M. Smith

1.8k citations

29 papers · 1.3k indexed · h-index 18

Impact in

Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research
Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities

Papers in ⓘ

Genetics 14
- Genetics and Neurodevelopmental Disorders 6
- Genomic variations and chromosomal abnormalities 3
- Diabetes and associated disorders 2
Molecular Biology 8
- Biochemical and Molecular Research 2

Co-authors: Pamela Flodman (9 shared papers)M. Anne Spence (7 shared papers)G. Wesley Hatfield (2 shared papers)Gregg Duester (2 shared papers)Robert J. Desnick (6 shared papers)Virginia Bilanchone (1 shared paper)F X Arredondo-Vega (4 shared papers)Susan L. Smalley (2 shared papers)
Journals: Cytogenetic and Genome Research (6 papers)Molecular Psychiatry (4 papers)Annals of the New York Academy of Sciences (3 papers)Proceedings of the National Academy of Sciences (3 papers)Annals of Human Genetics (2 papers)
Partner nations: United States United Kingdom Netherlands

In The Last Decade

M. Smith

29 papers receiving 1.2k citations

Peers

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-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 29 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease Nature Genetics ·R.S. Kandt, Jonathan L. Haines, M. Smith, Hope Northrup, R. J. M. Gardner, M. Priscilla Short, K. Dumars, E. Steve Roach, S. Steingold, S. A. Wall, Susan H. Blanton, Pamela Flodman, David J. Kwiatkowski, Ann Jewell, J L Weber, Allen D. Roses, Margaret A. Pericak‐Vance	1992	248
2	Autism and the serotonin transporter: the long and short of it Molecular Psychiatry ·Bernie Devlin, Edwin H. Cook, Hilary Coon, Géraldine Dawson, Elena L. Grigorenko, William McMahon, Nancy J. Minshew, David L. Pauls, M. Smith, M. Anne Spence, Patricia M. Rodier, Chris Stodgell, (unknown), (unknown)	2005	152
3	Molecular analysis of the human class I alcohol dehydrogenase gene family and nucleotide sequence of the gene encoding the beta subunit. Journal of Biological Chemistry ·Gregg Duester, M. Smith, Virginia Bilanchone, G. Wesley Hatfield	1986	120
4	High prevalence of rare dopamine receptor D4 alleles in children diagnosed with attention-deficit hyperactivity disorder Molecular Psychiatry ·Deborah Grady, H-C Chi, Y.-C. Ding, M. Smith, Eunice S. Wang, Sabrina Schuck, Pamela Flodman, M. Anne Spence, James M. Swanson, Robert K. Moyzis	2003	104
5	Evidence for multiple loci from a genome scan of autism kindreds Molecular Psychiatry ·Gerard D. Schellenberg, Géraldine Dawson, Yun Ju Sung, Annette Estes, Jeff Munson, Elisabeth A. Rosenthal, Joseph H. Rothstein, Pamela Flodman, M. Smith, Hilary Coon, L. Leong, C-E Yu, Chris Stodgell, Patricia M. Rodier, M. Anne Spence, Nancy J. Minshew, William M. McMahon, Ellen M. Wijsman	2006	94
6	Assignment of human alpha 1-antitrypsin to chromosome 14 by somatic cell hybrid analysis. Proceedings of the National Academy of Sciences ·G.J. Darlington, Kenneth H. Astrin, S P Muirhead, Robert J. Desnick, M. Smith	1982	50
7	Regional gene assignment of human porphobilinogen deaminase and esterase A4 to chromosome 11q23 leads to 11qter. Proceedings of the National Academy of Sciences ·Ai-li Wang, F X Arredondo-Vega, Philip F. Giampietro, M. Smith, W. French Anderson, Robert J. Desnick	1981	50
8	Human placental and intestinal alkaline phosphatase genes map to 2q34-q37. PubMed ·C.A. Griffin, M. Smith, Paula S. Henthorn, H. Harris, Mitchell J. Weiss, M Raducha, Beverly S. Emanuel	1987	47
9	Molecular genetic delineation of a deletion of chromosome 13q12→q13 in a patient with autism and auditory processing deficits Cytogenetic and Genome Research ·M. Smith, Abigail Woodroffe, R. Smith, S. Holguin, Josefina Lozano Martínez, Pauline A. Filipek, Charlotte Modahl, B. P. L. Moore, Maureen Bocian, Lee Z. Mays, Tracy M. Laulhere, Pamela Flodman, M. Anne Spence	2002	40
