Joseph F. Cubells

9.3k total citations
109 papers, 5.4k citations indexed

About

Joseph F. Cubells is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Genetics. According to data from OpenAlex, Joseph F. Cubells has authored 109 papers receiving a total of 5.4k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Cellular and Molecular Neuroscience, 32 papers in Molecular Biology and 27 papers in Genetics. Recurrent topics in Joseph F. Cubells's work include Neurotransmitter Receptor Influence on Behavior (29 papers), Autism Spectrum Disorder Research (16 papers) and Genetics and Neurodevelopmental Disorders (16 papers). Joseph F. Cubells is often cited by papers focused on Neurotransmitter Receptor Influence on Behavior (29 papers), Autism Spectrum Disorder Research (16 papers) and Genetics and Neurodevelopmental Disorders (16 papers). Joseph F. Cubells collaborates with scholars based in United States, Germany and Japan. Joseph F. Cubells's co-authors include Joel Gelernter, Henry R. Kranzler, Yi‐lang Tang, Charles F. Gillespie, Kerry J. Ressler, Alicia K. Smith, Karen N. Conneely, Bekh Bradley, Cyrus P. Zabetian and Elisabeth B. Binder and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Joseph F. Cubells

105 papers receiving 5.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joseph F. Cubells United States 38 1.3k 1.3k 1.2k 827 800 109 5.4k
Peter Zill Germany 39 1.8k 1.3× 1.2k 0.9× 944 0.8× 1.0k 1.3× 606 0.8× 131 5.1k
Helen Fox United Kingdom 43 1.7k 1.2× 665 0.5× 1.2k 1.0× 595 0.7× 411 0.5× 112 6.1k
Sue Z. Sabol United States 7 2.3k 1.7× 1.2k 1.0× 1.5k 1.2× 946 1.1× 614 0.8× 7 5.3k
Mary‐Anne Enoch United States 37 1.3k 1.0× 849 0.7× 931 0.8× 361 0.4× 440 0.6× 60 4.3k
Jerzy Samochowiec Poland 36 1.3k 0.9× 1.3k 1.0× 870 0.7× 1.3k 1.6× 422 0.5× 321 5.4k
Ina Giegling Germany 39 1.1k 0.9× 1.3k 1.0× 1.2k 1.0× 1.2k 1.4× 724 0.9× 133 5.0k
Brigitta Bondy Germany 45 2.3k 1.7× 1.5k 1.2× 960 0.8× 1.5k 1.9× 517 0.6× 160 6.1k
Ru‐Band Lu Taiwan 37 942 0.7× 977 0.8× 594 0.5× 1.1k 1.3× 593 0.7× 146 5.2k
David A. Nielsen United States 43 2.2k 1.7× 2.4k 1.9× 814 0.7× 670 0.8× 829 1.0× 118 6.4k
Bao‐Zhu Yang United States 33 902 0.7× 842 0.7× 1.1k 0.9× 295 0.4× 655 0.8× 68 3.6k

