Kimiaki Uetake

471 total citations
16 papers, 175 citations indexed

About

Kimiaki Uetake is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Kimiaki Uetake has authored 16 papers receiving a total of 175 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Kimiaki Uetake's work include Genetic Syndromes and Imprinting (2 papers), Renal Diseases and Glomerulopathies (2 papers) and Tuberous Sclerosis Complex Research (1 paper). Kimiaki Uetake is often cited by papers focused on Genetic Syndromes and Imprinting (2 papers), Renal Diseases and Glomerulopathies (2 papers) and Tuberous Sclerosis Complex Research (1 paper). Kimiaki Uetake collaborates with scholars based in Japan, Netherlands and Iran. Kimiaki Uetake's co-authors include Shinji Saitoh, Kenji Kurosawa, Tsutomu Ogata, Kana Hosoki, Mitsuhiro Kato, Shinobu Kohsaka, Masako Kohsaka, Jun Tohyama, Masayo Kagami and Masaya Kubota and has published in prestigious journals such as Brain Research, The Journal of Pediatrics and Epilepsia.

In The Last Decade

Kimiaki Uetake

15 papers receiving 171 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kimiaki Uetake Japan	7	88	61	40	25	24	16	175
Jillene Kogan United States	9	94 1.1×	105 1.7×	34 0.8×	55 2.2×	29 1.2×	13	217
Anne-Marie Van Der Kevie-Kersemaekers Netherlands	7	124 1.4×	92 1.5×	61 1.5×	3 0.1×	10 0.4×	13	212
Joshua L. Deignan United States	7	155 1.8×	79 1.3×	15 0.4×	4 0.2×	27 1.1×	8	249
Christopher I. Amos United States	3	200 2.3×	111 1.8×	6 0.1×	12 0.5×	7 0.3×	3	328
N. Logghe Belgium	9	85 1.0×	104 1.7×	37 0.9×	5 0.2×	9 0.4×	14	243
Koen Devriendt Belgium	9	137 1.6×	205 3.4×	61 1.5×	6 0.2×	8 0.3×	13	290
Frédérique Tihy Canada	11	215 2.4×	120 2.0×	146 3.6×	41 1.6×	23 1.0×	18	384
Taku Omata Japan	7	57 0.6×	119 2.0×	12 0.3×	3 0.1×	14 0.6×	29	221
Shreya Raman United States	7	156 1.8×	174 2.9×	48 1.2×	29 1.2×	28 1.2×	15	257
Abeer Al Tuwaijri Saudi Arabia	12	131 1.5×	230 3.8×	40 1.0×	9 0.4×	9 0.4×	23	368

Countries citing papers authored by Kimiaki Uetake

Since Specialization

Citations

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

Fields of papers citing papers by Kimiaki Uetake

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kimiaki Uetake

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

Takahashi, Toshiyuki, Takayuki Okamoto, Isao Yokota, et al.. (2021). The effect of rituximab on the quality of life of children with refractory nephrotic syndrome. Pediatrics International. 64(1). e14725–e14725. 3 indexed citations

Maruo, Yuji, et al.. (2021). Hemodynamics and cerebral perfusion in vasovagal syncope: A case series. Pediatrics International. 63(2). 235–237.

Hattori, Atsushi, Erina Suzuki, Hirohito Shima, et al.. (2019). DNA Methylation Status of SHOX-Flanking CpG Islands in Healthy Individuals and Short Stature Patients with Pseudoautosomal Copy Number Variations. Cytogenetic and Genome Research. 158(2). 56–62. 5 indexed citations

Takahashi, Toshiyuki, Takayuki Okamoto, Yasuyuki Sato, et al.. (2018). Periodically repeated rituximab administrations in children with refractory nephrotic syndrome: 2-year multicenter observational study. Pediatric Nephrology. 34(1). 87–96. 22 indexed citations

Yamamoto, Sayaka, Kimiaki Uetake, Masafumi Yamada, et al.. (2017). Relapsing Polychondritis With Increased Bone Marrow Signal on Magnetic Resonance Imaging in a 13-Year-Old Girl. JCR Journal of Clinical Rheumatology. 24(1). 52–54. 1 indexed citations

Sasaki, Daisuke, et al.. (2016). Stroke During Norovirus Infection as the Initial Episode of Antiphospholipid Syndrome. Global Pediatric Health. 3. 1 indexed citations

Kawano, Osamu, Akie Nakamura, Shuntaro Morikawa, et al.. (2015). Spondyloepiphyseal dysplasia congenita caused by double heterozygous mutations in COL2A1. American Journal of Medical Genetics Part A. 167(7). 1578–1581. 3 indexed citations

Kishimoto, Kenji, Ryōji Kobayashi, Hiroshi Yamamoto, et al.. (2014). Refractory Sacrococcygeal Germ Cell Tumor in Schinzel-Giedion Syndrome. Journal of Pediatric Hematology/Oncology. 37(4). e238–e241. 7 indexed citations

Suzuki, Masahiko, et al.. (2014). Newborn hypocarnitinemia due to long‐term transplacental pivalic acid passage. Pediatrics International. 56(5). 772–774. 4 indexed citations

10.

Kobayashi, Ryōji, et al.. (2012). Retinitis from cytomegalovirus during maintenance treatment for acute lymphoblastic leukemia. Pediatrics International. 54(2). 288–290. 18 indexed citations

11.

Hosoki, Kana, Masayo Kagami, Masaya Kubota, et al.. (2009). Maternal Uniparental Disomy 14 Syndrome Demonstrates Prader-Willi Syndrome-Like Phenotype. The Journal of Pediatrics. 155(6). 900–903.e1. 41 indexed citations

12.

Kurotaki, Naohiro, Joseph Shen, Tatsuro Kondoh, et al.. (2005). Phenotypic consequences of genetic variation at hemizygous alleles: Sotos syndrome is a contiguous gene syndrome incorporating coagulation factor twelve (FXII) deficiency. Genetics in Medicine. 7(7). 479–483. 33 indexed citations

13.

Takano, Kyoko, et al.. (2003). Cerebellar and brainstem involvement in familial juvenile nephronophthisis type I. Pediatric Neurology. 28(2). 142–144. 11 indexed citations

14.

Kohsaka, Shinobu, et al.. (1999). Brainstem triggers absence seizures in human generalized epilepsy. Brain Research. 837(1-2). 277–288. 18 indexed citations

15.

Kohsaka, Shinobu, et al.. (1996). Inter‐ and Intrahemispheric Phase of Diffuse 3‐Hz Spike‐and‐Wave (SW) Complex: SW Complex Versus Spike Component.. Epilepsia. 37(s3). 79–79. 2 indexed citations

16.

Nezu, Atsuo, Kimiaki Uetake, Yoshiko Nomura, & Masaya Segawa. (1991). Roles of a Subependymal Nodule of Tuberous Sclerosis on Pathophysiology of Epilepsy. Psychiatry and Clinical Neurosciences. 45(2). 372–377. 6 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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