Wakaba Endo

569 total citations
38 papers, 365 citations indexed

About

Wakaba Endo is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Wakaba Endo has authored 38 papers receiving a total of 365 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Genetics and 7 papers in Psychiatry and Mental health. Recurrent topics in Wakaba Endo's work include Genetics and Neurodevelopmental Disorders (9 papers), Metabolism and Genetic Disorders (6 papers) and Neurogenetic and Muscular Disorders Research (5 papers). Wakaba Endo is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Metabolism and Genetic Disorders (6 papers) and Neurogenetic and Muscular Disorders Research (5 papers). Wakaba Endo collaborates with scholars based in Japan and United States. Wakaba Endo's co-authors include Takehiko Inui, Kazuhiro Haginoya, Shigeo Kure, Noriko Togashi, Hirotomo Saitsu, Naomichi Matsumoto, Mitsugu Uematsu, Ryo Sato, Atsuo Kikuchi and Akira Onuma and has published in prestigious journals such as Journal of the Neurological Sciences, Pediatric Neurology and Brain and Development.

In The Last Decade

Wakaba Endo

33 papers receiving 362 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wakaba Endo Japan 12 151 108 82 66 50 38 365
Clara DM van Karnebeek Canada 7 190 1.3× 105 1.0× 40 0.5× 32 0.5× 78 1.6× 7 349
Michelle Demos Canada 13 270 1.8× 145 1.3× 64 0.8× 31 0.5× 50 1.0× 23 482
I. Desguerre France 12 194 1.3× 69 0.6× 98 1.2× 64 1.0× 111 2.2× 37 400
Iris Noyman Israel 9 207 1.4× 64 0.6× 104 1.3× 71 1.1× 23 0.5× 26 455
Noboru Fueki Japan 10 207 1.4× 76 0.7× 44 0.5× 51 0.8× 65 1.3× 24 356
Dimitar N. Azmanov Australia 12 191 1.3× 122 1.1× 41 0.5× 53 0.8× 26 0.5× 23 336
Ewa Emich‐Widera Poland 12 96 0.6× 39 0.4× 118 1.4× 66 1.0× 22 0.4× 55 353
Rosario Berardi Italy 14 146 1.0× 189 1.8× 84 1.0× 108 1.6× 33 0.7× 29 422
Francisca Millan United States 11 261 1.7× 250 2.3× 50 0.6× 49 0.7× 34 0.7× 19 479
Rosario Domingo‐Jiménez Spain 14 224 1.5× 145 1.3× 64 0.8× 77 1.2× 34 0.7× 48 648

Countries citing papers authored by Wakaba Endo

Since Specialization
Citations

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

Fields of papers citing papers by Wakaba Endo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wakaba Endo

