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"They're Not Going to Do Nothing for Me": Research Participants' Attitudes towards Elective Genetic Counseling

artículo científico publicado en 2020

A Clinical Decision Support Tool for Familial Hypercholesterolemia Based on Physician Input

scientific article published on 24 May 2018

A NOVEL GENOMIC SUSCEPTIBILITY LOCUS FOR PERIPHERAL ARTERIAL DISEASE ON CHROMOSOME 12

A Network-Biology Informed Computational Drug Repositioning Strategy to Target Disease Risk Trajectories and Comorbidities of Peripheral Artery Disease

artículo científico publicado en 2018

A Template for Authoring and Adapting Genomic Medicine Content in the eMERGE Infobutton Project

artículo científico publicado en 2014

A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids.

artículo científico publicado en 2019

A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium

scientific journal article

A collaborative approach to developing an electronic health record phenotyping algorithm for drug-induced liver injury

artículo científico publicado en 2013

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

artículo científico publicado en 2015

A conceptual model for translating omic data into clinical action

artículo científico publicado en 2015

A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects

artículo científico publicado en 2013

A genome-wide association study of red blood cell traits using the electronic medical record.

artículo científico publicado en 2010

A genome-wide linkage scan for ankle-brachial index in African American and non-Hispanic white subjects participating in the GENOA study

artículo científico publicado en 2005

A multi-locus genetic risk score for abdominal aortic aneurysm

artículo científico publicado en 2016

A novel quantitative trait locus on chromosome 1 with pleiotropic effects on HDL-cholesterol and LDL particle size in hypertensive sibships

artículo científico publicado en 2005

A patient-centered approach to the development and pilot of a warfarin pharmacogenomics patient education tool for health professionals

artículo científico publicado en 2015

A phenome-wide association study to discover pleiotropic effects of , , and

A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm

artículo científico publicado en 2013

A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers

artículo científico publicado en 2018

Adverse effects of long-term weight gain on microvascular endothelial function

scientific article published on 28 June 2018

An Implementation Science Framework to Develop a Clinical Decision Support Tool for Familial Hypercholesterolemia

artículo científico publicado en 2020

An analytical approach to characterize morbidity profile dissimilarity between distinct cohorts using electronic medical records.

artículo científico publicado en 2010

An electronic medical record-linked biorepository to identify novel biomarkers for atherosclerotic cardiovascular disease

artículo científico publicado en 2013

An information extraction framework for cohort identification using electronic health records

scientific article published on 18 March 2013

Analyzing the heterogeneity and complexity of Electronic Health Record oriented phenotyping algorithms.

artículo científico publicado en 2011

Antibody-based protein multiplex platforms: technical and operational challenges

artículo científico publicado en 2009

Aortic Pulse Wave Velocity Is Associated With Measures of Subclinical Target Organ Damage

artículo científico publicado el 1 de julio de 2011

Aortic augmentation index is associated with the ankle-brachial index: a community-based study

artículo científico publicado en 2007

Aortic augmentation index is inversely associated with cardiorespiratory fitness in men without known coronary heart disease

artículo científico publicado en 2006

Aortic pulse wave velocity is associated with the presence and quantity of coronary artery calcium: a community-based study

artículo científico publicado en 2005

Arterial dysfunction and functional performance in patients with peripheral artery disease: A review

artículo científico publicado el 29 de marzo de 2011

Arterial stiffness is associated with increase in blood pressure over time in treated hypertensives

artículo científico publicado en 2014

Arterial ultrasonography and tonometry as adjuncts to cardiovascular risk stratification

artículo científico publicado en 2007

Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies

artículo científico publicado en 2011

Association between metabolic syndrome and subclinical coronary atherosclerosis in asymptomatic adults

artículo científico publicado en 2004

Association of Ankle-Brachial Indices With Limb Revascularization or Amputation in Patients With Peripheral Artery Disease

scholarly article published 7 December 2018

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records

artículo científico publicado en 2016

Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian Randomization

artículo científico publicado en 2020

Association of a Family History of Coronary Heart Disease With Initiation of Statin Therapy in Individuals at Intermediate Risk

scientific article published on 01 June 2016

Association of novel risk factors with the ankle brachial index in African American and non-Hispanic white populations

