K. Paulsson

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Short communication Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a multicolor and locus-specific fluorescence in situ hybridization study

H. Tanke, B. Johansson, T. Fioretos, 2003 .

Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a multicolor and locus-specific fluorescence in situ hybridization study.

H. Tanke, B. Johansson, T. Fioretos, 2003, Cancer genetics and cytogenetics.

High Resolution Genome-Wide Array-Based Comparative Genome Hybridization Reveals Cryptic Chromosome Changes in AML and MDS Cases with Trisomy 8 as the Sole Cytogenetic Aberration.

Å. Borg, B. Johansson, T. Fioretos, 2005 .

High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration

Å. Borg, B. Johansson, T. Fioretos, 2006, Leukemia.

Tapasin Is Required for Efficient Peptide Binding to Transporter Associated with Antigen Processing*

H. Sjögren, Shangwu Chen, K. Paulsson, 2000, The Journal of Biological Chemistry.

Genetic predisposition to B-cell acute lymphoblastic leukemia at 14q11.2 is mediated by a CEBPE promoter polymorphism

J. Vijayakrishnan, R. Houlston, James B. Studd, 2018, Leukemia.

Proteogenomics and Hi-C reveal transcriptional dysregulation in high hyperdiploid childhood acute lymphoblastic leukemia

D. Odom, T. Fioretos, R. Jafari, 2019, Nature Communications.

Proteogenomics and Hi-C reveal transcriptional dysregulation in high hyperdiploid childhood acute lymphoblastic leukemia

D. Odom, T. Fioretos, R. Jafari, 2019, Nature Communications.

Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpression of genes in 1q22-32.3.

Å. Borg, B. Johansson, T. Fioretos, 2007, Human molecular genetics.

Tiling resolution array CGH, expression, and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpression of genes in 1q22-32.3

Å. Borg, B. Johansson, A. Andersson, 2007 .

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

B. Johansson, A. Castor, K. Paulsson, 2014, Leukemia.

Risk of RAS in relapsed childhood ALL.

K. Paulsson, 2014, Blood.

Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations

B. Johansson, T. Fioretos, A. Nordgren, 2010, Leukemia.

Cooperative genetic changes in pediatric B‐cell precursor acute lymphoblastic leukemia with deletions or mutations of IKZF1

B. Johansson, A. Castor, K. Paulsson, 2015, Genes, chromosomes & cancer.

Quality control of MHC class I maturation

K. Paulsson, Ping Wang, 2004, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Chaperones and folding of MHC class I molecules in the endoplasmic reticulum.

K. Paulsson, Ping Wang, 2003, Biochimica et biophysica acta.

Association of Tapasin and COPI Provides a Mechanism for the Retrograde Transport of Major Histocompatibility Complex (MHC) Class I Molecules from the Golgi Complex to the Endoplasmic Reticulum*

H. Sjögren, P. Anderson, M. Kleijmeer, 2002, The Journal of Biological Chemistry.

Assembly of tapasin-associated MHC class I in the absence of the transporter associated with antigen processing (TAP).

H. Ljunggren, H. Sjögren, P. Anderson, 2001, International immunology.

Peptide-bound Major Histocompatibility Complex Class I Molecules Associate with Tapasin before Dissociation from Transporter Associated with Antigen Processing*

H. Sjögren, K. Paulsson, Suling Li, 1999, The Journal of Biological Chemistry.

A novel human in vitro papillomavirus type 16 positive tonsil cancer cell line with high sensitivity to radiation and cisplatin

J. Dillner, D. Bzhalava, E. Hultin, 2019, BMC Cancer.

Distinct differences in association of MHC class I with endoplasmic reticulum proteins in wild-type, and beta 2-microglobulin- and TAP-deficient cell lines.

