Ayako Hattori

1.3k total citations
60 papers, 546 citations indexed

About

Ayako Hattori is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Ayako Hattori has authored 60 papers receiving a total of 546 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 21 papers in Genetics and 8 papers in Psychiatry and Mental health. Recurrent topics in Ayako Hattori's work include Genetics and Neurodevelopmental Disorders (8 papers), Genomics and Rare Diseases (6 papers) and Metabolism and Genetic Disorders (5 papers). Ayako Hattori is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Genomics and Rare Diseases (6 papers) and Metabolism and Genetic Disorders (5 papers). Ayako Hattori collaborates with scholars based in Japan, United Kingdom and Australia. Ayako Hattori's co-authors include Shinji Saitoh, Ikumi Hori, Yutaka Negishi, N Ando, Daisuke Ieda, Hajime Togari, Akihisa Iguchi, Tatsuya Ishikawa, Satoru Kobayashi and Kei Ohashi and has published in prestigious journals such as Journal of Neurochemistry, Journal of the American Geriatrics Society and Epilepsia.

In The Last Decade

Ayako Hattori

55 papers receiving 532 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ayako Hattori Japan 15 203 165 108 69 55 60 546
Jie Yin United States 14 201 1.0× 178 1.1× 88 0.8× 36 0.5× 67 1.2× 25 712
Radhika Dhamija United States 16 222 1.1× 193 1.2× 144 1.3× 76 1.1× 104 1.9× 64 721
Paola Nicolaides United Kingdom 11 188 0.9× 63 0.4× 107 1.0× 130 1.9× 33 0.6× 19 507
Peter Herkenrath Germany 16 207 1.0× 102 0.6× 146 1.4× 180 2.6× 58 1.1× 37 717
Felippe Borlot Canada 14 120 0.6× 228 1.4× 235 2.2× 105 1.5× 46 0.8× 36 543
Hamìt Özyürek Türkiye 10 223 1.1× 221 1.3× 61 0.6× 97 1.4× 35 0.6× 34 461
Allan Bayat Denmark 13 205 1.0× 233 1.4× 167 1.5× 111 1.6× 48 0.9× 61 557
Grace Vassallo United Kingdom 13 101 0.5× 86 0.5× 120 1.1× 58 0.8× 35 0.6× 36 532
Jolanta Wierzba Poland 17 383 1.9× 265 1.6× 42 0.4× 117 1.7× 69 1.3× 91 758
Nicholas M. Allen Ireland 12 223 1.1× 194 1.2× 167 1.5× 64 0.9× 15 0.3× 44 616

