Gordon C. Gowans

2.9k total citations
22 papers, 850 citations indexed

About

Gordon C. Gowans is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Gordon C. Gowans has authored 22 papers receiving a total of 850 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 13 papers in Genetics and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Gordon C. Gowans's work include Genomic variations and chromosomal abnormalities (9 papers), Congenital heart defects research (7 papers) and Chromosomal and Genetic Variations (4 papers). Gordon C. Gowans is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Congenital heart defects research (7 papers) and Chromosomal and Genetic Variations (4 papers). Gordon C. Gowans collaborates with scholars based in United States, Israel and Italy. Gordon C. Gowans's co-authors include David M. Grilly, Vazken M. Der Kaloustian, D. Ross McLeod, Stephen R. Williams, Helga V. Toriello, Micheala A. Aldred, Elaine H. Zackai, Sarah H. Elsea, Fahed Halal and R. Ellen Magenis and has published in prestigious journals such as Nature Genetics, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Gordon C. Gowans

22 papers receiving 801 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gordon C. Gowans United States 12 554 452 119 99 98 22 850
A. Moncla France 17 748 1.4× 633 1.4× 121 1.0× 174 1.8× 97 1.0× 29 1.1k
Audrey Labalme France 19 704 1.3× 629 1.4× 89 0.7× 123 1.2× 178 1.8× 66 1.2k
Liesbeth Rooms Belgium 17 593 1.1× 388 0.9× 118 1.0× 133 1.3× 67 0.7× 26 749
Bruno Delobel France 19 481 0.9× 366 0.8× 92 0.8× 91 0.9× 28 0.3× 37 804
Britt‐Marie Anderlid Sweden 22 813 1.5× 607 1.3× 200 1.7× 209 2.1× 51 0.5× 56 1.3k
Lars Riff Jensen Germany 11 927 1.7× 895 2.0× 211 1.8× 75 0.8× 66 0.7× 12 1.3k
R. Curtis Rogers United States 13 674 1.2× 492 1.1× 243 2.0× 75 0.8× 37 0.4× 20 882
A Nicod United Kingdom 8 679 1.2× 363 0.8× 61 0.5× 116 1.2× 68 0.7× 10 938
Eva Rossier Germany 13 392 0.7× 406 0.9× 74 0.6× 73 0.7× 39 0.4× 21 644
Mihailo Vujic Sweden 11 466 0.8× 797 1.8× 76 0.6× 97 1.0× 159 1.6× 14 1.1k

Countries citing papers authored by Gordon C. Gowans

Since Specialization
Citations

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

Fields of papers citing papers by Gordon C. Gowans

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gordon C. Gowans. 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 Gordon C. Gowans. The network helps show where Gordon C. Gowans may publish in the future.

Co-authorship network of co-authors of Gordon C. Gowans

This figure shows the co-authorship network connecting the top 25 collaborators of Gordon C. Gowans. A scholar is included among the top collaborators of Gordon C. Gowans 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 Gordon C. Gowans. Gordon C. Gowans 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.
Bain, Jennifer, Megan T. Cho, Aida Telegrafi, et al.. (2016). Variants in HNRNPH2 on the X Chromosome Are Associated with a Neurodevelopmental Disorder in Females. The American Journal of Human Genetics. 99(3). 728–734. 43 indexed citations
2.
Vanderver, Adeline, Davide Tonduti, Sarah Auerbach, et al.. (2012). Neurotransmitter abnormalities and response to supplementation in SPG11. Molecular Genetics and Metabolism. 107(1-2). 229–233. 11 indexed citations
3.
Gowans, Gordon C., Satyanarayana Gedela, David Q. Beversdorf, et al.. (2012). NF1 microduplications: identification of seven nonrelated individuals provides further characterization of the phenotype. Genetics in Medicine. 14(5). 508–514. 17 indexed citations
4.
Balasubramanian, Meena, Kath Smith, Lina Basel‐Vanagaite, et al.. (2011). Case series: 2q33.1 microdeletion syndrome—further delineation of the phenotype. Journal of Medical Genetics. 48(5). 290–298. 64 indexed citations
5.
Williams, Stephen R., Micheala A. Aldred, Vazken M. Der Kaloustian, et al.. (2010). Haploinsufficiency of HDAC4 Causes Brachydactyly Mental Retardation Syndrome, with Brachydactyly Type E, Developmental Delays, and Behavioral Problems. The American Journal of Human Genetics. 87(2). 219–228. 216 indexed citations
6.
Das, Bibhuti B., et al.. (2010). A Two-Month-Old Infant with Respiratory Distress and Left Ventricular Hypertrophy. The Journal of Pediatrics. 158(1). 149–154. 2 indexed citations
7.
Pani, Ariel M., Holly H. Hobart, Colleen A. Morris, et al.. (2010). Genome Rearrangements Detected by SNP Microarrays in Individuals with Intellectual Disability Referred with Possible Williams Syndrome. PLoS ONE. 5(8). e12349–e12349. 10 indexed citations
8.
Keaton, Amelia A., Kênia Balbi El-Jaick, Andrea Gropman, et al.. (2010). TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and Phenotype. Molecular Syndromology. 1(5). 211–222. 15 indexed citations
9.
10.
Gowans, Gordon C., et al.. (2009). Cornelia de Lange Syndrome: a case report with clinical review and recommended anticipatory guidance for the general practitioner.. PubMed. 107(9). 351–4. 2 indexed citations
11.
Ballif, Blake C., Aaron Theisen, Justine Coppinger, et al.. (2008). Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication. Molecular Cytogenetics. 1(1). 8–8. 176 indexed citations
12.
Ballif, Blake C., Elizabeth S. Jenkins, Suneeta Madan‐Khetarpal, et al.. (2007). Discovery of a previously unrecognized microdeletion syndrome of 16p11.2–p12.2. Nature Genetics. 39(9). 1071–1073. 140 indexed citations
13.
Angle, Brad, et al.. (2002). Partial duplication 4q and deletion 1p36 in monozygotic twins with discordant phenotypes. American Journal of Medical Genetics. 111(3). 307–312. 5 indexed citations
14.
Angle, Brad, et al.. (2002). Patient with terminal duplication 3q and terminal deletion 5q: comparison with the 3q duplication syndrome and distal 5q deletion syndrome. American Journal of Medical Genetics Part A. 116A(4). 376–380. 13 indexed citations
15.
Hersh, Joseph H., et al.. (2002). Developmental field defects: Coming together of associations and sequences during blastogenesis. American Journal of Medical Genetics. 110(4). 320–323. 11 indexed citations
16.
Grilly, David M., et al.. (1989). Effects of cocaine and d-amphetamine on sustained and selective attention in rats. Pharmacology Biochemistry and Behavior. 33(4). 733–739. 39 indexed citations
17.
Grilly, David M. & Gordon C. Gowans. (1988). Effects of naltrexone, andd-amphetamine, and their interaction on the stimulus control of choice behavior of rats. Psychopharmacology. 96(1). 73–80. 19 indexed citations
18.
Grilly, David M. & Gordon C. Gowans. (1986). Acute morphine dependence: Effects observed in shock and light discrimination tasks. Psychopharmacology. 88(4). 500–4. 13 indexed citations
19.
Grilly, David M. & Gordon C. Gowans. (1986). Comparison of the effects of morphine and immobilization stress on discrimination performance of rats.. Behavioral Neuroscience. 100(4). 512–524. 6 indexed citations
20.
Grilly, David M. & Gordon C. Gowans. (1986). Comparison of the effects of morphine and immobilization stress on discrimination performance of rats.. Behavioral Neuroscience. 100(4). 512–524. 6 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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