J. Catanese

发表

Initial sequencing and analysis of the human genome.

J. V. Moran, V. J. Pollara, D. Haussler, 2001, Nature.

A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis.

Steven J. Schrodi, Annette Lee, P. Gregersen, 2004, American journal of human genetics.

DAPK1 variants are associated with Alzheimer's disease and allele-specific expression.

Taylor J. Maxwell, M. Owen, J. Morris, 2006, Human molecular genetics.

A physical map of the mouse genome

Parvaneh Saeedi, William C. Nierman, Ewan Birney, 2002, Nature.

A BAC-based physical map of the major autosomes of Drosophila melanogaster.

G M Rubin, S E Celniker, S E Scherer, 2000, Science.

An improved approach for construction of bacterial artificial chromosome libraries.

P. D. de Jong, K. Osoegawa, J. Catanese, 1998, Genomics.

A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes.

Steven J. Schrodi, M. Leppert, K. Ardlie, 2007, American journal of human genetics.

Erratum: Initial sequencing and analysis of the human genome: International Human Genome Sequencing Consortium (Nature (2001) 409 (860-921))

Ronald W. Davis, J. V. Moran, V. J. Pollara, 2001 .

Identification of four gene variants associated with myocardial infarction.

E. Topol, J. Catanese, Diane U. Leong, 2005, American journal of human genetics.

Common variants at CD40 and other loci confer risk of rheumatoid arthritis

Jing Cui, Kristin G Ardlie, Elizabeth W Karlson, 2008, Nature Genetics.

Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants.

M. Gill, M. Owen, R. Segurado, 2007, Human molecular genetics.

Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease.

M. Owen, R. Segurado, J. Morris, 2008, Human molecular genetics.

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.

Taylor J. Maxwell, Peter Holmans, John Hardy, 2006, American journal of human genetics.

Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci

Jing Cui, Kristin G Ardlie, B Paul Wordsworth, 2010, Nature Genetics.

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.

Taylor J. Maxwell, M. Owen, J. Morris, 2006, American journal of human genetics.

An arrayed human not I-EcoRV boundary library as a tool for RLGS spot analysis.

P. Dejong, C. Plass, J. Catanese, 1997, DNA research : an international journal for rapid publication of reports on genes and genomes.

Construction and characterization of a new bovine bacterial artificial chromosome library with 10 genome-equivalent coverage

Timothy P. L. Smith, P. D. de Jong, J. Catanese, 2000, Mammalian Genome.

Development and Validation of a 34-Gene Inherited Cancer Predisposition Panel Using Next-Generation Sequencing

Y. Liu, J. Catanese, A. Gerasimova, 2020, BioMed research international.

Brief Report: Single-nucleotide polymorphisms in VKORC1 are risk factors for systemic lupus erythematosus in Asians.

J. Catanese, M. Petri, J. Reveille, 2013, Arthritis and rheumatism.

A physical map of the human genome

D. Haussler, B. Trask, R. Wilson, 2001, Nature.

Polymorphisms and Noncardioembolic Stroke in Three Case-Control Studies

E. Ringelstein, J. Catanese, V. Garcia, 2011, Cerebrovascular Diseases.

Identification of the cleavage sites resulting from enzymatic inactivation of human antithrombin III by Crotalus adamanteus proteinase II in the the presence and absence of heparin.

J. Catanese, L. F. Kress, 1981, Biochemistry.

Enzymatic inactivation of human antithrombin III. Limited proteolysis of the inhibitor by snake venom proteinases in the presence of heparin.

J. Catanese, L. F. Kress, 1980, Biochimica et biophysica acta.

SNPs in VKORC1 are Risk Factors for Systemic Lupus Erythematosus in Asians: Genetic risk factors for Lupus

Joanne, J. Catanese, M. Petri, 2013 .

Improving the Positive Predictive Value of Non-Invasive Prenatal Screening (NIPS)

J. Catanese, Weimin Sun, C. Strom, 2017, PloS one.

Analysis of the effects of snake venom proteinases on the activity of human plasma C1 esterase inhibitor, α1-antichymotrypsin and α2-antiplasmin

J. Catanese, T. Hirayama, L. F. Kress, 1983 .

Primary structure of the reactive site of human C1-inhibitor.

