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Nakagawanosato Hospital for the Disabled

InstitutionResearch output, impact & collaborations

Nakagawanosato Hospital for the Disabled is a institution indexed in ScholarIQ from OpenAlex.

What is known about Nakagawanosato Hospital for the Disabled?

ScholarIQrecord summary

Nakagawanosato Hospital for the Disabled is a research organisation in Saitama, JP. OpenAlex records 33 works and 1,352 citations for it.

How many works does Nakagawanosato Hospital for the Disabled have?

ScholarIQindexed works

Nakagawanosato Hospital for the Disabled has 33 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Nakagawanosato Hospital for the Disabled have?

ScholarIQcitation count

Nakagawanosato Hospital for the Disabled has 1,352 citations in the OpenAlex counts ScholarIQ stores.

What is the average h-index at Nakagawanosato Hospital for the Disabled?

ScholarIQavg h-index

Nakagawanosato Hospital for the Disabled has an average h-index of 49 in OpenAlex.

What is the ROR of Nakagawanosato Hospital for the Disabled?

ScholarIQror

The ROR for Nakagawanosato Hospital for the Disabled is on the source record.

What is the OpenAlex record for Nakagawanosato Hospital for the Disabled?

ScholarIQopenalex

The OpenAlex for Nakagawanosato Hospital for the Disabled is on the source record.

Who are the most-cited researchers behind Nakagawanosato Hospital for the Disabled?

ScholarIQtop researchers by citations
1
Toshiro Nagai · Genetic Syndromes and Imprinting
224 works9,078 citations

What are the most-cited papers on Nakagawanosato Hospital for the Disabled?

ScholarIQmost cited works
Haploinsufficiency of NSD1 causes Sotos syndrome
Naohiro Kurotaki, Kiyoshi Imaizumi, Naoki Harada, Mitsuo Masuno, Tatsuro Kondoh, Toshiro Nagai, Hirofumi Ohashi, Kenji Naritomi, Masato Tsukahara, Yoshio Makita, Tateo Sugimoto, Tohru Sonoda, Tomoko Hasegawa, Yasuaki Chinen, Hiroaki Tomita, Akira Kinoshita, Tsuyoshi Mizuguchi, Koh-ichiro Yoshiura, Tohru Ohta, Tatsuya Kishino, Yoshimitsu Fukushima, Norio Niikawa, Naomichi Matsumoto
Nature Genetics. 2002660 Citations
Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome
Yoshinori Tsurusaki, Nobuhiko Okamoto, Hirofumi Ohashi, Tomoki Kosho, Yoko Imai, Yumiko Hibi‐Ko, Tadashi Kaname, Kenji Naritomi, Hiroshi Kawame, Keiko Wakui, Yoshimitsu Fukushima, Tomomi Homma, Mitsuhiro Kato, Yoko Hiraki, Takanori Yamagata, Shoji Yano, Seiji Mizuno, Satoru Sakazume, Takuma Ishii, Toshiro Nagai, Masaaki Shiina, Kazuhiro Ogata, Tohru Ohta, Norio Niikawa, Satoko Miyatake, Ippei Okada, Takeshi Mizuguchi, Hiroshi Doi, Hirotomo Saitsu, Noriko Miyake, Naomichi Matsumoto
Nature Genetics. 2012526 Citations
ITPKC functional polymorphism associated with Kawasaki disease susceptibility and formation of coronary artery aneurysms
Yoshihiro Onouchi, Tomohiko Gunji, Jane C. Burns, Chisato Shimizu, Jane W. Newburger, Mayumi Yashiro, Yoshikazu Nakamura, Hiroshi Yanagawa, Keiko Wakui, Yoshimitsu Fukushima, Fumio Kishi, Kunihiro Hamamoto, Masaru Terai, Yoshitake Sato, Kazunobu Ouchi, Tsutomu Saji, Akiyoshi Nariai, Yoichi Kaburagi, Tetsushi Yoshikawa, Kyoko Suzuki, Takeo Tanaka, Toshiro Nagai, Hideo Cho, Akihiro Fujino, Akihiro Sekine, Reiichiro Nakamichi, Tatsuhiko Tsunoda, Tomisaku Kawasaki, Yusuke Nakamura, Akira Hata
Nature Genetics. 2007523 CitationsOPEN ACCESS
A genome-wide association study identifies three new risk loci for Kawasaki disease
Yoshihiro Onouchi, Kouichi Ozaki, Jane C. Burns, Chisato Shimizu, Masaru Terai, Hiromichi Hamada, Takafumi Honda, Hiroyuki Suzuki, Tomohiro Suenaga, Takashi Takeuchi, Norishige Yoshikawa, Yoichi Suzuki, Kumi Yasukawa, Ryota Ebata, Kouji Higashi, Tsutomu Saji, Yasushi Kemmotsu, Shinichi Takatsuki, Kazunobu Ouchi, Fumio Kishi, Tetsushi Yoshikawa, Toshiro Nagai, Kunihiro Hamamoto, Yoshitake Sato, Akihito Honda, Hironobu Kobayashi, Junichi Sato, Shoichi Shibuta, Masakazu Miyawaki, Ko Oishi, H. Yamaga, Noriyuki Aoyagi, Seiji Iwahashi, Ritsuko Miyashita, Yuji Murata, Kumiko Sasago, Atsushi Takahashi, Naoyuki Kamatani, Michiaki Kubo, Tatsuhiko Tsunoda, Akira Hata, Yusuke Nakamura, Toshihiro Tanaka
Nature Genetics. 2012339 Citations
Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia
Matthew J. Rock, Jean Prenen, Vincent Funari, Tara Funari, Barry Merriman, Stanley F. Nelson, Ralph S. Lachman, William R. Wilcox, Soraya Reyno, Roberto Quadrelli, Alicia Vaglio, Grzegorz Owsianik, Annelies Janssens, Thomas Voets, Shiro Ikegawa, Toshiro Nagai, David L. Rimoin, Bernd Nilius, Daniel H. Cohn
Nature Genetics. 2008236 CitationsOPEN ACCESS

How much of the research on Nakagawanosato Hospital for the Disabled is open access?

ScholarIQopen access share
55%OPEN ACCESS
Gold
0%
Green
18%
Hybrid
0%
Bronze
36%
Closed
45%

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