Junko Kanno

1.3k total citations · 1 hit paper
33 papers, 850 citations indexed

About

Junko Kanno is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Junko Kanno has authored 33 papers receiving a total of 850 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 13 papers in Genetics and 8 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Junko Kanno's work include Sexual Differentiation and Disorders (7 papers), Metabolism and Genetic Disorders (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Junko Kanno is often cited by papers focused on Sexual Differentiation and Disorders (7 papers), Metabolism and Genetic Disorders (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Junko Kanno collaborates with scholars based in Japan, United States and Israel. Junko Kanno's co-authors include Shigeo Kure, Yoichi Matsubara, Yoko Aoki, Fumiaki Kamada, Ayumi Narisawa, Tetsuya Niihori, Shigeru Tsuchiya, Teiji Tominaga, Atsuo Kikuchi and Naoto Ishii and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Annals of Neurology and Brain Research.

In The Last Decade

Junko Kanno

31 papers receiving 844 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.

A genome-wide association study identifies RNF213 as the first Moyamoya disease gene

2010 514 citations Fumiaki Kamada, Yoko Aoki et al. Journal of Human Genetics profile →

Peers

Junko Kanno

RHEUM

NEURO

PMH

GENET

Fumiaki Kamada Japan

David Kronn United States

Shoko Komatsuzaki Germany

Yu Abe Japan

Yoichi Mashimo Japan

Peter Huppke Germany

Ting‐Rong Hsu Taiwan

Argirios Dinopoulos Greece

Thorsten Rosenbaum Germany

Davide Tonduti Italy

Fumiaki Kamada Japan

Junko Kanno

483 ×1.0

RHEUM

328 ×1.0

NEURO

249 ×0.9

238 ×1.0

PMH

112 ×0.6

GENET

Citations per year, relative to Junko Kanno Junko Kanno (= 1×) peers Fumiaki Kamada

Countries citing papers authored by Junko Kanno

Since Specialization

Citations

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

Fields of papers citing papers by Junko Kanno

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Junko Kanno

This figure shows the co-authorship network connecting the top 25 collaborators of Junko Kanno. A scholar is included among the top collaborators of Junko Kanno 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 Junko Kanno. Junko Kanno 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

Kanno, Junko, Sayaka Kawashima, Hirohito Shima, et al.. (2024). A case of 49,XXXYY followed-up from infancy to adulthood with review of literature. Endocrine Journal. 71(7). 721–727.

Kitaoka, Taichi, Takuo Kubota, Junko Kanno, et al.. (2024). Clinical outcomes and medical management of achondroplasia in Japanese children: A retrospective medical record review of clinical data. American Journal of Medical Genetics Part A. 194(8). e63612–e63612. 3 indexed citations

Nakagawa, Tomohiro, et al.. (2024). Hearing loss with two pathogenic SLC26A4 variants and positive thyroid autoantibody: A case report. Clinical Pediatric Endocrinology. 33(4). 219–223. 1 indexed citations

Takayama, Jun, et al.. (2024). Idiopathic infantile hypercalcemia with a CYP24A1 variant triggered by vitamin D supplementation in fortified milk: A case report. Clinical Pediatric Endocrinology. 34(1). 60–65.

Suzuki, Dai, et al.. (2024). Trends in endogenous insulin secretion capacity and anti-islet autoantibody titers in two childhood-onset slowly progressive insulin-dependent diabetes mellitus cases. Clinical Pediatric Endocrinology. 33(4). 238–243. 2 indexed citations

Kawashima, Sayaka, et al.. (2024). Severe growth retardation during carbohydrate restriction in type 1 diabetes mellitus: A case report. Clinical Pediatric Endocrinology. 33(3). 181–186. 2 indexed citations

