Mari Matsuo

1.1k total citations
23 papers, 346 citations indexed

About

Mari Matsuo is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Mari Matsuo has authored 23 papers receiving a total of 346 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 11 papers in Molecular Biology and 5 papers in Surgery. Recurrent topics in Mari Matsuo's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Syndromes and Imprinting (2 papers). Mari Matsuo is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Syndromes and Imprinting (2 papers). Mari Matsuo collaborates with scholars based in Japan. Mari Matsuo's co-authors include Kenji Kurosawa, Toshiyuki Yamamoto, Kayoko Saito, Keiko Shimojima, Kiyoshi Imaizumi, Yoshikazu Kuroki, Tsutomu Ogata, Mitsuo Masuno, Koji Muroya and Yoshimitsu Fukushima and has published in prestigious journals such as Human Genetics, Nutrition and Epilepsy Research.

In The Last Decade

Mari Matsuo

22 papers receiving 340 citations

Peers

Countries citing papers authored by Mari Matsuo

Since Specialization

Citations

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

Fields of papers citing papers by Mari Matsuo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mari Matsuo

This figure shows the co-authorship network connecting the top 25 collaborators of Mari Matsuo. A scholar is included among the top collaborators of Mari Matsuo 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 Mari Matsuo. Mari Matsuo 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	Analysis of SMN protein in umbilical cord blood and postnatal peripheral blood of neonates with SMA: a rationale for prompt treatment initiation to prevent SMA development 2025 ·Orphanet Journal of Rare Diseases ·Noriko Otsuki, Tamaki Kato, (unknown), (unknown), Mari Matsuo, Emiko Kobayashi, Kazuhiro Haginoya, Hiroyuki Awano, Yasuhiro Takeshima, Toshio Saito, Kayoko Saito	2
2	Epidemiological investigation of spinal muscular atrophy in Japan 2021 ·Brain and Development ·(unknown), (unknown), (unknown), Tamaki Kato, Mari Matsuo, Kenji Nakashima, Kayoko Saito	19
3	Acromegaloid facial appearance syndrome 2020 ·Definitions ·Mari Matsuo	0
4	Effect of dietary fatty acid and micronutrient intake/energy ratio on serum diamine oxidase activity in healthy women 2017 ·Nutrition ·Makoto Miyoshi, (unknown), Mari Matsuo, Yasuhiro Hamada, Michiko Takahashi, Masashi Yamamoto, (unknown), (unknown), (unknown), (unknown), (unknown), Midori Hirai, Makoto Usami	4
5	Mandibulofacial dysostosis with microcephaly: A case presenting with seizures 2016 ·Brain and Development ·Mari Matsuo, (unknown), Yasushi Ito, Masako Sakauchi, Toshiyuki Yamamoto, Nobuhiko Okamoto, Yoshinori Tsurusaki, Noriko Miyake, Naomichi Matsumoto, Kayoko Saito	16
6	Genetic Counseling for Couples Seeking Noninvasive Prenatal Testing in Japan: Experiences of Pregnant Women and their Partners 2016 ·Journal of Genetic Counseling ·(unknown), Mari Matsuo, Masaki Ogawa, (unknown), Satoru Shimizu, Naoko Iwasaki, (unknown), (unknown), Hironao Numabe, Kayoko Saito	11
7	De novo triplication of 11q12.3 in a patient with developmental delay and distinctive facial features 2013 ·Molecular Cytogenetics ·Toshiyuki Yamamoto, Mari Matsuo, Shino Shimada, Noriko Sangu, Keiko Shimojima, (unknown), Kayoko Saito	3
