Markus Mayrhofer

Publikationer
Populärvetenskap och samverkan

Artiklar

Article: CANCER DISCOVERY. 2015;5(5):488-505
Genomic Complexity Profiling Reveals That HORMAD1 Overexpression Contributes to Homologous Recombination Deficiency in Triple-Negative Breast Cancers.
Watkins J; Weekes D; Shah V; Gazinska P; Joshi S; Sidhu B; Gillett C; Pinder S; Vanoli F; Jasin M; Mayrhofer M; Isaksson A; Cheang MCU; Mirza H; Frankum J; Lord CJ; Ashworth A; Vinayak S; Ford JM; Telli ML; Grigoriadis A; Tutt ANJ
Article: BMC CANCER. 2015;15:125
Microsatellite instability and mutations in BRAF and KRAS are significant predictors of disseminated disease in colon cancer.
Birgisson H; Edlund K; Wallin U; Påhlman L; Kultima HG; Mayrhofer M; Micke P; Isaksson A; Botling J; Glimelius B; Sundström M
Article: NATURE COMMUNICATIONS. 2015;6:6125
Intratumoral genome diversity parallels progression and predicts outcome in pediatric cancer
Mengelbier LH; Karlsson J; Lindgren D; Valind A; Lilljebjorn H; Jansson C; Bexell D; Braekeveldt N; Ameur A; Jonson T; Kultima HG; Isaksson A; Asmundsson J; Versteeg R; Rissler M; Fioretos T; Sandstedt B; Borjesson A; Backman T; Pal N; Ora I; Mayrhofer M; Gisselsson D
Article: BMC CANCER. 2014;14:872
1p36 deletion is a marker for tumour dissemination in microsatellite stable stage II-III colon cancer.
Mayrhofer M; Kultima HG; Birgisson H; Sundström M; Mathot L; Edlund K; Viklund B; Sjöblom T; Botling J; Micke P; Påhlman L; Glimelius B; Isaksson A
Article: GENOME BIOLOGY. 2013;14(3):R24
Patchwork: allele-specific copy number analysis of whole-genome sequenced tumor tissue.
Mayrhofer M; DiLorenzo S; Isaksson A
Article: BMC CANCER. 2012;12:407
Loss-of-heterozygosity on chromosome 19q in early-stage serous ovarian cancer is associated with recurrent disease.
Skirnisdottir I; Mayrhofer M; Rydåker M; Akerud H; Isaksson A
Article: AMERICAN JOURNAL OF HEMATOLOGY. 2012;87(7):737-740
Next generation RNA-sequencing in prognostic subsets of chronic lymphocytic leukemia
Mansouri L; Gunnarsson R; Sutton L-A; Ameur A; Hooper SD; Mayrhofer M; Juliusson G; Isaksson A; Gyllensten U; Rosenquist R
Article: GENOME BIOLOGY. 2011;12(10):R108
Allele-specific copy number analysis of tumor samples with aneuploidy and tumor heterogeneity
Rasmussen M; Sundstrom M; Kultima HG; Botling J; Micke P; Birgisson H; Glimelius B; Isaksson A
Article: HAEMATOLOGICA. 2011;96(8):1161-1169
Array-based genomic screening at diagnosis and during follow-up in chronic lymphocytic leukemia
Gunnarsson R; Mansouri L; Isaksson A; Goransson H; Cahill N; Jansson M; Rasmussen M; Lundin J; Norin S; Buhl AM; Smedby KE; Hjalgrim H; Karlsson K; Jurlander J; Geisler C; Juliusson G; Rosenquist R
Article: HAEMATOLOGICA. 2010;95(9):1519-1525
High-density screening reveals a different spectrum of genomic aberrations in chronic lymphocytic leukemia patients with 'stereotyped' IGHV3-21 and IGHV4-34 B-cell receptors
Marincevic M; Cahill N; Gunnarsson R; Isaksson A; Mansouri M; Goransson H; Rasmussen M; Jansson M; Ryan F; Karlsson K; Adami H-O; Davi F; Jurlander J; Juliusson G; Stamatopoulos K; Rosenquist R
Article: GENOME RESEARCH. 2010;20(7):899-907
Characterization of the RNA content of chromatin.
Mondal T; Rasmussen M; Pandey GK; Isaksson A; Kanduri C
Article: PLOS ONE. 2009;4(6):e6057
Quantification of Normal Cell Fraction and Copy Number Neutral LOH in Clinical Lung Cancer Samples Using SNP Array Data
Goransson H; Edlund K; Rydaker M; Rasmussen M; Winquist J; Ekman S; Bergqvist M; Thomas A; Lambe M; Rosenquist R; Holmberg L; Micke P; Botling J; Isaksson A

Alla övriga publikationer

Letter: LEUKEMIA. 2010;24(1):211-215
Large but not small copy-number alterations correlate to high-risk genomic aberrations and survival in chronic lymphocytic leukemia: a high-resolution genomic screening of newly diagnosed patients
Gunnarsson R; Isaksson A; Mansouri M; Goransson H; Jansson M; Cahill N; Rasmussen M; Staaf J; Lundin J; Norin S; Buhl AM; Smedby KE; Hjalgrim H; Karlsson K; Jurlander J; Juliusson G; Rosenquist R

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