Username

Password

Forgot Password?

Preview

Sign-in free and Explore the Exciting World of BiomedExperts:

Over 1.500.000 Profiles
More than 1.800 Organizations worldwide
State of the Art Network Visualizations

Manage your own Profile
Locate Experts in your Country/Region
Locate Experts in your 1. and 2. Level Network
Connect to Experts Worldwide

NetworkView

Bertil Johansson

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Disorders

Procedures

Anatomy

Chemicals & Drugs

Physiology

Gene Rearrangement

Living Beings

Infant

Sign-in to see full Profile

Network (preview)

Co-Publications
Name
108
Mitelman, Felix
45
Heim, Sverre
43
Fioretos, Thoas
38
Höglund, Mattias
35
Mertens, Fredrik
29
Mandahl, Nils
28
Billström, Rolf
22
Strömbeck, Bodil
20
Andrén-Sandberg, Ake
17
Gorunova, Ludmila
17
Panagopoulos, Ioannis
17
Paulsson, Kajsa
17
Bardi, Georgia
14
Pandis, Nikos
14
Lassen, Carin

Sign-in to see all Coauthors

Publications

TOP 3
Davidsson Josef; Lilljebjörn Henrik; Andersson Anna; Veerla Srinivas; Heldrup Jesper; Behrendtz Mikael; Fioretos Thoas; Johansson Bertil
The DNA methylome of pediatric acute lymphoblastic leukemia.
Karrman Kristina; Forestier Erik; Heyman Mats; Andersen Mette K; Autio Kirsi; Blennow Elisabeth; Borgström Georg; Ehrencrona Hans; Golovleva Irina; Heim Sverre; Heinonen Kristiina; Hovland Randi; Johannsson Johann H; Kerndrup Gitte; Nordgren Ann; Palmqvist Lars; Johansson Bertil;
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.
Paulsson Kajsa; Johansson Bertil
High hyperdiploid childhood acute lymphoblastic leukemia.

Sign-in to see all Publications

Sign in free and see...

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the visualized research activity
of experts around the globe

Sign-in to see more

Geonetwork of Bertil Johansson (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

