Maruyama H, Morino H, Izumi Y, Noda K, Kawakami H. Convenient diagnosis of spinal and bulbar muscular atrophy using a microchip electrophoresis system. Am J Neurodegener Dis. 2013;2(1):35-9.

Takeda I, Takahashi T, Ueno H, Morino H, Ochi K, Nakamura T, Hosomi N, Kawakami H, Hashimoto K, Matsumoto M. Autosomal recessive Andersen–Tawil syndrome with a novel mutation L94P in Kir2.1. Neurol Clin Neurosci. Jul;1(4):131-7. 2013

Miyashiro A, Sugihara K, Kawarai T, Miyamoto R, Izumi Y, Morino H, Maruyama H, Orlacchio A, Kawakami H, Kaji R. Oromandibular dystonia associated with SCA36. Mov Disord. 2013 Apr;28(4):558-9.

Izumi Y, Miyamoto R, Morino H, Yoshizawa A, Nishinaka K, Udaka F, Kameyama M, Maruyama H, Kawakami H. Cerebellar ataxia with SYNE1 mutation accompanying motor neuron disease. Neurology. 2013 Feb 5;80(6):600-1.

Keisuke Kajita, Yuki Kuwano*, Naruka Kitamura, Yuzuru Satake, Kensei Nishida, Ken Kurokawa, Yoko Akaike, Manami Honda, Kiyoshi Masuda and Kazuhito Rokutan : Ets1 and heat shock factor 1 regulate transcription of the Transformer 2β gene in human colon cancer cells, Journal of Gastroenterology, Vol.48, No.11, 1222-1233, 2013.

Manami Honda, Yuki Kuwano*, Sakurako Katsuura-Kamano, Kinuyo Fujita, Yoko Akaike, Shizuka Kano, Kensei Nishida, Kiyoshi Masuda and Kazuhito Rokutan : Chronic academic stress increases a group of microRNAs in peripheral blood, PLoS ONE, Vol.8, No.10, e75960, 2013.

Kiyoshi Masuda, Yuki Kuwano, Kensei Nishida, Kazuhito Rokutan and Issei Imoto : NF90 in Posttranscriptional Gene Regulation and MicroRNA Biogenesis., International Journal of Molecular Sciences, Vol.14, No.8, 17111-17121, 2013.

Naoko Yamagishi, Shigetada Kondo, Kiyoshi Masuda, Kensei Nishida, Yuki Kuwano, Duyen T Dang, Long H Dang, Takeshi Nikawa and Kazuhito Rokutan : Chronic inhibition of tumor cell-derived VEGF enhances the malignant phenotype of colorectal cancer cells, BMC Cancer, Vol.13, 229, 2013.

Shizuka Kano, Kensei Nishida, Chihiro Nishiyama, Yoko Akaike, Keisuke Kajita, Ken Kurokawa, Kiyoshi Masuda, Yuki Kuwano, Toshihito Tanahashi and Kazuhito Rokutan : Truncated serine/arginine-rich splicing factor 3 accelerates cell growth through up-regulating c-Jun expression, The Journal of Medical Investigation : JMI, Vol.60, No.3-4, 228-235, 2013.

Kiyoshi Masuda, Yuki Kuwano, Kensei Nishida and Kazuhito Rokutan : Application of DNA microarray technology to gerontological studies, Methods in Molecular Biology, Vol.1048, 285-308, 2013.

Sugihara K, Maruyama H, Morino H, Miyamoto R, Ueno H, Matsumoto M, Kaji R, Kitaguchi H, Yukitake M, Higashi Y, Nishinaka K, Oda M, Izumi Y, Kawakami H. The clinical characteristics of spinocerebellar ataxia 36: a study of 2121 Japanese ataxia patients. Mov Disord. 2012 Aug;27(9):1158-63.

