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Author Details

Linnea M Baudhuin
Mayo Clinic
1999
72
23
PMIDPaper TitleJournal TitlePublished Year
36598548Evolutions in Clinical Chemistry.Clin Chem2023
37883600A Year in Review: 2023.Clin Chem2023
37566393Confirmation of Insertion, Deletion, and Deletion-Insertion Variants Detected by Next-Generation Sequencing.Clin Chem2023
37045502Genetic-Guided Oral P2Y<sub>12</sub> Inhibitor Selection and Cumulative Ischemic Events After Percutaneous Coronary Intervention.JACC Cardiovasc Interv2023
37373874Determination of the Duplicated <i>CYP2D6</i> Allele Using Real-Time PCR Signal: An Alternative Approach.J Pers Med2023
36896471COL1A1 and COL1A2 variants in Ehlers-Danlos syndrome phenotypes and COL1-related overlap disorder.Am J Med Genet C Semin Med Genet2023
35449399Point of care CYP2C19 genotyping after percutaneous coronary intervention.Pharmacogenomics J2022
33257948The Dynamic and Multifaceted Nature of Cardiovascular Disease and Using Genetic Testing to Inform Clinical Care: An International Perspective.Clin Chem2021
33631351Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM): A Study from the ClinGen Cardiomyopathy Variant Curation Expert Panel.J Mol Diagn2021
34746741Genomics Integration Into Nephrology Practice.Kidney Med2021
34503679Hypertrophic Cardiomyopathy in the General Population: Leveraging the UK Biobank Database and Machine Learning Phenotyping.J Am Coll Cardiol2021
32609853All Clinical Exomes Are Not Alike: Coverage Matters.Clin Chem2020
31843866Predictive and Precision Medicine with Genomic Data.Clin Chem2020
30819664Privacy in Direct-to-Consumer Genetic Testing.Clin Chem2019
31227806Variability in gene-based knowledge impacts variant classification: an analysis of FBN1 missense variants in ClinVar.Eur J Hum Genet2019
30998396Clopidogrel Pharmacogenetics.Circ Cardiovasc Interv2019
30724853International survey of patients undergoing percutaneous coronary intervention and their attitudes toward pharmacogenetic testing.Pharmacogenet Genomics2019
29210320Genetic variation in statin intolerance and a possible protective role for UGT1A1.Pharmacogenomics2018
29903731Plasma Ceramides.Arterioscler Thromb Vasc Biol2018
27977017Effect of genetic variants of bilirubin metabolism on the degree of hyperbilirubinemia in African-American newborns.J Perinatol2017
28077442Miniaturized Nanopore DNA Sequencing: Accelerating the Path to Precision Medicine.Clin Chem2017
28213806Clinical UGT1A1 Genetic Analysis in Pediatric Patients: Experience of a Reference Laboratory.Mol Diagn Ther2017
28145427Variability in assigning pathogenicity to incidental findings: insights from LDLR sequence linked to the electronic health record in 1013 individuals.Eur J Hum Genet2017
29237689Technical Advances for the Clinical Genomic Evaluation of Sudden Cardiac Death: Verification of Next-Generation Sequencing Panels for Hereditary Cardiovascular Conditions Using Formalin-Fixed Paraffin-Embedded Tissues and Dried Blood Spots.Circ Cardiovasc Genet2017
26947514Preemptive Pharmacogenomic Testing for Precision Medicine: A Comprehensive Analysis of Five Actionable Pharmacogenomic Genes Using Next-Generation DNA Sequencing and a Customized CYP2D6 Genotyping Cascade.J Mol Diagn2016
26861553Classifying Germline Sequence Variants in the Era of Next-Generation Sequencing.Clin Chem2016
25101912Increased frequency of FBN1 truncating and splicing variants in Marfan syndrome patients with aortic events.Genet Med2015
26487761"Big Data" in Laboratory Medicine.Clin Chem2015
26483113What Is the True Prevalence of Hypertrophic Cardiomyopathy?J Am Coll Cardiol2015
25960255Confirming Variants in Next-Generation Sequencing Panel Testing by Sanger Sequencing.J Mol Diagn2015
25652356Decreased frequency of FBN1 missense variants in Ghent criteria-positive Marfan syndrome and characterization of novel FBN1 variants.J Hum Genet2015
25671637Relationship of genetic variation in the serotonin transporter gene (SLC6A4) and congenital and acquired cardiovascular diseases.Genet Test Mol Biomarkers2015
