Yo Niida

2.2k total citations
93 papers, 1.6k citations indexed

About

Yo Niida is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Yo Niida has authored 93 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 23 papers in Genetics and 22 papers in Physiology. Recurrent topics in Yo Niida's work include Tuberous Sclerosis Complex Research (14 papers), Histiocytic Disorders and Treatments (8 papers) and Genomic variations and chromosomal abnormalities (8 papers). Yo Niida is often cited by papers focused on Tuberous Sclerosis Complex Research (14 papers), Histiocytic Disorders and Treatments (8 papers) and Genomic variations and chromosomal abnormalities (8 papers). Yo Niida collaborates with scholars based in Japan, United States and Poland. Yo Niida's co-authors include Vijaya Ramesh, Hiroki Ura, Sumihito Togi, Katherine B. Sims, David J. Kwiatkowski, Mia MacCollin, Anat Stemmer‐Rachamimov, Akihiro Yachie, Roberta L. Beauchamp and Takanori Tsuji and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Yo Niida

88 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yo Niida Japan 21 453 432 338 334 244 93 1.6k
José Boucraut France 31 625 1.4× 246 0.6× 711 2.1× 125 0.4× 145 0.6× 97 2.8k
Stefan Wieczorek Germany 26 682 1.5× 289 0.7× 286 0.8× 100 0.3× 90 0.4× 60 1.8k
Pierre Labauge France 23 716 1.6× 265 0.6× 141 0.4× 147 0.4× 103 0.4× 119 2.4k
Barbara A. Christy United States 23 1.4k 3.2× 148 0.3× 210 0.6× 280 0.8× 435 1.8× 47 2.4k
Cyril Mignot France 26 844 1.9× 520 1.2× 137 0.4× 464 1.4× 90 0.4× 101 2.0k
Alfredo Brusco Italy 32 2.2k 4.9× 203 0.5× 223 0.7× 799 2.4× 198 0.8× 141 3.3k
Christina Chen United States 21 343 0.8× 267 0.6× 136 0.4× 122 0.4× 51 0.2× 48 1.4k
Yuko Tanabe Japan 25 671 1.5× 127 0.3× 105 0.3× 227 0.7× 572 2.3× 107 1.8k
Veronica A. Kinsler United Kingdom 21 492 1.1× 269 0.6× 306 0.9× 411 1.2× 791 3.2× 53 1.7k
Phillip J. Dexheimer United States 19 664 1.5× 175 0.4× 321 0.9× 326 1.0× 93 0.4× 36 1.5k

Countries citing papers authored by Yo Niida

Since Specialization
Citations

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

Fields of papers citing papers by Yo Niida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yo Niida

