Diana Chase

2.5k total citations
28 papers, 1.1k citations indexed

About

Diana Chase is a scholar working on Psychiatry and Mental health, Pediatrics, Perinatology and Child Health and Cellular and Molecular Neuroscience. According to data from OpenAlex, Diana Chase has authored 28 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Psychiatry and Mental health, 5 papers in Pediatrics, Perinatology and Child Health and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Diana Chase's work include Growth Hormone and Insulin-like Growth Factors (4 papers), Stress Responses and Cortisol (3 papers) and Cardiac pacing and defibrillation studies (2 papers). Diana Chase is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (4 papers), Stress Responses and Cortisol (3 papers) and Cardiac pacing and defibrillation studies (2 papers). Diana Chase collaborates with scholars based in United Kingdom, Hungary and United States. Diana Chase's co-authors include Gabriella Juhász, J.F.W. Deakin, Ian Anderson, Darragh Downey, Zoltán Tóth, Rebecca Elliott, Ruairidh Milne, Krisztina Mekli, Antony Payton and Hazel Platt and has published in prestigious journals such as Nature Genetics, Biological Psychiatry and The British Journal of Psychiatry.

In The Last Decade

Diana Chase

28 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Diana Chase United Kingdom 16 219 201 165 156 148 28 1.1k
Aryeh I. Herman United States 22 551 2.5× 167 0.8× 169 1.0× 384 2.5× 214 1.4× 35 1.4k
Nicholas Graham United Kingdom 19 210 1.0× 225 1.1× 205 1.2× 76 0.5× 79 0.5× 28 1.7k
Henriette N. Buttenschøn Denmark 19 217 1.0× 156 0.8× 146 0.9× 156 1.0× 92 0.6× 42 1.1k
Jun Sung Koh South Korea 19 169 0.8× 143 0.7× 79 0.5× 180 1.2× 64 0.4× 70 1.2k
Jinguo Zhai China 19 160 0.7× 154 0.8× 121 0.7× 84 0.5× 63 0.4× 55 971
Sarah Cohen‐Woods Australia 24 259 1.2× 283 1.4× 334 2.0× 142 0.9× 68 0.5× 55 1.5k
Susanne Höfels Germany 17 331 1.5× 400 2.0× 153 0.9× 384 2.5× 84 0.6× 22 1.7k
Eric Peters United States 18 335 1.5× 229 1.1× 262 1.6× 332 2.1× 367 2.5× 39 1.5k
Amy Ferguson United Kingdom 16 113 0.5× 181 0.9× 124 0.8× 68 0.4× 87 0.6× 25 919
Marike Polak Netherlands 14 103 0.5× 129 0.6× 287 1.7× 201 1.3× 76 0.5× 41 1.1k

Countries citing papers authored by Diana Chase

Since Specialization
Citations

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

Fields of papers citing papers by Diana Chase

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Diana Chase

This figure shows the co-authorship network connecting the top 25 collaborators of Diana Chase. A scholar is included among the top collaborators of Diana Chase 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 Diana Chase. Diana Chase 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.
Pap, Dorottya, Xénia Gonda, Eszter Molnár, et al.. (2012). Genetic variants in the catechol‐o‐methyltransferase gene are associated with impulsivity and executive function: Relevance for major depression. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 159B(8). 928–940. 15 indexed citations
2.
Anderson, Ian, Gabriella Juhász, Diana Chase, et al.. (2011). State-dependent alteration in face emotion recognition in depression. The British Journal of Psychiatry. 198(4). 302–308. 101 indexed citations
3.
Juhász, Gabriella, Jason S. Dunham, Shane McKie, et al.. (2011). The CREB1-BDNF-NTRK2 Pathway in Depression: Multiple Gene-Cognition-Environment Interactions. Biological Psychiatry. 69(8). 762–771. 136 indexed citations
4.
Hoyle, David C., Gabriella Juhász, Ester Aso, et al.. (2010). Shared changes in gene expression in frontal cortex of four genetically modified mouse models of depression. European Neuropsychopharmacology. 21(1). 3–10. 13 indexed citations
5.
Bagdy, György, Pál Riba, Valéria Kecskeméti, Diana Chase, & Gabriella Juhász. (2010). Headache‐type adverse effects of NO donors: vasodilation and beyond. British Journal of Pharmacology. 160(1). 20–35. 39 indexed citations
6.
Juhász, Gabriella, Diana Chase, Darragh Downey, et al.. (2009). CNR1 Gene is Associated with High Neuroticism and Low Agreeableness and Interacts with Recent Negative Life Events to Predict Current Depressive Symptoms. Neuropsychopharmacology. 34(8). 2019–2027. 136 indexed citations
7.
Juhász, Gabriella, Judit Lazáry, Diana Chase, et al.. (2009). Variations in the cannabinoid receptor 1 gene predispose to migraine. Neuroscience Letters. 461(2). 116–120. 49 indexed citations
8.
Juhász, Gabriella, Darragh Downey, Neal Hinvest, et al.. (2009). Risk-Taking Behavior in a Gambling Task Associated with Variations in the Tryptophan Hydroxylase 2 Gene: Relevance to Psychiatric Disorders. Neuropsychopharmacology. 35(5). 1109–1119. 29 indexed citations
9.
Benkő, Anita, Judit Lazáry, Eszter Molnár, et al.. (2009). Significant association between the C(−1019)G functional polymorphism of the HTR1A gene and impulsivity. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(2). 592–599. 55 indexed citations
10.
Chase, Diana, et al.. (2008). Is there unmet need for implantable cardioverter defibrillators? Findings from a post-mortem series of sudden cardiac death. EP Europace. 10(6). 741–746. 7 indexed citations
11.
Chase, Diana, et al.. (2006). Case series of sudden cardiac death. ePrints Soton (University of Southampton). 2 indexed citations
12.
13.
Butcher, Lee M, et al.. (2002). MSX1 and high cognitive ability. American Journal of Medical Genetics Part A. 114(7). 1 indexed citations
14.
Bryant, J, Emma Loveman, C Cave, Diana Chase, & Ruairidh Milne. (2002). Endocrinology trial design: adverse event reporting in randomised controlled trials of recombinant human GH in GH-deficient adults. Journal of Endocrinology. 175(2). 545–552. 12 indexed citations
15.
Relton, Caroline L., et al.. (2002). Polymorphisms of the DNA repair gene XRCC1 and the frequency of somatic mutations at the glycophorin A locus in newborns. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 502(1-2). 61–68. 20 indexed citations
16.
Bryant, J, Emma Loveman, Diana Chase, et al.. (2002). The clinical effectiveness and cost effectiveness of the use of human growth hormones in adults. Health Technology Assessment. 6(19). 7 indexed citations
17.
Healey, Catherine S., Alison M. Dunning, M. Dawn Teare, et al.. (2000). A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability. Nature Genetics. 26(3). 362–364. 135 indexed citations
18.
Chase, Diana, et al.. (1999). rhDNase therapy for the treatment of cystic fibrosis patients with mild to moderate lung disease. Journal of Clinical Pharmacy and Therapeutics. 24(6). 415–426. 17 indexed citations
19.
Leatherman, Sheila & Diana Chase. (1994). Using report cards to grade health plan quality.. PubMed. 4(1). 32–40. 5 indexed citations
20.
Chase, Diana, et al.. (1986). Genetics of Hunter Syndrome: carrier detection, new mutations, segregation and linkage analysis. Annals of Human Genetics. 50(4). 349–360. 19 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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