About: Stephan Ripke

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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
field of work	wds:Q56959255-6E8D8487-458A-4EC0-8CEE-2BB3FC915343
field of work	statistical genetics
owl:sameAs	Stephan Ripke
description	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) ricercatore (it) 研究者 (ja) araştırmacı (tr) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) statisticus (nl)
rdfs:label	Stephan Ripke (en) Stephan Ripke (es) Stephan Ripke (nl) Stephan Ripke (sq) Stephan Ripke (ast)
skos:prefLabel	Stephan Ripke (en) Stephan Ripke (es) Stephan Ripke (nl) Stephan Ripke (sq) Stephan Ripke (ast)
name	Stephan Ripke (en) Stephan Ripke (es) Stephan Ripke (nl) Stephan Ripke (sq) Stephan Ripke (ast)
given name	wds:Q56959255-C2F82C89-3CD2-435E-BDB0-F4AB6F1ABFA7
given name	Stephan
instance of	wds:Q56959255-4F5BAE08-1479-4E6E-A390-51FACBDEECE8
instance of	Homo sapiens
Google Knowledge Graph ID	wds:Q56959255-32730738-AEEE-4CCB-A021-F520B98043B7
Google Knowledge Graph ID	http://g.co/kg/g/11h2mdsqj2
Google Knowledge Graph ID	/g/11h2mdsqj2
ResearchGate profile ID	wds:Q56959255-06FD32CC-7570-462B-B21D-753F6E379765
ResearchGate profile ID	Stephan_Ripke
Google Scholar author ID	wds:Q56959255-CAC6902A-7B13-4785-AFD7-0B31EBC67B59
Google Scholar author ID	trMrAoUAAAAJ
occupation	wds:Q56959255-12A8BD0D-4557-4A2E-A067-7ED2D2F064EC wds:Q56959255-19A45BE6-6933-46F6-997D-9A849A821BAC wds:Q56959255-F955B071-1999-4FD8-8741-D3C691B2CA4A
employer	wds:Q56959255-79DAB90C-47E9-4F08-ABA5-893805B459B7 wds:Q56959255-D4E86A22-3CB5-43D0-9A95-9C84A58C41A5 wds:Q56959255-DAC79CFC-2668-4B2B-8098-0402B24F87F2
place of birth	wds:Q56959255-A7A9ACAB-365C-438C-8FA7-347399A93612
sex or gender	wds:Q56959255-e47ea3e3-4e7c-5426-601b-f8647a745de5
VIAF ID	wds:Q56959255-b156be0e-4af9-89a7-f664-82d630e27c7f
GND ID	wds:Q56959255-4b7b71d3-80ba-44ef-ae27-930ca5be28c4
date of birth	wds:Q56959255-567830c1-47b0-4ffa-a7b4-e51ae101dafd
educated at	wds:Q56959255-2add397b-09c5-489d-83e0-ad812bd812e2 wds:Q56959255-CD2B52DB-32B9-4EA2-B19C-4EBBD461FB7D
family name	wds:Q56959255-A74165A3-8C17-4421-B92B-022628683DE0
WorldCat Identities ID (superseded)	wds:Q56959255-5BD2EB0C-6CFF-4A74-A2E7-1A31BD144C69
VIAF ID	http://viaf.org/viaf/304939559
GND ID	https://d-nb.info/gnd/1228751943
occupation	statistician researcher geneticist
employer	Broad Institute Massachusetts General Hospital Charité
place of birth	Heidelberg
sex or gender	male
VIAF ID	304939559
GND ID	1228751943
date of birth	1973-01-01 00:00:00Z (xsd:dateTime)
educated at	University of Hamburg Utrecht University
family name	Ripke
WorldCat Identities ID (superseded)	viaf-304939559
ORCID iD	wds:Q56959255-0CD21C04-096E-4DA8-BE39-00788CE4A142
ORCID iD	https://orcid.org/0000-0003-3622-835X
ORCID iD	0000-0003-3622-835X
is about of	Stephan Ripke https://www.wikidata.org/wiki/Special:EntityData/Q56959255 Stephan Ripke
is author of	Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC) Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms Seven new loci associated with age-related macular degeneration Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome Genetic studies of body mass index yield new insights for obesity biology The GABA transporter 1 (SLC6A1): a novel candidate gene for anxiety disorders Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores Polygenic Risk Score, Parental Socioeconomic Status, Family History of Psychiatric Disorders, and the Risk for Schizophrenia: A Danish Population-Based Study and Meta-analysis. Estimation of SNP heritability from dense genotype data Polymorphisms in the GAD2 gene-region are associated with susceptibility for unipolar depression and with a risk factor for anxiety disorders Most genetic risk for autism resides with common variation Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders

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