About: Erwin Böttinger

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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	ikertzailea (eu) researcher (en) 연구원 (ko) investigador (es) araştırmacı (tr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) deutscher Mediziner (de)
rdfs:label	Erwin Böttinger (de) Erwin Böttinger (en) Erwin Böttinger (nl) Erwin Böttinger (ast)
skos:prefLabel	Erwin Böttinger (de) Erwin Böttinger (en) Erwin Böttinger (nl) Erwin Böttinger (ast)
name	Erwin Böttinger (de) Erwin Böttinger (en) Erwin Böttinger (nl) Erwin Böttinger (ast)
LinkedIn personal profile ID	wds:Q56298167-88da5eb5-47e1-f2f7-8c2c-bac4e606a839
LinkedIn personal profile ID	erwin-böttinger-8b3524138
given name	wds:Q56298167-AACA237F-9793-446D-8D1E-BDF5C9505F29
given name	Erwin
instance of	wds:Q56298167-489FF113-E435-4768-9EA0-7D453EEEFA7D
instance of	Homo sapiens
Google Knowledge Graph ID	wds:Q56298167-05D7E3F7-BB73-4082-AA5D-16FD4725DCBF
Google Knowledge Graph ID	http://g.co/kg/g/11f53qt7j4
Google Knowledge Graph ID	/g/11f53qt7j4
skos:altLabel	Erwin Bottinger (en) Erwin P Bottinger (en) Erwin P Bottinger (nl) Erwin P. Böttinger (de) Erwin Paul Böttinger (de)
occupation	wds:Q56298167-D71C08F3-0282-47CA-973B-3FFC4F4E0636
employer	wds:Q56298167-4f7a9799-2a2e-49ce-b1e3-1526dc7d46af
languages spoken, written or signed	wds:Q56298167-06F0C9FC-4A71-4F26-8056-3A0D98B22986
sex or gender	wds:Q56298167-75E13603-EC56-4580-B6D2-349BBE169A65
VIAF ID	wds:Q56298167-2507c268-47ae-e88a-a038-8b62037d8c38
GND ID	wds:Q56298167-adc4c108-4e77-1a1d-e7c9-ee3b8408dff8
Library of Congress authority ID	wds:Q56298167-0159F2CF-9506-4021-9973-01C272C25648
DBLP author ID	wds:Q56298167-75E4EEF4-5CCE-4348-B076-7571FB5488EC
date of birth	wds:Q56298167-d0fe363b-be06-43a5-bfb1-69ce8e21a4d5
educated at	wds:Q56298167-22604B9B-318A-4E91-BD70-58F9A3BCC9FD
VIAF ID	http://viaf.org/viaf/8114156012420049700006
GND ID	https://d-nb.info/gnd/1187840890
Library of Congress authority ID	http://id.loc.gov/authorities/names/n2020185990
DBLP author ID	https://dblp.org/pid/95/821.rdf
occupation	researcher
employer	University of Potsdam
languages spoken, written or signed	German
sex or gender	male
VIAF ID	8114156012420049700006
GND ID	1187840890
Library of Congress authority ID	n2020185990
DBLP author ID	95/821
date of birth	1950-01-01 00:00:00Z (xsd:dateTime)
educated at	University of Erlangen–Nuremberg
ORCID iD	wds:Q56298167-80EF8326-1586-472C-BB59-96ED5D9AD5AC wds:Q56298167-ac89ada4-4bd5-88e6-622a-5fd37442d1b2
ORCID iD	https://orcid.org/0000-0001-6868-6676 https://orcid.org/0000-0003-1357-7995
ORCID iD	0000-0001-6868-6676 0000-0003-1357-7995
is owl:sameAs of	Erwin Böttinger
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56298167 https://de.wikipedia.org/wiki/Erwin_B%C3%B6ttinger
is author of	Genetic studies of body mass index yield new insights for obesity biology Keratinocyte-specific Smad2 ablation results in increased epithelial-mesenchymal transition during skin cancer formation and progression A collaborative approach to developing an electronic health record phenotyping algorithm for drug-induced liver injury No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis Endothelial mitochondrial oxidative stress determines podocyte depletion in segmental glomerulosclerosis Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry Return of results in the genomic medicine projects of the eMERGE network Utility of endogenous creatinine clearance as a measure of renal function in mice Mouse models of diabetic nephropathy Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility Testing the role of predicted gene knockouts in human anthropometric trait variation Effect of Genetic African Ancestry on eGFR and Kidney Disease Genetic variation in APOL1 and MYH9 genes is associated with chronic kidney disease among Nigerians Smad2-dependent downregulation of miR-30 is required for TGF-β-induced apoptosis in podocytes Crossing the omic chasm: a time for omic ancillary systems Genome-wide molecular profiles of HCV-induced dysplasia and hepatocellular carcinoma Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study Transforming growth factor-β, bioenergetics, and mitochondria in renal disease Epithelial cell TGFβ signaling induces acute tubular injury and interstitial inflammation Podocyte-selective deletion of dicer induces proteinuria and glomerulosclerosis Identification of type 2 diabetes subgroups through topological analysis of patient similarity Loss-of-function mutations in APOC3, triglycerides, and coronary disease BAMBI regulates angiogenesis and endothelial homeostasis through modulation of alternative TGFβ signaling The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol

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