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Author Details

Terrie Kitchner
Center for Precision Medicine Research, Marshfield Clinic Research Institute
2007
37
17
PMIDPaper TitleJournal TitlePublished Year
38020121Estimating the efficacy of pharmacogenomics over a lifetime.Front Med (Lausanne)2023
37758833Genetic risk score in multiple sclerosis is associated with unique gut microbiome.Sci Rep2023
31386280Development of an Integrated Platform Using Multidisciplinary Real-World Data to Facilitate Biomarker Discovery for Medical Products.Clin Transl Sci2020
30590688Enrichment sampling for a multi-site patient survey using electronic health records and census data.J Am Med Inform Assoc2019
30814063A gene-based recessive diplotype exome scan discovers <i>FGF6</i>, a novel hepcidin-regulating iron-metabolism gene.Blood2019
28968884Applying family analyses to electronic health records to facilitate genetic research.Bioinformatics2018
27908689PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study.Lancet Diabetes Endocrinol2017
28190457Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.Am J Hum Genet2017
29079728PLATO software provides analytic framework for investigating complexity beyond genome-wide association studies.Nat Commun2017
28639489Healthcare provider education to support integration of pharmacogenomics in practice: the eMERGE Network experience.Pharmacogenomics2017
26691988A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.Nat Genet2016
26514439Comparing Mammography Abnormality Features to Genetic Variants in the Prediction of Breast Cancer in Women Recommended for Breast Biopsy.Acad Radiol2016
26587656CYP2C19 and CES1 polymorphisms and efficacy of clopidogrel and aspirin dual antiplatelet therapy in patients with symptomatic intracranial atherosclerotic disease.J Neurosurg2016
27881091Conducting a large, multi-site survey about patients' views on broad consent: challenges and solutions.BMC Med Res Methodol2016
27777502Analysis of <i>CYP1B1</i> in pediatric and adult glaucoma and other ocular phenotypes.Mol Vis2016
26746457Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.JAMA2016
26857349Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network.Clin Pharmacol Ther2016
25266681A polymorphism in HLA-G modifies statin benefit in asthma.Pharmacogenomics J2015
26413716A GWAS Study on Liver Function Test Using eMERGE Network Participants.PLoS One2015
26247077Long-Term Recall of Elements of Informed Consent: A Pilot Study Comparing Traditional and Computer-Based Consenting.IRB2015
26342218Desiderata for computable representations of electronic health records-driven phenotype algorithms.J Am Med Inform Assoc2015
26365338Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network.Am J Hum Genet2015
26734457CMTR1 is associated with increased asthma exacerbations in patients taking inhaled corticosteroids.Immun Inflamm Dis2015
25982363Biology-Driven Gene-Gene Interaction Analysis of Age-Related Cataract in the eMERGE Network.Genet Epidemiol2015
26030142Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy.PLoS One2015
25741542Next-generation analysis of cataracts: determining knowledge driven gene-gene interactions using biofilter, and gene-environment interactions using the Phenx Toolkit*.Pac Symp Biocomput2015
24423110Validation of PhenX measures in the personalized medicine research project for use in gene/environment studies.BMC Med Genomics2014
25250975Use of an electronic medical record to create the marshfield clinic twin/multiple birth cohort.Genet Epidemiol2014
25014365Cone structure in subjects with known genetic relative risk for AMD.Optom Vis Sci2014
23424120Next-generation analysis of cataracts: determining knowledge driven gene-gene interactions using Biofilter, and gene-environment interactions using the PhenX Toolkit.Pac Symp Biocomput2013
22024213A novel gene-environment interaction involved in endometriosis.Int J Gynaecol Obstet2012
21276236Dietary intake in the Personalized Medicine Research Project: a resource for studies of gene-diet interaction.Nutr J2011
21402364Apolipoprotein e4 genotype increases the risk of being diagnosed with posttraumatic fibromyalgia.PM R2011
19506792The role of cigarette smoking and statins in the development of postmenopausal osteoporosis: a pilot study utilizing the Marshfield Clinic Personalized Medicine Cohort.Osteoporos Int2010
19476582Use of an electronic medical record to characterize cases of intermediate statin-induced muscle toxicity.Prev Cardiol2009
18703947Intraocular pressure response to medication in a clinical setting: the Marshfield Clinic Personalized Medicine Research Project.J Glaucoma2008
17456828Use of an electronic medical record for the identification of research subjects with diabetes mellitus.Clin Med Res2007
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Collaborators

Catherine A McCarty
University of Minnesota Medical School, 1035 University Drive duluth
Co-authored papers 21
Murray H Brilliant
Marshfield Clinic Research Institute
Co-authored papers 18
Marylyn D Ritchie
Center for Systems Genomics, Pennsylvania State University, University Park
Co-authored papers 10
Gail P Jarvik
University of Washington Medical Center
Co-authored papers 9
Joshua C Denny
Vanderbilt University
Co-authored papers 9
Dan M Roden
Vanderbilt University Medical Center
Co-authored papers 9
Richard L Berg
Marshfield Clinic Research Institute
Co-authored papers 8
David S Carrell
Kaiser Permanente Washington Health Research Institute
Co-authored papers 8
John J Connolly
Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 7
Eric B Larson
University of Washington
Co-authored papers 6
Marc S Williams
University of Washington Medical Center
Co-authored papers 6
John R Wallace
The University of Alabama at Birmingham
Co-authored papers 6
Maureen E Smith
Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University
Co-authored papers 6
Sarah C Stallings
Vanderbilt University Medical Center
Co-authored papers 6
Peggy L Peissig
Center for Precision Medicine Research, Marshfield Clinic Research Institute
Co-authored papers 5
Ingrid A Holm
Harvard Medical School
Co-authored papers 5
Shefali S Verma
University of Pennsylvania
Co-authored papers 5
Scott J Hebbring
Marshfield Clinic Research Institute
Co-authored papers 5
David R Crosslin
University of Washington Medical Center
Co-authored papers 5
Rongling Li
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 5
James G Linneman
Marshfield Clinic Research Institute
Co-authored papers 4
Carol Waudby
Center for Human Genetics, Marshfield Clinic Research Foundation
Co-authored papers 4
Kyle B Brothers
Norton Children's Research Institute Affiliated with the University of Louisville
Co-authored papers 4
Sarah A Pendergrass
Biomedical and Translational Informatics Institute
Co-authored papers 4
Christian M Shaffer
Vanderbilt University
Co-authored papers 4
Kimberly F Doheny
Center for Inherited Disease Research, Johns Hopkins School of Medicine
Co-authored papers 4
Iftikhar J Kullo
Mayo Clinic
Co-authored papers 4
E Clayton
Harvard Medical School, Vanderbilt University, Yale University Yale Law School
Co-authored papers 3
Valerie D McManus
Biomedical Informatics Research Center, Marshfield Clinic Research Foundation
Co-authored papers 3
Martha J Shrubsole
Vanderbilt University Medical Center
Co-authored papers 3
Release 1.2