Yoko Aoki

9.8k citations

170 papers · 4.8k indexed · 1 hit paper · h-index 36

Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders 16
Rheumatology top 1%
Molecular Biology top 2%
- Protein Tyrosine Phosphatases 47
- RNA modifications and cancer 12
- RNA regulation and disease 10
- Mitochondrial Function and Pathology 8
Immunology top 5%
- Galectins and Cancer Biology 30
Neurology top 2%
Cell Biology
- Biotin and Related Studies 13
Oncology
- Peptidase Inhibition and Analysis 13

Co-authors: Yoichi Matsubara Tetsuya Niihori Shigeo Kure Yoichi Suzuki Shinichi Inoue Yoko Narumi Kenji Kurosawa Hirofumi Ohashi
Cited by: Clinical Biochemistry Rheumatology Molecular Biology
Journals: Brain and Development (7 papers)Molecular Genetics and Metabolism (6 papers)Human Mutation (6 papers)
Partner nations: Japan United States Spain

In The Last Decade

Yoko Aoki

165 papers receiving 4.7k citations

Hit Papers

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Peers

Countries citing papers authored by Yoko Aoki

Since Specialization

Citations

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

Fields of papers citing papers by Yoko Aoki

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Yoko Aoki, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Yoko Aoki Line = papers co-authored together Yoko Aoki links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Updated Genetic Analysis of Japanese Familial ALS Patients Carrying SOD1 Variants Revealed Phenotypic Differences for Common Variants Neurology Genetics ·Ayumi Nishiyama,Tetsuya Niihori,Naoki Suzuki,Rumiko Izumi,Tetsuya Akiyama,Masaaki Kato,Ryo Funayama,Keiko Nakayama,Hitoshi Warita,Yoko Aoki,Masashi Aoki	2024	1
2	Genetic backgrounds and genotype-phenotype relationships in anthropometric parameters of 116 Japanese individuals with Noonan syndrome Clinical Pediatric Endocrinology ·Yasuko Shoji,Aboudramane Camara,박부용,Barrie Thomas Dickie,Annie Delienne,Eriko Nishi,Shinobu Ida,Yuri Etani,Tetsuya Niihori,Yoko Aoki,Nobuhiko Okamoto,Masanobu Kawai	2024	1
3	Electrocardiographic Changes with Age in Japanese Patients with Noonan Syndrome Journal of Cardiovascular Development and Disease ·Yasuhiro Ichikawa,Hiroyuki Kuroda,Cristina Vaz Pereira,Roberto Tenório,谢宏,Florence E. Taylor,方晓蕾,Kenji Kurosawa,Yoko Aoki,Mari Iwamoto,Marina Tchomakova	2023	1
4	Nuclear pore pathology underlying multisystem proteinopathy type 3‐related inclusion body myopathy Annals of Clinical and Translational Neurology ·Rumiko Izumi,Kensuke Ikeda,Tetsuya Niihori,Naoki Suzuki,Matsuyuki Shirota,Ryo Funayama,Keiko Nakayama,Hitoshi Warita,M. Tateyama,Yoko Aoki,Masashi Aoki	2023	1
5	Mecom mutation related to radioulnar synostosis with amegakaryocytic thrombocytopenia reduces HSPCs in mice Blood Advances ·姚文军,Tetsuya Niihori,Akihiko Muto,Yoshikazu Hayashi,Taiki Abe,Kazuhiko Igarashi,Yoko Aoki	2023	2
6	Multidisciplinary Management of Costello Syndrome: Current Perspectives Journal of Multidisciplinary Healthcare ·Chiara Leoni,Christian Benno Stabernack,Marco Tartaglia,Yoko Aoki,Giuseppe Zampino	2022	12
7	Novel POLE mutations identified in patients with IMAGE-I syndrome cause aberrant subcellular localisation and protein degradation in the nucleus Journal of Medical Genetics ·Tomohiro Nakano,Yoji Sasahara,Atsuo Kikuchi,Kunihiko Moriya,Hidetaka Niizuma,Tetsuya Niihori,Matsuyuki Shirota,Ryo Funayama,Keiko Nakayama,Yoko Aoki,Shigeo Kure	2022	3
8	A novel deletion in the C-terminal region of HSPB8 in a family with rimmed vacuolar myopathy Journal of Human Genetics ·Guangran Dong,Tetsuya Niihori,Michio Kobayashi,Naoki Suzuki,Rumiko Izumi,Hitoshi Warita,Kenju Hara,Matsuyuki Shirota,Ryo Funayama,Keiko Nakayama,Ichizo Nishino,Masashi Aoki,Yoko Aoki	2021	7
9	A somatic activating KRAS variant identified in an affected lesion of a patient with Gorham–Stout disease Journal of Human Genetics ·Akifumi Nozawa,Michio Ozeki,Tetsuya Niihori,Natsuko Suzui,Tatsuhiko Miyazaki,Yoko Aoki	2020	38
10	Co‐occurrence of hypertrophic cardiomyopathy and juvenile myelomonocytic leukemia in a neonate with Noonan syndrome, leading to premature death Clinical Case Reports ·Akihiro Tamura,Wang ShengXue,Kousaku Matsubara,Sister Frances Sauvé,Yuma Takanashi,Givaldo Nascimento Júnior,Bhavana Kandukuri,R. van der Plank,Toshiaki Ishida,Daiichiro Hasegawa,Miria Elisabete Bairros Camargo,Tetsuya Niihori,Yozo Nakazawa,Kenichi Koike,Yoko Aoki,Yoshiyuki Kosaka	2018	2
