About: Bernardino F. Ghetti

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

neuropathologist

Attributes	Values
rdf:type	Item
description	연구원 (ko) 研究者 (ja) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) neuropatholoog (nl) neuropathologist (en)
rdfs:label	Bernardino F. Ghetti (en) Bernardino F. Ghetti (es) Bernardino F. Ghetti (it) Bernardino F. Ghetti (nl) Bernardino F. Ghetti (sq) Bernardino F. Ghetti (ast)
skos:prefLabel	Bernardino F. Ghetti (en) Bernardino F. Ghetti (es) Bernardino F. Ghetti (it) Bernardino F. Ghetti (nl) Bernardino F. Ghetti (sq) Bernardino F. Ghetti (ast)
name	Bernardino F. Ghetti (en) Bernardino F. Ghetti (es) Bernardino F. Ghetti (it) Bernardino F. Ghetti (nl) Bernardino F. Ghetti (sq) Bernardino F. Ghetti (ast)
affiliation	wds:Q56863342-2C12ED36-4353-46D5-B0A0-514E19C2292E
affiliation	Indiana University School of Medicine
Scopus author ID	wds:Q56863342-f2440ac3-465e-e1fc-45cd-e1ab5145640d
Scopus author ID	7101805049
given name	wds:Q56863342-4B6B9267-D315-4100-86DB-74FD4D20D263
given name	Bernardino
instance of	wds:Q56863342-337a8b77-40f8-8929-7370-db595cd439fa
instance of	Homo sapiens
award received	wds:Q56863342-1d06dd82-4b12-227f-c1b6-114d860ed4b5 wds:Q56863342-c5e33fa4-4aa3-1e5f-d61c-2888008a2693 wds:Q56863342-d8133d45-40bd-692f-d887-40334f6c2ea5
award received	Potamkin Prize Fellow of the American Association for the Advancement of Science Bengt Winblad Lifetime Achievement Award in Alzheimer’s Disease Research
work location	wds:Q56863342-5C211B21-858A-4AFD-A668-6E1DD0C5CB3B
work location	Indianapolis
skos:altLabel	Bernardino Ghetti (en) Bernardino Ghetti (nl)
occupation	wds:Q56863342-21fca320-4a49-3e65-dd23-38a39f436f47 wds:Q56863342-55B5DBF3-8BF7-4473-A907-736EABD86140 wds:Q56863342-CF310170-414C-4EE4-A7D4-62159027D8FD
employer	wds:Q56863342-15d42760-4cc2-df21-fa64-57ffb7d62bef wds:Q56863342-5B5B07E1-3E0A-4951-9C02-1701AB9828AF wds:Q56863342-e12b886e-4356-3056-be83-243093667b22
languages spoken, written or signed	wds:Q56863342-F1094A42-BD50-439A-B1A3-43A531E71954
sex or gender	wds:Q56863342-2e466e14-40f5-bbf1-e7a1-e9db21e791e2
VIAF ID	wds:Q56863342-aacaaf71-4983-904a-8baa-f2ebe2c99ddf
Library of Congress authority ID	wds:Q56863342-5dd45cb2-4201-f5aa-b88b-e3510fd0870d
on focus list of Wikimedia project	wds:Q56863342-1DE5D3E4-553F-4849-ACC2-0A72B08FB6D3
educated at	wds:Q56863342-e2d3ee27-4779-44aa-327d-a6b959a890c9
WorldCat Identities ID (superseded)	wds:Q56863342-71625925-2660-4AEF-A8B5-8B052E33AEC7
National Library of Israel J9U ID	wds:Q56863342-75CDFE5D-F8B1-4DCE-AB6D-DDD79C92E7CC
official website	wds:Q56863342-da319201-49cd-c540-a36d-7a9bfe5a61fd
VIAF ID	http://viaf.org/viaf/54044905
Library of Congress authority ID	http://id.loc.gov/authorities/names/nr96006599
occupation	neuropathologist university teacher researcher
employer	Indiana University School of Medicine Albert Einstein College of Medicine Indiana University – Purdue University Indianapolis
languages spoken, written or signed	English
sex or gender	male
VIAF ID	54044905
Library of Congress authority ID	nr96006599
on focus list of Wikimedia project	Wikidata:WikiProject IUPUI University Library
educated at	University of Pisa
WorldCat Identities ID (superseded)	lccn-nr96006599
National Library of Israel J9U ID	987012501669505171
official website	https://medicine.iu.edu/faculty/13352/ghetti-bernardino/
ORCID iD	wds:Q56863342-9F277662-C5F4-49E7-BAEA-D8D3634B74C2
ORCID iD	https://orcid.org/0000-0002-1842-8019
ORCID iD	0000-0002-1842-8019
is owl:sameAs of	Bernardino F. Ghetti Bernardino F. Ghetti
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56863342
is author of	Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies Association of a presenilin 1 S170F mutation with a novel Alzheimer disease molecular phenotype. Rarity of the Alzheimer disease-protective APP A673T variant in the United States Amino-terminally truncated Abeta peptide species are the main component of cotton wool plaques SNARE protein redistribution and synaptic failure in a transgenic mouse model of Parkinson's disease Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases Abeta42-driven cerebral amyloidosis in transgenic mice reveals early and robust pathology Neurodegeneration caused by proteins with an aberrant carboxyl-terminus Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea. Regional variability of imaging biomarkers in autosomal dominant Alzheimer's disease Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias Clinical and biomarker changes in dominantly inherited Alzheimer's disease Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE A novel mutation (G217D) in the Presenilin 1 gene ( PSEN1) in a Japanese family: presenile dementia and parkinsonism are associated with cotton wool plaques in the cortex and striatum

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