Shoji Tsuji

Research.com Recognitions

• 2024 - Research.com Genetics and Molecular Biology in Japan Leader Award

Overview

Best Publications

• Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

  Ellen Sidransky;Michael A. Nalls;Jan O. Aasly;Judith Aharon-Peretz

  2380
  Citations

• Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA)

  R. Koide;T. Ikeuchi;O. Onodera;H. Tanaka

  1384
  Citations

• Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

  Elisa Majounie;Alan E. Renton;Kin Mok;Elise G. P. Dopper;Elise G. P. Dopper

  1367
  Citations

• Interference by Huntingtin and Atrophin-1 with CBP-Mediated Transcription Leading to Cellular Toxicity

  Frederick C. Nucifora;Masayuki Sasaki;Matthew F. Peters;Hui Huang

  1340
  Citations

• Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene

  Hiroshi Ichinose;Tamae Ohye;Ei ichi Takahashi;Ei ichi Takahashi;Naohiko Seki

  941
  Citations

• Charcot-Marie-Tooth Disease Type 2A Caused by Mutation in a Microtubule Motor KIF1Bβ

  Chunjie Zhao;Junko Takita;Yosuke Tanaka;Mitsutoshi Setou

  927
  Citations

• Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.

  K Sanpei;H Takano;S Igarashi;T Sato

  894
  Citations

• A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2–q13.1

  Manabu Funayama;Kazuko Hasegawa;Hisayuki Kowa;Masaaki Saito

  885
  Citations

• α-Synuclein immunoreactivity in glial cytoplasmic inclusions in multiple system atrophy

  Koichi Wakabayashi;Makoto Yoshimoto;Shoji Tsuji;Hitoshi Takahashi

  860
  Citations

• SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein

  Koichiro Nakamura;Seon-Yong Jeong;Toshiki Uchihara;Midori Anno

  854
  Citations

• Safety and efficacy of edaravone in well defined patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial

  Koji Abe;Masashi Aoki;Shoji Tsuji;Yasuto Itoyama

  838
  Citations

• A rescue factor abolishing neuronal cell death by a wide spectrum of familial Alzheimer's disease genes and Aβ

  Yuichi Hashimoto;Takako Niikura;Hirohisa Tajima;Takashi Yasukawa

  746
  Citations

• Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease

  Shoji Tsuji;Osamu Onodera

  603
  Citations

• Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27

  H Matsumine;M Saito;S Shimoda-Matsubayashi;H Tanaka

  531
  Citations

• Expanded polyglutamine stretches interact with TAFII130, interfering with CREB-dependent transcription.

  Takayoshi Shimohata;Toshihiro Nakajima;Mitsunori Yamada;Chiharu Uchida

  491
  Citations

• A Neurological Disease Caused By an Expanded CAG Trinucleotide Repeat in The TATA-Binding Protein Gene: A New Polyglutamine Disease?

  Reiji Koide;Shigeichi Kobayashi;Takayoshi Shimohata;Takeshi Ikeuchi

  459
  Citations

• Mutations in COQ2 in familial and sporadic multiple-system atrophy the multiple-system atrophy research collaboration

  Jun Mitsui;Takashi Matsukawa;Hiroyuki Ishiura;Yoko Fukuda;Yoko Fukuda

  429
  Citations

• Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene

  Hidetoshi Date;Osamu Onodera;Hajime Tanaka;Kiyoshi Iwabuchi

  429
  Citations

• Familial juvenile parkinsonism: clinical and pathologic study in a family.

  H. Takahashi;E. Ohama;S. Suzuki;Y. Horikawa

  409
  Citations

• Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretch.

  Shuichi Igarashi;Reiji Koide;Takayoshi Shimohata;Mitsunori Yamada

  408
  Citations