Gina Kang

466 total citations
14 papers, 281 citations indexed

About

Gina Kang is a scholar working on Molecular Biology, Cognitive Neuroscience and Genetics. According to data from OpenAlex, Gina Kang has authored 14 papers receiving a total of 281 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Cognitive Neuroscience and 5 papers in Genetics. Recurrent topics in Gina Kang's work include Congenital heart defects research (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Autism Spectrum Disorder Research (5 papers). Gina Kang is often cited by papers focused on Congenital heart defects research (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Autism Spectrum Disorder Research (5 papers). Gina Kang collaborates with scholars based in United States, Japan and Canada. Gina Kang's co-authors include Noboru Hiroi, Takeshi Hiramoto, Go Suzuki, Yasuhiro Watanabe, Raju Kucherlapati, Yasushi Satoh, Kenji Tanigaki, Takeshi Izumi, William S. Trimble and Kathryn M. Harper and has published in prestigious journals such as Biological Psychiatry, Human Molecular Genetics and Molecular Psychiatry.

In The Last Decade

Gina Kang

13 papers receiving 269 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gina Kang United States	8	152	114	83	45	35	14	281
Yohan Yee Canada	10	127 0.8×	85 0.7×	129 1.6×	53 1.2×	24 0.7×	17	415
Masako Taniike Japan	6	94 0.6×	43 0.4×	36 0.4×	102 2.3×	33 0.9×	13	295
Tsukasa Sasaki Japan	9	168 1.1×	160 1.4×	35 0.4×	42 0.9×	68 1.9×	19	469
Jasmin Roohi United States	9	93 0.6×	158 1.4×	239 2.9×	17 0.4×	16 0.5×	10	391
Ismo Makkonen Finland	7	113 0.7×	219 1.9×	232 2.8×	26 0.6×	14 0.4×	7	370
Terri M. Driessen United States	14	120 0.8×	56 0.5×	47 0.6×	157 3.5×	12 0.3×	23	400
Dea Adamsen Denmark	9	85 0.6×	57 0.5×	65 0.8×	40 0.9×	10 0.3×	11	279
Michelle A. Cheh United States	6	139 0.9×	230 2.0×	263 3.2×	47 1.0×	14 0.4×	8	441
Bruno Gegenhuber United States	9	98 0.6×	81 0.7×	22 0.3×	74 1.6×	19 0.5×	11	341
Rena Vanzo United States	14	186 1.2×	302 2.6×	74 0.9×	33 0.7×	8 0.2×	25	504

Countries citing papers authored by Gina Kang

Since Specialization

Citations

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

Fields of papers citing papers by Gina Kang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gina Kang

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

All Works

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14 of 14 papers shown

Ageta‐Ishihara, Natsumi, Kazuki Fujii, Kenji Tanigaki, et al.. (2025). Septin5 deficiency impairs both recent and remote contextual fear memory. Molecular Brain. 18(1). 85–85.

Hiramoto, Takeshi, Akira Sumiyoshi, Takahira Yamauchi, et al.. (2024). Highly demarcated structural alterations in the brain and impaired social incentive learning in Tbx1 heterozygous mice. Molecular Psychiatry. 30(5). 1876–1886. 5 indexed citations

Hiramoto, Takeshi, Akira Sumiyoshi, Takahira Yamauchi, et al.. (2021). Tbx1, a gene encoded in 22q11.2 copy number variant, is a link between alterations in fimbria myelination and cognitive speed in mice. Molecular Psychiatry. 27(2). 929–938. 12 indexed citations

Nomoto, Kensaku, Gina Kang, Takeshi Hiramoto, et al.. (2020). Maternal approach behaviors toward neonatal calls are impaired by mother's experiences of raising pups with a risk gene variant for autism. Developmental Psychobiology. 63(1). 108–113. 7 indexed citations

Marttinen, Mikael, Catarina B. Ferreira, Kaisa M. A. Paldanius, et al.. (2020). Presynaptic Vesicle Protein SEPTIN5 Regulates the Degradation of APP C-Terminal Fragments and the Levels of Aβ. Cells. 9(11). 2482–2482. 9 indexed citations

Yamauchi, Takahira, Gina Kang, & Noboru Hiroi. (2020). Heterozygosity of murine Crkl does not recapitulate behavioral dimensions of human 22q11.2 hemizygosity. Genes Brain & Behavior. 20(5). e12719–e12719. 7 indexed citations

Broin, Pilib Ó, Michael Beckert, Takeshi Izumi, et al.. (2018). Computational Analysis of Neonatal Mouse Ultrasonic Vocalization. PubMed. 8(2). e46–e46. 5 indexed citations

Boku, Shuken, Takeshi Izumi, Akira Nishi, et al.. (2017). Copy number elevation of 22q11.2 genes arrests the developmental maturation of working memory capacity and adult hippocampal neurogenesis. Molecular Psychiatry. 23(4). 985–992. 17 indexed citations

Solís, Óscar, Patricia García‐Sanz, Antonio S. Herranz, et al.. (2017). Human COMT over-expression confers a heightened susceptibility to dyskinesia in mice. Neurobiology of Disease. 102. 133–139. 18 indexed citations

10.

Nomaru, Hiroko, Kenny Ye, Akira Nishi, et al.. (2015). Molecular Histochemistry Identifies Peptidomic Organization and Reorganization Along Striatal Projection Units. Biological Psychiatry. 79(5). 415–420. 6 indexed citations

11.

Okabe, Shota, Pilib Ó Broin, Akira Nishi, et al.. (2015). Structure and function of neonatal social communication in a genetic mouse model of autism. Molecular Psychiatry. 21(9). 1208–1214. 66 indexed citations

12.

Harper, Kathryn M., Takeshi Hiramoto, Kenji Tanigaki, et al.. (2012). Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain. Human Molecular Genetics. 21(15). 3489–3499. 41 indexed citations

13.

Yoshida, Atsuhiro, Norio Yamamoto, Makoto Kinoshita, et al.. (2012). Localization of septin proteins in the mouse cochlea. Hearing Research. 289(1-2). 40–51. 10 indexed citations

14.

Hiramoto, Takeshi, Gina Kang, Go Suzuki, et al.. (2011). Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model. Human Molecular Genetics. 20(24). 4775–4785. 78 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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