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Haematologica|January 18, 2020
Expanded circulating hematopoietic stem/progenitor cells as novel cell source for the treatment of TCIRG1 osteopetrosisValentina Capo, Sara Penna, Ivan Merelli, et al.Genome Medicine|December 20, 2015
Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosisBianca Tesi, Kristina Lagerstedt-Robinson, Samuel C C Chiang, et al.Allergy|October 10, 2019
ILC3 deficiency and generalized ILC abnormalities in DOCK8-deficient patientsAhmet Eken, Murat Cansever, Fatma Zehra Okus, et al.European Journal of Haematology|March 31, 2024
Identification of the molecular etiology in rare congenital hemolytic anemias using next-generation sequencing with exome-based copy number variant analysisEsra Isik, Yesim Aydinok, Canan Albayrak, et al.Journal of Clinical Immunology|August 9, 2024
DIAPH1-Deficiency is Associated with Major T, NK and ILC Defects in HumansZehra Busra Azizoglu, Royala Babayeva, Zehra Sule Haskologlu, et al.Clinical Immunology (Orlando, Fla.)|September 23, 2023
C-terminal variants in CDC42 drive type I interferon-dependent autoinflammation in NOCARH syndrome reversible by ruxolitinibFriedrich G Kapp, Stefanie Kretschmer, Cora C A Beckmann, et al.Frontiers in Immunology|April 11, 2022
Preclinical Studies on Convalescent Human Immune Plasma-Derived Exosome: Omics and Antiviral Properties to SARS-CoV-2Neslihan Pakize Taşlı, Zeynep Burçin Gönen, Oğuz Kaan Kırbaş, et al.Blood|October 12, 2022
Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changesMonika I Linder, Yoko Mizoguchi, Sebastian Hesse, et al.Blood|July 3, 2024
Efficacy of T-cell assays for the diagnosis of primary defects in cytotoxic lymphocyte exocytosisSamuel C C Chiang, Laura E Covill, Bianca Tesi, et al.Blood|September 11, 2019
CD137 deficiency causes immune dysregulation with predisposition to lymphomagenesisIdo Somekh, Marini Thian, David Medgyesi, et al.Pageof 16