Richard Rosenquist

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...

Outcome of ETV6/RUNX1-positive childhood acute lymphoblastic leukaemia in the NOPHO-ALL-1992 protocol: frequent late relapses but good overall survival. (2008)

Forestier, Erik, Heyman, Mats, Andersen, Mette K, Autio, Kirsi, Blennow, Elisabeth, Borgström, Georg, ...

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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 (2008)

Forestier, Erik, Gauffin, Fredrika, Andersen, Mette K, Autio, Kirsi, Borgström, Georg, Golovleva, Irina, ...

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Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature. (2007)

Forestier, Erik, Andersen, Mette K, Autio, Kirsi, Blennow, Elisabeth, Borgström, Georg, Golovleva, Irina, ...

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A hypothesis-generating search for new genetic breast cancer syndromes - a national study in 803 Swedish families (2007)

Von Wachenfeldt, Anna, Lindblom, Annika, Grönberg, Henrik, Einbeigi, Zakaria, Rosenquist, Richard, ...

Abstract Among Swedish families with an inherited predisposition for breast cancer, less than one third segregate mutations in genes known to be associated with an increased risk of breast cancer in...

Signal (2005)

Susann Fält, Mats Merup, Gerard Tobin, Ulf Thunberg, Gösta Gahrton, Richard Rosenquist, ...

doi:10.1182/blood-2004-10-4073 Distinctive gene expression pattern in VH3-21 utilizing B-cell chronic lymphocytic leukemia

Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO-93-AML trial between 1993 and 2001. (2003)

Forestier, Erik, Heim, Sverre, Blennow, Elisabeth, Borgström, Georg, Holmgren, Gösta, Heinonen, Kristiina, ...

Abstract is not available

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.

Quantification of Normal Cell Fraction and Copy Number Neutral LOH in Clinical Lung Cancer Samples Using SNP Array Data

Göransson, Hanna, Edlund, Karolina, Rydåker, Maria, Rasmussen, Markus, Winquist, Johan, Ekman, Simon, ...