Daniel J. Driscoll - Concepedia

Author

Daniel J. Driscoll

Also Known As

D DRISCOLL, D J Driscoll, D. J Driscoll, D. J. DRISCOLL, D. J. Driscoll, D.J. Driscoll, Daniel Driscoll, Daniel J Driscoll, Daniel J. Driscoll, Jennifer Miller

152

Publications

10.4K

Citations

H-Index

116

Concepts

All Affiliations

University of Florida Florida College University of Kansas Medical Center University of California, Irvine Philips (United States)

About

Daniel J. Driscoll is an author at University of Florida specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	26	35	3.3K
2	Natural Sciences	4	4	490
3	Public Health	4	4	257
4	Education	1	1	38
5	Health Sciences	1	1	34

Daniel J. Driscoll

Publications

8.2K

Citations

H-Index

Page 1

	Year	Citations
Prader–Willi syndrome Suzanne B. Cassidy, Daniel J. Driscoll European Journal of Human Genetics	2008	587
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, The American Journal of Human Genetics	2009	513
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, Proceedings of the National Academy of Sciences	1999	406
Allele-specific replication timing of imprinted gene regions Danny Kitsberg, Sara Selig, M. Brandels, Nature GeneticsAllele-specific Replication TimingGenomic MechanismDna ReplicationGene Structure	1993	382
Angelman syndrome: Consensus for diagnostic criteria Charles A. Williams, Harry Angelman, Jill Clayton‐Smith, American Journal of Medical Genetics Clinical FindingAngelman SyndromeMedicineDiagnosisNeuropathology	1995	362
Chromosome Breakage in the Prader-Willi and Angelman Syndromes Involves Recombination between Large, Transcribed Repeats at Proximal and Distal Breakpoints James Amos‐Landgraf, Yonggang Ji, Wayne Gottlieb, The American Journal of Human Genetics Transcribed RepeatsMendelian DisorderGenetic DisorderGeneticsPathology	1999	280
Imprinting-Mutation Mechanisms in Prader-Willi Syndrome Tohru Ohta, Todd A. Gray, Peter K. Rogan, The American Journal of Human Genetics Developmental BiologyGenetic DisorderGeneticsMolecular GeneticsImprinting-mutation Mechanisms	1999	276
Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene. Christopher C. Glenn, Shinji Saitoh, M T Jong, PubMed	1996	236
A Novel Imprinted Gene, Encoding a RING Zinc-Finger Protein, and Overlapping Antisense Transcript in the Prader-Willi Syndrome Critical Region M T Jong, Todd A. Gray, Yazhong Ji, Human Molecular Genetics	1999	229
A DNA methylation imprint, determined by the sex of the parent, distinguishes the angelman and Prader-Willi syndromes Daniel J. Driscoll, Michael F. Waters, Charles A. Williams, Genomics Developmental BiologyGenetic DisorderEpigenetic ChangeGeneticsDna Methylation	1992	211

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