Year of Publication | Publication | Programmcode and/or Input data |
| under review | Mendelian Randomization Analysis of the Relationship between Native American Ancestry and Gallbladder Cancer Risk | Programmcode - Mendelian Randomization Analysis of the Relationship between Native American Ancestry and Gallbladder Cancer Risk
Input data - Mendelian Randomization Analysis of the Relationship between Native American Ancestry and Gallbladder Cancer Risk |
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 |
