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

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

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20 of 20 papers shown

#	Work	Indexed citations
1	The Clinical Course and Treatment of a Case of Refractory Systemic Juvenile Myasthenia Gravis Successfully Treated with Thymectomy 2023 ·The Tohoku Journal of Experimental Medicine ·(unknown), (unknown), (unknown), (unknown), (unknown), Ryo Sato, (unknown), Wakaba Endo, Takehiko Inui, Noriko Togashi, (unknown), (unknown), Takatoshi Sato, Masato Kanzaki, Osamu Segawa, Kenta Masui, Keiko Ishigaki, Kazuhiro Haginoya	0
2	Neonatal developmental and epileptic encephalopathy with movement disorders and arthrogryposis: A case report with a novel missense variant of SCN1A 2023 ·Brain and Development ·(unknown), (unknown), Haruhiko Nakamura, (unknown), (unknown), Wakaba Endo, Takehiko Inui, Noriko Togashi, (unknown), Matsuyuki Shirota, Ryo Funayama, Tetsuya Niihori, Atsushi Fujita, Keiko Nakayama, Yoko Aoki, Naomichi Matsumoto, Shigeo Kure, Atsuo Kikuchi, Kazuhiro Haginoya	2
3	A first case of childhood chronic inflammatory demyelinating polyneuropathy associated with alopecia universalis 2022 ·Brain and Development ·(unknown), (unknown), Ryo Sato, Wakaba Endo, Takehiko Inui, Noriko Togashi, Kazuhiro Haginoya	0
4	Successful treatment with dimethyl fumarate in a child with relapsing-remitting multiple sclerosis 2022 ·Brain and Development ·(unknown), Yu Abe, Yoshitsugu Oikawa, (unknown), Wakaba Endo, (unknown), Toshiyuki Takahashi, Mitsugu Uematsu	2
5	The effect of dietary protein restriction in a case of molybdenum cofactor deficiency with MOCS1 mutation 2021 ·Molecular Genetics and Metabolism Reports ·Yu Abe, (unknown), Wakaba Endo, Hiroshi Hasegawa, Kimiyoshi Ichida, Mitsugu Uematsu, Shigeo Kure	10
6	A 23-year follow-up report of juvenile-onset Sandhoff disease presenting with a motor neuron disease phenotype and a novel variant 2021 ·Brain and Development ·(unknown), (unknown), Akira Onuma, (unknown), Wakaba Endo, (unknown), Takehiko Inui, Noriko Togashi, Ichiro Nakashima, Naomi Hino‐Fukuyo, Hiroyuki Ida, Satoko Miyatake, Naomichi Matsumoto, Kazuhiro Haginoya	0
7	Two cases of persistent falcine and occipital sinuses 2020 ·Brain and Development ·Takehiko Inui, (unknown), (unknown), Ryo Sato, (unknown), Wakaba Endo, Noriko Togashi, (unknown), Harushi Mori, Kazuhiro Haginoya	2
8	Fifteen-year follow-up of a patient with a DHDDS variant with non-progressive early onset myoclonic tremor and rare generalized epilepsy 2020 ·Brain and Development ·Noriko Togashi, Atsushi Fujita, (unknown), (unknown), (unknown), Ryo Sato, (unknown), Wakaba Endo, Takehiko Inui, Kazutaka Jin, Naomichi Matsumoto, Kazuhiro Haginoya	11
9	Two males with sick sinus syndrome in a family with 0.6 kb deletions involving major domains in MECP2 2019 ·European Journal of Medical Genetics ·Takehiko Inui, Kazuhiro Iwama, (unknown), Ryo Sato, (unknown), Wakaba Endo, Noriko Togashi, Yosuke Kakisaka, Atsuo Kikuchi, Takeshi Mizuguchi, Shigeo Kure, Naomichi Matsumoto, Kazuhiro Haginoya	1
10	Leucine-485 deletion variant of BRAF may exhibit the severe end of the clinical spectrum of CFC syndrome 2019 ·Journal of Human Genetics ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Ryo Sato, (unknown), Wakaba Endo, Takehiko Inui, Noriko Togashi, Atsuo Kikuchi, Tetsuya Niihori, Yoko Aoki, Shigeo Kure, Kazuhiro Haginoya	3
