Yoko Narumi

1.7k total citations
14 papers, 520 citations indexed

About

Yoko Narumi is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Yoko Narumi has authored 14 papers receiving a total of 520 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Immunology. Recurrent topics in Yoko Narumi's work include Hedgehog Signaling Pathway Studies (3 papers), Protein Tyrosine Phosphatases (3 papers) and Galectins and Cancer Biology (3 papers). Yoko Narumi is often cited by papers focused on Hedgehog Signaling Pathway Studies (3 papers), Protein Tyrosine Phosphatases (3 papers) and Galectins and Cancer Biology (3 papers). Yoko Narumi collaborates with scholars based in Japan, South Korea and Germany. Yoko Narumi's co-authors include Yoko Aoki, Tetsuya Niihori, Shigeo Kure, Yoichi Matsubara, Yoshimitsu Fukushima, Tomoki Kosho, Keiko Wakui, Makoto Yoshida, Satoru Sakazume and Yoshio Makita and has published in prestigious journals such as Human Mutation, Chemical and Pharmaceutical Bulletin and Clinical Genetics.

In The Last Decade

Yoko Narumi

14 papers receiving 512 citations

Peers

Countries citing papers authored by Yoko Narumi

Since Specialization

Citations

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

Fields of papers citing papers by Yoko Narumi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yoko Narumi

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

All Works

Sort: Min cites: Since: Top N: Style:

14 of 14 papers shown

#	Work	Indexed citations
1	Identification of a novel missense mutation of MAF in a Japanese family with congenital cataract by whole exome sequencing: A clinical report and review of literature 2014 ·American Journal of Medical Genetics Part A ·Yoko Narumi, Sachiko Nishina, (unknown), Yoko Aoki, Rika Kosaki, Keiko Wakui, Noriyuki Azuma, Toshinori Murata, Fumio Takada, Yoshimitsu Fukushima, Tomoki Kosho	28
2	Clinical consequences in truncating mutations in exon 34 of NOTCH2: Report of six patients with Hajdu–Cheney syndrome and a patient with serpentine fibula polycystic kidney syndrome 2013 ·American Journal of Medical Genetics Part A ·Yoko Narumi, (unknown), Kenji Shimizu, (unknown), (unknown), Kōichi Nakamura, Tomoki Kosho, Yumie Rhee, Yoon‐Sok Chung, Ok‐Hwa Kim, Yoshimitsu Fukushima, Woong‐Yang Park, Gen Nishimura	23
3	Microarray and FISH‐based genotype–phenotype analysis of 22 Japanese patients with Wolf–Hirschhorn syndrome 2013 ·American Journal of Medical Genetics Part A ·Kenji Shimizu, Keiko Wakui, Tomoki Kosho, Nobuhiko Okamoto, Seiji Mizuno, Kazuya Itomi, (unknown), (unknown), Osamu Samura, Yoshiyuki Kobayashi, Yuko Kako, Takashi Arai, Tsutomu Oh‐ishi, Hiroshi Kawame, Yoko Narumi, Hirofumi Ohashi, Yoshimitsu Fukushima	21
4	Exome sequencing in a family with an X‐linked lethal malformation syndrome: clinical consequences of hemizygous truncating OFD1 mutations in male patients 2012 ·Clinical Genetics ·Yoshinori Tsurusaki, Tomoki Kosho, (unknown), Yoko Narumi, Keiko Wakui, Yoshimitsu Fukushima, Hiroshi Doi, Hirotomo Saitsu, Noriko Miyake, Naomichi Matsumoto	21
5	Hypomyelination with atrophy of the basal ganglia and cerebellum in an infant with Down syndrome 2011 ·Clinical Dysmorphology ·Yoko Narumi, Takashi Shiihara, Hiroshi Yoshihashi, Satoru Sakazume, Marjo S. van der Knaap, (unknown), Naomichi Matsumoto, Yoshimitsu Fukushima	2
6	Implantable cardioverter defibrillator for progressive hypertrophic cardiomyopathy in a patient with LEOPARD syndrome and a novel PTPN11 mutation Gln510His 2011 ·American Journal of Medical Genetics Part A ·Yasushi Wakabayashi, (unknown), Yoko Narumi, (unknown), (unknown), Keiko Wakui, Yoshimitsu Fukushima, Yoichi Matsubara, Yoko Aoki, Tomoki Kosho	6
7	Myelodysplastic syndrome in a child with 15q24 deletion syndrome 2011 ·American Journal of Medical Genetics Part A ·Yoko Narumi, Masaaki Shiohara, Keiko Wakui, Asahito Hama, Seiji Kojima, Kentaro Yoshikawa, Yoshiro Amano, Tomoki Kosho, Yoshimitsu Fukushima	6
8	A variant of Desbuquois dysplasia characterized by advanced carpal bone age, short metacarpals, and elongated phalanges: Report of seven cases 2010 ·American Journal of Medical Genetics Part A ·Ok‐Hwa Kim, Gen Nishimura, Hae‐Ryong Song, Yoshito Matsui, Satoru Sakazume, Masanobu Yamada, Yoko Narumi, Yasemin Alanay, Sheila Unger, Tae‐Joon Cho, Sung Sup Park, Shiro Ikegawa, Peter Meinecke, Andrea Superti‐Furga	30
9	Genital abnormalities in Pallister–Hall syndrome: Report of two patients and review of the literature 2010 ·American Journal of Medical Genetics Part A ·Yoko Narumi, Tomoki Kosho, (unknown), Masaaki Shiohara, (unknown), Tetsuo Mori, Ayako Shimizu, Yasuhiko Igawa, (unknown), Kimiyo Takagi, Rie Kawamura, Keiko Wakui, Yoshimitsu Fukushima	19
10	A patient with early onset Huntington disease and severe cerebellar atrophy 2009 ·American Journal of Medical Genetics Part A ·Satoru Sakazume, (unknown), Eiji Oguma, (unknown), Takuma Ishii, Yoko Narumi, Takashi Shiihara, Hirofumi Ohashi	19
11	The RAS/MAPK syndromes: novel roles of the RAS pathway in human genetic disorders 2008 ·Human Mutation ·Yoko Aoki, Tetsuya Niihori, Yoko Narumi, Shigeo Kure, Yoichi Matsubara	256
12	Leukemia in Cardio-facio-cutaneous (CFC) Syndrome: A Patient With a Germline Mutation in BRAF Proto-oncogene 2007 ·Journal of Pediatric Hematology/Oncology ·Yoshio Makita, Yoko Narumi, Makoto Yoshida, Tetsuya Niihori, Shigeo Kure, Kenji Fujieda, Yoichi Matsubara, Yoko Aoki	40
13	A novel KCNQ4 one-base deletion in a large pedigree with hearing loss: implication for the genotype–phenotype correlation 2006 ·Journal of Human Genetics ·Fumiaki Kamada, Shigeo Kure, Takayuki Kudo, Yoichi Suzuki, Takeshi Oshima, Akiko Ichinohe, Kanako Kojima, Tetsuya Niihori, Junko Kanno, Yoko Narumi, Ayumi Narisawa, (unknown), Yoko Aoki, Katsuhisa Ikeda, Toshimitsu Kobayashi, Yoichi Matsubara	40
14	Comparative studies on the constituents of a parasitic plant and its host. III. On the constituents of Boschniakia rossica FEDTSCH. et FLEROV. (2). 1987 ·Chemical and Pharmaceutical Bulletin ·Tenji Konishi, Yoko Narumi, Kazuaki Watanabe, Shiu Kiyosawa, JUNZO SHOJI	9

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.

Explore authors with similar magnitude of impact