Erik Forestier

Research qualifications: Docent

Contact

erik.forestier@umu.se

Works at

Affiliated as research fellow at Department of Medical Biosciences Section: Medical and Clinical Genetics

By 6M, Sjukhusområdet Umeå universitet, 901 85 Umeå

Publications Publications

Multimodal classification of molecular subtypes in pediatric acute lymphoblastic leukemia

npj Precision Oncology, Nature Publishing Group 2023, Vol. 7, (1)

Krali, Olga; Marincevic-Zuniga, Yanara; Arvidsson, Gustav; et al.

DNA methylation holds prognostic information in relapsed precursor B-cell acute lymphoblastic leukemia

Clinical Epigenetics, BioMed Central 2018, Vol. 10

Borssén, Magnus; Nordlund, Jessica; Haider, Zahra; et al.

Quantification of Fusion Transcripts Reveals Slower Treatment Kinetics As Compared with Multiparameter Flow Cytometry during Induction Treatment of Acute Myeloid Leukemia in Children

Blood, American Society of Hematology 2018, Vol. 132

Karlsson, Lene; Nyvold, Charlotte Guldborg; Palmqvist, Lars; et al.

Pediatric Blood & Cancer, Vol. 65, (4)

Oskarsson, Trausti; Söderhäll, Stefan; Arvidson, Johan; et al.

Outcome after intensive reinduction therapy and allogeneic stem cell transplant in paediatric relapsed acute myeloid leukaemia

British Journal of Haematology, WILEY 2017, Vol. 178, (4) : 592-602

Karlsson, Lene; Forestier, Erik; Hasle, Henrik; et al.

Transcriptome sequencing in pediatric acute lymphoblastic leukemia identifies fusion genes associated with distinct DNA methylation profiles

Journal of Hematology & Oncology, BIOMED CENTRAL LTD 2017, Vol. 10

Marincevic-Zuniga, Yanara; Dahlberg, Johan; Nilsson, Sara; et al.

Children with low-risk acute lymphoblastic leukemia are at highest risk of second cancers

Pediatric Blood & Cancer, Wiley-Blackwell 2017, Vol. 64, (10)

Nielsen, Stine N.; Eriksson, Frank; Rosthoej, Susanne; et al.

Hyperleucocytosis in paediatric acute myeloid leukaemia - the challenge of white blood cell counts above 200 x 10(9)/l. The NOPHO experience 1984-2014

British Journal of Haematology, WILEY 2017, Vol. 178, (3) : 448-456

Zeller, Bernward; Glosli, Heidi; Forestier, Erik; et al.

DNA Methylation Adds Prognostic Value to Minimal Residual Disease Status in Pediatric T-Cell Acute Lymphoblastic Leukemia

Pediatric Blood & Cancer, Vol. 63, (7) : 1185-1192

Borssén, Magnus; Haider, Zahra; Landfors, Mattias; et al.

Deep targeted sequencing in pediatric acute lymphoblastic leukemia unveils distinct mutational patterns between genetic subtypes and novel relapse-associated genes

Oncotarget, Vol. 7, (39) : 64071-64088

Lindqvist, C. Marten; Lundmark, Anders; Nordlund, Jessica; et al.

Trisomy 8 in pediatric acute myeloid leukemia: A NOPHO-AML study

Genes, Chromosomes and Cancer, Wiley-Blackwell 2016, Vol. 55, (9) : 719-726

Lund Laursen, Anne Cathrine; Sandahl, Julie Damgaard; Kjeldsen, Eigil; et al.

PAX5-ESRRB is a recurrent fusion gene in B-cell precursor pediatric acute lymphoblastic leukemia

Haematologica, Vol. 101, (1) : E20-E23

Marincevic-Zuniga, Yanara; Zachariadis, Vasilios; Cavelier, Lucia; et al.

The genetic landscape of paediatric de novo acute myeloid leukaemia as defined by single nucleotide polymorphism array and exon sequencing of 100 candidate genes

British Journal of Haematology, Wiley-Blackwell 2016, Vol. 174, (2) : 292-301

Olsson, Linda; Zettermark, Sofia; Biloglav, Andrea; et al.

Relapsed childhood acute lymphoblastic leukemia in the Nordic countries: prognostic factors, treatment and outcome

Haematologica, Vol. 101, (1) : 68-76

Oskarsson, Trausti; Soderhall, Stefan; Arvidson, Johan; et al.

