Published in Am J Med Genet A on November 22, 2013
Interactive multimedia consent for biobanking: a randomized trial. Genet Med (2015) 0.95
The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies. BMC Med Genomics (2011) 9.20
Community consultation and communication for a population-based DNA biobank: the Marshfield clinic personalized medicine research project. Am J Med Genet A (2008) 2.74
Informed consent and subject motivation to participate in a large, population-based genomics study: the Marshfield Clinic Personalized Medicine Research Project. Community Genet (2007) 2.48
'Even if they ask you to stand by a tree all day, you will have to do it (laughter)...!': community voices on the notion and practice of informed consent for biomedical research in developing countries. Soc Sci Med (2005) 2.21
Improvement of informed consent and the quality of consent documents. Lancet Oncol (2008) 2.21
The effect of format modifications and reading comprehension on recall of informed consent information by low-income parents: a comparison of print, video, and computer-based presentations. Patient Educ Couns (2004) 1.55
Experiences with community engagement and informed consent in a genetic cohort study of severe childhood diseases in Kenya. BMC Med Ethics (2010) 1.54
Developing a simplified consent form for biobanking. PLoS One (2010) 1.45
The use of multimedia in the informed consent process. J Am Med Inform Assoc (1998) 1.43
Using computer agents to explain medical documents to patients with low health literacy. Patient Educ Couns (2009) 1.30
Informed versus uninformed consent for prostate surgery: the value of electronic consents. J Urol (2006) 1.05
Understanding of genetics among older adults. J Nurs Scholarsh (2006) 0.86
The role of nonverbal and verbal communication in a multimedia informed consent process. Appl Clin Inform (2011) 0.81
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Nat Genet (2007) 22.96
The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies. BMC Med Genomics (2011) 9.20
A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). Nat Genet (2009) 8.39
Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. Nat Genet (2009) 7.30
Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data. Nat Biotechnol (2013) 4.85
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies. Am J Hum Genet (2011) 3.85
New models for large prospective studies: is there a better way? Am J Epidemiol (2012) 3.85
Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network. Genet Med (2012) 3.29
Validation of electronic medical record-based phenotyping algorithms: results and lessons learned from the eMERGE network. J Am Med Inform Assoc (2013) 3.00
Clinical genetics provider real-time workflow study. Genet Med (2008) 2.49
Use of an electronic medical record for the identification of research subjects with diabetes mellitus. Clin Med Res (2007) 2.48
Quality control procedures for genome-wide association studies. Curr Protoc Hum Genet (2011) 2.48
Genome-wide association of lipid-lowering response to statins in combined study populations. PLoS One (2010) 2.43
An evaluation of the NQF Quality Data Model for representing Electronic Health Record driven phenotyping algorithms. AMIA Annu Symp Proc (2012) 2.29
Interactions between genetic variants and breast cancer risk factors in the breast and prostate cancer cohort consortium. J Natl Cancer Inst (2011) 2.09
Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk. Circulation (2013) 2.06
Five-year incidence of open-angle glaucoma: the visual impairment project. Ophthalmology (2002) 2.05
Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network. Hum Genet (2011) 2.00
Serum levels of vitamin D metabolites and breast cancer risk in the prostate, lung, colorectal, and ovarian cancer screening trial. Cancer Epidemiol Biomarkers Prev (2008) 1.80
Risk factors associated with the incidence of open-angle glaucoma: the visual impairment project. Invest Ophthalmol Vis Sci (2003) 1.79
Importance of multi-modal approaches to effectively identify cataract cases from electronic health records. J Am Med Inform Assoc (2012) 1.79
Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate. Am J Hum Genet (2011) 1.66
Genetic variants associated with angiotensin-converting enzyme inhibitor-associated angioedema. Pharmacogenet Genomics (2013) 1.65
