Inga Sakovich

Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis

Marita Bosticardo, Yasuhiro Yamazaki, Jennifer E. Cowan et al. · The American Journal of Human Genetics · 2019 · 78 citations · Full text

Immunogenetics, Lymphocyte Development, Genetics +9

Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity

Maria Elena Maccari, Martin Wolkewitz, Charlotte Schwab et al. · Journal of Allergy and Clinical Immunology · 2023 · 58 citations · Full text

Autoimmune Disease, Immune Cell Development, Immunodeficiencies +11

Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients

Christoph B. Geier, Maryssa Ellison, Rachel Cruz et al. · Journal of Clinical Immunology · 2022 · 40 citations · Full text

Geographical Distribution, Incidence, Malignancies, and Outcome of 136 Eastern Slavic Patients With Nijmegen Breakage Syndrome and NBN Founder Variant c.657_661del5

Svetlana Sharapova, Olga Pashchenko, Svetlana Vakhlyarskaya et al. · Frontiers in Immunology · 2021 · 39 citations · Full text

Heterozygous activating mutation in RAC2 causes infantile-onset combined immunodeficiency with susceptibility to viral infections

Svetlana Sharapova, Emma Haapaniemi, Inga Sakovich et al. · Clinical Immunology · 2019 · 34 citations

Primary Immunodeficiency, Human Retrovirus, Pathogenesis +7