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Wolff Schmiegel

Universitätsklinikum Knappschaftskrankenhaus Bochum · DE
Area of research
Oncology · Pathology and Forensic Medicine
Research interest
Research interests include Colorectal Cancer Treatments and Studies, Genetic factors in colorectal cancer, Pancreatic and Hepatic Oncology Research, and Colorectal Cancer Screening and Detection.
h-index
78
citations
26,096
works
1,213
NIH funding
primary concept
email

Recent publications

Baseline Liquid Biopsy in Relation to Tissue-Based Parameters in Metastatic Colorectal Cancer: Results From the Randomized FIRE-4 (AIO-KRK-0114) Study
Journal of Clinical Oncology 2025cited by 16position: middledoi
Evaluation of circulating tumor <scp>DNA</scp> as a prognostic and predictive biomarker in <i>BRAF</i> <scp>V600E</scp> mutated colorectal cancer—results from the <scp>FIRE</scp> ‐4.5 study
Molecular Oncology 2024cited by 8position: middledoi
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
EClinicalMedicine 2023cited by 103position: middledoi
Coinhibition of topoisomerase 1 and BRD4-mediated pause release selectively kills pancreatic cancer via readthrough transcription
Science Advances 2023cited by 15position: middledoi
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium
Hereditary Cancer in Clinical Practice 2022cited by 56position: middledoi
Chemoradiotherapy Plus Induction or Consolidation Chemotherapy as Total Neoadjuvant Therapy for Patients With Locally Advanced Rectal Cancer
JAMA Oncology 2021cited by 345position: middledoi
Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report
European Journal of Cancer 2021cited by 21position: middledoi
No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study
Journal of Clinical Medicine 2021cited by 19position: middledoi
Secondary resistance to anti-EGFR therapy by transcriptional reprogramming in patient-derived colorectal cancer models
Genome Medicine 2021cited by 15position: middledoi
Early detection of duodenal cancer by upper <scp>gastrointestinal</scp>‐endoscopy in Lynch syndrome
International Journal of Cancer 2021cited by 8position: middledoi
Cancer risks in Lynch syndrome, Lynch-like syndrome, and familial colorectal cancer type X: a prospective cohort study
BMC Cancer 2020cited by 50position: middledoi
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report
Genetics in Medicine 2020cited by 41position: middledoi
Value of upper <scp>gastrointestinal</scp> endoscopy for gastric cancer surveillance in patients with Lynch syndrome
International Journal of Cancer 2020cited by 40position: middledoi
Age‐dependent performance of <scp> <i>BRAF</i> </scp> mutation testing in Lynch syndrome diagnostics
International Journal of Cancer 2020cited by 30position: middledoi
Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
Genetics in Medicine 2020cited by 10position: middledoi
Perioperative chemotherapy with fluorouracil plus leucovorin, oxaliplatin, and docetaxel versus fluorouracil or capecitabine plus cisplatin and epirubicin for locally advanced, resectable gastric or gastro-oesophageal junction adenocarcinoma (FLOT4): a randomised, phase 2/3 trial
The Lancet 2019cited by 2,538position: middledoi
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
Genetics in Medicine 2019cited by 638position: middledoi
Randomized Phase II Trial of Chemoradiotherapy Plus Induction or Consolidation Chemotherapy as Total Neoadjuvant Therapy for Locally Advanced Rectal Cancer: CAO/ARO/AIO-12
Journal of Clinical Oncology 2019cited by 531position: middledoi
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report
Hereditary Cancer in Clinical Practice 2019cited by 63position: middledoi
<i>BRAF</i> mutation testing of MSI CRCs in Lynch syndrome diagnostics: performance and efficiency according to patient’s age
medRxiv 2019cited by 1position: middledoi
&lt;i&gt;BRAF&lt;/i&gt; Mutation Testing in Lynch Syndrome Diagnostics: Performance and Efficiency According to Patient's Age
SSRN Electronic Journal 2019cited by 0position: middledoi
No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies
Gastroenterology 2018cited by 150position: middledoi
Screening and surveillance in hereditary gastrointestinal cancers: Recommendations from the European Society of Digestive Oncology (ESDO) expert discussion at the 20th European Society for Medical Oncology (ESMO)/World Congress on Gastrointestinal Cancer, Barcelona, June 2018
European Journal of Cancer 2018cited by 68position: lastdoi
Risk of Malignancy in Adenomas Detected During Screening Colonoscopy
Clinical Gastroenterology and Hepatology 2018cited by 18position: middledoi
S3-Leitlinie – Kolorektales Karzinom
Zeitschrift für Gastroenterologie 2017cited by 243position: firstdoi
Perioperative chemotherapy with docetaxel, oxaliplatin, and fluorouracil/leucovorin (FLOT) versus epirubicin, cisplatin, and fluorouracil or capecitabine (ECF/ECX) for resectable gastric or gastroesophageal junction (GEJ) adenocarcinoma (FLOT4-AIO): A multicenter, randomized phase 3 trial.
Journal of Clinical Oncology 2017cited by 239position: middledoi
Genomic and transcriptomic heterogeneity of colorectal tumours arising in Lynch syndrome
The Journal of Pathology 2017cited by 56position: middledoi
Histopathological regression after neoadjuvant docetaxel, oxaliplatin, fluorouracil, and leucovorin versus epirubicin, cisplatin, and fluorouracil or capecitabine in patients with resectable gastric or gastro-oesophageal junction adenocarcinoma (FLOT4-AIO): results from the phase 2 part of a multicentre, open-label, randomised phase 2/3 trial
The Lancet Oncology 2016cited by 732position: middledoi
Outcome according to KRAS-, NRAS- and BRAF-mutation as well as KRAS mutation variants: pooled analysis of five randomized trials in metastatic colorectal cancer by the AIO colorectal cancer study group
Annals of Oncology 2016cited by 343position: middledoi
Impact of Age and Midostaurin-Dose on Response and Outcome in Acute Myeloid Leukemia with FLT3-ITD: Interim-Analyses of the AMLSG 16-10 Trial
Blood 2016cited by 22position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

· 5 papers (2012–2021)Deepak Vangala · Universitätsklinikum Knappschaftskrankenhaus Bochum5 papers (2018–2023) · 4 papers (2014–2023)Jürgen Weitz · University Medical Center Hamburg-Eppendorf4 papers (2019–2021)Sebastian Stintzing · German Cancer Research Center4 papers (2013–2025)Volker Heinemann · LMU Klinikum4 papers (2013–2025) · 4 papers (2014–2025)Dominik Paul Modest · Berliner Hochschule für Technik4 papers (2013–2025)L Altenhofen · Moffitt Cancer Center3 papers (2012–2018)Claudia Perne · Institute of Human Genetics3 papers (2020–2021)Stefan Aretz · Dutch Expert Centre for Screening3 papers (2020–2021)Karsten Schulmann · Universitätsklinikum Knappschaftskrankenhaus Bochum3 papers (2020–2021)Karolin Bucksch · Hamburg Wasser (Germany)3 papers (2020–2021)Alexander Baraniskin · Medizinische Hochschule Hannover3 papers (2015–2025)Nils Rahner · Amedes Genetics (Germany)3 papers (2020–2021) · 3 papers (2013–2017)Christoph Engel · University of Regensburg3 papers (2020–2021)Ralf‐Dieter Hofheinz · Heidelberg University3 papers (2017–2025)Jacob Nattermann · Marymount University3 papers (2020–2021)Monika Morak · Medical Genetics Center3 papers (2020–2021)