Daniel L Kastner


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Person Info

NAME

Daniel L

SURNAME

Kastner

Publications in SciGraph latest 50 shown

  • 2017-08 The monogenic autoinflammatory diseases define new pathways in human innate immunity and inflammation in NATURE IMMUNOLOGY
  • 2017-03 Dense genotyping of immune-related loci implicates host responses to microbial exposure in Behcet's disease susceptibility in NATURE GENETICS
  • 2016-12 Evaluation of KIR3DL1/KIR3DS1 polymorphism in Behçet’s disease in GENES & IMMUNITY
  • 2015-12 Update on CECR1 molecular diagnostics: new mutations in the deficiency of ADA2 (DADA2) and the North American polyarteritis nodosa (PAN) cohort in PEDIATRIC RHEUMATOLOGY
  • 2015-12 Identification of pyrin targets by CHiP-Seq in PEDIATRIC RHEUMATOLOGY
  • 2015-12 Cofilin-1 is an essential redox sensor for NLRP3 inflammasome activation in PEDIATRIC RHEUMATOLOGY
  • 2015-12 A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein in PEDIATRIC RHEUMATOLOGY
  • 2015-12 HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis in PEDIATRIC RHEUMATOLOGY
  • 2015-12 Immune dysregulation in patients with TRNT1 deficiency in PEDIATRIC RHEUMATOLOGY
  • 2015-12 Use of TNF inhibitors in the treatment of PAPA syndrome in PEDIATRIC RHEUMATOLOGY
  • 2015-10 Reply to Stoimenis et al in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-05 Identification of possible pathogenic pathways in Behçet’s disease using genome-wide association study data from two different populations in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-03 A small-molecule inhibitor of the NLRP3 inflammasome for the treatment of inflammatory diseases in NATURE MEDICINE
  • 2015 Pathogenesis in FAMILIAL MEDITERRANEAN FEVER
  • 2013-11 PW03-014 - TLR4 and MEFV variants are Behçet's risk factors in PEDIATRIC RHEUMATOLOGY
  • 2013-11 OR9-001 - Exome sequencing in monogenic Behçet-like disease in PEDIATRIC RHEUMATOLOGY
  • 2013-11 PW03-017 – Combination TNF and IL-1 blockade in PAPA syndrome in PEDIATRIC RHEUMATOLOGY
  • 2013-11 P02-003 - HIDS in a consanguineous family form Saudi Arabia? in PEDIATRIC RHEUMATOLOGY
  • 2013-11 OR10-001 - Altered mitochondrial ROS and metabolism in TRAPS in PEDIATRIC RHEUMATOLOGY
  • 2013-11 PW02-002 - Single MVK mutation and recurrent fevers in PEDIATRIC RHEUMATOLOGY
  • 2013-11 OR13-001 Loss-of-function mutations in CECR1, encoding adenosine deaminase 2 (ADA2), cause recurrent fevers and early onset strokes in PEDIATRIC RHEUMATOLOGY
  • 2013-02 Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1 in NATURE GENETICS
  • 2012-08 Lighting the fires within: the cell biology of autoinflammatory diseases in NATURE REVIEWS IMMUNOLOGY
  • 2011-08 Genetics of monogenic autoinflammatory diseases: past successes, future challenges in NATURE REVIEWS RHEUMATOLOGY
  • 2011-02 Autoinflammation in 2010: Expanding clinical spectrum and broadening therapeutic horizons in NATURE REVIEWS RHEUMATOLOGY
  • 2010-08 Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease in NATURE GENETICS
  • 2010-06 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci in NATURE GENETICS
  • 2009-12 Data for Genetic Analysis Workshop 16 Problem 1, association analysis of rheumatoid arthritis data in BMC PROCEEDINGS
  • 2009-12 Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk in NATURE GENETICS
  • 2009-07 REL, encoding a member of the NF-κB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis in NATURE GENETICS
  • 2008-10 Common variants at CD40 and other loci confer risk of rheumatoid arthritis in NATURE GENETICS
  • 2008 Periodic Syndromes in PRIMER ON THE RHEUMATIC DISEASES
  • 2006 The Systemic Autoinflammatory Diseases: Inborn Errors of the Innate Immune System in CURRENT CONCEPTS IN AUTOIMMUNITY AND CHRONIC INFLAMMATION
  • 2004-03 Haplotypes and DNA sequence variation within and surrounding the transthyretin gene: genotype–phenotype correlations in familial amyloid polyneuropathy (V30M) in Portugal and Sweden in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2001-03 Episodic evolution of pyrin in primates: human mutations recapitulate ancestral amino acid states in NATURE GENETICS
  • 2000-06 Isolation, genomic organization, and expression analysis of the mouse and rat homologs of MEFV, the gene for familial Mediterranean fever in MAMMALIAN GENOME
  • 1999-07 Genetic anticipation in Portuguese kindreds with familial amyloidotic polyneuropathy is unlikely to be caused by triplet repeat expansions in HUMAN GENETICS
  • 1996-04 CARNEY COMPLEX : CONFIRMATION OF THE CHROMOSOME 2p16 LOCUS, EXCLUSION OF THE hMSH-2, -6, & CALNB1 GENES AND CONSTRUCTION OF A GENETIC AND PHYSICAL MAP OF THE REGION. • 584 in PEDIATRIC RESEARCH
  • 1994-04 Localization of a gene causing cystinuria to chromosome 2p in NATURE GENETICS
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