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E. Schröck · SciRah

Researcher profile · Semantic Scholar

E. Schröck

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E. Schröck — researcher profile on SciRah

h-index: 55
Works: 254
Citations: 15K

Most-cited papers

Integrative genomic and transcriptomic analysis of leiomyosarcoma
Priya Chudasama, S. Mughal, M. Sanders, D. Hübschmann +37 more
2018Nature Communications268 citations Open access
Semantic Scholar
NRG1 Fusions in KRAS Wild-Type Pancreatic Cancer.
C. Heining, P. Horák, S. Uhrig, Paula L Codo +35 more
2018Cancer Discovery203 citations
Semantic Scholar
The landscape of chromothripsis across adult cancer types
N. Voronina, John K. L. Wong, D. Hübschmann, M. Hlevnjak +26 more
2020Nature Communications125 citations Open access
Semantic Scholar
Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database
M. Dominguez-Valentin, Saskia Haupt, T. Seppälä, J. Sampson +112 more
2023EClinicalMedicine110 citations Open access
Semantic Scholar
ATM Deficiency Generating Genomic Instability Sensitizes Pancreatic Ductal Adenocarcinoma Cells to Therapy-Induced DNA Damage.
L. Perkhofer, A. Schmitt, M. C. Romero Carrasco, M. Ihle +22 more
2017Cancer Research95 citations
Semantic Scholar
Defective homologous recombination DNA repair as therapeutic target in advanced chordoma
S. Gröschel, D. Hübschmann, Francesco Raimondi, P. Horák +35 more
2019Nature Communications79 citations Open access
Semantic Scholar
The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants
Stephanie A. Schubert, Jana L. Luttikhuizen, B. Auber, G. Schmidt +14 more
2019International Journal of Cancer55 citations Open access
Semantic Scholar
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings
A. Schmidt, M. Danyel, K. Grundmann, T. Brunet +168 more
2024Nature Genetics50 citations Open access
Semantic Scholar
Comprehensive genomic and epigenomic analysis in cancer of unknown primary guides molecularly-informed therapies despite heterogeneity
L. Möhrmann, M. Werner, M. Oleś, A. Mock +40 more
2022Nature Communications50 citations Open access
Semantic Scholar
Proteogenomic analysis reveals RNA as a source for tumor-agnostic neoantigen identification
Celina Tretter, N. de Andrade Krätzig, M. Pecoraro, S. Lange +35 more
2023Nature Communications42 citations Open access
Semantic Scholar
Response to olaparib in a PALB2 germline mutated prostate cancer and genetic events associated with resistance
P. Horák, J. Weischenfeldt, G. von Amsberg, B. Beyer +20 more
2019Cold Spring Harbor molecular case studies37 citations Open access
Semantic Scholar
Community-driven development of a modified progression-free survival ratio for precision oncology
A. Mock, C. Heilig, S. Kreutzfeldt, D. Huebschmann +101 more
2019ESMO Open36 citations Open access
Semantic Scholar
NCT/DKFZ MASTER handbook of interpreting whole-genome, transcriptome, and methylome data for precision oncology
A. Mock, Maria-Veronica Teleanu, S. Kreutzfeldt, C. Heilig +28 more
2023npj Precision Oncology35 citations Open access
Semantic Scholar
Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes
J. Garcia-Pelaez, Rita Barbosa-Matos, Silvana Lobo, A. Dias +65 more
2022The Lancet Oncology35 citations Open access
Semantic Scholar
Targetable ERBB2 mutations identified in neurofibroma/schwannoma hybrid nerve sheath tumors.
M. Ronellenfitsch, P. Harter, M. Kirchner, C. Heining +20 more
2020Journal of Clinical Investigation34 citations Open access
Semantic Scholar
Optimizing Genetic Workup in Pheochromocytoma and Paraganglioma by Integrating Diagnostic and Research Approaches
L. Gieldon, D. William, K. Hackmann, Winnie Jahn +19 more
2019Cancers33 citations Open access
Semantic Scholar
Mutant IDH1 Differently Affects Redox State and Metabolism in Glial Cells of Normal and Tumor Origin
Julia Biedermann, Matthias Preussler, Marina Conde, M. Peitzsch +16 more
2019Cancers33 citations Open access
Semantic Scholar
