Robert D. Nicholls

Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome

Robert D. Nicholls, Joan H.M. Knoll, Merlin G. Butler et al. · Nature · 1989 · 884 citations

Infertility, Genetic Testing, Developmental Biology +8

Genome of the marsupial Monodelphis domestica reveals innovation in non-coding sequences

Tarjei S. Mikkelsen, Matthew J. Wakefield, Bronwen Aken et al. · Nature · 2007 · 720 citations · Full text

Biology, Phylogenetics, Genome Study +12

A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16

Stephen T. Reeders, M.H. Breuning, Kay E. Davies et al. · Nature · 1985 · 703 citations

Genetic Disorder, Medicine, Genetics +11

Development of type 2 diabetes following intrauterine growth retardation in rats is associated with progressive epigenetic silencing of Pdx1

Jun Hyung Park, Doris A. Stoffers, Robert D. Nicholls et al. · Journal of Clinical Investigation · 2008 · 633 citations · Full text

Chromatin, Developmental Biology, Progressive Epigenetic Silencing +15

Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15

Karin Buiting, Shinji Saitoh, Bärbel Dittrich et al. · Nature Genetics · 1995 · 598 citations

Developmental Biology, Genetic Disorder, Developmental Genetics +8