R. Pettersson, P. Anderson, K. Paulsson, 2001, International immunology.

Inducing synthetic lethality for selective targeting of acute myeloid leukemia cells harboring STAG2 mutations

T. Fioretos, K. Paulsson, J. Larsson, 2022, bioRxiv.

Global RNA Expression and DNA Methylation Patterns in Primary Anaplastic Thyroid Cancer

Minjun Yang, K. Paulsson, N. Ravi, 2020, Cancers.

Chromosome gains drive childhood ALL

K. Paulsson, 2015, Oncotarget.

Single base substitution and insertion/deletion mutational signatures in adult core binding factor acute myeloid leukemia

B. Johansson, V. Lazarevic, Minjun Yang, 2022, Leukemia.

Novel gene targets detected by genomic profiling in a consecutive series of 126 adults with acute lymphoblastic leukemia

B. Johansson, K. Paulsson, M. Hansson, 2015, Haematologica.

The outermost N‐terminal region of tapasin facilitates folding of major histocompatibility complex class I

G. Røder, S. Buus, M. Harndahl, 2009, European journal of immunology.

The Double Lysine Motif of Tapasin Is a Retrieval Signal for Retention of Unstable MHC Class I Molecules in the Endoplasmic Reticulum1

K. Paulsson, Suling Li, Ping Wang, 2006, The Journal of Immunology.

13q12.2 deletions in acute lymphoblastic leukemia lead to upregulation of FLT3 through enhancer hijacking.

B. Johansson, T. Fioretos, M. Sigvardsson, 2020, Blood.

SNP array analysis of leukemic relapse samples after allogeneic hematopoietic stem cell transplantation with a sibling donor identifies meiotic recombination spots and reveals possible correlation with the breakpoints of acquired genetic aberrations

B. Johansson, D. Lindgren, K. Paulsson, 2011, Leukemia.

Distinct patterns of gained chromosomes in high hyperdiploid acute lymphoblastic leukemia with t(1;19)(q23;p13), t(9;22)(q34;q22) or MLL rearrangements

B. Johansson, A. Nordgren, M. Andersen, 2013, Leukemia.

Cytotoxic effect of menadione and sodium orthovanadate in combination on human glioma cells

J. Yakisich, Y. Hua, K. Paulsson, 2012, Investigational New Drugs.

Single nucleotide polymorphism array analysis of clonal evolution in younger adult acute lymphoblastic leukemia

T. Žvirblis, K. Paulsson, L. Griškevičius, 2016, Leukemia & lymphoma.

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

B. Johansson, A. Nordgren, M. Heyman, 2015, British journal of haematology.

Methylation of tumour suppressor gene promoters in the presence and absence of transcriptional silencing in high hyperdiploid acute lymphoblastic leukaemia

F. Ross, C. Harrison, A. Moorman, 2009, British journal of haematology.

Outcome of Children With Hypodiploid Acute Lymphoblastic Leukemia: A Retrospective Multinational Study.

C. Pui, R. Pieters, A. Baruchel, 2019, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Near-haploid and low-hypodiploid acute lymphoblastic leukemia: two distinct subtypes with consistently poor prognosis.

K. Paulsson, S. Safavi, 2017, Blood.

Tapasin and human leukocyte antigen class I dysregulation correlates with survival in glioblastoma multiforme.

K. Paulsson, L. Geironson, C. Thuring, 2014, Anti-cancer agents in medicinal chemistry.

Searching for cryptic chromosomal aberrations in high hyperdiploid childhood acute lymphoblastic leukaemias

B. Johansson, J. Davidsson, K. Paulsson, 2006, European journal of haematology.

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

B. Johansson, A. Nordgren, L. Cavelier, 2013, Haematologica.

Allelic variants of PRDM9 associated with high hyperdiploid childhood acute lymphoblastic leukaemia

B. Johansson, Eleanor L. Woodward, K. Paulsson, 2014, British journal of haematology.

Substantial intrinsic variability in chemoradiosensitivity of newly established anaplastic thyroid cancer cell-lines

Å. Borg, E. Brun, K. Paulsson, 2020, Acta oto-laryngologica.

