Author details

Full Name

Joseph J Catanese

Affiliation

ORCID

Career Start Year

1980

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
32090079	Development and Validation of a 34-Gene Inherited Cancer Predisposition Panel Using Next-Generation Sequencing.	BioMed Research International	2020
28248967	Improving the Positive Predictive Value of Non-Invasive Prenatal Screening (NIPS).	PLoS ONE	2017
28097184	719Arg Genetic Variant and Risk for Thoracic Aortic Dissection.	AORTA	2016
27084556	Mutation Yield of a 34-Gene Solid Tumor Panel in Community-Based Tumor Samples.		2016
26392438	Risk prediction by genetic risk scores for coronary heart disease is independent of self-reported family history.	European Heart Journal	2016
25903422	Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility.	Nat Commun	2015
25123217	Twelve-single nucleotide polymorphism genetic risk score identifies individuals at increased risk for future atrial fibrillation and stroke.	Stroke	2014
24743685	Genetic variants in FBN-1 and risk for thoracic aortic aneurysm and dissection.	PLoS ONE	2014
23124848	Brief Report: Single-nucleotide polymorphisms in VKORC1 are risk factors for systemic lupus erythematosus in Asians.	Arthritis Rheum	2013
22134093	Polymorphisms and noncardioembolic stroke in three case-control studies.	Cerebrovascular Diseases	2012
22707612	Genetic risk factors for thrombosis in systemic lupus erythematosus.	J Rheumatol	2012
22666496	Genome-wide study of gene variants associated with differential cardiovascular event reduction by pravastatin therapy.	PLoS ONE	2012
20668468	Carriers of rare missense variants in IFIH1 are protected from psoriasis.	J Invest Dermatol	2010
20927332	Investigation of KIF6 Trp719Arg in a case-control study of myocardial infarction: a Costa Rican population.	PLoS ONE	2010
20215968	KIF6 Trp719Arg polymorphism and the effect of statin therapy in elderly patients: results from the PROSPER study.		2010
20128871	Gene variants associated with venous thrombosis: confirmation in the MEGA study.	Journal of Thrombosis and Haemostasis	2010
20213474	West African and Amerindian ancestry and risk of myocardial infarction and metabolic syndrome in the Central Valley population of Costa Rica.	Human Genetics	2010
20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Nat Genet	2010
18775538	Polymorphism in the apolipoprotein(a) gene, plasma lipoprotein(a), cardiovascular disease, and low-dose aspirin therapy.	Atherosclerosis	2009
19644859	Association of a single-nucleotide polymorphism in CD40 with the rate of joint destruction in rheumatoid arthritis.	Arthritis Rheum	2009
19586676	Multiple variants in toll-like receptor 4 gene modulate risk of liver fibrosis in Caucasians with chronic hepatitis C infection.	Journal of Hepatology	2009
19583818	Genetic variants associated with deep vein thrombosis: the F11 locus.	Journal of Thrombosis and Haemostasis	2009
19286883	F9 MalmÃ¶, factor IX and deep vein thrombosis.	Haematologica	2009
19421222	Factor V Leiden and thrombosis in patients with systemic lupus erythematosus: a meta-analysis.	Genes Immun	2009
19752551	Polymorphisms associated with both noncardioembolic stroke and coronary heart disease: vienna stroke registry.	Cerebrovasc Dis	2009
19898481	Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk.	Nat Genet	2009
19822714	Association of IL2RA and IL2RB with rheumatoid arthritis: a replication study in a Dutch population.	Ann Rheum Dis	2009
18923449	Further genetic evidence for three psoriasis-risk genes: ADAM33, CDKAL1, and PTPN22.	J Invest Dermatol	2009
18682748	Analysis of 17,576 potentially functional SNPs in three case-control studies of myocardial infarction.	PLoS ONE	2008
17949987	SORL1 variants and risk of late-onset Alzheimer's disease.	Neurobiol Dis	2008
18628988	Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's disease.	PLoS One	2008
18349091	Gene variants associated with deep vein thrombosis.	JAMA - Journal of the American Medical Association	2008
18614543	The 5q31 variants associated with psoriasis and Crohn's disease are distinct.	Hum Mol Genet	2008
18650833	Detailed genetic characterization of the interleukin-23 receptor in psoriasis.	Genes Immun	2008
18794853	Common variants at CD40 and other loci confer risk of rheumatoid arthritis.	Nat Genet	2008
18648537	A large-scale rheumatoid arthritis genetic study identifies association at chromosome 9q33.2.	PLoS Genet	2008
18075513	Variants in the 5q31 cytokine gene cluster are associated with psoriasis.	Genes Immun	2008
18222355	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
18063669	Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease.	Hum Mol Genet	2008
18082575	The autoimmune disease-associated IL12B and IL23R polymorphisms in multiple sclerosis.	Hum Immunol	2007
17461418	A 7 gene signature identifies the risk of developing cirrhosis in patients with chronic hepatitis C.	Hepatology	2007
17317784	Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants.	Hum Mol Genet	2007
17236132	A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes.	Am J Hum Genet	2007
17569884	A polymorphism in the protease-like domain of apolipoprotein(a) is associated with severe coronary artery disease.	Arterioscler Thromb Vasc Biol	2007
16385451	A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.	Am J Hum Genet	2006
16917932	Genetic evidence for ubiquitin-specific proteases USP24 and USP40 as candidate genes for late-onset Parkinson disease.	Hum Mutat	2006
16697732	Identification of two gene variants associated with risk of advanced fibrosis in patients with chronic hepatitis C.	Gastroenterology	2006
16690874	Gene variants of VAMP8 and HNRPUL1 are associated with early-onset myocardial infarction.	Arterioscler Thromb Vasc Biol	2006
17008591	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
16685663	A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.	Am J Hum Genet	2006