Sign-in to see more

All Publications

2009: Davidsson Josef; Lilljebjörn Henrik; Andersson Anna; Veerla Srinivas; Heldrup Jesper; Behrendtz Mikael; Fioretos Thoas; Johansson Bertil
The DNA methylome of pediatric acute lymphoblastic leukemia.
Human molecular genetics 2009;18(21):4054-65.
2009: Karrman Kristina; Forestier Erik; Heyman Mats; Andersen Mette K; Autio Kirsi; Blennow Elisabeth; Borgström Georg; Ehrencrona Hans; Golovleva Irina; Heim Sverre; Heinonen Kristiina; Hovland Randi; Johannsson Johann H; Kerndrup Gitte; Nordgren Ann; Palmqvist Lars; Johansson Bertil;
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.
Genes, chromosomes & cancer 2009;48(9):795-805.
2009: Paulsson Kajsa; Johansson Bertil
High hyperdiploid childhood acute lymphoblastic leukemia.
Genes, chromosomes & cancer 2009;48(8):637-60.
2009: Lundin Catarina; Davidsson Josef; Hjorth Lars; Behrendtz Mikael; Johansson Bertil
Tiling resolution array-based comparative genomic hybridisation analyses of acute lymphoblastic leukaemias in children with Down syndrome reveal recurrent gain of 8q and deletions of 7p and 9p.
British journal of haematology 2009;146(1):113-5.
2009: Björk Jonas; Johansson Bertil; Broberg Karin; Albin Maria
Smoking as a risk factor for myelodysplastic syndromes and acute myeloid leukemia and its relation to cytogenetic findings: a case-control study.
Leukemia research 2009;33(6):788-91.
2009: Karrman Kristina; Kjeldsen Eigil; Lassen Carin; Isaksson Margareth; Davidsson Josef; Andersson Anna; Hasle Henrik; Fioretos Thoas; Johansson Bertil
The t(X;7)(q22;q34) in paediatric T-cell acute lymphoblastic leukaemia results in overexpression of the insulin receptor substrate 4 gene through illegitimate recombination with the T-cell receptor beta locus.
British journal of haematology 2009;144(4):546-51.
2008: Forestier Erik; Heyman Mats; Andersen Mette K; Autio Kirsi; Blennow Elisabeth; Borgström Georg; Golovleva Irina; Heim Sverre; Heinonen Kristina; Hovland Randi; Johannsson Johann H; Kerndrup Gitte; Nordgren Ann; Rosenquist Richard; Swolin Birgitta; Johansson Bertil;
Outcome of ETV6/RUNX1-positive childhood acute lymphoblastic leukaemia in the NOPHO-ALL-1992 protocol: frequent late relapses but good overall survival.
British journal of haematology 2008;140(6):665-72.
2008: Forestier Erik; Gauffin Fredrika; Andersen Mette K; Autio Kirsi; Borgström Georg; Golovleva Irina; Gustafsson Britt; Heim Sverre; Heinonen Kristina; Heyman Mats; Hovland Randi; Johannsson Johann H; Kerndrup Gitte; Rosenquist Richard; Schoumans Jacqueline; Swolin Birgitta; Johansson Bertil; Nordgren Ann;
Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)-positive B-cell precursor acute lymphoblastic leukemias: a Nordic series of 24 cases and review of the literature.
Genes, chromosomes & cancer 2008;47(2):149-58.
2008: Forestier Erik; Izraeli Shai; Beverloo Berna; Haas Oskar; Pession Andrea; Michalová Kyra; Stark Batia; Harrison Christine J; Teigler-Schlegel Andrea; Johansson Bertil
Cytogenetic features of acute lymphoblastic and myeloid leukemias in pediatric patients with Down syndrome: an iBFM-SG study.
Blood 2008;111(3):1575-83.
2008: Andersson Anna; Paulsson Kajsa; Lilljebjörn Henrik; Lassen Carin; Strömbeck Bodil; Heldrup Jesper; Behrendtz Mikael; Johansson Bertil; Fioretos Thoas
FLT3 mutations in a 10 year consecutive series of 177 childhood acute leukemias and their impact on global gene expression patterns.
Genes, chromosomes & cancer 2008;47(1):64-70.
2008: Paulsson Kajsa; Horvat Andrea; Strömbeck Bodil; Nilsson Fredrik; Heldrup Jesper; Behrendtz Mikael; Forestier Erik; Andersson Anna; Fioretos Thoas; Johansson Bertil
Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia.
Genes, chromosomes & cancer 2008;47(1):26-33.
2007: Lilljebjörn H; Heidenblad M; Nilsson B; Lassen C; Horvat A; Heldrup J; Behrendtz M; Johansson B; Andersson A; Fioretos T
Combined high-resolution array-based comparative genomic hybridization and expression profiling of ETV6/RUNX1-positive acute lymphoblastic leukemias reveal a high incidence of cryptic Xq duplications and identify several putative target genes within the commonly gained region.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2007;21(10):2137-44.
2007: Nilsson Lars; Edén Patrik; Olsson Eleonor; Månsson Robert; Astrand-Grundström Ingbritt; Strömbeck Bodil; Theilgaard-Mönch Kim; Anderson Kristina; Hast Robert; Hellström-Lindberg Eva; Samuelsson Jan; Bergh Gösta; Nerlov Claus; Johansson Bertil; Sigvardsson Mikael; Borg Ake; Jacobsen Sten Eirik W
The molecular signature of MDS stem cells supports a stem-cell origin of 5q myelodysplastic syndromes.
Blood 2007;110(8):3005-14.
2007: Davidsson Josef; Andersson Anna; Paulsson Kajsa; Heidenblad Markus; Isaksson Margareth; Borg Ake; Heldrup Jesper; Behrendtz Mikael; Panagopoulos Ioannis; Fioretos Thoas; Johansson Bertil
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.
Human molecular genetics 2007;16(18):2215-25.
2007: Paulsson Kajsa; Jonson Tord; Ora Ingrid; Olofsson Tor; Panagopoulos Ioannis; Johansson Bertil
Characterisation of genomic translocation breakpoints and identification of an alternative TCF3/PBX1 fusion transcript in t(1;19)(q23;p13)-positive acute lymphoblastic leukaemias.
British journal of haematology 2007;138(2):196-201.
2007: Agerstam Helena; Lilljebjörn Henrik; Lassen Carin; Swedin Agneta; Richter Johan; Vandenberghe Peter; Johansson Bertil; Fioretos Thoas
Fusion gene-mediated truncation of RUNX1 as a potential mechanism underlying disease progression in the 8p11 myeloproliferative syndrome.
Genes, chromosomes & cancer 2007;46(7):635-43.
2007: Andersson A; Ritz C; Lindgren D; Edén P; Lassen C; Heldrup J; Olofsson T; Råde J; Fontes M; Porwit-Macdonald A; Behrendtz M; Höglund M; Johansson B; Fioretos T
Microarray-based classification of a consecutive series of 121 childhood acute leukemias: prediction of leukemic and genetic subtype as well as of minimal residual disease status.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2007;21(6):1198-203.
2007: Forestier Erik; Andersen Mette K; Autio Kirsi; Blennow Elisabeth; Borgström Georg; Golovleva Irina; Heim Sverre; Heinonen Kristina; Hovland Randi; Johannsson Johann H; Kerndrup Gitte; Nordgren Ann; Rosenquist Richard; Swolin Birgitta; Johansson Bertil;
Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature.
Genes, chromosomes & cancer 2007;46(5):440-50.
2007: Karrman K; Sallerfors B; Lenhoff S; Fioretos T; Johansson B
Cytogenetic evolution patterns in CML post-SCT.
Bone marrow transplantation 2007;39(3):165-71.
2007: Paulsson K; Johansson B
Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes.
Pathologie-biologie 2007;55(1):37-48.
