Stephen J. Glatt

41.7k total citations
156 papers, 7.1k citations indexed

About

Stephen J. Glatt is a scholar working on Genetics, Psychiatry and Mental health and Molecular Biology. According to data from OpenAlex, Stephen J. Glatt has authored 156 papers receiving a total of 7.1k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Genetics, 52 papers in Psychiatry and Mental health and 41 papers in Molecular Biology. Recurrent topics in Stephen J. Glatt's work include Genetic Associations and Epidemiology (47 papers), Genetics and Neurodevelopmental Disorders (24 papers) and Attention Deficit Hyperactivity Disorder (21 papers). Stephen J. Glatt is often cited by papers focused on Genetic Associations and Epidemiology (47 papers), Genetics and Neurodevelopmental Disorders (24 papers) and Attention Deficit Hyperactivity Disorder (21 papers). Stephen J. Glatt collaborates with scholars based in United States, Japan and Australia. Stephen J. Glatt's co-authors include Stephen V. Faraone, Ming T. Tsuang, Denise Jackson, Daniel S. Tylee, Jessica Lasky‐Su, Ian Everall, Hamid M. Abdolmaleky, Rahim Shafa, Carlos A. Bolaños and Cassandra L. Smith and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Psychological Bulletin.

In The Last Decade

Stephen J. Glatt

153 papers receiving 6.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stephen J. Glatt United States	45	2.4k	2.2k	2.0k	1.4k	1.1k	156	7.1k
Gerome Breen United Kingdom	50	1.7k 0.7×	2.3k 1.0×	2.4k 1.2×	1.1k 0.8×	1.2k 1.1×	280	8.6k
John R. Kelsoe United States	47	2.7k 1.1×	1.8k 0.8×	2.0k 1.0×	1.5k 1.0×	1.3k 1.2×	167	8.1k
Ryota Hashimoto Japan	52	2.5k 1.0×	3.2k 1.5×	1.9k 1.0×	2.1k 1.5×	2.6k 2.3×	314	10.0k
James B. Potash United States	46	1.9k 0.8×	3.5k 1.6×	2.3k 1.2×	721 0.5×	719 0.6×	136	8.4k
Erik G. Jönsson Sweden	42	2.2k 0.9×	1.4k 0.6×	1.1k 0.5×	1.3k 0.9×	1.9k 1.6×	180	6.3k
Francis J. McMahon United States	54	3.4k 1.4×	2.4k 1.1×	3.1k 1.6×	790 0.5×	1.4k 1.3×	188	9.1k
Vishwajit L. Nimgaonkar United States	48	2.2k 0.9×	1.8k 0.9×	1.6k 0.8×	1.1k 0.7×	1.1k 1.0×	238	6.9k
Lourdes Fañanás Spain	41	1.7k 0.7×	979 0.5×	1.1k 0.6×	965 0.7×	928 0.8×	192	5.4k
Bart P. F. Rutten Netherlands	48	1.9k 0.8×	2.7k 1.3×	1.1k 0.6×	875 0.6×	1.2k 1.1×	243	9.3k
Marco P. Boks Netherlands	49	2.2k 0.9×	2.1k 1.0×	1.0k 0.5×	1.8k 1.3×	591 0.5×	204	8.4k

Countries citing papers authored by Stephen J. Glatt

Since Specialization

Citations

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

Fields of papers citing papers by Stephen J. Glatt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephen J. Glatt. 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 Stephen J. Glatt. The network helps show where Stephen J. Glatt may publish in the future.

Co-authorship network of co-authors of Stephen J. Glatt

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

All Works

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20 of 20 papers shown

Fennema‐Notestine, Christine, et al.. (2025). Neuroimaging Predictors of Cognitive Resilience against Alzheimer's Disease Pathology. Annals of Neurology. 97(6). 1038–1050. 1 indexed citations

Gillespie, Nathan A., Randy Notestine, Anthony Gamst, et al.. (2024). The genetic and environmental etiology of novel frequency‐driven regional parcellations of abnormal white matter. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 198(1). e33004–e33004. 1 indexed citations

Glatt, Stephen J., et al.. (2024). Inconsistent Methods Used to Set Airway Pressure Release Ventilation in Acute Respiratory Distress Syndrome: A Systematic Review and Meta-Regression Analysis. Journal of Clinical Medicine. 13(9). 2690–2690. 2 indexed citations

