Yoriko Watanabe

3.5k total citations
88 papers, 1.3k citations indexed

About

Yoriko Watanabe is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Yoriko Watanabe has authored 88 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 23 papers in Clinical Biochemistry and 23 papers in Genetics. Recurrent topics in Yoriko Watanabe's work include Metabolism and Genetic Disorders (23 papers), Neonatal Health and Biochemistry (9 papers) and Amino Acid Enzymes and Metabolism (9 papers). Yoriko Watanabe is often cited by papers focused on Metabolism and Genetic Disorders (23 papers), Neonatal Health and Biochemistry (9 papers) and Amino Acid Enzymes and Metabolism (9 papers). Yoriko Watanabe collaborates with scholars based in Japan, United States and United Kingdom. Yoriko Watanabe's co-authors include Jeffrey C. Murray, Shoji Yano, Takeharu Tsuge, Mary L. Marazita, Makoto Yoshino, Sandra Daack‐Hirsch, Hideki Abe, Azusa Saika, Naomichi Matsumoto and Satoshi Iwase and has published in prestigious journals such as SHILAP Revista de lepidopterología, PEDIATRICS and International Journal of Molecular Sciences.

In The Last Decade

Yoriko Watanabe

82 papers receiving 1.3k citations

Peers

Countries citing papers authored by Yoriko Watanabe

Since Specialization

Citations

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

Fields of papers citing papers by Yoriko Watanabe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yoriko Watanabe

