S. D. Smith

2.4k total citations · 1 hit paper
19 papers, 1.9k citations indexed

About

S. D. Smith is a scholar working on Genetics, Molecular Biology and Developmental and Educational Psychology. According to data from OpenAlex, S. D. Smith has authored 19 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Molecular Biology and 6 papers in Developmental and Educational Psychology. Recurrent topics in S. D. Smith's work include Genetics and Neurodevelopmental Disorders (6 papers), Reading and Literacy Development (5 papers) and Hearing, Cochlea, Tinnitus, Genetics (3 papers). S. D. Smith is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Reading and Literacy Development (5 papers) and Hearing, Cochlea, Tinnitus, Genetics (3 papers). S. D. Smith collaborates with scholars based in United States, Netherlands and United Kingdom. S. D. Smith's co-authors include J.L. Hamerton, M. Ray, William J. Kimberling, Marshall M. Haith, Philip M. Kelley, Bruce F. Pennington, Trent Fowler, James W. Askew, Guy C. Van Orden and Patrick A. Green and has published in prestigious journals such as Child Development, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

S. D. Smith

19 papers receiving 1.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A cytogenetic survey of 14,069 newborn infants

1975 441 citations J.L. Hamerton, M. Ray et al. Clinical Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
S. D. Smith United States	15	635	629	605	464	447	19	1.9k
Jeffrey R. Gruen United States	32	725 1.1×	865 1.4×	996 1.6×	26 0.1×	446 1.0×	93	3.0k
Joseph H. French United States	21	325 0.5×	350 0.6×	256 0.4×	27 0.1×	380 0.9×	39	1.7k
I. Rapin United States	23	601 0.9×	650 1.0×	372 0.6×	73 0.2×	1.3k 3.0×	48	2.5k
Dianne F. Newbury United Kingdom	25	728 1.1×	1.5k 2.3×	1.5k 2.4×	50 0.1×	1.0k 2.3×	55	2.8k
Maricela Alarcón United States	18	627 1.0×	1.3k 2.1×	572 0.9×	24 0.1×	1.2k 2.7×	24	2.4k
A. J. Lincoln United States	9	574 0.9×	1.4k 2.3×	166 0.3×	39 0.1×	1.8k 4.0×	11	2.4k
Jérôme Nicod United Kingdom	14	687 1.1×	696 1.1×	331 0.5×	51 0.1×	351 0.8×	21	1.7k
Silvia Paracchini United Kingdom	28	813 1.3×	1.6k 2.5×	1.3k 2.2×	24 0.1×	1.0k 2.2×	63	3.1k
Zona Lai United States	13	445 0.7×	468 0.7×	327 0.5×	17 0.0×	833 1.9×	16	2.4k
Ilana S. Warsofsky United States	15	379 0.6×	502 0.8×	142 0.2×	14 0.0×	679 1.5×	16	1.5k

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-authorship network of co-authors of S. D. Smith

This figure shows the co-authorship network connecting the top 25 collaborators of S. D. Smith. A scholar is included among the top collaborators of S. D. Smith based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with S. D. Smith. S. D. Smith is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

Devanna, Paolo, Ho J, S. D. Smith, et al.. (2017). Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders. Molecular Psychiatry. 23(5). 1375–1384. 38 indexed citations

Eicher, John D., Catherine M. Stein, Allison Avrich Ciesla, et al.. (2015). The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains. Genes Brain & Behavior. 14(4). 377–385. 8 indexed citations

Gialluisi, Alessandro, Dianne F. Newbury, Richard K. Olson, et al.. (2014). Genome‐wide screening for DNA variants associated with reading and language traits. Genes Brain & Behavior. 13(7). 686–701. 77 indexed citations

Deupree, Jean D., S. D. Smith, Christopher J. Kratochvil, et al.. (2006). Possible involvement of alpha‐2A adrenergic receptors in attention deficit hyperactivity disorder: Radioligand binding and polymorphism studies. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(8). 877–884. 32 indexed citations

Gayán, Javier, Erik G. Willcutt, Simon E. Fisher, et al.. (2005). Bivariate linkage scan for reading disability and attention‐deficit/hyperactivity disorder localizes pleiotropic loci. Journal of Child Psychology and Psychiatry. 46(10). 1045–1056. 69 indexed citations

Gayán, Javier, Jungho Ahn, David L. Pauls, et al.. (2002). Evidence for Linkage and Association with Reading Disability, on 6p21.3-22. The American Journal of Human Genetics. 70(5). 1287–1298. 106 indexed citations

Leenheer, Els De, R.J.H. Ensink, Henricus P. M. Kunst, et al.. (2002). DFNA2/<i>KCNQ4</i> and Its Manifestations. Advances in oto-rhino-laryngology. 61. 41–46. 15 indexed citations

Kelley, Philip M., David J. Harris, James W. Askew, et al.. (1998). Novel Mutations in the Connexin 26 Gene (GJB2) That Cause Autosomal Recessive (DFNB1) Hearing Loss. The American Journal of Human Genetics. 62(4). 792–799. 409 indexed citations

Smith, S. D., Philip M. Kelley, & Amy Brower. (1998). Molecular approaches to the genetic analysis of specific reading disability.. PubMed. 70(2). 239–56. 27 indexed citations

10.

Brown, Matthew, L. Van Laer, S. D. Smith, et al.. (1997). A Novel Locus for Autosomal Dominant Nonsyndromic Hearing Loss, DFNA13, Maps to Chromosome 6p. The American Journal of Human Genetics. 61(4). 924–927. 36 indexed citations

11.

Camp, Guy Van, Paul Coucke, Wendy Balemans, et al.. (1995). Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15. Human Molecular Genetics. 4(11). 2159–2163. 79 indexed citations

12.

Heeckt, P. F., et al.. (1994). Bacterial translocation and the role of postoperative selective bowel decontamination in small intestinal transplantation.. PubMed. 26(3). 1688–1688. 2 indexed citations

13.

Smith, S. D.. (1992). Identification of genetic influences.. PubMed. 2(4). 73–85. 4 indexed citations

14.

DeFries, J. C., Richard K. Olson, Bruce F. Pennington, & S. D. Smith. (1991). Colorado Reading Project: Past, Present, and Future. 2(2). 25 indexed citations

15.

Fulker, David W., Lon R. Cardon, J. C. DeFries, et al.. (1991). Multiple regression analysis of sib-pair data on reading to detect quantitative trait loci. Reading and Writing. 3(3-4). 299–313. 89 indexed citations

16.

Pennington, Bruce F., Guy C. Van Orden, S. D. Smith, Patrick A. Green, & Marshall M. Haith. (1990). Phonological Processing Skills and Deficits in Adult Dyslexics. Child Development. 61(6). 1753–1778. 290 indexed citations

17.

Pennington, Bruce F., et al.. (1987). Left-Handedness and Immune Disorders in Familial Dyslexics. Archives of Neurology. 44(6). 634–639. 110 indexed citations

18.

Heal, David J., S. D. Smith, & C.K. Atterwill. (1984). Effects of thyroid status on clonidine-induced hypo-activity responses in the developing rat. Journal of Neural Transmission. 60(3-4). 295–302. 4 indexed citations

19.

Hamerton, J.L., et al.. (1975). A cytogenetic survey of 14,069 newborn infants. Clinical Genetics. 8(4). 223–243. 441 indexed citations breakdown →

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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