Toru Momoi

1.3k total citations
40 papers, 921 citations indexed

About

Toru Momoi is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Physiology. According to data from OpenAlex, Toru Momoi has authored 40 papers receiving a total of 921 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Endocrinology, Diabetes and Metabolism and 10 papers in Physiology. Recurrent topics in Toru Momoi's work include Lysosomal Storage Disorders Research (9 papers), Growth Hormone and Insulin-like Growth Factors (8 papers) and Sexual Differentiation and Disorders (6 papers). Toru Momoi is often cited by papers focused on Lysosomal Storage Disorders Research (9 papers), Growth Hormone and Insulin-like Growth Factors (8 papers) and Sexual Differentiation and Disorders (6 papers). Toru Momoi collaborates with scholars based in Japan, United States and Greece. Toru Momoi's co-authors include Tohru Yorifuji, Chutaro Yamanaka, Masahiko Kawai, Masayuki Kaji, Masakatsu Sudo, Junko Muroi, Harukí Mikawa, Ayumi Uematsu, Hiroshi Sasaki and Henry L. Nadler and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Biochemical Journal and The Journal of Pediatrics.

In The Last Decade

Toru Momoi

39 papers receiving 872 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Toru Momoi Japan 17 334 310 218 159 155 40 921
A J Perlman United States 19 399 1.2× 665 2.1× 348 1.6× 151 0.9× 41 0.3× 22 1.4k
Chutaro Yamanaka Japan 14 222 0.7× 252 0.8× 175 0.8× 123 0.8× 42 0.3× 32 683
Chong Kun Cheon South Korea 18 384 1.1× 135 0.4× 395 1.8× 119 0.7× 76 0.5× 81 865
C. Charlton Mabry United States 14 317 0.9× 143 0.5× 133 0.6× 105 0.7× 228 1.5× 41 777
Luigi Garibaldi United States 17 219 0.7× 323 1.0× 181 0.8× 74 0.5× 59 0.4× 43 662
Harry J. Hirsch Israel 22 412 1.2× 412 1.3× 531 2.4× 248 1.6× 36 0.2× 70 1.3k
Richard Pang China 19 324 1.0× 385 1.2× 108 0.5× 49 0.3× 34 0.2× 45 1.1k
Ζ. Josefsberg Israel 16 529 1.6× 712 2.3× 278 1.3× 88 0.6× 42 0.3× 60 1.4k
Michèle G. Brunette Canada 15 318 1.0× 102 0.3× 93 0.4× 73 0.5× 66 0.4× 34 722
Yasuhiro Naiki Japan 16 510 1.5× 279 0.9× 356 1.6× 106 0.7× 130 0.8× 39 918

Countries citing papers authored by Toru Momoi

Since Specialization
Citations

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

Fields of papers citing papers by Toru Momoi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Toru Momoi