In silico peptide-binding predictions of passerine MHC class I reveal similarities across distantly related species, suggesting convergence on the level of protein function

C. Lundegaard, M. Nielsen, S. Wallin, 2013, Immunogenetics.

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

B. Johansson, C. Harrison, A. Moorman, 2013, Leukemia.

Improved cytogenetic characterization and risk stratification of pediatric acute lymphoblastic leukemia using single nucleotide polymorphism array analysis: A single center experience of 296 cases

B. Johansson, A. Castor, K. Paulsson, 2018, Genes, chromosomes & cancer.

Cytogenetic and molecular genetic characterization of the ‘high hyperdiploid’ B‐cell precursor acute lymphoblastic leukaemia cell line MHH‐CALL‐2 reveals a near‐haploid origin

B. Johansson, K. Paulsson, A. Biloglav, 2011, British journal of haematology.

NUP 98 / PSIP 1 ] is a poor prognostic marker associated with de novo acute myeloid leukaemia expressing both mature and immature surface antigens

K. Paulsson, K. Karlsson, C. Lundin, 2011 .

The insulin receptor substrate 4 gene (IRS4) is mutated in paediatric T‐cell acute lymphoblastic leukaemia

B. Johansson, K. Paulsson, M. Isaksson, 2011, British journal of haematology.

Microdeletions are a general feature of adult and adolescent acute lymphoblastic leukemia: Unexpected similarities with pediatric disease

T. Lister, J. Cazier, K. Paulsson, 2008, Proceedings of the National Academy of Sciences.

Pankiller effect of prolonged exposure to menadione on glioma cells: potentiation by vitamin C

M. Vita, J. Yakisich, K. Paulsson, 2010, Investigational New Drugs.

Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia

B. Johansson, T. Fioretos, A. Isaksson, 2018, Leukemia.

FLT3 mutations in a 10 year consecutive series of 177 childhood acute leukemias and their impact on global gene expression patterns

B. Johansson, C. Lassen, T. Fioretos, 2008, Genes, chromosomes & cancer.

Characterisation of genomic translocation breakpoints and identification of an alternative TCF3/PBX1 fusion transcript in t(1;19)(q23;p13)‐positive acute lymphoblastic leukaemias

B. Johansson, I. Øra, I. Panagopoulos, 2007, British journal of haematology.

De novo activating mutations drive clonal evolution and enhance clonal fitness in KMT2A-rearranged leukemia

J. Downing, Jing Ma, Guangchun Song, 2018, Nature Communications.

Inhibition of the transcription factors AP-1 and NF-kappaB in CD4 T cells by peroxisome proliferator-activated receptor gamma ligands.

P. Anderson, Shangwu Chen, K. Paulsson, 2001, International immunopharmacology.

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

B. Johansson, A. Castor, K. Paulsson, 2016, British journal of haematology.

Pan-Genomic Sequencing Reveals Actionable CDKN2A/2B Deletions and Kataegis in Anaplastic Thyroid Carcinoma

A. Stenman, Minjun Yang, J. Zedenius, 2021, Cancers.

Trisomies in Hematologic Malignancies

K. Paulsson, 2005 .

Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia

B. Johansson, T. Fioretos, A. Andersson, 2008, Genes, chromosomes & cancer.

Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia

B. Johansson, F. Mitelman, T. Fioretos, 2016, Nature Communications.

A population‐based single nucleotide polymorphism array analysis of genomic aberrations in younger adult acute lymphoblastic leukemia patients

T. Žvirblis, K. Paulsson, L. Griškevičius, 2015, Genes, chromosomes & cancer.

High hyperdiploid childhood acute lymphoblastic leukemia

Bertil Johansson, B. Johansson, K. Paulsson, 2009, Genes, chromosomes & cancer.

Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes.