Residual disease detected by flow cytometry is an independent predictor of survival in childhood acute myeloid leukaemia; results of the NOPHO-AML 2004 study

British Journal of Haematology, Vol. 174, (4) : 600-609

Tierens, Anne; Bjørklund, Elizabeth; Siitonen, Sanna; et al.

DNA methylome analysis of acute lymphoblastic leukemia cells reveals stochastic de novo DNA methylation in CpG islands

Epigenomics, Vol. 8, (10) : 1367-1387

Wahlberg, Per; Lundmark, Anders; Nordlund, Jessica; et al.

Acute Myeloid Leukemia in Adolescents and Young Adults Treated in Pediatric and Adult Departments in the Nordic Countries

Pediatric Blood & Cancer, Wiley-Blackwell 2016, Vol. 63, (1) : 83-92

Wennström, Lovisa; Edslev, Pernille Wendtland; Abrahamsson, Jonas; et al.

Heterogeneous cytogenetic subgroups and outcomes in childhood acute megakaryoblastic leukemia: a retrospective international study

Blood, American Society of Hematology 2015, Vol. 126, (13) : 1575-1584

Inaba, Hiroto; Zhou, Yinmei; Abla, Oussama; et al.

Deep sequencing and SNP array analyses of pediatric T-cell acute lymphoblastic leukemia reveal NOTCH1 mutations in minor subclones and a high incidence of uniparental isodisomies affecting CDKN2A

Journal of Hematology & Oncology, Vol. 8

Karrman, Kristina; Castor, Anders; Behrendtz, Mikael; et al.

The Mutational Landscape in Pediatric Acute Lymphoblastic Leukemia Deciphered by Whole Genome Sequencing

Human Mutation, Vol. 36, (1) : 118-128

Lindqvist, Carl Marten; Nordlund, Jessica; Ekman, Diana; et al.

DNA methylation-based subtype prediction for pediatric acute lymphoblastic leukemia

Clinical Epigenetics, Vol. 7

Nordlund, Jessica; Backlin, Christofer L.; Zachariadis, Vasilios; et al.

Normal karyotype is a poor prognostic factor in myeloid leukemia of Down syndrome: a retrospective, international study

Haematologica, Ferrata Storti Foundation 2014, Vol. 99, (2) : 299-307

Blink, Marjolein; Zimmermann, Martin; von Neuhoff, Christine; et al.

Acute lymphoblastic leukemia in children with Down syndrome: a retrospective analysis from the Ponte di Legno study group

Blood, American Society of Hematology 2014, Vol. 123, (1) : 70-77

Buitenkamp, Trudy D.; Izraeli, Shai; Zimmermann, Martin; et al.

Immortalization of T-Cells Is Accompanied by Gradual Changes in CpG Methylation Resulting in a Profile Resembling a Subset of T-Cell Leukemias

Neoplasia, Vol. 16, (7) : 606-615

Degerman, Sofie; Landfors, Mattias; Siwicki, Jan Konrad; et al.

Prognostic Implications of Mutations in NOTCH1 and FBXW7 in Childhood T-ALL Treated According to the NOPHO ALL-1992 and ALL-2000 Protocols

Pediatric Blood & Cancer, Wiley-Blackwell 2014, Vol. 61, (3) : 424-430

Fogelstrand, Linda; Staffas, Anna; Wasslavik, Carina; et al.

An international study of intrachromosomal amplification of chromosome 21 (iAMP21): cytogenetic characterization and outcome

Leukemia, Vol. 28, (5) : 1015-1021

Harrison, C. J.; Moorman, A. V.; Schwab, C.; et al.

Anthracycline Type during Induction Associated with Outcome in Pediatric t(8;21) and Inv(16) AML

Blood, Vol. 124, (21)

Hasle, Henrik; Abrahamsson, Jonas; De Bont, Evelina S.; et al.

Pediatric Acute Megakaryoblastic Leukemia without Down Syndrome: A Retrospective Study by the International Berlin-Frankfurt-Munster Study Group (I-BFMSG)

Blood, Vol. 124, (21)

Inaba, Hiroto; Zhou, Yinmei; Abla, Oussama; et al.

Clinical features and early treatment response of central nervous system involvement in childhood acute lymphoblastic leukemia

Pediatric Blood & Cancer, Vol. 61, (8) : 1416-1421

Levinsen, Mette; Taskinen, Mervi; Abrahamsson, Jonas; 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.