This figure shows the co-authorship network connecting the top 25 collaborators of Yoriko Watanabe. A scholar is included among the top collaborators of Yoriko Watanabe 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 Yoriko Watanabe. Yoriko Watanabe 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	Hemizygous SMARCA1 variants cause X-linked intellectual disability 2025 ·Journal of Human Genetics ·(unknown), Takeshi Mizuguchi, Keisuke Hamada, Kotaro Yuge, (unknown), Naomi Tsuchida, Yuri Uchiyama, Atsushi Fujita, Eriko Koshimizu, Kazuharu Misawa, Satoko Miyatake, Yoriko Watanabe, Hitoshi Osaka, Koh-ichiro Yoshiura, Kazuhiro Ogata, Naomichi Matsumoto	0
2	The c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease 2024 ·Journal of Human Genetics ·Tadashi Inoue, (unknown), Keiko Uchida, Kazuki Kodo, Kenji Suda, Yoriko Watanabe, Koh-ichiro Yoshiura, (unknown), (unknown), Kenko Azuma, Kei Inai, Jun Muneuchi, Yoshiyuki Furutani, (unknown), Hiroyuki Yamagishi	3
3	Ultra-widefield and anterior-segment optical coherence tomography in Alagille syndrome 2021 ·American Journal of Ophthalmology Case Reports ·(unknown), Masatoshi Haruta, (unknown), Yoriko Watanabe, Shigeo Yoshida	1
4	Case Report: Rituximab Improved Epileptic Spasms and EEG Abnormalities in an Infant With West Syndrome and Anti-NMDAR Encephalitis Associated With APECED 2021 ·Frontiers in Neurology ·(unknown), (unknown), Ryuta Nishikomori, Yoriko Watanabe, (unknown), Yukitoshi Takahashi, Haruo Shintaku, Toyojiro Matsuishi	1
5	Cystic biliary atresia with paucity of bile ducts and gene mutation in KDM6A: a case report 2019 ·SHILAP Revista de lepidopterología ·(unknown), Suguru Fukahori, Tatsuki Mizuochi, Yoriko Watanabe, (unknown), (unknown), (unknown), Naoki Hashizume, (unknown), (unknown), (unknown), Koh-ichiro Yoshiura, Yoshiaki Tanaka, Minoru Yagi	4
6	Three Cases of KCNT1 Mutations: Malignant Migrating Partial Seizures in Infancy with Massive Systemic to Pulmonary Collateral Arteries 2017 ·The Journal of Pediatrics ·Yuki Kawasaki, Ichiro Kuki, Eiji Ehara, Yosuke Murakami, Shin Okazaki, Hisashi Kawawaki, Munetsugu Hara, Yoriko Watanabe, (unknown), Kenji Suda, Hirotomo Saitsu, Naomichi Matsumoto	20
7	Fatigue and quality of life in citrin deficiency during adaptation and compensation stage 2013 ·Molecular Genetics and Metabolism ·Yoshiyuki Okano, Kyoko Kobayashi, Kenji Ihara, Tetsuya Ito, Makoto Yoshino, Yoriko Watanabe, Shunsaku Kaji, Toshihiro Ohura, Masayoshi Nagao, Atsuko Noguchi, Sotaro Mushiake, (unknown), Tomoko Hashimoto-Tamaoki	20
8	Enhanced Incorporation of 3-Hydroxy-4-Methylvalerate Unit into Biosynthetic Polyhydroxyalkanoate Using Leucine as a Precursor 2011 ·AMB Express ·Azusa Saika, Yoriko Watanabe, Kumar Sudesh, Hideki Abe, Takeharu Tsuge	24
9	Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies 2010 ·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	35
10	Familial Simpson-Golabi-Behmel syndrome: studies of X-chromosome inactivation and clinical phenotypes in two female individuals with GPC3 mutations 2010 ·Clinical Genetics ·Shoji Yano, Berivan Baskin, Abdolreza Bagheri, Yoriko Watanabe, Kathryn Moseley, Agnes L. Nishimura, Naomichi Matsumoto, (unknown)	25
11	Screening for Alagille Syndrome Mutations in the JAG1 and NOTCH2 Genes Using Denaturing High-Performance Liquid Chromatography 2007 ·Genetic Testing ·(unknown), Chiharu Torii, Rika Kosaki, Kenji Kurosawa, Hiroshi Yoshihashi, Koji Muroya, Nobuhiko Okamoto, Yoriko Watanabe, Tomoki Kosho, (unknown), Osamu Matsuda, (unknown), Kosuke Izumi, Takao Takahashi, Kenjiro Kosaki	7
12	Late‐onset ornithine transcarbamylase deficiency in male patients: Prognostic factors and characteristics of plasma amino acid profile 2006 ·Pediatrics International ·(unknown), Atsushi Nishiyori, Yasuyuki Tokunaga, Yoriko Watanabe, Norikazu Kuriya, Ryukichi Kumashiro, (unknown), Ryuichi Kuromaru, Shinichi Hirose, (unknown), Makoto Yoshino	26
13	Biokinetics of radiotellurium in rats 2003 ·Radiation Protection Dosimetry ·Y. Nishimura, Saroj Kumar Sahoo, (unknown), Shino Homma‐Takeda, Yoriko Watanabe, Jiro Inaba	2
14	Effect of supplementation with l-carnitine at a small dose on acylcarnitine profiles in serum and urine and the renal handling of acylcarnitines in a patient with multiple acyl-coenzyme A dehydrogenation defect 2003 ·Journal of Chromatography B ·Makoto Yoshino, (unknown), Yoriko Watanabe, Ichiro Yoshida, (unknown), Ikue Hata, Yosuke Shigematsu, Masahiko Kimura, Seiji Yamaguchi	3
15	The proportion of cells with functional X disomy is associated with the severity of mental retardation in mosaic ring X Turner syndrome females 2002 ·Cytogenetic and Genome Research ·Takeo Kubota, Keiko Wakui, Takamitsu Nakamura, Haruhiko Ohashi, Yoriko Watanabe, Makoto Yoshino, (unknown), Nobuhiko Okamoto, (unknown), Koji Muroya, Tsutomu Ogata, Y. Goto, Y. Fukushima	27
16	Thermoregulatory Responses to Different Moisture Transfer Rates of Clothing Material during Exercise 2001 ·Journal of the Textile Institute ·(unknown), Yoriko Watanabe, (unknown), H. Tokura, (unknown)	1
17	Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41 2001 ·Human Mutation ·Yoriko Watanabe, Jeffrey C. Murray, Bryan C. Bjork, Christine Bird, (unknown), Simon G. Gregory, David M. Kurnit, Brian C. Schutte	1
18	Effects of Inflammatory Cytokines Induced by Helicobacter pylori Infection on Aminopyrine Accumulation in Parietal Cells Isolated from Guinea Pigs 1999 ·Digestive Diseases and Sciences ·(unknown), Yoriko Watanabe, (unknown), Shin‐ichi Muramatsu, (unknown), Naruhiro Kimura, Takashi Miwa	5
19	AUTOLYSIS DURING TRACHEARY ELEMENTDIFFERENTIATION-ANALYSIS WITH INHIBITORS- 1995 ·Plant and Cell Physiology ·Yoriko Watanabe, Hiroo Fukuda	1
20	Basic Studies on the Prevention of Decubitus Sore 1990 ·Journal of Japan Academy of Nursing Science ·(unknown), (unknown), Yoriko Watanabe	0

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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