Daniel J. Driscoll

Prader–Willi syndrome

Suzanne B. Cassidy, Daniel J. Driscoll · European Journal of Human Genetics · 2008 · 587 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 · 513 citations · Full text

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 · 406 citations · Full text

Allele-specific replication timing of imprinted gene regions

Danny Kitsberg, Sara Selig, M. Brandels et al. · Nature · 1993 · 382 citations

Genetics, Allele-specific Replication Timing, Genomic Mechanism +7

Angelman syndrome: Consensus for diagnostic criteria

Charles A. Williams, Harry Angelman, Jill Clayton‐Smith et al. · American Journal of Medical Genetics · 1995 · 362 citations

Clinical Finding, Angelman Syndrome, Medicine +4