Deletions of IKZF1 and SPRED1 are associated with poor prognosis in a population-based series of pediatric B-cell precursor acute lymphoblastic leukemia diagnosed between 1992 and 2011

Leukemia, Vol. 28, (2) : 302-310

Olsson, L; Castor, A; Behrendtz, M; et al.

Pediatric Blood & Cancer, Wiley-Blackwell 2014, Vol. 61 2, (Supplement: 2 Meeting Abstract: EP-045) : S264-S264

Oskarsson, T.; Soderhall, S.; Arvidson, J.; et al.

t(6;9)(p22; q34)/DEK-NUP214-rearranged pediatric myeloid leukemia: an international study of 62 patients

Haematologica, Vol. 99, (5) : 865-872

Sandahl, Julie Damgaard; Coenen, Eva A.; Forestier, Erik; et al.

Ploidy and clinical characteristics of childhood acute myeloid leukemia: A NOPHO-AML study

Genes, Chromosomes and Cancer, Vol. 53, (8) : 667-675

Sandahl, Julie Damgaard; Kjeldsen, Eigil; Abrahamsson, Jonas; et al.

Detecting dic(9;20)(p13.2;p11.2)-positive B-cell precursor acute lymphoblastic leukemia in a clinical setting using fluorescence in situ hybridization

Leukemia, Nature Publishing Group 2014, Vol. 28, (1) : 196-198

Zachariadis, V.; Schoumans, J.; Ofverholm, I.; et al.

Accurate detection of subclonal single nucleotide variants in whole genome amplified and pooled cancer samples using HaloPlex target enrichment

BMC Genomics, BioMed Central 2013, Vol. 14 : 856-

Berglund, Eva C.; Lindqvist, Carl Mårten; Hayat, Shahina; et al.

Promoter DNA methylation pattern identifies prognostic subgroups in childhood T-cell acute lymphoblastic leukemia

PLOS ONE, Vol. 8, (6) : e65373-

Borssen, Magnus; Palmqvist, Lars; Karrman, Kristina; et al.

Genome-wide signatures of differential DNA methylation in pediatric acute lymphoblastic leukemia

Genome Biology, BioMed Central 2013, Vol. 14, (9) : Article number: r105-

Nordlund, Jessica; Backlin, Christofer L.; Wahlberg, Per; 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.

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.

Outcome of poor response paediatric AML using early SCT

European Journal of Haematology, Vol. 90, (3) : 187-194

Wareham, Neval E.; Heilmann, Carsten; Abrahamsson, Jonas; 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.

KI, WU, and Merkel Cell Polyomavirus DNA was not Detected in Guthrie Cards of Children who Later Developed Acute Lymphoblastic Leukemia

Journal of pediatric hematology/oncology (Print), Vol. 34, (5) : 364-367

Gustafsson, Britt; Honkaniemi, Emma; Goh, Shan; et al.

Gemtuzumab ozogamicin as postconsolidation therapy does not prevent relapse in children with AML: results from NOPHO-AML 2004

Blood, Vol. 120, (5) : 978-984

Hasle, Henrik; Abrahamsson, Jonas; Forestier, Erik; et al.

High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome

Genes, Chromosomes and Cancer, Malden: Wiley-Blackwell 2012, Vol. 51, (2) : 196-206

Lundin, Catarina; Hjorth, Lars; Behrendtz, Mikael; et al.

The DNA Methylation Landscape of Paediatric Acute Lymphoblastic Leukemia

European Journal of Cancer, Elsevier 2012, Vol. 48 : S141-S141

Nordlund, J.; Backlin, C.; Wahlberg, P.; et al.

Digital gene expression profiling of primary acute lymphoblastic leukemia cells

Leukemia, Vol. 26, (6) : 1218-1227

Nordlund, J.; Kiialainen, A.; Karlberg, O.; et al.

Relapsed acute lymphoblastic leukemia in the nordic countries - prognostic factors, treatment and outcome

Pediatric Blood & Cancer, Vol. 59, (6) : 1007-1008

Oskarsson, Trausti; Söderhall, Stefan; Arvidson, Johan; et al.

High ERG gene expression is an unfavorable prognostic marker in pediatric acute myeloid leukemia Response

Blood, Washington DC: The American Society of Hematology 2012, Vol. 119, (4) : 1087-1088

Staffas, Anna; Kanduri, Meena; Hovland, Randi; et al.

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