Masaki Noda

7.7k total citations · 1 hit paper
150 papers, 6.2k citations indexed

About

Masaki Noda is a scholar working on Molecular Biology, Oncology and Rheumatology. According to data from OpenAlex, Masaki Noda has authored 150 papers receiving a total of 6.2k indexed citations (citations by other indexed papers that have themselves been cited), including 118 papers in Molecular Biology, 44 papers in Oncology and 30 papers in Rheumatology. Recurrent topics in Masaki Noda's work include Bone Metabolism and Diseases (64 papers), Bone health and treatments (38 papers) and TGF-β signaling in diseases (28 papers). Masaki Noda is often cited by papers focused on Bone Metabolism and Diseases (64 papers), Bone health and treatments (38 papers) and TGF-β signaling in diseases (28 papers). Masaki Noda collaborates with scholars based in Japan, United States and Sri Lanka. Masaki Noda's co-authors include Akira Nifuji, Yoichi Ezura, Kunikazu Tsuji, Kazuhisa Nakashima, Gideon A. Rodan, Tadayoshi Hayata, Gérard Karsenty, Shu Takeda, Hisataka Kondo and Jong Deok Ahn and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Masaki Noda

149 papers receiving 6.1k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Leptin regulation of bone resorption by the sympathetic nervous system and CART

2005 1.0k citations Shu Takeda, Masaki Noda et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Masaki Noda Japan	41	3.7k	1.3k	824	765	692	150	6.2k
Michael W. Starbuck United States	19	3.2k 0.9×	1.2k 0.9×	611 0.7×	498 0.7×	703 1.0×	24	4.8k
Timothy R. Arnett United Kingdom	42	2.2k 0.6×	1.5k 1.1×	947 1.1×	516 0.7×	556 0.8×	85	5.7k
K.‐H. William Lau United States	43	2.9k 0.8×	937 0.7×	973 1.2×	746 1.0×	573 0.8×	165	5.8k
Eiichi Hinoi Japan	37	3.5k 0.9×	1.2k 0.9×	1.3k 1.6×	638 0.8×	591 0.9×	159	7.4k
Xiangli Yang United States	26	3.3k 0.9×	952 0.7×	436 0.5×	537 0.7×	698 1.0×	49	5.0k
Florent Elefteriou United States	35	2.2k 0.6×	962 0.7×	1.0k 1.3×	498 0.7×	592 0.9×	74	5.8k
Matthias Priemel Germany	30	2.1k 0.6×	1.1k 0.8×	1.4k 1.7×	738 1.0×	697 1.0×	76	5.6k
Jong Deok Ahn South Korea	10	2.3k 0.6×	1.0k 0.8×	1.2k 1.4×	334 0.4×	526 0.8×	11	4.5k
Hong Zhou Australia	45	3.0k 0.8×	2.7k 2.0×	860 1.0×	711 0.9×	640 0.9×	162	6.9k
Xiang‐Hang Luo China	43	3.5k 0.9×	863 0.7×	1.2k 1.4×	486 0.6×	397 0.6×	127	6.2k

Countries citing papers authored by Masaki Noda

Since Specialization

Citations

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

Fields of papers citing papers by Masaki Noda

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Masaki Noda

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

Kohara, Yukihiro, et al.. (2024). Gprc5a is a novel parathyroid hormone‐inducible gene and negatively regulates osteoblast proliferation and differentiation. Journal of Cellular Physiology. 239(8). e31297–e31297. 2 indexed citations

Tsuji, Kunikazu, Yoshinori Asou, Hideyuki Koga, et al.. (2023). Osteolytic Bone Loss and Skeletal Deformities in a Mouse Model for Early-Onset Paget’s Disease of Bone with PFN1 Mutation Are Treatable by Alendronate. Pharmaceuticals. 16(10). 1395–1395. 1 indexed citations

Hayashi, Naoki, Tsuyoshi Sato, Shoichiro Kokabu, et al.. (2018). Possible association of oestrogen and Cryba4 with masticatory muscle tendon‐aponeurosis hyperplasia. Oral Diseases. 25(1). 274–281. 5 indexed citations

Suzuki, Kazuhiro, et al.. (2016). Adrenergic control of the adaptive immune response by diurnal lymphocyte recirculation through lymph nodes. The Journal of Experimental Medicine. 213(12). 2567–2574. 144 indexed citations

