Takeo Kubota

5.5k total citations
130 papers, 3.6k citations indexed

About

Takeo Kubota is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Takeo Kubota has authored 130 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 80 papers in Molecular Biology, 62 papers in Genetics and 19 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Takeo Kubota's work include Epigenetics and DNA Methylation (43 papers), Genetics and Neurodevelopmental Disorders (35 papers) and Genetic Syndromes and Imprinting (17 papers). Takeo Kubota is often cited by papers focused on Epigenetics and DNA Methylation (43 papers), Genetics and Neurodevelopmental Disorders (35 papers) and Genetic Syndromes and Imprinting (17 papers). Takeo Kubota collaborates with scholars based in Japan, United States and China. Takeo Kubota's co-authors include Kunio Miyake, Takae Hirasawa, David H. Ledbetter, Susan L. Christian, Kazuki Mochizuki, Keiko Wakui, Yoichi Sakurada, Hiroyuki Iijima, Fumihiko Mabuchi and Lee Chuin Chen and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Takeo Kubota

129 papers receiving 3.5k citations

Peers

Countries citing papers authored by Takeo Kubota

Since Specialization

Citations

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

Fields of papers citing papers by Takeo Kubota

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Takeo Kubota

This figure shows the co-authorship network connecting the top 25 collaborators of Takeo Kubota. A scholar is included among the top collaborators of Takeo Kubota 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 Takeo Kubota. Takeo Kubota 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	Plasticity of histone modifications around Cidea and Cidec genes with secondary bile in the amelioration of developmentally-programmed hepatic steatosis 2019 ·Scientific Reports ·(unknown), Hiroaki Itoh, (unknown), (unknown), (unknown), (unknown), Naoaki Tamura, Toshiyuki Uchida, Kazunao Suzuki, Yoshihiro Ogawa, Nobuaki Shiraki, Kazuki Mochizuki, Takeo Kubota, Naohiro Kanayama	9
2	Epigenetic alterations induced by environmental stress associated with metabolic and neurodevelopmental disorders 2016 ·Current Zoology ·Takeo Kubota	19
3	Long-term imipramine treatment increases N-methyl-d-aspartate receptor activity and expression via epigenetic mechanisms 2015 ·European Journal of Pharmacology ·(unknown), Takae Hirasawa, Hirotake Kasai, (unknown), Kohji Moriishi, Kazuki Mochizuki, Schuichi Koizumi, Takeo Kubota	22
4	Epigenomic-Basis of Preemptive Medicine for Neurodevelopmental Disorders 2015 ·Current Genomics ·Takeo Kubota, Kunio Miyake, (unknown), Kazuki Mochizuki	6
5	Pre-B-Cell Acute Lymphoblastic Leukemia in a Boy with Hereditary Multiple Exostoses Caused byEXT1Deletion 2014 ·Pediatric Hematology and Oncology ·Takaya Nakane, Kumiko Goi, (unknown), Chihiro Kobayashi, Hidenori Sato, Takeo Kubota, Kanji Sugita	2
6	Sequence-specific microscopic visualization of DNA methylation status at satellite repeats in individual cell nuclei and chromosomes 2013 ·Nucleic Acids Research ·Yufeng Li, Yusuke Miyanari, Kenjiro Shirane, Hirohisa Nitta, Takeo Kubota, Hirofumi Ohashi, Akimitsu Okamoto, Hiroyuki Sasaki	30
7	An Xp22.12 microduplication including RPS6KA3 identified in a family with variably affected intellectual and behavioral disabilities 2013 ·Journal of Human Genetics ·Ayumi Matsumoto, (unknown), Kunio Miyake, Karin Kojima, Naomi Nakashima, Eriko F. Jimbo, Takeo Kubota, Mariko Y. Momoi, Takanori Yamagata	13