Yoshiko Kamezaki, Sakurako Katsuura, Yuki Kuwano, Toshihito Tanahashi and Kazuhito Rokutan : Circulating cytokine signatures in healthy medical students exposed to academic examination stress., Psychophysiology, Vol.49, No.7, 991-997, 2012.

Sakurako Katsuura, Yuki Kuwano, Naoko Yamagishi, Ken Kurokawa, Keisuke Kajita, Yoko Akaike, Kensei Nishida, Kiyoshi Masuda, Toshihito Tanahashi and Kazuhito Rokutan : MicroRNAs miR-144/144* and miR-16 in peripheral blood are potential biomarkers for naturalistic stress in healthy Japanese medical students., Neuroscience Letters, Vol.516, No.1, 79-84, 2012.

Ken Kurokawa, Toshihito Tanahashi, Tsutomu Iima, Yuta Yamamoto, Yoko Akaike, Kensei Nishida, Kiyoshi Masuda, Yuki Kuwano, Yoshiki Murakami, Masakazu Fukushima and Kazuhito Rokutan : Role of miR-19b and its target mRNAs in 5-fluorouracil resistance in colon cancer cells., Journal of Gastroenterology, Vol.47, No.8, 883-895, 2012.

Kiyoshi Masuda, Yuki Kuwano, Kensei Nishida and Kazuhito Rokutan : General RBP expression in human tissues as a function of age., Ageing Research Reviews, Vol.11, No.4, 423-431, 2012.

Ueno H, Kobatake K, Matsumoto M, Morino H, Maruyama H, Kawakami H. Severe brain atrophy after long-term survival seen in siblings with familial amyotrophic lateral sclerosis and a mutation in the optineurin gene: a case series. J Med Case Rep. 2011 Dec 12;5(1):573.

Hagiwara K, Morino H, Shiihara J, Tanaka T, Miyazawa H, Suzuki T, Kohda M, Okazaki Y, Seyama K, Kawakami H. Homozygosity mapping on homozygosity haplotype analysis to detect recessive disease-causing genes from a small number of unrelated, outbred patients. PLoS One. 2011;6(9):e25059.

Sugihara K, Maruyama H, Kamada M, Morino H, Kawakami H. Screening for OPTN mutations in amyotrophic lateral sclerosis in a mainly Caucasian population. Neurobiol Aging. 2011 Oct;32(10):1923.e9-10.

Tanaka E, Maruyama H, Morino H, Kawakami H. Detection of large expansions in SCA8 using a fluorescent repeat-primed PCR assay. Hiroshima J Med Sci. 2011 Sep;60(3):63-6.

Snapinn KW, Larson EB, Kawakami H, Ujike H, Borenstein AR, Izumi Y, Kaji R, Maruyama H, Mata IF, Morino H, Oda M, Tsuang DW, Yearout D, Edwards KL, Zabetian CP. The UCHL1 S18Y polymorphism and Parkinson's disease in a Japanese population. Parkinsonism Relat Disord. 2011 Jul;17(6):473-5.

Yuki Kuwano, Yoko Kamio, Tomoko Kawai, Sakurako Katsuura, Naoko Inada, Akiko Takaki and Kazuhito Rokutan : Autism-associated gene expression in peripheral leucocytes commonly observed between subjects with autism and healthy women having autistic children., PLoS ONE, Vol.6, No.9, e24723, 2011.

Yoko Akaike, Ken Kurokawa, Keisuke Kajita, Yuki Kuwano, Kiyoshi Masuda, Kensei Nishida, Seung Kang Wan, Toshihito Tanahashi and Kazuhito Rokutan : Skipping of an alternative intron in the srsf1 3' untranslated region increases transcript stability., The Journal of Medical Investigation : JMI, Vol.58, No.3-4, 180-187, 2011.

