Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
In: BMC Medical Genetics 18 (2017).
- Schlagwort
-
-
Hautkrankheit
Dermatologie
- Ereignis
-
Veröffentlichung
- (wo)
-
Erlangen
- (wer)
-
Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
- (wann)
-
2017
- Urheber
-
Uebe, Steffen
Ehrlicher, Maria
Ekici, Arif Bülent
Behrens, Frank
Böhm, Beate
Homuth, Georg
Schurmann, Claudia
Völker, Uwe
Jünger, Michael
Nauck, Matthias
Völzke, Henry
Traupe, Heiko
Krawczak, Michael
Burkhardt, Harald
Reis, André
Hüffmeier, Ulrike
- URN
-
urn:nbn:de:bvb:29-opus4-88840
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
25.03.2025, 13:44 MEZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Uebe, Steffen
- Ehrlicher, Maria
- Ekici, Arif Bülent
- Behrens, Frank
- Böhm, Beate
- Homuth, Georg
- Schurmann, Claudia
- Völker, Uwe
- Jünger, Michael
- Nauck, Matthias
- Völzke, Henry
- Traupe, Heiko
- Krawczak, Michael
- Burkhardt, Harald
- Reis, André
- Hüffmeier, Ulrike
- Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
Entstanden
- 2017
Ähnliche Objekte (12)
Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder
Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder
Strategies for Genome-Wide Association Analyses of Raw Copy Number Variation Data
Strategies for genome-wide association analyses of raw copy number variation data
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals
Genome-wide analyses of stallion fertility
Genome-wide analysis of mutually exclusive splicing
Genome-wide response patterns in stressed hepatocytes
Genome-wide mapping of the inflammation methylome
Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder
Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder
Strategies for Genome-Wide Association Analyses of Raw Copy Number Variation Data
Strategies for genome-wide association analyses of raw copy number variation data
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals
Genome-wide analyses of stallion fertility
Genome-wide analysis of mutually exclusive splicing
Genome-wide response patterns in stressed hepatocytes
Genome-wide mapping of the inflammation methylome
Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder
Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder
Strategies for Genome-Wide Association Analyses of Raw Copy Number Variation Data
Strategies for genome-wide association analyses of raw copy number variation data
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals
Genome-wide analyses of stallion fertility
Genome-wide analysis of mutually exclusive splicing
Genome-wide response patterns in stressed hepatocytes