Hironao Numabe

677 total citations
32 papers, 281 citations indexed

About

Hironao Numabe is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Hironao Numabe has authored 32 papers receiving a total of 281 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 12 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Hironao Numabe's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Prenatal Screening and Diagnostics (5 papers) and Connective tissue disorders research (4 papers). Hironao Numabe is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Prenatal Screening and Diagnostics (5 papers) and Connective tissue disorders research (4 papers). Hironao Numabe collaborates with scholars based in Japan, Spain and United States. Hironao Numabe's co-authors include Yutaka Nakahori, Yasuo Nakagome, Kenji Kurosawa, Takashi Tamura, Satoru Sakazume, Shigeo Nagafuchi, Nobuhiko Okamoto, Kenjiro Kosaki, Gen Nishimura and Hisashi Kawashima and has published in prestigious journals such as Human Molecular Genetics, Genomics and Human Genetics.

In The Last Decade

Hironao Numabe

30 papers receiving 267 citations

Peers

Countries citing papers authored by Hironao Numabe

Since Specialization

Citations

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

Fields of papers citing papers by Hironao Numabe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hironao Numabe

This figure shows the co-authorship network connecting the top 25 collaborators of Hironao Numabe. A scholar is included among the top collaborators of Hironao Numabe 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 Hironao Numabe. Hironao Numabe 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	Complex chromosomal 6q rearrangements revealed by combined long-molecule genomics technologies 2024 ·Genomics ·(unknown), Hironao Numabe, Satomi Mitsuhashi, Naomi Tsuchida, Yuri Uchiyama, Eriko Koshimizu, Kohei Hamanaka, Kazuharu Misawa, Satoko Miyatake, (unknown), Atsushi Fujita, Naomichi Matsumoto	1
2	De novo non-synonymous DPYSL2 (CRMP2) variants in two patients with intellectual disabilities and documentation of functional relevance through zebrafish rescue and cellular transfection experiments 2022 ·Human Molecular Genetics ·Hisato Suzuki, (unknown), (unknown), (unknown), Miyuki Takahashi, Mamiko Yamada, Hironobu Okuno, Fuyuki Miya, Toshiki Takenouchi, Hironao Numabe, Kenjiro Kosaki, Toshio Ohshima	7
3	Development of individuals with thanatophoric dysplasia surviving beyond infancy 2021 ·Pediatrics International ·(unknown), Hideaki Sawai, Hironao Numabe, Gen Nishimura, Hiroaki Shibahara	4
4	National survey of prevalence and prognosis of thanatophoric dysplasia in Japan 2019 ·Pediatrics International ·Hideaki Sawai, Kaname Oka, (unknown), Gen Nishimura, Takashi Omori, Hironao Numabe, Shinji Kosugi	11
5	Self-perceptions from people with Down syndrome in Japan 2018 ·Journal of Human Genetics ·(unknown), Rina Takahashi, (unknown), (unknown), Junko Yotsumoto, Hironao Numabe	4
6	Novel compound heterozygous DPH1 mutations in a patient with the unique clinical features of airway obstruction and external genital abnormalities 2018 ·Journal of Human Genetics ·(unknown), Shingo Oana, (unknown), Mitsuko Nakashima, Hironao Numabe, Hisashi Kawashima, Naomichi Matsumoto, Noriko Miyake	7
7	The severe clinical phenotype for a heterozygous Fabry female patient correlates to the methylation of non-mutated allele associated with chromosome 10q26 deletion syndrome 2017 ·Molecular Genetics and Metabolism ·Mohammad Arif Hossain, Hiroko Yanagisawa, Takashi Miyajima, (unknown), Ayumi Takamura, (unknown), (unknown), (unknown), Takeo Iwamoto, (unknown), Kenji Kurosawa, Hironao Numabe, Yoshikatsu Eto	14
