Steven P. Hamilton

17.9k total citations
78 papers, 3.6k citations indexed

About

Steven P. Hamilton is a scholar working on Genetics, Psychiatry and Mental health and Clinical Psychology. According to data from OpenAlex, Steven P. Hamilton has authored 78 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 19 papers in Psychiatry and Mental health and 18 papers in Clinical Psychology. Recurrent topics in Steven P. Hamilton's work include Child and Adolescent Psychosocial and Emotional Development (15 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Treatment of Major Depression (12 papers). Steven P. Hamilton is often cited by papers focused on Child and Adolescent Psychosocial and Emotional Development (15 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Treatment of Major Depression (12 papers). Steven P. Hamilton collaborates with scholars based in United States, Canada and United Kingdom. Steven P. Hamilton's co-authors include Susan L. Slager, Renée D. Goodwin, Patrick J. McGrath, Jeffrey Kraft, Eric Peters, James A. Knowles, Myrna M. Weissman, Stanley I. Shyn, Megan S. Reinalda and Gary A. Heiman and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neuron and PLoS ONE.

In The Last Decade

Steven P. Hamilton

75 papers receiving 3.5k citations

Peers

Steven P. Hamilton

GENET

CMN

PMH

Laura Mandelli Italy

Joseph F. Cubells United States

Peter Zill Germany

Lourdes Fañanás Spain

Yung‐yu Huang United States

Jens R. Wendland United States

Rael D. Strous Israel

Stephen Kanes United States

Susanne Lucae Germany

Ina Giegling Germany

Laura Mandelli Italy

Steven P. Hamilton

586 ×0.7

456 ×0.6

GENET

645 ×0.9

CMN

1.5k ×2.0

1.5k ×2.2

PMH

Citations per year, relative to Steven P. Hamilton Steven P. Hamilton (= 1×) peers Laura Mandelli

Countries citing papers authored by Steven P. Hamilton

Since Specialization

Citations

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

Fields of papers citing papers by Steven P. Hamilton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Steven P. Hamilton. 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 Steven P. Hamilton. The network helps show where Steven P. Hamilton may publish in the future.

Co-authorship network of co-authors of Steven P. Hamilton

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Stanco, Amelia, Ramón Pla, Daniel Vogt, et al.. (2014). NPAS1 Represses the Generation of Specific Subtypes of Cortical Interneurons. Neuron. 84(5). 940–953. 56 indexed citations

Yang, Xiaoyong, Ernest T. Lam, Jeremy S. Rabinowitz, et al.. (2013). A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation. Translational Psychiatry. 3(9). e301–e301. 32 indexed citations

Talati, Ardesheer, et al.. (2013). Genotyping serotonin transporter polymorphisms 5-HTTLPR and rs25531 in European- and African-American subjects from the National Institute of Mental Health’s Collaborative Center for Genomic Studies. Translational Psychiatry. 3(9). e307–e307. 49 indexed citations

Hamilton, Steven P.. (2011). A New Lead From Genetic Studies in Depressed Siblings: Assessing Studies of Chromosome 3. American Journal of Psychiatry. 168(8). 783–789. 17 indexed citations

Garriock, Holly A., Michael Tanowitz, Jeffrey Kraft, et al.. (2010). Association of Mu-Opioid Receptor Variants and Response to Citalopram Treatment in Major Depressive Disorder. American Journal of Psychiatry. 167(5). 565–573. 54 indexed citations

Huang, Jie, Roy H. Perlis, Sang Hyuck Lee, et al.. (2010). Cross-Disorder Genomewide Analysis of Schizophrenia, Bipolar Disorder, and Depression. American Journal of Psychiatry. 167(10). 1254–1263. 148 indexed citations

Seddon, Jennifer M., et al.. (2010). Phylogenetics of the pademelons (Macropodidae: Thylogale) and historical biogeography of the Australo-Papuan region. Molecular Phylogenetics and Evolution. 57(3). 1134–1148. 38 indexed citations

Peters, Eric, Victor I. Reus, & Steven P. Hamilton. (2009). The ABCB1 transporter gene and antidepressant response. F1000 Biology Reports. 1. 23–23. 7 indexed citations

Garriock, Holly A. & Steven P. Hamilton. (2009). Genetic Studies of Drug Response and Side Effects in the STAR*D Study, Part 1. The Journal of Clinical Psychiatry. 70(8). 1186–1187. 7 indexed citations

10.

Garriock, Holly A. & Steven P. Hamilton. (2009). Genetic Studies of Drug Response and Side Effects in the STAR*D Study, Part 2. The Journal of Clinical Psychiatry. 70(9). 1323–1325. 3 indexed citations

11.

Peters, Eric, Susan L. Slager, G. Douglas Jenkins, et al.. (2008). Resequencing of serotonin-related genes and association of tagging SNPs to citalopram response. Pharmacogenetics and Genomics. 19(1). 1–10. 68 indexed citations

12.

Hodges, Laura M., Myrna M. Weissman, Fatemeh Haghighi, et al.. (2008). Association and linkage analysis of candidate genes GRP, GRPR, CRHR1, and TACR1 in panic disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(1). 65–73. 19 indexed citations

13.

Kraft, Jeffrey, Eric Peters, Susan L. Slager, et al.. (2006). Analysis of Association Between the Serotonin Transporter and Antidepressant Response in a Large Clinical Sample. Biological Psychiatry. 61(6). 734–742. 113 indexed citations

14.

Goodwin, Renée D. & Steven P. Hamilton. (2003). Lifetime comorbidity of antisocial personality disorder and anxiety disorders among adults in the community. Psychiatry Research. 117(2). 159–166. 136 indexed citations

15.

Hamilton, Steven P., Susan L. Slager, Ada Baisre, et al.. (2003). Evidence for Genetic Linkage Between a Polymorphism in the Adenosine 2A Receptor and Panic Disorder. Neuropsychopharmacology. 29(3). 558–565. 110 indexed citations

16.

Hamilton, Steven P., Susan L. Slager, David J. Mayo, et al.. (2003). Investigation of polymorphisms in the CREM gene in panic disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 126B(1). 111–115. 13 indexed citations

17.

Goodwin, Renée D. & Steven P. Hamilton. (2002). Cigarette Smoking and Panic: The Role of Neuroticism. American Journal of Psychiatry. 159(7). 1208–1213. 75 indexed citations

18.

Hamilton, Steven P., Susan L. Slager, Gary A. Heiman, et al.. (2002). Evidence for a susceptibility locus for panic disorder near the catechol-O-methyltransferase gene on chromosome 22. Biological Psychiatry. 51(7). 591–601. 98 indexed citations

19.

Hamilton, Steven P., Gary A. Heiman, Fatemeh Haghighi, et al.. (1999). Lack of genetic linkage or association between a functional serotonin transporter polymorphism and panic disorder. Psychiatric Genetics. 9(1). 1–6. 55 indexed citations

20.

Rome, Leonard H., et al.. (1990). Matrix Interactions Regulating Myelinogenesis in Cultured Oligodendrocytes. Advances in experimental medicine and biology. 265. 157–167. 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.

Explore authors with similar magnitude of impact