Sophia Peters

1.0k total citations
12 papers, 178 citations indexed

About

Sophia Peters is a scholar working on Pathology and Forensic Medicine, Cancer Research and Surgery. According to data from OpenAlex, Sophia Peters has authored 12 papers receiving a total of 178 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Pathology and Forensic Medicine, 4 papers in Cancer Research and 3 papers in Surgery. Recurrent topics in Sophia Peters's work include Genetic factors in colorectal cancer (5 papers), Cancer Genomics and Diagnostics (4 papers) and Genomics and Rare Diseases (2 papers). Sophia Peters is often cited by papers focused on Genetic factors in colorectal cancer (5 papers), Cancer Genomics and Diagnostics (4 papers) and Genomics and Rare Diseases (2 papers). Sophia Peters collaborates with scholars based in Germany, Thailand and United States. Sophia Peters's co-authors include Stefan Aretz, Markus M. Nöthen, Isabel Spier, R. Adam, Sukanya Horpaopan, Stefanie Holzapfel, Michal R. Schweiger, Richard P. Lifton, Bernd Timmermann and Elke Holinski‐Feder and has published in prestigious journals such as PLoS ONE, European Journal of Cancer and Journal of Medical Genetics.

In The Last Decade

Sophia Peters

12 papers receiving 178 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sophia Peters Germany	8	67	66	46	42	35	12	178
Clévia Rosset Brazil	8	52 0.8×	81 1.2×	58 1.3×	32 0.8×	17 0.5×	27	256
Lara Rodríguez‐Laguna Spain	8	34 0.5×	52 0.8×	25 0.5×	59 1.4×	12 0.3×	19	154
Takaaki Yoshikawa Japan	6	28 0.4×	112 1.7×	82 1.8×	14 0.3×	36 1.0×	17	196
Ninad Oak United States	8	29 0.4×	131 2.0×	20 0.4×	126 3.0×	69 2.0×	14	260
Giulia Busonero Italy	4	45 0.7×	69 1.0×	60 1.3×	123 2.9×	59 1.7×	5	420
Marta Ferreira Portugal	6	27 0.4×	87 1.3×	39 0.8×	17 0.4×	47 1.3×	16	177
Changmi Deng China	8	18 0.3×	76 1.2×	51 1.1×	12 0.3×	61 1.7×	22	154
Loreall Pooler United States	8	13 0.2×	87 1.3×	41 0.9×	80 1.9×	39 1.1×	13	207
Yanlai Lu China	8	18 0.3×	89 1.3×	30 0.7×	16 0.4×	44 1.3×	10	228
Hélene Schlecht United Kingdom	7	27 0.4×	100 1.5×	60 1.3×	69 1.6×	28 0.8×	27	199

Countries citing papers authored by Sophia Peters

Since Specialization

Citations

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

Fields of papers citing papers by Sophia Peters

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sophia Peters

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

All Works

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12 of 12 papers shown

Schmidt, Axel, Nicolaus Schwerk, Diane M. Renz, et al.. (2023). Variants in FGF10 cause early onset of severe childhood interstitial lung disease: A detailed description of four affected children. Pediatric Pulmonology. 58(11). 3095–3105. 7 indexed citations

Hsieh, Tzung‐Chien, Axel Schmidt, Sophia Peters, et al.. (2022). Next‐generation phenotyping contributing to the identification of a 4.7 kb deletion in KANSL1 causing Koolen‐de Vries syndrome. Human Mutation. 43(11). 1659–1665. 4 indexed citations

Schmidt, Axel, Sophia Peters, Alexej Knaus, et al.. (2021). TBK1 and TNFRSF13B mutations and an autoinflammatory disease in a child with lethal COVID-19. npj Genomic Medicine. 6(1). 55–55. 28 indexed citations

Perne, Claudia, Sophia Peters, Maria Cartolano, et al.. (2021). Variant profiling of colorectal adenomas from three patients of two families with MSH3-related adenomatous polyposis. PLoS ONE. 16(11). e0259185–e0259185. 8 indexed citations

Spier, Isabel, R. Adam, Stefanie Holzapfel, et al.. (2019). Diagnostic yield and clinical utility of a comprehensive gene panel for hereditary tumor syndromes. Hereditary Cancer in Clinical Practice. 17(1). 5–5. 8 indexed citations

Kuechler, Alma, Mona Grimmel, Jessica Becker, et al.. (2018). De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies. Human Genetics. 137(5). 401–411. 16 indexed citations

Sharma, Amit, Sophia Peters, Stefan Aretz, et al.. (2018). Basal cell carcinomas developing independently from BAP1‐tumor predisposition syndrome in a patient with bilateral uveal melanoma. Genes Chromosomes and Cancer. 58(6). 357–364. 9 indexed citations

Horpaopan, Sukanya, Jutta Kirfel, Sophia Peters, et al.. (2017). Exome sequencing characterizes the somatic mutation spectrum of early serrated lesions in a patient with serrated polyposis syndrome (SPS). Hereditary Cancer in Clinical Practice. 15(1). 22–22. 5 indexed citations

Spier, Isabel, Martin Kerick, Dmitriy Drichel, et al.. (2016). Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis. Familial Cancer. 15(2). 281–288. 40 indexed citations

10.

Spier, Isabel, Dmitriy Drichel, Martin Kerick, et al.. (2015). Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases. Journal of Medical Genetics. 53(3). 172–179. 43 indexed citations

11.

Dafni, Urania, Kornelius Schulze, Erik Thunnissen, et al.. (2015). 3001 Prevalence and clinical association of gene mutations through Multiplex Mutation Testing in patients with NSCLC: Results from the ETOP Lungscape Project. European Journal of Cancer. 51. S595–S596. 6 indexed citations

12.

Chatzitomaris, Apostolos, et al.. (2015). A novel de novo mutation in the thyroid hormone receptor-beta gene. Experimental and Clinical Endocrinology & Diabetes. 122(3). 4 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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