8	Background of couples undergoing non‐invasive prenatal testing in Japan 2016 ·Journal of obstetrics and gynaecology research ·Eri Takeda, Nobuhiro Suzumori, Kyoko Kumagai, (unknown), Takeshi Ebara, Junko Yotsumoto, Hironao Numabe, Mayumi Sugiura‐Ogasawara	5
9	Hypergonadotropic hypogonadism and hypersegmented neutrophils in a patient with ataxia‐telangiectasia‐like disorder: Potential diagnostic clues? 2014 ·American Journal of Medical Genetics Part A ·Takeshi Yoshida, Tomonari Awaya, Minoru Shibata, Takeo Kato, Hironao Numabe, Junya Kobayashi, (unknown), Toshio Heike	9
10	Compound heterozygous deletions in pseudoautosomal region 1 in an infant with mild manifestations of langer mesomelic dysplasia 2013 ·American Journal of Medical Genetics Part A ·Takayoshi Tsuchiya, Minoru Shibata, Hironao Numabe, (unknown), Kazuhiko Nakabayashi, Gen Nishimura, Toshiro Nagai, Tsutomu Ogata, Maki Fukami	11
11	High concentration of middle chain fatty acid in a case of Duchenne muscular dystrophy with severe mental retardation 2012 ·Pediatrics International ·Hisashi Kawashima, Kiyoko Watanabe, (unknown), Hiroaki Ioi, Yasuyo Kashiwagi, Tasuku Miyajima, Kouji Takekuma, Ichizo Nishino, Hironao Numabe	2
12	GPC3 mutations in seven patients with Simpson–Golabi–Behmel syndrome 2007 ·American Journal of Medical Genetics Part A ·Satoru Sakazume, Nobuhiko Okamoto, Toshiyuki Yamamoto, Kenji Kurosawa, Hironao Numabe, Yuko Ohashi, Yuko Kako, Toshiro Nagai, (unknown)	23
13	Comprehensive screening of CREB‐binding protein gene mutations among patients with Rubinstein‐Taybi syndrome using denaturing high‐performance liquid chromatography 2005 ·Congenital Anomalies ·Toru Udaka, (unknown), Rika Kosaki, Kenji Kurosawa, Nobuhiko Okamoto, Seiji Mizuno, Yoshio Makita, Hironao Numabe, Joaquín Fernández Toral, Takao Takahashi, Kenjiro Kosaki	19
14	Children Behavior Checklist (CBCL)/2−3 in children with febrile episodes under 3 months of age and enterovirus infection 2002 ·Pediatrics International ·Hisashi Kawashima, (unknown), Yasuyo Kashiwagi, (unknown), (unknown), Takeshi Takami, Hironao Numabe, Kouji Takekuma, Akinori Hoshika	2
15	Introduction of a security system based on fingerprint authentication, a encipherment device an virtual private network(VPN) technology. 2000 ·Medical Informatics ·(unknown), (unknown), (unknown), (unknown), (unknown), Masayuki Kitamura, Hironao Numabe	0
16	Squamous cell carcinoma‐related antigen in children with atopic dermatitis 2000 ·Pediatrics International ·Hisashi Kawashima, Shigeo Nishimata, Yasuyo Kashiwagi, Hironao Numabe, (unknown), (unknown), Kouji Takekuma, Akinori Hoshika	17
17	PCR detection of structurally abnormal Y chromosomes 1992 ·The Japanese Journal of Human Genetics ·Shigeo Nagafuchi, Satoko Seki, Yutaka Nakahori, Takashi Tamura, Hironao Numabe, Yasuo Nakagome	24
18	The majority of the marker chromosomes in Japanese patients with stigmata of turner syndrome are derived from Y chromosomes 1992 ·Human Genetics ·(unknown), Takashi Tamura, Yutaka Nakahori, Kazue Takano, Yoshikazu Nishi, Noritaka Iwatani, (unknown), (unknown), Susumu Konda, Tomoko Hasegawa, Hironao Numabe, Kenji Fujieda, (unknown), Itsuro Hibi, Yasuo Nakagome	35
19	Localization of 24 cosmid clones on the human Y chromosome 1992 ·The Japanese Journal of Human Genetics ·Shigeo Nagafuchi, Yutaka Nakahori, Yusuke Nakamura, Sarah England, Takashi Tamura, Hironao Numabe, Yasuo Nakagome	1
20	DNA analyses of XX and XX-hypospadiac males 1992 ·Human Genetics ·Hironao Numabe, Shigeo Nagafuchi, Yutaka Nakahori, Takashi Tamura, (unknown), Mikio Namiki, (unknown), Yoshimitsu Fukushima, Hideki Fuse, (unknown), Takayuki Arai, Yutaka Matsuzaki, Keiko Fukutani, Koichiro Isurugi, Yoshikazu Kuroki, Tatsuro Ikeuchi, Masahiko Yoshida, Shigeru Minowada, Yasuo Nakagome	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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