2007: Panagopoulos Ioannis; Kerndrup Gitte; Carlsen Niels; Strömbeck Bodil; Isaksson Margareth; Johansson Bertil
Fusion of NUP98 and the SET binding protein 1 (SETBP1) gene in a paediatric acute T cell lymphoblastic leukaemia with t(11;18)(p15;q12).
British journal of haematology 2007;136(2):294-6.
2007: Lundin C; Heidenblad M; Strombeck B; Borg A; Hovland R; Heim S; Johansson B
Tiling resolution array CGH of dic(7;9)(p11 approximately 13;p11 approximately 13) in B-cell precursor acute lymphoblastic leukemia reveals clustered breakpoints at 7p11.2 approximately 12.1 and 9p13.1.
Cytogenetic and genome research 2007;118(1):13-8.
2006: Schoumans Jacqueline; Johansson Bertil; Corcoran Martin; Kuchinskaya Ekaterina; Golovleva Irina; Grandér Dan; Forestier Erik; Staaf Johan; Borg Ake; Gustafsson Britt; Blennow Elisabeth; Nordgren Ann
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.
British journal of haematology 2006;135(4):492-9.
2006: Paulsson K; Heidenblad M; Mörse H; Borg A; Fioretos T; Johansson B
Identification of cryptic aberrations and characterization of translocation breakpoints using array CGH in high hyperdiploid childhood acute lymphoblastic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2006;20(11):2002-7.
2006: Karrman Kristina; Forestier Erik; Andersen Mette K; Autio Kirsi; Borgström Georg; Heim Sverre; Heinonen Kristina; Hovland Randi; Kerndrup Gitte; Johansson Bertil;
High incidence of the ETV6/RUNX1 fusion gene in paediatric precursor B-cell acute lymphoblastic leukaemias with trisomy 21 as the sole cytogenetic change: a Nordic series of cases diagnosed 1989-2005.
British journal of haematology 2006;135(3):352-4.
2006: Panagopoulos Ioannis; Lilljebjörn Henrik; Strömbeck Bodil; Hjorth Lars; Olofsson Tor; Johansson Bertil
MLL/GAS7 fusion in a pediatric case of t(11;17)(q23;p13)-positive precursor B-cell acute lymphoblastic leukemia.
Haematologica 2006;91(9):1287-8.
2006: Davidsson Josef; Heidenblad Markus; Borg Ake; Johansson Bertil
Array-based comparative genomic hybridization characterization of cytogenetically polyclonal myeloid malignancies.
Cancer genetics and cytogenetics 2006;169(2):179-80.
2006: Karrman Kristina; Andersson Anna; Björgvinsdóttir Helga; Strömbeck Bodil; Lassen Carin; Olofsson Tor; Nguyen-Khac Florence; Berger Roland; Bernard Olivier; Fioretos Thoas; Johansson Bertil
Deregulation of cyclin D2 by juxtaposition with T-cell receptor alpha/delta locus in t(12;14)(p13;q11)-positive childhood T-cell acute lymphoblastic leukemia.
European journal of haematology 2006;77(1):27-34.
2006: Broliden Per Anders; Dahl Inger-Marie; Hast Robert; Johansson Bertil; Juvonen Eeva; Kjeldsen Lars; Porwit-MacDonald Anna; Sjoo Malvin; Tangen Jon-Magnus; Uggla Bertil; Oberg Gunnar; Hellstrom-Lindberg Eva
Antithymocyte globulin and cyclosporine A as combination therapy for low-risk non-sideroblastic myelodysplastic syndromes.
Haematologica 2006;91(5):667-70.
2006: Panagopoulos Ioannis; Strömbeck Bodil; Isaksson Margareth; Heldrup Jesper; Olofsson Tor; Johansson Bertil
Fusion of ETV6 with an intronic sequence of the BAZ2A gene in a paediatric pre-B acute lymphoblastic leukaemia with a cryptic chromosome 12 rearrangement.
British journal of haematology 2006;133(3):270-5.
2006: Paulsson K; Heidenblad M; Strömbeck B; Staaf J; Jönsson G; Borg A; Fioretos T; Johansson B
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.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2006;20(5):840-6.
2006: Davidsson Josef; Paulsson Kajsa; Johansson Bertil
Searching for cryptic chromosomal aberrations in high hyperdiploid childhood acute lymphoblastic leukaemias.
European journal of haematology 2006;76(5):449-50.
2006: Paulsson K; Békássy A N; Olofsson T; Mitelman F; Johansson B; Panagopoulos I
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.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2006;20(2):224-9.
2006: Schaad K; Strömbeck B; Mandahl N; Andersen M K; Heim S; Mertens F; Johansson B
FISH mapping of i(7q) in acute leukemias and myxoid liposarcoma reveals clustered breakpoints in 7p11.2: implications for formation and pathogenetic outcome of the idic(7)(p11.2).
Cytogenetic and genome research 2006;114(2):126-30.
2005: Andersson Anna; Olofsson Tor; Lindgren David; Nilsson Björn; Ritz Cecilia; Edén Patrik; Lassen Carin; Råde Johan; Fontes Magnus; Mörse Helena; Heldrup Jesper; Behrendtz Mikael; Mitelman Felix; Höglund Mattias; Johansson Bertil; Fioretos Thoas
Molecular signatures in childhood acute leukemia and their correlations to expression patterns in normal hematopoietic subpopulations.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(52):19069-74.
2005: Davidsson Josef; Paulsson Kajsa; Johansson Bertil
Multicolor fluorescence in situ hybridization characterization of cytogenetically polyclonal hematologic malignancies.
Cancer genetics and cytogenetics 2005;163(2):180-3.
2005: Paulsson Kajsa; Mörse Helena; Fioretos Thoas; Behrendtz Mikael; Strömbeck Bodil; Johansson Bertil
Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia.
Genes, chromosomes & cancer 2005;44(2):113-22.
2005: Mitelman Felix; Mertens Fredrik; Johansson Bertil
Prevalence estimates of recurrent balanced cytogenetic aberrations and gene fusions in unselected patients with neoplastic disorders.
Genes, chromosomes & cancer 2005;43(4):350-66.
2005: Castor Anders; Nilsson Lars; Astrand-Grundström Ingbritt; Buitenhuis Miranda; Ramirez Carole; Anderson Kristina; Strömbeck Bodil; Garwicz Stanislaw; Békássy Albert N; Schmiegelow Kjeld; Lausen Birgitte; Hokland Peter; Lehmann Sören; Juliusson Gunnar; Johansson Bertil; Jacobsen Sten Eirik W
Distinct patterns of hematopoietic stem cell involvement in acute lymphoblastic leukemia.
Nature medicine 2005;11(6):630-7.
2005: Andersson A; Edén P; Lindgren D; Nilsson J; Lassen C; Heldrup J; Fontes M; Borg A; Mitelman F; Johansson B; Höglund M; Fioretos T
Gene expression profiling of leukemic cell lines reveals conserved molecular signatures among subtypes with specific genetic aberrations.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2005;19(6):1042-50.
2005: Paulsson Kajsa; Horvat Andrea; Fioretos Thoas; Mitelman Felix; Johansson Bertil
Formation of der(19)t(1;19)(q23;p13) in acute lymphoblastic leukemia.
Genes, chromosomes & cancer 2005;42(2):144-8.
2004: Panagopoulos Ioannis; Kitagawa Ashly; Isaksson Margareth; Mörse Helena; Mitelman Felix; Johansson Bertil
MLL/GRAF fusion in an infant acute monocytic leukemia (AML M5b) with a cytogenetically cryptic ins(5;11)(q31;q23q23).
Genes, chromosomes & cancer 2004;41(4):400-4.
2004: Nilsson Therese; Nilsson Lars; Lenhoff Stig; Rylander Lars; Astrand-Grundström Ingbritt; Strömbeck Bodil; Höglund Mattias; Turesson Ingemar; Westin Jan; Mitelman Felix; Jacobsen Sten E W; Johansson Bertil