artículo científico publicado en 2007

Association of plasma resistin with glomerular filtration rate and albuminuria in hypertensive adults

scientific article published on 04 September 2007

Association of polymorphisms in NOS3 with the ankle-brachial index in hypertensive adults

artículo científico publicado en 2007

Association of serum myeloperoxidase with the ankle-brachial index and peripheral arterial disease

artículo científico publicado en 2009

Association of serum osteoprotegerin with ankle-brachial index and urine albumin: creatinine ratio in African-Americans and non-Hispanic whites

artículo científico publicado en 2009

Association of serum osteoprotegerin with left ventricular mass in African American adults with hypertension

artículo científico publicado en 2010

Association of soluble cell adhesion molecules with ankle-brachial index in a biethnic cohort of predominantly hypertensive individuals

artículo científico publicado en 2008

Associations Between Inflammation and Physical Function in African Americans and European Americans with Prevalent Cardiovascular Risk Factors

artículo científico publicado en 2016

Associations Between Serum Inflammatory Markers and Hippocampal Volume in a Community Sample.

artículo científico publicado en 2016

Associations between inflammation and cognitive function in African Americans and European Americans

artículo científico publicado en 2014

Associations of Candidate Biomarkers of Vascular Disease with the Ankle-Brachial Index and Peripheral Arterial Disease

artículo científico publicado el 11 de enero de 2013

Associations of Genetically Predicted Lp(a) (Lipoprotein [a]) Levels With Cardiovascular Traits in Individuals of European and African Ancestry

artículo científico publicado en 2021

Associations of serum uric acid with markers of inflammation, metabolic syndrome, and subclinical coronary atherosclerosis

scientific article published on 01 January 2007

Atherogenic lipoprotein subprofiling.

artículo científico publicado en 2008

Biomarkers Associated With Pulse Pressure in African-Americans and Non-Hispanic Whites

artículo científico publicado el 20 de octubre de 2011

Biomarkers of Left Ventricular Hypertrophy and Remodeling in Blacks

artículo científico publicado el 10 de octubre de 2011

Brachial artery diameter and vasodilator response to nitroglycerine, but not flow-mediated dilatation, are associated with the presence and quantity of coronary artery calcium in asymptomatic adults

artículo científico publicado en 2007

Brachial-ankle pulse wave velocity is associated with walking distance in patients referred for peripheral arterial disease evaluation

artículo científico publicado en 2009

Burden of hospitalization in clinically diagnosed peripheral artery disease: A community-based study

artículo científico publicado en 2017

C-reactive Protein among Community-Dwelling Hypertensives on Single-agent Antihypertensive Treatment

artículo científico publicado en 2009

C-reactive protein is related to arterial wave reflection and stiffness in asymptomatic subjects from the community

artículo científico publicado en 2005

Challenges in returning results in a genomic medicine implementation study: the Return of Actionable Variants Empirical (RAVE) study

scientific article published on 04 May 2020

Challenges in translating plasma proteomics from bench to bedside: update from the NHLBI Clinical Proteomics Programs.

artículo científico publicado en 2008

Child-Parent Familial Hypercholesterolemia Screening in Primary Care

Clinical Correlates of Autosomal Chromosomal Abnormalities in an Electronic Medical Record-Linked Genome-Wide Association Study: A Case Series

artículo científico publicado en 2013

Clinical Correlates of Autosomal Chromosomal Abnormalities in an Electronic Medical Record-Linked Genome-Wide Association Study: A Case Series.

artículo científico publicado en 2013

Clinical Decision Support to Implement CYP2D6 Drug-Gene Interaction

artículo científico publicado en 2015

Comorbidity Characterization Among eMERGE Institutions: A Pilot Evaluation with the Johns Hopkins Adjusted Clinical Groups® System.

artículo científico publicado en 2019

Comparative and evolutionary pharmacogenetics of ABCB1: complex signatures of positive selection on coding and regulatory regions.

