Standout Papers
- PhenoScanner V2: an expanded tool for searching human genotype–phenotype associations (2019)
- PhenoScanner: a database of human genotype–phenotype associations (2016)
- A robust and efficient method for Mendelian randomization with hundreds of genetic variants (2020)
- A fast and efficient colocalization algorithm for identifying shared genetic risk factors across multiple traits (2021)
Immediate Impact
5 from Science/Nature 70 standout
Citing Papers
Global Effect of Cardiovascular Risk Factors on Lifetime Estimates
2025 Standout
Mass-spectrometry-based proteomics: from single cells to clinical applications
2025 StandoutNature
Works of James R Staley being referenced
PhenoScanner V2: an expanded tool for searching human genotype–phenotype associations
2019 Standout
PhenoScanner: a database of human genotype–phenotype associations
2016 Standout
Author Peers
| Author | Last Decade | Papers | Cites | ||||
|---|---|---|---|---|---|---|---|
| James R Staley | 855 | 1465 | 226 | 458 | 17 | 3.1k | |
| Veronika Skrivankova | 630 | 1041 | 114 | 419 | 12 | 2.6k | |
| Benjamin Woolf | 682 | 1125 | 127 | 459 | 39 | 2.9k | |
| Allan Motyer | 1151 | 2113 | 205 | 439 | 14 | 4.3k | |
| Niki Dimou | 820 | 1204 | 135 | 509 | 40 | 3.5k | |
| Praveen Surendran | 693 | 1040 | 103 | 329 | 25 | 2.3k | |
| Vanessa Y. Tan | 1182 | 2169 | 220 | 674 | 12 | 4.4k | |
| Mark Effingham | 1155 | 2113 | 210 | 447 | 7 | 4.2k | |
| Charles Laurin | 1222 | 2479 | 262 | 704 | 14 | 4.7k | |
| Valeriia Haberland | 1161 | 2138 | 217 | 659 | 7 | 4.2k | |
| Ryan Langdon | 1364 | 2281 | 336 | 722 | 21 | 4.8k |
All Works
Login with ORCID to disown or claim papers
Loading papers...