Kanno, Junko, Dai Suzuki, Sayaka Kawashima, et al.. (2019). A Follow-Up from Infancy to Puberty in a Japanese Male with SRY-Negative 46,XX Testicular Disorder of Sex Development Carrying a p.Arg92Trp Mutation in NR5A1. Sexual Development. 13(2). 60–66. 3 indexed citations

Kanno, Junko, et al.. (2017). Responsiveness to pamidronate treatment is not related to the genotype of type I collagen in patients with osteogenesis imperfecta. Journal of Bone and Mineral Metabolism. 36(3). 344–351. 5 indexed citations

Shima, Hirohito, Junko Kanno, Erina Suzuki, et al.. (2017). Xp22.31 Microdeletion due to Microhomology-Mediated Break-Induced Replication in a Boy with Contiguous Gene Deletion Syndrome. Cytogenetic and Genome Research. 151(1). 1–4. 12 indexed citations

10.

Igarashi, Maki, Kei Takasawa, Junko Kanno, et al.. (2016). IdenticalNR5A1Missense Mutations in Two Unrelated 46,XX Individuals with Testicular Tissues. Human Mutation. 38(1). 39–42. 41 indexed citations

11.

Miyado, Mami, Masafumi Inui, Maki Igarashi, et al.. (2016). The p.R92W variant of NR5A1/Nr5a1 induces testicular development of 46,XX gonads in humans, but not in mice: phenotypic comparison of human patients and mutation-induced mice. Biology of Sex Differences. 7(1). 56–56. 19 indexed citations

12.

Fujiwara, Ikuma, Yoshiko Murakami, Tetsuya Niihori, et al.. (2015). Mutations in PIGL in a patient with Mabry syndrome. American Journal of Medical Genetics Part A. 167(4). 777–785. 26 indexed citations

13.

Kamada, Fumiaki, Yoko Aoki, Ayumi Narisawa, et al.. (2010). A genome-wide association study identifies RNF213 as the first Moyamoya disease gene. Journal of Human Genetics. 56(1). 34–40. 514 indexed citations breakdown →

14.

Kiyoshige, Yoshiro, Shigeo Kure, Kaoru Goto, et al.. (2007). Inherited risk factors for deep venous thrombosis following total hip arthroplasty in Japanese patients: matched control study. Journal of Orthopaedic Science. 12(2). 118–122. 3 indexed citations

15.

Sato, Kenichi, Junko Kanno, Teiji Tominaga, Yoichi Matsubara, & Shigeo Kure. (2006). De novo and salvage pathways of DNA synthesis in primary cultured neurall stem cells. Brain Research. 1071(1). 24–33. 12 indexed citations

16.

Kure, Shigeo, Stanley H. Korman, Junko Kanno, et al.. (2006). Rapid diagnosis of glycine encephalopathy by ¹³C‐glycine breath test. Annals of Neurology. 59(5). 862–867. 14 indexed citations

17.

Kamada, Fumiaki, Shigeo Kure, Takayuki Kudo, et al.. (2006). A novel KCNQ4 one-base deletion in a large pedigree with hearing loss: implication for the genotype–phenotype correlation. Journal of Human Genetics. 51(5). 455–460. 40 indexed citations

18.

Korman, Stanley H., Isaiah D. Wexler, Alisa Gutman, et al.. (2006). Treatment from birth of nonketotic hyperglycinemia due to a novel GLDC mutation. Annals of Neurology. 59(2). 411–415. 41 indexed citations

19.

Boneh, Avihu, Stanley H. Korman, Ken‐ichi Sato, et al.. (2005). A single nucleotide substitution that abolishes the initiator methionine codon of the GLDC gene is prevalent among patients with glycine encephalopathy in Jerusalem. Journal of Human Genetics. 50(5). 230–234. 19 indexed citations

20.

Nakazawa, Chifuyu, et al.. (1997). A Comparative Study of 95 Previous Cases with Kawasaki Disease and 101 Recent Cases The Relation between Coronary Arterial Lesions and Gamma-globulin Therapy. 101(12). 1686–1692. 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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