This figure shows the co-authorship network connecting the top 25 collaborators of Toru Momoi. A scholar is included among the top collaborators of Toru Momoi 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 Toru Momoi. Toru Momoi 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.
Nagasaka, Hironori, Tohru Yorifuji, Toru Momoi, et al.. (2009). Lipoprotein profiles in children with two common cholesteryl ester transfer protein gene mutations, D442G and I14A, during the first year of life. Clinica Chimica Acta. 406(1-2). 52–56. 4 indexed citations
2.
Nagasaka, Hironori, Yoshiyuki Okano, Hirokazu Tsukahara, et al.. (2009). Sustaining hypercitrullinemia, hypercholesterolemia and augmented oxidative stress in Japanese children with aspartate/glutamate carrier isoform 2-citrin-deficiency even during the silent period. Molecular Genetics and Metabolism. 97(1). 21–26. 28 indexed citations
3.
Mamada, Mitsukazu, Tohru Yorifuji, Keiji Kurokawa, et al.. (2006). Fibrillin I gene polymorphism is associated with tall stature of normal individuals. Human Genetics. 120(5). 733–735. 9 indexed citations
4.
Tsukahara, Hirokazu, Ikue Hata, Yukiko Todoroki, et al.. (2003). Formation of Advanced Glycosylation End Products and Oxidative Stress in Young Patients with Type 1 Diabetes. Pediatric Research. 54(3). 419–424. 75 indexed citations
5.
Uematsu, Ayumi, Tohru Yorifuji, Junko Muroi, et al.. (2002). Parental origin of normal X chromosomes in Turner syndrome patients with various karyotypes: Implications for the mechanism leading to generation of a 45,X karyotype. American Journal of Medical Genetics. 111(2). 134–139. 78 indexed citations
6.
Hiraoka, Masahiro, Hirokazu Tsukahara, Yusei Ohshima, et al.. (2000). Efficacy of long-term azathioprine for relapsing nephrotic syndrome. Pediatric Nephrology. 14(8-9). 776–778. 4 indexed citations
7.
Yorifuji, Tohru, Junko Muroi, Ayumi Uematsu, Hidefumi Hiramatsu, & Toru Momoi. (1999). Hyperinsulinism-hyperammonemia syndrome caused by mutant glutamate dehydrogenase accompanied by novel enzyme kinetics. Human Genetics. 104(6). 476–479. 61 indexed citations
8.
Uematsu, Ayumi, Tohru Yorifuji, Junko Muroi, Chutaro Yamanaka, & Toru Momoi. (1999). Relatively longer hand in patients with Ullrich-Turner syndrome. American Journal of Medical Genetics. 82(3). 254–256. 2 indexed citations
9.
Kawai, Masahiko, Tohru Yorifuji, Chutaro Yamanaka, et al.. (1997). A Case of Robinow Syndrome Accompanied by Partial Growth Hormone Insufficiency Treated with Growth Hormone. Hormone Research. 48(1). 41–43. 4 indexed citations
10.
Kinoshita, Eiichi, et al.. (1997). <i>DAX</i><i>-</i>1 Gene Mutations and Deletions in Japanese Patients with Adrenal Hypoplasia Congenita and Hypogonadotropic Hypogonadism. Hormone Research. 48(1). 29–34. 20 indexed citations
11.
Momoi, Toru, Chutaro Yamanaka, Rieko Tanaka, et al.. (1995). Elevation of serum creatine phosphokinase during growth hormone treatment in patients with multiple pituitary hormone deficiency. European Journal of Pediatrics. 154(11). 886–889. 4 indexed citations
12.
Tanaka, Rieko, et al.. (1995). Type 3 GM I gangliosidosis: clinical and neuroradiological findings in an 11-year-old girl. Journal of Neurology. 242(5). 299–303. 12 indexed citations
13.
Kaji, Masayuki, Masatoshi Ito, Takehiko Okuno, et al.. (1992). Serum Copper and Zinc Levels in Epileptic Children with Valproate Treatment. Epilepsia. 33(3). 555–557. 31 indexed citations
14.
Yamanaka, Chutaro, Toru Momoi, Ichiro Fujisawa, et al.. (1990). Neurohypophyseal function of an ectopic posterior lobe in patients with growth hormone deficiency. European Journal of Endocrinology. 122(5). 664–670. 20 indexed citations
15.
Kawai, Masahiko, et al.. (1990). The syndrome of Möbius sequence, peripheral neuropathy, and hypogonadotropic hypogonadism. American Journal of Medical Genetics. 37(4). 578–582. 15 indexed citations
16.
Yorifuji, Tohru, Toru Momoi, Chutaro Yamanaka, et al.. (1989). Y Chromosome Specific DNA Probe in the Diagnosis of a Patient with mos 45, X/46, XYnf. Pediatrics International. 31(1). 85–89. 1 indexed citations
17.
Kikuchi, Kiyoshi, Ichiro Fujisawa, Toru Momoi, et al.. (1988). Hypothalamic-Pituitary Function in Growth Hormone-Deficient Patients With Pituitary Stalk Transection. The Journal of Clinical Endocrinology & Metabolism. 67(4). 817–823. 110 indexed citations
18.
Shimatsu, Akira, et al.. (1988). Nocturnal urinary growth hormone excretion in children with short stature. European Journal of Endocrinology. 119(1). 113–117. 13 indexed citations
19.
Sudo, Masakatsu, et al.. (1978). Identification of fatty acid methyl esters in kidneys and livers of two patients with Reye's syndrome. Clinica Chimica Acta. 84(1-2). 179–184. 5 indexed citations
20.
Momoi, Toru, et al.. (1977). Simplified assay method of α-l-iduronidase activity in leukocytes for detection of hurler syndrome and its carriers. Clinica Chimica Acta. 81(3). 311–313. 5 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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