Octupole-driven magnetoresistance in an antiferromagnetic tunnel junction by Chen, Xianzhe, Higo, Tomoya, Tanaka, Katsuhiro, Nomoto, Takuya, Tsai, Hanshen, Idzuchi, Hiroshi, Shiga, Masanobu, Sakamoto, Shoya, Ando, Ryoya, Kosaki, Hidetoshi, Matsuo, Takumi, Nishio-Hamane, Daisuke, Arita, Ryotaro, Miwa, Shinji, Nakatsuji, Satoru

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Magnon–Photon Coupling in a Spinel Ferrite with Large Gilbert Damping by Kosaki, Hidetoshi, Umeda, Maki, Saitoh, Eiji, Shiomi, Yuki

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Impact of a SLC24A5 variant on the retinal pigment epithelium of a Japanese patient with oculocutaneous albinism type 6 by Saito, Toru, Okamura, Ken, Kosaki, Rika, Wakamatsu, Kazumasa, Ito, Shosuke, Nakajima, Osamu, Yamashita, Hidetoshi, Hozumi, Yutaka, Suzuki, Tamio

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Six years’ accomplishment of the Initiative on Rare and Undiagnosed Diseases: nationwide project in Japan to discover causes, mechanisms, and cures by Takahashi, Yuji, Date, Hidetoshi, Oi, Hideki, Adachi, Takeya, Imanishi, Noriaki, Kimura, En, Takizawa, Hotake, Kosugi, Shinji, Matsumoto, Naomichi, Kosaki, Kenjiro, Matsubara, Yoichi, Ando, Yukio, Anzai, Toshihisa, Ariga, Tadashi, Fukushima, Yoshimitsu, Furusawa, Yoshihiko, Ganaha, Akira, Goto, Yuichi, Hata, Kenichiro, Honda, Masataka, Iijima, Kazumoto, Ikka, Tsunakuni, Imoto, Issei, Kaname, Tadashi, Kobayashi, Masao, Kojima, Seiji, Kurahashi, Hiroki, Kure, Shigeo, Kurosawa, Kenji, Maegaki, Yoshihiro, Makita, Yoshio, Morio, Tomohiro, Narita, Ichiei, Nomura, Fumio, Ogata, Tsutomu, Ozono, Keiichi, Oka, Akira, Okamoto, Nobuhiko, Saitoh, Shinji, Sakurai, Akihiro, Takada, Fumio, Takahashi, Tsutomu, Tamaoka, Akira, Umezawa, Akihiro, Yachie, Akihiro, Yoshiura, Kouichiro, Chinen, Yasutsugu, Eguchi, Mariko, Fujio, Keishi, Hosoda, Kiminori, Ichikawa, Tomohiko, Kawarai, Toshitaka, Kosho, Tomoki, Masuno, Mitsuo, Nakamura, Akie, Nakane, Takaya, Ogi, Tomoo, Okada, Satoshi, Sakata, Yasushi, Seto, Toshiyuki, Takahashi, Yoshiyuki, Takano, Tadao, Ueda, Mitsuharu, Yagasaki, Hideaki, Yamamoto, Toshiyuki, Watanabe, Atsushi, Hotta, Yoshihiro, Kubo, Akiharu, Maruyama, Hirofumi, Moriyama, Keiji, Nanba, Eiji, Sakai, Norio, Sekijima, Yoshiki, Shimosegawa, Toru, Takeuchi, Tsutomu, Usami, Shinichi, Yamamoto, Kazuhiko, Mizusawa, Hidehiro

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Identification of a novel splice‐site WWOX variant with paternal uniparental isodisomy in a patient with infantile epileptic encephalopathy by Nishino, Megumi, Tanaka, Mai, Imagawa, Kazuo, Yaita, Katsuyuki, Enokizono, Takashi, Ohto, Tatsuyuki, Suzuki, Hisato, Yamada, Mamiko, Takenouchi, Toshiki, Kosaki, Kenjiro, Takada, Hidetoshi

