Eri Kondo-Iida

1.2k total citations · 1 hit paper
13 papers, 939 citations indexed

About

Eri Kondo-Iida is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Eri Kondo-Iida has authored 13 papers receiving a total of 939 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 3 papers in Cellular and Molecular Neuroscience and 2 papers in Genetics. Recurrent topics in Eri Kondo-Iida's work include Muscle Physiology and Disorders (13 papers), RNA modifications and cancer (8 papers) and Mitochondrial Function and Pathology (4 papers). Eri Kondo-Iida is often cited by papers focused on Muscle Physiology and Disorders (13 papers), RNA modifications and cancer (8 papers) and Mitochondrial Function and Pathology (4 papers). Eri Kondo-Iida collaborates with scholars based in Japan and Belgium. Eri Kondo-Iida's co-authors include Tatsushi Toda, Kazuhiro Kobayashi, Kayoko Saito, Yusuke Nakamura, Makiko Ōsawa, Yutaka Nakahori, Yasuo Nakagome, Yoshiko Nomura, Ikuya Nonaka and Kiichiro Matsumura and has published in prestigious journals such as Nature, FEBS Letters and Human Molecular Genetics.

In The Last Decade

Eri Kondo-Iida

13 papers receiving 927 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

1998 624 citations Kazuhiro Kobayashi, Yutaka Nakahori et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Eri Kondo-Iida Japan	8	842	209	113	107	105	13	939
K Hart United Kingdom	12	703 0.8×	113 0.5×	104 0.9×	59 0.6×	182 1.7×	15	786
Lau A.J. Blonden Netherlands	12	727 0.9×	93 0.4×	114 1.0×	64 0.6×	172 1.6×	15	861
Sophie Currier United States	7	682 0.8×	141 0.7×	94 0.8×	122 1.1×	79 0.8×	7	811
Paola Prandini Italy	11	799 0.9×	152 0.7×	81 0.7×	144 1.3×	189 1.8×	15	1.0k
Alice Steinbrecher Germany	5	638 0.8×	125 0.6×	85 0.8×	118 1.1×	83 0.8×	7	725
Michał Milewski Poland	12	605 0.7×	107 0.5×	93 0.8×	253 2.4×	26 0.2×	34	1.1k
Jeffrey Murray United Kingdom	7	605 0.7×	100 0.5×	51 0.5×	30 0.3×	90 0.9×	8	766
Pierre Miniou France	13	611 0.7×	87 0.4×	51 0.5×	51 0.5×	16 0.2×	15	752
H.M. Kozman Australia	15	483 0.6×	64 0.3×	86 0.8×	77 0.7×	112 1.1×	23	706
Yeliz Yuva United Kingdom	8	567 0.7×	202 1.0×	51 0.5×	124 1.2×	149 1.4×	9	653

Countries citing papers authored by Eri Kondo-Iida

Since Specialization

Citations

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

Fields of papers citing papers by Eri Kondo-Iida

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eri Kondo-Iida

This figure shows the co-authorship network connecting the top 25 collaborators of Eri Kondo-Iida. A scholar is included among the top collaborators of Eri Kondo-Iida 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 Eri Kondo-Iida. Eri Kondo-Iida is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

Kobayashi, Kazuhiro, Reiko Kato, Eri Kondo-Iida, et al.. (2017). Deep-intronic variant of fukutin is the most prevalent point mutation of Fukuyama congenital muscular dystrophy in Japan. Journal of Human Genetics. 62(11). 945–948. 9 indexed citations

Kobayashi, Kazuhiro, Junko Sasaki, Eri Kondo-Iida, et al.. (2001). Structural organization, complete genomic sequences and mutational analyses of the Fukuyama‐type congenital muscular dystrophy gene, fukutin. FEBS Letters. 489(2-3). 192–196. 35 indexed citations

Saito, Kayoko, Makiko Ōsawa, Zhiping Wang, et al.. (2000). Haplotype-Phenotype correlation in Fukuyama congenital muscular dystrophy. American Journal of Medical Genetics. 92(3). 184–190. 32 indexed citations

Matsui, T, Kumiko Ando, Eri Kondo-Iida, et al.. (2000). A case of Walker–Warburg syndrome. Brain and Development. 22(7). 454–457. 6 indexed citations

Matsuzaka, Tetsuo, Osamu Kobayashi, Eri Kondo-Iida, et al.. (2000). Walker–Warburg syndrome is genetically distinct from Fukuyama type congenital muscular dystrophy. Journal of the Neurological Sciences. 177(2). 150–153. 6 indexed citations

Toda, Tatsushi, et al.. (2000). The Fukuyama congenital muscular dystrophy story. Neuromuscular Disorders. 10(3). 153–159. 57 indexed citations

Saito, Kayoko, Yukio Fukuyama, Eri Kondo-Iida, et al.. (1999). Congenital muscular dystrophy with central and peripheral nervous system involvement in a Belgian patient. Neuromuscular Disorders. 9(4). 251–256. 7 indexed citations

Kondo-Iida, Eri, Kazuhiro Kobayashi, Masao Watanabe, et al.. (1999). Novel Mutations and Genotype-Phenotype Relationships in 107 Families With Fukuyama-Type Congenital Muscular Dystrophy (FCMD). Human Molecular Genetics. 8(12). 2303–2309. 134 indexed citations

Kobayashi, Kazuhiro, Yutaka Nakahori, Masashi Miyake, et al.. (1998). An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy. Nature. 394(6691). 388–392. 624 indexed citations breakdown →

10.

Saito, Kayoko, Eri Kondo-Iida, Juan Du, et al.. (1998). Prenatal diagnosis of Fukuyama type congenital muscular dystrophy in eight Japanese families by haplotype analysis using new markers closest to the gene. American Journal of Medical Genetics. 77(4). 310–316. 9 indexed citations

11.

Kondo-Iida, Eri, Kayoko Saito, Hajime Tanaka, et al.. (1997). Molecular genetic evidence of clinical heterogeneity in Fukuyama-type congenital muscular dystrophy. Human Genetics. 99(4). 427–432. 16 indexed citations

12.

Saito, Kayoko, Eri Kondo-Iida, Kiyoko Ikeya, et al.. (1997). Molecular evidence of clinical heterogeneity in Fukuyama type congenital muscular dystrophy. Neuromuscular Disorders. 7(6-7). 429–429. 1 indexed citations

13.

Kondo-Iida, Eri, Kayoko Saito, Makiko Ōsawa, et al.. (1997). Polymorphism analysis of Fukuyama type congenital muscular dystrophy (FCMD) siblings with different phenotypes. Brain and Development. 19(3). 181–186. 3 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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