Retinitis Pigmentosa Patients Identifies Novel LCA5 Mutations and New Genotype-Phenotype Correlations

2013 · Donna S. Mackay, Arundhati Dev Borman, et al. · Human Mutation · 37

High levels of the AR-V7 Splice Variant and Co-Amplification of the Golgi Protein CodingYIPF6inARAmplified Prostate Cancer Bone Metastases

2017 · Erik Djusberg, Emma Jernberg, et al. · The Prostate · 35

Works count: 121

Citation count: 2,854

H-index: 29

I10-index: 68