artículo científico publicado en 2007

Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate

artículo científico publicado en 2011

Complexity in the genetic architecture of leukoaraiosis in hypertensive sibships from the GENOA Study

artículo científico publicado en 2009

Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study

artículo científico publicado en 2017

Coronary Heart Disease Risk Associated with Primary Isolated Hypertriglyceridemia; a Population-Based Study

artículo científico publicado en 2021

Coronary artery calcification progression is heritable

artículo científico publicado en 2007

DIFFERENCES IN PREVALENCE OF PHENOTYPICALLY AND GENOTYPICALLY ASCERTAINED FAMILIAL HYPERCHOLESTEROLEMIA IN A COHORT WITH HYPERCHOLESTEROLEMIA

artículo científico publicado en 2018

Defining a Contemporary Ischemic Heart Disease Genetic Risk Profile Using Historical Data

artículo científico publicado en 2016

Design of a Controlled Trial of Cascade Screening for Hypercholesterolemia: The (CASH) Study

Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE network

Developing a Process for Returning Medically Actionable Genomic Variants to Latino Patients in a Federally Qualified Health Center

artículo científico publicado en 2018

Discovering Novel Biochemical and Genetic Markers for Coronary Heart Disease in Qatari Individuals: The Initiative Qatar Cardiovascular Biorepository

scientific article published on 23 January 2020

Discovering peripheral arterial disease cases from radiology notes using natural language processing

artículo científico publicado el 13 de noviembre de 2010

Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals

artículo científico publicado en 2017

Disease location is associated with survival in patients with peripheral arterial disease

artículo científico publicado en 2013

Do research participants share genomic screening results with family members?

artículo científico publicado en 2021

Early-onset peripheral arterial occlusive disease: clinical features and determinants of disease severity and location

artículo científico publicado el 1 de mayo de 2003

Electronic health record access by patients as an indicator of information seeking and sharing for cardiovascular health promotion in social networks: Secondary analysis of a randomized clinical trial

article

Electronic medical records for genetic research: results of the eMERGE consortium

artículo científico publicado en 2011

Elevated serum osteoprotegerin is associated with increased left ventricular mass index and myocardial stiffness

artículo científico publicado en 2017

Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example

artículo científico publicado en 2018

Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records

artículo científico publicado en 2013

Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience

artículo científico publicado en 2018

Ethical, legal, and social implications of incorporating genomic information into electronic health records

artículo científico publicado en 2013

Ethnic differences in low-density lipoprotein particle size in hypertensive adults

artículo científico publicado en 2007

Ethnic differences in peripheral arterial disease in the NHLBI Genetic Epidemiology Network of Arteriopathy (GENOA) study

artículo científico publicado en 2003

Evaluation of the MC4R gene across eMERGE network identifies many unreported obesity-associated variants

scientific article published on 20 September 2020

Evidence for positive selection in the C-terminal domain of the cholesterol metabolism gene PCSK9 based on phylogenetic analysis in 14 primate species

artículo científico publicado en 2007

Evolutionary genetics of coronary heart disease.

artículo científico publicado en 2009

Facilitating phenotype transfer using a common data model

scientific article published on 17 July 2019

Failure to follow up on a medically actionable finding from direct to consumer genetic testing: A case report

artículo científico publicado en 2020

Family history as a risk factor for carotid artery stenosis

artículo científico publicado en 2014

Family history as a risk factor for peripheral arterial disease

artículo científico publicado en 2014

Family history of atherosclerotic vascular disease is associated with the presence of abdominal aortic aneurysm

artículo científico publicado en 2015

Forearm vascular reactivity and arterial stiffness in asymptomatic adults from the community

artículo científico publicado en 2008

Frailty Across the Spectrum of Ankle-Brachial Index

artículo científico publicado el 6 de julio de 2011

GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network

scientific article published on 17 July 2019

Gene expression profiling of peripheral blood mononuclear cells in the setting of peripheral arterial disease.

