Mamoru Ozaki

521 total citations
38 papers, 389 citations indexed

About

Mamoru Ozaki is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Mamoru Ozaki has authored 38 papers receiving a total of 389 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 14 papers in Molecular Biology and 9 papers in Surgery. Recurrent topics in Mamoru Ozaki's work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (8 papers) and Genetic Syndromes and Imprinting (4 papers). Mamoru Ozaki is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (8 papers) and Genetic Syndromes and Imprinting (4 papers). Mamoru Ozaki collaborates with scholars based in Japan, United States and France. Mamoru Ozaki's co-authors include Yo Niida, Shogo Katsuda, Yoshimichi Ueda, Katsuaki Sato, Hiroaki Kakinuma, Hideaki Chiyo, Hiroaki Takahashi, Shiro Miwa, Koji Suzuki and Tomomi Tanaka and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Obstetrics and Gynecology and European Urology.

In The Last Decade

Mamoru Ozaki

37 papers receiving 379 citations

Peers

Countries citing papers authored by Mamoru Ozaki

Since Specialization

Citations

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

Fields of papers citing papers by Mamoru Ozaki

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mamoru Ozaki

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

#	Work	Indexed citations
1	Establishment of human induced pluripotent stem cell lines, KMUGMCi006, from a patient with Tuberous sclerosis complex (TSC) bearing mosaic nonsense mutations in the Tuberous sclerosis complex 2 (TSC2) gene 2023 ·Stem Cell Research ·Hiroki Ura, Sumihito Togi, Mamoru Ozaki, (unknown), Yo Niida	1
2	Establishment of a human induced pluripotent stem cell line, KMUGMCi001-A, from a patient bearing a heterozygous c.772 + 3_772 + 4dup mutation in the ACVRL1 gene leading Telangiectasia, hereditary hemorrhagic, type 2 (HHT2) 2022 ·Stem Cell Research ·Hiroki Ura, Sumihito Togi, (unknown), Mamoru Ozaki, Yo Niida	3
3	Neonatal Death Caused by Interrupted Aortic Arch Associated With 22q11.2 Deletion Syndrome 2018 ·American Journal of Forensic Medicine & Pathology ·(unknown), Masatoshi Yamaguchi, Mamoru Ozaki, Nobuhiro Yukawa	2
4	Human Malformation Syndromes of Defective <b><i>GLI</i></b>: Opposite Phenotypes of 2q14.2 (<b><i>GLI2</i></b>) and 7p14.2 (<b><i>GLI3</i></b>) Microdeletions and a GLIA/R Balance Model 2017 ·Cytogenetic and Genome Research ·Yo Niida, Mika Inoue, Mamoru Ozaki, (unknown)	9
5	PCS/MVA syndrome caused by an Alu insertion in the BUB1B gene 2017 ·Human Genome Variation ·(unknown), Takema Kato, (unknown), (unknown), (unknown), Mamoru Ozaki, (unknown), Hiroshi Sameshima, Hiroki Kurahashi	10
6	Angelman Syndrome Caused by Chromosomal Rearrangements: A Case Report of 46,XX,+der(13)t(13;15)(q14.1;q12)mat,-15 with an Atypical Phenotype and Review of the Literature 2016 ·Cytogenetic and Genome Research ·Yo Niida, Hitoshi Sato, Mamoru Ozaki, (unknown), (unknown), (unknown)	2
7	A Girl with Greig Cephalopolysyndactyly Contiguous Gene Deletion Syndrome: The Importance and Usefulness of DNA Microarray Analysis 2015 ·Yo Niida, Mamoru Ozaki, (unknown)	1
