Ohiko Hashimoto

896 total citations
28 papers, 659 citations indexed

About

Ohiko Hashimoto is a scholar working on Cognitive Neuroscience, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Ohiko Hashimoto has authored 28 papers receiving a total of 659 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Cognitive Neuroscience, 17 papers in Genetics and 6 papers in Psychiatry and Mental health. Recurrent topics in Ohiko Hashimoto's work include Genetics and Neurodevelopmental Disorders (15 papers), Autism Spectrum Disorder Research (15 papers) and Genomic variations and chromosomal abnormalities (5 papers). Ohiko Hashimoto is often cited by papers focused on Genetics and Neurodevelopmental Disorders (15 papers), Autism Spectrum Disorder Research (15 papers) and Genomic variations and chromosomal abnormalities (5 papers). Ohiko Hashimoto collaborates with scholars based in Japan, United States and Russia. Ohiko Hashimoto's co-authors include Nobumasa Kato, Shinko Koishi, Yukiko Kano, Hisami Nishida, Tsukasa Sasaki, Toshiro Sugiyama, Tetsuya Marui, Eiji Nanba, Kiyoto Kasai and Kenji Yamamoto and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Psychiatry and Biochemical and Biophysical Research Communications.

In The Last Decade

Ohiko Hashimoto

28 papers receiving 640 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ohiko Hashimoto Japan	12	261	229	159	158	97	28	659
D Gonen United States	8	375 1.4×	358 1.6×	167 1.1×	160 1.0×	111 1.1×	9	658
Christopher L. Muller United States	10	493 1.9×	276 1.2×	146 0.9×	261 1.7×	98 1.0×	10	929
Aaron J. Towers United States	10	265 1.0×	328 1.4×	291 1.8×	516 3.3×	102 1.1×	11	1.2k
Loyse Hippolyte Switzerland	17	683 2.6×	320 1.4×	94 0.6×	150 0.9×	197 2.0×	22	939
Ashley A. Scott‐Van Zeeland United States	11	640 2.5×	310 1.4×	87 0.5×	204 1.3×	203 2.1×	13	1.0k
Ellen J. Hoffman United States	12	204 0.8×	196 0.9×	49 0.3×	314 2.0×	170 1.8×	22	838
Andreas G. Chiocchetti Germany	17	284 1.1×	335 1.5×	104 0.7×	474 3.0×	125 1.3×	50	983
Rhinda Goedken United States	10	170 0.7×	272 1.2×	134 0.8×	144 0.9×	67 0.7×	15	536
Annette Milnik Switzerland	15	326 1.2×	75 0.3×	96 0.6×	195 1.2×	89 0.9×	37	835
Dionisio A. Amodeo United States	14	346 1.3×	191 0.8×	134 0.8×	159 1.0×	71 0.7×	24	627

Countries citing papers authored by Ohiko Hashimoto

Since Specialization

Citations

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

Fields of papers citing papers by Ohiko Hashimoto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ohiko Hashimoto

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

Nakamura, Masayuki, Takeshi Yasuda, Teiichi Onuma, et al.. (2020). DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A. Journal of Human Genetics. 66(4). 419–429. 10 indexed citations

Yanagi, Kumiko, Tadashi Kaname, Keiko Wakui, et al.. (2012). Identification of Four Novel Synonymous Substitutions in the X-Linked GenesNeuroligin 3andNeuroligin 4Xin Japanese Patients with Autistic Spectrum Disorder. SHILAP Revista de lepidopterología. 2012. 1–5. 21 indexed citations

Marui, Tetsuya, Ikuko Funatogawa, Shinko Koishi, et al.. (2010). The NADH‐ubiquinone oxidoreductase 1 alpha subcomplex 5 (NDUFA5) gene variants are associated with autism. Acta Psychiatrica Scandinavica. 123(2). 118–124. 26 indexed citations

Marui, Tetsuya, Ikuko Funatogawa, Shinko Koishi, et al.. (2009). Association between autism and variants in the wingless-type MMTV integration site family member 2 ( WNT2) gene. The International Journal of Neuropsychopharmacology. 13(4). 443–443. 27 indexed citations

