List of works - Volker Endris

Ataxia-telangiectasia-mutated protein kinase levels stratify patients with pancreatic adenocarcinoma into prognostic subgroups with loss being a strong indicator of poor survival

scientific article

Combined targeted DNA and RNA sequencing of advanced NSCLC in routine molecular diagnostics: Analysis of the first 3,000 Heidelberg cases

scientific article published on 19 February 2019

Comparative genetic profiling aids diagnosis and clinical decision making in challenging cases of CUP syndrome

scientific article published on 29 April 2019

Comprehensive analysis of clinico-pathological data reveals heterogeneous relations between atherosclerosis and cancer

scientific article

Distinctive Spatiotemporal Stability of Somatic Mutations in Metastasized Microsatellite-stable Colorectal Cancer

scientific article published on August 2015

Genetic changes of non-small cell lung cancer under neoadjuvant therapy

scientific article published on 20 April 2016

Genetic profiling of melanoma in routine diagnostics: assay performance and molecular characteristics in a consecutive series of 274 cases

scientific article published on 20 October 2018

Genomic architecture of FGFR2 fusions in cholangiocarcinoma and its implication for molecular testing

scientific article published in 2022

Global DNA methylation reflects spatial heterogeneity and molecular evolution of lung adenocarcinomas

article

High SIRT1 expression is a negative prognosticator in pancreatic ductal adenocarcinoma

scientific article

Identification of a highly lethal V3+ TP53+ subset in ALK+ lung adenocarcinoma

scientific article published on 30 October 2018

Integrated clinicomolecular characterization identifies RAS activation and CDKN2A deletion as independent adverse prognostic factors in cancer of unknown primary

scientific article published on 11 March 2020

Ioncopy: a novel method for calling copy number alterations in amplicon sequencing data including significance assessment

scientific article

Measurement of tumor mutational burden (TMB) in routine molecular diagnostics: in silico and real-life analysis of three larger gene panels

scientific article published on 04 February 2019

Molecular diagnostic profiling of lung cancer specimens with a semiconductor-based massive parallel sequencing approach: feasibility, costs, and performance compared with conventional sequencing

scientific article

Mutations in POLE and survival of colorectal cancer patients--link to disease stage and treatment

scientific article

Mutations in genes encoding PI3K-AKT and MAPK signaling define anogenital papillary hidradenoma

scientific article published on 23 October 2015

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation

scientific article

Prevalence of somatic mitochondrial mutations and spatial distribution of mitochondria in non-small cell lung cancer

scientific article published on 30 May 2017

RNA-Based Detection of Gene Fusions in Formalin-Fixed and Paraffin-Embedded Solid Cancer Samples

scientific article published on 05 September 2019

SHANK1 Deletions in Males with Autism Spectrum Disorder

scientific article

Size matters: Dissecting key parameters for panel-based tumor mutational burden analysis

scientific article published on 04 December 2018

Targeted molecular profiling reveals genetic heterogeneity of poromas and porocarcinomas

scientific article published on 18 December 2017

Targeted ultra-deep sequencing reveals recurrent and mutually exclusive mutations of cancer genes in blastic plasmacytoid dendritic cell neoplasm

scientific article

Targeting rare and non-canonical driver variants in NSCLC – An uncharted clinical field

scientific article published on 21 February 2021

Tubular, lactating, and ductal adenomas are devoid of MED12 Exon2 mutations, and ductal adenomas show recurrent mutations in GNAS and the PI3K-AKT pathway

scientific article published on 20 July 2016

Variant classification in precision oncology

scientific article published on 21 May 2019

List of works by Volker Endris

Ataxia-telangiectasia-mutated protein kinase levels stratify patients with pancreatic adenocarcinoma into prognostic subgroups with loss being a strong indicator of poor survival

Combined targeted DNA and RNA sequencing of advanced NSCLC in routine molecular diagnostics: Analysis of the first 3,000 Heidelberg cases

Comparative genetic profiling aids diagnosis and clinical decision making in challenging cases of CUP syndrome

Comprehensive analysis of clinico-pathological data reveals heterogeneous relations between atherosclerosis and cancer

Distinctive Spatiotemporal Stability of Somatic Mutations in Metastasized Microsatellite-stable Colorectal Cancer

Genetic changes of non-small cell lung cancer under neoadjuvant therapy

Genetic profiling of melanoma in routine diagnostics: assay performance and molecular characteristics in a consecutive series of 274 cases

Genomic architecture of FGFR2 fusions in cholangiocarcinoma and its implication for molecular testing

Global DNA methylation reflects spatial heterogeneity and molecular evolution of lung adenocarcinomas

High SIRT1 expression is a negative prognosticator in pancreatic ductal adenocarcinoma

Identification of a highly lethal V3+ TP53+ subset in ALK+ lung adenocarcinoma

Integrated clinicomolecular characterization identifies RAS activation and CDKN2A deletion as independent adverse prognostic factors in cancer of unknown primary

Ioncopy: a novel method for calling copy number alterations in amplicon sequencing data including significance assessment

Measurement of tumor mutational burden (TMB) in routine molecular diagnostics: in silico and real-life analysis of three larger gene panels

Molecular diagnostic profiling of lung cancer specimens with a semiconductor-based massive parallel sequencing approach: feasibility, costs, and performance compared with conventional sequencing

Mutations in POLE and survival of colorectal cancer patients--link to disease stage and treatment

Mutations in genes encoding PI3K-AKT and MAPK signaling define anogenital papillary hidradenoma

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation

Prevalence of somatic mitochondrial mutations and spatial distribution of mitochondria in non-small cell lung cancer

RNA-Based Detection of Gene Fusions in Formalin-Fixed and Paraffin-Embedded Solid Cancer Samples

SHANK1 Deletions in Males with Autism Spectrum Disorder

Size matters: Dissecting key parameters for panel-based tumor mutational burden analysis

Targeted molecular profiling reveals genetic heterogeneity of poromas and porocarcinomas

Targeted ultra-deep sequencing reveals recurrent and mutually exclusive mutations of cancer genes in blastic plasmacytoid dendritic cell neoplasm

Targeting rare and non-canonical driver variants in NSCLC – An uncharted clinical field

Tubular, lactating, and ductal adenomas are devoid of MED12 Exon2 mutations, and ductal adenomas show recurrent mutations in GNAS and the PI3K-AKT pathway

Variant classification in precision oncology