GD
| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome | Genome research |  | 2013 | 714 | 518 | ||
| Transcriptional and post-transcriptional profile of human chromosome 21 | Genome research |  | 2009 | 676 | 0 | ||
| Specific BACE1 genotypes provide additional risk for late-onset Alzheimer disease in APOE epsilon 4 carriers | American journal of medical genetics. Part B, Neuropsychiatric genetics | | 2003 | 536 | 1 | ||
| Isolation of the human BACH1 transcription regulator gene, which maps to chromosome 21q22.1 | Human genetics | | 1998 | 527 | 0 | ||
| Mapping of the human holocarboxylase synthetase gene (HCS) to the Down syndrome critical region of chromosome 21q22 | Annales de génétique | 1996 | 564 | 0 | |||
| Mapping of the gene for the p60 subunit of the human chromatin assembly factor (CAF1A) to the Down syndrome region of chromosome 21 | Genomics | | 1996 | 521 | 0 |
