Robert D. Nicholls - Concepedia

Author

Robert D. Nicholls

Also Known As

Nicholls, R.D., Nicholls, Robert, R D Nicholls, R Nicholls, R. D. Nicholls, R. NICHOLLS, R. Nicholls, R.D. Nicholls, ROBERT D. NICHOLLS, Robert D Nicholls

164

Publications

16.7K

Citations

H-Index

130

Concepts

All Affiliations

Case Western Reserve University University Hospitals of Cleveland Center for Human Genetics University of Florida Florida College

About

Robert D. Nicholls is an author at Case Western Reserve University specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	42	58	9.6K
2	Natural Sciences	16	17	2.5K
3	Health Sciences	3	3	182
4	Public Health	2	2	224
5	Engineering	1	1	202

Robert D. Nicholls

101

Publications

14.3K

Citations

H-Index

Page 1

	Year	Citations
Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome Robert D. Nicholls, Joan H.M. Knoll, Merlin G. Butler, Nature InfertilityGenetic TestingDevelopmental BiologyGenetic ImprintingGenetic Disorder	1989	884
Genome of the marsupial Monodelphis domestica reveals innovation in non-coding sequences Tarjei S. Mikkelsen, Matthew J. Wakefield, Bronwen Aken, Nature BiologyPhylogeneticsGenome StudyComparative GenomicsGenetics	2007	720
A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16 Stephen T. Reeders, M.H. Breuning, Kay E. Davies, Nature Genetic DisorderMedicineGeneticsRenal PathologyPolymorphic Dna Marker	1985	703
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, Journal of Clinical Investigation ChromatinDevelopmental BiologyProgressive Epigenetic SilencingMedicineGenetics	2008	633
Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15 Karin Buiting, Shinji Saitoh, Bärbel Dittrich, Nature Genetics Developmental BiologyGenetic DisorderDevelopmental GeneticsGeneticsChromosome Biology	1995	598
Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion Joan H.M. Knoll, Robert D. Nicholls, R.E. Magenis, American Journal of Medical Genetics	1989	581
A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism Eugene M. Rinchik, Scott J. Bultman, Bernhard Horsthemke, Nature Ocular DiseaseExperimental OphthalmologyOphthalmologyGenetic DisorderGenetics	1993	413
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
Recombination at the human α-globin gene cluster: Sequence features and topological constraints Robert D. Nicholls, Nathan Fischel‐Ghodsian, Douglas R. Higgs Cell Linkage DisequilibriumTopological ConstraintsGeneticsMolecular BiologyMolecular Genetics	1987	344

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