Dependent data methods are widely used in practice to conduct analyses for hierarchical and longitudinal studies. Formally, their use depends on a variety of assumptions, for example, parametric distributional assumptions or assumptions about the sampling mechanism. The overarching goal of our research program is to quantify sensitivity to these assumptions, identifying scenarios in which they are and are not important and developing new, more robust methods when necessary. Our focus is on assumptions surrounding the sampling mechanism, including missing data and outcome dependent sampling. Our research has four aims.
Our first aim considers the performance of commonly used methods that are used to avoid cluster level confounding. However, they may be sensitive to data which are missing at random (MAR), but not missing completely at random (MCAR).
Aims 2 through 4 consider outcome dependent sampling mechanisms that are frequently encountered in practice.
In Aim 2 we consider the use of parametric mixed models in situations such as for outcome dependent family studies.
Aim 3 considers the situation in which the timing of measurements may be dependent on previous results (e.g., more frequent exams in prostate cancer patients with rising prostate specific antigen (PSA) test results).
Aim 4 considers a general and unifying context in which to imbed the work on Aims 2 and 3, derive optimality results, and develop a platform for creation of new statistical methods for outcome dependent sampling. Results from our research will directly inform current statistical practice for these commonly used methods.
Longitudinal and dependent data analysis methods are used in a wide variety of biomedical research investigations. If the assumptions on which the models are based are incorrect in important ways, it could give rise to misleading research conclusions. Knowing for which assumptions the results are sensitive and by how much is important to their proper use.
|McCulloch, Charles E; Neuhaus, John M; Olin, Rebecca L (2016) Biased and unbiased estimation in longitudinal studies with informative visit processes. Biometrics 72:1315-1324|
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|McCulloch, Charles E; Neuhaus, John M (2011) Prediction of random effects in linear and generalized linear models under model misspecification. Biometrics 67:270-9|
|Neuhaus, John M; McCulloch, Charles E (2011) The effect of misspecification of random effects distributions in clustered data settings with outcome-dependent sampling. Can J Stat 39:488-497|
|Neuhaus, John M; McCulloch, Charles E; Boylan, Ross (2010) A Note on Type II Error Under Random Effects Misspecification in Generalized Linear Mixed Models. Biometrics :|
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