Eric W. Klee - Concepedia

Author

Eric W. Klee

Also Known As

Asad, Sarah, Brendan C. Lanpher, Bruno Dallapiccola, E Klee, E. Klee, E. W. Klee, E.W. Klee, Eric Gamazon, Eric Klee, Eric W Klee

456

Publications

10.7K

Citations

H-Index

218

Concepts

All Affiliations

Mayo Clinic Mayo Clinic in Florida Mayo Clinic in Arizona WinnMed Inserm

About

Eric W. Klee is an author at Mayo Clinic specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	35	64	4.3K
2	Engineering	9	9	307
3	Public Health	7	7	368
4	Natural Sciences	6	6	382
5	Health Sciences	4	4	113

Eric W. Klee

154

Publications

8.1K

Citations

H-Index

Page 1

	Year	Citations
Integrated Genomic Characterization Reveals Novel, Therapeutically Relevant Drug Targets in FGFR and EGFR Pathways in Sporadic Intrahepatic Cholangiocarcinoma Mitesh J. Borad, Mia D. Champion, Jan B. Egan, PLoS Genetics Fgfr InhibitorsPathologySporadic Intrahepatic CholangiocarcinomaCholangiopathiesTumor Biology	2014	334
Preemptive Genotyping for Personalized Medicine: Design of the Right Drug, Right Dose, Right Time—Using Genomic Data to Individualize Treatment Protocol Suzette J. Bielinski, Janet E. Olson, Jyotishman Pathak, Mayo Clinic Proceedings Patient SelectionRight DrugPersonalized TreatmentRight DosePharmacotherapy	2014	298
Sentieon DNASeq Variant Calling Workflow Demonstrates Strong Computational Performance and Accuracy Katherine I. Kendig, Saurabh Baheti, Matthew A. Bockol, Frontiers in Genetics GeneticsGenome Analysis ToolkitMolecular BiologyGenomicsHigh Throughput Sequencing	2019	264
Distinct epigenetic landscapes underlie the pathobiology of pancreatic cancer subtypes Gwen Lomberk, Yuna Blum, Rémy Nicolle, Nature Communications	2018	258
Genome-wide detection of tandem DNA repeats that are expanded in autism Brett Trost, Worrawat Engchuan, Charlotte Nguyen, Nature Tandem DnaDna SequencingSyndromic AutismGeneticsMolecular Biology	2020	246
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders Vincenzo Salpietro, Christine L. Dixon, Hui Guo, Nature Communications	2019	236
Genomic and Phenotypic Characterization of a Broad Panel of Patient-Derived Xenografts Reflects the Diversity of Glioblastoma Rachael A. Vaubel, Shulan Tian, Dioval Remonde, Clinical Cancer Research	2019	223
Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development Ashley L. Lennox, Mariah L. Hoye, Ruiji Jiang, Neuron Developmental BiologyBrain DevelopmentDevelopmental GeneticsGeneticsRna Biology	2020	205
Preemptive Pharmacogenomic Testing for Precision Medicine Yuan Ji, Jennifer M. Skierka, Joseph H. Blommel, Journal of Molecular Diagnostics MedicinePharmacologyPreemptive Pharmacogenomic TestingOmicsPharmacogenomics	2016	191
Bi-allelic Alterations in AEBP1 Lead to Defective Collagen Assembly and Connective Tissue Structure Resulting in a Variant of Ehlers-Danlos Syndrome Patrick R. Blackburn, Xu Zhi, Kathleen E. Tumelty, The American Journal of Human Genetics Ehlers-danlos SyndromeDefective Collagen AssemblyFibrosisAutoimmune DiseaseGenetic Disorder	2018	167

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