About: Bruno Reversade

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

American geneticist

Attributes	Values
rdf:type	Item
owl:sameAs	Bruno Reversade
description	wetenschapper (nl) дослідник (uk) American geneticist (en) genetista estadounidense (es) عالم وراثة أمريكي (ar) Biologiste américain, Bruno Reversade est spécialisé en génétique humaine (fr)
rdfs:label	Bruno Reversade (de) Bruno Reversade (en) Bruno Reversade (es) Bruno Reversade (fr) Bruno Reversade (it) Bruno Reversade (nl) Bruno Reversade (pt) Bruno Reversade (pt-br)
skos:prefLabel	Bruno Reversade (de) Bruno Reversade (en) Bruno Reversade (es) Bruno Reversade (fr) Bruno Reversade (it) Bruno Reversade (nl) Bruno Reversade (pt) Bruno Reversade (pt-br)
name	Bruno Reversade (de) Bruno Reversade (en) Bruno Reversade (es) Bruno Reversade (fr) Bruno Reversade (it) Bruno Reversade (nl) Bruno Reversade (pt) Bruno Reversade (pt-br)
given name	wds:Q85566689-1C427F8C-5BA0-4C8D-8A6A-7C15F10EC7E0
given name	Bruno
instance of	wds:Q85566689-07E24CD0-F169-4131-8984-09F941A3FDA7
instance of	Homo sapiens
Google Knowledge Graph ID	wds:Q85566689-AB8C9E22-AFF0-4A1E-A2B1-7E5328349BFC
Google Knowledge Graph ID	http://g.co/kg/g/11j8kdt_9f
Google Knowledge Graph ID	/g/11j8kdt_9f
Google Scholar author ID	wds:Q85566689-ea476355-4935-d85f-1d3b-3f217c626ea4
Google Scholar author ID	4vuCuLYAAAAJ
skos:altLabel	Reversade (en)
occupation	wds:Q85566689-4a7b15f1-9ecd-48b4-81fb-03ee7130e114
employer	wds:Q85566689-deb8b62e-503e-4226-94e0-53910d5ea371
languages spoken, written or signed	wds:q85566689-5ab1aaa4-456f-bd16-9748-f714a04ac839
sex or gender	wds:Q85566689-02DBBCB7-411B-4858-95DE-35E7DC645E2C
ISNI	wds:Q85566689-8a7fa614-4d1c-9547-425c-d4913ad66a7f
VIAF ID	wds:Q85566689-dbf308df-4951-2380-5514-0bc2af9430eb
IdRef ID	wds:Q85566689-2c6d7068-4a89-7565-a01f-40b591e705b4
country of citizenship	wds:Q85566689-79DC7363-0109-4578-AADE-5AAD354A6D39
date of birth	wds:Q85566689-CEDB409F-1633-4DDD-B435-65D0AA3D38DF
writing language	wds:q85566689-79630336-41c4-2da1-b21d-8a73c8ca9472
educated at	wds:Q85566689-33aff683-4ef7-46f6-a6f2-0e1c6e01c9ac
WorldCat Identities ID (superseded)	wds:Q85566689-18873D03-1689-4D16-A7C2-20B9581706BA
official website	wds:Q85566689-bf0def69-4c80-93ce-081b-c7c42a8c2f2f
VIAF ID	http://viaf.org/viaf/202165911
IdRef ID	http://www.idref.fr/109134621/id
occupation	biologist
employer	Koç University
languages spoken, written or signed	English
sex or gender	male
ISNI	0000000357788567
VIAF ID	202165911
IdRef ID	109134621
country of citizenship	France
date of birth	1978-01-01 00:00:00Z (xsd:dateTime)
writing language	English
educated at	Pierre and Marie Curie University
WorldCat Identities ID (superseded)	viaf-202165911
official website	http://www.reversade.com
ORCID iD	wds:Q85566689-F4A90C47-506D-457A-B325-1D0D069536BD
Dimensions author ID	wds:Q85566689-19D3F3E5-13FA-42FF-8849-54352E250F83
ORCID iD	https://orcid.org/0000-0002-4070-7997
ORCID iD	0000-0002-4070-7997
Dimensions author ID	01172221021.14
is owl:sameAs of	Bruno Reversade
is about of	Bruno Reversade https://www.wikidata.org/wiki/Special:EntityData/Q85566689 Bruno Reversade https://fr.wikipedia.org/wiki/Bruno_Reversade
is author of	The Apelin receptor enhances Nodal/TGFβ signaling to ensure proper cardiac development. Quantitative imaging reveals real-time Pou5f3-Nanog complexes driving dorsoventral mesendoderm patterning in zebrafish ELABELA deficiency promotes preeclampsia and cardiovascular malformations in mice Structural basis of RIP2 activation and signaling Mitochondrial peptide BRAWNIN is essential for vertebrate respiratory complex III assembly Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability. Mitchell-Riley syndrome iPSC exhibit reduced pancreatic endoderm differentiation due to an RFX6 mutation Leveraging ancestry to improve causal variant identification in exome sequencing for monogenic disorders Inactivation of DRG1, encoding a translation factor GTPase, causes a recessive neurodevelopmental disorder Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology Enteroviral 3C protease activates the human NLRP1 inflammasome in airway epithelia HOX epimutations driven by maternal SMCHD1/LRIF1 haploinsufficiency trigger homeotic transformations in genetically wildtype offspring A Micropatterned Human-Specific Neuroepithelial Tissue for Modeling Gene and Drug-Induced Neurodevelopmental Defects R-spondin signalling is essential for the maintenance and differentiation of mouse nephron progenitors Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity
is author of	wds:Q59327258-2322B52F-4591-49FA-AE32-E9B1AE4261AA wds:Q90245532-1EA60852-E21D-4A6F-B6C8-1B73003BCCC5 wds:Q100503527-C0F3808B-BC67-476C-80AD-DE518D0449C0

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