B. Johansson, K. Paulsson, 2007, Pathologie-biologie.

Genetic and epigenetic characterization of hypodiploid acute lymphoblastic leukemia

B. Johansson, Srinivas Veerla, A. Castor, 2015, Oncotarget.

Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies.

M. Rocchi, B. Johansson, C. Lassen, 2004, Human molecular genetics.

Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia

Bertil Johansson, Henrik Lilljebjörn, Bryan D. Young, 2010, Proceedings of the National Academy of Sciences.

HLA-I antigen presentation and tapasin influence immune responses against malignant brain tumors - considerations for successful immunotherapy.

K. Paulsson, A. Darabi, C. Thuring, 2014, Anti-Cancer Agents in Medicinal Chemistry.

Low Concentration of Salinomycin Prevents Regrowth and Partially Depletes Human Glioma Cells Surviving High Concentrations of Alkylating Agents.

J. Yakisich, K. Paulsson, Å. Sidén, 2013 .

Genomic Heterogeneity in Acute Leukemia

K. Paulsson, 2013, Cytogenetic and Genome Research.

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

B. Johansson, A. Nordgren, L. Palmqvist, 2012, Genes, chromosomes & cancer.

A novel and cytogenetically cryptic t(7;21)(p22;q22) in acute myeloid leukemia results in fusion of RUNX1 with the ubiquitin-specific protease gene USP42

B. Johansson, F. Mitelman, I. Panagopoulos, 2006, Leukemia.

Genomic complexity and targeted genes in anaplastic thyroid cancer cell lines.

Minjun Yang, Eleanor L. Woodward, K. Paulsson, 2017, Endocrine-related cancer.

Tapasin Facilitation of Natural HLA-A and -B Allomorphs Is Strongly Influenced by Peptide Length, Depends on Stability, and Separates Closely Related Allomorphs

G. Røder, S. Buus, M. Harndahl, 2013, The Journal of Immunology.

The idic(X)(q13) in myeloid malignancies: breakpoint clustering in segmental duplications and association with TET2 mutations.

B. Johansson, A. Hagemeijer, M. Slovak, 2010, Human molecular genetics.

10 MHC Class I Quality Control

G. Røder, K. Paulsson, L. Geironson, 2018 .

MHC Class I Quality Control

G. Røder, K. Paulsson, Linda Geironson Ulfsson, 2012 .

Viral Proteins Interfering with Antigen Presentation Target the Major Histocompatibility Complex Class I Peptide-Loading Complex

G. Røder, K. Paulsson, I. Bressendorff, 2008, Journal of Virology.

Evolutionary and functional perspectives of the major histocompatibility complex class I antigen-processing machinery

K. Paulsson, Kajsa M Paulsson, 2004, Cellular and Molecular Life Sciences CMLS.

Retained heterodisomy is associated with high gene expression in hyperhaploid inflammatory leiomyosarcoma.

F. Mertens, Srinivas Veerla, N. Mandahl, 2012, Neoplasia.

Correction: Clonal Evolution through Loss of Chromosomes and Subsequent Polyploidization in Chondrosarcoma

K. Paulsson, J. Bovée, K. H. Nord, 2011, PLoS ONE.

Clonal Evolution through Loss of Chromosomes and Subsequent Polyploidization in Chondrosarcoma

K. Paulsson, J. Bovée, K. H. Nord, 2011, PloS one.

Evidence for a single‐step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia

B. Johansson, T. Fioretos, K. Paulsson, 2005, Genes, chromosomes & cancer.

Proteogenomics and Hi-C reveal transcriptional dysregulation in high hyperdiploid childhood acute lymphoblastic leukemia

D. Odom, T. Fioretos, R. Jafari, 2019, Nature Communications.

Genomic complexity and targeted genes in anaplastic thyroid cancer cell lines.

Minjun Yang, Eleanor L. Woodward, K. Paulsson, 2017, Endocrine-related cancer.