J. Catanese, G. Salvesen, J. Travis, 1985, The Journal of biological chemistry.

Enzymatic inactivation of human plasma C1-inhibitor and alpha 1-antichymotrypsin by Pseudomonas aeruginosa proteinase and elastase.

J. Catanese, L. F. Kress, 1984, Biochimica et biophysica acta.

Opossum serum alpha 1-proteinase inhibitor: purification, linear sequence, and resistance to inactivation by rattlesnake venom metalloproteinases.

J. Catanese, L. F. Kress, 1993, Biochemistry.

Isolation from opossum serum of a metalloproteinase inhibitor homologous to human alpha 1B-glycoprotein.

J. Catanese, L. F. Kress, 1992, Biochemistry.

Genetic variants associated with deep vein thrombosis: the F11 locus

P. Reitsma, J. Catanese, F. Rosendaal, 2009, Journal of thrombosis and haemostasis : JTH.

F9 Malmö, factor IX and deep vein thrombosis

P. Reitsma, J. Catanese, F. Rosendaal, 2009, Haematologica.

West African and Amerindian ancestry and risk of myocardial infarction and metabolic syndrome in the Central Valley population of Costa Rica

J. Catanese, E. Ruiz-Narváez, H. Campos, 2010, Human Genetics.

Effects of human plasma alpha2 macroglobulin on the proteolytic activity of snake venoms.

J. Catanese, L. F. Kress, 1981, Toxicon : official journal of the International Society on Toxinology.

Mutation Yield of a 34-Gene Solid Tumor Panel in Community-Based Tumor Samples

F. Waldman, J. Catanese, J. Sninsky, 2016, Molecular Diagnosis & Therapy.

The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X

P. Deloukas, R. Durbin, J. Sulston, 2001, Nature.

A bacterial artificial chromosome library for sequencing the complete human genome.

P. D. de Jong, K. Osoegawa, J. Catanese, 2001, Genome research.

Construction and characterization of a 10-fold genome equivalent rat P1-derived artificial chromosome library.

A. Monaco, G. Lathrop, P. D. de Jong, 1998, Genomics.

Bacterial artificial chromosome libraries for mouse sequencing and functional analysis.

P. D. de Jong, K. Osoegawa, Y. Hayashizaki, 2000, Genome research.

Genetic Risk Factors for Thrombosis in Systemic Lupus Erythematosus

J. Catanese, M. Petri, J. Reveille, 2012, The Journal of Rheumatology.

Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility

X. Estivill, M. Weichenthal, A. Bowcock, 2015, Nature Communications.

Carriers of rare missense variants in IFIH1 are protected from psoriasis.

P. Kwok, M. Leppert, A. Bowcock, 2010, The Journal of investigative dermatology.

Genetic evidence for ubiquitin‐specific proteases USP24 and USP40 as candidate genes for late‐onset Parkinson disease

J. Catanese, S. Schrodi, Yonghong Li, 2006, Human mutation.

Association of a single-nucleotide polymorphism in CD40 with the rate of joint destruction in rheumatoid arthritis.

P. Gregersen, S. Raychaudhuri, J. Catanese, 2009, Arthritis and rheumatism.

An AscI boundary library for the studies of genetic and epigenetic alterations in CpG islands.

Dieter Weichenhan, Christoph Plass, Ramana V Davuluri, 2002, Genome research.

A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.

J. Catanese, S. Schrodi, Diane U. Leong, 2006, American journal of human genetics.

Common variants at CD 40 and other loci confer risk of rheumatoid arthritis

M. Daly, Annette Lee, P. Gregersen, 2008 .

A Large-Scale Rheumatoid Arthritis Genetic Study Identifies Association at Chromosome 9q33.2

Christopher I. Amos, Michael F. Seldin, Kristin G. Ardlie, 2008, PLoS genetics.