11	Craniosynostosis in patients with RASopathies: Accumulating clinical evidence for expanding the phenotype American Journal of Medical Genetics Part A ·Kimiko Ueda,Dong Yeul Lee,Tetsuya Niihori,Yoko Aoki,Nobuhiko Okamoto	2017	31
12	Long-term outcome of a 26-year-old woman with West syndrome and an nuclear receptor subfamily 2 group F member 1 gene (NR2F1) mutation Seizure ·Naomi Hino‐Fukuyo,Atsuo Kikuchi,Hiroyuki Yokoyama,Kazuie Iinuma,Shunwang Zhao,Kazuhiro Haginoya,Tetsuya Niihori,Keiko Nakayama,Yoko Aoki,Shigeo Kure	2017	11
13	Identification of a novel missense mutation of MAF in a Japanese family with congenital cataract by whole exome sequencing: A clinical report and review of literature American Journal of Medical Genetics Part A ·Yoko Narumi,Sachiko Nishina,Penny Woodberry,Yoko Aoki,Rika Kosaki,Keiko Wakui,Noriyuki Azuma,Toshinori Murata,Fumio Takada,Yoshimitsu Fukushima,Tomoki Kosho	2014	28
14	Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies Journal of Human Genetics ·Shoko Komatsuzaki,Yoko Aoki,Tetsuya Niihori,Nobuhiko Okamoto,Raoul C. M. Hennekam,Saskia Hopman,Hirofumi Ohashi,Seiji Mizuno,Yoriko Watanabe,Hotaka Kamasaki,Ikuko Kondo,Nobuko Moriyama,Kenji Kurosawa,Hiroshi Kawame,Ryuhei Okuyama,Masue Imaizumi,Takeshi Rikiishi,Shigeru Tsuchiya,Shigeo Kure,Yoichi Matsubara	2010	35
15	Resolution of anti-neutrophil cytoplasmic antibody-associated vasculitis after resection of gastric cancer Modern Rheumatology ·Yoshinori Hosoya,Seiji Minota,Alan Kawarai Lefor,Kazuya Sakuma,Yoko Aoki,Takeshi Kamimura,Tingyan Lu,育子岡本,Nobuyuki Kanai,Yoshikazu Yasuda	2009	7
16	Mutation spectrum of the PCCA and PCCB genes in Japanese patients with propionic acidemia Molecular Genetics and Metabolism ·S. Maekawa,Osamu Sakamoto,Yoichi Matsubara,Shigeo Kure,Yoichi Suzuki,Yoko Aoki,Seiji Yamaguchi,Yukihiro Takahashi,Toshiya Nishikubo,Laura Lidia Villaba,Akira Yoshioka,Toshiyuki Kimura,Kiyoshi Hayasaka,Yoshinori Kohno,Kazuie Iinuma,Toshihiro Ohura	2004	29
17	Lack of evidence for a significant association between nonsyndromic cleft lip with or without cleft palate and the retinoic acid receptor alpha gene in the Japanese population Journal of Human Genetics ·隆雄加地,Youichi Suzuki,Xiaoyuan Yang,Atsushi Yamada,Yoko Aoki,Shigeo Kure,Yoichi Matsubara	2002	13
18	Identification and characterization of mutations in patients with holocarboxylase synthetase deficiency Human Genetics ·Yoko Aoki,D. J. Manson,Osamu Sakamoto,Masahiro Hiratsuka,Christelle Bachi Gedeon,张志飞 Zhifei Zhang,Paz Briones,Terttu Suormala,E. R. Baumgartner,Yoichi Suzuki,Kuniaki Narisawa	1999	19
19	TwoCPT2 mutations in three Japanese patients with carnitine palmitoyltransferase II deficiency: Functional analysis and association with polymorphic haplotypes and two clinical phenotypes Human Mutation ·Min Ah Han,Jun Akanuma,Patrizia Cavadini,Yoko Aoki,Shigeo Kure,Federica Invernizzi,Ichiro Yoshida,Jun‐ichi Kira,Franco Taroni,Yoichi Matsubara,Kuniaki Narisawa	1998	49
20	Skin Cancer ·Ghali Gz,Yoko Aoki,F. Ståhlberg,A. Hafner,А. В. Голуб	1986	5

About Yoko Aoki

Yoko Aoki is a scholar working on Clinical Biochemistry, Immunology and Molecular Biology, having authored 170 papers that have together received 4.8k indexed citations. Recurring topics across this work include Protein Tyrosine Phosphatases (47 papers), Galectins and Cancer Biology (30 papers), Metabolism and Genetic Disorders (16 papers), Biotin and Related Studies (13 papers), Peptidase Inhibition and Analysis (13 papers), RNA modifications and cancer (12 papers), RNA regulation and disease (10 papers) and Mitochondrial Function and Pathology (8 papers). The work is most often cited by research in Clinical Biochemistry (408 citations), Rheumatology (762 citations) and Molecular Biology (2.9k citations). Yoko Aoki has collaborated with scholars based in Japan, United States and Spain. Frequent co-authors include Yoichi Matsubara, Tetsuya Niihori, Shigeo Kure, Yoichi Suzuki, Shinichi Inoue, Yoko Narumi, Kenji Kurosawa, Hirofumi Ohashi, Hiroshi Kawame and Yukichi Tanaka. Their work appears in journals such as Brain and Development, Molecular Genetics and Metabolism, Human Mutation, Human Molecular Genetics and Journal of Pediatric Hematology/Oncology.

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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