Monika Morak

5.1k total citations
36 papers, 793 citations indexed

About

Monika Morak is a scholar working on Pathology and Forensic Medicine, Cancer Research and Molecular Biology. According to data from OpenAlex, Monika Morak has authored 36 papers receiving a total of 793 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Pathology and Forensic Medicine, 16 papers in Cancer Research and 14 papers in Molecular Biology. Recurrent topics in Monika Morak's work include Genetic factors in colorectal cancer (30 papers), Cancer Genomics and Diagnostics (16 papers) and Colorectal Cancer Screening and Detection (8 papers). Monika Morak is often cited by papers focused on Genetic factors in colorectal cancer (30 papers), Cancer Genomics and Diagnostics (16 papers) and Colorectal Cancer Screening and Detection (8 papers). Monika Morak collaborates with scholars based in Germany, United States and United Kingdom. Monika Morak's co-authors include Elke Holinski‐Feder, Andreas Laner, Gisela Keller, Brigitte Royer‐Pokora, Verena Steinke, Stefan Aretz, Magnus von Knebel Doeberitz, Heather Hampel, Albert de la Chapelle and Dietlinde Stienen and has published in prestigious journals such as Journal of Clinical Oncology, Scientific Reports and International Journal of Cancer.

In The Last Decade

Monika Morak

36 papers receiving 790 citations

Peers

Countries citing papers authored by Monika Morak

Since Specialization

Citations

This map shows the geographic impact of Monika Morak's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Monika Morak with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Monika Morak more than expected).

Fields of papers citing papers by Monika Morak

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Monika Morak. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Monika Morak. The network helps show where Monika Morak may publish in the future.

