Valerie Greger
Muscular Dystrophy Association(US)
Publications by Year
Research Areas
Ocular Oncology and Treatments, Cystic Fibrosis Research Advances, Cancer-related Molecular Pathways, Prenatal Screening and Diagnostics, Genetic Syndromes and Imprinting
Most-Cited Works
- → Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastoma(1989)564 cited
- Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.(1994)
- → Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma(1994)185 cited
- → 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(1995)67 cited
- → Carrier screening by next‐generation sequencing: health benefits and cost effectiveness(2016)61 cited
- → A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromes.(1992)47 cited
- → Next-generation carrier screening(2013)46 cited
- → Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locus(1987)45 cited
- → Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastoma(1991)45 cited
- → 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(2014)45 cited