Shelley D. Smith - Concepedia

Author

Shelley D. Smith

Also Known As

D. Smith, Shelley, S D Smith, S Smith, SHELLEY D. SMITH, Shelley D Smith, Shelley D. Smith, Shelley D.Smith, Shelley Smith, Smith, Shelley

110

Publications

6.5K

Citations

H-Index

103

Concepts

All Affiliations

University of Denver University of Nebraska Medical Center University of Colorado Boulder Nebraska Medical Center University of Oxford

About

Shelley D. Smith is an author at University of Denver specializing in medicine, genetics, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Education	5	5	539
2	Language Studies	5	5	536
3	Arts	4	4	148
4	Health Sciences	4	4	169
5	Business	1	1	20

Shelley D. Smith

Publications

5.6K

Citations

H-Index

Page 1

	Year	Citations
Quantitative Trait Locus for Reading Disability on Chromosome 6 Lon R. Cardon, Shelley D. Smith, David W. Fulker, Science Haplotype DeterminationQuantitative GeneticsGenotype-phenotype AssociationGenetic DisorderMedicine	1994	540
<i>DCDC2</i> is associated with reading disability and modulates neuronal development in the brain Haiying Meng, Shelley D. Smith, Karl Hager, Proceedings of the National Academy of Sciences	2005	389
Specific Reading Disability: Identification of an Inherited Form Through Linkage Analysis Shelley D. Smith, William J. Kimberling, Bruce F. Pennington, Science Family MedicineDevelopmental DisabilityChromosome 15Genetic DisorderMedicine	1983	333
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia Simon E. Fisher, Clyde Francks, Angela J. Marlow, Nature Genetics Genetic DisorderGeneticsChromosome 18NeuroscienceNeurology	2001	270
Phonological Processing Skills and Deficits in Adult Dyslexics Bruce F. Pennington, Guy C. Van Orden, Shelley D. Smith, Child Development	1990	258
Quantitative-Trait Locus for Specific Language and Reading Deficits on Chromosome 6p Javier Gayán, Shelley D. Smith, Stacey S. Cherny, The American Journal of Human Genetics Reading DeficitsLanguage DisorderGenetic DisorderGeneticsNeurolinguistics	1999	252
A 77-Kilobase Region of Chromosome 6p22.2 Is Associated with Dyslexia in Families From the United Kingdom and From the United States Clyde Francks, Silvia Paracchini, Shelley D. Smith, The American Journal of Human Genetics Down SyndromeGenetic DisorderMedicineGeneticsChromosome 6P22.2	2004	240
Joint Analysis of the DRD5 Marker Concludes Association with Attention-Deficit/Hyperactivity Disorder Confined to the Predominantly Inattentive and Combined Subtypes Naomi Lowe, Aiveen Kirley, Ziarih Hawi, The American Journal of Human Genetics AdhdPsychopathologyPsychiatryBrain FunctionCombined Subtypes	2004	184
Tietz syndrome (hypopigmentation/deafness) caused by mutation of<i>MITF</i>: Figure 1 Shelley D. Smith, Philip M. Kelley, Judith B. Kenyon, Journal of Medical Genetics	2000	151
Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention‐deficit/hyperactivity disorder Erik G. Willcutt, Bruce F. Pennington, Shelley D. Smith, American Journal of Medical Genetics GeneticsGenetic EpidemiologyLinkage AnalysisAttention‐deficit/hyperactivity DisorderSocial Sciences	2002	143

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