About: Stéphanie Baulac

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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) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) wetenschapper (nl) дослідниця (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtuese (sq) ricercatrice (it)
rdfs:label	Stéphanie Baulac (en) Stéphanie Baulac (es) Stéphanie Baulac (fr) Stéphanie Baulac (nl) Stéphanie Baulac (sl) Stéphanie Baulac (ast)
skos:prefLabel	Stéphanie Baulac (en) Stéphanie Baulac (es) Stéphanie Baulac (fr) Stéphanie Baulac (nl) Stéphanie Baulac (sl) Stéphanie Baulac (ast)
name	Stéphanie Baulac (en) Stéphanie Baulac (es) Stéphanie Baulac (fr) Stéphanie Baulac (nl) Stéphanie Baulac (sl) Stéphanie Baulac (ast)
given name	wds:Q47402324-70BD48CB-50D4-4C44-A772-AB753743D893
given name	Stéphanie
instance of	wds:Q47402324-336ED9EE-0658-40EF-B7F7-33E2FB8118C8
instance of	Homo sapiens
Loop ID	wds:Q47402324-B346D723-B0D2-486E-BBC9-4762A84B979F
Loop ID	559375
doctoral student	wds:Q47402324-21465FED-7455-491B-8BE0-5579A96223BE
doctoral student	Alexandre Carpentier
occupation	wds:Q47402324-49C448AC-B8F0-4800-A508-5064EC8E46C1
employer	wds:Q47402324-DD4EA118-8792-49C6-976A-493BE0E4E1D7
sex or gender	wds:Q47402324-E446C9E2-789B-40B5-8D58-CE9114DD88F8
ISNI	wds:Q47402324-81A39F49-709E-4A95-9E2C-AD36F0304008 wds:Q47402324-D3EAE1E8-996B-4386-A0A4-2FF7715DA1CC
VIAF ID	wds:Q47402324-0DBCEEF1-A4CD-4A4C-9330-91B102B0BC83 wds:Q47402324-60497340-CF2B-417B-902E-770729FE0FB3
Bibliothèque nationale de France ID	wds:Q47402324-9FB247DB-79B3-4104-9C6E-BC8576E27209
IdRef ID	wds:Q47402324-79029526-9E2E-4672-8F6D-CD63346220BE wds:Q47402324-A730984E-712D-4912-B482-48D6C53EF6CC
Persée author ID	wds:Q47402324-D35D555F-D1A5-4C21-8976-864F6B08D8C2
date of birth	wds:Q47402324-E6524A99-E84A-42C7-B762-A75B97E7D7BC
educated at	wds:Q47402324-CFC7602E-B151-4753-9568-E81447609AE5
WorldCat Identities ID (superseded)	wds:Q47402324-A18E5DDC-28E7-4036-BA85-799D68D2DF29
VIAF ID	http://viaf.org/viaf/129743 http://viaf.org/viaf/219297397
Bibliothèque nationale de France ID	http://data.bnf.fr/ark:/12148/cb125884480#about
IdRef ID	http://www.idref.fr/059711310/id http://www.idref.fr/074176234/id
Persée author ID	http://data.persee.fr/person/70835
occupation	researcher
employer	Brain and Spine Institute
sex or gender	female organism
ISNI	0000000006496239 0000000359599866
VIAF ID	129743 219297397
Bibliothèque nationale de France ID	125884480
IdRef ID	059711310 074176234
Persée author ID	70835
date of birth	1975-01-01 00:00:00Z (xsd:dateTime)
educated at	Paris Descartes University
WorldCat Identities ID (superseded)	viaf-219297397
ORCID iD	wds:Q47402324-CAB00456-17EF-4990-8A6F-F385D717D3B2
ORCID iD	https://orcid.org/0000-0001-6430-4693
ORCID iD	0000-0001-6430-4693
ResearcherID	wds:Q47402324-C1FB6A0C-0774-4F6D-87E3-2AF774A05FBE
ResearcherID	O-2099-2016
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q47402324
is author of	Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene Dominant partial epilepsies: A clinical, electrophysiological and genetic study of 19 European families De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2 Dimerization of Parkinson's disease-causing DJ-1 and formation of high molecular weight complexes in human brain. Mutations of DEPDC5 cause autosomal dominant focal epilepsies De novo mutations in HCN1 cause early infantile epileptic encephalopathy DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy. GABAA Receptor 2 Subunit Mutations Linked to Human Epileptic Syndromes Differentially Affect Phasic and Tonic Inhibition Fever, genes, and epilepsy Mutations and deletions in PCDH19 account for various familial or isolated epilepsies in females A rat model for LGI1-related epilepsies Increased DJ-1 expression under oxidative stress and in Alzheimer's disease brains Role of the phosphoinositide phosphatase FIG4 gene in familial epilepsy with polymicrogyria Zebrafish lacking Alzheimer presenilin enhancer 2 (Pen-2) demonstrate excessive p53-dependent apoptosis and neuronal loss. New locus for febrile seizures with absence epilepsy on 3p and a possible modifier gene on 18p. Functional gamma-secretase complex assembly in Golgi/trans-Golgi network: interactions among presenilin, nicastrin, Aph1, Pen-2, and gamma-secretase substrates Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy

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