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- Publications
- Influence
Identification of a CpG island methylator phenotype that defines a distinct subgroup of glioma.
- H. Noushmehr, D. Weisenberger, +24 authors K. Aldape
- Biology, Medicine
- Cancer cell
- 18 May 2010
We have profiled promoter DNA methylation alterations in 272 glioblastoma tumors in the context of The Cancer Genome Atlas (TCGA). We found that a distinct subset of samples displays concerted… Expand
Subtype and pathway specific responses to anticancer compounds in breast cancer
- Laura M. Heiser, A. Sadanandam, +40 authors P. Spellman
- Biology, Medicine
- Proceedings of the National Academy of Sciences
- 14 October 2011
Breast cancers are comprised of molecularly distinct subtypes that may respond differently to pathway-targeted therapies now under development. Collections of breast cancer cell lines mirror many of… Expand
Exploration, normalization, and genotype calls of high-density oligonucleotide SNP array data.
- B. Carvalho, H. Bengtsson, T. Speed, R. Irizarry
- Biology, Medicine
- Biostatistics
- 1 April 2007
In most microarray technologies, a number of critical steps are required to convert raw intensity measurements into the data relied upon by data analysts, biologists, and clinicians. These data… Expand
Serotonin autoreceptor function and antidepressant drug action
- S. Hjorth, H. Bengtsson, A. Kullberg, D. Carlzon, H. Peilot, S. Auerbach
- Psychology, Medicine
- Journal of psychopharmacology
- 1 March 2000
This article briefly summarizes, within the context of a brief review of the relevant literature, the outcome of our recent rat microdialysis studies on (1) the relative importance of serotonin… Expand
DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly.
- I. Scheinin, D. Sie, +12 authors B. Ylstra
- Biology, Medicine
- Genome research
- 1 December 2014
Detection of DNA copy number aberrations by shallow whole-genome sequencing (WGS) faces many challenges, including lack of completion and errors in the human reference genome, repetitive sequences,… Expand
Estimation and assessment of raw copy numbers at the single locus level
- H. Bengtsson, R. Irizarry, B. Carvalho, T. Speed
- Biology, Computer Science
- Bioinform.
- 1 March 2008
TLDR
Type I Collagen α1 Sp1 Polymorphism and the Risk of Cruciate Ligament Ruptures or Shoulder Dislocations
- S. Khoschnau, H. Melhus, +6 authors K. Michaëlsson
- Medicine
- The American journal of sports medicine
- 1 December 2008
Background Cruciate ligament ruptures and shoulder dislocations are often caused by trauma, but predisposing intrinsic factors might also influence the risk. These injuries are more common in those… Expand
aroma.affymetrix: A generic framework in R for analyzing small to very large Affymetrix data sets in bounded memory
Summary: We have developed a cross-platform open-source framework for analyzing Affymetrix data sets consisting of 1 to 1,000s of arrays. By working directly with CDF and CEL files (standard… Expand
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Parent-specific copy number in paired tumor-normal studies using circular binary segmentation
- A. Olshen, H. Bengtsson, P. Neuvial, P. Spellman, R. Olshen, V. Seshan
- Biology, Computer Science
- Bioinform.
- 1 August 2011
TLDR
Clonal expansion and epigenetic reprogramming following deletion or amplification of mutant IDH1
- T. Mazor, C. Chesnelong, +24 authors J. Costello
- Biology, Medicine
- Proceedings of the National Academy of Sciences
- 15 September 2017
Significance Identifying the drivers of tumorigenesis provides insight into mechanisms of transformation and can suggest novel therapeutic targets. IDH1 mutations in gliomas are one such promising… Expand
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