Stanley F. Nelson

4.9k total citations
16 papers, 1.1k citations indexed

About

Stanley F. Nelson is a scholar working on Molecular Biology, Cognitive Neuroscience and Genetics. According to data from OpenAlex, Stanley F. Nelson has authored 16 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Cognitive Neuroscience and 4 papers in Genetics. Recurrent topics in Stanley F. Nelson's work include Attention Deficit Hyperactivity Disorder (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomics and Rare Diseases (2 papers). Stanley F. Nelson is often cited by papers focused on Attention Deficit Hyperactivity Disorder (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomics and Rare Diseases (2 papers). Stanley F. Nelson collaborates with scholars based in United States, Japan and France. Stanley F. Nelson's co-authors include Timothy F. Cloughesy, Paul S. Mischel, Linda M. Liau, Susan L. Smalley, James J. McGough, James T. McCracken, Marc Carlson, Cho-Lea Tso, Zugen Chen and Koji Yoshimoto and has published in prestigious journals such as Nature Genetics, PLoS ONE and Radiology.

In The Last Decade

Stanley F. Nelson

16 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stanley F. Nelson United States	12	391	245	197	195	168	16	1.1k
Sharon K. Michelhaugh United States	24	606 1.5×	189 0.8×	99 0.5×	287 1.5×	128 0.8×	49	1.5k
Wang Zheng China	21	721 1.8×	31 0.1×	111 0.6×	121 0.6×	54 0.3×	43	1.5k
Romina Combi Italy	19	496 1.3×	349 1.4×	155 0.8×	104 0.5×	150 0.9×	38	1.1k
Louis N. Manganas United States	16	775 2.0×	102 0.4×	104 0.5×	65 0.3×	63 0.4×	24	1.3k
David A. Rempe United States	16	559 1.4×	167 0.7×	185 0.9×	29 0.1×	67 0.4×	20	1.2k
Jelle Praet Belgium	18	295 0.8×	45 0.2×	119 0.6×	145 0.7×	37 0.2×	33	1.2k
Maria Cristina D’Adamo Italy	25	1.2k 3.1×	134 0.5×	97 0.5×	66 0.3×	162 1.0×	61	1.6k
Hiroki Kitaura Japan	16	312 0.8×	117 0.5×	123 0.6×	32 0.2×	111 0.7×	35	703
Yumiko Nishikawa Japan	21	151 0.4×	238 1.0×	265 1.3×	15 0.1×	89 0.5×	40	1.1k
Beatrice Paradiso Italy	17	321 0.8×	165 0.7×	111 0.6×	66 0.3×	157 0.9×	36	966

Countries citing papers authored by Stanley F. Nelson

Since Specialization

Citations

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

Fields of papers citing papers by Stanley F. Nelson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stanley F. Nelson. 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 Stanley F. Nelson. The network helps show where Stanley F. Nelson may publish in the future.

Co-authorship network of co-authors of Stanley F. Nelson

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

All Works

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16 of 16 papers shown

Mis, Emily K., Rebecca Signer, Weizhen Ji, et al.. (2021). Expansion of NEUROD2 phenotypes to include developmental delay without seizures. American Journal of Medical Genetics Part A. 185(4). 1076–1080. 7 indexed citations

Mitra, Ileena, Christine Ladd‐Acosta, Lisa Croen, et al.. (2016). Pleiotropic Mechanisms Indicated for Sex Differences in Autism. PLoS Genetics. 12(11). e1006425–e1006425. 56 indexed citations

Ye, Fei, Yibei Zhang, Yue Liu, et al.. (2013). Protective Properties of Radio-Chemoresistant Glioblastoma Stem Cell Clones Are Associated with Metabolic Adaptation to Reduced Glucose Dependence. PLoS ONE. 8(11). e80397–e80397. 50 indexed citations

Al‐Gazali, Lihadh, et al.. (2013). X chromosome exome sequencing reveals a novel ALG13 mutation in a nonsyndromic intellectual disability family with multiple affected male siblings. American Journal of Medical Genetics Part A. 164(1). 164–169. 20 indexed citations

Mick, Eric, Alexandre A. Todorov, Susan L. Smalley, et al.. (2010). Family-Based Genome-Wide Association Scan of Attention-Deficit/Hyperactivity Disorder. Journal of the American Academy of Child & Adolescent Psychiatry. 49(9). 898–905.e3. 99 indexed citations

Carlson, Marc, et al.. (2008). Genetically defined EWS/FLI1 model system suggests mesenchymal origin of Ewing's family tumors. Laboratory Investigation. 88(12). 1291–1302. 22 indexed citations

Pope, Whitney B., Jun Dong, Marc Carlson, et al.. (2008). Relationship between Gene Expression and Enhancement in Glioblastoma Multiforme: Exploratory DNA Microarray Analysis. Radiology. 249(1). 268–277. 124 indexed citations

Rock, Matthew J., Jean Prenen, Vincent Funari, et al.. (2008). Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia. Nature Genetics. 40(8). 999–1003. 176 indexed citations

Loo, Sandra K., et al.. (2008). Cognitive functioning in affected sibling pairs with ADHD: familial clustering and dopamine genes. Journal of Child Psychology and Psychiatry. 49(9). 950–957. 34 indexed citations

10.

Tso, Cho-Lea, Peter Shintaku, James Chen, et al.. (2006). Primary Glioblastomas Express Mesenchymal Stem-Like Properties. Molecular Cancer Research. 4(9). 607–619. 184 indexed citations

11.

Saghizadeh, Mehrnoosh, Andrei A. Kramerov, Jian Tajbakhsh, et al.. (2005). Proteinase and Growth Factor Alterations Revealed by Gene Microarray Analysis of Human Diabetic Corneas. Investigative Ophthalmology & Visual Science. 46(10). 3604–3604. 72 indexed citations

12.

Kim, Chang‐Jin, et al.. (2004). Silicon Microarray Pin With Selective Hydrophobic Coating. 443–446. 3 indexed citations

13.

Ogdie, Matthew N., I. Laurence MacPhie, Sonia L. Minassian, et al.. (2003). A Genomewide Scan for Attention-Deficit/Hyperactivity Disorder in an Extended Sample: Suggestive Linkage on 17p11. The American Journal of Human Genetics. 72(5). 1268–1279. 147 indexed citations

14.

Nishitani, Junko, Zugen Chen, Min Qin, et al.. (2002). Identification of genes required for immortalization in human papillomavirus-infected human oral keratinocytes.. PubMed. 48 Online Pub. OL331–41. 4 indexed citations

15.

McCracken, James T., Stanley F. Nelson, & Susan L. Smalley. (2001). The dopamine receptor DRD4 gene. Trends in Pharmacological Sciences. 22(2). 56–56. 2 indexed citations

16.

Yue, Qing, et al.. (1998). De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxia. American Journal of Medical Genetics. 77(4). 298–301. 60 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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