10	Molecular cloning and characterization of a cDNA for the beta subunit of human alcohol dehydrogenase. Proceedings of the National Academy of Sciences ·Gregg Duester, G. Wesley Hatfield, R. Bühler, J Hempel, Hans Jörnvall, M. Smith	1984	40
11	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 ·M. Smith, Julienne Escamilla, Pauline A. Filipek, Maureen Bocian, Charlotte Modahl, Pamela Flodman, M. Anne Spence	2001	38
12	Phenotypic variation of tuberous sclerosis in a single extended kindred. Journal of Medical Genetics ·Susan L. Smalley, F J Burger, M. Smith	1994	37
13	Mild “Unstable Haemoglobin Haemolytic Anaemia” caused by Haemoglobin Shepherds Bush (B74 (E18) Gly→Asp) Nature ·Jason M. White, M. C. Brain, P.A. Lorkin, H. Lehmann, M. Smith	1970	35
14	Assignment of the gene for acid beta-glucosidase to human chromosome 1. PubMed ·Bridget Shafit‐Zagardo, E.A. Devine, M. Smith, F X Arredondo-Vega, Robert J. Desnick	1981	34
15	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 ·Deborah Grady, Ante Harxhi, M. Smith, Pamela Flodman, M. Anne Spence, James M. Swanson, Robert K. Moyzis	2005	32
16	REPORT on the First International Workshop on Chromosome 9 held at Girton College Cambridge, UK, 22–24 March, 1992 Annals of Human Genetics ·Sue Povey, M. Smith, Jonathan L. Haines, Damian Kwiatkowski, Jane W. Fountain, A E Bale, Catherine M. Abbott, I Jackson, Martin Lawrie, M.A. Hultén	1992	27
17	A Comparative Study on Genetic Heterogeneity in Tuberous Sclerosis: Evidence for One Gene on 9q34 and a Second Gene on 11q22–23^a Annals of the New York Academy of Sciences ·L. A. J. JANSSEN, Sue Povey, (unknown), L. A. Sandkuyl, Dick Lindhout, Pamela Flodman, M. Smith, Julian R. Sampson, J. L. HAINES, E. C. MERKENS, P Fleury, Priscilla Short, J. Amos, D. J. J. Halley	1991	22
18	Autism and Psychiatric Disorders in Tuberous Sclerosis Annals of the New York Academy of Sciences ·Susan L. Smalley, M. Smith, Peter E. Tanguay	1991	17
19	Assignment of the gene locus for human ?-l-fucosidase to chromosome 1 by analysis of somatic cell hybrids Somatic Cell and Molecular Genetics ·Bryan M. Turner, M. Smith, V. S. Turner, Raju Kucherlapati, F.H. Ruddle, Kurt Hirschhorn	1978	16
20	An Attempt to Map Two Genes for Tuberous Sclerosis Using Novel Two‐Point Methods^a Annals of the New York Academy of Sciences ·Sue Povey, (unknown), L. A. J. JANSSEN, Mari‐Wyn Burley, M. Smith, Pamela Flodman, N.E. Morton, J. H. Edwards, Julian R. Sampson, John R.W. Yates, J. L. Haines, J. Amos, M. Priscilla Short, L. A. Sandkuyl, D. J. J. Halley, Alan Fryer, Torben Bech-Hansen, Rolf Mueller, L. AL‐GHAZALI, M Super, J. OSBORNE	1991	16

About M. Smith

M. Smith is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Surgery and Oncology, having authored 29 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (5 papers), Tuberous Sclerosis Complex Research (4 papers), Pancreatic function and diabetes (4 papers), Genomic variations and chromosomal abnormalities (3 papers), T-cell and B-cell Immunology (2 papers), Diabetes and associated disorders (2 papers) and Biochemical and Molecular Research (2 papers). The work is most often cited by research in Cognitive Neuroscience (328 citations), Genetics (415 citations), Physiology (352 citations), Psychiatry and Mental health (152 citations) and Pathology and Forensic Medicine (164 citations). M. Smith has collaborated with scholars based in United States, United Kingdom and Netherlands. Frequent co-authors include Pamela Flodman, M. Anne Spence, G. Wesley Hatfield, Gregg Duester, Robert J. Desnick, Virginia Bilanchone, F X Arredondo-Vega, Susan L. Smalley, Jonathan L. Haines and Nancy J. Minshew. Their work appears in journals such as Cytogenetic and Genome Research, Molecular Psychiatry, Annals of the New York Academy of Sciences, Proceedings of the National Academy of Sciences and Annals of Human 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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