T. Jonson

发表

Retained heterodisomy for chromosome 12 in atypical lipomatous tumors: implications for ring chromosome formation

D. Gisselsson, F. Mertens, N. Mandahl, 2004, Cytogenetic and Genome Research.

Four evolutionary trajectories underlie genetic intratumoral variation in childhood cancer

Anders Isaksson, Johan Staaf, Jenny Karlsson, 2018, Nature Genetics.

Cytogenetic and FISH analyses of pancreatic carcinoma reveal breaks in 18q11 with consistent loss of 18q12-qter and frequent gain of 18p.

B. Johansson, L. Gorunova, G. Stenman, 1998, British Journal of Cancer.

Convergent evolution of 11p allelic loss in multifocal Wilms tumors arising in WT1 mutation carriers

J. Karlsson, D. Gisselsson, B. Sandstedt, 2018, Pediatric blood & cancer.

Detailed genomic mapping and expression analyses of 12p amplifications in pancreatic carcinomas reveal a 3.5‐Mb target region for amplification

M. Höglund, B. Johansson, M. Heidenblad, 2002, Genes, chromosomes & cancer.

Neuroblastoma patient-derived orthotopic xenografts retain metastatic patterns and geno- and phenotypes of patient tumours

D. Gisselsson, S. Navarro, I. Tadeo, 2014, International journal of cancer.

PREPL deficiency: delineation of the phenotype and development of a functional blood assay

N. Voermans, E. Kamsteeg, D. Lederer, 2017, Genetics in Medicine.

Telomeric associations correlate with telomere length reduction and clonal chromosome aberrations in giant cell tumor of bone

D. Gisselsson, F. Mertens, L. Gorunova, 2009, Cytogenetic and Genome Research.

Tissue variations of mosaic genome-wide paternal uniparental disomy and phenotype of multi-syndromal congenital hyperinsulinism.

S. Detlefsen, H. Christesen, K. Brøndum‐Nielsen, 2020, European journal of medical genetics.

Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU

J. Stoler, C. Garel, C. Depienne, 2017, Human Genetics.

Distinct Mitotic Segregation Errors Mediate Chromosomal Instability in Aggressive Urothelial Cancers

D. Gisselsson, M. Höglund, D. Lindgren, 2007, Clinical Cancer Research.

Tiling resolution array CGH and high density expression profiling of urothelial carcinomas delineate genomic amplicons and candidate target genes specific for advanced tumors

Mattias Höglund, Srinivas Veerla, Åke Borg, 2008, BMC Medical Genomics.

Microarray analyses reveal strong influence of DNA copy number alterations on the transcriptional patterns in pancreatic cancer: implications for the interpretation of genomic amplifications

Mattias Höglund, David Lindgren, J. Veltman, 2005, Oncogene.

Genome-wide array-based comparative genomic hybridization reveals multiple amplification targets and novel homozygous deletions in pancreatic carcinoma cell lines.

J. Veltman, M. Höglund, A. V. van Kessel, 2004, Cancer research.

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.

Molecular characterization of jumping translocations reveals spatial and temporal breakpoint heterogeneity

M. Höglund, B. Johansson, F. Mitelman, 1998, Leukemia.

Oncogenes hijack a constitutively activeTP53promoter in osteosarcoma

J. Staaf, F. Foijer, L. Magnusson, 2020 .

Pancreatic carcinoma cell lines with SMAD4 inactivation show distinct expression responses to TGFB1

M. Höglund, B. Johansson, T. Fioretos, 2003, Genes, chromosomes & cancer.

Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors

D. Gisselsson, M. Höglund, F. Mitelman, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Structural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity.

D. Gisselsson, M. Höglund, F. Mitelman, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Extended genetic diagnostics for children with profound sensorineural hearing loss by implementing massive parallel sequencing. Diagnostic outcome, family experience and clinical implementation.

Tove Ullmark, T. Jonson, P. Piccinelli, 2022, International Journal of Pediatric Otorhinolaryngology.

Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU

J. Stoler, C. Garel, C. Depienne, 2017, Human Genetics.

Dysregulated gene expression through TP53 promoter swapping in osteosarcoma

J. Staaf, F. Foijer, L. Magnusson, 2023, bioRxiv.

Characterization of genomically amplified segments using PCR: Optimizing relative‐PCR for reliable and simple gene expression and gene copy analyses

M. Höglund, B. Johansson, L. Gorunova, 2000, Genes, chromosomes & cancer.

Four evolutionary trajectories underlie genetic intratumoral variation in childhood cancer

J. Karlsson, Linda Holmquist Mengelbier, D. Gisselsson, 2018, Nature Genetics.

Intratumoral genome diversity parallels progression and predicts outcome in pediatric cancer

J. Karlsson, D. Gisselsson, A. Ameur, 2015, Nature Communications.

Genomic profiling and directed ex vivo drug analysis of an unclassifiable myelodysplastic/myeloproliferative neoplasm progressing into acute myeloid leukemia

A. Andersson, M. Ehinger, T. Jonson, 2016, Genes, chromosomes & cancer.

Centrosomal abnormalities, multipolar mitoses, and chromosomal instability in head and neck tumours with dysfunctional telomeres

D. Gisselsson, F. Mertens, J. Wiegant, 2002, British Journal of Cancer.

Altered expression of TGFB receptors and mitogenic effects of TGFB in pancreatic carcinomas.

B Johansson, M. Höglund, B. Johansson, 2001, International journal of oncology.

Genetic heterogeneity in rhabdomyosarcoma revealed by SNP array analysis

D. Gisselsson, F. Mertens, N. Mandahl, 2016, Genes, chromosomes & cancer.

Molecular analyses of the 15q and 18q SMAD genes in pancreatic cancer

A. Andrén-sandberg, M. Höglund, B. Johansson, 1999, Genes, chromosomes & cancer.

Tiling resolution array CGH and high density expression profiling of urothelial carcinomas delineate genomic amplicons and candidate target genes specific for advanced tumors

Å. Borg, M. Höglund, D. Lindgren, 2008 .

ZMIZ1-associated neurodevelopmental disorder and Hirschsprung disease

E. Eklund, T. Jonson, Anders Valind, 2021 .

Mechanisms and Consequences of Chromosomal Instability in Malignant tumours

H. Tanke, M. Höglund, F. Mitelman, 2008 .

Intratumoral genome diversity parallels progression and predicts outcome in pediatric cancer

J. Karlsson, D. Gisselsson, A. Ameur, 2015, Nature Communications.

Telomeric associations correlate with telomere length reduction and clonal chromosome aberrations in giant cell tumor of bone

D. Gisselsson, F. Mertens, L. Gorunova, 2009, Cytogenetic and Genome Research.