Targeted capture-based NGS is superior to multiplex PCR-based NGS for hereditary BRCA1 and BRCA2 gene analysis in FFPE tumor samples
F. Zakrzewski, L. Gieldon, A. Rump, Michael Seifert +13 more
2019BMC Cancer29 citations Open access
Semantic Scholar
Boosting care and knowledge about hereditary cancer: European Reference Network on Genetic Tumour Risk Syndromes
J. Vos, Lisette Giepmans, C. Röhl, Nicoline Geverink +40 more
2018Familial Cancer27 citations Open access
Semantic Scholar
Validating Comprehensive Next-Generation Sequencing Results for Precision Oncology: The NCT/DKTK Molecularly Aided Stratification for Tumor Eradication Research Experience.
A. Lier, R. Penzel, C. Heining, P. Horák +40 more
2018JCO Precision Oncology25 citations Open access
Semantic Scholar
Twist exome capture allows for lower average sequence coverage in clinical exome sequencing
B. Yaldiz, Erdi Kucuk, J. Hampstead, T. Hofste +296 more
2023Human Genomics24 citations Open access
Semantic Scholar
Successful BRAF/MEK inhibition in a patient with BRAFV600E-mutated extrapancreatic acinar cell carcinoma
Elena Busch, S. Kreutzfeldt, A. Agaimy, G. Mechtersheimer +13 more
2020Cold Spring Harbor molecular case studies23 citations Open access
Semantic Scholar
Identification of novel snoRNA-based biomarkers for clear cell renal cell carcinoma from urine-derived extracellular vesicles
Konrad Grützmann, K. Salomo, Alexander Krüger, A. Lohse-Fischer +8 more
2024Biology Direct22 citations Open access
Semantic Scholar
Metastatic adult pancreatoblastoma: Multimodal treatment and molecular characterization of a very rare disease.
A. Berger, S. Mughal, M. Allgäuer, C. Springfeld +14 more
2020Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]22 citations
Semantic Scholar
Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study
C. Meisel, C. E. Sadowski, D. Kohlstedt, K. Keller +9 more
2017Archives of Gynecology and Obstetrics21 citations
Semantic Scholar
Investigating the effects of additional truncating variants in DNA-repair genes on breast cancer risk in BRCA1-positive women
I. Sepahi, U. Faust, M. Sturm, K. Bosse +23 more
2019BMC Cancer20 citations Open access
Semantic Scholar
Whole exome sequencing identifies mTOR and KEAP1 as potential targets for radiosensitization of HNSCC cells refractory to EGFR and β1 integrin inhibition
E. Klapproth, Ellen Dickreuter, F. Zakrzewski, Michael Seifert +5 more
2018OncoTarget20 citations Open access
Semantic Scholar
Translational and clinical comparison of whole genome and transcriptome to panel sequencing in precision oncology
I. Kerle, Thomas Gross, A. Kögler, J. Arnold +20 more
2025npj Precision Oncology19 citations Open access
Semantic Scholar
Genomic landscape and molecularly informed therapy in thymic carcinoma and other advanced thymic epithelial tumors.
L. Möhrmann, L. Rostock, M. Werner, M. Oleś +45 more
2025i Medicina18 citations Open access
Semantic Scholar
Signaling-induced systematic repression of miRNAs uncovers cancer vulnerabilities and targeted therapy sensitivity
A. Wurm, S. Brilloff, Sofia Kolovich, Silvia Schäfer +23 more
2023Cell Reports Medicine13 citations Open access
Semantic Scholar
Different Effects of RNAi-Mediated Downregulation or Chemical Inhibition of NAMPT in an Isogenic IDH Mutant and Wild-Type Glioma Cell Model
Maximilian Clausing, D. William, Matthias Preussler, Julia Biedermann +6 more
2022International Journal of Molecular Sciences13 citations Open access
Semantic Scholar
Molecular Characterization of Astrocytoma Progression Towards Secondary Glioblastomas Utilizing Patient-Matched Tumor Pairs
Michael Seifert, G. Schackert, A. Temme, E. Schröck +2 more
2020Cancers13 citations Open access
Semantic Scholar
Novel dominant-negative NR2F1 frameshift mutation and a phenotypic expansion of the Bosch-Boonstra-Schaaf optic atrophy syndrome.
Sonja Walsh, Sophie Gößwein, A. Rump, M. von der Hagen +4 more
2020European Journal of Medical Genetics12 citations
Semantic Scholar
