Mastodon
Kliniken &… Institute Medizinische… Forschung Arbeitsgruppen Statistical… Software and Data

Software and data

Year of PublicationPublicationProgrammcode and/or Input data
2024Cholecystectomy and digestive cancer in Chile: Complementary results from interrupted time series and aggregated data analysesProgrammcode

 
2023Gallstones, cholecystectomy and kidney cancer: observational and mendelian randomisation results based on large cohortsInput data – Mendelian Randomization Analysis of Gallstones and Cholecystectomy with Kidney Cancer Risk
2023Gallbladder Cancer Risk and Indigenous South American Mapuche Ancestry: Instrumental Variable Analysis Using Ancestry-Informative MarkersProgrammcode 
Input data
2022Identification of circulating lncRNAs associated with gallbladder cancer risk by tissue-based preselection, cis-eQTL validation, and analysis of association with genotype-based expressionProgrammcode - Identification of circulating lncRNAs associated with gallbladder cancer risk
Input data - Identification of circulating lncRNAs associated with gallbladder cancer risk
2021Robust Huber-LASSO for improved prediction of protein, metabolite, and gene expression levels relying on individual genotype dataProgrammcode Robust Huber-LASSO for improved prediction of protein, metabolite and gene expression levels relying on individual genotype data
2020Optimal selection of genetic variants for adjustment of population stratification in European association studiesProgrammcode Optimal selection of genetic variants for adjustment of population stratification in European association studies
2017Imputation of missing genotypes within LD-blocks relying on the basic coalescent and beyondProgrammcode Imputation of Missing Genotypes within LD-Blocks Relying on the Basic Coalescent and Beyond
2017Robust logistic regression to narrow down the winner’s curse for rare and recessive susceptibility variantsProgrammcode Robust Logistic Regression to Narrow Down the Winners Curse
2017Subtypes 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

2014Tailored selection of study individuals to be sequenced in order to improve the accuracy of genotype imputationProgrammcode Tailored Selection of Study Individuals to be Sequenced in Order to Improve the Accuracy of Genotype Imputation
2007Constraints for genetic association studies imposed by attributable fraction and familial riskCalculation of Population attributable fraction Familial relative risk and Statistical power