11	Rett-like features and cortical visual impairment in a Japanese patient with HECW2 mutation 2018 ·Brain and Development ·Haruhiko Nakamura, Mitsugu Uematsu, (unknown), Yu Abe, Wakaba Endo, Atsuo Kikuchi, (unknown), Ryo Funayama, Matsuyuki Shirota, Keiko Nakayama, Tetsuya Niihori, Yoko Aoki, Kazuhiro Haginoya, Shigeo Kure	7
12	A novel mutation in the proteolytic domain of LONP1 causes atypical CODAS syndrome 2017 ·Journal of Human Genetics ·Takehiko Inui, (unknown), (unknown), Wakaba Endo, Yosuke Kakisaka, Atsuo Kikuchi, Akira Onuma, Shigeo Kure, Ichizo Nishino, Chihiro Ohba, Hirotomo Saitsu, Naomichi Matsumoto, Kazuhiro Haginoya	15
13	A severe female case of arthrogryposis multiplex congenita with brain atrophy, spastic quadriplegia and intellectual disability caused by ZC4H2 mutation 2017 ·Brain and Development ·(unknown), Wakaba Endo, Takehiko Inui, (unknown), (unknown), Noriko Togashi, Ryo Sato, Natsuko Arai‐Ichinoi, Atsuo Kikuchi, Shigeo Kure, Kazuhiro Haginoya	9
14	FDG-PET study of patients with Leigh syndrome 2016 ·Journal of the Neurological Sciences ·(unknown), Tomohiro Kaneta, Noriko Togashi, Naomi Hino‐Fukuyo, Tomoko Kobayashi, Mitsugu Uematsu, Taro Kitamura, Takehiko Inui, (unknown), (unknown), (unknown), Wakaba Endo, Noriko Miyake, Hirotomo Saitsu, Naomichi Matsumoto, Shigeo Kure	12
15	The first report of Japanese patients with asparagine synthetase deficiency 2016 ·Brain and Development ·Takahiro Yamamoto, Wakaba Endo, Hidenori Ohnishi, Kazuo Kubota, Norio Kawamoto, Takehiko Inui, Atsushi Imamura, Jun‐ichi Takanashi, Masaaki Shiina, Hirotomo Saitsu, Kazuhiro Ogata, Naomichi Matsumoto, Kazuhiro Haginoya, Toshiyuki Fukao	25
16	First Japanese variant of late infantile neuronal ceroid lipofuscinosis caused by novel CLN6 mutations 2016 ·Brain and Development ·Ryo Sato, Takehiko Inui, Wakaba Endo, (unknown), (unknown), (unknown), Hiroyuki Morita, Hirotomo Saitsu, Naomichi Matsumoto, Kazuhiro Haginoya	9
17	Outcome of hemiplegic cerebral palsy born at term depends on its etiology 2015 ·Brain and Development ·(unknown), Kazuhiro Haginoya, (unknown), (unknown), K Ogura, Takehiko Inui, Wakaba Endo, (unknown), (unknown), (unknown), Hiroshi Arai	19
18	Two cases of early-onset myoclonic seizures with continuous parietal delta activity caused by EEF1A2 mutations 2015 ·Brain and Development ·Takehiko Inui, Satoru Kobayashi, (unknown), Ryo Sato, Wakaba Endo, Mitsugu Uematsu, Hiroshi Oba, Hirotomo Saitsu, Naomichi Matsumoto, Shigeo Kure, Kazuhiro Haginoya	26
19	Neuroepidemiology of Porencephaly, Schizencephaly, and Hydranencephaly in Miyagi Prefecture, Japan 2015 ·Pediatric Neurology ·Naomi Hino‐Fukuyo, Noriko Togashi, (unknown), Junko Saito, Takehiko Inui, Wakaba Endo, Ryo Sato, (unknown), Hirotomo Saitsu, Kazuhiro Haginoya	17
20	A girl with Cardio-facio-cutaneous syndrome complicated with status epilepticus and acute encephalopathy 2013 ·Brain and Development ·Keisuke Wakusawa, Satoru Kobayashi, Yu Abe, Soichiro Tanaka, Wakaba Endo, Takehiko Inui, (unknown), (unknown), Noriko Togashi, Takahiro Nara, Tetsuya Niihori, Yoko Aoki, Kazuhiro Haginoya	8

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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