Monika Maringa

1.0k total citations
7 papers, 691 citations indexed

About

Monika Maringa is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Monika Maringa has authored 7 papers receiving a total of 691 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Surgery and 4 papers in Molecular Biology. Recurrent topics in Monika Maringa's work include Pancreatic function and diabetes (4 papers), Diabetes and associated disorders (3 papers) and BRCA gene mutations in cancer (2 papers). Monika Maringa is often cited by papers focused on Pancreatic function and diabetes (4 papers), Diabetes and associated disorders (3 papers) and BRCA gene mutations in cancer (2 papers). Monika Maringa collaborates with scholars based in Germany, Spain and Serbia. Monika Maringa's co-authors include Rita K. Schmutzler, Eva Wardelmann, Andrea Hocke, C Leutner, Hans H. Schild, Christiane Kühl, Dieter Krebs, Andrea Kempe, U. Pfeifer and George D. Yancopoulos and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Radiology.

In The Last Decade

Monika Maringa

7 papers receiving 673 citations

Peers

Monika Maringa

RNMI

GENET

PFM

MB

CR

Robin Parker Canada

Francesca Pietribiasi Italy

Angela Cramer United Kingdom

Sari Tuupanen Finland

Umut Aypar United States

Malinda L. Butz United States

Andrea Kempe Germany

Katherine Chung United States

Lucía Hernández Spain

Alissa Minkovsky United States

Robin Parker Canada

Monika Maringa

170 ×0.6

RNMI

84 ×0.3

GENET

85 ×0.4

PFM

315 ×1.5

MB

144 ×1.3

CR

Citations per year, relative to Monika Maringa Monika Maringa (= 1×) peers Robin Parker

Countries citing papers authored by Monika Maringa

Since Specialization

Citations

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

Fields of papers citing papers by Monika Maringa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Monika Maringa

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

All Works

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7 of 7 papers shown

1.

Keupp, Katharina, Stephanie Hampp, Monika Maringa, et al.. (2019). Biallelic germline BRCA1 mutations in a patient with early onset breast cancer, mild Fanconi anemia‐like phenotype, and no chromosome fragility. Molecular Genetics & Genomic Medicine. 7(9). e863–e863. 20 indexed citations

2.

Datz, Nicolin, et al.. (2011). Molekulargenetische Diagnostik bei Verdacht auf Maturity Onset Diabetes of the Young (MODY): Klinische Parameter zur Entscheidungshilfe. DMW - Deutsche Medizinische Wochenschrift. 136(21). 1111–1115. 2 indexed citations

3.

Raile, Klemens, Eva Klopocki, Martin Holder, et al.. (2009). Expanded Clinical Spectrum in Hepatocyte Nuclear Factor 1B-Maturity-Onset Diabetes of the Young. The Journal of Clinical Endocrinology & Metabolism. 94(7). 2658–2664. 73 indexed citations

4.

Meißner, Thomas, Jan Marquard, Nadia Cobo‐Vuilleumier, et al.. (2008). Diagnostic Difficulties in Glucokinase Hyperinsulinism. Hormone and Metabolic Research. 41(4). 320–326. 22 indexed citations

5.

Maringa, Monika, et al.. (2008). A case of new mutation in maturity-onset diabetes of the young type 3 (MODY 3) responsive to a low dose of sulphonylurea. Diabetes Research and Clinical Practice. 81(1). e1–e3. 5 indexed citations

6.

Oldridge, Michael, Ana María Fortuna, Monika Maringa, et al.. (2000). Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B. Nature Genetics. 24(3). 275–278. 163 indexed citations

7.

Kühl, Christiane, Rita K. Schmutzler, C Leutner, et al.. (2000). Breast MR Imaging Screening in 192 Women Proved or Suspected to Be Carriers of a Breast Cancer Susceptibility Gene: Preliminary Results. Radiology. 215(1). 267–279. 406 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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