This figure shows the co-authorship network connecting the top 25 collaborators of Wakaba Endo. A scholar is included among the top collaborators of Wakaba Endo 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 Wakaba Endo. Wakaba Endo 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.
Sato, Ryo, Wakaba Endo, Takehiko Inui, et al.. (2023). The Clinical Course and Treatment of a Case of Refractory Systemic Juvenile Myasthenia Gravis Successfully Treated with Thymectomy. The Tohoku Journal of Experimental Medicine. 262(1). 29–31.
2.
Nakamura, Haruhiko, Wakaba Endo, Takehiko Inui, et al.. (2023). Neonatal developmental and epileptic encephalopathy with movement disorders and arthrogryposis: A case report with a novel missense variant of SCN1A. Brain and Development. 45(9). 505–511. 2 indexed citations
3.
4.
Abe, Yu, et al.. (2022). Successful treatment with dimethyl fumarate in a child with relapsing-remitting multiple sclerosis. Brain and Development. 44(5). 353–356. 2 indexed citations
5.
Abe, Yu, Wakaba Endo, Hiroshi Hasegawa, et al.. (2021). The effect of dietary protein restriction in a case of molybdenum cofactor deficiency with MOCS1 mutation. Molecular Genetics and Metabolism Reports. 26. 100716–100716. 10 indexed citations
6.
Onuma, Akira, Wakaba Endo, Takehiko Inui, et al.. (2021). A 23-year follow-up report of juvenile-onset Sandhoff disease presenting with a motor neuron disease phenotype and a novel variant. Brain and Development. 43(10). 1029–1032.
7.
Inui, Takehiko, Ryo Sato, Wakaba Endo, et al.. (2020). Two cases of persistent falcine and occipital sinuses. Brain and Development. 43(1). 170–173. 2 indexed citations
8.
Togashi, Noriko, Atsushi Fujita, Ryo Sato, et al.. (2020). Fifteen-year follow-up of a patient with a DHDDS variant with non-progressive early onset myoclonic tremor and rare generalized epilepsy. Brain and Development. 42(9). 696–699. 11 indexed citations
9.
Inui, Takehiko, Kazuhiro Iwama, Ryo Sato, et al.. (2019). Two males with sick sinus syndrome in a family with 0.6 kb deletions involving major domains in MECP2. European Journal of Medical Genetics. 63(3). 103769–103769. 1 indexed citations
10.
Sato, Ryo, Wakaba Endo, Takehiko Inui, et al.. (2019). Leucine-485 deletion variant of BRAF may exhibit the severe end of the clinical spectrum of CFC syndrome. Journal of Human Genetics. 64(5). 499–504. 3 indexed citations
11.
Nakamura, Haruhiko, Mitsugu Uematsu, Yu Abe, et al.. (2018). Rett-like features and cortical visual impairment in a Japanese patient with HECW2 mutation. Brain and Development. 40(5). 410–414. 7 indexed citations
12.
Inui, Takehiko, Wakaba Endo, Yosuke Kakisaka, et al.. (2017). A novel mutation in the proteolytic domain of LONP1 causes atypical CODAS syndrome. Journal of Human Genetics. 62(6). 653–655. 15 indexed citations
13.
Endo, Wakaba, Takehiko Inui, Noriko Togashi, et al.. (2017). A severe female case of arthrogryposis multiplex congenita with brain atrophy, spastic quadriplegia and intellectual disability caused by ZC4H2 mutation. Brain and Development. 40(4). 334–338. 9 indexed citations
14.
Kaneta, Tomohiro, Noriko Togashi, Naomi Hino‐Fukuyo, et al.. (2016). FDG-PET study of patients with Leigh syndrome. Journal of the Neurological Sciences. 362. 309–313. 12 indexed citations
15.
Yamamoto, Takahiro, Wakaba Endo, Hidenori Ohnishi, et al.. (2016). The first report of Japanese patients with asparagine synthetase deficiency. Brain and Development. 39(3). 236–242. 25 indexed citations
16.
Sato, Ryo, Takehiko Inui, Wakaba Endo, et al.. (2016). First Japanese variant of late infantile neuronal ceroid lipofuscinosis caused by novel CLN6 mutations. Brain and Development. 38(9). 852–856. 9 indexed citations
17.
Haginoya, Kazuhiro, et al.. (2015). Outcome of hemiplegic cerebral palsy born at term depends on its etiology. Brain and Development. 38(3). 267–273. 19 indexed citations
18.
Inui, Takehiko, Satoru Kobayashi, Ryo Sato, et al.. (2015). Two cases of early-onset myoclonic seizures with continuous parietal delta activity caused by EEF1A2 mutations. Brain and Development. 38(5). 520–524. 26 indexed citations
19.
Hino‐Fukuyo, Naomi, Noriko Togashi, Junko Saito, et al.. (2015). Neuroepidemiology of Porencephaly, Schizencephaly, and Hydranencephaly in Miyagi Prefecture, Japan. Pediatric Neurology. 54. 39–42.e1. 17 indexed citations
20.
Wakusawa, Keisuke, Satoru Kobayashi, Yu Abe, et al.. (2013). A girl with Cardio-facio-cutaneous syndrome complicated with status epilepticus and acute encephalopathy. Brain and Development. 36(1). 61–63. 8 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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