Countries citing papers authored by Joseph F. Cubells

Since Specialization
Citations

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

Fields of papers citing papers by Joseph F. Cubells

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joseph F. Cubells

This figure shows the co-authorship network connecting the top 25 collaborators of Joseph F. Cubells. A scholar is included among the top collaborators of Joseph F. Cubells 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 Joseph F. Cubells. Joseph F. Cubells 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.
2.
Ousley, Opal, et al.. (2024). Reduced amplitude and slowed latency of the acoustic startle response in adolescents and adults with 22q11.2 deletion syndrome. Schizophrenia Research. 269. 9–17. 1 indexed citations
3.
Duan, Kuaikuai, Adam Goldman-Yassen, Derek M. Novacek, et al.. (2024). Beyond IQ: executive function deficits and their relation to functional, clinical, and neuroimaging outcomes in 3q29 deletion syndrome. Psychological Medicine. 54(14). 3876–3887.
4.
Andari, Elissar, Shota Nishitani, Michael J. Morrier, et al.. (2020). Epigenetic modification of the oxytocin receptor gene: implications for autism symptom severity and brain functional connectivity. Neuropsychopharmacology. 45(7). 1150–1158. 64 indexed citations
5.
Ousley, Opal, Samuel Fernàndez‐Carriba, Erica Smearman, et al.. (2017). Examining the Overlap between Autism Spectrum Disorder and 22q11.2 Deletion Syndrome. International Journal of Molecular Sciences. 18(5). 1071–1071. 33 indexed citations
6.
Gillespie, Charles F., Lynn M. Almli, Alicia K. Smith, et al.. (2013). Sex dependent influence of a functional polymorphism in steroid 5‐α‐reductase type 2 (SRD5A2) on post‐traumatic stress symptoms. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(3). 283–292. 31 indexed citations
7.
Schroeder, James W., Alicia K. Smith, Patricia A. Brennan, et al.. (2012). DNA methylation in neonates born to women receiving psychiatric care. Epigenetics. 7(4). 409–414. 53 indexed citations
8.
Dunlop, Boadie W., Elisabeth B. Binder, Joseph F. Cubells, et al.. (2012). Predictors of remission in depression to individual and combined treatments (PReDICT): study protocol for a randomized controlled trial. Trials. 13(1). 106–106. 88 indexed citations
9.
Hunter, Jessica Ezzell, Mary Leslie, Debra Hamilton, et al.. (2012). Depression and anxiety symptoms among women who carry the FMR1 premutation: Impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 159B(5). 549–559. 32 indexed citations
10.
Tang, Yi‐lang, et al.. (2011). Validation of the Autism Spectrum Screening Questionnaire, Mandarin Chinese Version (CH-ASSQ) in Beijing, China. Autism. 15(6). 713–727. 26 indexed citations
11.
Ji, Ning, Lan Shuai, Yun Chen, et al.. (2011). Dopamine β‐hydroxylase gene associates with stroop color‐word task performance in Han Chinese children with attention deficit/hyperactivity disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(6). 730–736. 14 indexed citations
12.
Binder, Elisabeth B., D. Jeffrey Newport, Alicia K. Smith, et al.. (2010). A serotonin transporter gene polymorphism predicts peripartum depressive symptoms in an at-risk psychiatric cohort. Journal of Psychiatric Research. 44(10). 640–646. 51 indexed citations
13.
Niciu, Mark J., Grace Chan, Joel Gelernter, et al.. (2009). Subtypes of major depression in substance dependence. Addiction. 104(10). 1700–1709. 21 indexed citations
14.
Gillespie, Charles F., Bekh Bradley, Alicia K. Smith, et al.. (2009). Trauma exposure and stress-related disorders in inner city primary care patients. General Hospital Psychiatry. 31(6). 505–514. 396 indexed citations
15.
Bradley, Rebekah, Elisabeth B. Binder, Michael P. Epstein, et al.. (2008). Influence of Child Abuse on Adult Depression. Archives of General Psychiatry. 65(2). 190–190. 487 indexed citations
16.
Ousley, Opal, et al.. (2007). A review of neurocognitive and behavioral profiles associated with 22q11 deletion syndrome: Implications for clinical evaluation and treatment. Current Psychiatry Reports. 9(2). 148–158. 39 indexed citations
17.
Tang, Yi‐lang, et al.. (2006). Opiate addiction in China: current situation and treatments. Addiction. 101(5). 657–665. 117 indexed citations
18.
Cho, Sonhae, Chun‐Hyung Kim, Joseph F. Cubells, et al.. (2003). Variations in the dopamine β‐hydroxylase gene are not associated with the autonomic disorders, pure autonomic failure, or multiple system atrophy. American Journal of Medical Genetics Part A. 120A(2). 234–236. 10 indexed citations
19.
Kim, Chun‐Hyung, Heesun Kim, Joseph F. Cubells, & Kwangsoo Kim. (1999). A Previously Undescribed Intron and Extensive 5′ Upstream Sequence, but Not Phox2a-mediated Transactivation, Are Necessary for High Level Cell Type-specific Expression of the Human Norepinephrine Transporter Gene. Journal of Biological Chemistry. 274(10). 6507–6518. 109 indexed citations
20.

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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