Daniel J. Driscoll

Prader–Willi syndrome

Suzanne B. Cassidy, Daniel J. Driscoll · European Journal of Human Genetics · 2008 · 589 citations · Full text

Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations

Paweł Stankiewicz, Partha Sen, Samarth Bhatt et al. · The American Journal of Human Genetics · 2009 · 536 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

Nutritional phases in Prader–Willi syndrome

Jennifer Miller, Christy H. Lynn, Danielle C. Driscoll et al. · American Journal of Medical Genetics Part A · 2011 · 433 citations · Full text

Agriculture, Nutrition, Pediatrics +17

A maternally methylated CpG island in <i>KvLQT1</i> is associated with an antisense paternal transcript and loss of imprinting in Beckwith–Wiedemann syndrome

Nancy J. Smilinich, Colleen D. Day, Galina V. Fitzpatrick et al. · Proceedings of the National Academy of Sciences · 1999 · 407 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Allele-specific replication timing of imprinted gene regions

Danny Kitsberg, Sara Selig, M. Brandels et al. · Nature · 1993 · 383 citations

Life Sciences, Genetics, Molecular Genetics +12