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The Genomic Medicine at VA Study (GenoVA)
Clinical Trial ID NCT04331535
PubWeight™ 0.00
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🔗 Visit the ClinicalTrials.gov page for NCT04331535
Top papers
Rank
Title
Journal
Year
PubWeight™
‹?›
101
Impact of Genetic Testing and Family Health History Based Risk Counseling on Behavior Change and Cognitive Precursors for Type 2 Diabetes.
J Genet Couns
2016
0.75
102
Impact of a Genetic Risk Score for Coronary Artery Disease on Reducing Cardiovascular Risk: A Pilot Randomized Controlled Study.
Front Cardiovasc Med
2017
0.75
103
Binge drinking modifies the association between lifetime alcohol intake and breast cancer risk in moderate drinkers.
Am J Epidemiol
2017
0.75
104
Association analysis identifies 65 new breast cancer risk loci.
Nature
2017
0.75
105
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.
Nat Genet
2017
0.75
106
The infinitesimal model: Definition, derivation, and implications.
Theor Popul Biol
2017
0.75
107
Temporal Trends in the Incidence, Prevalence, and Survival of Patients With Atrial Fibrillation From 2004 to 2016.
Am J Cardiol
2017
0.75
108
Outcomes of colon resection in patients with metastatic colon cancer.
Am J Surg
2016
0.75
109
The use of breast-conserving surgery for women treated for breast cancer in the Department of Veterans Affairs.
Am J Surg
2013
0.75
110
Challenges and strategies for implementing genomic services in diverse settings: experiences from the Implementing GeNomics In pracTicE (IGNITE) network.
BMC Med Genomics
2017
0.75
111
National Trends in Atrial Fibrillation Hospitalization, Readmission, and Mortality for Medicare Beneficiaries, 1999-2013.
Circulation
2017
0.75
112
Effect of the Tool to Reduce Inappropriate Medications on Medication Communication and Deprescribing.
J Am Geriatr Soc
2017
0.75
113
Veterans Healthcare Administration providers' attitudes and perceptions regarding pragmatic trials embedded at the point of care.
Clin Trials
2014
0.75
114
Developing a common framework for evaluating the implementation of genomic medicine interventions in clinical care: the IGNITE Network's Common Measures Working Group.
Genet Med
2017
0.75
115
Surrogate-assisted feature extraction for high-throughput phenotyping.
J Am Med Inform Assoc
2017
0.75
116
The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.
Ann Intern Med
2017
0.75
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