Software and data
| Year of Publication | Publication | Programmcode and/or Input data |
| 2024 | Cholecystectomy and digestive cancer in Chile: Complementary results from interrupted time series and aggregated data analyses | Programmcode |
| 2023 | Gallstones, cholecystectomy and kidney cancer: observational and mendelian randomisation results based on large cohorts | Input data – Mendelian Randomization Analysis of Gallstones and Cholecystectomy with Kidney Cancer Risk |
| 2023 | Gallbladder Cancer Risk and Indigenous South American Mapuche Ancestry: Instrumental Variable Analysis Using Ancestry-Informative Markers | Programmcode Input data |
| 2022 | Identification of circulating lncRNAs associated with gallbladder cancer risk by tissue-based preselection, cis-eQTL validation, and analysis of association with genotype-based expression | Programmcode - Identification of circulating lncRNAs associated with gallbladder cancer risk Input data - Identification of circulating lncRNAs associated with gallbladder cancer risk |
| 2021 | Robust Huber-LASSO for improved prediction of protein, metabolite, and gene expression levels relying on individual genotype data | Programmcode Robust Huber-LASSO for improved prediction of protein, metabolite and gene expression levels relying on individual genotype data |
| 2020 | Optimal selection of genetic variants for adjustment of population stratification in European association studies | Programmcode Optimal selection of genetic variants for adjustment of population stratification in European association studies |
| 2017 | Imputation of missing genotypes within LD-blocks relying on the basic coalescent and beyond | Programmcode Imputation of Missing Genotypes within LD-Blocks Relying on the Basic Coalescent and Beyond |
| 2017 | Robust logistic regression to narrow down the winner’s curse for rare and recessive susceptibility variants | Programmcode Robust Logistic Regression to Narrow Down the Winners Curse |
| 2017 | Subtypes of Native American ancestry and leading causes of death | Aggregate-data Subtypes of Native American Ancestry and Death Validation data Subtypes of Native American Ancestry and Death |
| 2014 | Tailored selection of study individuals to be sequenced in order to improve the accuracy of genotype imputation | Programmcode Tailored Selection of Study Individuals to be Sequenced in Order to Improve the Accuracy of Genotype Imputation |
| 2007 | Constraints for genetic association studies imposed by attributable fraction and familial risk | Calculation of Population attributable fraction Familial relative risk and Statistical power |