Marui, Tetsuya, Ikuko Funatogawa, Shinko Koishi, et al.. (2008). Association of the neuronal cell adhesion molecule (NRCAM) gene variants with autism. The International Journal of Neuropsychopharmacology. 12(1). 1–1. 93 indexed citations

Kato, Chieko, Mamoru Tochigi, Jun Ohashi, et al.. (2008). Association study of the 15q11‐q13 maternal expression domain in Japanese autistic patients. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(7). 1008–1012. 10 indexed citations

Kato, Chieko, Mamoru Tochigi, Shinko Koishi, et al.. (2008). Association study of the commonly recognized breakpoints in chromosome 15q11–q13 in Japanese autistic patients. Psychiatric Genetics. 18(3). 133–136. 2 indexed citations

Tochigi, Mamoru, Chieko Kato, Jun Ohashi, et al.. (2008). No association between the ryanodine receptor 3 gene and autism in a Japanese population. Psychiatry and Clinical Neurosciences. 62(3). 341–344. 6 indexed citations

Tochigi, Mamoru, Chieko Kato, Shinko Koishi, et al.. (2007). No evidence for significant association between GABA receptor genes in chromosome 15q11–q13 and autism in a Japanese population. Journal of Human Genetics. 52(12). 985–989. 11 indexed citations

10.

Marui, Tetsuya, Shinko Koishi, Ikuko Funatogawa, et al.. (2007). No association between the Neuronal Pentraxin II gene polymorphism and autism. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 31(4). 940–943. 7 indexed citations

11.

Kasai, Kiyoto, Ohiko Hashimoto, Yuki Kawakubo, et al.. (2005). Delayed automatic detection of change in speech sounds in adults with autism: A magnetoencephalographic study. Clinical Neurophysiology. 116(7). 1655–1664. 67 indexed citations

12.

Marui, Tetsuya, Shinko Koishi, Ikuko Funatogawa, et al.. (2005). No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population. Neuroscience Research. 53(1). 91–94. 24 indexed citations

13.

Higaki, Katsumi, Yumiko Sakamoto, Ohiko Hashimoto, et al.. (2005). Polyhistidine tract expansions in HOXA1 result in intranuclear aggregation and increased cell death. Biochemical and Biophysical Research Communications. 336(4). 1033–1039. 14 indexed citations

14.

Marui, Tetsuya, Ohiko Hashimoto, Eiji Nanba, et al.. (2004). Association between the neurofibromatosis‐1 (NF1) locus and autism in the Japanese population. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 131B(1). 43–47. 45 indexed citations

15.

Marui, Tetsuya, Ohiko Hashimoto, Eiji Nanba, et al.. (2003). Gastrin-releasing peptide receptor (GRPR) locus in Japanese subjects with autism. Brain and Development. 26(1). 5–7. 10 indexed citations

16.

Honjo, Shuji, Hitoshi Kaneko, Tatsuo Ujiie, et al.. (2003). Antenatal Depression and Maternal-Fetal Attachment. Psychopathology. 36(6). 304–311. 59 indexed citations

17.

Sasaki, Tsukasa, Rie Akaho, Yuji Okazaki, et al.. (2000). Human Leukocyte Antigen and Season of Birth in Japanese Patients With Schizophrenia. American Journal of Psychiatry. 157(7). 1173–1175. 31 indexed citations

18.

Fukuda, Masato, et al.. (1999). A Family with an atonic variant of paroxysmal kinesigenic choreoathetosis and hypercalcitoninemia. Movement Disorders. 14(2). 342–344. 4 indexed citations

19.

Hashimoto, Ohiko, Yasuo Shimizu, & Yoko Kawasaki. (1993). Brief report: Low frequency of the fragile X syndrome among Japanese autistic subjects. Journal of Autism and Developmental Disorders. 23(1). 201–209. 8 indexed citations

20.

Hashimoto, Ohiko, Makoto Honda, Shin‐Ichi Niwa, et al.. (1993). Linkage Analysis between Familial Myoclonus Epilepsy and Short Arm of Chromosome 6 Using HLA Phenotype as Genetic Marker. Psychiatry and Clinical Neurosciences. 47(2). 275–277. 3 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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