MDS/AML-associated cytogenetic abnormalities in multiple myeloma and monoclonal gammopathy of undetermined significance: evidence for frequent de novo occurrence and multipotent stem cell involvement of del(20q).
Genes, chromosomes & cancer 2004;41(3):223-31.
2004: Nilsson Therese; Lenhoff Stig; Rylander Lars; Höglund Mattias; Turesson Ingemar; Mitelman Felix; Westin Jan; Johansson Bertil
High frequencies of chromosomal aberrations in multiple myeloma and monoclonal gammopathy of undetermined significance in direct chromosome preparation.
British journal of haematology 2004;126(4):487-94.
2004: Storlazzi Clelia T; Fioretos Thoas; Paulsson Kajsa; Strömbeck Bodil; Lassen Carin; Ahlgren Tomas; Juliusson Gunnar; Mitelman Felix; Rocchi Mariano; Johansson Bertil
Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies.
Human molecular genetics 2004;13(14):1479-85.
2004: Andersson Anna; Johansson Bertil; Lassen Carin; Mitelman Felix; Billström Rolf; Fioretos Thoas
Clinical impact of internal tandem duplications and activating point mutations in FLT3 in acute myeloid leukemia in elderly patients.
European journal of haematology 2004;72(5):307-13.
2004: Mitelman Felix; Johansson Bertil; Mertens Fredrik
Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer.
Nature genetics 2004;36(4):331-4.
2004: Dykes J H; Lindmark A; Lenhoff S; Winqvist I; Johansson B; Olofsson T; Olsson M L
Autologous del(20q)-positive erythroid progenitor cells, re-emerging after DLI treatment of an MDS patient relapsing after allo-SCT, can provide a normal peripheral red blood cell count.
Bone marrow transplantation 2004;33(5):559-63.
2004: Barbouti Aikaterini; Stankiewicz Pawel; Nusbaum Chad; Cuomo Christina; Cook April; Höglund Mattias; Johansson Bertil; Hagemeijer Anne; Park Sung-Sup; Mitelman Felix; Lupski James R; Fioretos Thoas
The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats.
American journal of human genetics 2004;74(1):1-10.
2004: Johansson Bertil; Mertens Fredrik; Mitelman Felix
Clinical and biological importance of cytogenetic abnormalities in childhood and adult acute lymphoblastic leukemia.
Annals of medicine 2004;36(7):492-503.
2003: Albin Maria; Björk Jonas; Welinder Hans; Tinnerberg Håkan; Mauritzson Nils; Billström Rolf; Strömberg Ulf; Mikoczy Zoli; Johansson Bertil; Ahlgren Tomas; Nilsson Per-Gunnar; Mitelman Felix; Hagmar Lars
Cytogenetic and morphologic subgroups of myelodysplastic syndromes in relation to occupational and hobby exposures.
Scandinavian journal of work, environment & health 2003;29(5):378-87.
2003: Paulsson Kajsa; Panagopoulos Ioannis; Knuutila Sakari; Jee Kowan Ja; Garwicz Stanislaw; Fioretos Thoas; Mitelman Felix; Johansson Bertil
Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia.
Blood 2003;102(8):3010-5.
2003: Barbouti Aikaterini; Ahlgren Tomas; Johansson Bertil; Höglund Mattias; Lassen Carin; Turesson Ingemar; Mitelman Felix; Fioretos Thoas
Clinical and genetic studies of ETV6/ABL1-positive chronic myeloid leukaemia in blast crisis treated with imatinib mesylate.
British journal of haematology 2003;122(1):85-93.
2003: Forestier Erik; Heim Sverre; Blennow Elisabeth; Borgström Georg; Holmgren Gösta; Heinonen Kristiina; Johannsson Johann; Kerndrup Gitte; Andersen Mette Klarskov; Lundin Catarina; Nordgren Ann; Rosenquist Richard; Swolin Birgitta; Johansson Bertil;
Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO-93-AML trial between 1993 and 2001.
British journal of haematology 2003;121(4):566-77.
2003: Jonson Tord; Heidenblad Markus; Håkansson Petra; Gorunova Ludmila; Johansson Bertil; Fioretos Thoas; Höglund Mattias
Pancreatic carcinoma cell lines with SMAD4 inactivation show distinct expression responses to TGFB1.
Genes, chromosomes & cancer 2003;36(4):340-52.
2003: Barbouti Aikaterini; Höglund Mattias; Johansson Bertil; Lassen Carin; Nilsson Per-Gunnar; Hagemeijer Anne; Mitelman Felix; Fioretos Thoas
A novel gene, MSI2, encoding a putative RNA-binding protein is recurrently rearranged at disease progression of chronic myeloid leukemia and forms a fusion gene with HOXA9 as a result of the cryptic t(7;17)(p15;q23).
Cancer research 2003;63(6):1202-6.
2003: Nilsson Thérèse; Höglund Mattias; Lenhoff Stig; Rylander Lars; Turesson Ingemar; Westin Jan; Mitelman Felix; Johansson Bertil
A pooled analysis of karyotypic patterns, breakpoints and imbalances in 783 cytogenetically abnormal multiple myelomas reveals frequently involved chromosome segments as well as significant age- and sex-related differences.
British journal of haematology 2003;120(6):960-9.
2003: Paulsson Kajsa; Fioretos Thoas; Strömbeck Bodil; Mauritzson Nils; Tanke Hans J; Johansson Bertil
Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a multicolor and locus-specific fluorescence in situ hybridization study.
Cancer genetics and cytogenetics 2003;140(1):66-9.
2003: Panagopoulos Ioannis; Isaksson Margareth; Billström Rolf; Strömbeck Bodil; Mitelman Felix; Johansson Bertil
Fusion of the NUP98 gene and the homeobox gene HOXC13 in acute myeloid leukemia with t(11;12)(p15;q13).
Genes, chromosomes & cancer 2003;36(1):107-12.
2003: Panagopoulos Ioannis; Isaksson Margareth; Lindvall Charlotta; Hagemeijer Anna; Mitelman Felix; Johansson Bertil
Genomic characterization of MOZ/CBP and CBP/MOZ chimeras in acute myeloid leukemia suggests the involvement of a damage-repair mechanism in the origin of the t(8;16)(p11;p13).
Genes, chromosomes & cancer 2003;36(1):90-8.
2002: Mauritzson N; Albin M; Rylander L; Billström R; Ahlgren T; Mikoczy Z; Björk J; Strömberg U; Nilsson P G; Mitelman F; Hagmar L; Johansson B
Pooled analysis of clinical and cytogenetic features in treatment-related and de novo adult acute myeloid leukemia and myelodysplastic syndromes based on a consecutive series of 761 patients analyzed 1976-1993 and on 5098 unselected cases reported in the literature 1974-2001.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2002;16(12):2366-78.
2002: Barbouti Aikaterini; Johansson Bertil; Höglund Mattias; Mauritzson Nils; Strömbeck Bodil; Nilsson Per-Gunnar; Tanke Hans J; Hagemeijer Anne; Mitelman Felix; Fioretos Thoas
Multicolor COBRA-FISH analysis of chronic myeloid leukemia reveals novel cryptic balanced translocations during disease progression.
Genes, chromosomes & cancer 2002;35(2):127-37.
2002: Billström R; Ahlgren T; Békássy A N; Malm C; Olofsson T; Höglund M; Mitelman F; Johansson B
Acute myeloid leukemia with inv(16)(p13q22): involvement of cervical lymph nodes and tonsils is common and may be a negative prognostic sign.
American journal of hematology 2002;71(1):15-9.
2002: Hallén Magnus; Parada Luis A; Gorunova Ludmila; Pålsson Birger; Dictor Michael; Johansson Bertil
