Standout Papers
- The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data (2010)
- A framework for variation discovery and genotyping using next-generation DNA sequencing data (2011)
- Absolute quantification of somatic DNA alterations in human cancer (2012)
- Whole-organism lineage tracing by combinatorial and cumulative genome editing (2016)
- Genomic sequencing of meningiomas identifies oncogenic SMO and AKT1 mutations (2013)
- Whole-exome sequencing identifies a recurrent NAB2-STAT6 fusion in solitary fibrous tumors (2013)
- Simultaneous single-cell profiling of lineages and cell types in the vertebrate brain (2018)
- Single-cell lineage tracing of metastatic cancer reveals selection of hybrid EMT states (2021)
Immediate Impact
3 by Nobel laureates 61 from Science/Nature 103 standout
Citing Papers
Y chromosome loss in cancer drives growth by evasion of adaptive immunity
2023 StandoutNature
CRISPR technology: A decade of genome editing is only the beginning
2023 StandoutScienceNobel
Works of Aaron McKenna being referenced
Massively parallel profiling and predictive modeling of the outcomes of CRISPR/Cas9-mediated double-strand break repair
2019
Simultaneous single-cell profiling of lineages and cell types in the vertebrate brain
2018 Standout
Author Peers
| Author | Last Decade | Papers | Cites | |||
|---|---|---|---|---|---|---|
| Aaron McKenna | 14055 | 4826 | 10495 | 26 | 27.8k | |
| Kristian Cibulskis | 13198 | 4695 | 10389 | 21 | 26.7k | |
| Kiran Garimella | 14092 | 4302 | 12020 | 45 | 29.0k | |
| Andrey Sivachenko | 14768 | 4294 | 10618 | 48 | 28.0k | |
| Andrew Kernytsky | 12510 | 3728 | 10073 | 12 | 24.9k | |
| Eric Banks | 18118 | 5181 | 17798 | 29 | 39.1k | |
| Mark A. DePristo | 19141 | 5142 | 17599 | 22 | 41.7k | |
| Mark Chaisson | 19583 | 4503 | 4181 | 30 | 30.9k | |
| Julian Maller | 10767 | 2656 | 17518 | 15 | 34.8k | |
| Davis J. McCarthy | 20482 | 6059 | 3976 | 37 | 34.2k | |
| Carrie Davis | 20105 | 5203 | 3773 | 22 | 31.5k |
All Works
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