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List of works by Teresita Díaz de Ståhl

A segmental maximum a posteriori approach to genome-wide copy number profiling.

scientific article published on 19 January 2008

Characterization of novel and complex genomic aberrations in glioblastoma using a 32K BAC array

scientific article

Chromosome 22 array-CGH profiling of breast cancer delimited minimal common regions of genomic imbalances and revealed frequent intra-tumoral genetic heterogeneity

scientific article published in October 2006

Chromosome 22 tiling-path array-CGH analysis identifies germ-line- and tumor-specific aberrations in patients with glioblastoma multiforme

scientific article

Copy-number polymorphisms: mining the tip of an iceberg

scientific article

Distal 22q11.2 microduplication encompassing the BCR gene

scientific article published in December 2008

Frequent genetic differences between matched primary and metastatic breast cancer provide an approach to identification of biomarkers for disease progression

scientific article

High-resolution array-CGH profiling of germline and tumor-specific copy number alterations on chromosome 22 in patients affected with schwannomas

scientific article published on 28 October 2005

Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2.

scientific article

Microarray-based survey of CpG islands identifies concurrent hyper- and hypomethylation patterns in tissues derived from patients with breast cancer

scientific article published on 01 July 2006

Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter).

scientific article published in August 2007

Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles

scientific article published on 14 February 2008

Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array

scientific article published in March 2008

Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis.

scientific article published on 3 June 2010

Somatic mosaicism for copy number variation in differentiated human tissues

scientific article published on 01 September 2008

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