Ezura, Yoichi, Makiri Kawasaki, Takayuki Yamada, et al.. (2015). BMP‐2 Enhances Lgr4 Gene Expression in Osteoblastic Cells. Journal of Cellular Physiology. 231(4). 887–895. 25 indexed citations

Nakai, Akiko, et al.. (2014). Control of lymphocyte egress from lymph nodes through β2-adrenergic receptors. The Journal of Experimental Medicine. 211(13). 2583–2598. 222 indexed citations

Hayata, Tadayoshi, Takuya Notomi, Yayoi Izu, et al.. (2014). PTH Regulates β2‐Adrenergic Receptor Expression in Osteoblast‐Like MC3T3‐E1 Cells. Journal of Cellular Biochemistry. 116(1). 142–148. 16 indexed citations

Ezura, Yoichi & Masaki Noda. (2013). [Parathyroid hormone : its anabolic action on bone].. PubMed. 23(2). 203–9. 1 indexed citations

Wehbi, Vanessa L., Tadayoshi Hayata, Timothy N. Feinstein, et al.. (2012). Anabolic action of parathyroid hormone regulated by the β ₂ -adrenergic receptor. Proceedings of the National Academy of Sciences. 109(19). 7433–7438. 53 indexed citations

10.

Kawamata, Aya, Akane Inoue, Hiroaki Hemmi, et al.. (2011). Dok-1 and Dok-2 deficiency induces osteopenia via activation of osteoclasts. Journal of Cellular Physiology. 226(12). 3087–3093. 8 indexed citations

11.

Hayashi, Chikako, Urara Hasegawa, Yoshitomo Saita, et al.. (2009). Osteoblastic bone formation is induced by using nanogel‐crosslinking hydrogel as novel scaffold for bone growth factor. Journal of Cellular Physiology. 220(1). 1–7. 75 indexed citations

12.

Nakamura, Takahisa, Michihiko Usui, Mitsuhiro Yoneda, et al.. (2007). Cnot7-Null Mice Exhibit High Bone Mass Phenotype and Modulation of BMP Actions. Journal of Bone and Mineral Research. 22(8). 1217–1223. 28 indexed citations

13.

Saita, Yoshitomo, Tsuyoshi Takagi, Michihiko Usui, et al.. (2007). Lack of Schnurri-2 Expression Associates with Reduced Bone Remodeling and Osteopenia. Journal of Biological Chemistry. 282(17). 12907–12915. 26 indexed citations

14.

Ono, Noriaki, Kazuhisa Nakashima, Ernestina Schipani, et al.. (2007). Constitutively Active Parathyroid Hormone Receptor Signaling in Cells in Osteoblastic Lineage Suppresses Mechanical Unloading-induced Bone Resorption. Journal of Biological Chemistry. 282(35). 25509–25516. 21 indexed citations

15.

Kato, Norihiko, Susan R. Rittling, Kazuhisa Nakashima, et al.. (2007). Osteopontin deficiency enhances anabolic action of EP4 agonist at a sub-optimal dose in bone. Journal of Endocrinology. 193(1). 171–182. 6 indexed citations

16.

Kato, Norihiko, Urara Hasegawa, Nobuyuki Morimoto, et al.. (2007). Nanogel‐based delivery system enhances PGE₂ effects on bone formation. Journal of Cellular Biochemistry. 101(5). 1063–1070. 41 indexed citations

17.

Yoshida, Yutaka, Sakae Tanaka, Hisashi Umemori, et al.. (2000). Negative Regulation of BMP/Smad Signaling by Tob in Osteoblasts. Cell. 103(7). 1085–1097. 265 indexed citations

18.

Yamashita, Toshihide, et al.. (1998). Elongation of the epiphyseal trabecular bone in transgenic mice carrying a klotho gene locus mutation that leads to a syndrome resembling aging. Journal of Endocrinology. 159(1). 1–8. 45 indexed citations

19.

Liu, Ying, Hideto Watanabe, Akira Nifuji, et al.. (1997). Overexpression of a Single Helix-Loop-Helix-type Transcription Factor, Scleraxis, Enhances Aggrecan Gene Expression in Osteoblastic Osteosarcoma ROS17/2.8 Cells. Journal of Biological Chemistry. 272(47). 29880–29885. 60 indexed citations

20.

Tamura, Masato & Masaki Noda. (1994). Identification of a DNA sequence involved in osteoblast-specific gene expression via interaction with helix-loop-helix (HLH)-type transcription factors.. The Journal of Cell Biology. 126(3). 773–782. 74 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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