| Steven C et al (2009) |
114 TOF Trios 398 TOF |
Affymetrix Human Genome Wide SNP Array 6.0 |
PRKAB2, CHDIL, BCL9, GJA5 |
potential TOF candidate gene |
| Douglas C Bittel et al (2011) |
19 TOF |
Applied Microarrays Inc. CodeLink Human Whole Genome Bioarray |
A2BP1, VEGF, NPPA, NPPB, |
potential relevance for TOF |
| Amy Rodemoyer et al (2011) |
16 TOF |
Affymetrix Human Exon 1.0 ST v2 |
NEFH, SST, TF, KRT6A, KRT7, NTRK2, MYL2, PPBP, NRGN, APOC3
|
dysregulated network in TOF |
| Goodship et al (2012) |
362 TOF |
SEQUENOM MALDI-TOF |
PTPN11 |
risk allele for TOF |
| Candice K et al (2012) |
433 TOF |
Affymetrix Genome-Wide Human SNP Array 6.0 |
GJA5, PLXNA2 |
potential TOF candidate gene |
| Rachel Soemedi et al (2012) |
283 TOF Trios |
Illumina 660W SNP Array 6.0 |
GJA5, HAND2, EDIL3, CNOT6 |
potential TOF candidate gene |
| Heather J.Cordell et al (2013) |
798 TOF |
Illumina 600W QUAD array |
PTPN11, GPC5, NRP1 |
risk allele for TOF |
| Marcel Grunert et al (2014) |
22 TOF |
NimbleGen sequence capture 365K array Genome Sequencer FLX Illumina Genome Analyzer |
deleterious SNPs in BARX1, BCCIP, DAG1, EDN1, FANCL, FANCM, FMR1, FOXK1, HCN2, MYOM2, PEX6, ROCK1, TCEB3, TP53BP2, TTN, WBSCR16
|
imbalance of functional networks in TOF |
| Tan ZP et al (2015) |
1 TOF |
Illumina Hiseq2000 |
SCN5A |
a possible cause of TOF |
| LaHaye S et al (2016) |
2 TOF |
Illumina Hiseq2000 |
MYBPC3, SOS1 |
uncertain significance |
