Hideshi Kawakami

Overview

Best Publications

• CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

  Yoshiya Kawaguchi;Toshihiro Okamoto;Masafumi Taniwaki;Megumi Aizawa

  2108
  Citations

• Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

  Wataru Satake;Yuko Nakabayashi;Yuko Nakabayashi;Ikuko Mizuta;Ikuko Mizuta;Yushi Hirota;Yushi Hirota

  1499
  Citations

• Mutations of optineurin in amyotrophic lateral sclerosis

  Hirofumi Maruyama;Hiroyuki Morino;Hidefumi Ito;Hidefumi Ito;Yuishin Izumi

  1476
  Citations

• Self-Organization of Polarized Cerebellar Tissue in 3D Culture of Human Pluripotent Stem Cells

  Keiko Muguruma;Ayaka Nishiyama;Hideshi Kawakami;Kouichi Hashimoto

  668
  Citations

• Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease.

  Demetrius M. Maraganore;Mariza De Andrade;Alexis Elbaz;Matthew J. Farrer

  620
  Citations

• High frequency of open-angle glaucoma in Japanese patients with Alzheimer's disease

  Hiroki Tamura;Hideshi Kawakami;Takashi Kanamoto;Tomoko Kato

  296
  Citations

• Molecular features of the CAG repeats and clinical manifestation of Machado—Joseph disease

  Hirofumi Maruyama;Shigenobu Nakamura;Zenjiro Matsuyama;Tetsuo Sakai

  256
  Citations

• Generation of transgenic mice with elevated blood pressure by introduction of the rat renin and angiotensinogen genes.

  H Ohkubo;H Kawakami;Y Kakehi;T Takumi

  211
  Citations

• Lack of an association of estrogen receptor α gene polymorphisms and transcriptional activity with Alzheimer disease

  Hirofumi Maruyama;Hiromasa Toji;Charles R. Harrington;Ken Sasaki

  205
  Citations

• Molecular Features of the CAG Repeats of Spinocerebellar Ataxia 6 (SCA6)

  Zenjiro Matsuyama;Hideshi Kawakami;Hirofumi Maruyama;Yuishin Izumi

  186
  Citations

• Characteristic Magnetic Resonance Imaging Findings in Machado-Joseph Disease

  Yoshio Murata;Shinya Yamaguchi;Hideshi Kawakami;Yukari Imon

  159
  Citations

• Linear ubiquitination is involved in the pathogenesis of optineurin-associated amyotrophic lateral sclerosis

  Seshiru Nakazawa;Daisuke Oikawa;Daisuke Oikawa;Ryohei Ishii;Takashi Ayaki

  137
  Citations

• Direct Alteration of the P/Q-Type Ca2+ Channel Property by Polyglutamine Expansion in Spinocerebellar Ataxia 6

  Zenjiro Matsuyama;Minoru Wakamori;Yasuo Mori;Hideshi Kawakami

  134
  Citations

• Structure and organization of the gene encoding human dopamine transporter.

  Toshitaka Kawarai;Hideshi Kawakami;Yasuhiro Yamamura;Shigenobu Nakamura

  133
  Citations

• Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: A study of 1,286 Japanese patients

  Hirofumi Maruyama;Yuishin Izumi;Hiroyuki Morino;Masaya Oda

  130
  Citations

• Mutations in Twinkle primase-helicase cause Perrault syndrome with neurologic features.

  Hiroyuki Morino;Sarah B. Pierce;Yukiko Matsuda;Tom Walsh

  127
  Citations

• Vulnerability of Purkinje Cells Generated from Spinocerebellar Ataxia Type 6 Patient-Derived iPSCs

  Yoshihito Ishida;Hideshi Kawakami;Hiroyuki Kitajima;Ayaka Nishiyama

  126
  Citations

• Optineurin suppression causes neuronal cell death via NF-κB pathway.

  Mayumi Akizuki;Hirofumi Yamashita;Kengo Uemura;Hirofumi Maruyama

  109
  Citations

• Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study

  Alexis Elbaz;Lorene M Nelson;Haydeh Payami;John P A Ioannidis

  106
  Citations

• Mutations of optineurin in amyotrophic lateral

  Hirofumi Maruyama;Hiroyuki Morino;Hidefumi Ito;Yuishin Izumi

  1
  Citations