Tissue architecture delineates field cancerization in BRAFV600E-induced tumor development.

M. Bergo, Shawn Liang, J. Kero, 2021, Disease models & mechanisms.

Cytokine-Induced Src Homology 2 Protein (Cis) Promotes T Cell Receptor–Mediated Proliferation and Prolongs Survival of Activated T Cells

S. Karlsson, P. Anderson, Shangwu Chen, 2000, The Journal of experimental medicine.

Genetic and regulatory mechanism of susceptibility to high-hyperdiploid acute lymphoblastic leukaemia at 10q21.2

J. Vijayakrishnan, R. Houlston, James B. Studd, 2017, Nature Communications.

Identification of cryptic aberrations and characterization of translocation breakpoints using array CGH in high hyperdiploid childhood acute lymphoblastic leukemia

Å. Borg, B. Johansson, T. Fioretos, 2006, Leukemia.

Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia.

B. Johansson, F. Mitelman, T. Fioretos, 2003, Blood.

The incidence of trisomy 8 as a sole chromosomal aberration in myeloid malignancies varies in relation to gender, age, prior iatrogenic genotoxic exposure, and morphology.

B. Johansson, F. Mitelman, T. Fioretos, 2001, Cancer genetics and cytogenetics.

Sister chromatid cohesion defects are associated with chromosomal copy number heterogeneity in high hyperdiploid childhood acute lymphoblastic leukemia

A. Castor, Minjun Yang, K. Paulsson, 2020, Genes, chromosomes & cancer.

The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia

B. Johansson, T. Fioretos, A. Nordgren, 2015, Nature Genetics.

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

B. Johansson, T. Fioretos, M. Ehinger, 2015, Journal of Hematology & Oncology.

Dendritic cell dysfunction and implications for dendritic cell-based therapy in colorectal cancer

K. Paulsson, M. Josiassen, 2011 .

Multicolor fluorescence in situ hybridization characterization of cytogenetically polyclonal hematologic malignancies.

B. Johansson, J. Davidsson, K. Paulsson, 2005, Cancer genetics and cytogenetics.

MYC is not overexpressed in a case of chronic myelomonocytic leukemia with MYC-containing double minutes

H. Tanke, B. Johansson, C. Lassen, 2003, Leukemia.

Extraordinary peptide-binding mode of a songbird MHC class-I molecule suggests mechanism to counter pathogen immune evasion

M. Nielsen, S. Buus, K. Lindkvist-Petersson, 2023, bioRxiv.

Stability of peptide–HLA‐I complexes and tapasin folding facilitation – tools to define immunogenic peptides

G. Røder, K. Paulsson, L. Geironson, 2012, FEBS letters.

Tapasin Discriminates Peptide-Human Leukocyte Antigen-A*02:01 Complexes Formed with Natural Ligands*

G. Røder, S. Buus, M. Harndahl, 2011, The Journal of Biological Chemistry.

HLA class I is most tightly linked to levels of tapasin compared with other antigen-processing proteins in glioblastoma

S. Buus, M. Harndahl, K. Paulsson, 2015, British Journal of Cancer.

t(9;11)(p22;p15) [NUP98/PSIP1] is a poor prognostic marker associated with de novo acute myeloid leukaemia expressing both mature and immature surface antigens.

B. Johansson, K. Paulsson, T. Olofsson, 2011, Leukemia research.

Partial 17q gain resulting from isochromosomes, unbalanced translocations and complex rearrangements is associated with gene overexpression, older age and shorter overall survival in high hyperdiploid childhood acute lymphoblastic leukemia

B. Johansson, K. Paulsson, A. Biloglav, 2013, Leukemia.

Single base substitution mutational signatures in pediatric acute myeloid leukemia based on whole genome sequencing

B. Johansson, A. Castor, Minjun Yang, 2021, Leukemia.

Clonal origin and development of high hyperdiploidy in childhood acute lymphoblastic leukaemia

B. Johansson, J. Zuna, F. Foijer, 2023, Nature Communications.

Identification of Targetable Lesions in Anaplastic Thyroid Cancer by Genome Profiling

Minjun Yang, Eleanor L. Woodward, K. Paulsson, 2019, Cancers.

