Inga Hinrichsen

695 total citations
16 papers, 314 citations indexed

About

Inga Hinrichsen is a scholar working on Pathology and Forensic Medicine, Cancer Research and Molecular Biology. According to data from OpenAlex, Inga Hinrichsen has authored 16 papers receiving a total of 314 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Pathology and Forensic Medicine, 11 papers in Cancer Research and 9 papers in Molecular Biology. Recurrent topics in Inga Hinrichsen's work include Genetic factors in colorectal cancer (15 papers), Cancer Genomics and Diagnostics (11 papers) and RNA Research and Splicing (6 papers). Inga Hinrichsen is often cited by papers focused on Genetic factors in colorectal cancer (15 papers), Cancer Genomics and Diagnostics (11 papers) and RNA Research and Splicing (6 papers). Inga Hinrichsen collaborates with scholars based in Germany, Spain and Chile. Inga Hinrichsen's co-authors include Guido Plotz, Angela Brieger, Stefan Zeuzem, Jan Kosiński, Peter Friedhoff, Janusz M. Bujnicki, Stefan Zeuzem, Marta Pineda, Conxi Lázaro and Gabriel Capellá and has published in prestigious journals such as PLoS ONE, Clinical Cancer Research and Molecular Cancer.

In The Last Decade

Inga Hinrichsen

16 papers receiving 311 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Inga Hinrichsen Germany	11	208	200	143	80	43	16	314
D. Nguyen United States	4	252 1.2×	209 1.0×	158 1.1×	155 1.9×	37 0.9×	7	356
Erin E. Henninger United States	5	143 0.7×	213 1.1×	167 1.2×	63 0.8×	34 0.8×	5	333
Isabella Gazzoli Netherlands	8	235 1.1×	247 1.2×	164 1.1×	162 2.0×	71 1.7×	13	444
Hiromi O. Shiwaku Japan	5	106 0.5×	146 0.7×	67 0.5×	89 1.1×	30 0.7×	7	248
Mireia Menéndez Spain	10	110 0.5×	182 0.9×	135 0.9×	97 1.2×	158 3.7×	15	346
Nandy Hofland Netherlands	5	156 0.8×	228 1.1×	50 0.3×	83 1.0×	64 1.5×	7	325
Sukanya Horpaopan Thailand	6	206 1.0×	124 0.6×	113 0.8×	115 1.4×	65 1.5×	15	308
Junmei Hao China	6	62 0.3×	193 1.0×	105 0.7×	104 1.3×	29 0.7×	14	311
Pablo Herrero-Jimenez United States	6	54 0.3×	273 1.4×	139 1.0×	59 0.7×	48 1.1×	8	374
Daniel Serber United States	6	162 0.8×	293 1.5×	47 0.3×	64 0.8×	30 0.7×	7	400

Countries citing papers authored by Inga Hinrichsen

Since Specialization

Citations

This map shows the geographic impact of Inga Hinrichsen'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 Inga Hinrichsen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Inga Hinrichsen more than expected).

Fields of papers citing papers by Inga Hinrichsen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Inga Hinrichsen. 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 Inga Hinrichsen. The network helps show where Inga Hinrichsen may publish in the future.

Co-authorship network of co-authors of Inga Hinrichsen

This figure shows the co-authorship network connecting the top 25 collaborators of Inga Hinrichsen. A scholar is included among the top collaborators of Inga Hinrichsen 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 Inga Hinrichsen. Inga Hinrichsen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Hinrichsen, Inga, et al.. (2019). Validation of an in Vitro Mismatch Repair Assay Used in the Functional Characterization of Mismatch Repair Variants. Journal of Molecular Diagnostics. 22(3). 376–385. 3 indexed citations

Brieger, Angela, et al.. (2019). Analysis of MUTYH alternative transcript expression, promoter function, and the effect of human genetic variants. Human Mutation. 40(4). 472–482. 5 indexed citations

Hinrichsen, Inga, Sebastian Funke, Thomas Oellerich, et al.. (2018). DNA mismatch repair activity of MutLα is regulated by CK2‐dependent phosphorylation of MLH1 (S477). Molecular Carcinogenesis. 57(12). 1723–1734. 12 indexed citations

López‐Köstner, Francisco, Adriana Della Valle, Carlos Vaccaro, et al.. (2018). Evaluation of MLH1 variants of unclear significance. Genes Chromosomes and Cancer. 57(7). 350–358. 5 indexed citations

Hinrichsen, Inga, et al.. (2017). Phosphorylation‐dependent signaling controls degradation of DNA mismatch repair protein PMS2. Molecular Carcinogenesis. 56(12). 2663–2668. 14 indexed citations

Hinrichsen, Inga, et al.. (2017). Loss of MLH1 sensitizes colon cancer cells to DNA‐PKcs inhibitor KU60648. Molecular Carcinogenesis. 56(7). 1816–1824. 11 indexed citations

Hinrichsen, Inga, Dieter Schäfer, David Langer, et al.. (2014). Functional testing strategy for coding genetic variants of unclear significance in MLH1 in Lynch syndrome diagnosis. Carcinogenesis. 36(2). 202–211. 9 indexed citations

Hinrichsen, Inga, Benjamin Philipp Ernst, Dieter Schäfer, et al.. (2014). Reduced migration of MLH1 deficient colon cancer cells depends on SPTAN1. Molecular Cancer. 13(1). 11–11. 29 indexed citations

Hinrichsen, Inga, et al.. (2014). Promoter Methylation of MLH1, PMS2, MSH2 and p16 Is a Phenomenon of Advanced-Stage HCCs. PLoS ONE. 9(1). e84453–e84453. 28 indexed citations

10.

Hinrichsen, Inga, Angela Brieger, Jörg Trojan, et al.. (2013). Expression Defect Size among Unclassified MLH1 Variants Determines Pathogenicity in Lynch Syndrome Diagnosis. Clinical Cancer Research. 19(9). 2432–2441. 26 indexed citations

11.

Borràs, Ester, Marta Pineda, Juan Cadiñanos, et al.. (2013). Refining the role of pms2 in Lynch syndrome: germline mutational analysis improved by comprehensive assessment of variants. Journal of Medical Genetics. 50(8). 552–563. 42 indexed citations

12.

Brieger, Angela, et al.. (2012). C-Terminal Fluorescent Labeling Impairs Functionality of DNA Mismatch Repair Proteins. PLoS ONE. 7(2). e31863–e31863. 17 indexed citations

13.

Plotz, Guido, Markus Casper, Jochen Raedle, et al.. (2012). MUTYHgene expression and alternative splicing in controls and polyposis patients. Human Mutation. 33(7). 1067–1074. 25 indexed citations

14.

Borràs, Ester, Marta Pineda, Angela Brieger, et al.. (2012). Comprehensive functional assessment ofMLH1variants of unknown significance. Human Mutation. 33(11). 1576–1588. 24 indexed citations

15.

Kosiński, Jan, Inga Hinrichsen, Janusz M. Bujnicki, Peter Friedhoff, & Guido Plotz. (2010). Identification of Lynch syndrome mutations in the MLH1-PMS2 interface that disturb dimerization and mismatch repair. Human Mutation. 31(8). 975–982. 54 indexed citations

16.

Hinrichsen, Inga, et al.. (2009). RNA processing in plant mitochondria is independent of transcription. Plant Molecular Biology. 70(6). 663–668. 10 indexed citations

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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