James M. Gabriel
Publications by Year
Research Areas
Genetic Syndromes and Imprinting, Epigenetics and DNA Methylation, Prenatal Screening and Diagnostics, Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → Imprinting-Mutation Mechanisms in Prader-Willi Syndrome(1999)276 cited
- → Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation(1997)141 cited
- → A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and Angelman syndromes(1999)121 cited
- → Report of the fourth international workshop on human chromosome 15 mapping 1997(1999)61 cited
- → A model system to study genomic imprinting of human genes(1998)56 cited
- → Structure and function correlations at the imprinted mouse Snrpn locus(1998)39 cited
- → Conserved characteristics of heterochromatin-forming DNA at the 15q11-q13 imprinting center(1999)37 cited
- → A common insertion/deletion polymorphism in the Prader—Willi syndrome minimal critical region(1994)6 cited
- → Clinical spectrum and molecular diagnosis of Angelman and Prader‐Willi syndrome patients with an imprinting mutation(1997)3 cited
- Fourth International Workshop on Human Chromosome 15 Mapping, Genome Database, Baltimore, MD, October 28 1997(1999)