8	Epigenetic understanding of gene-environment interactions in psychiatric disorders: a new concept of clinical genetics 2012 ·Clinical Epigenetics ·Takeo Kubota, Kunio Miyake, Takae Hirasawa	109
9	Role of Complement Factor H I62V and Age-Related Maculopathy Susceptibility 2 A69S Variants in the Clinical Expression of Polypoidal Choroidal Vasculopathy 2011 ·Ophthalmology ·Yoichi Sakurada, Takeo Kubota, Mitsuhiro Imasawa, Fumihiko Mabuchi, (unknown), Naohiko Tanabe, Hiroyuki Iijima	32
10	JAK2V617F Mutation-positive Childhood Essential Thrombocythemia Associated With Cerebral Venous Sinus Thrombosis 2009 ·Journal of Pediatric Hematology/Oncology ·Hidemitsu Kurosawa, (unknown), Takashi Matsushita, Takeo Kubota, (unknown), Shigeko Kuwashima, (unknown), Yuya Sato, Keitaro Fukushima, Kenichi Sugita, (unknown), Hyuntae Park, Yasuhide Hayashi, Osamu Arisaka	8
11	One Third of Japanese Patients with Multiple Osteochondromas May Have Mutations in Genes Other Than EXT1 or EXT2 2008 ·Genetic Testing ·(unknown), Takahito Wada, (unknown), Takeo Kubota, Keiko Wakui, Yoshimitsu Fukushima	5
12	Methyl CpG-Binding Protein 2 (a Mutation of Which Causes Rett Syndrome) Directly Regulates Insulin-Like Growth Factor Binding Protein 3 in Mouse and Human Brains 2007 ·Journal of Neuropathology & Experimental Neurology ·Masayuki Itoh, (unknown), Sachio Takashima, Shinichi Kudo, Yoshiko Nomura, Masaya Segawa, Takeo Kubota, Hideo Mori, Shigeki Tanaka, Hiroshi Horie, Yuzo Tanabe, Yu‐ichi Goto	68
13	Secreted protein-based reporter systems for monitoring inflammatory events: Critical interference by endoplasmic reticulum stress 2006 ·Journal of Immunological Methods ·Nobuhiko Hiramatsu, Ayumi Kasai, Kunihiro Hayakawa, Kaoru Nagai, Takeo Kubota, Jian Yao, Masanori Kitamura	26
14	A transcriptional repressor MeCP2 causing Rett syndrome is expressed in embryonic non-neuronal cells and controls their growth 2005 ·Developmental Brain Research ·Kaoru Nagai, Kunio Miyake, Takeo Kubota	27
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	Three novel DNMT3B mutations in Japanese patients with ICF syndrome 2002 ·American Journal of Medical Genetics ·(unknown), Takeo Kubota, (unknown), Takashi Sado, Takahito Chijiwa, (unknown), Isao Suetake, Shoji Tajima, Keiko Wakui, Yukio Miki, Masatoshi Hayashi, Yoshimitsu Fukushima, Hiroyuki Sasaki	82
17	Prenatal interphase FISH diagnosis of PLP1 duplication associated with Pelizaeus–Merzbacher disease 2001 ·Prenatal Diagnosis ·Ken Inoue, Makoto Kanai, Yuzo Tanabe, Takeo Kubota, Catherine D. Kashork, Keiko Wakui, Yoshimitsu Fukushima, James R. Lupski, Lisa G. Shaffer	21
18	Molecular genetic study of japanese patients with X-linked alpha-thalassemia/mental retardation syndrome (ATR-X). 2000 ·PubMed ·Takahito Wada, Takeo Kubota, (unknown), Shinji Saitoh	17
19	Methylation Analysis of the Fragile X Syndrome by PCR 1997 ·Genetic Testing ·Soma Das, Takeo Kubota, Min‐Ae Song, Richard A. Daniel, Elizabeth Berry‐Kravis, T. Prior, Bradley W. Popovich, (unknown), Tadao Arinami, David H. Ledbetter	36
20	Excess functional copy of allele at chromosomal region 11p15 may cause Widemann‐Beckwith (EMG) syndrome 1994 ·American Journal of Medical Genetics ·Takeo Kubota, Shinji Saitoh, Tadashi Matsumoto, Kouji Narahara, Yoshimitsu Fukushima, Yoshihiro Jinno, Norio Niikawa	18

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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