Standout Papers
- SNP Genotyping Using the Sequenom MassARRAY iPLEX Platform (2009)
- Common deletion polymorphisms in the human genome (2005)
- Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs (2008)
- De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly (2012)
Immediate Impact
9 by Nobel laureates 24 from Science/Nature 60 standout
Citing Papers
Human TKTL1 implies greater neurogenesis in frontal neocortex of modern humans than Neanderthals
2022 StandoutScienceNobel
A role of PIEZO1 in iron metabolism in mice and humans
2021 StandoutNobel
Works of Stacey B. Gabriel being referenced
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
2008 Standout
Common deletion polymorphisms in the human genome
2005 Standout
Author Peers
| Author | Last Decade | Papers | Cites | ||||
|---|---|---|---|---|---|---|---|
| Stacey B. Gabriel | 1676 | 1606 | 119 | 412 | 13 | 3.6k | |
| Huy Nguyen | 1941 | 2525 | 160 | 294 | 14 | 5.0k | |
| Matthew DeFelice | 1938 | 2344 | 166 | 504 | 7 | 5.0k | |
| Brendan Blumenstiel | 2064 | 2358 | 166 | 626 | 12 | 5.3k | |
| J Ott | 2059 | 2191 | 196 | 158 | 8 | 4.4k | |
| Giulio Genovese | 2511 | 1774 | 169 | 419 | 66 | 6.5k | |
| Nathalie Drouot | 1837 | 1400 | 89 | 242 | 36 | 3.4k | |
| Jin Yu | 2961 | 2959 | 201 | 738 | 15 | 5.7k | |
| Jennifer L. Moran | 2636 | 2252 | 151 | 264 | 62 | 4.7k | |
| Chang-En Yu | 2852 | 743 | 37 | 357 | 34 | 4.7k | |
| Sabine Fauré | 1889 | 1124 | 583 | 173 | 9 | 3.3k |
All Works
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