Items where Author is "Akiyama, Masato"

2021

Nishiguchi, Koji M. and Miya, Fuyuki and Mori, Yuka and Fujita, Kosuke and Akiyama, Masato and Kamatani, Takashi and Koyanagi, Yoshito and Sato, Kota and Takigawa, Toru and Ueno, Shinji and Tsugita, Misato and Kunikata, Hiroshi and Cisarova, Katarina and Nishino, Jo and Murakami, Akira and Abe, Toshiaki and Momozawa, Yukihide and Terasaki, Hiroko and Wada, Yuko and Sonoda, Koh-Hei and Rivolta, Carlo and Tsunoda, Tatsuhiko and Tsujikawa, Motokazu and Ikeda, Yasuhiro and Nakazawa, Toru. (2021) A hypomorphic variant in EYS detected by genome-wide association study contributes toward retinitis pigmentosa. Communications Biology, 4 (1). p. 140.

2019

Nikopoulos, Konstantinos and Cisarova, Katarina and Quinodoz, Mathieu and Koskiniemi-Kuendig, Hanna and Miyake, Noriko and Farinelli, Pietro and Rehman, Atta Ur and Khan, Muhammad Imran and Prunotto, Andrea and Akiyama, Masato and Kamatani, Yoichiro and Terao, Chikashi and Miya, Fuyuki and Ikeda, Yasuhiro and Ueno, Shinji and Fuse, Nobuo and Murakami, Akira and Wada, Yuko and Terasaki, Hiroko and Sonoda, Koh-Hei and Ishibashi, Tatsuro and Kubo, Michiaki and Cremers, Frans P. M. and Kutalik, Zoltán and Matsumoto, Naomichi and Nishiguchi, Koji M. and Nakazawa, Toru and Rivolta, Carlo. (2019) A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy. Nature Communications, 10 (1). p. 2884.

2018

Teumer, Alexander and Chaker, Layal and Groeneweg, Stefan and Li, Yong and Di Munno, Celia and Barbieri, Caterina and Schultheiss, Ulla T. and Traglia, Michela and Ahluwalia, Tarunveer S. and Akiyama, Masato and Appel, Emil Vincent R. and Arking, Dan E. and Arnold, Alice and Astrup, Arne and Beekman, Marian and Beilby, John P. and Bekaert, Sofie and Boerwinkle, Eric and Brown, Suzanne J. and De Buyzere, Marc and Campbell, Purdey J. and Ceresini, Graziano and Cerqueira, Charlotte and Cucca, Francesco and Deary, Ian J. and Deelen, Joris and Eckardt, Kai-Uwe and Ekici, Arif B. and Eriksson, Johan G. and Ferrrucci, Luigi and Fiers, Tom and Fiorillo, Edoardo and Ford, Ian and Fox, Caroline S. and Fuchsberger, Christian and Galesloot, Tessel E. and Gieger, Christian and Gögele, Martin and De Grandi, Alessandro and Grarup, Niels and Greiser, Karin Halina and Haljas, Kadri and Hansen, Torben and Harris, Sarah E. and van Heemst, Diana and den Heijer, Martin and Hicks, Andrew A. and den Hollander, Wouter and Homuth, Georg and Hui, Jennie and Ikram, M. Arfan and Ittermann, Till and Jensen, Richard A. and Jing, Jiaojiao and Jukema, J. Wouter and Kajantie, Eero and Kamatani, Yoichiro and Kasbohm, Elisa and Kaufman, Jean-Marc and Kiemeney, Lambertus A. and Kloppenburg, Margreet and Kronenberg, Florian and Kubo, Michiaki and Lahti, Jari and Lapauw, Bruno and Li, Shuo and Liewald, David C. M. and Lifelines Cohort Study, and Lim, Ee Mun and Linneberg, Allan and Marina, Michela and Mascalzoni, Deborah and Matsuda, Koichi and Medenwald, Daniel and Meisinger, Christa and Meulenbelt, Ingrid and De Meyer, Tim and Meyer Zu Schwabedissen, Henriette E. and Mikolajczyk, Rafael and Moed, Matthijs and Netea-Maier, Romana T. and Nolte, Ilja M. and Okada, Yukinori and Pala, Mauro and Pattaro, Cristian and Pedersen, Oluf and Petersmann, Astrid and Porcu, Eleonora and Postmus, Iris and Pramstaller, Peter P. and Psaty, Bruce M. and Ramos, Yolande F. M. and Rawal, Rajesh and Redmond, Paul and Richards, J. Brent and Rietzschel, Ernst R. and Rivadeneira, Fernando and Roef, Greet and Rotter, Jerome I. and Sala, Cinzia F. and Schlessinger, David and Selvin, Elizabeth and Slagboom, P. Eline and Soranzo, Nicole and Sørensen, Thorkild I. A. and Spector, Timothy D. and Starr, John M. and Stott, David J. and Taes, Youri and Taliun, Daniel and Tanaka, Toshiko and Thuesen, Betina and Tiller, Daniel and Toniolo, Daniela and Uitterlinden, Andre G. and Visser, W. Edward and Walsh, John P. and Wilson, Scott G. and Wolffenbuttel, Bruce H. R. and Yang, Qiong and Zheng, Hou-Feng and Cappola, Anne and Peeters, Robin P. and Naitza, Silvia and Völzke, Henry and Sanna, Serena and Köttgen, Anna and Visser, Theo J. and Medici, Marco. (2018) Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation. Nature communications, 9 (1). p. 4455.