Subramanya Srikantan, Kotb Abdelmohsen, Kyung Eun Lee, Kumiko Tominaga, S Sarah Subaran, Yuki Kuwano, Ritu Kulshrestha, Rohit Panchakshari, Ho Hyeon Kim, Xiaoling Yang, L Jennifer Martindale, S Bernard Marasa, M Mihee Kim, P Robert Wersto, E Fred Indig, Dipanjan Chowdhury and Myriam Gorospe : Translational control of TOP2A influences doxorubicin efficacy., Molecular and Cellular Biology, Vol.31, No.18, 3790-3801, 2011.

Sakurako Katsuura, Yoshiko Kamezaki, Naoko Yamagishi, Yuki Kuwano, Kensei Nishida, Kiyoshi Masuda, Toshihito Tanahashi, Tomoko Kawai, Kokichi Arisawa and Kazuhito Rokutan : Circulating vascular endothelial growth factor is independently and negatively associated with trait anxiety and depressive mood in healthy Japanese university students., International Journal of Psychophysiology, Vol.81, No.1, 38-43, 2011.

Ken Kurokawa, Toshihito Tanahashi, Akiho Murata, Yoko Akaike, Sakurako Katsuura, Kensei Nishida, Kiyoshi Masuda, Yuki Kuwano, Tomoko Kawai and Kazuhito Rokutan : Effects of chronic academic stress on mental state and expression of glucocorticoid receptor α and β isoforms in healthy Japanese medical students., Stress, Vol.14, No.4, 431-438, 2011.

Huqun, Fukuyama S, Morino H, Miyazawa H, Tanaka T, Suzuki T, Kohda M, Kawakami H, Okazaki Y, Seyama K, Hagiwara K. A quantitatively-modeled homozygosity mapping algorithm, qHomozygosityMapping, utilizing whole genome single nucleotide polymorphism genotyping data. BMC Bioinformatics. 2010 Oct 15;11 Suppl 7:S5.

Maruyama H, Morino H, Ito H, Izumi Y, Kato H, Watanabe Y, Kinoshita Y, Kamada M, Nodera H, Suzuki H, Komure O, Matsuura S, Kobatake K, Morimoto N, Abe K, Suzuki N, Aoki M, Kawata A, Hirai T, Kato T, Ogasawara K, Hirano A, Takumi T, Kusaka H, Hagiwara K, Kaji R, Kawakami H. Mutations of optineurin in amyotrophic lateral sclerosis. Nature. 2010 May 13;465(7295):223-6.

Ken Kurokawa, Yuki Kuwano*, Kumiko Tominaga, Tomoko Kawai, Sakurako Katsuura, Naoko Yamagishi, Yuzuru Satake, Keisuke Kajita, Toshihito Tanahashi and Kazuhito Rokutan : Brief naturalistic stress induces an alternative splice variant of SMG-1 lacking exon 63 in peripheral leukocytes., Neuroscience Letters, Vol.484, No.2, 128-132, 2010.

Yamamoto Y, Tanahashi T, Katsuura S, Kurokawa K, Nishida K, Kuwano Y, Kawai T, Teshima-Kondo S, Chikahisa S, Tsuruo Y, Sei H, Rokutan K. Interleukin-18 deficiency reduces neuropeptide gene expressions in the mouse amygdala related with behavioral change. J Neuroimmunol., Vol. 229 No.1-2, 129-39, 2010.

Abdelmohsen K, Hutchison ER, Lee EK, Kuwano Y, Kim MM, Masuda K, Srikantan S, Subaran SS, Marasa BS, Mattson MP, Gorospe M. miR-375 inhibits differentiation of neurites by lowering HuD levels. Mol Cell Biol. 2010 Vol. 30, No.17, 4197-210, 2010.

Lee EK, Kim HH, Kuwano Y, Abdelmohsen K, Srikantan S, Subaran SS, Gleichmann M, Mughal MR, Martindale JL, Yang X, Worley PF, Mattson MP, Gorospe M.hnRNP C promotes APP translation by competing with FMRP for APP mRNA recruitment to P bodies. Nat Struct Mol Biol. Vol. 17, No. 6, 732-9, 2010.

