Yuji Oto

480 total citations
29 papers, 331 citations indexed

About

Yuji Oto is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Yuji Oto has authored 29 papers receiving a total of 331 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 10 papers in Pediatrics, Perinatology and Child Health and 8 papers in Molecular Biology. Recurrent topics in Yuji Oto's work include Genetic Syndromes and Imprinting (17 papers), Prenatal Screening and Diagnostics (9 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Yuji Oto is often cited by papers focused on Genetic Syndromes and Imprinting (17 papers), Prenatal Screening and Diagnostics (9 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Yuji Oto collaborates with scholars based in Japan. Yuji Oto's co-authors include Nobuyuki Murakami, Toshiro Nagai, Kazuo Obata, Atsunori Yoshino, Yuriko Tanaka, Takayoshi Tsuchiya, Tadayuki Ayabe, Yoshiko Abe, Koji Muroya and Masanori Adachi and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Research in Developmental Disabilities.

In The Last Decade

Yuji Oto

26 papers receiving 323 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yuji Oto Japan	12	212	128	66	58	49	29	331
Sarah Bocchini Italy	9	243 1.1×	129 1.0×	58 0.9×	115 2.0×	47 1.0×	25	385
Frances Elmslie United Kingdom	10	99 0.5×	117 0.9×	43 0.7×	22 0.4×	50 1.0×	16	291
Junko Muroi Japan	12	172 0.8×	228 1.8×	79 1.2×	76 1.3×	58 1.2×	19	439
Christèle du Souich Canada	13	251 1.2×	141 1.1×	54 0.8×	128 2.2×	41 0.8×	25	459
Teresa De Toni Italy	9	111 0.5×	118 0.9×	28 0.4×	137 2.4×	72 1.5×	23	289
Andrea Guerin Canada	8	103 0.5×	99 0.8×	69 1.0×	57 1.0×	36 0.7×	30	336
Patricia Lopes Pereira France	11	180 0.8×	195 1.5×	24 0.4×	26 0.4×	15 0.3×	13	428
Jaina Patel Canada	8	193 0.9×	118 0.9×	37 0.6×	11 0.2×	16 0.3×	17	389
Nunzia Mollo Italy	10	84 0.4×	186 1.5×	27 0.4×	29 0.5×	20 0.4×	14	341
Anne Rochtus Belgium	10	217 1.0×	189 1.5×	75 1.1×	20 0.3×	12 0.2×	26	379

Countries citing papers authored by Yuji Oto

Since Specialization

Citations

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

Fields of papers citing papers by Yuji Oto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yuji Oto

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

Oto, Yuji, Takeshi Inoue, Akihisa Nitta, et al.. (2024). A case report of odonto-hypophosphatasia with a novel variant in the ALPL gene. Journal of Pediatric Endocrinology and Metabolism. 37(3). 276–279.

Oto, Yuji, Nobuyuki Murakami, Takeshi Inoue, et al.. (2023). Perinatal and neonatal characteristics of Prader–Willi syndrome in Japan. Pediatrics International. 65(1). e15540–e15540. 1 indexed citations

Murakami, Nobuyuki, et al.. (2022). Relationship Between Sensory Processing and Autism Spectrum Disorder-Like Behaviors in Prader-Willi Syndrome. American Journal on Intellectual and Developmental Disabilities. 127(3). 249–263.

Oto, Yuji, Takeshi Inoue, So Nagai, et al.. (2021). Successful treatment of Gaucher disease type 1 by enzyme replacement therapy over a 10-year duration in a Japanese pediatric patient: A case report. Experimental and Therapeutic Medicine. 21(3). 246–246. 5 indexed citations

Oto, Yuji, Nobuyuki Murakami, Takeshi Inoue, et al.. (2021). Psychiatric behavioral effect and characteristics of type 2 diabetes mellitus on Japanese patients with Prader-Willi syndrome: a preliminary retrospective study. Journal of Pediatric Endocrinology and Metabolism. 35(1). 89–96. 1 indexed citations

