About: Volker M. Lauschke

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) researcher (en) 연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq)
rdfs:label	Volker M Lauschke (es) Volker M Lauschke (nl) Volker M Lauschke (sl) Volker M. Lauschke (en)
skos:prefLabel	Volker M Lauschke (es) Volker M Lauschke (nl) Volker M Lauschke (sl) Volker M. Lauschke (en)
name	Volker M Lauschke (es) Volker M Lauschke (nl) Volker M Lauschke (sl) Volker M. Lauschke (en)
LinkedIn personal profile ID	wds:Q48289711-762DF6A4-9955-4752-9428-3687A84392E5
LinkedIn personal profile ID	vlauschke
Scopus author ID	wds:Q48289711-537618B3-F1B5-421C-A5EA-23E740F46246
Scopus author ID	56955751900
given name	wds:Q48289711-C664B27D-5F69-49D4-B928-A73AF0FD2962
given name	Volker
instance of	wds:Q48289711-0A3AE633-D785-4787-8ADE-E1AF8CEE79A2
instance of	Homo sapiens
Loop ID	wds:Q48289711-4EF85071-7188-4BE5-AF5B-441D706D3AC8
Loop ID	431725
skos:altLabel	Volker Lauschke (en)
occupation	wds:Q48289711-F5C10DED-C972-43B3-9F55-1A3DAE8B3BFA
employer	wds:Q48289711-93C0878E-9D27-4B26-BC12-332D6A2FDCD2 wds:Q48289711-F5C63909-4010-4842-A88D-BAC44E4DCE3A
sex or gender	wds:Q48289711-D766E5BC-695B-4AF1-A0CF-E9745829B7DA
VIAF ID	wds:Q48289711-414536FB-5351-4A1D-89A8-050FD821E76B
GND ID	wds:Q48289711-776eb9dc-cfd4-4436-bca4-31584905f16f
date of birth	wds:Q48289711-1ED46FF9-A968-45E2-95C3-A4F64134A838
educated at	wds:Q48289711-199160DD-5A02-40DA-AA02-2DBF82DEB245 wds:Q48289711-95F82E61-4995-44B1-B981-DF9E1FC4AEA3 wds:Q48289711-A4CC5628-FC31-4827-9EBC-9101A8AEF888 wds:Q48289711-DD05B152-2698-4693-B080-DB40BE682D9B wds:Q48289711-DD1F51BB-97A8-4E14-91F7-B633196194BC
WorldCat Identities ID (superseded)	wds:Q48289711-80C56AFE-718C-41BA-ABE0-A4C48E539A56
official website	wds:Q48289711-47AC99EC-1EF2-4F4F-9AAE-8AF387C88548
VIAF ID	http://viaf.org/viaf/305355298
GND ID	https://d-nb.info/gnd/1044411244
occupation	researcher
employer	Karolinska Institutet European Molecular Biology Laboratory
sex or gender	male
VIAF ID	305355298
GND ID	1044411244
date of birth	2000-01-01 00:00:00Z (xsd:dateTime)
educated at	FernUniversität in Hagen University of Bergen European Molecular Biology Laboratory University of Cologne University of Bonn
WorldCat Identities ID (superseded)	viaf-305355298
official website	http://ki.se/en/people/vollau
ORCID iD	wds:Q48289711-DAE7F2C5-5B02-46FE-934A-426C07D5246F
ORCID iD	https://orcid.org/0000-0002-1140-6204
ORCID iD	0000-0002-1140-6204
ResearcherID	wds:Q48289711-447BA13D-F1FD-4216-B9A2-5605F4EF9FFE
Publons author ID	wds:Q48289711-3d0e26ff-cc48-438e-83eb-d3ed6db33e6c
ResearcherID	O-3014-2017
Publons author ID	1229954
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q48289711
is author of	Novel 3D Culture Systems for Studies of Human Liver Function and Assessments of the Hepatotoxicity of Drugs and Drug Candidates The Importance of Patient-Specific Factors for Hepatic Drug Response and Toxicity Characterization of primary human hepatocyte spheroids as a model system for drug-induced liver injury, liver function and disease A multicenter assessment of single-cell models aligned to standard measures of cell health for prediction of acute hepatotoxicity Worldwide Distribution of Cytochrome P450 Alleles: A Meta-analysis of Population-scale Sequencing Projects. Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting. Rare genetic variants in cellular transporters, metabolic enzymes, and nuclear receptors can be important determinants of interindividual differences in drug response Genetic variation in the human cytochrome P450 supergene family Transcriptional, Functional, and Mechanistic Comparisons of Stem Cell-Derived Hepatocytes, HepaRG Cells, and Three-Dimensional Human Hepatocyte Spheroids as Predictive In Vitro Systems for Drug-Induced Liver Injury. Single base resolution analysis of 5-hydroxymethylcytosine in 188 human genes: implications for hepatic gene expression Pitfalls and Opportunities for Epigenomic Analyses Focused on Disease Diagnosis, Prognosis, and Therapy. Pharmacoepigenetics and Toxicoepigenetics: Novel Mechanistic Insights and Therapeutic Opportunities. Precision Medicine and Rare Genetic Variants Pharmacogenomic Biomarkers for Improved Drug Therapy-Recent Progress and Future Developments. How to Consider Rare Genetic Variants in Personalized Drug Therapy. Integrating rare genetic variants into pharmacogenetic drug response predictions. Genetic variability and population diversity of the human SLCO (OATP) transporter family Massive rearrangements of cellular MicroRNA signatures are key drivers of hepatocyte dedifferentiation. Comparison of hepatic 2D sandwich cultures and 3D spheroids for long-term toxicity applications: A multi-center study. Prediction of Drug-Induced Hepatotoxicity Using Long-Term Stable Primary Hepatic 3D Spheroid Cultures in Chemically Defined Conditions. Transcriptomic, Proteomic, and Functional Long-Term Characterization of Multicellular Three-Dimensional Human Liver Microtissues The impact of variants in ATP-binding cassette transporters on breast cancer treatment Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions An optimized prediction framework to assess the functional impact of pharmacogenetic variants

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