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Kühnisch, J.* ; Thiering, E. ; Heitmüller, D.* ; Tiesler, C.M. ; Grallert, H. ; Heinrich-Weltzien, R.* ; Hickel, R.* ; Heinrich, J. ; GINI-10 plus Study Group (Wichmann, H.-E. ; Heinrich, J. ; Sausenthaler, S. ; Zutavern, A. ; Chen, C.-M. ; Schnappinger, M. ; Rzehak, P.) ; LISA-10 plus Study Group (Wichmann, H.-E. ; Heinrich, J. ; Sausenthaler, S. ; Chen, C.-M. ; Schnappinger, M.)

Genome-Wide Association Study (GWAS) for Molar-Incisor Hypomineralization (MIH).

Clin. Oral Investig. 18, 677-682 (2014)
DOI PMC
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
OBJECTIVES: This genome-wide association study (GWAS) investigated the relationship between molar-incisor hypomineralization (MIH) and possible genetic loci. Clinical and genetic data from the 10-year follow-up of 668 children from the Munich GINI-plus and LISA-plus birth cohort studies were analyzed. MATERIAL AND METHODS: The dental examinations included the diagnosis of MIH according to the criteria of the European Academy of Paediatric Dentistry (EAPD). Children with MIH were categorized as those with a minimum of one hypomineralized first permanent molar. A GWAS was implemented following a quality-control step and an additive genetic effect was assumed. RESULTS: A total of 2,013,491 single-nucleotide polymorphisms (SNPs) were available for analysis. Rs13058467, which is located near the SCUBE1 gene on chromosome 22 (p < 3.72E-7), was identified as a possible locus linked to MIH when using a threshold of p value <1E-6. CONCLUSIONS: After considering the limitations of the present study (e.g., limited sample size and lack of an independent replication sample), it can be concluded that (1) replication analyses in an independent cohort study are strongly recommended and (2) large-scale and well-powered studies are needed to investigate a possible genetic link to MIH.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Genetics; GWAS; Dental anomaly; developmental disorder; Birth cohort study; Epidemiology; Genetic-basis; Inherited Anomalies; Molecular-genetics; Tooth Development; Morphogenesis; Scube1; Teeth; Mouse
Sprache englisch
Veröffentlichungsjahr 2014
Prepublished im Jahr 2013
HGF-Berichtsjahr 2013
ISSN (print) / ISBN 1432-6981
e-ISSN 1436-3771
Zeitschrift Clinical Oral Investigations
Quellenangaben Band: 18, Heft: 2, Seiten: 677-682 Artikelnummer: , Supplement: ,
Verlag Springer
Verlagsort Heidelberg
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Epidemiology (EPI)
Research Unit Molecular Epidemiology (AME)
POF Topic(s) 30503 - Chronic Diseases of the Lung and Allergies
30501 - Systemic Analysis of Genetic and Environmental Factors that Impact Health
Forschungsfeld(er) Genetics and Epidemiology
PSP-Element(e) G-503900-001
G-504200-002
PubMed ID 23918034
DOI 10.1007/s00784-013-1054-8
WOS ID WOS:000332317500040
Scopus ID 84894558165
Erfassungsdatum 2013-08-12
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