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Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2

Nature genetics, 1996-10, Vol.14 (2), p.185-187

1996

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Examinations of Methylenetetrahydrofolate Reductase C677T and A1298C Mutations—and In Utero Viability

American journal of human genetics, 2001-11, Vol.69 (5), p.1150-1152

2001

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Germ-Line Mutational Analysis of the TSC2 Gene in 90 Tuberous-Sclerosis Patients

American journal of human genetics, 1998-02, Vol.62 (2), p.286-294

1998

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Genetic Variants Identified in a European Genome-Wide Association Study That Were Found to Predict Incident Coronary Heart Disease in the Atherosclerosis Risk in Communities Study

American journal of epidemiology, 2010-01, Vol.171 (1), p.14-23

2010

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C78 FIBROSIS: MEDIATORS AND MODULATORS: Deregulation Of Cleavage Factor Im 25 (cfim25) Contributes To Pulmonary Fibrosis Through Alternative

American journal of respiratory and critical care medicine, 2017-01, Vol.195

2017

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A72 MECHANISMS DRIVING FIBROSIS: Contribution Of Transforming Growth Factor Beta1 (tgf1) Signaling To Pulmonary Fibrosis Through Alternative Polyadenlyation (apa) Of Mrna

American journal of respiratory and critical care medicine, 2017-01, Vol.195

2017

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D36 SEPSIS, ACUTE RESPIRATORY DISTRESS SYNDROME, AND ACUTE LUNG INJURY: Adenosine Signaling Through The A2b Receptor Is Protective In Bleomycin-Induced Acute Lung Injury

American journal of respiratory and critical care medicine, 2014-01, Vol.189, p.1

2014

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B108 BEYOND WHO GROUP I PULMONARY HYPERTENSION: Increased Hyaluronan And Altered Lymphangiogenesis In Group Iii Pulmonary Hypertension

American journal of respiratory and critical care medicine, 2015-01, Vol.191, p.1

2015

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A57 LUNG INJURY, REPAIR, AND FIBROSIS: THE PLOT THICKENS FOR THREE'S COMPANY: Adenosine Regulates The Resolution And Exacerbation Of Pulmonary Fibrosis

American journal of respiratory and critical care medicine, 2015-01, Vol.191, p.1

2015

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Promotor genotype of the platelet-derived growth factor receptor-α gene shows population stratification but not association with spina bifida meningomyelocele

American journal of medical genetics. Part A, 2005-12, Vol.139A (3), p.194-198

2005

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B97 A SCAR IS BORN: NEW INSIGHTS IN LUNG FIBROGENESIS: Adora2b Expression In Myeloid Cells Modulates The Severity Of Pulmonary Fibrosis

American journal of respiratory and critical care medicine, 2014-01, Vol.189, p.1

2014

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A57 WHO GROUP III/IV PULMONARY HYPERTENSION: Pulmonary Hypertension Secondary To Idiopathic Pulmonary Fibrosis: A Case For Adenosine?

American journal of respiratory and critical care medicine, 2014-01, Vol.189, p.1

2014

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Association of the Complement Factor H Y402H Polymorphism With Cardiovascular Disease Is Dependent Upon Hypertension Status: The ARIC Study

American journal of hypertension, 2008-05, Vol.21 (5), p.533-538

2008

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Interaction effects of high-density lipoprotein metabolism gene variation and alcohol consumption on coronary heart disease risk: the atherosclerosis risk in communities study

Journal of studies on alcohol and drugs, 2007-07, Vol.68 (4), p.485-492

2007

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Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease

Human genetics, 2008-05, Vol.123 (4), p.399-408

2008

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Methylenetetrahydrofolate reductase and spina bifida: Evaluation of level of defect and maternal genotypic risk in Hispanics

American journal of medical genetics, 2000-11, Vol.95 (1), p.21-27

2000

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Testing for genetic associations in a spina bifida population: Analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defects

American journal of medical genetics, 2002-07, Vol.110 (3), p.203-207

2002

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Promoter haplotype combinations for the human PDGFRA gene are associated with risk of neural tube defects

Molecular genetics and metabolism, 2004-02, Vol.81 (2), p.127-132

2004

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Testing for genetic associations with the PAX gene family in a spina bifida population

