Edwin H. Cook

71.1k total citations · 4 hit papers
314 papers, 28.4k citations indexed

About

Edwin H. Cook is a scholar working on Cognitive Neuroscience, Genetics and Molecular Biology. According to data from OpenAlex, Edwin H. Cook has authored 314 papers receiving a total of 28.4k indexed citations (citations by other indexed papers that have themselves been cited), including 152 papers in Cognitive Neuroscience, 118 papers in Genetics and 74 papers in Molecular Biology. Recurrent topics in Edwin H. Cook's work include Autism Spectrum Disorder Research (145 papers), Genetics and Neurodevelopmental Disorders (87 papers) and Attention Deficit Hyperactivity Disorder (51 papers). Edwin H. Cook is often cited by papers focused on Autism Spectrum Disorder Research (145 papers), Genetics and Neurodevelopmental Disorders (87 papers) and Attention Deficit Hyperactivity Disorder (51 papers). Edwin H. Cook collaborates with scholars based in United States, United Kingdom and Canada. Edwin H. Cook's co-authors include Bennett Leventhal, Catherine Lord, Susan Risi, Andrew Pickles, Michael Rutter, Jeremy Veenstra‐VanderWeele, Stephen W. Scherer, Camille W. Brune, Daniel W. Bradley and Eric Courchesne and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Edwin H. Cook

308 papers receiving 27.2k citations

Hit Papers

The Autism Diagnostic Observation Schedule—Generic: A Sta... 1995 2026 2005 2015 2000 1995 2000 1999 2.0k 4.0k 6.0k
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.

  1. The Autism Diagnostic Observation Schedule—Generic: A Standard Measure of Social and Communication Deficits Associated with the Spectrum of Autism
    2000 6.1k citations Catherine Lord, Susan Risi et al. profile →
  2. Association of attention-deficit disorder and the dopamine transporter gene.
    1995 796 citations Edwin H. Cook, Mark A. Stein et al. profile →
  3. Practice parameter: Screening and diagnosis of autism
    2000 753 citations Edwin H. Cook et al. profile →
  4. The Screening and Diagnosis of Autistic Spectrum Disorders
    1999 702 citations Edwin H. Cook et al. profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Edwin H. Cook United States 83 16.8k 9.4k 6.9k 6.4k 5.2k 314 28.4k
Declan Murphy United Kingdom 93 15.1k 0.9× 5.2k 0.6× 3.9k 0.6× 6.1k 1.0× 3.9k 0.7× 541 31.2k
Bennett Leventhal United States 57 12.6k 0.7× 4.8k 0.5× 7.6k 1.1× 4.9k 0.8× 1.6k 0.3× 177 20.6k
Nancy J. Minshew United States 84 17.4k 1.0× 5.9k 0.6× 4.2k 0.6× 5.2k 0.8× 1.5k 0.3× 213 20.2k
Marion Leboyer France 87 9.1k 0.5× 6.1k 0.7× 7.4k 1.1× 11.0k 1.7× 4.0k 0.8× 614 28.6k
Christopher Gillberg Sweden 111 27.7k 1.6× 12.1k 1.3× 16.4k 2.4× 16.6k 2.6× 3.8k 0.7× 727 45.6k
Éric Fombonne Canada 76 16.1k 1.0× 5.6k 0.6× 10.3k 1.5× 6.6k 1.0× 1.7k 0.3× 290 23.8k
Jan K. Buitelaar Netherlands 104 22.9k 1.4× 3.8k 0.4× 12.5k 1.8× 20.6k 3.2× 2.2k 0.4× 874 45.1k
Ming T. Tsuang United States 116 12.5k 0.7× 7.1k 0.8× 13.3k 1.9× 23.4k 3.7× 6.0k 1.1× 841 49.1k
John A. Sweeney United States 97 18.4k 1.1× 3.2k 0.3× 5.0k 0.7× 14.0k 2.2× 2.3k 0.4× 613 33.5k
Fred R. Volkmar United States 82 18.4k 1.1× 5.0k 0.5× 8.9k 1.3× 5.6k 0.9× 882 0.2× 281 22.5k

Countries citing papers authored by Edwin H. Cook

Since Specialization
Citations

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

Fields of papers citing papers by Edwin H. Cook

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edwin H. Cook. 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 Edwin H. Cook. The network helps show where Edwin H. Cook may publish in the future.