24388019Preemptive genotyping for personalized medicine: design of the right drug, right dose, right time-using genomic data to individualize treatment protocol.Mayo Clin Proc2014
24789092The FDA and 23andMe: violating the First Amendment or protecting the rights of consumers?Clin Chem2014
24420163Genetic and biochemical analyses in dyslipidemic patients undergoing LDL apheresis.J Clin Apher2014
23290513UGT1A1 genetic analysis as a diagnostic aid for individuals with unconjugated hyperbilirubinemia.J Pediatr2013
24049795PCSK9 and the road less traveled: how an unconventional approach led to a major discovery.Clin Chem2013
23757769Quality guidelines for next-generation sequencing.Clin Chem2013
23501331Effects of atorvastatin on CYP3A4 and CYP3A5 mRNA expression in mononuclear cells and CYP3A activity in hypercholeresterolemic patients.Clin Chim Acta2013
22133117How novel molecular diagnostic technologies and biomarkers are revolutionizing genetic testing and patient care.Expert Rev Mol Diagn2012
23430904A Non-classical Presentation of Tangier Disease with Three ABCA1 Mutations.JIMD Rep2012
22811991A new era of genetic testing and its impact on research and clinical care.Clin Chem2012
20876227Determining the optimal approach for government-regulated genetic testing.Clin Chem2011
20643254Relation of ADRB1, CYP2D6, and UGT1A1 polymorphisms with dose of, and response to, carvedilol or metoprolol therapy in patients with chronic heart failure.Am J Cardiol2010
20920651Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testing.Am J Cardiol2010
18648394LDLR promoter variant and exon 14 mutation on the same chromosome are associated with an unusually severe FH phenotype and treatment resistance.Eur J Hum Genet2009
19956433Genetics of coronary artery disease: focus on genome-wide association studies.Am J Transl Res2009
19955245Warfarin sensitivity genotyping: a review of the literature and summary of patient experience.Mayo Clin Proc2009
19967918Genetic markers for coronary artery disease.Clin Lab Sci2009
19694059Novel human pathological mutations. Gene symbol: LDLR. Disease: hypercholesterolemia.Hum Genet2009
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Collaborators

Eric W Klee
Mayo Clinic College of Medicine and Science
Co-authored papers 6
Jennifer M Skierka
Mayo Clinic
Co-authored papers 5
Stephen N Thibodeau
Mayo Clinic
Co-authored papers 5
John L Black
Mayo Clinic
Co-authored papers 5
Matthew J Ferber
Mayo Clinic
Co-authored papers 5
Naveen L Pereira
Mayo Clinic
Co-authored papers 4
Richard M Weinshilboum
Mayo Clinic
Co-authored papers 3
Kent R Bailey
Mayo Clinic
Co-authored papers 3
Suzette J Bielinski
Mayo Clinic
Co-authored papers 3
Pedro J Caraballo
Mayo Clinic
Co-authored papers 2
Yves Rosenberg
National Heart Lung and Blood Institute
Co-authored papers 2
William J Sandborn
University of California San Diego
Co-authored papers 2
Tamra L Veldhuizen
Mayo Clinic
Co-authored papers 2
Michael J Ackerman
Mayo Clinic, Windland Smith Rice Genetic Heart Rhythm Clinic)
Co-authored papers 2
Lisa G Peterson
Mayo Clinic
Co-authored papers 2
Malcolm R Bell
Mayo Clinic
Co-authored papers 2
Liang Wang
H. Lee Moffitt Cancer Center
Co-authored papers 2
Jamie K Bruflat
Mayo Clinic
Co-authored papers 2
Liewei Wang
Mayo Clinic
Co-authored papers 2
Joseph H Blommel
Mayo Clinic, Clemson University
Co-authored papers 2
Iftikhar J Kullo
Mayo Clinic
Co-authored papers 2
Birgit Funke
Partners Healthcare Center for Personalized Genetic Medicine
Co-authored papers 2
Janet E Olson
Mayo Clinic
Co-authored papers 2
Carolyn R Rohrer Vitek
Center for Individualized Medicine, College of Medicine, Mayo Clinic
Co-authored papers 1
Euijung Ryu
Mayo Clinic
Co-authored papers 1
Timothy Caulfield
Faculty of Law and School of Public Health, University of Alberta
Co-authored papers 1
John A Heit
Mayo Clinic
Co-authored papers 1
Leslie G Biesecker
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 1
Arjun K Manrai
Co-authored papers 1
Pavel N Pichurin
Mayo Clinic
Co-authored papers 1
Release 1.2