Calaluce R, Gubin MM, Davis JW, Magee JD, Chen J, Kuwano Y, Gorospe M, Atasoy U. The RNA binding protein HuR differentially regulates unique subsets of mRNAs in estrogen receptor negative and estrogen receptor positive breast cancer. BMC Cancer. Vol.10, 126, 2010.

Kamada M, Maruyama H, Tanaka E, Morino H, Wate R, Ito H, Kusaka H, Kawano Y, Miki T, Nodera H, Izumi Y, Kaji R, Kawakami H. Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosis. J Neurol Sci. 2009 Sep 15;284(1-2):69-71.

Zabetian CP, Yamamoto M, Lopez AN, Ujike H, Mata IF, Izumi Y, Kaji R, Maruyama H, Morino H, Oda M, Hutter CM, Edwards KL, Schellenberg GD, Tsuang DW, Yearout D, Larson EB, Kawakami H. LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease. Mov Disord. 2009 May 15;24(7):1034-41.

Shrestha I, Ohshita T, Naka H, Morino H, Matsumoto M. Cytotoxic edema in neuro-Behcet's disease ? Intern Med.;47(23):2073-6. 2008

Craig K, Takiyama Y, Soong BW, Jardim LB, Saraiva-Pereira ML, Lythgow K, Morino H, Maruyama H, Kawakami H, Chinnery PF. Pathogenic expansions of the SCA6 locus are associated with a common CACNA1A haplotype across the globe: founder effect or predisposing chromosome? Eur J Hum Genet. Jul;16(7):841-7. 2008

Tanaka E, Maruyama H, Morino H, Nakajima E, Kawakami H. The CNTN4 c.4256C>T mutation is rare in Japanese with inherited spinocerebellar ataxia. J Neurol Sci. Mar 15;266(1-2):180-1. 2008

Elbaz A, Nelson LM, Payami H, Ioannidis JP, Fiske BK, Annesi G, Carmine Belin A, Factor SA, Ferrarese C, Hadjigeorgiou GM, Higgins DS, Kawakami H, Krüger R, Marder KS, Mayeux RP, Mellick GD, Nutt JG, Ritz B, Samii A, Tanner CM, Van Broeckhoven C, Van Den Eeden SK, Wirdefeldt K, Zabetian CP, Dehem M, Montimurro JS, Southwick A, Myers RM, Trikalinos TA, Silburn PA, Nuytemans K, Pals P, Pickut B, Cras P, Paul De Deyn P, Theuns J, Tzourio C, Amouyel P, Lambert JC, Riess O, Bauer P, Gasser T, Berg D, Xiromerisiou G, Galbussera A, Zini M, Goldwurm S, Pezzoli G, Quattrone A, Annesi F, Tarantino P, Morino H, Maruyama H, Izumi Y, Kaji R, Pedersen NL, Olson L, Westerlund M, Galter D, Sydow O, McGuire V, Topol B, Wahner A, Bordelon YM, Tang MX, Bronstein J, Brady S, Aggarwal A, Liu X, Griffith A, Leis BC, Roberts JW. Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study. Lancet Neurol. Nov;5(11):917-23. 2006

Hiramoto K, Kawakami H, Inoue K, Seki T, Maruyama H, Morino H, Matsumoto M, Kurisu K, Sakai N. Identification of a new family of spinocerebellar ataxia type 14 in the Japanese spinocerebellar ataxia population by the screening of PRKCG exon 4. Mov Disord. Sep;21(9):1355-60. 2006

Zabetian CP, Morino H, Ujike H, Yamamoto M, Oda M, Maruyama H, Izumi Y, Kaji R, Griffith A, Leis BC, Roberts JW, Yearout D, Samii A, Kawakami H. Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease. Neurology. Aug 22;67(4):697-9. 2006