Construction of atorvastatin dose-response relationships using data from a large population-based DNA biobank. Basic Clin Pharmacol Toxicol (2007) 1.64
Eye health in rural Australia. Clin Experiment Ophthalmol (2002) 1.51
Vitamin E supplementation and cataract: randomized controlled trial. Ophthalmology (2004) 1.48
Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium. Genet Med (2010) 1.47
A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects. Hum Genet (2013) 1.47
Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks. PLoS One (2011) 1.42
Vitamin E supplementation and macular degeneration: randomised controlled trial. BMJ (2002) 1.41
Dietary intake in the Personalized Medicine Research Project: a resource for studies of gene-diet interaction. Nutr J (2011) 1.27
Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality. Genet Epidemiol (2011) 1.26
Vitamin D receptor polymorphisms and breast cancer risk: results from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium. Cancer Epidemiol Biomarkers Prev (2009) 1.23
Prevalence and associations of epiretinal membranes in the visual impairment project. Am J Ophthalmol (2005) 1.23
Apolipoprotein (APOE) gene is associated with progression of age-related macular degeneration (AMD). Hum Mutat (2006) 1.22
Estrogen receptor genotype is associated with risk of venous thromboembolism during tamoxifen therapy. Breast Cancer Res Treat (2008) 1.21
Gene-environment interaction in progression of AMD: the CFH gene, smoking and exposure to chronic infection. Hum Mol Genet (2008) 1.17
Population-based assessment of refractive error in India: the Andhra Pradesh eye disease study. Clin Experiment Ophthalmol (2002) 1.17
Cataract research using electronic health records. BMC Ophthalmol (2011) 1.17
Alcohol, tobacco, and drug use disorders and personality disorder symptoms. Exp Clin Psychopharmacol (2004) 1.16
Validity of eight integrated healthcare delivery organizations' administrative clinical data to capture breast cancer chemotherapy exposure. Cancer Epidemiol Biomarkers Prev (2012) 1.15
Practical challenges in integrating genomic data into the electronic health record. Genet Med (2013) 1.14
Quantification of the clinical modifiers impacting high-density lipoprotein cholesterol in the community: Personalized Medicine Research Project. Prev Cardiol (2010) 1.14
Genome-wide association study identifies common variants associated with circulating vitamin E levels. Hum Mol Genet (2011) 1.14
Development of cataract and associated risk factors: the Visual Impairment Project. Arch Ophthalmol (2006) 1.13
Prediction of breast cancer risk by genetic risk factors, overall and by hormone receptor status. J Med Genet (2012) 1.13
High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE. Clin Transl Sci (2012) 1.13
Five-year incidence of diabetic retinopathy in the Melbourne Visual Impairment Project. Clin Experiment Ophthalmol (2003) 1.12
Use of an electronic medical record to characterize cases of intermediate statin-induced muscle toxicity. Prev Cardiol (2009) 1.11
Implementation of workflow engine technology to deliver basic clinical decision support functionality. BMC Med Res Methodol (2011) 1.10
Characterization of low-density lipoprotein cholesterol-lowering efficacy for atorvastatin in a population-based DNA biorepository. Basic Clin Pharmacol Toxicol (2008) 1.09
Association of VEGF gene polymorphisms with diabetic retinopathy in a south Indian cohort. Ophthalmic Genet (2008) 1.06
Genetic variation associated with circulating monocyte count in the eMERGE Network. Hum Mol Genet (2013) 1.05
Five-year incidence of age-related maculopathy: the Visual Impairment Project. Ophthalmology (2004) 1.05
Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits. Mayo Clin Proc (2012) 1.05
Development of an optical character recognition pipeline for handwritten form fields from an electronic health record. J Am Med Inform Assoc (2011) 1.04
Population based allele frequencies of disease associated polymorphisms in the Personalized Medicine Research Project. BMC Genet (2010) 1.04
The impact of rubella immunization on the serological status of women of childbearing age: a retrospective longitudinal study in Melbourne, Australia. Am J Public Health (2003) 1.03
Five-year incidence of bilateral cause-specific visual impairment in the Melbourne Visual Impairment Project. Invest Ophthalmol Vis Sci (2003) 1.03
