Dietlinde Stienen

1.5k total citations
11 papers, 715 citations indexed

About

Dietlinde Stienen is a scholar working on Pathology and Forensic Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Dietlinde Stienen has authored 11 papers receiving a total of 715 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pathology and Forensic Medicine, 6 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Dietlinde Stienen's work include Genetic factors in colorectal cancer (7 papers), Cancer Genomics and Diagnostics (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Dietlinde Stienen is often cited by papers focused on Genetic factors in colorectal cancer (7 papers), Cancer Genomics and Diagnostics (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Dietlinde Stienen collaborates with scholars based in Germany, Netherlands and Italy. Dietlinde Stienen's co-authors include Stefan Aretz, Siegfried Uhlhaas, Peter Propping, Waltraut Friedl, Walter Back, Steffan Loff, Stefanie Vogt, Elke Holinski‐Feder, Elisabeth Mangold and René Santer and has published in prestigious journals such as International Journal of Cancer, Journal of Medical Genetics and Human Mutation.

In The Last Decade

Dietlinde Stienen

11 papers receiving 691 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dietlinde Stienen Germany	9	514	230	198	198	189	11	715
Isabel Spier Germany	13	307 0.6×	183 0.8×	293 1.5×	221 1.1×	145 0.8×	36	662
Margot G F van Lier Netherlands	9	667 1.3×	417 1.8×	142 0.7×	148 0.7×	317 1.7×	12	897
Pardeep Kaurah Canada	7	375 0.7×	233 1.0×	265 1.3×	192 1.0×	165 0.9×	11	712
Ingrid P. Vogelaar Netherlands	11	316 0.6×	204 0.9×	157 0.8×	110 0.6×	187 1.0×	13	545
Monique Goossens Netherlands	6	701 1.4×	496 2.2×	216 1.1×	131 0.7×	456 2.4×	7	873
Henry T. Lynch United States	9	455 0.9×	386 1.7×	154 0.8×	258 1.3×	154 0.8×	9	724
Yvonne Engwall Sweden	7	271 0.5×	160 0.7×	165 0.8×	161 0.8×	95 0.5×	9	508
Joan Shaw United Kingdom	6	275 0.5×	178 0.8×	218 1.1×	83 0.4×	109 0.6×	9	476
Anne Marie Jelsig Denmark	12	262 0.5×	128 0.6×	67 0.3×	115 0.6×	91 0.5×	43	424
Hamid Mehenni Switzerland	8	397 0.8×	179 0.8×	278 1.4×	127 0.6×	165 0.9×	10	603

Countries citing papers authored by Dietlinde Stienen

Since Specialization

Citations

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

Fields of papers citing papers by Dietlinde Stienen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dietlinde Stienen

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

All Works

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11 of 11 papers shown

Hofmann, Andrea, Alina C. Hilger, Dietlinde Stienen, et al.. (2016). Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVs. Journal of Neurodevelopmental Disorders. 8(1). 11–11. 19 indexed citations

Redler, Silke, Sandra M. Pasternack, Sabrina Wolf, et al.. (2015). A novelKRT86mutation in a Turkish family with monilethrix, and identification of maternal mosaicism. Clinical and Experimental Dermatology. 40(7). 781–785. 5 indexed citations

Spier, Isabel, Stefanie Holzapfel, Janine Altmüller, et al.. (2014). Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas. International Journal of Cancer. 137(2). 320–331. 103 indexed citations

Aretz, Stefan, Rossella Tricarico, Laura Papi, et al.. (2013). MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events. European Journal of Human Genetics. 22(7). 923–929. 36 indexed citations

Spier, Isabel, Sukanya Horpaopan, Stefanie Vogt, et al.. (2012). Deep intronicAPCmutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis. Human Mutation. 33(7). 1045–1050. 54 indexed citations

Draaken, Markus, Heiko Reutter, Charlotte Schramm, et al.. (2010). Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy. European Journal of Medical Genetics. 53(2). 55–60. 48 indexed citations

Kaufmann, Astrid, Stefanie Vogt, Siegfried Uhlhaas, et al.. (2009). Analysis of Rare APC Variants at the mRNA Level. Journal of Molecular Diagnostics. 11(2). 131–139. 17 indexed citations

Aretz, Stefan, Dietlinde Stienen, Siegfried Uhlhaas, et al.. (2007). High proportion of large genomic deletions and a genotype–phenotype update in 80 unrelated families with juvenile polyposis syndrome. Journal of Medical Genetics. 44(11). 702–709. 151 indexed citations

Aretz, Stefan, Dietlinde Stienen, Nicolaus Friedrichs, et al.. (2007). SomaticAPCmosaicism: a frequent cause of familial adenomatous polyposis (FAP). Human Mutation. 28(10). 985–992. 101 indexed citations

10.

Pagenstecher, Constanze, Dorothea Gadzicki, Dietlinde Stienen, et al.. (2007). A Complex Rearrangement in the APC Gene Uncovered by Multiplex Ligation-Dependent Probe Amplification. Journal of Molecular Diagnostics. 9(1). 122–126. 7 indexed citations

11.

Aretz, Stefan, Dietlinde Stienen, Siegfried Uhlhaas, et al.. (2005). High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome. Human Mutation. 26(6). 513–519. 174 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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