8	A sibling case of Wolfram syndrome with a novel mutation Y652X in WFS1 2013 ·Diabetology International ·Naoko Iwasaki, (unknown), Mari Matsuo, (unknown), (unknown), Yuko Ono, Katsuya Tanabe, Yukio Tanizawa, Makiko Ogata, (unknown), (unknown), Satoru Nagata, Makiko Ōsawa, Yasuko Uchigata, Kayoko Saito	1
9	Clinical manifestations of the deletion of Down syndrome critical region including DYRK1A and KCNJ6 2010 ·American Journal of Medical Genetics Part A ·Toshiyuki Yamamoto, Keiko Shimojima, Tsutomu Nishizawa, Mari Matsuo, Masahiro Ito, Katsumi Imai	41
10	Genomic copy number variations at 17p13.3 and epileptogenesis 2010 ·Epilepsy Research ·Keiko Shimojima, (unknown), Hiroka Takahashi, (unknown), Yukitoshi Takahashi, Kousaku Ohno, Mari Matsuo, Kayoko Saito, Toshiyuki Yamamoto	34
11	Clinical presentation, EEG studies, and novel mutations in two cases of GLUT1 deficiency syndrome in Japan 2004 ·Brain and Development ·Yasushi Ito, (unknown), Hirokazu Oguni, Tomohiro Nakayama, Mari Matsuo, Makoto Funatsuka, Thomas Voït, Jörg Klepper, Makiko Ōsawa	19
12	Further delineation of the behavioral and neurologic features in Costello syndrome 2003 ·American Journal of Medical Genetics Part A ·Hiroshi Kawame, (unknown), Kenji Kurosawa, Mari Matsuo, Mitsuo Masuno, Hirofumi Ohashi, Noboru Fueki, (unknown), (unknown), Kaoru Suzuki, Akira Akatsuka, (unknown), Yoshimitsu Fukushima	46
13	Paternal UPD14 is responsible for a distinctive malformation complex 2002 ·American Journal of Medical Genetics ·Kenji Kurosawa, Hiroyuki Sasaki, Yoshiaki Sato, Michiko Yamanaka, (unknown), Yuji Ito, Torayuki Okuyama, Mari Matsuo, Kiyoshi Imaizumi, Yoshikazu Kuroki, Gen Nishimura	45
14	Premature thelarche in Rubinstein‐Taybi syndrome 2002 ·American Journal of Medical Genetics ·Kenji Kurosawa, Mitsuo Masuno, Katsuhiko Tachibana, Kiyoshi Imaizumi, Mari Matsuo, Yoshikazu Kuroki	3
15	Sotos syndrome associated with a de novo balanced reciprocal translocation t(5;8)(q35;q24.1) 2001 ·American Journal of Medical Genetics ·Kiyoshi Imaizumi, Junko Kimura, Mari Matsuo, Kenji Kurosawa, Mitsuo Masuno, Norio Niikawa, Yoshikazu Kuroki	31
16	47,XXX male: A clinical and molecular study 2001 ·American Journal of Medical Genetics ·Tsutomu Ogata, Mari Matsuo, Koji Muroya, Yasuhiro Koyama, Keiko Fukutani	5
17	[Weaver syndrome(Weaver-Smith syndrome)]. 2001 ·PubMed ·Mari Matsuo	1
18	[Acrocallosal syndrome (Schinzel type)]. 2001 ·PubMed ·Mari Matsuo	1
19	Clinical and molecular studies in 15 females with ring X chromosomes: implications for r(X) formation and mental development 2000 ·Human Genetics ·Mari Matsuo, Koji Muroya, Masanori Adachi, Katsuhiko Tachibana, Yumi Asakura, Yoshiko Nakagomi, Keiichi Hanaki, Susumu Yokoya, (unknown), Yutaka Igarashi, Kunihiko Hanew, Nobutake Matsuo, Tsutomu Ogata	10
20	Random X-inactivation in a girl with duplication Xp11.21-p21.3: Report of a patient and review of the literature 1999 ·American Journal of Medical Genetics ·Mari Matsuo, Koji Muroya, Kenjiro Kosaki, Takashi Ishii, Yoshimitsu Fukushima, Makoto Anzo, Tsutomu Ogata	28

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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