Next-generation analysis of cataracts: determining knowledge driven gene-gene interactions using Biofilter, and gene-environment interactions using the PhenX Toolkit. Pac Symp Biocomput (2013) 1.02
Using Medical Text Extraction, Reasoning and Mapping System (MTERMS) to process medication information in outpatient clinical notes. AMIA Annu Symp Proc (2011) 1.01
Stakeholder engagement: a key component of integrating genomic information into electronic health records. Genet Med (2013) 1.00
KRAS testing and epidermal growth factor receptor inhibitor treatment for colorectal cancer in community settings. Cancer Epidemiol Biomarkers Prev (2012) 1.00
Iris colour, ethnic origin and progression of age-related macular degeneration. Clin Experiment Ophthalmol (2003) 0.99
Attachment, parental bonding and borderline personality disorder features in young adults. J Pers Disord (2002) 0.99
Mapping Partners Master Drug Dictionary to RxNorm using an NLP-based approach. J Biomed Inform (2011) 0.99
Utilization of eye care services by Victorians likely to benefit from eye care. Clin Experiment Ophthalmol (2004) 0.99
Environment-wide association study (EWAS) for type 2 diabetes in the Marshfield Personalized Medicine Research Project Biobank. Pac Symp Biocomput (2014) 0.98
Lutein and zeaxanthin and the risk of cataract: the Melbourne visual impairment project. Invest Ophthalmol Vis Sci (2006) 0.98
Evaluating standard terminologies for encoding allergy information. J Am Med Inform Assoc (2013) 0.98
Investigating Perceived Institutional Review Board Quality and Function Using the IRB Researcher Assessment Tool. J Empir Res Hum Res Ethics (2008) 0.95
Underutilization of Lynch syndrome screening in a multisite study of patients with colorectal cancer. Genet Med (2013) 0.95
Intron 4 VNTR of endothelial nitric oxide synthase (eNOS) gene and diabetic retinopathy in type 2 patients in southern India. Ophthalmic Genet (2007) 0.94
Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records. PLoS One (2013) 0.94
Hypothesis-independent pathway analysis implicates GABA and acetyl-CoA metabolism in primary open-angle glaucoma and normal-pressure glaucoma. Hum Genet (2014) 0.93
Pharmacogenomics: will the promise be fulfilled? Nat Rev Genet (2010) 0.92
Estrogen pathway polymorphisms in relation to primary open angle glaucoma: an analysis accounting for gender from the United States. Mol Vis (2013) 0.90
Validation of PhenX measures in the personalized medicine research project for use in gene/environment studies. BMC Med Genomics (2014) 0.90
Development of a fingerprinting panel using medically relevant polymorphisms. BMC Med Genomics (2009) 0.89
Psychosocial work characteristics predict cardiovascular disease risk factors and health functioning in rural women: the Wisconsin Rural Women's Health Study. J Rural Health (2005) 0.88
A pilot study of gene/gene and gene/environment interactions in Alzheimer disease. Clin Med Res (2010) 0.87
Circulating insulin-like growth factor (IGF)-I and IGF binding protein (IGFBP)-3 levels and postmenopausal breast cancer risk in the prostate, lung, colorectal, and ovarian cancer screening trial (PLCO) cohort. Horm Cancer (2010) 0.87
The need for routine eye examinations. Invest Ophthalmol Vis Sci (2004) 0.87
Progression of visual field loss in open angle glaucoma in the Melbourne Visual Impairment Project. Clin Experiment Ophthalmol (2006) 0.86
Diabetic retinopathy and IGF-1 gene polymorphic cytosine-adenine repeats in a Southern Indian cohort. Ophthalmic Res (2007) 0.85
Energy intake and risk of postmenopausal breast cancer: an expanded analysis in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial (PLCO) cohort. Cancer Epidemiol Biomarkers Prev (2009) 0.85
Genetic variation in CYP27B1 is associated with congestive heart failure in patients with hypertension. Pharmacogenomics (2009) 0.84
Vacations improve mental health among rural women: the Wisconsin Rural Women's Health Study. WMJ (2005) 0.83
Diabetic retinopathy: Validation study of ALR2, RAGE, iNOS and TNFB gene variants in a south Indian cohort. Ophthalmic Genet (2010) 0.83
CDKN2B-AS1 genotype-glaucoma feature correlations in primary open-angle glaucoma patients from the United States. Am J Ophthalmol (2012) 0.83
Health services utilization and cost of retinitis pigmentosa. Arch Ophthalmol (2012) 0.82
Utilization of HER2 genetic testing in a multi-institutional observational study. Am J Manag Care (2012) 0.82