Yumiko Ondo

598 total citations
19 papers, 450 citations indexed

About

Yumiko Ondo is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Yumiko Ondo has authored 19 papers receiving a total of 450 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Yumiko Ondo's work include Genomic variations and chromosomal abnormalities (9 papers), Genomics and Rare Diseases (4 papers) and Congenital heart defects research (4 papers). Yumiko Ondo is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Genomics and Rare Diseases (4 papers) and Congenital heart defects research (4 papers). Yumiko Ondo collaborates with scholars based in Japan and Australia. Yumiko Ondo's co-authors include Shinichi Kohsaka, Takae Hirasawa, Toshiyuki Yamamoto, Nobuhiko Okamoto, Y. Imai, Keiko Shimojima, Chihiro Akazawa, Shigeo Uchino, Yasuko Nakamura and Shizuyo Honda and has published in prestigious journals such as Blood, Biochemical and Biophysical Research Communications and Neuroscience.

In The Last Decade

Yumiko Ondo

19 papers receiving 445 citations

Peers

Countries citing papers authored by Yumiko Ondo

Since Specialization

Citations

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

Fields of papers citing papers by Yumiko Ondo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yumiko Ondo

This figure shows the co-authorship network connecting the top 25 collaborators of Yumiko Ondo. A scholar is included among the top collaborators of Yumiko Ondo 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 Yumiko Ondo. Yumiko Ondo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Molecular Profiles of Breast Cancer in a Single Institution 2020 ·Anticancer Research ·Takako Kamio, (unknown), Takako Aoki, Yumiko Ondo, (unknown), (unknown), (unknown), Takahiro Okamoto, Hitoshi Kanno, Toshiyuki Yamamoto	2
2	Complex chromosomal rearrangements of human chromosome 21 in a patient manifesting clinical features partially overlapped with that of Down syndrome 2020 ·Human Genetics ·(unknown), (unknown), (unknown), Yumiko Ondo, Eriko Nishi, Nobuhiko Okamoto, Toshiyuki Yamamoto	7
3	Analyses of breakpoint junctions of complex genomic rearrangements comprising multiple consecutive microdeletions by nanopore sequencing 2020 ·Journal of Human Genetics ·(unknown), (unknown), (unknown), Yumiko Ondo, Toshiyuki Yamamoto	10
4	MED13L haploinsufficiency syndrome: A de novo frameshift and recurrent intragenic deletions due to parental mosaicism 2017 ·American Journal of Medical Genetics Part A ·Toshiyuki Yamamoto, Keiko Shimojima, Yumiko Ondo, Shuichi Shimakawa, Nobuhiko Okamoto	24
5	A novel TUBB4A mutation G96R identified in a patient with hypomyelinating leukodystrophy onset beyond adolescence 2017 ·Human Genome Variation ·Yongping Lu, Yumiko Ondo, Keiko Shimojima, Hitoshi Osaka, Toshiyuki Yamamoto	13
6	A 15q14 microdeletion involving MEIS2 identified in a patient with autism spectrum disorder 2017 ·Human Genome Variation ·Keiko Shimojima, Yumiko Ondo, Nobuhiko Okamoto, Toshiyuki Yamamoto	9
7	Familial 9q33q34 microduplication in siblings with developmental disorders and macrocephaly 2017 ·European Journal of Medical Genetics ·Keiko Shimojima, Nobuhiko Okamoto, Himanshu Goel, Yumiko Ondo, Toshiyuki Yamamoto	2
8	Mutations in NSD1 and NFIX in Three Patients with Clinical Features of Sotos Syndrome and Malan Syndrome 2017 ·Journal of Pediatric Genetics ·Yongping Lu, Pin Fee Chong, Ryutaro Kira, Toshiyuki Seto, Yumiko Ondo, Keiko Shimojima, Toshiyuki Yamamoto	6
