Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastoma

Valerie Greger, Eberhard Passarge, Wolfgang H�pping, +2

Human Genetics

ChromatinLineage PlasticityEpigenetic ChangeGeneticsSpontaneous Regression +8

Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.

André Reis, Bärbel Dittrich, Valerie Greger, +5

PubMed

Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma

Valerie Greger, Nils Debus, Dietmar Lohmann, +3

Human Genetics

GeneticsMolecular GeneticsParental OriginMedicineCell Biology +1

The γ-aminobutyric acid receptor γ3 subunit gene (GABRG3) is tightly linked to the α5 subunit gene (GABRA5) on human chromosome 15q11–q13 and is transcribed in the same orientation

Valerie Greger, Joan H.M. Knoll, Elizabeth A. Woolf, +10

Genomics

Same OrientationG Protein-coupled ReceptorGenetic DisorderGeneticsHuman Polymorphism +6

Carrier screening by next‐generation sequencing: health benefits and cost effectiveness

Mohammad Hossein Azimi, Kyle Schmaus, Valerie Greger, +3

Molecular Genetics & Genomic Medicine

A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromes.

Karin Buiting, Valerie Greger, Bernard H. Brownstein, +5

Proceedings of the National Academy of Sciences

GeneticsPathologyGene CharacterizationMolecular GeneticsDisease Gene Identification +15

Validation for Clinical Use of, and Initial Clinical Experience with, a Novel Approach to Population-Based Carrier Screening using High-Throughput, Next-Generation DNA Sequencing

Stephanie Hallam, Heather H. Nelson, Valerie Greger, +10

Journal of Molecular Diagnostics

Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastoma

Kai Kloss, Petra Währisch, Valerie Greger, +5

American Journal of Medical Genetics

Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locus

Bernhard Horsthemke, Valerie Greger, H.J. Barnert, +2

Human Genetics

Retinoblastoma LocusSubmicroscopic DeletionsGenetic TestingGene Deletion DataOphthalmology +6

Newly established human retinoblastoma cell lines exhibit an “immortalized” but not an invasive phenotype <i>in vitro</i>

Sahine Griegel, Hong Chen, Roland Frötschl, +4

International Journal of Cancer