Enzymatic digestion of human plasma inter-α-trypsin inhibitor by snake venom metalloproteinases

J. Catanese, L. F. Kress, 1985 .

Genetic Variants in FBN-1 and Risk for Thoracic Aortic Aneurysm and Dissection

J. Catanese, J. Elefteriades, V. Garcia, 2014, PloS one.

Polymorphism in KIF6 gene and benefit from statins after acute coronary syndromes: results from the PROVE IT-TIMI 22 study.

M. Sabatine, E. Braunwald, C. Cannon, 2008, Journal of the American College of Cardiology.

Polymorphism in the apolipoprotein(a) gene, plasma lipoprotein(a), cardiovascular disease, and low-dose aspirin therapy.

Daniel I Chasman, Paul M Ridker, P. Ridker, 2009, Atherosclerosis.

A Polymorphism in the Protease-Like Domain of Apolipoprotein(a) Is Associated With Severe Coronary Artery Disease

E. Topol, Curtis Noordhof, M. Koschinsky, 2007, Arteriosclerosis, thrombosis, and vascular biology.

The autoimmune disease-associated IL12B and IL23R polymorphisms in multiple sclerosis.

J. Catanese, A. Begovich, Joanne H Wang, 2007, Human immunology.

Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family.

Steven J. Schrodi, M. Owen, J. Morris, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Twelve–Single Nucleotide Polymorphism Genetic Risk Score Identifies Individuals at Increased Risk for Future Atrial Fibrillation and Stroke

P. Ellinor, J. Catanese, S. Kathiresan, 2014, Stroke.

Genetic variants at CD28, PRDM1, and CD2/CD58 are associated with rheumatoid arthritis risk

M. Daly, Annette Lee, P. Gregersen, 2009, Nature Genetics.

Risk prediction by genetic risk scores for coronary heart disease is independent of self-reported family history

J. Catanese, S. Kathiresan, O. Melander, 2015, European heart journal.

Further genetic evidence for three psoriasis-risk genes: ADAM33, CDKAL1, and PTPN22.

P. Kwok, M. Leppert, A. Bowcock, 2009, The Journal of investigative dermatology.

A 7 gene signature identifies the risk of developing cirrhosis in patients with chronic hepatitis C

Olivia T. Abar, S. Friedman, J. Catanese, 2007, Hepatology.

PTPN 22 genetic variation : evidence for multiple variants associated with rheumatoid arthritis

Steven J. Schrodi, P. Gregersen, E. Beasley, 2016 .

PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.

Steven J. Schrodi, P. Gregersen, E. Beasley, 2005, American journal of human genetics.

Genetic Variation : Evidence for Multiple Variants Associated with Rheumatoid Arthritis

Steven J. Schrodi, P. Gregersen, E. Beasley, 2005 .

The 5q31 variants associated with psoriasis and Crohn's disease are distinct

M. Leppert, J. Catanese, A. Begovich, 2008, Human molecular genetics.

Semiautomated clone verification by real-time PCR using molecular beacons.

N. Nowak, P. D. de Jong, J. Catanese, 2000, BioTechniques.

Positional cloning of the combined hyperlipidemia gene Hyplip1

P. D. de Jong, J. Catanese, A. Lusis, 2002, Nature genetics.

SORL1 variants and risk of late-onset Alzheimer’s disease

M. Owen, J. Morris, A. Goate, 2008, Neurobiology of Disease.

Association of ABCA1 with late-onset Alzheimer’s disease is not observed in a case-control study

M. Owen, P. Holmans, L. Thal, 2004, Neuroscience Letters.

Analysis of 17,576 Potentially Functional SNPs in Three Case–Control Studies of Myocardial Infarction

Mary J. Malloy, John P. Kane, J. Catanese, 2008, PloS one.

Identification of two gene variants associated with risk of advanced fibrosis in patients with chronic hepatitis C.

Olivia T. Abar, S. Friedman, J. Catanese, 2006, Gastroenterology.

Gene variants associated with deep vein thrombosis.