Co-authorship network of co-authors of Monika Morak

This figure shows the co-authorship network connecting the top 25 collaborators of Monika Morak. A scholar is included among the top collaborators of Monika Morak based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Monika Morak. Monika Morak is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Transcript capture and ultradeep long-read RNA sequencing (CAPLRseq) to diagnose HNPCC/Lynch syndrome 2023 ·Journal of Medical Genetics ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Verena Steinke‐Lange, Andreas Laner, Monika Morak, Elke Holinski‐Feder, Dieter A Wolf	10
2	Long-term chemoprevention in patients with adenomatous polyposis coli: an observational study 2022 ·Familial Cancer ·Teresa Neuhann, (unknown), Verena Steinke‐Lange, Monika Morak, Andreas Laner, (unknown), Elke Holinski‐Feder	6
3	Splicing analyses for variants in MMR genes: best practice recommendations from the European Mismatch Repair Working Group 2022 ·European Journal of Human Genetics ·Monika Morak, Marta Pineda, Alexandra Martins, Pascaline Gaildrat, Hélène Tubeuf, Aurélie Drouet, Carolina de la Torre, (unknown), (unknown), Verena Steinke‐Lange, Udo Koehler, Andreas Laner, (unknown), (unknown), Elke Holinski‐Feder, Gabriel Capellá	5
4	Constitutional chromothripsis of the APC locus as a cause of genetic predisposition to colon cancer 2021 ·Journal of Medical Genetics ·(unknown), (unknown), Monika Morak, Alex Hastie, (unknown), (unknown), (unknown), (unknown), Andreas Laner, Verena Steinke‐Lange, Udo Koehler, Elke Holinski‐Feder, Dieter A Wolf	12
5	Prevalence of CNV-neutral structural genomic rearrangements in MLH1, MSH2, and PMS2 not detectable in routine NGS diagnostics 2020 ·Familial Cancer ·Monika Morak, Verena Steinke‐Lange, (unknown), Anna Benet‐Pagès, (unknown), Andreas Laner, Katrin Kayser, Stefan Aretz, Elke Holinski‐Feder	9
6	Results of multigene panel testing in familial cancer cases without genetic cause demonstrated by single gene testing 2019 ·Scientific Reports ·Mev Dominguez–Valentin, Sigve Nakken, Hélène Tubeuf, Daniel Vodák, Per Olaf Ekstrøm, (unknown), Monika Morak, Elke Holinski‐Feder, Arild Holth, Gabriel Capellá, Ben Davidson, D. Gareth Evans, Alexandra Martins, Pål Møller, Eivind Hovig	12
7	Targeted deep-intronic sequencing in a cohort of unexplained cases of suspected Lynch syndrome 2019 ·European Journal of Human Genetics ·(unknown), Monika Morak, Anna Benet‐Pagès, Andreas Laner, (unknown), Elke Holinski‐Feder	11
8	Identification of genetic variants for clinical management of familial colorectal tumors 2018 ·BMC Medical Genetics ·Mev Dominguez–Valentin, Sigve Nakken, Hélène Tubeuf, Daniel Vodák, Per Olaf Ekstrøm, (unknown), Monika Morak, Elke Holinski‐Feder, Alexandra Martins, Pål Møller, Eivind Hovig	16
9	Clinical characteristics and EGD surveillance in Lynch-syndrome patients with small bowel/duodenal carcinomas. 2018 ·Journal of Clinical Oncology ·Deepak Vangala, Christian Pox, (unknown), Christoph Engel, (unknown), Claudia Perne, Verena Steinke‐Lange, Nils Rahner, Hans K. Schackert, Matthias Kloor, Stefanie Holzapfel, (unknown), Christian P. Strassburg, Monika Morak, Elke Holinski‐Feder, Reinhard Büttner, Stefan Aretz, Markus Loeffler, Wolff Schmiegel, Karsten Schulmann	2
10	Value of EGD for gastric cancer surveillance in patients with hereditary non-polyposis colorectal cancer (HNPCC) or Lynch syndrome (LS). 2018 ·Journal of Clinical Oncology ·(unknown), Deepak Vangala, (unknown), Christian Pox, Christoph Engel, (unknown), Claudia Perne, Jacob Nattermann, Verena Steinke‐Lange, Nils Rahner, Hans K. Schackert, Matthias Kloor, (unknown), Monika Morak, Elke Holinski‐Feder, Reinhard Büttner, Stefan Aretz, Markus Loeffler, Wolff Schmiegel, Karsten Schulmann	3
11	Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: A comprehensive analysis of 3,671 families 2013 ·International Journal of Cancer ·Verena Steinke, Stefanie Holzapfel, Markus Loeffler, Elke Holinski‐Feder, Monika Morak, Hans K. Schackert, Heike Görgens, Christian Pox, Brigitte Royer‐Pokora, Magnus von Knebel Doeberitz, Reinhard Büttner, Peter Propping, Christoph Engel	19
12	Biallelic MLH1 SNP cDNA expression or constitutional promoter methylation can hide genomic rearrangements causing Lynch syndrome 2011 ·Journal of Medical Genetics ·Monika Morak, Udo Koehler, Hans K. Schackert, Verena Steinke, Brigitte Royer‐Pokora, Karsten Schulmann, Matthias Kloor, W. Höchter, J. Weingart, (unknown), (unknown), Elke Holinski‐Feder	54
13	An American founder mutation in MLH1 2011 ·International Journal of Cancer ·Jerneja Tomšič, Sandya Liyanarachchi, Heather Hampel, Monika Morak, Brittany C. Thomas, Victoria M. Raymond, Anu Chittenden, Hans K. Schackert, Stephen B. Gruber, Sapna Syngal, Alessandra Viel, Elke Holinski‐Feder, Stephen N. Thibodeau, Albert de la Chapelle	12
14	Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies 2011 ·Familial Cancer ·Karin Hardt, (unknown), Beate Betz, Timm O. Goecke, (unknown), (unknown), Kati Servan, Verena Steinke, Nils Rahner, Monika Morak, Elke Holinski‐Feder, Christoph Engel, Gabriela Möslein, (unknown), Magnus von Knebel Doeberitz, Christian Pox, Johannes H. Hegemann, Brigitte Royer‐Pokora	22
15	First evidence for digenic inheritance in hereditary colorectal cancer by mutations in the base excision repair genes 2010 ·European Journal of Cancer ·Monika Morak, (unknown), (unknown), (unknown), Elke Holinski‐Feder	26
16	MUTYH‐associated polyposis – variability of the clinical phenotype in patients with biallelic and monoallelic MUTYH mutations and report on novel mutations 2010 ·Clinical Genetics ·Monika Morak, Andreas Laner, Ulrike Bacher, (unknown), Elke Holinski‐Feder	37
17	Serum antibodies against frameshift peptides in microsatellite unstable colorectal cancer patients with Lynch syndrome 2009 ·Familial Cancer ·Miriam Reuschenbach, Matthias Kloor, Monika Morak, Nicolas Wentzensen, Anja Germann, Yvette Garbe, Mirjam Tariverdian, Peter Findeisen, Michael Neumaier, Elke Holinski‐Feder, Magnus von Knebel Doeberitz	44
18	A novel mitochondrial MTND5 frameshift mutation causing isolated complex I deficiency, renal failure and myopathy 2009 ·Neuromuscular Disorders ·Charlotte L. Alston, Monika Morak, Christopher Reid, Iain P. Hargreaves, Simon Pope, John M. Land, Simon J.R. Heales, Rita Horváth, Helen Mundy, Robert W. Taylor	31
19	Further evidence for heritability of an epimutation in one of 12 cases with MLH1 promoter methylation in blood cells clinically displaying HNPCC 2008 ·European Journal of Human Genetics ·Monika Morak, Hans Konrad Schackert, Nils Rahner, Beate Betz, Matthias Ebert, Constanze Walldorf, Brigitte Royer‐Pokora, Karsten Schulmann, Magnus von Knebel Doeberitz, Wolfgang Dietmaier, Gisela Keller, (unknown), (unknown), Elke Holinski‐Feder	79
20	Report on de-novo mutation in the MSH2 gene as a rare event in hereditary nonpolyposis colorectal cancer 2008 ·European Journal of Gastroenterology & Hepatology ·Monika Morak, Andreas Laner, Michael Scholz, (unknown), Elke Holinski‐Feder	10

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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