Hideaki Sawai

1.9k total citations
67 papers, 1.2k citations indexed

About

Hideaki Sawai is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Hideaki Sawai has authored 67 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 18 papers in Molecular Biology and 17 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Hideaki Sawai's work include Prenatal Screening and Diagnostics (13 papers), Connective tissue disorders research (12 papers) and Genomic variations and chromosomal abnormalities (6 papers). Hideaki Sawai is often cited by papers focused on Prenatal Screening and Diagnostics (13 papers), Connective tissue disorders research (12 papers) and Genomic variations and chromosomal abnormalities (6 papers). Hideaki Sawai collaborates with scholars based in Japan, United States and France. Hideaki Sawai's co-authors include Hiroyuki Yamamoto, Manuel Perucho, Shiro Ikegawa, Koji Koyama, Shinji Komori, Gen Nishimura, Miho Morioka, Minoru Okada, Noriyuki Tsumaki and Akihiro Yamashita and has published in prestigious journals such as Nature, Human Molecular Genetics and Molecular Biology and Evolution.

In The Last Decade

Hideaki Sawai

66 papers receiving 1.1k citations

Peers

Hideaki Sawai

GENET

PFM

SURGE

ONCOL

Takuya Naruto Japan

K. Morgan Canada

Alexandros Lambropoulos Greece

Masami Inoue Japan

Leo P. de Waal Netherlands

Susana Seixas Portugal

Katrin van der Ven Germany

Barbara A. Innes United Kingdom

D. McGibbon United Kingdom

Margaret G. Petroff United States

Takuya Naruto Japan

Hideaki Sawai

588 ×1.2

423 ×1.4

GENET

95 ×0.4

PFM

143 ×0.7

SURGE

143 ×0.9

ONCOL

Citations per year, relative to Hideaki Sawai Hideaki Sawai (= 1×) peers Takuya Naruto

Countries citing papers authored by Hideaki Sawai

Since Specialization

Citations

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

Fields of papers citing papers by Hideaki Sawai

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hideaki Sawai

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

Takahashi, H., Yoji Okamoto, Takashi Hamada, et al.. (2023). Soft- and Hard-Error Radiation Reliability of 228 KB $3\mathrm{T}+1\mathrm{C}$ Oxide Semiconductor Memory. 1–6. 2 indexed citations

Sawai, Hideaki, et al.. (2021). Development of individuals with thanatophoric dysplasia surviving beyond infancy. Pediatrics International. 64(1). e15007–e15007. 4 indexed citations

Setoh, Kazuya, Meiko Takahashi, Koichiro Higasa, et al.. (2019). Association of ALPL variants with serum alkaline phosphatase and bone traits in the general Japanese population: The Nagahama Study. Journal of Human Genetics. 65(3). 337–343. 3 indexed citations

Sawai, Hideaki, Kaname Oka, Gen Nishimura, et al.. (2019). National survey of prevalence and prognosis of thanatophoric dysplasia in Japan. Pediatrics International. 61(8). 748–753. 11 indexed citations

Wakimoto, Yu, et al.. (2018). A Case of a Pregnant Woman with Thrombosis in an Artificial Aortic Valve Resulting in Severe Cerebral Hemorrhage in the Newborn. Case Reports in Obstetrics and Gynecology. 2018(1). 6154382–6154382. 1 indexed citations

Saito, Tomoko, Keisuke Nagasaki, Gen Nishimura, et al.. (2016). Criteria for radiologic diagnosis of hypochondroplasia in neonates. Pediatric Radiology. 46(4). 513–518. 7 indexed citations

Miyake, Hidehiko, Shigehito Yamada, Yosuke Fujii, et al.. (2016). Nationwide survey for current clinical status of amniocentesis and maternal serum marker test in Japan. Journal of Human Genetics. 61(10). 879–884. 4 indexed citations

Suzumori, Nobuhiro, Takeshi Ebara, Takahiro Yamada, et al.. (2016). Fetal cell-free DNA fraction in maternal plasma is affected by fetal trisomy. Journal of Human Genetics. 61(7). 647–652. 46 indexed citations

Khor, Seik‐Soon, Wanling Yang, M. Kawashima, et al.. (2015). High-accuracy imputation for HLA class I and II genes based on high-resolution SNP data of population-specific references. The Pharmacogenomics Journal. 15(6). 530–537. 35 indexed citations

10.

Tsubamoto, Hiroshi, et al.. (2013). A large seminoma occurring 20years after diagnosis of complete androgen insensitivity syndrome: A case report. PubMed. 5. 16–18. 2 indexed citations

11.

Yamada, Takahiro, Masaki Takagi, Gen Nishimura, et al.. (2012). Recurrence of osteogenesis imperfecta due to maternal mosaicism of a novel COL1A1 mutation. American Journal of Medical Genetics Part A. 158A(11). 2969–2971. 1 indexed citations

12.

Tada, Noriko, Shiro Hinotsu, Hisashi Urushihara, et al.. (2011). The current status of umbilical cord blood collection in Japanese medical centers: Survey of obstetricians. Transfusion and Apheresis Science. 44(3). 263–268. 3 indexed citations

13.

Sawai, Hideaki, et al.. (2011). Prenatal diagnosis of Kniest dysplasia with three-dimensional helical computed tomography. The Journal of Maternal-Fetal & Neonatal Medicine. 24(9). 1181–1184. 9 indexed citations

14.

Watanabe, Atsushi, Tatsuki Karasugi, Hideaki Sawai, et al.. (2010). Prevalence of c.1559delT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypophosphatasia in Japanese and effects of the mutation on heterozygous carriers. Journal of Human Genetics. 56(2). 166–168. 56 indexed citations

15.

Hikosaka, Kenji, Yoh‐ichi Watanabe, Naotoshi Tsuji, et al.. (2009). Divergence of the Mitochondrial Genome Structure in the Apicomplexan Parasites, Babesia and Theileria. Molecular Biology and Evolution. 27(5). 1107–1116. 89 indexed citations

16.

Wada, Yuka, Gen Nishimura, Toshiro Nagai, et al.. (2009). Mutation analysis of SOX9 and single copy number variant analysis of the upstream region in eight patients with campomelic dysplasia and acampomelic campomelic dysplasia. American Journal of Medical Genetics Part A. 149A(12). 2882–2885. 13 indexed citations

17.

Maeda, Koichi, Yoshinari Miyamoto, Hideaki Sawai, et al.. (2006). A compound heterozygote harboring novel and recurrent DTDST mutations with intermediate phenotype between atelosteogenesis type II and diastrophic dysplasia. American Journal of Medical Genetics Part A. 140A(11). 1143–1147. 11 indexed citations

18.

Kataoka, Soromon, Hideaki Sawai, Hideto Yamada, et al.. (2004). Radiographic and genetic diagnosis of sporadic hypochondroplasia early in the neonatal period. Prenatal Diagnosis. 24(1). 45–49. 8 indexed citations

19.

Sawai, Hideaki, Minoru Shigeta, Shinji Komori, et al.. (1995). Direct Production of the Fab Fragment Derived From the Sperm Immobilizing Antibody Using Polymerase Chain Reaction and cDNA Expression Vectors. American Journal of Reproductive Immunology. 34(1). 26–34. 4 indexed citations

20.

Sawai, Hideaki, et al.. (1993). Stable Production of Recombinant Human Sperm Immobilizing Antibody Using cDNA Expression Vectors. American Journal of Reproductive Immunology. 29(2). 100–108. 2 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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