Maraganore DM, de Andrade M, Elbaz A, Farrer MJ, Ioannidis JP, Krüger R, Rocca WA, Schneider NK, Lesnick TG, Lincoln SJ, Hulihan MM, Aasly JO, Ashizawa T, Chartier-Harlin MC, Checkoway H, Ferrarese C, Hadjigeorgiou G, Hattori N, Kawakami H, Lambert JC, Lynch T, Mellick GD, Papapetropoulos S, Parsian A, Quattrone A, Riess O, Tan EK, Van Broeckhoven C, Amouyel P, Albanese A, Annesi G, Bogaerts V, Destée A, Gibson JM, Goldwurm S, Maruyama H, Morino H, Mouroux V, Nicoletti G, Pals P, Pavanni R, Perlmutter JS, Pezzoli G, Prigione A, Racette BA, Silburn PA, Tzourio C, Wong MC, Uhl GR, Xiromerisiou G, Yu XY. Collaborative analysis of α-synuclein gene promoter variability and Parkinson disease. JAMA. Aug 9;296(6):661-70. 2006

Terasawa H, Oda M, Morino H, Miyachi T, Izumi Y, Maruyama H, Matsumoto M, Kawakami H. A novel haplotype of spinocerebellar ataxia type 6 contributes to the highest prevalence in western Japan. Neurosci Lett. Mar 25;358(2):107-10. 2004

Oda M, Maruyama H, Komure O, Morino H, Terasawa H, Izumi Y, Imamura T, Yasuda M, Ichikawa K, Ogawa M, Matsumoto M, Kawakami H. Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17. Arch Neurol. Feb;61(2):209-12. 2004

Oda M, Maruyama H, Izumi Y, Morino H, Torii T, Nakamura S, Kawakami H. Dinucleotide repeat polymorphism in interferon-gamma gene is not associated with sporadic Alzheimer's disease. Am J Med Genet B Neuropsychiatr Genet. Jan 1;124B(1):48-9. 2004

Izumi Y, Maruyama H, Oda M, Morino H, Okada T, Ito H, Sasaki I, Tanaka H, Komure O, Udaka F, Nakamura S, Kawakami H. SCA8 repeat expansion: large CTA/CTG repeat alleles are more common in ataxic patients, including those with SCA6. Am J Hum Genet. Mar;72(3):704-9. 2003

Nishimura M, Kawakami H, Komure O, Maruyama H, Morino H, Izumi Y, Nakamura S, Kaji R, Kuno S. Contribution of the interleukin-1beta gene polymorphism in multiple system atrophy. Mov Disord. Jul;17(4):808-11. 2002

Maruyama H, Izumi Y, Morino H, Oda M, Toji H, Nakamura S, Kawakami H. Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: a study of 1,286 Japanese patients. Am J Med Genet. Jul 8;114(5):578-83. 2002

Oda M, Morino H, Maruyama H, Terasawa H, Izumi Y, Torii T, Sasaki K, Nakamura S, Kawakami H. Dinucleotide repeat polymorphisms in the neprilysin gene are not associated with sporadic Alzheimer's disease. Neurosci Lett. Mar 1;320(1-2):105-7. 2002

Maruyama H, Izumi Y, Oda M, Torii T, Morino H, Toji H, Sasaki K, Terasawa H, Nakamura S, Kawakami H. Lack of an association between cystatin C gene polymorphisms in Japanese patients with Alzheimer's disease. Neurology. Jul 24;57(2):337-9. 2001

Izumi Y, Morino H, Oda M, Maruyama H, Udaka F, Kameyama M, Nakamura S, Kawakami H. Genetic studies in Parkinson's disease with an alpha-synuclein/NACP gene polymorphism in Japan. Neurosci Lett. Mar 9;300(2):125-7. 2001

Morino H, Kawarai T, Izumi Y, Kazuta T, Oda M, Komure O, Udaka F, Kameyama M, Nakamura S, Kawakami H. A single nucleotide polymorphism of dopamine transporter gene is associated with Parkinson's disease. Ann Neurol. Apr;47(4):528-31. 2000