artículo científico publicado en 2012

Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program

scientific article published on 28 September 2020

Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits

artículo científico publicado en 2012

Genetic basis of hypercholesterolemia in adults

artículo científico publicado en 2021

Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases

artículo científico publicado en 2021

Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data

artículo científico publicado en 2009

Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network

artículo científico publicado en 2014

Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network

artículo científico publicado en 2011

Genetic variants that confer resistance to malaria are associated with red blood cell traits in African-Americans: an electronic medical record-based genome-wide association study

artículo científico publicado en 2013

Genetic variation associated with circulating monocyte count in the eMERGE Network

artículo científico publicado en 2013

Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk

artículo científico publicado en 2013

Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy

artículo científico publicado en 2015

Genome-wide association studies for atherosclerotic vascular disease and its risk factors

artículo científico publicado en 2009

Genome-wide study of resistant hypertension identified from electronic health records

artículo científico publicado en 2017

Genotype-informed estimation of risk of coronary heart disease based on genome-wide association data linked to the electronic medical record

artículo científico publicado en 2011

Geographic differences in allele frequencies of susceptibility SNPs for cardiovascular disease

artículo científico publicado en 2011

High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE

artículo científico publicado en 2012

Higher plasma leptin levels are associated with reduced left ventricular mass and left ventricular diastolic stiffness in black women: insights from the Genetic Epidemiology Network of Arteriopathy (GENOA) study

scientific article published on 15 June 2018

Hypertension in pregnancy is a risk factor for peripheral arterial disease decades after pregnancy.

artículo científico publicado en 2013

Hypertension in pregnancy is associated with elevated C-reactive protein levels later in life

artículo científico publicado en 2013

Hypertension in pregnancy is associated with elevated homocysteine levels later in life

artículo científico publicado en 2013

Identification of Four Novel Loci in Asthma in European American and African American Populations

artículo científico publicado en 2016

Identification of unique venous thromboembolism-susceptibility variants in African-Americans

artículo científico publicado en 2017

Identifying Abdominal Aortic Aneurysm Cases and Controls using Natural Language Processing of Radiology Reports

artículo científico publicado en 2013

Identifying Peripheral Arterial Disease Cases Using Natural Language Processing of Clinical Notes

scientific article published on 01 February 2016

Identifying gene-gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts

artículo científico publicado en 2016

Implementation Science to Increase Adoption of Genomic Medicine: An Urgent Need

artículo científico publicado en 2020

Implementation of preemptive DNA sequence–based pharmacogenomics testing across a large academic medical center: The Mayo-Baylor RIGHT 10K Study

artículo científico publicado en 2022

Inactivating mutations in NPC1L1 and protection from coronary heart disease

artículo científico publicado en 2014

Increased Serum N-Terminal Pro–B-Type Natriuretic Peptide Levels in Patients With Medial Arterial Calcification and Poorly Compressible Leg Arteries

artículo científico publicado el 14 de octubre de 2010

Integrating pharmacogenomics into the electronic health record by implementing genomic indicators

artículo científico publicado en 2020

Interleukin-6 Receptor Signaling and Abdominal Aortic Aneurysm Growth Rates

artículo científico publicado en 2019

Investigating the Genetic Architecture of the PR Interval Using Clinical Phenotypes

artículo científico publicado en 2017

Investigating the complex genetic architecture of ankle-brachial index, a measure of peripheral arterial disease, in non-Hispanic whites

artículo científico publicado en 2008

LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins

Lack of association between lipoprotein(a) and coronary artery calcification in the Genetic Epidemiology Network of Arteriopathy (GENOA) study

artículo científico publicado en 2004

Lessening the Burden of Familial Hypercholesterolemia Using Health Information Technology

artículo científico publicado en 2018

Leveraging informatics for genetic studies: use of the electronic medical record to enable a genome-wide association study of peripheral arterial disease

artículo científico publicado el 1 de septiembre de 2010

Leveraging the Electronic Health Record to Create an Automated Real-Time Prognostic Tool for Peripheral Arterial Disease

scientific article published on 01 December 2018

Leveraging the electronic health record to implement genomic medicine

artículo científico publicado en 2013

Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network

scientific article published on 22 September 2020

Low-density lipoprotein particle size and coronary atherosclerosis in subjects belonging to hypertensive sibships

artículo científico publicado en 2004

Making pretest genomic counseling optional: lessons from the RAVE study

artículo científico publicado en 2018

Making work visible for electronic phenotype implementation: Lessons learned from the eMERGE network

artículo científico publicado en 2019

Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels

artículo científico publicado en 2011

Measurement and quality control issues in multiplex protein assays: a case study

artículo científico publicado en 2009

Measures of arterial stiffness and wave reflection are associated with walking distance in patients with peripheral arterial disease.