Cytogenetic abnormalities in a hemangiopericytoma of the spleen.
Cancer genetics and cytogenetics 2002;136(1):62-5.
2002: Nilsson Lars; Astrand-Grundström Ingbritt; Anderson Kristina; Arvidsson Ingrid; Hokland Peter; Bryder David; Kjeldsen Lars; Johansson Bertil; Hellström-Lindberg Eva; Hast Robert; Jacobsen Sten Eirik W
Involvement and functional impairment of the CD34(+)CD38(-)Thy-1(+) hematopoietic stem cell pool in myelodysplastic syndromes with trisomy 8.
Blood 2002;100(1):259-67.
2002: Nilsson T; Lenhoff S; Turesson I; Rylander L; Mitelman F; Westin J; Höglund M; Johansson B
Cytogenetic features of multiple myeloma: impact of gender, age, disease phase, culture time, and cytokine stimulation.
European journal of haematology 2002;68(6):345-53.
2002: Panagopoulos Ioannis; Fioretos Thoas; Isaksson Margareth; Larsson Gun; Billström Rolf; Mitelman Felix; Johansson Bertil
Expression of NUP98/TOP1, but not of TOP1/NUP98, in a treatment-related myelodysplastic syndrome with t(10;20;11)(q24;q11;p15).
Genes, chromosomes & cancer 2002;34(2):249-54.
2002: Heidenblad Markus; Jonson Tord; Mahlamäki Eija H; Gorunova Ludmila; Karhu Ritva; Johansson Bertil; Höglund Mattias
Detailed genomic mapping and expression analyses of 12p amplifications in pancreatic carcinomas reveal a 3.5-Mb target region for amplification.
Genes, chromosomes & cancer 2002;34(2):211-23.
2002: Johansson Bertil; Fioretos Thoas; Mitelman Felix
Cytogenetic and molecular genetic evolution of chronic myeloid leukemia.
Acta haematologica 2002;107(2):76-94.
2001: Fioretos T; Panagopoulos I; Lassen C; Swedin A; Billström R; Isaksson M; Strömbeck B; Olofsson T; Mitelman F; Johansson B
Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: the first fusion gene involving BCR but not ABL.
Genes, chromosomes & cancer 2001;32(4):302-10.
2001: Björk J; Albin M; Welinder H; Tinnerberg H; Mauritzson N; Kauppinen T; Strömberg U; Johansson B; Billström R; Mikoczy Z; Ahlgren T; Nilsson P G; Mitelman F; Hagmar L
Are occupational, hobby, or lifestyle exposures associated with Philadelphia chromosome positive chronic myeloid leukaemia?
Occupational and environmental medicine 2001;58(11):722-7.
2001: Paulsson K; Säll T; Fioretos T; Mitelman F; Johansson B
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.
Cancer genetics and cytogenetics 2001;130(2):160-5.
2001: Björk J; Albin M; Mauritzson N; Strömberg U; Johansson B; Hagmar L
Smoking and acute myeloid leukemia: associations with morphology and karyotypic patterns and evaluation of dose-response relations.
Leukemia research 2001;25(10):865-72.
2001: Andersson A; Höglund M; Johansson B; Lassen C; Billström R; Garwicz S; Nilsson P G; Mitelman F; Fioretos T
Paired multiplex reverse-transcriptase polymerase chain reaction (PMRT-PCR) analysis as a rapid and accurate diagnostic tool for the detection of MLL fusion genes in hematologic malignancies.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2001;15(8):1293-300.
2001: Jonson T; Albrechtsson E; Axelson J; Heidenblad M; Gorunova L; Johansson B; Höglund M
Altered expression of TGFB receptors and mitogenic effects of TGFB in pancreatic carcinomas.
International journal of oncology 2001;19(1):71-81.
2001: Gorunova L; Dawiskiba S; Andrén-Sandberg A; Höglund M; Johansson B
Extensive cytogenetic heterogeneity in a benign retroperitoneal schwannoma.
Cancer genetics and cytogenetics 2001;127(2):148-54.
2001: Höglund M; Gisselsson D; Mandahl N; Johansson B; Mertens F; Mitelman F; Säll T
Multivariate analyses of genomic imbalances in solid tumors reveal distinct and converging pathways of karyotypic evolution.
Genes, chromosomes & cancer 2001;31(2):156-71.
2001: Mauritzson N; Johansson B; Rylander L; Albin M; Strömberg U; Billström R; Ahlgren T; Mikoczy Z; Mitelman F; Hagmar L; Nilsson P G
The prognostic impact of karyotypic subgroups in myelodysplastic syndromes is strongly modified by sex.
British journal of haematology 2001;113(2):347-56.
2001: Johansson B; Axelsson P; Billström R; Strömbeck B; Arheden K; Olofsson T; Cervin A; Adriansson M; Tanke H J; Mitelman F; Fioretos T
Isodicentric 7p, idic(7)(q11.2), in acute myeloid leukemia associated with older age and favorable response to induction chemotherapy: a new clinical entity?
Genes, chromosomes & cancer 2001;30(3):261-6.
2001: Panagopoulos I; Fioretos T; Isaksson M; Samuelsson U; Billström R; Strömbeck B; Mitelman F; Johansson B
Fusion of the MORF and CBP genes in acute myeloid leukemia with the t(10;16)(q22;p13).
Human molecular genetics 2001;10(4):395-404.
2000: Albin M; Björk J; Welinder H; Tinnerberg H; Mauritzson N; Johansson B; Billström R; Strömberg U; Mikoczy Z; Ahlgren T; Nilsson P G; Mitelman F; Hagmar L
Acute myeloid leukemia and clonal chromosome aberrations in relation to past exposure to organic solvents.
Scandinavian journal of work, environment & health 2000;26(6):482-91.
2000: Panagopoulos I; Teixeira M R; Micci F; Hammerstrøm J; Isaksson M; Johansson B; Mitelman F; Heim S
Acute myeloid leukemia with inv(8)(p11q13).
Leukemia & lymphoma 2000;39(5-6):651-6.
2000: Jonson T; Mahlamäki E H; Karhu R; Gorunova L; Johansson B; Höglund M
Characterization of genomically amplified segments using PCR: optimizing relative-PCR for reliable and simple gene expression and gene copy analyses.
Genes, chromosomes & cancer 2000;29(2):192-9.
2000: Panagopoulos I; Isaksson M; Lindvall C; Björkholm M; Ahlgren T; Fioretos T; Heim S; Mitelman F; Johansson B
RT-PCR analysis of the MOZ-CBP and CBP-MOZ chimeric transcripts in acute myeloid leukemias with t(8;16)(p11;p13).
Genes, chromosomes & cancer 2000;28(4):415-24.
2000: Forestier E; Johansson B; Gustafsson G; Borgström G; Kerndrup G; Johannsson J; Heim S
Prognostic impact of karyotypic findings in childhood acute lymphoblastic leukaemia: a Nordic series comparing two treatment periods. For the Nordic Society of Paediatric Haematology and Oncology (NOPHO) Leukaemia Cytogenetic Study Group.
British journal of haematology 2000;110(1):147-53.
2000: Andreasson P; Höglund M; Békássy A N; Garwicz S; Heldrup J; Mitelman F; Johansson B
Cytogenetic and FISH studies of a single center consecutive series of 152 childhood acute lymphoblastic leukemias.
European journal of haematology 2000;65(1):40-51.
2000: Mauritzson N; Johansson B; Albin M; Rylander L; Billström R; Ahlgren T; Mikoczy Z; Strömberg U; Mitelman F; Hagmar L; Nilsson P G
Survival time in a population-based consecutive series of adult acute myeloid leukemia--the prognostic impact of karyotype during the time period 1976-1993.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2000;14(6):1039-43.
2000: Björk J; Albin M; Mauritzson N; Strömberg U; Johansson B; Hagmar L
Smoking and myelodysplastic syndromes.
