M. Smith

1.8k total citations
29 papers, 1.3k citations indexed

About

M. Smith is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, M. Smith has authored 29 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Cognitive Neuroscience. Recurrent topics in M. Smith's work include Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (5 papers) and Tuberous Sclerosis Complex Research (4 papers). M. Smith is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (5 papers) and Tuberous Sclerosis Complex Research (4 papers). M. Smith collaborates with scholars based in United States, United Kingdom and Netherlands. M. Smith's co-authors include Pamela Flodman, M. Anne Spence, Gregg Duester, G. Wesley Hatfield, Robert J. Desnick, Virginia Bilanchone, F X Arredondo-Vega, Susan L. Smalley, Jonathan L. Haines and Géraldine Dawson and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

M. Smith

29 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Smith United States 18 446 415 352 328 164 29 1.3k
Athel Hockey Australia 19 833 1.9× 500 1.2× 408 1.2× 74 0.2× 110 0.7× 46 1.5k
Kira A. Dies United States 15 361 0.8× 553 1.3× 392 1.1× 228 0.7× 93 0.6× 26 1.2k
Agata Fiumara Italy 27 1.1k 2.4× 474 1.1× 1.0k 2.9× 240 0.7× 119 0.7× 131 2.4k
B. Ford United States 21 494 1.1× 122 0.3× 260 0.7× 76 0.2× 93 0.6× 36 1.8k
Elisabetta Bolognesi Italy 21 257 0.6× 207 0.5× 94 0.3× 202 0.6× 150 0.9× 50 973
Jesús Lascorz Germany 19 447 1.0× 273 0.7× 332 0.9× 182 0.6× 115 0.7× 25 1.7k
Mark D. Potter United States 16 611 1.4× 367 0.9× 70 0.2× 110 0.3× 43 0.3× 23 1.3k
Jillian S. Parboosingh Canada 29 936 2.1× 617 1.5× 165 0.5× 96 0.3× 66 0.4× 85 2.0k
Donna M. Krasnewich United States 28 1.3k 3.0× 362 0.9× 671 1.9× 111 0.3× 149 0.9× 59 2.4k
Jinong Feng United States 27 1.3k 2.8× 725 1.7× 72 0.2× 411 1.3× 77 0.5× 44 2.1k

Countries citing papers authored by M. Smith

Since Specialization
Citations

This map shows the geographic impact of M. 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 M. Smith with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Smith more than expected).

Fields of papers citing papers by M. Smith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Smith

