Ikuko Kondo

6.9k total citations
128 papers, 3.8k citations indexed

About

Ikuko Kondo is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ikuko Kondo has authored 128 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Molecular Biology, 44 papers in Genetics and 28 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ikuko Kondo's work include Genetic Neurodegenerative Diseases (21 papers), Genetics and Neurodevelopmental Disorders (21 papers) and Genomic variations and chromosomal abnormalities (15 papers). Ikuko Kondo is often cited by papers focused on Genetic Neurodegenerative Diseases (21 papers), Genetics and Neurodevelopmental Disorders (21 papers) and Genomic variations and chromosomal abnormalities (15 papers). Ikuko Kondo collaborates with scholars based in Japan, United States and Norway. Ikuko Kondo's co-authors include Tetsuro Miki, Hideo Hamaguchi, N Shimizu, Dennis Drayna, Richard Lawn, Mitsutoshi Yamamoto, Yasuharu Tabara, Keiko Kobayashi, Tomotsugu Yasuda and Mikio Iijima and has published in prestigious journals such as Nature Genetics, Neurology and Annals of Neurology.

In The Last Decade

Ikuko Kondo

126 papers receiving 3.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ikuko Kondo Japan 33 1.7k 1.2k 585 561 499 128 3.8k
Vardiella Meiner Israel 31 1.1k 0.7× 604 0.5× 156 0.3× 1.1k 2.0× 214 0.4× 128 3.2k
Mira Irons United States 30 1.8k 1.0× 632 0.5× 210 0.4× 1.4k 2.5× 102 0.2× 82 3.2k
R. Mark Gardiner United Kingdom 22 1.6k 0.9× 309 0.3× 188 0.3× 730 1.3× 499 1.0× 34 3.3k
Harvey W. Mohrenweiser United States 36 3.2k 1.8× 874 0.7× 86 0.1× 257 0.5× 772 1.5× 67 6.1k
Yair Anikster Israel 36 1.9k 1.1× 475 0.4× 977 1.7× 158 0.3× 247 0.5× 132 4.2k
Helena Stibler Sweden 38 2.3k 1.3× 237 0.2× 366 0.6× 275 0.5× 178 0.4× 95 4.1k
Kazuhiro Oka United States 34 1.9k 1.1× 770 0.6× 138 0.2× 844 1.5× 353 0.7× 74 3.8k
J. A. Maassen Netherlands 37 3.7k 2.1× 691 0.6× 1.2k 2.1× 1.1k 1.9× 206 0.4× 95 5.0k
Mary B. Davis United Kingdom 39 2.3k 1.3× 461 0.4× 292 0.5× 187 0.3× 1.8k 3.6× 111 4.3k
Daniel K. Burns United States 31 2.1k 1.2× 914 0.8× 110 0.2× 422 0.8× 143 0.3× 80 4.0k

Countries citing papers authored by Ikuko Kondo

Since Specialization
Citations

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

Fields of papers citing papers by Ikuko Kondo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ikuko Kondo

