Matthew Zawistowski

发表

Leveraging summary statistics to make inferences about complex phenotypes in large biobanks

Nathan L. Tintle, Jason Westra, Angela Gasdaska, 2018, PSB.

Corrected ROC analysis for misclassified binary outcomes.

Matthew Zawistowski, Jeremy B Sussman, Rodney A Hayward, 2017, Statistics in medicine.

Exploring Various Polygenic Risk Scores for Basal Cell Carcinoma, Cutaneous Squamous Cell Carcinoma and Melanoma in the Phenomes of the Michigan Genomics Initiative and the UK Biobank

Bhramar Mukherjee, Gonçalo R. Abecasis, Stephanie E. Moser, 2018 .

Methods for Association Analysis and Meta‐Analysis of Rare Variants in Families

Francesco Cucca, Dajiang J Liu, Matthew Zawistowski, 2015, Genetic epidemiology.

A Geometric Framework for Evaluating Rare Variant Tests of Association

Matthew Zawistowski, Shannon Fast, Keli Liu, 2013, Genetic epidemiology.

The influence of genomic context on mutation patterns in the human genome inferred from rare variants

John Novembre, Daniel Wegmann, Sebastian Zöllner, 2013, Genome research.

Extending rare-variant testing strategies: analysis of noncoding sequence and imputed genotypes.

Yun Li, Sebastian Zöllner, Shyam Gopalakrishnan, 2010, American journal of human genetics.

Exploring Various Polygenic Risk Scores for Skin Cancer in the Phenomes of the Michigan Genomics Initiative and the UK Biobank with a Visual Catalog: PRSWeb

Bhramar Mukherjee, Gonçalo R. Abecasis, Stephanie E. Moser, 2018, bioRxiv.

A Coalescent Model for Genotype Imputation

Noah A. Rosenberg, Ethan M. Jewett, Sebastian Zöllner, 2012, Genetics.