Publication

Publication 2016
  1. Nikitski A, Rogounovitch T, Bychkov A, Takahashi M, Yoshiura KI, Mitsutake N, Kawaguchi T, Matsuse M, Drozd VM, Demidchik YE, Nishihara E, Hirokawa M, Miyauchi A, Rubanovich AV, Matsuda F, Yamashita S, Saenko VA. Genotype analyses in the Japanese and Belarusian populations reveal independent effects of rs965513 and rs1867277 but do not support the role of FOXE1 polyalanine tract length in conferring risk for papillary thyroid carcinoma. Thyroid. 2016 Feb;27(2): 224-235. doi: 10.1089/thy.2015.0541. (IF: 3.784)
  2. Uchiyama Y, Nakashima M, Watanabe S, Miyajima M, Taguri M, Miyatake S, Miyake N, Saitsu H, Mishima H, Kinoshita A, Arai H, Yoshiura K, Matsumoto N. Ultra-sensitive droplet digital PCR for detecting a low-prevalence somatic GNAQ mutation in Sturge-Weber syndrome. Sci Rep. 2016 Mar 9;6:22985. doi: 10.1038/srep22985. (IF: 5.228)
  3. Koga T, Migita K, Sato S, Umeda M, Nonaka F, Kawashiri SY, Iwamoto N, Ichinose K, Tamai M, Nakamura H, Origuchi T, Ueki Y, Masumoto J, Agematsu K, Yachie A, Yoshiura K, Eguchi K, Kawakami A. Multiple Serum Cytokine Profiling to Identify Combinational Diagnostic Biomarkers in Attacks of Familial Mediterranean Fever. Medicine (Baltimore). 2016 Apr;95(16): e3449. doi: 10.1097/MD.0000000000003449. (IF: 2.133)
  4. Watanabe S, Shimizu K, Ohashi H, Kosaki R, Okamoto N, Shimojima K, Yamamoto T, Chinen Y, Mizuno S, Dowa Y, Shiomi N, Toda Y, Tashiro K, Shichijo K, Minatozaki K, Aso S, Minagawa K, Hiraki Y, Shimokawa O, Matsumoto T, Fukuda M, Moriuchi H, Yoshiura K, Kondoh T. Detailed analysis of 26 cases of 1q partial duplication/triplication syndrome. Am J Med Genet A. 2016 Apr;170(4): 908-917. doi: 10.1002/ajmg.a.37496. (IF: 2.082)
  5. Dateki S, Watanabe S, Nakatomi A, Kinoshita E, Matsumoto T, Yoshiura K, Moriuchi H. Genetic background of hyperphenylalaninemia in Nagasaki, Japan.  Pediatr Int. 2016 May;58(5): 431-433. doi: 10.1111/ped.12924. (IF: 0.868)
  6. Mussazhanova Z, Akazawa Y, Matsuda K, Shichijo K, Miura S, Otsubo R, Oikawa M, Yoshiura KI, Mitsutake N, Rogounovitch T, Saenko V, Kozykenova Z, Zhetpisbaev B, Shabdarbaeva D, Sayakenov N, Amantayev B, Kondo H, Ito M, Nakashima M. Association between p53-binding protein 1 expression and genomic instability in oncocytic follicular adenoma of the thyroid. Endocr J. 2016 May 31;63(5): 457-467. doi: 10.1507/endocrj.EJ15-0629. (IF: 1.895)
  7. Migita K, Izumi Y, Jiuchi Y, Iwanaga N, Kawahara C, Agematsu K, Yachie A, Masumoto J, Fujikawa K, Yamasaki S, Nakamura T, Ubara Y, Koga T, Nakashima Y, Shimizu T, Umeda M, Nonaka F, Yasunami M, Eguchi K, Yoshiura K, Kawakami A.  Familial Mediterranean fever is no longer a rare disease in Japan. Arthritis Res Ther. 2016 Jul 30;18: 175. doi: 10.1186/s13075-016-1071-5. (IF: 3.979)
  8. Wada H, Matsuda K, Akazawa Y, Yamaguchi Y, Miura S, Ueki N, Kinoshita A, Yoshiura K, Kondo H, Ito M, Nagayasu T, Nakashima M. Expression of Somatostatin Receptor Type 2A and PTEN in Neuroendocrine Neoplasms Is Associated with Tumor Grade but Not with Site of Origin. Endocr Pathol. 2016 Sep;27(3): 179-187. doi: 10.1007/s12022-016-9436-5. (IF: 1.817)
  9. Konomoto T, Imamura H, Orita M, Tanaka E, Moritake H, Sato Y, Fujimoto S, Harita Y, Hisano S, Yoshiura KI, Nunoi H. Clinical and histological findings of autosomal dominant renal-limited disease with LMX1B mutation. Nephrology (Carlton). 2016 Sep;21(9): 765-773. doi: 10.1111/nep.12666. (IF: 1.796)
  10. Miura K, Mishima H, Yasunami M, Kaneuchi M, Kitajima M, Abe S, Higashijima A, Fuchi N, Miura S, Yoshiura KI, Masuzaki H. A significant association between rs8067378 at 17q12 and invasive cervical cancer originally identified by a genome-wide association study in Han Chinese is replicated in a Japanese population. J Hum Genet. 2016 Sep;61(9): 793-796. doi: 10.1038/jhg.2016.50. (IF: 2.487)
  11. Matsuda K, Tateishi S, Akazawa Y, Kinoshita A, Yoshida S, Morisaki S, Fukushima A, Matsuwaki T, Yoshiura KI, Nakashima M. Rapid growth of mitotically active cellular fibroma of the ovary: a case report and review of the literature. Diagn Pathol. 2016 Oct 22;11(1): 101. doi:10.1186/s13000-016-0554-7  (IF: 1.895)