The TNFRSF13C H159Y Variant Is Associated with Severe COVID-19: A Retrospective Study of 500 Patients from Southern Italy

Common variants at 21q22.3 locus influence MX1 and TMPRSS2 gene expression and susceptibility to severe COVID-19

(2021) Immacolata Andolfo et al.   iScience

COVID-19 infection: the perspectives on immune responses

(2020) Yufang Shi et al.   CELL DEATH AND DIFFERENTIATION

A possible role for B cells in COVID-19? Lesson from patients with agammaglobulinemia

(2020) Isabella Quinti et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy

(2020) Rosanna Asselta et al.   Aging-US

ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population

(2020) Elisa Benetti et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Genomewide Association Study of Severe Covid-19 with Respiratory Failure

(2020) David Ellinghaus et al.   NEW ENGLAND JOURNAL OF MEDICINE

Deciphering the Role of Host Genetics in Susceptibility to Severe COVID-19

(2020) Madalina Elena Carter-Timofte et al.   Frontiers in Immunology

Genetic Analysis of the Coronavirus SARS-CoV-2 Host Protease TMPRSS2 in Different Populations

(2020) Roberta Russo et al.   Frontiers in Genetics

SARS-CoV-2 Infection of Pluripotent Stem Cell-Derived Human Lung Alveolar Type 2 Cells Elicits a Rapid Epithelial-Intrinsic Inflammatory Response

(2020) Jessie Huang et al.   Cell Stem Cell

Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

(2020) Qian Zhang et al.   SCIENCE

Genetic mechanisms of critical illness in Covid-19

(2020) Erola Pairo-Castineira et al.   NATURE

FAS‐mediated apoptosis impairment in patients with ALPS/ALPS‐like phenotype carrying variants on CASP10 gene

(2019) Maurizio Miano et al.   BRITISH JOURNAL OF HAEMATOLOGY

TNFRSF13C/BAFFR P21R and H159Y polymorphisms in multiple sclerosis

(2019) Panagiotis Ntellas et al.   Multiple Sclerosis and Related Disorders

Association of variants in BAFF (rs9514828 and rs1041569) and BAFF-R (rs61756766) genes with the risk of chronic lymphocytic leukemia

(2016) Monika Jasek et al.   TUMOR BIOLOGY

Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies

(2015) Vassilios Lougaris et al.   JOURNAL OF CLINICAL IMMUNOLOGY

A BAFF Receptor His159Tyr Mutation in Sjögren's Syndrome-Related Lymphoproliferation

(2015) Aristea Papageorgiou et al.   Arthritis & Rheumatology

BAFF-R mutations in Good's syndrome

(2014) Vassilios Lougaris et al.   CLINICAL IMMUNOLOGY

Three Different Classifications, B Lymphocyte Subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) Gene Mutations, CTLA-4 and ICOS Gene Polymorphisms in Turkish Patients with Common Variable Immunodeficiency

(2012) Necil Kutukculer et al.   JOURNAL OF CLINICAL IMMUNOLOGY

A BAFF-R mutation associated with non-Hodgkin lymphoma alters TRAF recruitment and reveals new insights into BAFF-R signaling

(2010) Joanne M. Hildebrand et al.   JOURNAL OF EXPERIMENTAL MEDICINE