Shelley D. Smith

6.6k citations

70 papers · 4.2k indexed · h-index 35

Developmental and Educational Psychology top 0.2%
- Reading and Literacy Development 27
- Language Development and Disorders 14
Statistics and Probability top 0.5%
- Cognitive and developmental aspects of mathematical skills 6
Sensory Systems top 1%
- Hearing, Cochlea, Tinnitus, Genetics 11
Cognitive Neuroscience top 2%
Genetics top 1%
- Genetics and Neurodevelopmental Disorders 28
- Genomic variations and chromosomal abnormalities 7
Education
- Child Development and Digital Technology 7
Psychiatry and Mental health
- Attention Deficit Hyperactivity Disorder 6

Co-authors: Bruce F. Pennington John C. DeFries William J. Kimberling Richard K. Olson Lon R. Cardon David W. Fulker Javier Gayán Herbert A. Lubs
Cited by: Developmental and Educational Psychology Statistics and Probability Sensory Systems
Journals: Science (2 papers)New England Journal of Medicine (1 paper)Proceedings of the National Academy of Sciences (1 paper)
Partner nations: United States United Kingdom Netherlands

In The Last Decade

Shelley D. Smith

67 papers receiving 3.9k citations

Peers

Countries citing papers authored by Shelley D. Smith

Since Specialization

Citations

This map shows the geographic impact of Shelley D. Smith's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Shelley D. Smith with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Shelley D. Smith more than expected).

