Carla Rosenberg

Non-recurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair (2008)

Friez, Michael J, Boespflug-Tanguy, Odile, Zenker, Martin, Vianna-Morgante, Angela M, ...

Recurrent submicroscopic genomic copy number changes are the result of non-allelic homologous recombination (NAHR). Non-recurrent aberrations however, can result from different non-exclusive...

Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair (2008)

Bauters, Marijke, Van Esch, Hilde, Friez, Michael J., Boespflug-Tanguy, Odile, Zenker, Martin, Vianna-Morgante, Angela M., ...

Recurrent submicroscopic genomic copy number changes are the result of nonallelic homologous recombination (NAHR). Nonrecurrent aberrations, however, can result from different nonexclusive...

Widening the clinical spectrum of Pitt-Rogers-Danks/Wolf-Hirschhorn syndromes (2007)

Mazzeu,Juliana F., Krepischi-Santos,Ana Cristina, Rosenberg,Carla, Lourenço,Charles M., Lezirovitz,Karina, Szuhai,Karoly, ...

Chromosomal rearrangements involving partial deletion of the short arm of chromosome 4 and partial duplication of the short arm of chromosome 8 have been described both in Pitt-Rogers-Danks syndrome...

Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation (2007)

Ullmann, Reinhard, Turner, Gillian, Kirchhoff, Maria, Chen, Wei, Tonge, Bruce, Rosenberg, Carla, ...

Autism and mental retardation (MR) are often associated, suggesting that these conditions are etiologically related. Recently, array-based comparative genomic hybridization (array CGH) has identified...

Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation (2007)

Ullmann, Reinhard, Turner, Gillian, Kirchhoff, Maria, Chen, Wei, Tonge, Bruce, Rosenberg, Carla, ...

Autism and mental retardation (MR) are often associated, suggesting that these conditions are etiologically related. Recently, array-based comparative genomic hybridization (array CGH) has identified...

An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome (2005)

Rosenberg, Carla, Krepischi-Santos, Ana Cristina, Kok, Fernando, Knijnenburg, Jeroen, ...

FG syndrome is an X-linked multiple congenital anomalies (MCA) syndrome. It has been mapped to four distinct loci FGS1-4, through linkage analysis (Xq13, Xp22.3, and Xp11.4-p11.3) and based on the...

Genomic profiling by DNA amplification of laser capture microdissected tissues and array CGH (2004)

Cardoso, Joana, Molenaar, Lia, De Menezes, Renée X., Rosenberg, Carla, Morreau, Hans, Möslein, Gabriela, ...

Comparative genomic hybridization by means of BAC microarrays (array CGH) allows high-resolution profiling of copy-number aberrations in tumor DNA. However, specific genetic lesions associated with...

Differentially Painting Human Chromosome Arms with Combined Binary Ratio-labeling Fluorescence In Situ Hybridization

Wiegant, Joop, Bezrookove, Vladimir, Rosenberg, Carla, Tanke, Hans J., Raap, Anton K., Zhang, Hongen, ...

Recently we developed a novel strategy for differentially painting all 24 human chromosomes. It is termed COBRA–FISH, short for combined binary ratio labeling–fluorescence in situ hybridization....

Genomic profiling by DNA amplification of laser capture microdissected tissues and array CGH

Cardoso, Joana, Molenaar, Lia, De Menezes, Renée X., Rosenberg, Carla, Morreau, Hans, Möslein, Gabriela, ...

Comparative genomic hybridization by means of BAC microarrays (array CGH) allows high-resolution profiling of copy-number aberrations in tumor DNA. However, specific genetic lesions associated with...

Differentially Painting Human Chromosome Arms with Combined Binary Ratio-labeling Fluorescence In Situ Hybridization

Wiegant, Joop, Bezrookove, Vladimir, Rosenberg, Carla, Tanke, Hans J., Raap, Anton K., Zhang, Hongen, ...

Recently we developed a novel strategy for differentially painting all 24 human chromosomes. It is termed COBRA–FISH, short for combined binary ratio labeling–fluorescence in situ hybridization....

Genomic profiling by DNA amplification of laser capture microdissected tissues and array CGH

Cardoso, Joana, Molenaar, Lia, De Menezes, Renée X., Rosenberg, Carla, Morreau, Hans, Möslein, Gabriela, ...

Comparative genomic hybridization by means of BAC microarrays (array CGH) allows high-resolution profiling of copy-number aberrations in tumor DNA. However, specific genetic lesions associated with...

Near-Haploidy and Subsequent Polyploidization Characterize the Progression of Peripheral Chondrosarcoma

Van Royen, Martin, Bardoel, Alfons F. J., Rosenberg, Carla, Cornelisse, Cees J., Cleton-Jansen, Anne-Marie, ...

Chondrosarcomas are malignant cartilaginous tumors arising centrally in bone (central chondrosarcoma), or secondarily within the cartilaginous cap of osteochondroma (peripheral chondrosarcoma). We...

Molecular Cytogenetic Evaluation of Gastric Cardia Adenocarcinoma and Precursor Lesions

Van Dekken, Herman, Alers, Janneke C., Riegman, Peter H. J., Rosenberg, Carla, Tilanus, Hugo W., Vissers, Kees

Analyses of cancer incidence data in the United States and Western Europe revealed steadily rising rates over the past decades of adenocarcinomas of the esophagus and gastric cardia. Genetic...

Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair

Bauters, Marijke, Van Esch, Hilde, Friez, Michael J., Boespflug-Tanguy, Odile, Zenker, Martin, Vianna-Morgante, Angela M., ...

Recurrent submicroscopic genomic copy number changes are the result of nonallelic homologous recombination (NAHR). Nonrecurrent aberrations, however, can result from different nonexclusive...