D Gonen

872 total citations
9 papers, 658 citations indexed

About

D Gonen is a scholar working on Cognitive Neuroscience, Genetics and Molecular Biology. According to data from OpenAlex, D Gonen has authored 9 papers receiving a total of 658 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Cognitive Neuroscience, 4 papers in Genetics and 3 papers in Molecular Biology. Recurrent topics in D Gonen's work include Autism Spectrum Disorder Research (5 papers), Obsessive-Compulsive Spectrum Disorders (2 papers) and Receptor Mechanisms and Signaling (2 papers). D Gonen is often cited by papers focused on Autism Spectrum Disorder Research (5 papers), Obsessive-Compulsive Spectrum Disorders (2 papers) and Receptor Mechanisms and Signaling (2 papers). D Gonen collaborates with scholars based in United States. D Gonen's co-authors include Bennett Leventhal, Edwin H. Cook, Jeremy Veenstra‐VanderWeele, Catherine Lord, Eric Courchesne, Nancy J. Cox, Richard Haas, Stephen J. Guter, Alan J. Lincoln and Thomas R. Insel and has published in prestigious journals such as Science, The American Journal of Human Genetics and Molecular Psychiatry.

In The Last Decade

D Gonen

9 papers receiving 626 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
D Gonen United States	8	375	358	167	160	111	9	658
Ohiko Hashimoto Japan	12	261 0.7×	229 0.6×	159 1.0×	158 1.0×	97 0.9×	28	659
Rhinda Goedken United States	10	170 0.5×	272 0.8×	134 0.8×	144 0.9×	67 0.6×	15	536
Shinko Koishi Japan	9	152 0.4×	156 0.4×	132 0.8×	109 0.7×	53 0.5×	12	395
A. Ting Wang United States	11	634 1.7×	565 1.6×	225 1.3×	293 1.8×	161 1.5×	14	1.1k
Loyse Hippolyte Switzerland	17	683 1.8×	320 0.9×	94 0.6×	150 0.9×	197 1.8×	22	939
Dionisio A. Amodeo United States	14	346 0.9×	191 0.5×	134 0.8×	159 1.0×	71 0.6×	24	627
Johann du Hoffmann United States	10	261 0.7×	156 0.4×	123 0.7×	193 1.2×	56 0.5×	13	519
Danielle Halpern United States	15	617 1.6×	618 1.7×	237 1.4×	350 2.2×	173 1.6×	30	1.2k
Danielle N. Abrams United States	6	431 1.1×	248 0.7×	88 0.5×	132 0.8×	39 0.4×	6	572
Suping Wu China	6	166 0.4×	183 0.5×	340 2.0×	129 0.8×	112 1.0×	9	599

Countries citing papers authored by D Gonen

Since Specialization

Citations

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

Fields of papers citing papers by D Gonen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of D Gonen

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

All Works

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9 of 9 papers shown

1.

Andrews, Lori B., David A. Stoney, R. E. Gaensslen, et al.. (2004). Constructing Ethical Guidelines for Biohistory. Science. 304(5668). 215–216. 6 indexed citations

2.

Young, Larry J., D Gonen, Jeremy Veenstra‐VanderWeele, et al.. (2002). Transmission disequilibrium testing of arginine vasopressin receptor 1A (AVPR1A) polymorphisms in autism. Molecular Psychiatry. 7(5). 503–507. 201 indexed citations

3.

Devlin, Bernie, Edwin H. Cook, Géraldine Dawson, et al.. (2002). No evidence for linkage of liability to autism toHOXA1in a sample from the CPEA network. American Journal of Medical Genetics. 114(6). 667–672. 21 indexed citations

4.

Veenstra‐VanderWeele, Jeremy, et al.. (2001). Genomic organization of the SLC1A1/EAAC1 gene and mutation screening in early-onset obsessive-compulsive disorder. Molecular Psychiatry. 6(2). 160–167. 55 indexed citations

5.

Veenstra‐VanderWeele, Jeremy, et al.. (2000). Mutation screening of human 5-HT2Breceptor gene in early-onset obsessive-compulsive disorder. Molecular and Cellular Probes. 14(1). 47–52. 22 indexed citations

6.

Gonen, D, et al.. (2000). Deletion polymorphism in the coding region of the human NESP55 alternative transcript of GNAS1. Molecular and Cellular Probes. 14(3). 191–194. 10 indexed citations

7.

Veenstra‐VanderWeele, Jeremy, et al.. (1999). Mutation screening of the UBE3A /E6-AP gene in autistic disorder. Molecular Psychiatry. 4(1). 64–67. 40 indexed citations

8.

Gonen, D, Jeremy Veenstra‐VanderWeele, Zhi-Yong Yang, Bennett Leventhal, & Edwin H. Cook. (1999). High throughput fluorescent CE-SSCP SNP genotyping. Molecular Psychiatry. 4(4). 339–343. 19 indexed citations

9.

Cook, Edwin H., Nancy J. Cox, Catherine Lord, et al.. (1998). Linkage-Disequilibrium Mapping of Autistic Disorder, with 15q11-13 Markers. The American Journal of Human Genetics. 62(5). 1077–1083. 284 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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