8	Development of a practical NF1 genetic testing method through the pilot analysis of five Japanese families with neurofibromatosis type 1 2014 ·Brain and Development ·Akiko Okumura, Mamoru Ozaki, Yo Niida	7
9	Paternal uniparental isodisomy of chromosome 22 in a patient with metachromatic leukodystrophy 2012 ·Journal of Human Genetics ·Yo Niida, (unknown), (unknown), (unknown), Mamoru Ozaki	9
10	Extrauterine endometrial stromal sarcoma with JAZF1/JJAZ1 fusion confirmed by RT-PCR and interphase FISH presenting as an inguinal tumor 2007 ·Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin ·Katsuaki Sato, Yoshimichi Ueda, (unknown), Mamoru Ozaki, Masanori Hisaoka, Shogo Katsuda	20
11	Rapid detection of trisomy 21 by gene dosage analysis using quantitative real‐time polymerase chain reaction 2006 ·Journal of obstetrics and gynaecology research ·Tomoko Tsujie, Masahiko Takemura, Tadashi Kimura, Koichiro Shimoya, Tateki Tsutsui, Kazuhide Ogita, Mamoru Ozaki, Yuji Murata	6
12	Pleomorphic adenoma (benign mixed tumor) of the breast: A case report and review of the literature 2005 ·Pathology - Research and Practice ·Katsuaki Sato, Yoshimichi Ueda, (unknown), Mamoru Ozaki, Naoki Nitta, Kiran Chada, (unknown), Shogo Katsuda	25
13	Incidence of Diffuse Large B-Cell Lymphoma of Germinal Center B-Cell Origin in Whole Diffuse Large B-Cell Lymphoma: Tissue Fluorescence In Situ Hybridization Using t(14;18) Compared with Immunohistochemistry 2005 ·International Journal of Hematology ·Yuko Hirose, Yasufumi Masaki, (unknown), Kumiko Shimoyama, Toshihiro Fukushima, Hiroshi Kawabata, Noriyoshi Ogawa, Yuji Wano, Mamoru Ozaki	11
14	Centrosome Hyperamplification and Chromosomal Damage after Exposure to Radiation 2004 ·Oncology ·Kenji Kawamura, (unknown), Mamoru Ozaki, Kuniyoshi Iwabuchi, Hideyuki Nakashima, (unknown), (unknown), Masao Inoue, Kenzo Tokunaga, (unknown), Ryosuke Ikeda, Koji Suzuki	21
15	Centrosome Hyperamplification and Chromosomal Instability in Bladder Cancer 2003 ·European Urology ·Kenji Kawamura, Manabu Moriyama, (unknown), Mamoru Ozaki, Takuji Tanaka, Takayuki Nojima, Kohzaburo Fujikawa‐Yamamoto, Ryosuke Ikeda, Koji Suzuki	26
16	Bilateral pleural effusion in the first trimester: A predictor of chromosomal abnormality and embryonic death? 1997 ·American Journal of Obstetrics and Gynecology ·Takashi Shimizu, Kazumasa Hashimoto, Michio SHIMIZU, Mamoru Ozaki, Yuji Murata	5
17	Elevated Cytokine Levels in Synovial Fluid of Rheumatoid Arthritis Correlates with the Presence of Cytomegalovirus Genome 1994 ·Autoimmunity ·T Murayama, Naoyuki Tsuchiya, (unknown), Mamoru Ozaki, Daitoku Sakamuro, Kanji Hirai, Shoichi Shimizu, Ko Ito, Kouji Matsushima, (unknown)	11
18	Papillary Renal Cell Carcinoma With Numeric Changes of Chromosomes in a Long-Term Hemodialysis Patient: A Karyotype Analysis 1993 ·American Journal of Kidney Diseases ·(unknown), (unknown), Mamoru Ozaki	18
19	A case of ring chromosome 15 accompanied by almost normal intelligence 1990 ·Human Genetics ·(unknown), Hiroaki Takahashi, Mamoru Ozaki, (unknown), (unknown)	10
20	Localization of the spherocytosis gene to chromosome segment 8p11.22?8p21.1 1988 ·Human Genetics ·(unknown), Hideaki Chiyo, Mamoru Ozaki, (unknown), Shiro Miwa	30

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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