Robert D. Nicholls
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
- → Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome(1989)884 cited
- → Genome of the marsupial Monodelphis domestica reveals innovation in non-coding sequences(2007)723 cited
- → A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16(1985)703 cited
- → Development of type 2 diabetes following intrauterine growth retardation in rats is associated with progressive epigenetic silencing of Pdx1(2008)633 cited
- → Genome Organization, Function, and Imprinting in Prader-Willi and Angelman Syndromes(2001)624 cited
- → Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15(1995)598 cited
- → Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion(1989)582 cited
- → Imprinting in Prader–Willi and Angelman syndromes(1998)452 cited
- → A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism(1993)414 cited
- → A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith–Wiedemann syndrome(1999)406 cited