Monogenic forms of systemic lupus erythematosus: new insights into SLE pathogenesis

IRF5 haplotypes demonstrate diverse serological associations which predict serum interferon alpha activity and explain the majority of the genetic association with systemic lupus erythematosus

(2011) Timothy B Niewold et al.   ANNALS OF THE RHEUMATIC DISEASES

B lymphocyte stimulator levels in systemic lupus erythematosus: Higher circulating levels in African American patients and increased production after influenza vaccination in patients with low baseline levels

(2011) Lauren L. Ritterhouse et al.   ARTHRITIS AND RHEUMATISM

A loss-of-function variant of the antiviral molecule MAVS is associated with a subset of systemic lupus patients

(2011) Julien Pothlichet et al.   EMBO Molecular Medicine

Evaluation of the TREX1 gene in a large multi-ancestral lupus cohort

(2011) B Namjou et al.   GENES AND IMMUNITY

The Autoimmune Disease Risk Allele of UBE2L3 in African American Patients with Systemic Lupus Erythematosus: A Recessive Effect Upon Subphenotypes

(2011) S. AGIK et al.   JOURNAL OF RHEUMATOLOGY

Type I interferon signature is high in lupus and neuromyelitis optica but low in multiple sclerosis

(2011) Xuan Feng et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature

(2011) Tracy A Briggs et al.   NATURE GENETICS

Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity

(2011) Ekkehart Lausch et al.   NATURE GENETICS

Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus

(2011) Sulaiman M Al-Mayouf et al.   NATURE GENETICS

Familial Aggregation of Autoimmune Disease in Juvenile Dermatomyositis

(2011) T. B. Niewold et al.   PEDIATRICS

Linkage of Type I Interferon Activity and TNF-Alpha Levels in Serum with Sarcoidosis Manifestations and Ancestry

(2011) Nadera J. Sweiss et al.   PLoS One

Homozygous mutation in SAMHD1 gene causes cerebral vasculopathy and early onset stroke

(2011) B. Xin et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Netting Neutrophils Are Major Inducers of Type I IFN Production in Pediatric Systemic Lupus Erythematosus

(2011) G. S. Garcia-Romo et al.   Science Translational Medicine

Chilblains as a Diagnostic Sign of Aicardi-Goutières Syndrome

(2010) G. M. H. Abdel-Salam et al.   NEUROPEDIATRICS

Primary Immunodeficiency and Autoimmunity: Lessons From Human Diseases

(2010) G. J. Arason et al.   SCANDINAVIAN JOURNAL OF IMMUNOLOGY

Age- and gender-specific modulation of serum osteopontin and interferon-α by osteopontin genotype in systemic lupus erythematosus

(2009) S N Kariuki et al.   GENES AND IMMUNITY

Aicardi-Goutieres syndrome and related phenotypes: linking nucleic acid metabolism with autoimmunity

(2009) Y. J. Crow et al.   HUMAN MOLECULAR GENETICS

Autoimmune manifestations in primary immune deficiencies

(2008) Guillaume Bussone et al.   AUTOIMMUNITY REVIEWS

Trex1 Prevents Cell-Intrinsic Initiation of Autoimmunity

(2008) Daniel B. Stetson et al.   CELL

Association of Systemic Lupus Erythematosus withC8orf13–BLKandITGAM–ITGAX

(2008) Geoffrey Hom et al.   NEW ENGLAND JOURNAL OF MEDICINE

Inhibition of G1P3 expression found in the differential display study on respiratory syncytial virus infection

(2008) Dong-chi Zhao et al.   Virology Journal