Epidemiology (Cambridge, Mass.) 2000;11(3):285-91.
2000: Forestier E; Johansson B; Borgström G; Kerndrup G; Johansson J; Heim S
Cytogenetic findings in a population-based series of 787 childhood acute lymphoblastic leukemias from the Nordic countries. The NOPHO Leukemia Cytogenetic Study Group.
European journal of haematology 2000;64(3):194-200.
2000: Parada L A; Limon J; Iliszko M; Czauderna P; Gisselsson D; Höglund M; Kullendorff C M; Wiebe T; Mertens F; Johansson B
Cytogenetics of hepatoblastoma: further characterization of 1q rearrangements by fluorescence in situ hybridization: an international collaborative study.
Medical and pediatric oncology 2000;34(3):165-70.
2000: Johansson B; Fioretos T; Kullendorff C M; Wiebe T; Békássy A N; Garwicz S; Forestier E; Roos G; Akerman M; Mitelman F; Billström R
Granulocytic sarcomas in body cavities in childhood acute myeloid leukemias with 11q23/MLL rearrangements.
Genes, chromosomes & cancer 2000;27(2):136-42.
1999: Gorunova L; Parada L A; Limon J; Jin Y; Hallén M; Hägerstrand I; Iliszko M; Wajda Z; Johansson B
Nonrandom chromosomal aberrations and cytogenetic heterogeneity in gallbladder carcinomas.
Genes, chromosomes & cancer 1999;26(4):312-21.
1999: Parada L A; Hallén M; Hägerstrand I; Tranberg K G; Johansson B
Clonal chromosomal abnormalities in congenital bile duct dilatation (Caroli's disease).
Gut 1999;45(5):780-2.
1999: Fioretos T; Strömbeck B; Sandberg T; Johansson B; Billström R; Borg A; Nilsson P G; Van Den Berghe H; Hagemeijer A; Mitelman F; Höglund M
Isochromosome 17q in blast crisis of chronic myeloid leukemia and in other hematologic malignancies is the result of clustered breakpoints in 17p11 and is not associated with coding TP53 mutations.
Blood 1999;94(1):225-32.
1999: Johansson B; Billström R; Broberg K; Fioretos T; Nilsson P G; Ahlgren T; Malm C; Samuelsson B O; Mitelman F
Cytogenetic polyclonality in hematologic malignancies.
Genes, chromosomes & cancer 1999;24(3):222-9.
1999: Jerkeman M; Johansson B; Akerman M; Cavallin-Ståhl E; Kristoffersson U; Mitelman F
Prognostic implications of cytogenetic aberrations in diffuse large B-cell lymphomas.
European journal of haematology 1999;62(3):184-90.
1999: Mauritzson N; Johansson B; Albin M; Billström R; Ahlgren T; Mikoczy Z; Nilsson P G; Hagmar L; Mitelman F
A single-center population-based consecutive series of 1500 cytogenetically investigated adult hematological malignancies: karyotypic features in relation to morphology, age and gender.
European journal of haematology 1999;62(2):95-102.
1999: Jonson T; Gorunova L; Dawiskiba S; Andrén-Sandberg A; Stenman G; ten Dijke P; Johansson B; Höglund M
Molecular analyses of the 15q and 18q SMAD genes in pancreatic cancer.
Genes, chromosomes & cancer 1999;24(1):62-71.
1998: Gorunova L; Höglund M; Andrén-Sandberg A; Dawiskiba S; Jin Y; Mitelman F; Johansson B
Cytogenetic analysis of pancreatic carcinomas: intratumor heterogeneity and nonrandom pattern of chromosome aberrations.
Genes, chromosomes & cancer 1998;23(2):81-99.
1998: Andreasson P; Höglund M; Jonson T; Békàssy A; Mitelman F; Johansson B
Molecular characterization of jumping translocations reveals spatial and temporal breakpoint heterogeneity.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1998;12(9):1411-6.
1998: Parada L A; Hallén M; Tranberg K G; Hägerstrand I; Bondeson L; Mitelman F; Johansson B
Frequent rearrangements of chromosomes 1, 7, and 8 in primary liver cancer.
Genes, chromosomes & cancer 1998;23(1):26-35.
1998: Nilsson T; Andreasson P; Höglund M; Fioretos T; Billström R; Garwicz S; Mitelman F; Johansson B
ETV6/ABL fusion is rare in Ph-negative chronic myeloid disorders.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1998;12(7):1167-8.
1998: Höglund M; Gorunova L; Jonson T; Dawiskiba S; Andrén-Sandberg A; Stenman G; Johansson B
Cytogenetic and FISH analyses of pancreatic carcinoma reveal breaks in 18q11 with consistent loss of 18q12-qter and frequent gain of 18p.
British journal of cancer 1998;77(11):1893-9.
1998: Johansson B; Moorman A V; Secker-Walker L M
Derivative chromosomes of 11q23-translocations in hematologic malignancies. European 11q23 Workshop participants.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1998;12(5):828-33.
1998: Johansson B; Moorman A V; Haas O A; Watmore A E; Cheung K L; Swanton S; Secker-Walker L M
Hematologic malignancies with t(4;11)(q21;q23)--a cytogenetic, morphologic, immunophenotypic and clinical study of 183 cases. European 11q23 Workshop participants.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1998;12(5):779-87.
1998: Andreasson P; Johansson B; Arheden K; Kristoffersson U; Akerman M; Mitelman F; Höglund M
Genomic amplification of CCND2 is rare in non-Hodgkin lymphomas.
Cancer genetics and cytogenetics 1998;102(1):81-2.
1998: Andreasson P; Johansson B; Billström R; Garwicz S; Mitelman F; Höglund M
Fluorescence in situ hybridization analyses of hematologic malignancies reveal frequent cytogenetically unrecognized 12p rearrangements.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1998;12(3):390-400.
1998: Höglund M; Gorunova L; Andrén-Sandberg A; Dawiskiba S; Mitelman F; Johansson B
Cytogenetic and fluorescence in situ hybridization analyses of chromosome 19 aberrations in pancreatic carcinomas: frequent loss of 19p13.3 and gain of 19q13.1-13.2.
Genes, chromosomes & cancer 1998;21(1):8-16.
1997: Mahlamäki E H; Höglund M; Gorunova L; Karhu R; Dawiskiba S; Andrén-Sandberg A; Kallioniemi O P; Johansson B
Comparative genomic hybridization reveals frequent gains of 20q, 8q, 11q, 12p, and 17q, and losses of 18q, 9p, and 15q in pancreatic cancer.
Genes, chromosomes & cancer 1997;20(4):383-91.
1997: Johansson B; Brøndum-Nielsen K; Billström R; Schiødt I; Mitelman F
Translocations between the long arms of chromosomes 1 and 5 in hematologic malignancies are strongly associated with neoplasms of the myeloid lineages.
Cancer genetics and cytogenetics 1997;99(2):97-101.
1997: Andreasson P; Johansson B; Carlsson M; Jarlsfelt I; Fioretos T; Mitelman F; Höglund M
BCR/ABL-negative chronic myeloid leukemia with ETV6/ABL fusion.
Genes, chromosomes & cancer 1997;20(3):299-304.
1997: Parada L A; Bardi G; Hallén M; Hägerstrand I; Tranberg K G; Mitelman F; Johansson B
Cytogenetic abnormalities and clonal evolution in an adult hepatoblastoma.
The American journal of surgical pathology 1997;21(11):1381-6.
1997: Johansson B; Billström R; Kristoffersson U; Akerman M; Garwicz S; Ahlgren T; Malm C; Mitelman F
Deletion of chromosome arm 3p in hematologic malignancies.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1997;11(8):1207-13.
1997: Bardi G; Parada L A; Bomme L; Pandis N; Johansson B; Willén R; Fenger C; Kronborg O; Mitelman F; Heim S