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A novel missense PTEN mutation identified in a patient with macrocephaly and developmental delay by Ueno, Yuichi, Enokizono, Takashi, Fukushima, Hiroko, Ohto, Tatsuyuki, Imagawa, Kazuo, Tanaka, Mai, Sakai, Aiko, Suzuki, Hisato, Uehara, Tomoko, Takenouchi, Toshiki, Kosaki, Kenjiro, Takada, Hidetoshi

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Novel ARX mutation identified in infantile spasm syndrome patient by Takeshita, Yohei, Ohto, Tatsuyuki, Enokizono, Takashi, Tanaka, Mai, Suzuki, Hisato, Fukushima, Hiroko, Uehara, Tomoko, Takenouchi, Toshiki, Kosaki, Kenjiro, Takada, Hidetoshi

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A case of autism spectrum disorder with cleft lip and palate carrying a mutation in exon 8 of AUTS2 by Saeki, Saki, Enokizono, Takashi, Imagawa, Kazuo, Fukushima, Hiroko, Kajikawa, Daigo, Sakai, Aiko, Tanaka, Mai, Ohto, Tatsuyuki, Suzuki, Hisato, Uehara, Tomoko, Takenouchi, Toshiki, Kenjiro, Kosaki, Takada, Hidetoshi

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Novel ARX mutation identified in infantile spasm syndrome patient by Takeshita, Yohei, Ohto, Tatsuyuki, Enokizono, Takashi, Tanaka, Mai, Suzuki, Hisato, Fukushima, Hiroko, Uehara, Tomoko, Takenouchi, Toshiki, Kosaki, Kenjiro, Takada, Hidetoshi

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Establishment of immunity against Epstein‐Barr virus infection in a patient with CHARGE/complete DiGeorge syndrome after peripheral blood lymphocyte transfusion by Hosaka, Sho, Kobayashi, Chie, Saito, Hirota, Imai-Saito, Ayako, Suzuki, Ryoko, Iwabuchi, Atsushi, Kato, Yoshiaki, Jimbo, Takahiro, Watanabe, Nobuyuki, Onodera, Masafumi, Imadome, Ken‐Ichi, Masumoto, Kouji, Nanmoku, Toru, Fukushima, Takashi, Kosaki, Kenjiro, Sumazaki, Ryo, Takada, Hidetoshi

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Successful cord blood transplantation for a CHARGE syndrome with CHD7 mutation showing DiGeorge sequence including hypoparathyroidism by Inoue, Hirosuke, Takada, Hidetoshi, Kusuda, Takeshi, Goto, Takako, Ochiai, Masayuki, Kinjo, Tadamune, Muneuchi, Jun, Takahata, Yasushi, Takahashi, Naomi, Morio, Tomohiro, Kosaki, Kenjiro, Hara, Toshiro

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A case of autism spectrum disorder with cleft lip and palate carrying a mutation in exon 8 of AUTS2 by Saeki, Saki, Enokizono, Takashi, Imagawa, Kazuo, Fukushima, Hiroko, Kajikawa, Daigo, Sakai, Aiko, Tanaka, Mai, Ohto, Tatsuyuki, Suzuki, Hisato, Uehara, Tomoko, Takenouchi, Toshiki, Kenjiro, Kosaki, Takada, Hidetoshi

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Establishment of immunity against Epstein-Barr virus infection in a patient with CHARGE/complete DiGeorge syndrome after peripheral blood lymphocyte transfusion by Hosaka, Sho, Kobayashi, Chie, Saito, Hirota, Imai-Saito, Ayako, Suzuki, Ryoko, Iwabuchi, Atsushi, Kato, Yoshiaki, Jimbo, Takahiro, Watanabe, Nobuyuki, Onodera, Masafumi, Imadome, Ken-Ichi, Masumoto, Kouji, Nanmoku, Toru, Fukushima, Takashi, Kosaki, Kenjiro, Sumazaki, Ryo, Takada, Hidetoshi

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