American journal of medical genetics, 2002-07, Vol.110 (3), p.195-202

2002

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Genetic variation in the proto-oncogene SKI and risk for orofacial clefting

Molecular genetics and metabolism, 2005-11, Vol.86 (3), p.412-416

2005

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Associations between polymorphisms within the thymidylate synthase gene and spina bifida

Birth defects research. A Clinical and molecular teratology, 2003-11, Vol.67 (11), p.924-928

2003

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Evaluation of infant methylenetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects

Birth defects research. A Clinical and molecular teratology, 2003-03, Vol.67 (3), p.154-157

2003

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Spina bifida and other neural tube defects

Current problems in pediatrics (English ed.), 2000-11, Vol.30 (10), p.313

2000

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Evaluation of the jumonji gene and risk for spina bifida and congenital heart defects

American journal of medical genetics, 2004-04, Vol.126A (2), p.215-217

2004

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Risk factors for neural tube defects: Associations between uncoupling protein 2 polymorphisms and spina bifida

Birth defects research. A Clinical and molecular teratology, 2003-03, Vol.67 (3), p.158-161

2003

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Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2

Examinations of Methylenetetrahydrofolate Reductase C677T and A1298C Mutations—and In Utero Viability

Germ-Line Mutational Analysis of the TSC2 Gene in 90 Tuberous-Sclerosis Patients

Genetic Variants Identified in a European Genome-Wide Association Study That Were Found to Predict Incident Coronary Heart Disease in the Atherosclerosis Risk in Communities Study

C78 FIBROSIS: MEDIATORS AND MODULATORS: Deregulation Of Cleavage Factor Im 25 (cfim25) Contributes To Pulmonary Fibrosis Through Alternative

A72 MECHANISMS DRIVING FIBROSIS: Contribution Of Transforming Growth Factor Beta1 (tgf1) Signaling To Pulmonary Fibrosis Through Alternative Polyadenlyation (apa) Of Mrna

D36 SEPSIS, ACUTE RESPIRATORY DISTRESS SYNDROME, AND ACUTE LUNG INJURY: Adenosine Signaling Through The A2b Receptor Is Protective In Bleomycin-Induced Acute Lung Injury

B108 BEYOND WHO GROUP I PULMONARY HYPERTENSION: Increased Hyaluronan And Altered Lymphangiogenesis In Group Iii Pulmonary Hypertension

A57 LUNG INJURY, REPAIR, AND FIBROSIS: THE PLOT THICKENS FOR THREE'S COMPANY: Adenosine Regulates The Resolution And Exacerbation Of Pulmonary Fibrosis

Promotor genotype of the platelet-derived growth factor receptor-α gene shows population stratification but not association with spina bifida meningomyelocele

B97 A SCAR IS BORN: NEW INSIGHTS IN LUNG FIBROGENESIS: Adora2b Expression In Myeloid Cells Modulates The Severity Of Pulmonary Fibrosis

A57 WHO GROUP III/IV PULMONARY HYPERTENSION: Pulmonary Hypertension Secondary To Idiopathic Pulmonary Fibrosis: A Case For Adenosine?

Association of the Complement Factor H Y402H Polymorphism With Cardiovascular Disease Is Dependent Upon Hypertension Status: The ARIC Study

Interaction effects of high-density lipoprotein metabolism gene variation and alcohol consumption on coronary heart disease risk: the atherosclerosis risk in communities study

Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease

Methylenetetrahydrofolate reductase and spina bifida: Evaluation of level of defect and maternal genotypic risk in Hispanics

Testing for genetic associations in a spina bifida population: Analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defects

Promoter haplotype combinations for the human PDGFRA gene are associated with risk of neural tube defects

Testing for genetic associations with the PAX gene family in a spina bifida population

Genetic variation in the proto-oncogene SKI and risk for orofacial clefting

Associations between polymorphisms within the thymidylate synthase gene and spina bifida

Evaluation of infant methylenetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects

Spina bifida and other neural tube defects

Evaluation of the jumonji gene and risk for spina bifida and congenital heart defects

Risk factors for neural tube defects: Associations between uncoupling protein 2 polymorphisms and spina bifida

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