Gunnar Juliusson

Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios (2008)

Staaf, Johan, Vallon-Christersson, Johan, Lindgren, David, Juliusson, Gunnar, Rosenquist, Richard, Höglund, Mattias, ...

Abstract Background Illumina Infinium whole genome genotyping (WGG) arrays are increasingly being applied in cancer genomics to study gene copy number alterations and allele-specific aberrations such...

Segmentation-based detection of allelic imbalance and loss-of-heterozygosity in cancer cells using whole genome SNP arrays (2008)

Staaf, Johan, Lindgren, David, Vallon-Christersson, Johan, Isaksson, Anders, Göransson, Hanna, Juliusson, Gunnar, ...

Abstract We present a strategy for detection of loss-of-heterozygosity and allelic imbalance in cancer cells from whole genome single nucleotide polymorphism genotyping data. Using a dilution series...

Rapid and effective CD3 T-cell depletion with a magnetic cell sorting program to produce peripheral blood progenitor cell products for haploidentical transplantation in children and adults. (2007)

Dykes, Josefina H, Toporski, Jacek, Juliusson, Gunnar, Békássy, Albert N, Lenhoff, Stig, Lindmark, Anders, ...

Abstract is not available

Impact of age on survival after intensive therapy for multiple myeloma: a population-based study by the Nordic Myeloma Study Group. (2006)

Lenhoff, Stig, Hjorth, Martin, Westin, Jan, Brinch, Lorentz, Backstrom, Bengt, Carlson, Kristina, ...

Abstract is not available

Purine analogues: rationale for development, mechanisms of action, and pharmacokinetics in hairy cell leukemia. (2006)

Juliusson, Gunnar, Liliemark, Jan

Abstract is not available.

Application of population pharmacokinetics to cladribine (2005)

Lindemalm, Synnöve, Savic, Radojka M, Karlsson, Mats O, Juliusson, Gunnar, Liliemark, Jan, Albertioni, Freidoun

Abstract Background The nucleoside analog cladribine is used for the treatment of a variety of indolent B- and T-cell lymphoid malignancies. The primary aim of the study was to evaluate the...

Distinct patterns of hematopoietic stem cell involvement in acute lymphoblastic leukemia. (2005)

Castor, Anders, Nilsson, Lars, Astrand-Grundström, Ingbritt, Buitenhuis, Miranda, Ramirez, Carole, Anderson, Kristina, ...

Abstract is not available

Identification of a commonly amplified 4.3 Mb region with overexpression of the C8FW gene, encoding a phosphoprotein regulated by mitogenic pathways, but not of the MYC gene in MYC-containing double minutes in myeloid malignancies. (2004)

Storlazzi, Clelia T., Fioretos, Thoas, Paulsson, Kajsa, Strömbeck, Bodil, Lassen, Carin, Ahlgren, Tomas, ...

Abstract is not available

Identification of a commonly amplified 4.3 Mb region with overexpression of the C8FW gene, encoding a phosphoprotein regulated by mitogenic pathways, but not of the MYC gene in MYC-containing double minutes in myeloid malignancies (2004)

Storlazzi, Clelia T., Fioretos, Thoas, Paulsson, Kajsa, Strömbeck, Bodil, Lassen, Carin, Ahlgren, Tomas, ...

Double minutes (dmin), the cytogenetic hallmark of genomic amplification, are found in approximately 1% of karyotypically abnormal acute myeloid leukemias (AML) and myelodysplastic syndromes (MDS)....

Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies (2004)

Storlazzi, Clelia T., Fioretos, Thoas, Paulsson, Kajsa, Strömbeck, Bodil, Lassen, Carin, Ahlgren, Tomas, ...

Double minutes (dmin), the cytogenetic hallmark of genomic amplification, are found in ∼1% of karyotypically abnormal acute myeloid leukemias (AML) and myelodysplastic syndromes (MDS). The...

Identification of a commonly amplified 4.3 Mb region with overexpression of the C8FW gene, encoding a phosphoprotein regulated by mitogenic pathways, but not of the MYC gene in MYC-containing double minutes in myeloid malignancies (2004)

Storlazzi, Clelia T., Fioretos, Thoas, Paulsson, Kajsa, Strömbeck, Bodil, Lassen, Carin, Ahlgren, Tomas, ...

Double minutes (dmin), the cytogenetic hallmark of genomic amplification, are found in approximately 1% of karyotypically abnormal acute myeloid leukemias (AML) and myelodysplastic syndromes (MDS)....

RT-PCR analysis of acute myeloid leukemia with t(8;16)(p11;p13): Identification of a novel MOZ/CBP transcript and absence of CBP/MOZ expression. (2002)

Panagopoulos, Ioannis, Fioretos, Thoas, Isaksson, Margareth, Mitelman, Felix, Johansson, Bertil, Theorin, Niklas, ...

Application of population pharmacokinetics to cladribine

Lindemalm, Synnöve, Savic, Radojka M, Karlsson, Mats O, Juliusson, Gunnar, Liliemark, Jan, Albertioni, Freidoun

Application of population pharmacokinetics to cladribine

Lindemalm, Synnöve, Savic, Radojka M, Karlsson, Mats O, Juliusson, Gunnar, Liliemark, Jan, Albertioni, Freidoun

Hypocholesterolaemia in hairy cell leukaemia: Authors’ reply

Juliusson, Gunnar, Vitols, Sigurd

Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios

Staaf, Johan, Vallon-Christersson, Johan, Lindgren, David, Juliusson, Gunnar, Rosenquist, Richard, Höglund, Mattias, ...

Segmentation-based detection of allelic imbalance and loss-of-heterozygosity in cancer cells using whole genome SNP arrays

Staaf, Johan, Lindgren, David, Vallon-Christersson, Johan, Isaksson, Anders, Göransson, Hanna, Juliusson, Gunnar, ...

A strategy is presented for detection of loss-of-heterozygosity and allelic imbalance in cancer cells from whole genome SNP genotyping data.