dc.contributor.author | MOLLOY, ANNE | en |
dc.date.accessioned | 2015-12-09T11:29:53Z | |
dc.date.available | 2015-12-09T11:29:53Z | |
dc.date.issued | 2012 | en |
dc.date.submitted | 2012 | en |
dc.identifier.citation | Minguzzi S, Molloy AM, Peadar K, Mills J, Scott JM, Troendle J, Pangilinan F, Brody L, Parle-McDermott A, Genotyping of a tri-allelic polymorphism by a novel melting curve assay in MTHFD1L: an association study of nonsyndromic Cleft in Ireland., BMC medical genetics, 13, 2012, 29 | en |
dc.identifier.issn | 1471-2350 | en |
dc.identifier.other | Y | en |
dc.description | PUBLISHED | en |
dc.description.abstract | Background:
Polymorphisms within the
MTHFD1L
gene were previously associated with risk of neural tube defects
in Ireland. We sought to test the most significant
MTHFD1L
polymorphisms for an association with risk of cleft in an
Irish cohort. This required the development of a new melting curve assay to genotype the technically challenging
MTHFD1L
triallelic deletion/insertion polymorphism (rs3832406).
Methods:
Melting curve analysis was used to genotype the
MTHFD1L
triallelic deletion/insertion polymorphism
(rs3832406) and a Single Nucleotide Polymorphism rs17080476 in an Irish cohort consisting of 981 Irish case-parent
trios and 1,008 controls. Tests for association with nonsyndromic cleft lip with or without cleft palate and cleft
palate included case/control analysis, mother/control analysis and Transmission Disequilibrium Tests of case-parent
trios.
Results:
A successful melting curve genotyping assay was developed for the deletion/insertion polymorphism
(rs3832406). The TDT analysis initially showed that the rs3832406 polymorphism was associated with isolated cleft
lip with or without cleft palate. However, corrected p-values indicated that this association was not significant.
Conclusions:
Melting Curve Analysis can be employed to successfully genotype challenging polymorphisms such
as the
MTHFD1L
triallelic deletion/insertion polymorphism (DIP) reported here (rs3832406) and is a viable alternative
to capillary electrophoresis. Corrected p-values indicate no association between
MTHFD1L
and risk of cleft in an Irish
cohort | en |
dc.description.sponsorship | This work was supported by the IRCSET Embark initiative. The authors
sincerely thank all the patients and families who participated in the study,
the Cleft Lip and Palate Association of Ireland, and the Dublin Cleft Centre
team. Recruitment of the Irish cleft cohort was supported by the Intramural
Research Program of the Eunice Kennedy Shriver National Institute of Child
Health and Human Development and the Health Research Board of Ireland. | en |
dc.format.extent | 29 | en |
dc.relation.ispartofseries | BMC medical genetics | en |
dc.relation.ispartofseries | 13 | en |
dc.rights | Y | en |
dc.subject | MTHFD1L gene | en |
dc.subject.lcsh | MTHFD1L gene | en |
dc.title | Genotyping of a tri-allelic polymorphism by a novel melting curve assay in MTHFD1L: an association study of nonsyndromic Cleft in Ireland. | en |
dc.type | Journal Article | en |
dc.type.supercollection | scholarly_publications | en |
dc.type.supercollection | refereed_publications | en |
dc.identifier.peoplefinderurl | http://people.tcd.ie/amolloy | en |
dc.identifier.rssinternalid | 84419 | en |
dc.identifier.doi | http://dx.doi.org/10.1186/1471-2350-13-29 | en |
dc.rights.ecaccessrights | openAccess | |
dc.subject.TCDTheme | Genes & Society | en |
dc.identifier.orcid_id | 0000-0002-1688-9049 | en |
dc.identifier.uri | http://hdl.handle.net/2262/75128 | |