| The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome | Genome research |  | | 2013 | 751 | 688 |
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| Transcriptional and post-transcriptional profile of human chromosome 21 | Genome research |  | | 2009 | 719 | 0 |
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| 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 | 568 | 1 |
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| Isolation of the human BACH1 transcription regulator gene, which maps to chromosome 21q22.1 | Human genetics | | | 1998 | 552 | 0 |
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| Mapping of the human holocarboxylase synthetase gene (HCS) to the Down syndrome critical region of chromosome 21q22 | Annales de génétique | | | 1996 | 602 | 0 |
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| 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 | 550 | 0 |
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