9	A novel <i>CASK</i> mutation identified in siblings exhibiting developmental disorders with/without microcephaly 2017 ·Intractable & Rare Diseases Research ·Toshiyuki Seto, Takashi Hamazaki, (unknown), Satoshi Kudo, Haruo Shintaku, Yumiko Ondo, Keiko Shimojima, Toshiyuki Yamamoto	17
10	Loss-of-function mutations and global rearrangements in GPC3 in patients with Simpson–Golabi–Behmel syndrome 2016 ·Human Genome Variation ·Keiko Shimojima, Yumiko Ondo, Eriko Nishi, Seiji Mizuno, (unknown), (unknown), (unknown), Maho Sato, Masami Inoue, Nobuhiko Okamoto, Toshiyuki Yamamoto	10
11	Challenges in detecting genomic copy number aberrations using next-generation sequencing data and the eXome Hidden Markov Model: a clinical exome-first diagnostic approach 2016 ·Human Genome Variation ·Toshiyuki Yamamoto, Keiko Shimojima, Yumiko Ondo, Katsumi Imai, Pin Fee Chong, Ryutaro Kira, (unknown), Akira Saito, Nobuhiko Okamoto	36
12	A de novo microdeletion in a patient with inner ear abnormalities suggests that the 10q26.13 region contains the responsible gene 2016 ·Human Genome Variation ·Noriko Sangu, Nobuhiko Okamoto, Keiko Shimojima, Yumiko Ondo, Masanori Nishikawa, Toshiyuki Yamamoto	8
13	Concurrent occurrence of an inherited 16p13.11 microduplication and a de novo 19p13.3 microdeletion involving MAP2K2 in a patient with developmental delay, distinctive facial features, and lambdoid synostosis 2016 ·European Journal of Medical Genetics ·Keiko Shimojima, Yumiko Ondo, (unknown), Nozomi Sano, (unknown), Tatsuki Oyoshi, Nayuta Higa, Hiroshi Tokimura, Kazunori Arita, Toshiyuki Yamamoto	4
14	The Novel Missense Mutation of GATA1 Caused Red Cell Adenosine Deaminase Overproduction Associated with Congenital Hemolytic Anemia 2016 ·Blood ·(unknown), Toshiyuki Yamamoto, Taiju Utsugisawa, Takako Aoki, Takuya Iwasaki, Yumiko Ondo, Takahiro Kawakami, Shinichiro Nakagawa, Shuichi Ozono, Hiroko Inada, Hitoshi Kanno	1
15	Novel variants of the SHANK3 gene in Japanese autistic patients with severe delayed speech development 2011 ·Psychiatric Genetics ·Chikako Waga, Nobuhiko Okamoto, Yumiko Ondo, (unknown), Yu‐ichi Goto, Shinichi Kohsaka, Shigeo Uchino	46
16	Inhibition of N-methyl-d-aspartate receptor activity resulted in aberrant neuronal migration caused by delayed morphological development in the mouse neocortex 2010 ·Neuroscience ·(unknown), Takae Hirasawa, Hidenori Tabata, (unknown), Chikako Waga, Yumiko Ondo, Kazunori Nakajima, Shinichi Kohsaka	10
17	Direct interaction of post‐synaptic density‐95/Dlg/ZO‐1 domain‐containing synaptic molecule Shank3 with GluR1 α‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazole propionic acid receptor 2006 ·Journal of Neurochemistry ·Shigeo Uchino, (unknown), Shizuyo Honda, Yasuko Nakamura, Yumiko Ondo, (unknown), Moe Tsutsumi, Eri Suzuki, Takae Hirasawa, Shinichi Kohsaka	77
18	Visualization of microglia in living tissues using Iba1‐EGFP transgenic mice 2005 ·Journal of Neuroscience Research ·Takae Hirasawa, (unknown), Y. Imai, Yumiko Ondo, Chihiro Akazawa, (unknown), Shinichi Kohsaka	141
19	Slo2 sodium-activated K+ channels bind to the PDZ domain of PSD-95 2003 ·Biochemical and Biophysical Research Communications ·Shigeo Uchino, (unknown), Shizuyo Honda, Takae Hirasawa, (unknown), Yasuko Nakamura, Yumiko Ondo, Shinichi Kohsaka	27

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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