S. D. Smith

2.4k citations
19 papers · 1.9k · 1 hit paper · h-index 15

Impact in

Papers in

    • Genetics and Neurodevelopmental Disorders 5
    • Genomic variations and chromosomal abnormalities 2
    • Genetic Associations and Epidemiology 2

S. D. Smith

19 papers receiving 1.7k citations

S. D. Smith's Hit Papers

A cytogenetic survey of 14,069 newborn infants 1975 · 441 citations
4410+17+34Years since publication100200300400

Peers

S. D. Smith
Comparison fields: 5 of 99
  • Sensory Systems 461
  • Developmental and Educational Psychology 579
  • Statistics and Probability 206
  • Genetics 576
  • Cognitive Neuroscience 392
Replace I. Rapin with:
I. Rapin United States
Jeffrey R. Gruen United States
Anna Maria Chilosi Italy
Elina Mäki‐Torkko Sweden
Dianne F. Newbury United Kingdom
Paola Cipriani Italy
Viviann Nordin Sweden
Maricela Alarcón United States
Gunilla Ahlsén Sweden
Jérôme Nicod United Kingdom
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Citations per field
00.5×10×17.2×
I. Rapin · 1×
Citations per year

Countries citing papers authored by S. D. Smith

Since Specialization
Citations

This map shows the geographic impact of S. 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 S. 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 S. D. Smith more than expected).

Fields of papers citing papers by S. D. Smith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S. 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 S. D. Smith. The network helps show where S. D. Smith may publish in the future.

Co-authors

The 25 scholars most cited alongside S. 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 S. D. Smith Line = papers co-authored together S. D. Smith links everyone, so they are left out of the graph.

All Works

19 of 19 papers shown
#Work
1
A cytogenetic survey of 14,069 newborn infants
Hit paper breakdown →
1975441
2 1998411
3 1990291
4 1987110
5 2002106
6 199189
7 199580
8 201477
9 200569
10 201740
11 199736
12 200632
13
Molecular approaches to the genetic analysis of specific reading disability.
199827
14
Colorado Reading Project: Past, Present, and Future
199125
15 200215
16 20158
17 19844
18
Identification of genetic influences.
19924
19
Bacterial translocation and the role of postoperative selective bowel decontamination in small intestinal transplantation.
19942

About S. D. Smith

S. D. Smith is a scholar working on Genetics, Molecular Biology, Developmental and Educational Psychology, Cognitive Neuroscience and Sensory Systems, having authored 19 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), Reading and Literacy Development (4 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers), Vestibular and auditory disorders (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Attention Deficit Hyperactivity Disorder (2 papers), Genetic Associations and Epidemiology (2 papers) and Hemispheric Asymmetry in Neuroscience (2 papers). The work is most often cited by research in Sensory Systems (461 citations), Developmental and Educational Psychology (579 citations), Statistics and Probability (206 citations), Genetics (576 citations) and Cognitive Neuroscience (392 citations). S. D. Smith has collaborated with scholars based in United States, Netherlands and United Kingdom. Frequent co-authors include Bruce F. Pennington, J.L. Hamerton, M. Ray, Marshall M. Haith, Philip M. Kelley, David J. Harris, James W. Askew, Trent Fowler, Guy C. Van Orden and J. C. DeFries. Their work appears in journals such as The American Journal of Human Genetics, Genes Brain & Behavior, Clinical Genetics, Reading and Writing and American Journal of Medical Genetics Part B Neuropsychiatric Genetics.

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.

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