Joseph J Catanese

Author PubWeight™ 77.68‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis. Am J Hum Genet 2004 13.71
2 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. Nat Genet 2010 9.90
3 A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes. Am J Hum Genet 2006 9.56
4 Common variants at CD40 and other loci confer risk of rheumatoid arthritis. Nat Genet 2008 7.07
5 A physical map of the mouse genome. Nature 2002 4.97
6 PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis. Am J Hum Genet 2005 3.95
7 Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk. Nat Genet 2009 3.52
8 A polymorphism in the protease-like domain of apolipoprotein(a) is associated with severe coronary artery disease. Arterioscler Thromb Vasc Biol 2007 2.47
9 A 7 gene signature identifies the risk of developing cirrhosis in patients with chronic hepatitis C. Hepatology 2007 2.16
10 Polymorphism in KIF6 gene and benefit from statins after acute coronary syndromes: results from the PROVE IT-TIMI 22 study. J Am Coll Cardiol 2008 2.12
11 KIF6 Trp719Arg polymorphism and the effect of statin therapy in elderly patients: results from the PROSPER study. Eur J Cardiovasc Prev Rehabil 2010 1.98
12 Identification of four gene variants associated with myocardial infarction. Am J Hum Genet 2005 1.89
13 Gene variants of VAMP8 and HNRPUL1 are associated with early-onset myocardial infarction. Arterioscler Thromb Vasc Biol 2006 1.60
14 A large-scale rheumatoid arthritis genetic study identifies association at chromosome 9q33.2. PLoS Genet 2008 1.53
15 Polymorphism in the apolipoprotein(a) gene, plasma lipoprotein(a), cardiovascular disease, and low-dose aspirin therapy. Atherosclerosis 2008 1.48
16 Identification of two gene variants associated with risk of advanced fibrosis in patients with chronic hepatitis C. Gastroenterology 2006 1.38
17 Association of a single-nucleotide polymorphism in CD40 with the rate of joint destruction in rheumatoid arthritis. Arthritis Rheum 2009 1.24
18 Analysis of 17,576 potentially functional SNPs in three case-control studies of myocardial infarction. PLoS One 2008 1.17
19 Asp92Asn polymorphism in the myeloid IgA Fc receptor is associated with myocardial infarction in two disparate populations: CARE and WOSCOPS. Arterioscler Thromb Vasc Biol 2006 1.07
20 Further genetic evidence for three psoriasis-risk genes: ADAM33, CDKAL1, and PTPN22. J Invest Dermatol 2008 1.04
21 Carriers of rare missense variants in IFIH1 are protected from psoriasis. J Invest Dermatol 2010 0.97
22 Polymorphisms associated with both noncardioembolic stroke and coronary heart disease: vienna stroke registry. Cerebrovasc Dis 2009 0.94
23 The 5q31 variants associated with psoriasis and Crohn's disease are distinct. Hum Mol Genet 2008 0.91
24 The autoimmune disease-associated IL12B and IL23R polymorphisms in multiple sclerosis. Hum Immunol 2007 0.89
25 Investigation of KIF6 Trp719Arg in a case-control study of myocardial infarction: a Costa Rican population. PLoS One 2010 0.87
26 Genome-wide study of gene variants associated with differential cardiovascular event reduction by pravastatin therapy. PLoS One 2012 0.84
27 Polymorphisms and noncardioembolic stroke in three case-control studies. Cerebrovasc Dis 2011 0.76