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Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|April 10, 2023
Systematic assays and resources for the functional annotation of non-coding variantsMartin Kircher, Kerstin U LudwigGenome Biology|August 18, 2009
Improved base calling for the Illumina Genome Analyzer using machine learning strategiesMartin Kircher, Udo Stenzel, Janet KelsoBMC Genomics|July 25, 2008
Structural conservation versus functional divergence of maternally expressed microRNAs in the Dlk1/Gtl2 imprinting regionMartin Kircher, Christoph Bock, Martina PaulsenGigascience|April 21, 2023
The Regulatory Mendelian Mutation score for GRCh38Max Schubach, Lusiné Nazaretyan, Martin KircherNucleic Acids Research|October 25, 2011
Double indexing overcomes inaccuracies in multiplex sequencing on the Illumina platformMartin Kircher, Susanna Sawyer, Matthias MeyerGenome Medicine|August 4, 2025
varCADD: large sets of standing genetic variation enable genome-wide pathogenicity predictionLusiné Nazaretyan, Philipp Rentzsch, Martin KircherBMC Genomics|August 2, 2011
Addressing challenges in the production and analysis of illumina sequencing dataMartin Kircher, Patricia Heyn, Janet KelsoAACN Clinical Issues|May 16, 2002
Restraint use in acute and critical care settings: changing practiceBeth MartinAACN Advanced Critical Care|May 3, 2007
Prevention of gastrointestinal complications in the critically ill patientBeth MartinPageof 16