Caterina Cancrini

Overview

Best Publications

• HLA-haploidentical stem cell transplantation after removal of αβ+ T and B cells in children with nonmalignant disorders

  Alice Bertaina;Pietro Merli;Sergio Rutella;Sergio Rutella;Daria Pagliara

  484
  Citations

• Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study.

  Tanya I Coulter;Anita Chandra;Chris M Bacon;Judith Babar

  468
  Citations

• A hypermorphic IκBα mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency

  Gilles Courtois;Asma Smahi;Janine Reichenbach;Rainer Döffinger

  414
  Citations

• Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome

  Cristina Woellner;E. Michael Gertz;Alejandro A. Schäffer;Macarena Lagos

  356
  Citations

• Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.

  Asbjørg Stray-Pedersen;Hanne Sørmo Sorte;Pubudu Samarakoon;Tomasz Gambin;Tomasz Gambin

  288
  Citations

• Accumulation of peripheral autoreactive B cells in the absence of functional human regulatory T cells

  Tuure Kinnunen;Nicolas Chamberlain;Henner Morbach;Jinyoung Choi

  214
  Citations

• Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency

  Jolan E. Walter;Lindsey B. Rosen;Krisztian Csomos;Jacob M. Rosenberg

  206
  Citations

• Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry

  Maria Elena Maccari;Hassan Abolhassani;Hassan Abolhassani;Asghar Aghamohammadi;Alessandro Aiuti

  203
  Citations

• A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function.

  Michael T Lam;Michael T Lam;Simona Coppola;Oliver H F Krumbach;Giusi Prencipe

  196
  Citations

• In vivo tracking of T cells in humans unveils decade-long survival and activity of genetically modified T memory stem cells.

  Luca Biasco;Serena Scala;Luca Basso Ricci;Francesca Dionisio

  193
  Citations

• Outcome of hematopoietic stem cell transplantation for adenosine deaminase–deficient severe combined immunodeficiency

  Amel Hassan;Claire Booth;Alex Brightwell;Zoe Allwood

  177
  Citations

• Clinical features and follow-up in patients with 22q11.2 deletion syndrome.

  Caterina Cancrini;Pamela Puliafito;Maria Cristina Digilio;Annarosa Soresina

  171
  Citations

• Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations.

  Julian Thalhammer;Gerhard Kindle;Alexandra Nieters;Stephan Rusch

  158
  Citations

• A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency.

  Yu Nee Lee;Francesco Frugoni;Kerry Dobbs;Jolan E. Walter

  153
  Citations

• X-linked agammaglobulinemia (XLA): Phenotype, diagnosis, and therapeutic challenges around the world

  Zeinab A. El-Sayed;Irina Abramova;Juan Carlos Aldave;Waleed Al-Herz

  118
  Citations

• Humoral immune responses and CD27+ B cells in children with DiGeorge syndrome (22q11.2 deletion syndrome).

  A. Finocchi;A. Finocchi;S. Di Cesare;M. L Romiti;C. Capponi

  111
  Citations

• Characterization of T and B cell repertoire diversity in patients with RAG deficiency

  Yu Nee Lee;Yu Nee Lee;Francesco Frugoni;Kerry Dobbs;Irit Tirosh

  105
  Citations

• Efficacy and Adverse Events During Janus Kinase Inhibitor Treatment of SAVI Syndrome.

  Stefano Volpi;Antonella Insalaco;Roberta Caorsi;Elettra Santori

  105
  Citations

• Human germline heterozygous gain-of-function<i>STAT6</i>variants cause severe allergic disease

  Unknown

  104
  Citations

• Demethylation analysis of the FOXP3 locus shows quantitative defects of regulatory T cells in IPEX-like syndrome.

  F. Barzaghi;L. Passerini;E. Gambineri;S. Ciullini Mannurita

  101
  Citations

• Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects.

  Emilia Cirillo;Giuliana Giardino;Vera Gallo;Pamela Puliafito

  100
  Citations

• Consensus statement of the Italian society of pediatric allergy and immunology for the pragmatic management of children and adolescents with allergic or immunological diseases during the COVID-19 pandemic.

  Fabio Cardinale;Giorgio Ciprandi;Salvatore Barberi;Roberto Bernardini

  90
  Citations