Author details

Full Name

Dominik Glodzik

Affiliation

ORCID

Career Start Year

2011

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36944408	Detection of Biallelic Loss of DNA Repair Genes in Formalin-Fixed, Paraffin-Embedded Tumor Samples Using a Novel Tumor-Only Sequencing Panel.	J Mol Diagn	2023
37914857	Chromoscope: interactive multiscale visualization for structural variation in human genomes.	Nat Methods	2023
37812025	Subclonal Somatic Copy-Number Alterations Emerge and Dominate in Recurrent Osteosarcoma.	Cancer Res	2023
36711976	Subclonal somatic copy number alterations emerge and dominate in recurrent osteosarcoma.	bioRxiv	2023
35469014	Functional patient-derived organoid screenings identify MCLA-158 as a therapeutic EGFR Ã¿ LGR5 bispecific antibody with efficacy in epithelial tumors.	Nat Cancer	2022
35585047	Feasibility of whole genome and transcriptome profiling in pediatric and young adult cancers.	Nat Commun	2022
35122044	Author Correction: A practical framework and online tool for mutational signature analyses show intertissue variation and driver dependencies.	Nat Cancer	2020
32320050	11p15.5 epimutations in children with Wilms tumor and hepatoblastoma detected in peripheral blood.	Cancer	2020
32118208	A practical framework and online tool for mutational signature analyses show inter-tissue variation and driver dependencies.	Nat Cancer	2020
33392515	Revealing the impact of structural variants in multiple myeloma.	Blood Cancer Discov	2020
33106634	Cancer therapy shapes the fitness landscape of clonal hematopoiesis.	Nat Genet	2020
32719340	Comprehensive molecular comparison of BRCA1 hypermethylated and BRCA1 mutated triple negative breast cancers.	Nat Commun	2020
30988298	Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation.	Nat Commun	2019
31570822	Whole-genome sequencing of triple-negative breast cancers in a population-based clinical study.	Nat Med	2019
31444325	Genomic landscape and chronological reconstruction of driver events in multiple myeloma.	Nat Commun	2019
30252041	Mutational mechanisms of amplifications revealed by analysis of clustered rearrangements in breast cancers.	Ann Oncol	2018
28112740	A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers.	Nat Genet	2017
28904067	Whole-Genome Sequencing Reveals Breast Cancers with Mismatch Repair Deficiency.	Cancer Res	2017
28977645	Short inverted repeats contribute to localized mutability in human somatic cells.	Nucleic Acids Res	2017
29074948	Corrigendum: A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers.	Nat Genet	2017
28288110	HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures.	Nat Med	2017
27049301	Whole-exome sequencing in an isolated population from the Dalmatian island of Vis.	Eur J Hum Genet	2016
27136393	The topography of mutational processes in breast cancer genomes.	Nat Commun	2016
27135926	Landscape of somatic mutations in 560 breast cancer whole-genome sequences.	Nature	2016
26099045	Subclonal diversification of primary breast cancer revealed by multiregion sequencing.	Nat Med	2015
26443852	The genome as a record of environmental exposure.	Mutagenesis	2015
25002714	Plasma vitamin D concentration influences survival outcome after a diagnosis of colorectal cancer.	Journal of Clinical Oncology	2014
23361219	Inference of identity by descent in population isolates and optimal sequencing studies.	European Journal of Human Genetics	2013
23874685	Local exome sequences facilitate imputation of less common variants and increase power of genome wide association studies.	PLoS One	2013
21461552	Utility of non-rule-based visual matching as a strategy to allow novices to achieve skin lesion diagnosis.	Acta Dermato-Venereologica	2011