Yitian Zhou, Volker M Lauschke. Clin Pharmacol Ther 2021
Times Cited: 10
Times Cited: 10
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Computational Methods for the Pharmacogenetic Interpretation of Next Generation Sequencing Data.
Yitian Zhou, Kohei Fujikura, Souren Mkrtchian, Volker M Lauschke. Front Pharmacol 2018
Yitian Zhou, Kohei Fujikura, Souren Mkrtchian, Volker M Lauschke. Front Pharmacol 2018
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Integrating rare genetic variants into pharmacogenetic drug response predictions.
Magnus Ingelman-Sundberg, Souren Mkrtchian, Yitian Zhou, Volker M Lauschke. Hum Genomics 2018
Magnus Ingelman-Sundberg, Souren Mkrtchian, Yitian Zhou, Volker M Lauschke. Hum Genomics 2018
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Rare genetic variants in cellular transporters, metabolic enzymes, and nuclear receptors can be important determinants of interindividual differences in drug response.
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Ethnogeographic and inter-individual variability of human ABC transporters.
Qingyang Xiao, Yitian Zhou, Volker M Lauschke. Hum Genet 2020
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Heritability of metoprolol and torsemide pharmacokinetics.
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Population-scale predictions of DPD and TPMT phenotypes using a quantitative pharmacogene-specific ensemble classifier.
Yitian Zhou, Carolina Dagli Hernandez, Volker M Lauschke. Br J Cancer 2020
Yitian Zhou, Carolina Dagli Hernandez, Volker M Lauschke. Br J Cancer 2020
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An optimized prediction framework to assess the functional impact of pharmacogenetic variants.
Yitian Zhou, Souren Mkrtchian, Masaki Kumondai, Masahiro Hiratsuka, Volker M Lauschke. Pharmacogenomics J 2019
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Pharmacogenomics of GPCR Drug Targets.
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Emerging strategies to bridge the gap between pharmacogenomic research and its clinical implementation.
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Volker M Lauschke, Magnus Ingelman-Sundberg. NPJ Genom Med 2020
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Cytochrome P450 enzymes in drug metabolism: regulation of gene expression, enzyme activities, and impact of genetic variation.
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Genetic variation in human drug-related genes.
Charlotta Pauline Irmgard Schärfe, Roman Tremmel, Matthias Schwab, Oliver Kohlbacher, Debora Susan Marks. Genome Med 2017
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The genetic landscape of the human solute carrier (SLC) transporter superfamily.
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Lena Schaller, Volker M Lauschke. Hum Genet 2019
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Genetic variability and population diversity of the human SLCO (OATP) transporter family.
Boyao Zhang, Volker M Lauschke. Pharmacol Res 2019
Boyao Zhang, Volker M Lauschke. Pharmacol Res 2019
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Rare genetic variability in human drug target genes modulates drug response and can guide precision medicine.
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Worldwide Distribution of Cytochrome P450 Alleles: A Meta-analysis of Population-scale Sequencing Projects.
Y Zhou, M Ingelman-Sundberg, V M Lauschke. Clin Pharmacol Ther 2017
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Gene-Specific Variant Classifier (DPYD-Varifier) to Identify Deleterious Alleles of Dihydropyrimidine Dehydrogenase.
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The mutational constraint spectrum quantified from variation in 141,456 humans.
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A method and server for predicting damaging missense mutations.
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The Pharmacogene Variation (PharmVar) Consortium: Incorporation of the Human Cytochrome P450 (CYP) Allele Nomenclature Database.
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Genetic variation in the human cytochrome P450 supergene family.
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The global spectrum of protein-coding pharmacogenomic diversity.
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Pharmacogenomic Biomarkers for Improved Drug Therapy-Recent Progress and Future Developments.
Volker M Lauschke, Lili Milani, Magnus Ingelman-Sundberg. AAPS J 2017
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Long-read human genome sequencing and its applications.
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Prediction of drug response and adverse drug reactions: From twin studies to Next Generation Sequencing.
Volker M Lauschke, Magnus Ingelman-Sundberg. Eur J Pharm Sci 2019
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Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions.
Sulev Reisberg, Kristi Krebs, Maarja Lepamets, Mart Kals, Reedik Mägi, Kristjan Metsalu, Volker M Lauschke, Jaak Vilo, Lili Milani. Genet Med 2019
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Germline variant burden in multidrug resistance transporters is a therapy-specific predictor of survival in breast cancer patients.
Qingyang Xiao, Yitian Zhou, Stefan Winter, Florian Büttner, Elke Schaeffeler, Matthias Schwab, Volker M Lauschke. Int J Cancer 2020
Qingyang Xiao, Yitian Zhou, Stefan Winter, Florian Büttner, Elke Schaeffeler, Matthias Schwab, Volker M Lauschke. Int J Cancer 2020
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Towards precision medicine: advances in computational approaches for the analysis of human variants.
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Analysis of protein-coding genetic variation in 60,706 humans.
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A model-based cost-effectiveness analysis of pharmacogenomic panel testing in cardiovascular disease management: preemptive, reactive, or none?
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Unveiling the guidance heterogeneity for genome-informed drug treatment interventions among regulatory bodies and research consortia.
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CADD-Splice-improving genome-wide variant effect prediction using deep learning-derived splice scores.
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Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting.
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PharmVar GeneFocus: CYP2B6.
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Cyrius: accurate CYP2D6 genotyping using whole-genome sequencing data.
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PharmVar GeneFocus: CYP2D6.
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Towards population-scale long-read sequencing.
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The ethnogeographic variability of genetic factors underlying G6PD deficiency.
Maria Koromina, Maria Theodora Pandi, Peter J van der Spek, George P Patrinos, Volker M Lauschke. Pharmacol Res 2021
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Cost-effectiveness of pharmacogenetic-guided treatment: are we there yet?
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.