Oto, Yuji, Takeshi Inoue, Akihisa Nitta, et al.. (2021). Primary hyperparathyroidism in a child with abdominal pain and hematuria. Clinical Pediatric Endocrinology. 30(2). 111–113. 1 indexed citations

Kobayashi, Sayuki, Nobuyuki Murakami, Yuji Oto, et al.. (2021). Subtle Cardiovascular Abnormalities in Prader-Willi Syndrome Might Begin in Young Adulthood. Internal Medicine. 60(21). 3377–3384. 7 indexed citations

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

Murakami, Nobuyuki, et al.. (2018). Aberrant, autistic, and food-related behaviors in adults with Prader-Willi syndrome. The comparison between young adults and adults. Research in Developmental Disabilities. 73. 126–134. 8 indexed citations

10.

Oto, Yuji, et al.. (2018). Early adiposity rebound in patients with Prader-Willi syndrome. Journal of Pediatric Endocrinology and Metabolism. 31(12). 1311–1314. 1 indexed citations

11.

Inoue, Takeshi, Nobuyuki Murakami, Tadayuki Ayabe, et al.. (2016). Pyruvate Improved Insulin Secretion Status in a Mitochondrial Diabetes Mellitus Patient. The Journal of Clinical Endocrinology & Metabolism. 101(5). 1924–1926. 21 indexed citations

12.

Oto, Yuji, et al.. (2015). The ratio of serum free triiodothyronine to free thyroxine in children: a retrospective database survey of healthy short individuals and patients with severe thyroid hypoplasia or central hypothyroidism. Thyroid Research. 8(1). 10–10. 11 indexed citations

13.

Sato, Yohei, Masako Fujiwara, Hiroshi Kobayashi, et al.. (2015). Residual glycosaminoglycan accumulation in mitral and aortic valves of a patient with attenuated MPS I (Scheie syndrome) after 6 years of enzyme replacement therapy: Implications for early diagnosis and therapy. SHILAP Revista de lepidopterología. 5. 94–97. 5 indexed citations

14.

Asakura, Yumi, Kiyomi Abe, Koji Muroya, et al.. (2015). Combined Growth Hormone and Thyroid-Stimulating Hormone Deficiency in a Japanese Patient with a Novel Frameshift Mutation in IGSF1. Hormone Research in Paediatrics. 84(5). 349–354. 19 indexed citations

15.

Kido, Yasuhiro, Satoru Sakazume, Yoshiko Abe, et al.. (2013). Testosterone replacement therapy to improve secondary sexual characteristics and body composition without adverse behavioral problems in adult male patients with Prader–Willi syndrome: An observational study. American Journal of Medical Genetics Part A. 161(9). 2167–2173. 29 indexed citations

16.

Murakami, Nobuyuki, Yukiko Hayashi, Yuji Oto, et al.. (2013). Congenital generalized lipodystrophy type 4 with muscular dystrophy: Clinical and pathological manifestations in early childhood. Neuromuscular Disorders. 23(5). 441–444. 26 indexed citations

17.

Murakami, Nobuyuki, Kazuo Obata, Yoshiko Abe, et al.. (2012). Scoliosis in Prader–Willi syndrome: Effect of growth hormone therapy and value of paravertebral muscle volume by CT in predicting scoliosis progression. American Journal of Medical Genetics Part A. 158A(7). 1628–1632. 22 indexed citations

18.

Oto, Yuji, Kazuo Obata, Keiko Matsubara, et al.. (2012). Growth hormone secretion and its effect on height in pediatric patients with different genotypes of Prader–Willi syndrome. American Journal of Medical Genetics Part A. 158A(6). 1477–1480. 16 indexed citations

19.

Tanaka, Yuriko, Yoshiko Abe, Yuji Oto, et al.. (2012). Characterization of fat distribution in Prader–Willi syndrome: Relationships with adipocytokines and influence of growth hormone treatment. American Journal of Medical Genetics Part A. 161(1). 27–33. 28 indexed citations

20.

Tanaka, Yuriko, et al.. (2011). Five cases of West syndrome complicated by nephrocalcinosis during combination therapy with ACTH and zonisamide. Japanese journal of pediatric nephrology. 24(1). 86–91.

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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