This figure shows the co-authorship network connecting the top 25 collaborators of Ikuko Kondo. A scholar is included among the top collaborators of Ikuko Kondo 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 Ikuko Kondo. Ikuko Kondo 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.
Komatsuzaki, Shoko, Yoko Aoki, Tetsuya Niihori, et al.. (2010). Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies. Journal of Human Genetics. 55(12). 801–809. 35 indexed citations
2.
Ishikawa, Kinya, M Sakamoto, Taiji Tsunemi, et al.. (2008). Direct and accurate measurement of CAG repeat configuration in the ataxin-1 (ATXN-1) gene by “dual-fluorescence labeled PCR-restriction fragment length analysis”. Journal of Human Genetics. 53(4). 287–295. 4 indexed citations
3.
Mitsuda, Noriaki, Hidehisa Yamagata, Wangtao Zhong, et al.. (2005). A novel alternative splice variant of nicastrin and its implication in Alzheimer disease. Life Sciences. 78(21). 2444–2448. 4 indexed citations
4.
Zhong, Wangtao, Hidehisa Yamagata, Keiko Taguchi, et al.. (2005). Lymphocyte-specific protein tyrosine kinase is a novel risk gene for Alzheimer disease. Journal of the Neurological Sciences. 238(1-2). 53–57. 7 indexed citations
5.
Taguchi, Keiko, Hidehisa Yamagata, Wangtao Zhong, et al.. (2005). Identification of hippocampus‐related candidate genes for Alzheimer's disease. Annals of Neurology. 57(4). 585–588. 35 indexed citations
6.
Shimizu, Atsushi, Shuichi Asakawa, Takashi Sasaki, et al.. (2003). A novel giant gene CSMD3 encoding a protein with CUB and sushi multiple domains: a candidate gene for benign adult familial myoclonic epilepsy on human chromosome 8q23.3–q24.1. Biochemical and Biophysical Research Communications. 309(1). 143–154. 63 indexed citations
7.
Yu, Yang, Katsuyuki Ohmori, Ikuko Kondo, et al.. (2002). Correlation of functional and structural alterations of the coronary arterioles during development of type II diabetes mellitus in rats. Cardiovascular Research. 56(2). 303–311. 36 indexed citations
8.
Yamagata, Hidehisa, Kouzin Kamino, Takuo Nomura, et al.. (2001). Genetic Association between Alzheimer Disease and the Alpha-Synuclein Gene. Dementia and Geriatric Cognitive Disorders. 12(2). 106–109. 20 indexed citations
9.
Watanabe, Masao, Ikuko Kondo, Koichi Okamoto, et al.. (1999). Analysis of spinocerebellar ataxia type 2 gene and haplotype analysis: (CCG)1- 2 polymorphism and contribution to founder effect. Journal of Medical Genetics. 36(2). 112–114.
10.
Kondo, Ikuko, Kiyomi Mizugishi, Tadafumi Hashimoto, et al.. (1999). Missense mutations in phosphomannomutase 2 gene in two Japanese families with carbohydrate‐deficient glycoprotein syndrome type 1. Clinical Genetics. 55(1). 50–54. 19 indexed citations
11.
Kondo, Ikuko & Mitsutoshi Yamamoto. (1998). Genetic polymorphism of paraoxonase 1 (PON1) and susceptibility to Parkinson's disease. Brain Research. 806(2). 271–273. 72 indexed citations
12.
Yamamoto, Mitsutoshi, Ikuko Kondo, Norio Ogawa, et al.. (1997). Genetic association between susceptibility to Parkinson's disease and α1-antichymotrypsin polymorphism. Brain Research. 759(1). 153–155. 28 indexed citations
13.
Hattori, Haruo, Yoshihisa Higuchi, Takehiko Okuno, et al.. (1997). Early‐Childhood Progressive Myoclonus Epilepsy Presenting as Partial Seizures in Dentatorubral‐Pallidoluysian Atrophy. Epilepsia. 38(3). 271–274. 6 indexed citations
14.
Uyama, Eiichiro, Ikuko Kondo, Makoto Uchino, et al.. (1995). Dentatorubral-pallidoluysian atrophy (DRPLA): clinical, genetic, and neuroradiologic studies in a family. Journal of the Neurological Sciences. 130(2). 146–153. 47 indexed citations
15.
Hadano, Shinji, Masahiko Watanabe, Haruhiko Yokoi, et al.. (1991). Laser microdissection and single unique primer PCR allow generation of regional chromosome DNA clones from a single human chromosome. Genomics. 11(2). 364–373. 48 indexed citations
16.
Kondo, Ikuko, et al.. (1991). Weaver syndrome in two Japanese children. American Journal of Medical Genetics. 41(2). 221–224. 8 indexed citations
17.
Kondo, Ikuko, et al.. (1990). The Cohen syndrome: Does mottled retina separate a finnish and a jewish type?. American Journal of Medical Genetics. 37(1). 109–113. 33 indexed citations
18.
Kondo, Ikuko, et al.. (1990). A Japanese male infant with the weaver syndrome. The Japanese Journal of Human Genetics. 35(3). 257–262. 5 indexed citations
19.
20.
Kobayashi, Yutaka, T Haruta, Takashi Fukaya, et al.. (1975). CLINICAL EVALUATION OF FOSFOMYCIN NATRIUM SALT IN CHILDREN. 23(11). 3433–3441. 1 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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