This figure shows the co-authorship network connecting the top 25 collaborators of Yo Niida. A scholar is included among the top collaborators of Yo Niida 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 Yo Niida. Yo Niida 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.
2.
Ura, Hiroki, et al.. (2025). Integrated Analysis of Somatic DNA Variants and DNA Methylation of Tumor Suppressor Genes in Colorectal Cancer. International Journal of Molecular Sciences. 26(4). 1642–1642. 1 indexed citations
3.
Niida, Yo, et al.. (2024). Investigation of a novel PROS1 splicing variant in a patient with protein S deficiency. Human Genome Variation. 11(1). 28–28.
4.
5.
Niida, Yo, Sumihito Togi, & Hiroki Ura. (2023). Streamlining Genetic Diagnosis With Long-Range Polymerase Chain Reaction (PCR)-Based Next-Generation Sequencing for Type I and Type II Collagenopathies. Cureus. 15(12). e50482–e50482. 1 indexed citations
6.
Togi, Sumihito, et al.. (2023). Schimmelpenning‐Feuerstein‐Mims syndrome induced by HRAS Gly12Ser somatic mosaic mutation: Case report and literature review. The Journal of Dermatology. 50(9). 1213–1215. 3 indexed citations
7.
Osawa, Takahiro, Mototsugu Oya, Tohru Okanishi, et al.. (2023). Clinical Practice Guidelines for tuberous sclerosis complex‐associated renal angiomyolipoma by the Japanese Urological Association: Summary of the update. International Journal of Urology. 30(10). 808–817. 4 indexed citations
8.
9.
Togi, Sumihito, Hiroki Ura, & Yo Niida. (2021). Optimization and Validation of Multimodular, Long-Range PCR–Based Next-Generation Sequencing Assays for Comprehensive Detection of Mutation in Tuberous Sclerosis Complex. Journal of Molecular Diagnostics. 23(4). 424–446. 21 indexed citations
10.
Sasaki, Tsuyoshi, Takehiro Uda, Ichiro Kuki, et al.. (2021). TSC2 somatic mosaic mutation, including extra-tumor tissue, may be the developmental cause of solitary subependymal giant cell astrocytoma. Child s Nervous System. 38(1). 77–83. 9 indexed citations
11.
Katô, Hajime, Yuka Kinoshita, Yuki Taniguchi, et al.. (2020). Identification of ENPP1 Haploinsufficiency in Patients With Diffuse Idiopathic Skeletal Hyperostosis and Early-Onset Osteoporosis. Journal of Bone and Mineral Research. 37(6). 1125–1135. 27 indexed citations
12.
Niida, Yo, et al.. (2020). Squamous cell carcinoma–like ungual fibroma as early diagnostic indicators of tuberous sclerosis complex in an elderly patient. SHILAP Revista de lepidopterología. 3(5). 111–112. 1 indexed citations
13.
Hata, Yukiko, Hiromichi Taneichi, Tomomi Tanaka, et al.. (2019). Two autopsy cases of sudden unexpected death from Dravet syndrome with novel de novo SCN1A variants. Brain and Development. 42(2). 171–178. 10 indexed citations
14.
15.
16.
Okuyama, Hiroshi, Yuki Matsui, H. Yamaya, et al.. (2013). Adult-onset renal failure in a family with Alagille syndrome with proteinuria and a novel JAG1 mutation. Clinical Kidney Journal. 6(3). 295–299. 4 indexed citations
17.
Shimizu, Masaki, Yo Niida, Shoichi Koizumi, & Akihiro Yachie. (2013). An infant with recurrent convulsive seizures of 3 weeks duration: Questions. Pediatric Nephrology. 29(10). 1951–1951. 4 indexed citations
18.
Wada, Taizo, et al.. (2011). A case of acute encephalopathy with hemophagocytic lymphohistiocytosis and clonal T-cell expansion. Brain and Development. 34(5). 376–379. 2 indexed citations
19.
Niida, Yo, Anat Stemmer‐Rachamimov, Marian L. Logrip, et al.. (2001). Survey of Somatic Mutations in Tuberous Sclerosis Complex (TSC) Hamartomas Suggests Different Genetic Mechanisms for Pathogenesis of TSC Lesions. The American Journal of Human Genetics. 69(3). 493–503. 148 indexed citations
20.
Niida, Yo, Janine Lewis, Roberta L. Beauchamp, et al.. (1999). Analysis of bothTSC1 andTSC2 for germline mutations in 126 unrelated patients with tuberous sclerosis. Human Mutation. 14(5). 412–422. 123 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by José Boucraut Breakdown of academic impact, for papers by Stefan Wieczorek Breakdown of academic impact, for papers by Pierre Labauge Breakdown of academic impact, for papers by Barbara A. Christy Breakdown of academic impact, for papers by Cyril Mignot Breakdown of academic impact, for papers by Alfredo Brusco Breakdown of academic impact, for papers by Christina Chen Breakdown of academic impact, for papers by Yuko Tanabe Breakdown of academic impact, for papers by Veronica A. Kinsler Breakdown of academic impact, for papers by Phillip J. Dexheimer
Rankless by CCL
2026