This figure shows the co-authorship network connecting the top 25 collaborators of M. Smith. A scholar is included among the top collaborators of M. 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 M. Smith. M. Smith is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Ryu, Jiyoon, M. Smith, Juli Bai, et al.. (2024). Diet-enhanced LRG1 expression promotes insulin hypersecretion and ER stress in pancreatic beta cells. Diabetologia. 68(3). 615–628. 2 indexed citations
2.
Schellenberg, Gerard D., Géraldine Dawson, Yun Ju Sung, et al.. (2006). Evidence for multiple loci from a genome scan of autism kindreds. Molecular Psychiatry. 11(11). 1049–1060. 94 indexed citations
3.
Grady, Deborah, Ante Harxhi, M. Smith, et al.. (2005). Sequence variants of theDRD4 gene in autism: Further evidence that rareDRD4 7R haplotypes are ADHD specific. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 136B(1). 33–35. 32 indexed citations
4.
Devlin, Bernie, Edwin H. Cook, Hilary Coon, et al.. (2005). Autism and the serotonin transporter: the long and short of it. Molecular Psychiatry. 10(12). 1110–1116. 152 indexed citations
5.
Grady, Deborah, M. Smith, Eunice S. Wang, et al.. (2003). High prevalence of rare dopamine receptor D4 alleles in children diagnosed with attention-deficit hyperactivity disorder. Molecular Psychiatry. 8(5). 536–545. 104 indexed citations
6.
Smith, M., Abigail Woodroffe, Josefina Lozano Martínez, et al.. (2002). Molecular genetic delineation of a deletion of chromosome 13q12→q13 in a patient with autism and auditory processing deficits. Cytogenetic and Genome Research. 98(4). 233–239. 40 indexed citations
7.
Smith, M., Pauline A. Filipek, Maureen Bocian, et al.. (2001). Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR. Cytogenetic and Genome Research. 94(1-2). 15–22. 38 indexed citations
8.
Leslie, T.A., N. J. Levell, Sally J. Cutler, et al.. (1994). Acrodermatitis chronica atrophicans: a case report and review of the literature. British Journal of Dermatology. 131(5). 687–693. 16 indexed citations
9.
Smalley, Susan L., F J Burger, & M. Smith. (1994). Phenotypic variation of tuberous sclerosis in a single extended kindred.. Journal of Medical Genetics. 31(10). 761–765. 37 indexed citations
10.
Kandt, R.S., Jonathan L. Haines, M. Smith, et al.. (1992). Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease. Nature Genetics. 2(1). 37–41. 248 indexed citations
11.
Smalley, Susan L., M. Smith, & Peter E. Tanguay. (1991). Autism and Psychiatric Disorders in Tuberous Sclerosis. Annals of the New York Academy of Sciences. 615(1). 382–383. 17 indexed citations
12.
Povey, Sue, Mari‐Wyn Burley, M. Smith, et al.. (1991). An Attempt to Map Two Genes for Tuberous Sclerosis Using Novel Two‐Point Methodsa. Annals of the New York Academy of Sciences. 615(1). 298–305. 16 indexed citations
13.
Povey, Sue, L. A. Sandkuyl, Dick Lindhout, et al.. (1991). A Comparative Study on Genetic Heterogeneity in Tuberous Sclerosis: Evidence for One Gene on 9q34 and a Second Gene on 11q22–23a. Annals of the New York Academy of Sciences. 615(1). 306–315. 22 indexed citations
14.
Martiniuk, Frank, M. Smith, Amy L. Ellenbogen, et al.. (1983). Assignment of the gene for neutral alpha-glucosidase AB to chromosome 11. Cytogenetic and Genome Research. 35(2). 110–116. 9 indexed citations
15.
Darlington, G.J., et al.. (1982). Assignment of human alpha 1-antitrypsin to chromosome 14 by somatic cell hybrid analysis.. Proceedings of the National Academy of Sciences. 79(3). 870–873. 50 indexed citations
16.
Shafit‐Zagardo, Bridget, et al.. (1981). Assignment of the gene for acid beta-glucosidase to human chromosome 1.. PubMed. 33(4). 564–75. 34 indexed citations
17.
Smith, M., Bryan M. Turner, Nobutaka Tanigaki, & Kurt Hirschhorn. (1978). Regional localization of <i>HLA, ME</i><sub>s</sub><i>, </i>and <i>SO</i><i>D</i><sub>M</sub> on chromosome 6. Cytogenetic and Genome Research. 22(1-6). 428–433. 8 indexed citations
18.
Turner, Bryan M., M. Smith, V. S. Turner, et al.. (1978). Assignment of the gene locus for human ?-l-fucosidase to chromosome 1 by analysis of somatic cell hybrids. Somatic Cell and Molecular Genetics. 4(1). 45–54. 16 indexed citations
19.
Smith, M., Kurt Hirschhorn, J. Shuster, & Phil Gold. (1976). The study of human immunoglobulins in hybrid cells: tentative assignment of the genes responsible for human heavy chain immunoglobulin production to chromosome 2. Cytogenetic and Genome Research. 16(1-5). 235–237. 2 indexed citations
20.
White, Jason M., M. C. Brain, P.A. Lorkin, H. Lehmann, & M. Smith. (1970). Mild “Unstable Haemoglobin Haemolytic Anaemia” caused by Haemoglobin Shepherds Bush (B74 (E18) Gly→Asp). Nature. 225(5236). 939–941. 35 indexed citations

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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