Hirohito Shima

639 total citations
29 papers, 313 citations indexed

About

Hirohito Shima is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Hirohito Shima has authored 29 papers receiving a total of 313 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 11 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Hirohito Shima's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Congenital Ear and Nasal Anomalies (6 papers) and Sexual Differentiation and Disorders (4 papers). Hirohito Shima is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Congenital Ear and Nasal Anomalies (6 papers) and Sexual Differentiation and Disorders (4 papers). Hirohito Shima collaborates with scholars based in Japan, United States and Germany. Hirohito Shima's co-authors include Maki Fukami, Satoshi Narumi, Tsutomu Ogata, Erina Suzuki, Keiko Matsubara, Akie Nakamura, Weizhen Ji, Akira Satoh, James McGrath and Ramona Jühlen and has published in prestigious journals such as PLoS ONE, Journal of Medical Genetics and European Journal of Endocrinology.

In The Last Decade

Hirohito Shima

27 papers receiving 299 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hirohito Shima Japan 11 149 140 65 40 34 29 313
P.M. Chou United States 9 192 1.3× 77 0.6× 65 1.0× 20 0.5× 13 0.4× 17 321
Teresa Vendrell Spain 12 160 1.1× 143 1.0× 45 0.7× 34 0.8× 11 0.3× 25 310
Juliana Godoy Assumpção Brazil 10 175 1.2× 101 0.7× 32 0.5× 10 0.3× 22 0.6× 19 304
Shu‐Chin Chien Taiwan 10 84 0.6× 73 0.5× 44 0.7× 9 0.2× 29 0.9× 32 309
Chantal Farra Lebanon 10 139 0.9× 120 0.9× 22 0.3× 8 0.2× 21 0.6× 29 337
F. H. Menko Netherlands 8 116 0.8× 137 1.0× 44 0.7× 28 0.7× 18 0.5× 12 396
M.G. Tibiletti Italy 11 142 1.0× 102 0.7× 49 0.8× 18 0.5× 13 0.4× 25 441
Ulrike Gamerdinger Germany 11 190 1.3× 105 0.8× 35 0.5× 60 1.5× 55 1.6× 20 398
Nicola Foster United Kingdom 9 155 1.0× 91 0.7× 43 0.7× 9 0.2× 14 0.4× 11 320
AnneMarie Vos Netherlands 7 169 1.1× 88 0.6× 196 3.0× 17 0.4× 17 0.5× 8 350

Countries citing papers authored by Hirohito Shima

Since Specialization
Citations

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

Fields of papers citing papers by Hirohito Shima

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hirohito Shima

This figure shows the co-authorship network connecting the top 25 collaborators of Hirohito Shima. A scholar is included among the top collaborators of Hirohito Shima 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 Hirohito Shima. Hirohito Shima 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.
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.
2.
Nakagawa, Tomohiro, et al.. (2024). Hearing loss with two pathogenic <i>SLC26A4</i> variants and positive thyroid autoantibody: A case report. Clinical Pediatric Endocrinology. 33(4). 219–223. 1 indexed citations
3.
4.
Sano, Shinichiro, Sayaka Kawashima, Akie Nakamura, et al.. (2023). (Epi)genetic and clinical characteristics in 84 patients with pseudohypoparathyroidism type 1B. European Journal of Endocrinology. 189(6). 590–600. 1 indexed citations
5.
Hattori, Atsushi, Hirohito Shima, Akira Ishiguro, et al.. (2019). Unbalanced Y;7 Translocation between Two Low-Similarity Sequences Leading to SRY-Positive 45,X Testicular Disorders of Sex Development. Cytogenetic and Genome Research. 158(3). 115–120. 2 indexed citations
6.
Hattori, Atsushi, Erina Suzuki, Hirohito Shima, et al.. (2019). DNA Methylation Status of SHOX-Flanking CpG Islands in Healthy Individuals and Short Stature Patients with Pseudoautosomal Copy Number Variations. Cytogenetic and Genome Research. 158(2). 56–62. 5 indexed citations
7.
Shima, Hirohito, Atsushi Hijikata, Yûkô Fukui, et al.. (2019). WDR11 is another causative gene for coloboma, cardiac anomaly and growth retardation in 10q26 deletion syndrome. European Journal of Medical Genetics. 63(1). 103626–103626. 11 indexed citations
8.
Suzuki, Erina, Hirohito Shima, Masayo Kagami, et al.. (2019). (Epi)genetic defects of MKRN3 are rare in Asian patients with central precocious puberty. Human Genome Variation. 6(1). 7–7. 9 indexed citations
9.
Shima, Hirohito, et al.. (2019). A case report and literature review of monoallelic mutation of GHR. Journal of Pediatric Endocrinology and Metabolism. 32(4). 415–419. 2 indexed citations
10.
Hachiya, Rumi, et al.. (2019). MIRAGE syndrome with recurrent pneumonia probably associated with gastroesophageal reflux and achalasia: A case report. Clinical Pediatric Endocrinology. 28(4). 147–153. 10 indexed citations
11.
Shima, Hirohito, Takashi Tachibana, Makoto Oshiro, et al.. (2018). MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiency. PLoS ONE. 13(11). e0206184–e0206184. 18 indexed citations
12.
Fukui, Yûkô, Shuichi Yatsuga, Hirohito Shima, et al.. (2018). An unclassified variant of CHD7 activates a cryptic splice site in a patient with CHARGE syndrome. Human Genome Variation. 5(1). 18006–18006. 6 indexed citations
13.
Nishioka, Junko, et al.. (2017). The first Japanese case of central precocious puberty with a novel MKRN3 mutation. Human Genome Variation. 4(1). 17017–17017. 14 indexed citations
14.
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
15.
Shima, Hirohito, Katrin Koehler, Kazuhiko Sugimoto, et al.. (2017). Two patients with MIRAGE syndrome lacking haematological features: role of somatic second-site reversion SAMD9 mutations. Journal of Medical Genetics. 55(2). 81–85. 40 indexed citations
16.
Shima, Hirohito, Weizhen Ji, James McGrath, et al.. (2017). A novel SAMD9 mutation causing MIRAGE syndrome: An expansion and review of phenotype, dysmorphology, and natural history. American Journal of Medical Genetics Part A. 176(2). 415–420. 26 indexed citations
17.
Shima, Hirohito, Shuichi Yatsuga, Akie Nakamura, et al.. (2016). <b><i>NR0B1</i></b> Frameshift Mutation in a Boy with Idiopathic Central Precocious Puberty. Sexual Development. 10(4). 205–209. 10 indexed citations
18.
Suzuki, Erina, Hirohito Shima, Kunihiko Hanew, et al.. (2016). Complex X-Chromosomal Rearrangements in Two Women with Ovarian Dysfunction: Implications of Chromothripsis/Chromoanasynthesis-Dependent and -Independent Origins of Complex Genomic Alterations. Cytogenetic and Genome Research. 150(2). 86–92. 15 indexed citations
19.
Nakamura, Yasuhiro, et al.. (1992). Elastofibroma dorsi. Cytologic, histologic, immunohistochemical and ultrastructural studies.. PubMed. 36(4). 559–62. 19 indexed citations
20.
Tanaka, Takuji, et al.. (1984). Glassy Cell Carcinoma of the Uterine Cervix. Pathology - Research and Practice. 178(4). 389–392. 8 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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