Cytogenetic findings in metastases from colorectal cancer.
International journal of cancer. Journal international du cancer 1997;72(4):604-7.
1997: Billström R; Johansson B; Fioretos T; Garwicz S; Malm C; Zettervall O; Mitelman F
Poor survival in t(8;21) (q22;q22)-associated acute myeloid leukaemia with leukocytosis.
European journal of haematology 1997;59(1):47-52.
1997: Andreasson P; Johansson B; Strömbeck B; Donnér M; Mitelman F; Höglund M
Childhood acute lymphoblastic leukaemia with ider(21)(q10)t(12;21)(p12;q22): a new recurrent abnormality showing ETV6/CBFA2 fusion.
British journal of haematology 1997;98(1):216-8.
1997: Mertens F; Johansson B; Höglund M; Mitelman F
Chromosomal imbalance maps of malignant solid tumors: a cytogenetic survey of 3185 neoplasms.
Cancer research 1997;57(13):2765-80.
1997: Andreasson P; Johansson B; Arheden K; Billström R; Mitelman F; Höglund M
Deletions of CDKN1B and ETV6 in acute myeloid leukemia and myelodysplastic syndromes without cytogenetic evidence of 12p abnormalities.
Genes, chromosomes & cancer 1997;19(2):77-83.
1997: Mitelman F; Johansson B; Mandahl N; Mertens F
Clinical significance of cytogenetic findings in solid tumors.
Cancer genetics and cytogenetics 1997;95(1):1-8.
1997: Mitelman F; Mertens F; Johansson B
A breakpoint map of recurrent chromosomal rearrangements in human neoplasia.
Nature genetics 1997;15 Spec No():417-74.
1997: Parada L A; Bardi G; Hallén M; Hägerstrand I; Tranberg K G; Mitelman F; Johansson B
Monosomy 22 in a case of biliary adenofibroma.
Cancer genetics and cytogenetics 1997;93(2):183-4.
1997: Billström R; Johansson B; Strömbeck B; el-Rifai W; Larramendy M; Olofsson T; Mitelman F; Knuutila S
Clonal CD5-positive B lymphocytes in myelodysplastic syndrome with systemic vasculitis and trisomy 8.
Annals of hematology 1997;74(1):37-40.
1997: Bardi G; Parada L A; Bomme L; Pandis N; Willén R; Johansson B; Jeppsson B; Beroukas K; Heim S; Mitelman F
Cytogenetic comparisons of synchronous carcinomas and polyps in patients with colorectal cancer.
British journal of cancer 1997;76(6):765-9.
1996: Mertens F; Johansson B; Mitelman F
Dichotomy of hyperdiploid acute lymphoblastic leukemia on the basis of the distribution of gained chromosomes.
Cancer genetics and cytogenetics 1996;92(1):8-10.
1996: Johansson B; Mertens F; Mitelman F
Primary vs. secondary neoplasia-associated chromosomal abnormalities--balanced rearrangements vs. genomic imbalances?
Genes, chromosomes & cancer 1996;16(3):155-63.
1996: Johansson B; Fioretos T; Billström R; Mitelman F
Abberant cytogenetic evolution pattern of Philadelphia-positive chronic myeloid leukemia treated with interferon-alpha.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1996;10(7):1134-8.
1996: Köhler M; Johansson B; Garwicz S; Heim S; Mitelman F
No FISH evidence for trisomy 7 in normal or leukemic bone marrow.
Cancer genetics and cytogenetics 1996;88(2):133-5.
1996: Andreasson P; Johansson B; Arheden K; Tedgård U; Ljung R; Heim S; Mitelmann F
Emergence of novel transient clonal chromosomal bone marrow changes in remission of acute lymphoblastic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1996;10(2):378-83.
1996: Johansson B; Fioretos T; Garwicz S; Heim S; Mitelman F
t(3;21)(q26;q22) with AML1 rearrangement in a de novo childhood acute monoblastic leukaemia.
British journal of haematology 1996;92(2):429-31.
1996: Panagopoulos I; Aman P; Johansson B; Malm C; Lenhoff S; Billström R; Mitelman F
NRAS mutations are rare in acute myeloid leukaemias with t(8;21) or inv(16).
European journal of haematology 1996;56(1-2):68-71.
1996: Höglund M; Johansson B; Pedersen-Bjergaard J; Marynen P; Mitelman F
Molecular characterization of 12p abnormalities in hematologic malignancies: deletion of KIP1, rearrangement of TEL, and amplification of CCND2.
Blood 1996;87(1):324-30.
1995: Gorunova L; Johansson B; Dawiskiba S; Andrén-Sandberg A; Jin Y; Mandahl N; Heim S; Mitelman F
Massive cytogenetic heterogeneity in a pancreatic carcinoma: fifty-four karyotypically unrelated clones.
Genes, chromosomes & cancer 1995;14(4):259-66.
1995: Richter J; Swedin A; Olofsson T; Johansson B; Akerman M; Winqvist I
Aggressive course of primary plasma cell leukemia with unusual morphological and cytogenetic features.
Annals of hematology 1995;71(6):307-10.
1995: Johansson B; Mertens F; Mitelman F
Cytogenetic evolution patterns in non-Hodgkin's lymphoma.
Blood 1995;86(10):3905-14.
1995: Johansson B; Arheden K; Höglund M; Othzén A; Békássy A N; Turesson I; Heim S; Mitelman F
Fluorescence in situ hybridization analysis of whole-arm 7;12 translocations in hematologic malignancies.
Genes, chromosomes & cancer 1995;14(1):56-62.
1995: Gorunova L; Johansson B; Dawiskiba S; Andrén-Sandberg A; Mandahl N; Heim S; Mitelman F
Cytogenetically detected clonal heterogeneity in a duodenal adenocarcinoma.
Cancer genetics and cytogenetics 1995;82(2):146-50.
1995: Johansson B; Waldenström J; Hasselblom S; Mitelman F
Waldenström's macroglobulinemia with the AML/MDS-associated t(1;3)(p36;q21).
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1995;9(7):1136-8.
1995: Pandis N; Jin Y; Gorunova L; Petersson C; Bardi G; Idvall I; Johansson B; Ingvar C; Mandahl N; Mitelman F
Chromosome analysis of 97 primary breast carcinomas: identification of eight karyotypic subgroups.
Genes, chromosomes & cancer 1995;12(3):173-85.
1994: Panagopoulos I; Aman P; Fioretos T; Höglund M; Johansson B; Mandahl N; Heim S; Behrendtz M; Mitelman F
Fusion of the FUS gene with ERG in acute myeloid leukemia with t(16;21)(p11;q22).
Genes, chromosomes & cancer 1994;11(4):256-62.
1994: Bardi G; Aman P; Johansson B; Pandis N; Mandahl N; Bak-Jensen E; Björkman A; Sjögren H O; Andrén-Sandberg A; Mitelman F
Cytogenetic characterization of a periampullary adenocarcinoma of the pancreas, its liver metastasis, and a cell line established from the metastasis and a cell line established from the metastasis in a patient with Gardner's syndrome.
Cancer genetics and cytogenetics 1994;76(1):29-32.
1994: Bardi G; Gorunova L; Limon J; Nedoszytko B; Johansson B; Pandis N; Mandahl N; Bak-Jensen E; Andrén-Sandberg A; Rys J
Abnormal karyotypes in three carcinomas of the gallbladder.
Cancer genetics and cytogenetics 1994;76(1):15-8.
1994: Mertens F; Johansson B; Mitelman F
Isochromosomes in neoplasia.
Genes, chromosomes & cancer 1994;10(4):221-30.
1994: Johansson B; Bardi G; Pandis N; Gorunova L; Bäckman P L; Mandahl N; Dawiskiba S; Andrén-Sandberg A; Heim S; Mitelman F
Karyotypic pattern of pancreatic adenocarcinomas correlates with survival and tumour grade.
International journal of cancer. Journal international du cancer 1994;58(1):8-13.