Countries citing papers authored by Ayako Hattori

Since Specialization
Citations

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

Fields of papers citing papers by Ayako Hattori

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ayako Hattori

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

All Works

20 of 20 papers shown
1.
Fujimoto, Masanori, Y. Nakamura, Daisuke Ieda, et al.. (2022). Angelman syndrome with mosaic paternal uniparental disomy suggestive of mitotic nondisjunction. Journal of Human Genetics. 68(2). 87–90. 1 indexed citations
2.
Suzuki, Takeshi, Yuji Ito, Tadashi Ito, et al.. (2022). Quantitative Three-Dimensional Gait Evaluation in Patients With Glucose Transporter 1 Deficiency Syndrome. Pediatric Neurology. 132. 23–26. 1 indexed citations
3.
Natsume, Jun, Naoko Ishihara, Yoshiteru Azuma, et al.. (2020). Lenticular nuclei to thalamic ratio on PET is useful for diagnosis of GLUT1 deficiency syndrome. Brain and Development. 43(1). 69–77. 2 indexed citations
4.
Iwayama, Hideyuki, Norimitsu Wakao, Hirokazu Kurahashi, et al.. (2020). Administration of nusinersen via paramedian approach for spinal muscular atrophy. Brain and Development. 43(1). 121–126. 2 indexed citations
5.
Suzuki, Hisato, Ayako Hattori, Ikumi Hori, et al.. (2020). De novo 2q36.3q37.1 deletion encompassing TRIP12 and NPPC yields distinct phenotypes. Human Genome Variation. 7(1). 19–19. 1 indexed citations
6.
Uematsu, Mitsugu, Tomoko Kobayashi, Noriko Togashi, et al.. (2020). Behavioral problems and family distress in tuberous sclerosis complex. Epilepsy & Behavior. 111. 107321–107321. 4 indexed citations
7.
Ogawa, Chikako, Hiroyuki Kidokoro, Naoko Ishihara, et al.. (2019). Splenial Lesions in Benign Convulsions With Gastroenteritis Associated With Rotavirus Infection. Pediatric Neurology. 109. 79–84. 8 indexed citations
8.
Hori, Ikumi, Koichi Ito, Ayako Hattori, et al.. (2019). Transition from Leigh syndrome to MELAS syndrome in a patient with heteroplasmic MT-ND3 m.10158T>C. Brain and Development. 41(9). 803–807. 7 indexed citations
9.
Hori, Ikumi, Fuyuki Miya, Yutaka Negishi, et al.. (2018). A novel homozygous missense mutation in the SH3-binding motif of STAMBP causing microcephaly-capillary malformation syndrome. Journal of Human Genetics. 63(9). 957–963. 10 indexed citations
10.
Ieda, Daisuke, Ikumi Hori, Y. Nakamura, et al.. (2018). A novel truncating mutation in FLNA causes periventricular nodular heterotopia, Ehlers-Danlos-like collagenopathy and macrothrombocytopenia. Brain and Development. 40(6). 489–492. 12 indexed citations
11.
Kato, Koji, Fuyuki Miya, Ikumi Hori, et al.. (2017). A novel missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria and cleft palate. Journal of Human Genetics. 62(9). 861–863. 18 indexed citations
12.
Hamada, Nanako, Yutaka Negishi, Makoto Mizuno, et al.. (2016). Role of a heterotrimeric G‐protein, Gi2, in the corticogenesis: possible involvement in periventricular nodular heterotopia and intellectual disability. Journal of Neurochemistry. 140(1). 82–95. 13 indexed citations
13.
Negishi, Yutaka, Fuyuki Miya, Ayako Hattori, et al.. (2015). Truncating mutation in NFIA causes brain malformation and urinary tract defects. Human Genome Variation. 2(1). 15007–15007. 19 indexed citations
14.
Hattori, Ayako, Hirofumi Komaki, Masao Kawatani, et al.. (2012). A novel mutation in the LMNA gene causes congenital muscular dystrophy with dropped head and brain involvement. Neuromuscular Disorders. 22(2). 149–151. 21 indexed citations
15.
Saito, Yoshiaki, Hirofumi Komaki, Ayako Hattori, et al.. (2011). Extramuscular manifestations in children with severe congenital myopathy due to ACTA1 gene mutations. Neuromuscular Disorders. 21(7). 489–493. 9 indexed citations
16.
Saito, Yoshiaki, Masaya Kubota, Kenji Kurosawa, et al.. (2010). Polymicrogyria and infantile spasms in a patient with 1p36 deletion syndrome. Brain and Development. 33(5). 437–441. 10 indexed citations
17.
Hussein, Mohamed Hamed, Hiroki Kakita, Ayako Hattori, et al.. (2007). THE SEX DIFFERENCES OF CEREBROSPINAL FLUID LEVELS OF INTERLEUKIN 8 AND ANTIOXIDANTS IN ASPHYXIATED NEWBORNS. Shock. 28(2). 154–159. 12 indexed citations
18.
Hattori, Ayako, N Ando, Mohamed Hamed Hussein, et al.. (2006). Short-Duration ACTH Therapy for Cryptogenic West Syndrome With Better Outcome. Pediatric Neurology. 35(6). 415–418. 8 indexed citations
19.
Umegaki, Hiroyuki, Ayako Hattori, Hisayuki Miura, et al.. (2004). Cognitive function in Japanese elderly with type 2 diabetes mellitus. Journal of Diabetes and its Complications. 18(1). 42–46. 35 indexed citations
20.
Nomura, Hideki, Toshio Hayashi, Teiji Esaki, et al.. (2002). Standardization of Plasma Brain Natriuretic Peptide Concentrations in Older Japanese—Relationship to Latent Renal Dysfunction and Ischemic Heart Disease. Journal of the American Geriatrics Society. 50(9). 1504–1509. 17 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

Breakdown of academic impact, for papers by Jie Yin Breakdown of academic impact, for papers by Radhika Dhamija Breakdown of academic impact, for papers by Paola Nicolaides Breakdown of academic impact, for papers by Peter Herkenrath Breakdown of academic impact, for papers by Felippe Borlot Breakdown of academic impact, for papers by Hamìt Özyürek Breakdown of academic impact, for papers by Allan Bayat Breakdown of academic impact, for papers by Grace Vassallo Breakdown of academic impact, for papers by Jolanta Wierzba Breakdown of academic impact, for papers by Nicholas M. Allen
Rankless by CCL
2026