P. Reitsma, J. Catanese, F. Rosendaal, 2008, Journal of the American Medical Association (JAMA).

Malmö , factor IX and deep vein thrombosis

P. Reitsma, J. Catanese, F. Rosendaal, 2009 .

F 9 Malmö , factor IX and deep vein thrombosis

P. Reitsma, J. Catanese, F. Rosendaal, 2022 .

Abbreviated Title ( Length 25 characters ) : Genetic risk for incident CHD 2

J. Pankow, J. Coresh, J. Catanese, 2007 .

Genome-Wide Study of Gene Variants Associated with Differential Cardiovascular Event Reduction by Pravastatin Therapy

N. Sattar, J. Catanese, F. Sacks, 2012, PloS one.

Association of a single-nucleotide polymorphism in CD 40 with the rate of joint destruction in rheumatoid arthritis

P. Gregersen, S. Cessie, S. Raychaudhuri, 2011 .

Multiple variants in toll-like receptor 4 gene modulate risk of liver fibrosis in Caucasians with chronic hepatitis C infection.

Olivia T. Abar, S. Friedman, J. Catanese, 2009, Journal of hepatology.

KIF6 Trp719Arg polymorphism and the effect of statin therapy in elderly patients: results from the PROSPER study

J. Catanese, J. Jukema, I. Ford, 2010, European journal of cardiovascular prevention and rehabilitation : official journal of the European Society of Cardiology, Working Groups on Epidemiology & Prevention and Cardiac Rehabilitation and Exercise Physiology.

KIF6 719Arg Genetic Variant and Risk for Thoracic Aortic Dissection

J. Catanese, J. Elefteriades, C. Rowland, 2016, AORTA.

Gene Variants of VAMP8 and HNRPUL1 Are Associated With Early-Onset Myocardial Infarction

E. Topol, J. Catanese, S. Ellis, 2006, Arteriosclerosis, thrombosis, and vascular biology.

Neither Replication nor Simulation Supports a Role for the Axon Guidance Pathway in the Genetics of Parkinson's Disease

J. Catanese, S. Schrodi, Yonghong Li, 2008, PloS one.

Asp92Asn Polymorphism in the Myeloid IgA Fc Receptor Is Associated With Myocardial Infarction in Two Disparate Populations: CARE and WOSCOPS

M. Sabatine, J. Catanese, F. Sacks, 2006, Arteriosclerosis, thrombosis, and vascular biology.

Variants in the 5q31 cytokine gene cluster are associated with psoriasis

M. Leppert, J. Catanese, A. Begovich, 2008, Genes and Immunity.

A porcine BAC library with tenfold genome coverage: a resource for physical and genetic map integration

P. D. de Jong, K. Osoegawa, J. Catanese, 2001, Mammalian Genome.

Novel genetic markers for structural coronary artery disease, myocardial infarction, and familial combined hyperlipidemia: candidate and genome scans of functional SNPs

J. Catanese, Diane U. Leong, L. McAllister, 2004 .

Investigation of KIF6 Trp719Arg in a Case-Control Study of Myocardial Infarction: A Costa Rican Population

J. Catanese, F. Sacks, C. Rowland, 2010, PloS one.

Genetic Risk Factors for Thrombosis in Systemic Lupus Erythematosus

J. Catanese, M. Petri, J. Reveille, 2012, Journal of Rheumatology.

Genetic variants at CD28, PRDM1, and CD2/CD58 are associated with rheumatoid arthritis risk

M. Daly, Annette Lee, P. Gregersen, 2009, Nature Genetics.

DAPK1 variants are associated with Alzheimer's disease and allele-specific expression.

Taylor J. Maxwell, M. Owen, L. Thal, 2006, Human molecular genetics.

Gene variants associated with deep vein thrombosis.

P. Reitsma, J. Catanese, F. Rosendaal, 2008, JAMA.

The BDNF val66met polymorphism is not associated with late onset Alzheimer's disease in three case–control samples

M. Owen, L. Thal, A. Goate, 2005, Molecular Psychiatry.

Improving the Positive Predictive Value of Non-Invasive Prenatal Screening (NIPS)

J. Catanese, Weimin Sun, C. Strom, 2017, PloS one.

Polymorphisms Associated with Both Noncardioembolic Stroke and Coronary Heart Disease: Vienna Stroke Registry

J. Catanese, C. Rowland, C. Mannhalter, 2009, Cerebrovascular Diseases.