Fields of papers citing papers by Shelley D. Smith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shelley D. Smith. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Shelley D. Smith. The network helps show where Shelley D. Smith may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Shelley D. Smith, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Shelley D. Smith Line = papers co-authored together Shelley D. Smith links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ Human Genetics ·John D. Eicher,Natalie R. Powers,Laura L. Miller,Kathryn L. Mueller,Sara Mascheretti,Cecilia Marino,Erik G. Willcutt,John C. DeFries,Richard K. Olson,Shelley D. Smith,Bruce F. Pennington,J. Bruce Tomblin,Susan M. Ring,Jeffrey R. Gruen	2014	29
2	Approach to epigenetic analysis in language disorders Journal of Neurodevelopmental Disorders ·Shelley D. Smith	2011	11
3	A Family Based Association Study of DRD4, DAT1, and 5HTT and Continuous Traits of Attention-Deficit Hyperactivity Disorder Behavior Genetics ·L. Cinnamon Bidwell,Erik G. Willcutt,Matthew B. McQueen,John C. DeFries,Richard K. Olson,Shelley D. Smith,Bruce F. Pennington	2011	44
4	Etiologies and Molecular Mechanisms of Communication Disorders Journal of Developmental & Behavioral Pediatrics ·Shelley D. Smith,Elena L. Grigorenko,Erik G. Willcutt,Bruce F. Pennington,Richard K. Olson,John C. DeFries	2010	8
5	Genes, language development, and language disorders Mental Retardation and Developmental Disabilities Research Reviews ·Shelley D. Smith	2007	43
6	Gene × Environment interactions in speech sound disorder predict language and preliteracy outcomes Development and Psychopathology ·Lauren M. McGrath,Bruce F. Pennington,Erik G. Willcutt,Richard Boada,Lawrence D. Shriberg,Shelley D. Smith	2007	28
7	DCDC2 is associated with reading disability and modulates neuronal development in the brain Proceedings of the National Academy of Sciences ·Haiying Meng,Shelley D. Smith,Karl Hager,Matthew A. Held,Jonathan Liu,Richard K. Olson,Bruce F. Pennington,John C. DeFries,Joel Gelernter,Thomas O’Reilly-Pol,Stefan Somlo,Pawel Skudlarski,Sally E. Shaywitz,Bennett A. Shaywitz,Karen E. Marchione,Yu Wang,Murugan Paramasivam,Joseph J. LoTurco,Grier P. Page,Jeffrey R. Gruen	2005	310
8	A 77-Kilobase Region of Chromosome 6p22.2 Is Associated with Dyslexia in Families From the United Kingdom and From the United States The American Journal of Human Genetics ·Clyde Francks,Silvia Paracchini,Shelley D. Smith,A.J. Richardson,Tom S. Scerri,Lon R. Cardon,Angela J. Marlow,I. Laurence MacPhie,Janet G. Walter,Bruce F. Pennington,Simon E. Fisher,Richard K. Olson,John C. DeFries,John Stein,Anthony P. Monaco	2004	190
9	Differential Genetic Etiology of Reading Component Processes as a Function of IQ Behavior Genetics ·Valerie S. Knopik,Shelley D. Smith,Lon R. Cardon,Bruce F. Pennington,Javier Gayán,Richard K. Olson,John C. DeFries	2002	30
10	Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention‐deficit/hyperactivity disorder American Journal of Medical Genetics ·Erik G. Willcutt,Bruce F. Pennington,Shelley D. Smith,Lon R. Cardon,Javier Gayán,Valerie S. Knopik,Richard K. Olson,John C. DeFries	2002	103
11	Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1 Psychiatric Genetics ·Clyde Francks,Simon E. Fisher,Richard K. Olson,Bruce F. Pennington,Shelley D. Smith,John C. DeFries,Anthony P. Monaco	2002	59
12	Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia Nature Genetics ·Simon E. Fisher,Clyde Francks,Angela J. Marlow,I. Laurence MacPhie,Dianne F. Newbury,Lon R. Cardon,Yumiko Ishikawa-Brush,A.J. Richardson,Joel B. Talcott,Javier Gayán,Richard K. Olson,Bruce F. Pennington,Shelley D. Smith,John C. DeFries,John Stein,Anthony P. Monaco	2001	204
13	Etiology of Reading Difficulties and Rapid Naming: The Colorado Twin Study of Reading Disability Behavior Genetics ·Chayna Davis,Javier Gayán,Valerie S. Knopik,Shelley D. Smith,Lon R. Cardon,Bruce F. Pennington,Richard K. Olson,John C. DeFries	2001	45
14	A Twin and Family Study of the Association Between Immune System Dysfunction and Dyslexia Using Blood Serum Immunoassay and Survey Data Brain and Cognition ·Jeffrey W. Gilger,Bruce F. Pennington,Ronald J. Harbeck,John C. DeFries,Brian L. Kotzin,Phyllis Green,Shelley D. Smith	1998	15
15	Single gene influences on radiologically-detectable malformations of the inner ear Journal of Communication Disorders ·Shelley D. Smith,Lee A. Harker	1998	12
16	Genetic analysis of dyslexia and other complex behavioral phenotypes Current Opinion in Pediatrics ·Bruce F. Pennington,Shelley D. Smith	1997	3
17	Differential risk for developmental reading disorders in the offspring of compensated versus noncompensated parents Reading and Writing ·Jeffrey W. Gilger,Elizabeth Hanebuth,Shelley D. Smith,Bruce F. Pennington	1996	18
18	Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q Human Molecular Genetics ·Kunihiro Fukushima,Arabandi Ramesh,C. R. Srikumari Srisailapathy,Li Ni,Achih Chen,Marsha E. O'Neill,Guy Van Camp,Paul Coucke,Shelley D. Smith,Judith B. Kenyon,Pawain Jain,Ed.R. Wilcox,Ross I. S. Zbar,Richard J. Smith	1995	41
19	Familial Dyslexia: Use of Genetic Linkage Data to Define Subtypes Journal of the American Academy of Child & Adolescent Psychiatry ·Shelley D. Smith,Bruce F. Pennington,William J. Kimberling,Paul S. Ing	1990	88
20	Spelling Errors in Adults with a Form of Familial Dyslexia Child Development ·Bruce F. Pennington,Linda L. McCabe,Shelley D. Smith,Dianne L. Lefly,Myra O. Bookman,William J. Kimberling,Herbert A. Lubs	1986	82

About Shelley D. Smith

Shelley D. Smith is a scholar working on Developmental and Educational Psychology, Sensory Systems and Genetics, having authored 70 papers that have together received 4.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (28 papers), Reading and Literacy Development (27 papers), Language Development and Disorders (14 papers), Hearing, Cochlea, Tinnitus, Genetics (11 papers), Genomic variations and chromosomal abnormalities (7 papers), Child Development and Digital Technology (7 papers), Cognitive and developmental aspects of mathematical skills (6 papers) and Attention Deficit Hyperactivity Disorder (6 papers). The work is most often cited by research in Developmental and Educational Psychology (2.5k citations), Statistics and Probability (848 citations) and Sensory Systems (359 citations). Shelley D. Smith has collaborated with scholars based in United States, United Kingdom and Netherlands. Frequent co-authors include Bruce F. Pennington, John C. DeFries, William J. Kimberling, Richard K. Olson, Lon R. Cardon, David W. Fulker, Javier Gayán, Herbert A. Lubs, Erik G. Willcutt and Guy C. Van Orden. Their work appears in journals such as Science, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact