About: Neil J. Sebire

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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) ikertzailea (eu) 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	Neil J. Sebire (en) Neil J. Sebire (es) Neil J. Sebire (nl) Neil J. Sebire (sl) Neil J. Sebire (ast)
skos:prefLabel	Neil J. Sebire (en) Neil J. Sebire (es) Neil J. Sebire (nl) Neil J. Sebire (sl) Neil J. Sebire (ast)
name	Neil J. Sebire (en) Neil J. Sebire (es) Neil J. Sebire (nl) Neil J. Sebire (sl) Neil J. Sebire (ast)
Scopus author ID	wds:Q38549176-90FA9A5D-62B9-4E5F-A855-23C844893C69
Scopus author ID	7004794073
given name	wds:Q38549176-51C87049-5441-45C7-9ABC-A7CA01F8E272
given name	Neil
instance of	wds:Q38549176-9B55315F-3032-427E-8D70-93634CB28BCF
instance of	Homo sapiens
skos:altLabel	Neil Sebire (en)
Nationale Thesaurus voor Auteursnamen ID	wds:Q38549176-a8ecb1d1-3953-416e-b504-80854579f250
occupation	wds:Q38549176-2A785C66-BB6F-461D-BCC4-41207DEB7F4B
employer	wds:Q38549176-16D06DA0-8445-4073-86E8-CF1C3440C273
NUKAT ID	wds:Q38549176-6C3D325C-0C28-464C-9B5B-7289591DF977
sex or gender	wds:Q38549176-82E176F5-E7B0-42A3-8C2B-AF805B3A8A5A
ISNI	wds:Q38549176-643182CC-1554-4CEF-9E91-1EFECC8E7CC0
VIAF ID	wds:Q38549176-F04F7E6F-FE03-4D92-A9D5-B105A731B7A5
GND ID	wds:Q38549176-f462e894-4f80-4516-8330-6991cb585546
Library of Congress authority ID	wds:Q38549176-EE5DE2CD-E3D7-49F1-B512-24E9A4CE900A
IdRef ID	wds:Q38549176-F09B5178-8E4C-4CD9-A109-669F2B1AF4A2
on focus list of Wikimedia project	wds:Q38549176-E7C29598-F10E-4C21-90FE-971A66633EF7
date of birth	wds:Q38549176-33404F36-44DB-4101-87B3-4553A014DB8B
family name	wds:Q38549176-4725719D-11F1-4854-9586-17152B3DA547
WorldCat Identities ID (superseded)	wds:Q38549176-4ED68B1E-8464-4A0C-A128-AF941F9A0F54
National Library of Israel J9U ID	wds:Q38549176-61B2A7A1-641A-43CE-8E0F-813B7ABB6347
official website	wds:Q38549176-EDA93300-5EB1-4ABB-B4F9-5117686EEF2F
Nationale Thesaurus voor Auteursnamen ID	http://data.bibliotheken.nl/id/thes/p304865753
VIAF ID	http://viaf.org/viaf/16483065
GND ID	https://d-nb.info/gnd/173024262
Library of Congress authority ID	http://id.loc.gov/authorities/names/n95801358
IdRef ID	http://www.idref.fr/116773766/id
Nationale Thesaurus voor Auteursnamen ID	304865753
occupation	researcher
employer	University College London
NUKAT ID	n2010121304
sex or gender	male
ISNI	0000000108739254
VIAF ID	16483065
GND ID	173024262
Library of Congress authority ID	n95801358
IdRef ID	116773766
on focus list of Wikimedia project	WikiProject COVID-19
date of birth	1968-01-01 00:00:00Z (xsd:dateTime)
family name	Sebire
WorldCat Identities ID (superseded)	lccn-n95801358
National Library of Israel J9U ID	987007366592305171
official website	http://iris.ucl.ac.uk/iris/browse/profile?upi=NJSEB45
ORCID iD	wds:Q38549176-B73A8C28-6C58-4E25-94A8-908CC5373F2D
ORCID iD	https://orcid.org/0000-0001-5348-9063
ORCID iD	0000-0001-5348-9063
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q38549176
is author of	Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes Imaging Invasion: Micro-CT imaging of adamantinomatous craniopharyngioma highlights cell type specific spatial relationships of tissue invasion DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndrome Diagnosis of Neuronal Ceroid Lipofuscinosis (Batten Disease) by Electron Microscopy in Peripheral Blood Specimens Natural history of testicular regression syndrome and consequences for clinical management Prenatal determination of chorionicity in triplet pregnancy by ultrasonographic examination of the ipsilon zone Infant colitis—it's in the genes Less invasive perinatal autopsies and the future of postmortem science Clusterin, a haploinsufficient tumor suppressor gene in neuroblastomas First-trimester ultrasound screening for chromosomal defects UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal-translucency thickness at 10–14 weeks of gestation Review: Neuropathological features of unexplained sudden unexpected death in infancy: current evidence and controversies A molecular map of mesenchymal tumors Infection and sudden unexpected death in infancy: a systematic retrospective case review. EVERREST prospective study: a 6-year prospective study to define the clinical and biological characteristics of pregnancies affected by severe early onset fetal growth restriction Placental villus morphology in relation to maternal hypoxia at high altitude Perilobar nephrogenic rests are nonobligate molecular genetic precursor lesions of insulin-like growth factor-II-associated Wilms tumors Gestational Choriocarcinoma Mimicking a Uterine Adenocarcinoma Is maternal underweight really a risk factor for adverse pregnancy outcome? A population-based study in London. Tumors in Pediatric Patients at Diffusion-weighted MR Imaging: Apparent Diffusion Coefficient and Tumor Cellularity Obstetric risks of pregnancy in women less than 18 years old

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