Gary A. Heiman

7.8k total citations
62 papers, 2.4k citations indexed

About

Gary A. Heiman is a scholar working on Genetics, Clinical Psychology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Gary A. Heiman has authored 62 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 19 papers in Clinical Psychology and 17 papers in Cellular and Molecular Neuroscience. Recurrent topics in Gary A. Heiman's work include Autism Spectrum Disorder Research (16 papers), Obsessive-Compulsive Spectrum Disorders (14 papers) and Neurological disorders and treatments (13 papers). Gary A. Heiman is often cited by papers focused on Autism Spectrum Disorder Research (16 papers), Obsessive-Compulsive Spectrum Disorders (14 papers) and Neurological disorders and treatments (13 papers). Gary A. Heiman collaborates with scholars based in United States, Netherlands and Cyprus. Gary A. Heiman's co-authors include Susan E. Hodge, Susan Bressman, Laurie J. Ozelius, Myrna M. Weissman, Abby J. Fyer, Deborah Raymond, Steven P. Hamilton, James A. Knowles, Prakash Gorroochurn and Rachel Saunders‐Pullman and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Neurology.

In The Last Decade

Gary A. Heiman

62 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gary A. Heiman United States	33	888	868	434	430	381	62	2.4k
Carol Dobson‐Stone Australia	36	725 0.8×	982 1.1×	681 1.6×	428 1.0×	300 0.8×	86	4.2k
Thomas Brücke Austria	35	1.8k 2.0×	1.3k 1.5×	265 0.6×	149 0.3×	453 1.2×	77	3.5k
Virginia L. Willour United States	24	168 0.2×	408 0.5×	346 0.8×	788 1.8×	608 1.6×	45	2.3k
Alain Rougier France	29	899 1.0×	1.1k 1.3×	460 1.1×	95 0.2×	735 1.9×	76	2.7k
Souhel Najjar United States	21	346 0.4×	587 0.7×	140 0.3×	185 0.4×	661 1.7×	37	2.5k
Carlo Cianchetti Italy	26	322 0.4×	466 0.5×	167 0.4×	250 0.6×	698 1.8×	103	2.4k
Linda E. Nee United States	26	836 0.9×	611 0.7×	351 0.8×	226 0.5×	387 1.0×	57	2.7k
Francesca Bisulli Italy	33	670 0.8×	736 0.8×	88 0.2×	593 1.4×	1.6k 4.2×	165	3.1k
Dominique Endres Germany	22	610 0.7×	161 0.2×	420 1.0×	235 0.5×	321 0.8×	126	1.8k
Lan Xiong Canada	24	564 0.6×	139 0.2×	142 0.3×	298 0.7×	340 0.9×	58	1.5k

Countries citing papers authored by Gary A. Heiman

Since Specialization

Citations

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

Fields of papers citing papers by Gary A. Heiman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gary A. Heiman. 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 Gary A. Heiman. The network helps show where Gary A. Heiman may publish in the future.

Co-authorship network of co-authors of Gary A. Heiman

This figure shows the co-authorship network connecting the top 25 collaborators of Gary A. Heiman. A scholar is included among the top collaborators of Gary A. Heiman 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 Gary A. Heiman. Gary A. Heiman 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

Heiman, Gary A., et al.. (2025). Evaluating pregnancy termination rates for fetal chromosome and single gene disorders. Journal of Genetic Counseling. 34(4). e70099–e70099. 1 indexed citations

Nasello, Cara, Junbing Wu, Joshua K. Thackray, et al.. (2024). Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in mice. Proceedings of the National Academy of Sciences. 121(19). e2307156121–e2307156121. 8 indexed citations

Abdulkadir, Mohamed, Jay A. Tischfield, Gary A. Heiman, Pieter J. Hoekstra, & Andrea Dietrich. (2022). Polygenic and environmental determinants of tics in the Avon Longitudinal Study of Parents and Children. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 192(5-6). 73–84. 1 indexed citations

Abdulkadir, Mohamed, Carol A. Mathews, Jeremiah M. Scharf, et al.. (2018). Polygenic Risk Scores Derived From a Tourette Syndrome Genome-wide Association Study Predict Presence of Tics in the Avon Longitudinal Study of Parents and Children Cohort. Biological Psychiatry. 85(4). 298–304. 16 indexed citations

Gorroochurn, Prakash, Susan E. Hodge, Gary A. Heiman, & David A. Greenberg. (2011). An Improved Delta-Centralization Method for Population Stratification. Human Heredity. 71(3). 180–185. 1 indexed citations

Heiman, Gary A., Richard Gill, Sergey Kalachikov, et al.. (2010). Evaluation of depression risk in LGI1 mutation carriers. Epilepsia. 51(9). 1685–1690. 20 indexed citations

Sanokawa‐Akakura, Reiko, Weihuan Cao, Gary A. Heiman, et al.. (2010). Control of Alzheimer's Amyloid Beta Toxicity by the High Molecular Weight Immunophilin FKBP52 and Copper Homeostasis in Drosophila. PLoS ONE. 5(1). e8626–e8626. 53 indexed citations

Choi, Hyunmi, John B. Wong, Anil Mendiratta, Gary A. Heiman, & Marla J. Hamberger. (2010). Numeracy and framing bias in epilepsy. Epilepsy & Behavior. 20(1). 29–33. 10 indexed citations

Bressman, Susan, Deborah Raymond, Tania Fuchs, et al.. (2009). Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study. The Lancet Neurology. 8(5). 441–446. 119 indexed citations

10.

Heiman, Gary A., Robert A. King, & Jay A. Tischfield. (2008). New Jersey Center for Tourette Syndrome Sharing Repository: methods and sample description. BMC Medical Genomics. 1(1). 58–58. 6 indexed citations

11.

Heiman, Gary A., Elizabeth L. Ogburn, Prakash Gorroochurn, Katherine M. Keyes, & Deborah S. Hasin. (2007). Evidence for a two-stage model of dependence using the NESARC and its implications for genetic association studies. Drug and Alcohol Dependence. 92(1-3). 258–266. 29 indexed citations

12.

Heiman, Gary A., Susan E. Hodge, Prakash Gorroochurn, Junying Zhang, & David A. Greenberg. (2004). Effect of Population Stratification on Case-Control Association Studies. Human Heredity. 58(1). 30–39. 38 indexed citations

13.

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

14.

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

15.

Ahsan, Habibul, Susan E. Hodge, Gary A. Heiman, Melissa D. Begg, & Ezra Susser. (2002). Relative risk for genetic associations: the case-parent triad as a variant of case-cohort design. International Journal of Epidemiology. 31(3). 669–678. 9 indexed citations

16.

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

17.

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

18.

Nygaard, Torbjoern G., Deborah Raymond, Caiping Chen, et al.. (1999). Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31. Annals of Neurology. 46(5). 794–798. 71 indexed citations

19.

Bressman, Susan, Ann Hunt, Gary A. Heiman, et al.. (1994). Exclusion of the DYT1 locus in a non‐Jewish family with early‐onset dystonia. Movement Disorders. 9(6). 626–632. 29 indexed citations

20.

Nygaard, Torbjoern G., Hirohide Takahashi, Gary A. Heiman, et al.. (1992). Long‐term treatment response and fluorodopa positron emission tomographic scanning of parkinsonism in a family with dopa‐responsive dystonia. Annals of Neurology. 32(5). 603–608. 73 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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