Monika Morak

LMU Klinikum — Germany

Medicine · Health Sciences

31h-index5.0kcitations88works1.52yr avg
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Research Topics

Genetic factors in colorectal cancer(60), Cancer Genomics and Diagnostics(30), Colorectal Cancer Screening and Detection(21), Aortic aneurysm repair treatments(11), Colorectal Cancer Treatments and Studies(10)

Publications74 total

1039 Evaluating the prognostic impact of tebentafusp-associated cutaneous toxicities on survival in 83 uveal melanoma patients: a multi-institutional cohort study
Regular and Young Investigator Award Abstracts·2025Open Access
Adenomas Are Frequent in PMS2 Lynch Syndrome patients but Rarely Mismatch Repair Deficient
2025Open Access
Retrospective multicenter analysis of real-life toxicity and outcome of ipilimumab and nivolumab in metastatic uveal melanoma
The Oncologist·2025· 3 citedOpen Access
Interleukin-4 and -13 Gene Expression Profiles in Immune-Related Bullous Pemphigoid Indicate Efficacy of IL-4/IL-13 Inhibitors
Cancers·2025· 3 citedOpen Access
Transcript capture and ultradeep long-read RNA sequencing (CAPLRseq) to diagnose HNPCC/Lynch syndrome
Journal of Medical Genetics·2023· 16 citedOpen Access
Impact of the COVID-19 pandemic on surgical care in the Netherlands
British journal of surgery·2022· 22 citedOpen Access
Splicing analyses for variants in MMR genes: best practice recommendations from the European Mismatch Repair Working Group
European Journal of Human Genetics·2022· 10 citedOpen Access
Long-term chemoprevention in patients with adenomatous polyposis coli: an observational study
Familial Cancer·2022· 7 cited
Constitutional chromothripsis of the <i>APC</i> locus as a cause of genetic predisposition to colon cancer
Journal of Medical Genetics·2021· 17 citedOpen Access
Adenoma and colorectal cancer risks in Lynch syndrome, Lynch‐like syndrome and familial colorectal cancer type X
International Journal of Cancer·2021· 8 citedOpen Access
Early detection of duodenal cancer by upper <scp>gastrointestinal</scp>‐endoscopy in Lynch syndrome
International Journal of Cancer·2021· 7 citedOpen Access
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·2021· 19 citedOpen Access
No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study
Kölner Universitäts PublikationsServer (Universität zu Köln)·2021Open Access
Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report
European Journal of Cancer·2021· 19 citedOpen Access
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report
Genetics in Medicine·2020· 38 citedOpen Access
Value of upper <scp>gastrointestinal</scp> endoscopy for gastric cancer surveillance in patients with Lynch syndrome
International Journal of Cancer·2020· 38 citedOpen Access
Age‐dependent performance of <scp> <i>BRAF</i> </scp> mutation testing in Lynch syndrome diagnostics
International Journal of Cancer·2020· 29 citedOpen Access
CAH-X Syndrome in a german cohort of patients with 21--hydroxylase deficiency
Endocrine Abstracts·2020
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·2020· 8 citedOpen Access
Cancer risks in Lynch syndrome, Lynch-like syndrome, and familial colorectal cancer type X: a prospective cohort study
BMC Cancer·2020· 49 citedOpen Access
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Frequent Co-authors

Elke Holinski‐Feder(44), Nils Rahner(20), Christoph Engel(18), Gabriela Möslein(16), Stefan Aretz(15), Hans K. Schackert(15), Verena Steinke‐Lange(15), Matthias Kloor(15), Reinhard Büttner(13), Magnus von Knebel Doeberitz(13), Pål Møller(13), Gabriel Capellá(12), Eivind Hovig(12), Toni T. Seppälä(11), Sigve Nakken(11), Stefanie Holzapfel(11), Kirsi Pylvänäinen(11), Laura Renkonen‐Sinisalo(11), Marta Pineda(11), Hans F. A. Vasen(11)