T Momoi

672 total citations
16 papers, 498 citations indexed

About

T Momoi is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, T Momoi has authored 16 papers receiving a total of 498 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Endocrinology, Diabetes and Metabolism and 5 papers in Genetics. Recurrent topics in T Momoi's work include Growth Hormone and Insulin-like Growth Factors (6 papers), Metabolism and Genetic Disorders (3 papers) and Pituitary Gland Disorders and Treatments (3 papers). T Momoi is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (6 papers), Metabolism and Genetic Disorders (3 papers) and Pituitary Gland Disorders and Treatments (3 papers). T Momoi collaborates with scholars based in Japan, United States and Canada. T Momoi's co-authors include Ichiro Fujisawa, Kiyoshi Kikuchi, Kaori Togashi, K Nishimura, S Noma, T Sagoh, Kyo Itoh, Shunsuke Minami, Tohru Yorifuji and Chutaro Yamanaka and has published in prestigious journals such as Radiology, Clinical Chemistry and American Journal of Kidney Diseases.

In The Last Decade

T Momoi

16 papers receiving 470 citations

Peers

Countries citing papers authored by T Momoi

Since Specialization

Citations

This map shows the geographic impact of T 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 T Momoi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T Momoi more than expected).

Fields of papers citing papers by T Momoi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T Momoi

This figure shows the co-authorship network connecting the top 25 collaborators of T Momoi. A scholar is included among the top collaborators of T 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 T Momoi. T Momoi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

#	Title	Journal	Authors	Indexed citations
1	A randomized study of two long-course prednisolone regimens for nephrotic syndrome in children	American Journal of Kidney Diseases	Masahiro Hiraoka, Hirokazu Tsukahara et al.	51
2	Uniparental and functional X disomy in Turner syndrome patients with unexplained mental retardation and X derived marker chromosomes.	Journal of Medical Genetics	Tohru Yorifuji, Junko Muroi et al.	23
3	Nephropathy and growth hormone deficiency in a patient with mitochondrial tRNA(Leu(UUR)) mutation.	Journal of Medical Genetics	Tohru Yorifuji, Masahiko Kawai et al.	36
4	Rotavirus encephalitis: detection of the virus genomic RNA in the cerebrospinal fluid of a child.	PubMed	Akira Yoshida, Ryuichi Tanaka et al.	49
5	Acquired growth hormone deficiency due to pituitary stalk transection after head trauma in childhood	European Journal of Pediatrics	Chutaro Yamanaka, T Momoi et al.	35
6	Protein‐losing gastroenteropathy with facial anomaly and growth retardation: A mild case of Hennekam syndrome	American Journal of Medical Genetics	Chutaro Yamanaka, Mitsufumi Mayumi et al.	13
7	Short stature with normal growth hormone and elevated IGF-I	European Journal of Pediatrics	T Momoi, Chutaro Yamanaka et al.	10
8	Leukocyte and plasma N‐laurylsphingosine deacylase (ceramidase) in Farber disease	Clinical Genetics	Yoav Ben‐Yoseph, R. Gagné et al.	15
9	Wilms tumour in a patient with growth hormone replacement therapy	European Journal of Pediatrics	T Momoi, Chutaro Yamanaka et al.	3
10	Magnetic Resonance Imaging in Growth Hormone Deficiency	Acta Paediatrica	T Momoi, Kiyoshi Kikuchi et al.	4
11	Transection of the pituitary stalk: development of an ectopic posterior lobe assessed with MR imaging.	Radiology	Ichiro Fujisawa, Kiyoshi Kikuchi et al.	202
12	Clinical Trial with Authentic Recombinant Somatropin in Japan	Acta Paediatrica	Kazue Takano, KAZUO SHIZUME et al.	5
13	Treatment of Pituitary Dwarfism with Authentic Recombinant Human Growth Hormone (SM-9500)	Endocrinologia Japonica	Kazue Takano, KAZUO SHIZUME et al.	7
14	Thermal activation of hexosaminidase A in a genetic compound with Tay‐Sachs disease	Journal of Inherited Metabolic Disease	Yoav Ben‐Yoseph, T Momoi et al.	10
15	Organic acids and branched‐chain amino acids in body fluids before and after multiple exchange transfusions in maple syrup urine disease	Journal of Inherited Metabolic Disease	Yosuke Shigematsu, Kiyoshi Kikuchi et al.	16
16	(omega-1)-Hydroxymonocarboxylic acids in urine of infants fed medium-chain triglycerides.	Clinical Chemistry	T Momoi, M. Sudo et al.	19

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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