1994: Johansson B; Mertens F; Mitelman F
Secondary chromosomal abnormalities in acute leukemias.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1994;8(6):953-62.
1994: Johansson B; Billström R; Mauritzson N; Mitelman F
Trisomy 19 as the sole chromosomal anomaly in hematologic neoplasms.
Cancer genetics and cytogenetics 1994;74(1):62-5.
1994: Köhler M; Johansson B; Ludvigsson J; Aman P; Heim S; Mitelman F
Acute myeloid leukemia (AML-M1) with multiple trisomies and t(8;21)(q22;q22).
Cancer genetics and cytogenetics 1994;73(1):79-81.
1993: Johansson B; Mertens F; Mitelman F
Cytogenetic deletion maps of hematologic neoplasms: circumstantial evidence for tumor suppressor loci.
Genes, chromosomes & cancer 1993;8(4):205-18.
1993: Mertens F; Johansson B; Mitelman F
Age- and gender-related heterogeneity of cancer chromosome aberrations.
Cancer genetics and cytogenetics 1993;70(1):6-11.
1993: Bardi G; Johansson B; Pandis N; Mandahl N; Bak-Jensen E; Lindström C; Törnqvist A; Frederiksen H; Andrén-Sandberg A; Mitelman F
Cytogenetic analysis of 52 colorectal carcinomas--non-random aberration pattern and correlation with pathologic parameters.
International journal of cancer. Journal international du cancer 1993;55(3):422-8.
1993: Bardi G; Johansson B; Pandis N; Mandahl N; Bak-Jensen E; Andrén-Sandberg A; Mitelman F; Heim S
Karyotypic abnormalities in tumours of the pancreas.
British journal of cancer 1993;67(5):1106-12.
1993: Johansson B; Heim S; Mandahl N; Mertens F; Mitelman F
Trisomy 7 in nonneoplastic cells.
Genes, chromosomes & cancer 1993;6(4):199-205.
1993: Bardi G; Johansson B; Pandis N; Bak-Jensen E; Orndal C; Heim S; Mandahl N; Andrén-Sandberg A; Mitelman F
Cytogenetic aberrations in colorectal adenocarcinomas and their correlation with clinicopathologic features.
Cancer 1993;71(2):306-14.
1992: Bardi G; Johansson B; Pandis N; Heim S; Mandahl N; Hägerstrand I; Holmin T; Andrén-Sandberg A; Mitelman F
Trisomy 7 in nonneoplastic focal steatosis of the liver.
Cancer genetics and cytogenetics 1992;63(1):22-4.
1992: Bardi G; Johansson B; Pandis N; Heim S; Mandahl N; Bak-Jensen E; Frederiksen H; Andrén-Sandberg A; Mitelman F
Recurrent chromosome aberrations in abdominal smooth muscle tumors.
Cancer genetics and cytogenetics 1992;62(1):43-6.
1992: Johansson B; Bardi G; Heim S; Mandahl N; Mertens F; Bak-Jensen E; Andrén-Sandberg A; Mitelman F
Nonrandom chromosomal rearrangements in pancreatic carcinomas.
Cancer 1992;69(7):1674-81.
1992: Bardi G; Johansson B; Pandis N; Heim S; Mandahl N; Andrén-Sandberg A; Hägerstrand I; Mitelman F
Cytogenetic findings in three primary hepatocellular carcinomas.
Cancer genetics and cytogenetics 1992;58(2):191-5.
1992: Bardi G; Johansson B; Pandis N; Heim S; Mandahl N; Békássy A; Hägerstrand I; Mitelman F
Trisomy 2 as the sole chromosomal abnormality in a hepatoblastoma.
Genes, chromosomes & cancer 1992;4(1):78-80.
1991: Mertens F; Sallerfors B; Heim S; Johansson B; Kristoffersson U; Malm C; Mitelman F
Trisomy 13 as a primary chromosome aberration in acute leukemia.
Cancer genetics and cytogenetics 1991;56(1):39-44.
1991: Johansson B; Mertens F; Heim S; Kristoffersson U; Mitelman F
Cytogenetics of secondary myelodysplasia (sMDS) and acute nonlymphocytic leukemia (sANLL).
European journal of haematology 1991;47(1):17-27.
1991: Bardi G; Johansson B; Pandis N; Heim S; Mandahl N; Andrén-Sandberg A; Hägerstrand I; Mitelman F
Trisomy 7 in short-term cultures of colorectal adenocarcinomas.
Genes, chromosomes & cancer 1991;3(2):149-52.
1991: Mertens F; Johansson B; Heim S; Kristoffersson U; Mitelman F
Karyotypic patterns in chronic myeloproliferative disorders: report on 74 cases and review of the literature.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1991;5(3):214-20.
1991: Mertens F; Heim S; Mandahl N; Johansson B; Mertens O; Persson B; Salemark L; Wennerberg J; Jonsson N; Mitelman F
Cytogenetic analysis of 33 basal cell carcinomas.
Cancer research 1991;51(3):954-7.
1991: Johansson B; Mertens F; Mitelman F
Geographic heterogeneity of neoplasia-associated chromosome aberrations.
Genes, chromosomes & cancer 1991;3(1):1-7.
1990: Johansson B; Mertens F; Heim S; Kristoffersson U; Mandahl N; Nilsson P G; Mitelman F
Cytogenetic findings in acute megakaryoblastic leukemia (ANLL-M7).
Cancer genetics and cytogenetics 1990;48(1):119-23.
1990: Johansson B; Mertens F; Fioretos T; Heim S; Kristoffersson U; Mandahl N; Bartram C R; Mitelman F
Remarkably long survival of a patient with Ph1-positive chronic myeloid leukemia and 5' bcr rearrangement.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1990;4(6):448-9.
1990: Mertens F; Johansson B; Heim S; Kristoffersson U; Mandahl N; Turesson I; Malm C; Othzén A; Bartram C R; Catovsky D
Trisomy 14 in atypical chronic myeloid leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1990;4(2):117-20.
1989: Heim S; Johansson B; Mertens F
Constitutional chromosome instability and cancer risk.
Mutation research 1989;221(1):39-51.
1989: Mertens F; Heim S; Mandahl N; Johansson B; Rydholm A; Biörklund A; Wennerberg J; Jonsson N; Mitelman F
Clonal chromosome aberrations in a keratoacanthoma and a basal cell papilloma.
Cancer genetics and cytogenetics 1989;39(2):227-32.
1989: Heim S; Mertens F; Jin Y S; Mandahl N; Johansson B; Biörklund A; Wennerberg J; Jonsson N; Mitelman F
Diverse chromosome abnormalities in squamous cell carcinomas of the skin.
Cancer genetics and cytogenetics 1989;39(1):69-76.
1989: Mertens F; Heim S; Jin Y S; Johansson B; Mandahl N; Biörklund A; Wennerberg J; Jonsson N; Mitelman F
Basosquamous papilloma. A benign epithelial skin tumor with multiple cytogenetic clones.
Cancer genetics and cytogenetics 1989;37(2):235-9.
1989: Johansson B; Mandahl N; Heim S; Mertens F; Andrén-Sandberg A; Mitelam F
Chromosome abnormalities in a pancreatic adenocarcinoma.
Cancer genetics and cytogenetics 1989;37(2):209-13.
1989: Mertens F; Johansson B
Frequency and distribution of N-methyl-N'-nitro-N-nitrosoguanidine (MNNG)-induced structural chromosome aberrations in fibroblasts from sarcoma and non-Hodgkin's lymphoma patients.
Mutation research 1989;210(1):63-70.
1988: Mertens F; Johansson B; Heim S; Mandahl N; Rydholm A; Mitelman F
Normal frequency of chromosome breakage in lymphocytes from patients with musculoskeletal sarcoma.
Cancer genetics and cytogenetics 1988;33(2):299-304.
1988: Johansson B; Mertens F
Normal level of spontaneous chromosome breakage in lymphocytes from patients with non-Hodgkin's lymphoma.
Cancer genetics and cytogenetics 1988;33(1):51-7.
1988: Johansson B; Mertens F; Palm L; Englesson I; Kristoffersson U
Duplication 18p with mild influence on the phenotype.
American journal of medical genetics 1988;29(4):871-4.

Sign-in to see more