artículo científico publicado en 2006

Mechanisms of disease: The genetic basis of coronary heart disease.

artículo científico publicado en 2007

Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS data

artículo científico publicado en 2013

Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci

artículo científico publicado en 2016

Methods for the selection of tagging SNPs: a comparison of tagging efficiency and performance

artículo científico publicado en 2006

Mid-regional pro-adrenomedullin is associated with pulse pressure, left ventricular mass, and albuminuria in African Americans with hypertension

artículo científico publicado en 2009

Mining peripheral arterial disease cases from narrative clinical notes using natural language processing

artículo científico publicado en 2017

Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study

artículo científico publicado en 2020

Molecular evolution of 5' flanking regions of 87 candidate genes for atherosclerotic cardiovascular disease.

artículo científico publicado en 2006

Molecular population genetics of PCSK9: a signature of recent positive selection.

artículo científico publicado en 2008

Motivation, Perception, and Treatment Beliefs in the Myocardial Infarction Genes (MI-GENES) Randomized Clinical Trial

artículo científico publicado en 2017

Multidisciplinary model to implement pharmacogenomics at the point of care.

artículo científico publicado en 2016

My Approach to the Patient With Familial Hypercholesterolemia

artículo científico publicado en 2016

Neutral, Negative, or Negligible? Changes in Patient Perceptions of Disease Risk Following Receipt of a Negative Genomic Screening Result

artículo científico publicado en 2020

Novel genomic loci influencing plasma homocysteine levels

artículo científico publicado en 2006

Novel markers of peripheral arterial disease

artículo científico publicado en 2009

Osteocalcin and type 2 diabetes risk in Latinos: a life course approach.

artículo científico publicado en 2015

PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance.

artículo científico publicado en 2016

Participant choices for return of genomic results in the eMERGE Network

artículo científico publicado en 2020

Patient and Provider Perspectives on a Decision Aid for Familial Hypercholesterolemia

artículo científico publicado en 2018

Patient reactions to receiving negative genomic screening results by mail

artículo científico publicado en 2020

Patterns of population differentiation of candidate genes for cardiovascular disease

artículo científico publicado en 2007

Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network

artículo científico publicado en 2015

Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index

artículo científico publicado en 2014

Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality

artículo científico publicado en 2011

Plasma C-terminal pro-endothelin-1 is associated with target-organ damage in African Americans with hypertension

artículo científico publicado en 2010

Plasma carboxy-terminal provasopressin (copeptin): a novel marker of insulin resistance and metabolic syndrome

scientific article published on 14 April 2009

Plasma midregional pro-atrial natriuretic peptide is associated with blood pressure indices and hypertension severity in adults with hypertension

scientific article published on 12 February 2009

Pleiotropic genetic effects contribute to the correlation between HDL cholesterol, triglycerides, and LDL particle size in hypertensive sibships

artículo científico publicado en 2005

Polygenic Risk Scores for Diverse Ancestries: Making Genomic Medicine Equitable

artículo científico publicado en 2020

Practical considerations in genomic decision support: The eMERGE experience

artículo científico publicado en 2015

Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups

scientific article published on 01 May 2020

Preemptive genotyping for personalized medicine: design of the right drug, right dose, right time-using genomic data to individualize treatment protocol

artículo científico publicado en 2014

Probing the Virtual Proteome to Identify Novel Disease Biomarkers

artículo científico publicado en 2018

Progression of subclinical coronary atherosclerosis: does obesity make a difference?

artículo científico publicado en 2005

Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network

artículo científico publicado en 2015

Quality control procedures for genome-wide association studies

artículo científico publicado en 2011

Quantitative trait loci influencing low density lipoprotein particle size in African Americans

artículo científico publicado en 2006

Rapid identification of familial hypercholesterolemia from electronic health records: The SEARCH study

artículo científico publicado en 2016

Relation of C-reactive protein and fibrinogen to coronary artery calcium in subjects with systemic hypertension

scientific article published on 01 July 2003

Relation of plasma midregional proatrial natriuretic peptide to target organ damage in adults with systemic hypertension

artículo científico publicado en 2009

Reply: To PMID 23122799.

