Additional file 1: of Coronary risk in relation to genetic variation in MEOX2 and TCF15 in a Flemish population ...

Table S1. Common tagging SNPs in MEOX2. Table S2. MEOX2 and TCF15 SNPs and allele and genotype frequencies in unrelated founders. Table S3. MEOX2 and TCF15 allele and genotype frequencies in 2027 analysed participants. Table S4. Sex- and age-standardised CHD rates by MEOX2 SNPs. Table S5. Hazard ratios for CHD by MEOX2 SNPs in participants free of CHD at baseline. Table S6. Sex- and age-standardised CHD rates by MEOX2 haplotypes. Table S7. Hazard ratios for CHD by MEOX2 haplotypes reconstructed while accounting for pedigree information. Table S8. Hazard ratios for CHD by MEOX2 haplotypes in pa... Mehr ...

Verfasser: Yang, Wen-Yi
Petit, Thibault
Lutgarde Thijs
Zhang, Zhen-Yu
Jacobs, Lotte
Hara, Azusa
Wei, Fang-Fei
Salvi, Erika
Citterio, Lorena
Carpini, Simona Delli
Gu, Yu-Mei
Knez, Judita
Cauwenberghs, Nicholas
Barcella, Matteo
Barlassina, Cristina
Manunta, Paolo
Coppiello, Giulia
Aranguren, Xabier
Kuznetsova, Tatiana
Cusi, Daniele
Verhamme, Peter
Luttun, Aernout
Staessen, Jan
Dokumenttyp: Scholarlyarticle
Erscheinungsdatum: 2015
Verlag/Hrsg.: Figshare
Schlagwörter: Space Science / Medicine / Genetics / FOS: Biological sciences / Neuroscience / Pharmacology / Biotechnology / Evolutionary Biology / 69999 Biological Sciences not elsewhere classified / 111714 Mental Health / FOS: Health sciences
Sprache: unknown
Permalink: https://search.fid-benelux.de/Record/base-29060262
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : https://dx.doi.org/10.6084/m9.figshare.c.3623990_d1.v1

Table S1. Common tagging SNPs in MEOX2. Table S2. MEOX2 and TCF15 SNPs and allele and genotype frequencies in unrelated founders. Table S3. MEOX2 and TCF15 allele and genotype frequencies in 2027 analysed participants. Table S4. Sex- and age-standardised CHD rates by MEOX2 SNPs. Table S5. Hazard ratios for CHD by MEOX2 SNPs in participants free of CHD at baseline. Table S6. Sex- and age-standardised CHD rates by MEOX2 haplotypes. Table S7. Hazard ratios for CHD by MEOX2 haplotypes reconstructed while accounting for pedigree information. Table S8. Hazard ratios for CHD by MEOX2 haplotypes in participants free of CHD at baseline. Table S9. Baseline characteristics of participants without blood left for genotyping compared with those included in the analyses. Figure S1. Plot of the MEOX2 gene and flanking regions on chromosome 7. Figure S2. Plot of the TCF15 gene and flanking regions on chromosome 20. Figure S3. Interaction between TCF15 rs12624577 and MEOX2 rs4532497. Figure S4. Incidence of coronary ...