Formation of der(19)t(1;19)(q23;p13) in acute lymphoblastic leukemia

Thoas Fioretos, Bertil Johansson, B. Johansson, 2005, Genes, chromosomes & cancer.

Patterns and frequencies of acquired and constitutional uniparental isodisomies in pediatric and adult B‐cell precursor acute lymphoblastic leukemia

B. Johansson, K. Paulsson, L. Olsson, 2016, Genes, chromosomes & cancer.

De novo activating mutations drive clonal evolution and enhance clonal fitness in KMT2A-rearranged leukemia

J. Downing, Jing Ma, Guangchun Song, 2018, Nature Communications.

High hyperdiploid childhood acute lymphoblastic leukemia: Chromosomal gains as the main driver event

K. Paulsson, 2016, Molecular & cellular oncology.

The structure of songbird MHC class I reveals antigen binding that is flexible at the N-terminus and static at the C-terminus

M. Nielsen, S. Buus, K. Lindkvist-Petersson, 2023, Frontiers in immunology.

Genetic and regulatory mechanism of susceptibility to high-hyperdiploid acute lymphoblastic leukaemia at 10p21.2.

J. Vijayakrishnan, R. Houlston, James B. Studd, 2017 .

Genetic and epigenetic characterization of hypodiploid acute lymphoblastic leukemia

B. Johansson, Srinivas Veerla, A. Castor, 2015, Oncotarget.

Molecular characterisation of a recurrent, semi‐cryptic RUNX1 translocation t(7;21) in myelodysplastic syndrome and acute myeloid leukaemia

M. Sales, K. Paulsson, M. Groves, 2010, British journal of haematology.

Cooperative genetic changes in pediatric B‐cell precursor acute lymphoblastic leukemia with deletions or mutations of IKZF1

B. Johansson, A. Castor, K. Paulsson, 2015, Genes, Chromosomes and Cancer.

Novel gene targets detected by genomic profiling in a consecutive series of 126 adults with acute lymphoblastic leukemia

B. Johansson, K. Paulsson, M. Hansson, 2015, Haematologica.

Clonal Evolution through Loss of Chromosomes and Subsequent Polyploidization in Chondrosarcoma

K. Paulsson, J. Bovée, K. H. Nord, 2011, PLoS ONE.

Genomic complexity and targeted genes in anaplastic thyroid cancer cell lines.

Minjun Yang, Eleanor L. Woodward, K. Paulsson, 2017, Endocrine-related cancer.

B. Johansson, M. Heyman, K. Paulsson, 2015, British journal of haematology.

Chromosomal Gains as a Favorable Prognostic Factor in Pediatric ALL.

K. Paulsson, 2023, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Patterns and frequencies of acquired and constitutional uniparental isodisomies in pediatric and adult B‐cell precursor acute lymphoblastic leukemia

B. Johansson, K. Paulsson, L. Olsson, 2016, Genes, chromosomes & cancer.

Ethnicity, deprivation and screening: survival from breast cancer among screening-eligible women in the West Midlands diagnosed from 1989 to 2011

B. Rachet, D. Nicol, D. Fitzpatrick, 2015, British Journal of Cancer.

Drug-resilient Cancer Cell Phenotype Is Acquired via Polyploidization Associated with Early Stress Response Coupled to HIF2α Transcriptional Regulation

K. Pienta, F. Foijer, D. Spierings, 2024, Cancer research communications.

Constitutional and acquired genetic variants in ARID5B in pediatric B‐cell precursor acute lymphoblastic leukemia

B. Johansson, T. Fioretos, J. Zuna, 2024, Genes, chromosomes & cancer.