About: Graeme Black

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

British academic

Attributes	Values
rdf:type	Item
description	wetenschapper (nl) дослідник (uk) United Kingdom karimba ŋun nyɛ doo (dag) հետազոտող (hy) hulumtues (sq) académico británico (es) أكاديمي بريطاني (ar) British academic (en)
rdfs:label	Graeme Black (en) Graeme Black (es) Graeme Black (fr) Graeme Black (it) Graeme Black (nl) Graeme Black (ast) Graeme Black (sl) Graeme Black (sq)
skos:prefLabel	Graeme Black (en) Graeme Black (es) Graeme Black (fr) Graeme Black (it) Graeme Black (nl) Graeme Black (ast) Graeme Black (sl) Graeme Black (sq)
name	Graeme Black (en) Graeme Black (es) Graeme Black (fr) Graeme Black (it) Graeme Black (nl) Graeme Black (ast) Graeme Black (sl) Graeme Black (sq)
ResearchGate contributions ID	wds:Q30429957-4080c3dd-41c5-fcdf-a6d3-fca2b2350255
ResearchGate contributions ID	2080424920
Scopus author ID	wds:Q30429957-77AAB6E8-DA10-448D-9AC4-1253B5E9783C
Scopus author ID	7102294178
given name	wds:Q30429957-56509D91-1A03-4C6F-ACDF-E5826EB11442
given name	Graeme
instance of	wds:Q30429957-1C11A744-1C78-49A9-889F-E77B4A54F3A8
instance of	Homo sapiens
award received	wds:Q30429957-3EE9420B-B1F9-497B-9920-1CC42A2D5B99 wds:Q30429957-BDB1119C-4263-4954-8305-1B98F8A1F930
award received	Officer of the Order of the British Empire Fellow of the Academy of Medical Sciences
skos:altLabel	Graeme Charles Mackinlay Black (en)
occupation	wds:Q30429957-3392822D-F008-4240-A52C-6A9B7A39D299 wds:Q30429957-95171C38-C71E-4356-9061-6307C994420A wds:Q30429957-F84D2360-DD20-4872-8668-71DD08DCDD8D
employer	wds:Q30429957-3bed8110-4573-7a3e-58d9-86a1cd3f6681
languages spoken, written or signed	wds:Q30429957-C5F472BA-DBD6-4EC0-BBD8-D0AB1195EB76
sex or gender	wds:Q30429957-293A60A4-837B-41FD-B2BE-B452A9B5C523
DBLP author ID	wds:Q30429957-4BB6197F-5666-4B40-826D-D403E4415525
country of citizenship	wds:Q30429957-27E1C5E5-FED5-4512-8C01-8B69B68A9C7F
Who's Who UK ID	wds:Q30429957-2fb83a04-4c84-ea1e-ee88-93d63dc97b5d
academic degree	wds:Q30429957-12E692CD-0A1C-4414-9994-8F478433F948
date of birth	wds:Q30429957-127AB11D-6171-4FD2-BB87-87910BC00D16
educated at	wds:Q30429957-6380F5CA-0B2C-4805-B3A8-2590F345C51E wds:Q30429957-7B3BC512-7229-42F2-B0BA-9C931725CC9B wds:Q30429957-B4D4791D-0CAC-450E-9FB9-944F48BB7655 wds:Q30429957-E33F92F4-1777-4C9D-9597-70B3D0DC7FC6
family name	wds:Q30429957-CD5B4876-A6B8-4DE4-8B76-E34E0D38ABAA
official website	wds:Q30429957-C156EBF2-342D-4BC7-88AB-DC6432DA03A2
DBLP author ID	https://dblp.org/pid/141/5506.rdf
occupation	university teacher ophthalmologist geneticist
employer	University of Manchester
languages spoken, written or signed	English
sex or gender	male
DBLP author ID	141/5506
country of citizenship	United Kingdom
Who's Who UK ID	U288848
academic degree	Doctor of Philosophy
date of birth	1962-09-06 00:00:00Z (xsd:dateTime)
educated at	University of Oxford John Ffowcs Williams Royal College of Ophthalmologists
family name	Black
official website	http://www.human-development.manchester.ac.uk/staff/GraemeBlack/
Springer Nature person ID	wds:Q30429957-F3784A8E-1148-4B0C-8379-8482E4BBDE2B
ORCID iD	wds:Q30429957-814975EF-D0CF-42F9-A744-EED659F52B69
Dimensions author ID	wds:Q30429957-9F20EE57-5AB2-4E26-A0E1-BDD3EA3817B6
ORCID iD	https://orcid.org/0000-0001-8727-6592
Springer Nature person ID	01223043246.10
ORCID iD	0000-0001-8727-6592
Dimensions author ID	01223043246.10
ResearcherID	wds:Q30429957-52D2DCAD-2690-40F8-8BEB-82D134A08D21
Publons author ID	wds:Q30429957-90494ce5-f3c1-4b8b-8682-4abc74178e0f
ResearcherID	K-7374-2015
Publons author ID	2367652
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q30429957
is author of	Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR. Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q. BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects RPGR mutation analysis and disease: an update. Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding protein Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in males Molecular genetic analysis of the NF2 gene in young patients with unilateral vestibular schwannomas. Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene.

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