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The american rheumatism association 1987 revised criteria for the classification of rheumatoid arthritis

1988 • 19,632 citations

Revised Criteria for the Classification of Rheumatoid Arthritis

1990 • 7,730 citations

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

2001 • 5,526 citations

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

2001 • 4,997 citations

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

2001 • 2,948 citations

Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle–Wells syndrome

2001 • 1,593 citations

Ancient Missense Mutations in a New Member of the RoRet Gene Family Are Likely to Cause Familial Mediterranean Fever

1997 • 1,502 citations

A candidate gene for familial Mediterranean fever

1997 • 1,481 citations

Germline Mutations in the Extracellular Domains of the 55 kDa TNF Receptor, TNFR1, Define a Family of Dominantly Inherited Autoinflammatory Syndromes

1999 • 1,363 citations

CARD15 mutations in Blau syndrome

2001 • 945 citations

A physical map of the human genome

2001 • 927 citations

Hereditary Periodic Fever

2001 • 456 citations

URTICARIA, DEAFNESS, AND AMYLOIDOSIS: A NEW HEREDO-FAMILIAL SYNDROME

1962 • 368 citations

The Tumor-Necrosis-Factor Receptor–Associated Periodic Syndrome: New Mutations in TNFRSF1A, Ancestral Origins, Genotype-Phenotype Studies, and Evidence for Further Genetic Heterogeneity of Periodic Fevers

2001 • 338 citations

Familial cold autoinflammatory syndrome: Phenotype and genotype of an autosomal dominant periodic fever

2001 • 315 citations

PYPAF1, a PYRIN-containing Apaf1-like Protein That Assembles with ASC and Regulates Activation of NF-κB

2002 • 267 citations

TNFRSF1A mutations and autoinflammatory syndromes

2000 • 243 citations

The PYRIN domain: A member of the death domain‐fold superfamily

2001 • 149 citations

Identification of a Locus on Chromosome 1q44 for Familial Cold Urticaria

2000 • 138 citations

Genetic Linkage of the Muckle-Wells Syndrome to Chromosome 1q44

1999 • 128 citations

An autosomal dominant periodic fever associated with AA amyloidosis in a North Indian family maps to distal chromosome 1q

2000 • 50 citations

Familial cold urticaria

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Hereditary periodic fever syndromes

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An Israeli Arab patient with a de novoTNFRSF1A mutation causing tumor necrosis factor receptor-associated periodic syndrome

2002 • 36 citations