Standout Papers
- The MR-Base platform supports systematic causal inference across the human phenome (2018)
- LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis (2016)
- Use of genetic variation to separate the effects of early and later life adiposity on disease risk: mendelian randomisation study (2020)
- Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation (2022)
Immediate Impact
12 from Science/Nature 61 standout
Citing Papers
Trans-ancestry genome-wide study of depression identifies 697 associations implicating cell types and pharmacotherapies
2025 Standout
A comprehensive spatio-cellular map of the human hypothalamus
2025 StandoutNature
Works of Benjamin Elsworth being referenced
Use of genetic variation to separate the effects of early and later life adiposity on disease risk: mendelian randomisation study
2020 Standout
The MR-Base platform supports systematic causal inference across the human phenome
2018 Standout
Author Peers
| Author | Last Decade | Papers | Cites | ||||
|---|---|---|---|---|---|---|---|
| Benjamin Elsworth | 1519 | 2696 | 428 | 781 | 25 | 5.4k | |
| Ryan Langdon | 1364 | 2281 | 413 | 722 | 21 | 4.8k | |
| Marie Verbanck | 1387 | 2373 | 377 | 853 | 19 | 5.3k | |
| Denis Baird | 1265 | 2474 | 350 | 759 | 16 | 4.8k | |
| Charles Laurin | 1222 | 2479 | 310 | 704 | 14 | 4.7k | |
| Fabiola Del Greco M | 1520 | 3037 | 420 | 958 | 38 | 6.3k | |
| Damjan Vukcevic | 2034 | 3097 | 420 | 620 | 19 | 6.2k | |
| Vanessa Y. Tan | 1182 | 2169 | 343 | 674 | 12 | 4.4k | |
| James Yarmolinsky | 1658 | 3035 | 570 | 1022 | 30 | 6.6k | |
| Hashem A. Shihab | 2902 | 3346 | 707 | 752 | 23 | 6.8k | |
| Adrián Cortés | 1588 | 2468 | 303 | 569 | 30 | 5.7k |
All Works
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