Junichiro Machida

2.0k total citations
32 papers, 1.0k citations indexed

About

Junichiro Machida is a scholar working on Molecular Biology, Genetics and Oral Surgery. According to data from OpenAlex, Junichiro Machida has authored 32 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 18 papers in Genetics and 12 papers in Oral Surgery. Recurrent topics in Junichiro Machida's work include Cleft Lip and Palate Research (15 papers), dental development and anomalies (14 papers) and Oral and Maxillofacial Pathology (12 papers). Junichiro Machida is often cited by papers focused on Cleft Lip and Palate Research (15 papers), dental development and anomalies (14 papers) and Oral and Maxillofacial Pathology (12 papers). Junichiro Machida collaborates with scholars based in Japan, United States and United Kingdom. Junichiro Machida's co-authors include Kazuo Shimozato, Jeffrey C. Murray, Masahiko Toyama, Hidemichi Yuasa, K. Kurita, Nobumi Ogi, P L Westesson, Sandra Daack‐Hirsch, Andrew C. Lidral and Aurora A. Burds and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Junichiro Machida

32 papers receiving 966 citations

Peers

Junichiro Machida

GENET

RHEUM

CMT

Domenico Scopelliti Italy

Koji Hanada Japan

Naoya Izumi Japan

Shushu He China

Mohong Deng China

Eliane H. Dutra United States

H.J.J. Blackwood United Kingdom

Qinggong Meng China

Chang-Hyeon An South Korea

Sawa Kaneko Japan

Domenico Scopelliti Italy

Junichiro Machida

226 ×0.4

GENET

396 ×0.8

36 ×0.1

57 ×0.3

RHEUM

42 ×0.2

CMT

Citations per year, relative to Junichiro Machida Junichiro Machida (= 1×) peers Domenico Scopelliti

Countries citing papers authored by Junichiro Machida

Since Specialization

Citations

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

Fields of papers citing papers by Junichiro Machida

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Junichiro Machida

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

Izumi, Hiroto, Takeshi Nishiyama, Atsuo Nakayama, et al.. (2023). Novel WNT10A variant in a Japanese case of nonsyndromic oligodontia. Human Genome Variation. 10(1). 3–3. 2 indexed citations

Goto, Hiroki, Atsuo Nakayama, Takeshi Nishiyama, et al.. (2021). Novel MSX1 frameshift mutation in a Japanese family with nonsyndromic oligodontia. Human Genome Variation. 8(1). 29–29. 3 indexed citations

Goto, Hiroki, Masashi Kimura, Junichiro Machida, et al.. (2021). A novel LRP6 variant in a Japanese family with oligodontia. Human Genome Variation. 8(1). 30–30. 6 indexed citations

Machida, Junichiro, Hiroaki Goto, Akio Shibata, et al.. (2017). WNT10A variants isolated from Japanese patients with congenital tooth agenesis. Human Genome Variation. 4(1). 17047–17047. 18 indexed citations

Goto, Hiroki, Junichiro Machida, Akio Shibata, et al.. (2016). Novel RUNX2/CBFA1 mutation in the runt domain in a Japanese patient with cleidocranial dysplasia. Journal of Oral and Maxillofacial Surgery Medicine and Pathology. 29(3). 222–224. 1 indexed citations

Nagao, Toru, Saman Warnakulasuriya, Shogo Hasegawa, et al.. (2016). Elucidating risk factors for oral leukoplakia affecting gingivae in Japanese subjects. SHILAP Revista de lepidopterología. 1. 8 indexed citations

Kimura, Masashi, Mitsuko Nakashima, Junichiro Machida, et al.. (2015). An Aberrant Splice Acceptor Site Due to a Novel Intronic Nucleotide Substitution in MSX1 Gene Is the Cause of Congenital Tooth Agenesis in a Japanese Family. PLoS ONE. 10(6). e0128227–e0128227. 21 indexed citations

Lidral, Andrew C., Huan Liu, Steven A. Bullard, et al.. (2015). A single nucleotide polymorphism associated with isolated cleft lip and palate, thyroid cancer and hypothyroidism alters the activity of an oral epithelium and thyroid enhancer near FOXE1. Human Molecular Genetics. 24(14). 3895–3907. 34 indexed citations

Shibata, Akio, Junichiro Machida, Masashi Kimura, et al.. (2015). Characterisation of novel RUNX2 mutation with alanine tract expansion from Japanese cleidocranial dysplasia patient. Mutagenesis. 31(1). gev057–gev057. 17 indexed citations

10.

Machida, Junichiro, Masashi Kimura, Akio Shibata, et al.. (2014). Characterization of Novel MSX1 Mutations Identified in Japanese Patients with Nonsyndromic Tooth Agenesis. PLoS ONE. 9(8). e102944–e102944. 27 indexed citations

11.

Kimura, Masashi, Yoshihito Tokita, Junichiro Machida, et al.. (2014). A novel PITX2 mutation causing iris hypoplasia. Human Genome Variation. 1(1). 14005–14005. 8 indexed citations

12.

Kimura, Masashi, Toru Nagao, Junichiro Machida, & Saman Warnakulasuriya. (2012). Mutation of keratin 4 gene causing white sponge nevus in a Japanese family. International Journal of Oral and Maxillofacial Surgery. 42(5). 615–618. 21 indexed citations

13.

Machida, Junichiro, Masashi Kimura, Takao Ono, et al.. (2011). Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia. European Journal of Human Genetics. 19(8). 844–850. 21 indexed citations

14.

Machida, Junichiro, et al.. (2010). Massive immature teratoma in a neonate. International Journal of Oral and Maxillofacial Surgery. 39(10). 1020–1023. 12 indexed citations

15.

Mizuno, Seiji, Kenjiro Kosaki, Junichiro Machida, et al.. (2006). Monopolar preparation of human lymphocytes for evaluation of the metaphase chromosome alignment. Chromosome science. 9(3). 75–83. 1 indexed citations

16.

Yoshiura, Koh-ichiro, Junichiro Machida, Teruyuki Niimi, et al.. (2004). Two missense mutations in the IRF6 gene in two Japanese families with Van der Woude syndrome. Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology. 98(4). 414–417. 17 indexed citations

17.

Suzuki, Yasushi, Peter A. Jezewski, Junichiro Machida, et al.. (2004). In a Vietnamese population, MSX1 variants contribute to cleft lip and palate. Genetics in Medicine. 6(3). 117–125. 97 indexed citations

18.

Machida, Junichiro, et al.. (1999). Transforming Growth Factor-α (TGFA): Genomic Structure, Boundary Sequences, and Mutation Analysis in Nonsyndromic Cleft Lip/Palate and Cleft Palate Only. Genomics. 61(3). 237–242. 38 indexed citations

19.

Yoshiura, Koh-ichiro, Junichiro Machida, Sandra Daack‐Hirsch, et al.. (1998). Characterization of a Novel Gene Disrupted by a Balanced Chromosomal Translocation t(2;19)(q11.2;q13.3) in a Family with Cleft Lip and Palate. Genomics. 54(2). 231–240. 57 indexed citations

20.

Lidral, Andrew C., Paul A. Romitti, Ann M. Basart, et al.. (1998). Association of MSX1 and TGFB3 with Nonsyndromic Clefting in Humans. The American Journal of Human Genetics. 63(2). 557–568. 255 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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