Novel VPS33B mutation in a patient with autosomal recessive keratoderma‐ichthyosis‐deafness syndrome
S. Alter, A. Hotz, A. Jahn, N. Di Donato +9 more
2018American Journal of Medical Genetics. Part A12 citations
Semantic Scholar
A clinical screening tool to detect genetic cancer predisposition in pediatric oncology shows high sensitivity but can miss a substantial percentage of affected children.
U. Friedrich, M. Bienias, C. Zinke, M. Prazenicova +15 more
2023Genetics in Medicine11 citations Open access
Semantic Scholar
Germany’s national genomDE strategy
Andreas Till, R. Siddiqui, C. Altbürger, Roland F. Schwarz +45 more
2025Nature Medicine10 citations
Semantic Scholar
Overview of the Clinical Features of Li-Fraumeni Syndrome and the Current European ERN GENTURIS Guideline
C. Kratz, V. Steinke-Lange, I. Spier, S. Aretz +2 more
2021Geburtshilfe und Frauenheilkunde8 citations Open access
Semantic Scholar
Comprehensive genomic characterization of gene therapy-induced T-cell acute lymphoblastic leukemia
P. Horák, S. Uhrig, Maximilian Witzel, Irene Gil-Farina +18 more
2020Leukemia8 citations Open access
Semantic Scholar
Exploring evolutionary trajectories in ovarian cancer patients by longitudinal analysis of ctDNA
Oliver Kutz, S. Drukewitz, Alexander Krüger, Daniela E. Aust +7 more
2024Clinical Chemistry and Laboratory Medicine6 citations
Semantic Scholar
PUF60-SCRIB fusion transcript in a patient with 8q24.3 microdeletion and atypical Verheij syndrome.
Dalia Abdin, A. Rump, A. Tzschach, Katharina Sarnow +3 more
2019European Journal of Medical Genetics6 citations
Semantic Scholar
Posterior amorphous corneal dystrophy in a patient with 12q21.33 deletion
J. Lenk, J. Porrmann, M. Smitka, Ines Eger +5 more
2018Ophthalmic Genetics6 citations
Semantic Scholar
A quiescence-like/TGF-β1-specific CRISPRi screen reveals drug uptake transporters as secondary targets of kinase inhibitors in AML.
E. Rahimian, M. Koochak, S. Traikov, Michael Schroeder +14 more
2025Drug resistance updates5 citations Open access
Semantic Scholar
Identification of epigenetically regulated genes distinguishing intracranial from extracranial melanoma metastases.
D. Westphal, M. Meinhardt, Konrad Grützmann, Lisa Schöne +19 more
2023Journal of Investigative Dermatology5 citations Open access
Semantic Scholar
Gene expression-based prediction of pazopanib efficacy in sarcoma.
C. Heilig, A. Lassmann, S. Mughal, A. Mock +43 more
2022European Journal of Cancer5 citations
Semantic Scholar
Case Report: ANXA2 Associated Life-Threatening Coagulopathy With Hyperfibrinolysis in a Patient With Non-APL Acute Myeloid Leukemia
L. Ruhnke, F. Stölzel, Lisa Wagenführ, H. Altmann +7 more
2021Frontiers in Oncology5 citations Open access
Semantic Scholar
Germline SDHB‐inactivating mutation in gastric spindle cell sarcoma
C. Heilig, P. Horák, D. Lipka, A. Mock +22 more
2020Genes, Chromosomes and Cancer5 citations
Semantic Scholar
Identifying risk factors for metachronous colorectal cancer in Lynch syndrome.
R. Hüneburg, K. Weber, S. Aretz, V. Steinke-Lange +12 more
2025Clinical Gastroenterology and Hepatology4 citations Open access
Semantic Scholar
Cerebral organoids expressing mutant actin genes reveal cellular mechanism underlying microcephaly
I. Niehaus, Michaela Wilsch-Bräuninger, Felipe Mora-Bermúdez, Mihaela Bobić-Rasonja +15 more
2024bioRxiv4 citations Open access
Semantic Scholar
OnkoRiskNET: a multicenter, interdisciplinary, telemedicine-based model to improve care for patients with a genetic tumor risk syndrome
Johanna Tecklenburg, B. Vajen, S. Morlot, Petra Anders +7 more
2022BMC Health Services Research4 citations Open access
Semantic Scholar
Solving the genetic aetiology of hereditary gastrointestinal tumour syndromes- a collaborative multicentre endeavour within the project Solve-RD.
Anna K. Sommer, Iris B. A. W. Te Paske, J. Garcia-Pelaez, A. Laner +22 more
2022European Journal of Medical Genetics4 citations Open access
Semantic Scholar

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