Mazza, Tommaso, Jonathan Hess, Steven D. Blatt, et al.. (2023). Novel genome‐wide associations for effort valuation and psychopathology in children and adults. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 195(4). e32964–e32964. 2 indexed citations

Hess, Jonathan, Manuel Mattheisen, Tiffany A. Greenwood, et al.. (2023). A polygenic resilience score moderates the genetic risk for schizophrenia: Replication in 18,090 cases and 28,114 controls from the Psychiatric Genomics Consortium. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 195(2). e32957–e32957. 5 indexed citations

Glatt, Stephen J., et al.. (2022). Bipolar Disorder, Religion, and Spirituality: A Scoping Review. Journal of Religion and Health. 61(5). 3589–3614. 9 indexed citations

Rees, Elliott, Hugo Creeth, Hai‐Gwo Hwu, et al.. (2021). Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations. Nature Communications. 12(1). 5353–5353. 50 indexed citations

Hess, Jonathan, et al.. (2020). Autophagy, apoptosis, and neurodevelopmental genes might underlie selective brain region vulnerability in attention-deficit/hyperactivity disorder. Molecular Psychiatry. 26(11). 6643–6654. 22 indexed citations

Tylee, Daniel S., Jonathan Hess, Thomas P. Quinn, et al.. (2016). Blood transcriptomic comparison of individuals with and without autism spectrum disorder: A combined‐samples mega‐analysis. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 174(3). 181–201. 37 indexed citations

10.

Hess, Jonathan, et al.. (2015). The influence of genes on “positive valence systems” constructs: A systematic review. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 171(1). 92–110. 12 indexed citations

11.

Glatt, Stephen J., et al.. (2014). GRIK4 Polymorphism and its Association with Antidepressant Response in Depressed Patients: A Meta-Analysis. Pharmacogenomics. 15(11). 1451–1459. 19 indexed citations

12.

Glatt, Stephen J., Sharon D. Chandler, Caroline M. Nievergelt, et al.. (2013). Blood‐based gene‐expression predictors of PTSD risk and resilience among deployed marines: A pilot study. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(4). 313–326. 61 indexed citations

13.

Bulayeva, Kazima, Todd Lencz, Stephen J. Glatt, et al.. (2012). [Mapping genes related to early onset major depressive disorder in Dagestan genetic isolates].. PubMed. 23(3). 161–70. 7 indexed citations

14.

Faraone, Stephen V. & Stephen J. Glatt. (2009). A Comparison of the Efficacy of Medications for Adult Attention-Deficit/Hyperactivity Disorder Using Meta-Analysis of Effect Sizes. The Journal of Clinical Psychiatry. 71(6). 754–763. 279 indexed citations

15.

Glatt, Stephen J., et al.. (2008). The tryptophan hydroxylase gene influences risk for bipolar disorder but not major depressive disorder: results of meta‐analyses. Bipolar Disorders. 10(7). 816–821. 21 indexed citations

16.

Abdolmaleky, Hamid M., Kuang‐Hung Cheng, Stephen V. Faraone, et al.. (2006). Hypomethylation of MB-COMT promoter is a major risk factor for schizophrenia and bipolar disorder. Human Molecular Genetics. 15(21). 3132–3145. 346 indexed citations

17.

Faraone, Stephen V., Jessica Lasky‐Su, Stephen J. Glatt, Paul Van Eerdewegh, & Ming T. Tsuang. (2006). Early onset bipolar disorder: possible linkage to chromosome 9q34. Bipolar Disorders. 8(2). 144–151. 31 indexed citations

18.

Seidman, Larry J., Anthony J. Giuliano, Clyde W. Smith, et al.. (2005). Neuropsychological Functioning in Adolescents and Young Adults at Genetic Risk for Schizophrenia and Affective Psychoses: Results from the Harvard and Hillside Adolescent High Risk Studies. Schizophrenia Bulletin. 32(3). 507–524. 120 indexed citations

19.

Tsuang, Ming T., et al.. (2005). Assessing the validity of blood‐based gene expression profiles for the classification of schizophrenia and bipolar disorder: A preliminary report. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 133B(1). 1–5. 173 indexed citations

20.

Glatt, Stephen J., Carlos A. Bolaños, George H. Trksak, & Denise Jackson. (2000). Effects of prenatal cocaine exposure on dopamine system development: a meta-analysis. Neurotoxicology and Teratology. 22(5). 617–629. 50 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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