Anne‐Laure Mathieu

Pivotal role of exogenous pyruvate in human natural killer cell metabolism

Haploinsufficiency in PTPN2 leads to early-onset systemic autoimmunity from Evans syndrome to lupus

Mendelian Causes of Autoimmunity: the Lupus Phenotype

Tumor-induced natural killer cell dysfunction is a rapid and reversible process uncoupled from the expression of immune checkpoints

mTOR Activation Underlies Enhanced B Cell Proliferation and Autoimmunity in <i>PrkcdG510S/G510S</i> Mice

DNASE1L3 deficiency, new phenotypes, and evidence for a transient type I IFN signaling

Polyclonal expansion of TCR Vβ 21.3 ⁺ CD4 ⁺ and CD8 ⁺ T cells is a hallmark of multisystem inflammatory syndrome in children

Sequential actions of EOMES and T-BET promote stepwise maturation of natural killer cells

LACC1 deficiency links juvenile arthritis with autophagy and metabolism in macrophages

Early-onset autoimmunity associated with SOCS1 haploinsufficiency

Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts

DEF6 deficiency, a mendelian susceptibility to EBV infection, lymphoma, and autoimmunity

Monogenic lupus: Dissecting heterogeneity

T‐bet and Eomes govern differentiation and function of mouse and human NK cells and ILC1

Comparison of RT-qPCR and Nanostring in the measurement of blood interferon response for the diagnosis of type I interferonopathies

Antigen-Induced but Not Innate Memory CD8 T Cells Express NKG2D and Are Recruited to the Lung Parenchyma upon Viral Infection

S1PR5 is essential for human natural killer cell migration toward sphingosine-1 phosphate

Human Naive and Memory T Cells Display Opposite Migratory Responses to Sphingosine-1 Phosphate

Terminal NK cell maturation is controlled by concerted actions of T-bet and Zeb2 and is essential for melanoma rejection

PRKDC mutations associated with immunodeficiency, granuloma, and autoimmune regulator–dependent autoimmunity

Inherited anomalies of innate immune receptors in pediatric-onset inflammatory diseases

Mutations in CECR1 associated with a neutrophil signature in peripheral blood