The DOI matches its Crossref record; 61 of the 62 references it cites were found in a registry or an index.
Instrumental Variables Estimation With Some Invalid Instruments and its Application to Mendelian Randomization.
Abstract
Instrumental variables have been widely used for estimating the causal effect between exposure and outcome. Conventional estimation methods require complete knowledge about all the instruments’ validity; a valid instrument must not have a direct effect on the outcome and not be related to unmeasured confounders. Often, this is impractical as highlighted by Mendelian randomization studies where genetic markers are used as instruments and complete knowledge about instruments’ validity is equivalent to complete knowledge about the involved genes’ functions. In this article, we propose a method for estimation of causal effects when this complete knowledge is absent. It is shown that causal effects are identified and can be estimated as long as less than 50% of instruments are invalid, without knowing which of the instruments are invalid. We also introduce conditions for identification when the 50% threshold is violated. A fast penalized ℓ1 estimation method, called sisVIVE, is introduced for estimating the causal effect without knowing which instruments are valid, with theoretical guarantees on its performance. The proposed method is demonstrated on simulated data and a real Mendelian randomization study concerning the effect of body mass index(BMI) on health-related quality of life (HRQL) index. An R package sisVIVE is available on CRAN. Supplementary materials for this article are available online.
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“Variable selection and dimension reduction approaches have been proposed to maximize the proportion of variance in the exposure explained by the selected variants while avoiding instability due to multicollinearity 63 .”
From Guidelines for performing Mendelian randomization investigations (2020) · cites this paper as [63]
Citations
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Bowden, J., Davey Smith, G., & Burgess, S. (2015) · International Journal of Epidemiology · doi:10.1093/ije/dyv080 · Cited by 9,816
Bowden, J., Davey Smith, G., Haycock, P. C., & Burgess, S. (2016) · Genetic Epidemiology · doi:10.1002/gepi.21965 · Cited by 8,922
The MR-Base platform supports systematic causal inference across the human phenome
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Metadata
- Authors
- Kang, H., Zhang, A., Cai, T. T., & Small, D. S.
- Venue
- Journal of the American Statistical Association
- Publisher
- Informa UK Limited
- Published
- 2016-01-02
- Volume
- 111
- Issue
- 513
- Pages
- 132-144
- ISSN
- 0162-1459 (ISSN-L)
- 1537-274X
- OpenAlex
- W1991587639
- Cited by
- 265
- References
- 62
- Citations by year
- 2026: 16 · 2025: 20 · 2024: 28 · 2023: 27 · 2022: 29 · 2021: 18 · 2020: 35 · 2019: 26 · 2018: 26 · 2017: 14 · 2016: 16
- FWCI
- 19.10
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of the American Statistical Association (publishedVersion)
- ScholarlyCommons (University of Pennsylvania) (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Topics
- Physical Sciences › Mathematics › Statistics and Probability › Advanced Causal Inference Techniques
- Physical Sciences › Mathematics › Statistics and Probability › Statistical Methods and Inference
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Keywords
- instrumental variables, invalid instruments, Mendelian randomization, causal effect estimation, causal identification, genetic instruments, body mass index, health-related quality of life, unmeasured confounding
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