artículo científico publicado en 2013

Return of genomic results to research participants: the floor, the ceiling, and the choices in between

artículo científico publicado en 2014

Return of results in the genomic medicine projects of the eMERGE network

artículo científico publicado en 2014

Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network

artículo científico publicado en 2020

Returning genomic results in a Federally Qualified Health Center: the intersection of precision medicine and social determinants of health

scientific article published on 06 May 2020

Risk Factors for Polyvascular Involvement in Patients With Peripheral Artery Disease: A Mendelian Randomization Study

artículo científico publicado en 2020

Risk factor profile for chronic kidney disease is similar to risk factor profile for small artery disease

artículo científico publicado en 2011

Serum N-Terminal Pro-B-Type Natriuretic Peptide Levels Are Associated With Functional Capacity in Patients With Peripheral Arterial Disease

artículo científico publicado el 17 de noviembre de 2011

Serum osteocalcin is associated with measures of insulin resistance, adipokine levels, and the presence of metabolic syndrome

artículo científico publicado en 2010

Sex and ethnic differences in 47 candidate proteomic markers of cardiovascular disease: the Mayo Clinic proteomic markers of arteriosclerosis study

artículo científico publicado en 2010

Sex-specific associations of lipoprotein(a) with presence and quantity of coronary artery calcification in an asymptomatic population

artículo científico publicado en 2004

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

artículo científico publicado en 2016

Should pretest genetic counselling be required for patients pursuing genomic sequencing? Results from a survey of participants in a large genomic implementation study

artículo científico publicado en 2018

Surveillance of Peripheral Arterial Disease Cases Using Natural Language Processing of Clinical Notes

artículo científico publicado en 2017

Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data

artículo científico publicado en 2013

Targeted Sequencing Study to Uncover Shared Genetic Susceptibility Between Peripheral Artery Disease and Coronary Heart Disease-Brief Report

scientific article published on 01 June 2019

Temporal trends in lipid testing among children and adolescents: A population based study

artículo científico publicado en 2017

The ATXN2-SH2B3 locus is associated with peripheral arterial disease: an electronic medical record-based genome-wide association study

artículo científico publicado en 2014

The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future

artículo científico publicado el 6 de junio de 2013

The Return of Actionable Variants Empirical (RAVE) Study, a Mayo Clinic Genomic Medicine Implementation Study: Design and Initial Results

artículo científico publicado en 2018

The association between cigarette smoking and inflammation: The Genetic Epidemiology Network of Arteriopathy (GENOA) study

artículo científico publicado en 2017

The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies

artículo científico publicado en 2011

The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype

scientific article published on 08 October 2018

The phenotypic legacy of admixture between modern humans and Neandertals

artículo científico publicado en 2016

The polygenic architecture of left ventricular mass mirrors the clinical epidemiology

scientific article published on 05 May 2020

Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network

artículo científico publicado en 2020

Usefulness of Red Cell Distribution Width to Predict Mortality in Patients With Peripheral Artery Disease

artículo científico publicado el 4 de febrero de 2011

Using the electronic health record for genomics research

scientific article published on 01 April 2020

Validation of electronic medical record-based phenotyping algorithms: results and lessons learned from the eMERGE network

artículo científico publicado en 2013

Variability in assigning pathogenicity to incidental findings: insights from LDLR sequence linked to the electronic health record in 1013 individuals

artículo científico publicado en 2017

Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies

artículo científico publicado en 2011

Web-Based Tool (FH Family Share) to Increase Uptake of Cascade Testing for Familial Hypercholesterolemia: Development and Evaluation

artículo científico publicado en 2022

White blood cell count predicts all-cause mortality in patients with suspected peripheral arterial disease

artículo científico publicado en 2009

Whole exome sequencing implicates an INO80D mutation in a syndrome of aortic hypoplasia, premature atherosclerosis, and arterial stiffness

artículo científico publicado en 2014

eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants

artículo científico publicado en 2016

eMERGEing progress in genomics-the first seven years

artículo científico publicado en 2014

ePhenotyping for Abdominal Aortic Aneurysm in the Electronic Medical Records and Genomics (eMERGE) Network: Algorithm Development and Konstanz Information Miner Workflow

artículo científico publicado en 2015