Co-authorship network of co-authors of Edwin H. Cook

This figure shows the co-authorship network connecting the top 25 collaborators of Edwin H. Cook. A scholar is included among the top collaborators of Edwin H. Cook 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 Edwin H. Cook. Edwin H. Cook 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.
Anderson, George P., Edwin H. Cook, Randy Blakely, James S. Sutcliffe, & Jeremy Veenstra‐VanderWeele. (2024). Long COVID-19 and Peripheral Serotonin: A Commentary and Reconsideration. Journal of Inflammation Research. Volume 17. 2169–2172. 6 indexed citations
2.
Bishop, Jeffrey R., Chuan Zhou, Andrea Gaedigk, et al.. (2024). Dopamine Transporter and CYP2D6 Gene Relationships with Attention-Deficit/Hyperactivity Disorder Treatment Response in the Methylphenidate and Atomoxetine Crossover Study. Journal of Child and Adolescent Psychopharmacology. 34(10). 458–469. 2 indexed citations
3.
Saravanapandian, Vidya, Joel Frohlich, Joerg F. Hipp, et al.. (2020). Properties of beta oscillations in Dup15q syndrome. Journal of Neurodevelopmental Disorders. 12(1). 22–22. 16 indexed citations
4.
Wang, Quan, Rui Chen, Feixiong Cheng, et al.. (2019). A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data. Nature Neuroscience. 22(5). 691–699. 84 indexed citations
5.
Owley, Thomas, Matthew W. Mosconi, Suma Jacob, et al.. (2015). Pharmacogenetic Study of Serotonin Transporter and 5HT2A Genotypes in Autism. Journal of Child and Adolescent Psychopharmacology. 25(6). 467–474. 10 indexed citations
6.
Wassenaar, Catherine A., David V. Conti, Soma Das, et al.. (2014). UGT1A and UGT2B Genetic Variation Alters Nicotine and Nitrosamine Glucuronidation in European and African American Smokers. Cancer Epidemiology Biomarkers & Prevention. 24(1). 94–104. 25 indexed citations
7.
Merikangas, Alison, Ricardo Segurado, Elizabeth A. Heron, et al.. (2014). The phenotypic manifestations of rare genic CNVs in autism spectrum disorder. Molecular Psychiatry. 20(11). 1366–1372. 23 indexed citations
8.
Urraca, Nora, Lea K. Davis, Edwin H. Cook, N. Carolyn Schanen, & Lawrence T. Reiter. (2010). A Single-Tube Quantitative High-Resolution Melting Curve Method for Parent-of-Origin Determination of 15q Duplications. Genetic Testing and Molecular Biomarkers. 14(4). 571–576. 8 indexed citations
9.
Kumar, Revati, Jyotsna Sudi, Camille W. Brune, et al.. (2009). A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism. Journal of Medical Genetics. 47(2). 81–90. 39 indexed citations
10.
Gruber, Reut, Ridha Joober, Natalie Grizenko, et al.. (2009). Dopamine Transporter Genotype and Stimulant Side Effect Factors in Youth Diagnosed with Attention-Deficit/Hyperactivity Disorder. Journal of Child and Adolescent Psychopharmacology. 19(3). 233–239. 24 indexed citations
11.
Kumar, Revati, Samer Karamohamed, Jyotsna Sudi, et al.. (2007). Recurrent 16p11.2 microdeletions in autism. Human Molecular Genetics. 17(4). 628–638. 487 indexed citations
12.
Geller, Barbara, Rebecca Tillman, Kristine Bolhofner, Kathleen Hennessy, & Edwin H. Cook. (2007). GAD1 Single Nucleotide Polymorphism Is in Linkage Disequilibrium with a Child Bipolar I Disorder Phenotype. Journal of Child and Adolescent Psychopharmacology. 18(1). 25–29. 20 indexed citations
13.
Hus, Vanessa, Andrew Pickles, Edwin H. Cook, Susan Risi, & Catherine Lord. (2006). Using the ADI-R to increase phenotypic homogeneity in genetic studies of autism. Biological Psychiatry. 1 indexed citations
14.
Berry‐Kravis, Elizabeth, Sandra S. Block, Stephen J. Guter, et al.. (2006). Effect of CX516, an AMPA-Modulating Compound, on Cognition and Behavior in Fragile X Syndrome: AControlled Trial. Journal of Child and Adolescent Psychopharmacology. 16(5). 525–540. 124 indexed citations
15.
Owley, Thomas, Jeff Salt, Stephen J. Guter, et al.. (2006). AProspective, Open-Label Trial of Memantine in the Treatment of Cognitive, Behavioral, and Memory Dysfunction in Pervasive Developmental Disorders. Journal of Child and Adolescent Psychopharmacology. 16(5). 517–524. 88 indexed citations
16.
French, Deborah, Mark R. Wilkinson, Wenjian Yang, et al.. (2005). Global gene expression as a function of germline genetic variation. Human Molecular Genetics. 14(12). 1621–1629. 13 indexed citations
17.
Wagner, Karen Dineen, Edwin H. Cook, Henry Chung, & Michael Messig. (2003). Remission Status After Long-Term Sertraline Treatment of Pediatric Obsessive-Compulsive Disorder. Journal of Child and Adolescent Psychopharmacology. 13(supplement 1). 53–60. 45 indexed citations
18.
Owley, Thomas, et al.. (2002). Case Series: Adderall ® Augmentation of Serotonin Reuptake Inhibitors in Childhood-Onset Obsessive Compulsive Disorder. Journal of Child and Adolescent Psychopharmacology. 12(2). 165–171. 11 indexed citations
19.
20.
Mullé, Jennifer G., et al.. (1993). 3q29 Recurrent Deletion. 4 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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