Shigeaki Nonoyama

Overview

Best Publications

• The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome

  Alejandro Aruffo;Alejandro Aruffo;Mary Farrington;Diane Hollenbaugh;Xu Li

  1008
  Citations

• International consensus document (icon): common variable immunodeficiency disorders

  Francisco A. Bonilla;Isil Barlan;Helen Chapel;Beatriz Tavares Costa-Carvalho

  888
  Citations

• Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015

  Capucine Picard;Waleed Al-Herz;Aziz Bousfiha;Jean Laurent Casanova

  857
  Citations

• Human Tyrosine Kinase 2 Deficiency Reveals Its Requisite Roles in Multiple Cytokine Signals Involved in Innate and Acquired Immunity

  Yoshiyuki Minegishi;Masako Saito;Tomohiro Morio;Ken Watanabe

  804
  Citations

• Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination.

  Kohsuke Imai;Geir Slupphaug;Wen I. Lee;Wen I. Lee;Patrick Revy

  764
  Citations

• Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency

  Waleed Al-Herz;Aziz Bousfiha;Jean-Laurent Casanova;Jean-Laurent Casanova;Helen Chapel

  694
  Citations

• Primary immunodeficiencies: 2009 update

  Luigi D. Notarangelo;Alain Fischer;Raif S. Geha;Jean-Laurent Casanova

  630
  Citations

• Primary immunodeficiency diseases: An update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee

  Raif S. Geha;Luigi D. Notarangelo;Jean Laurent Casanova;Helen Chapel

  610
  Citations

• Common defects of ABCG2, a high-capacity urate exporter, cause gout: A function-based genetic analysis in a Japanese population

  Hirotaka Matsuo;Tappei Takada;Kimiyoshi Ichida;Kimiyoshi Ichida;Takahiro Nakamura

  521
  Citations

• Clinical Features and Outcome of Patients With IRAK-4 and MyD88 Deficiency

  Capucine Picard;Capucine Picard;Horst Von Bernuth;Horst Von Bernuth;Horst Von Bernuth;Pegah Ghandil;Pegah Ghandil;Pegah Ghandil;Maya Chrabieh;Maya Chrabieh

  488
  Citations

• Clinical course of patients with WASP gene mutations

  Kohsuke Imai;Tomohiro Morio;Yi Zhu;Yinzhu Jin

  466
  Citations

• Mutations in glucose transporter 9 gene SLC2A9 cause renal hypouricemia.

  Hirotaka Matsuo;Toshinori Chiba;Shushi Nagamori;Akiyoshi Nakayama

  456
  Citations

• AID mutant analyses indicate requirement for class-switch-specific cofactors

  Van-Thanh Ta;Hitoshi Nagaoka;Nadia Catalan;Anne Durandy

  382
  Citations

• Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome

  Alexandra Y. Kreins;Alexandra Y. Kreins;Michael J. Ciancanelli;Satoshi Okada;Xiao Fei Kong

  352
  Citations

• Functional STAT3 deficiency compromises the generation of human T follicular helper cells

  Cindy S. Ma;Cindy S. Ma;Danielle T. Avery;Anna Chan;Marcel Batten;Marcel Batten

  350
  Citations

• CD40 ligand expression is defective in a subset of patients with common variable immunodeficiency.

  Mary Farrington;Laura S. Grosmaire;Shigeaki Nonoyama;Susanna H. Fischer

  314
  Citations

• The 2015 IUIS Phenotypic Classification for Primary Immunodeficiencies

  Aziz Bousfiha;Leïla Jeddane;Waleed Al-Herz;Fatima Ailal

  312
  Citations

• Absence of IgD-CD27(+) memory B cell population in X-linked hyper-IgM syndrome.

  Kazunaga Agematsu;Haruo Nagumo;Koji Shinozaki;Sho Hokibara

  293
  Citations

• Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study

  Elodie Elkaim;Elodie Elkaim;Benedicte Neven;Benedicte Neven;Benedicte Neven;Julie Bruneau;Julie Bruneau;Kanako Mitsui-Sekinaka

  283
  Citations

• Induction of the high-affinity IgE receptor (FcɛRI) on human mast cells by IL-4

  Hano Toru;Chisel Ra;Shigeaki Nonoyama;Katsuhiro Suzuki

  274
  Citations