Dietlinde Stienen

1.5k citations

11 papers · 715 indexed · h-index 9

Co-authors: Stefan Aretz Siegfried Uhlhaas Peter Propping Waltraut Friedl Steffan Loff Walter Back Stefanie Vogt Elke Holinski‐Feder
Topics: Genetic factors in colorectal cancer (7 papers)Cancer Genomics and Diagnostics (3 papers)Genomic variations and chromosomal abnormalities (3 papers)
Cited by: Pathology and Forensic Medicine Cancer Research Oncology
Journals: International Journal of Cancer Journal of Medical Genetics Human Mutation
Partner nations: Germany Netherlands Denmark

In The Last Decade

Dietlinde Stienen

11 papers receiving 691 citations

Peers

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

#	Work	Indexed citations
1	Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVs 2016 ·Journal of Neurodevelopmental Disorders ·(unknown),Andrea Hofmann,(unknown),Alina C. Hilger,(unknown),Dietlinde Stienen,U. Gembruch,Michael Ludwig,Waltraut M. Merz,Heiko Reutter	19
2	A novelKRT86mutation in a Turkish family with monilethrix, and identification of maternal mosaicism 2015 ·Clinical and Experimental Dermatology ·Silke Redler,Sandra M. Pasternack,Sabrina Wolf,Dietlinde Stienen,Joerg Wenzel,Markus M. Nöthen,Regina C. Betz	5
3	Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas 2014 ·International Journal of Cancer ·Isabel Spier,Stefanie Holzapfel,Janine Altmüller,Bixiao Zhao,Sukanya Horpaopan,Stefanie Vogt,Sophia Chen,Monika Morak,(unknown),Katrin Kayser,Dietlinde Stienen,R. Adam,Peter Nürnberg,Guido Plotz,Elke Holinski‐Feder,Richard P. Lifton,Hölger Thiele,Per Hoffmann,Verena Steinke,Stefan Aretz	103
4	MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events 2013 ·European Journal of Human Genetics ·Stefan Aretz,Rossella Tricarico,Laura Papi,Isabel Spier,Elisa Pin,Sukanya Horpaopan,Emanuela Lucci‐Cordisco,Monica Pedroni,Dietlinde Stienen,Annamaria Gentile,Anna Panza,Ada Piepoli,Maurizio Ponz de Leòn,Waltraut Friedl,Alessandra Viel,Maurizio Genuardi	36
5	Deep intronicAPCmutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis 2012 ·Human Mutation ·Isabel Spier,Sukanya Horpaopan,Stefanie Vogt,Siegfried Uhlhaas,Monika Morak,Dietlinde Stienen,Markus Draaken,Michael Ludwig,Elke Holinski‐Feder,Markus M. Nöthen,Per Hoffmann,Stefan Aretz	54
6	Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy 2010 ·European Journal of Medical Genetics ·Markus Draaken,Heiko Reutter,Charlotte Schramm,Enrika Bartels,Thomas M. Boemers,Anne‐Karoline Ebert,Wolfgang Rösch,Annette Schröder,Raimund Stein,Susanne Moebus,Dietlinde Stienen,Per Hoffmann,Markus M. Nöthen,Michael Ludwig	48
7	Analysis of Rare APC Variants at the mRNA Level 2009 ·Journal of Molecular Diagnostics ·Astrid Kaufmann,Stefanie Vogt,Siegfried Uhlhaas,Dietlinde Stienen,Ingo Kurth,H. Hameister,Elisabeth Mangold,(unknown),(unknown),Peter Propping,Waltraut Friedl,Stefan Aretz	17
8	High proportion of large genomic deletions and a genotype–phenotype update in 80 unrelated families with juvenile polyposis syndrome 2007 ·Journal of Medical Genetics ·Stefan Aretz,Dietlinde Stienen,Siegfried Uhlhaas,M. Stolte,Mark M. Entius,Steffan Loff,Walter Back,Astrid Kaufmann,(unknown),Stefan Blaas,Reiner Siebert,Stefanie Vogt,S Spranger,Elke Holinski‐Feder,Lone Sunde,Peter Propping,(unknown)	151
9	SomaticAPCmosaicism: a frequent cause of familial adenomatous polyposis (FAP) 2007 ·Human Mutation ·Stefan Aretz,Dietlinde Stienen,Nicolaus Friedrichs,Susanne Stemmler,Siegfried Uhlhaas,Nils Rahner,Peter Propping,Waltraut Friedl	101
10	A Complex Rearrangement in the APC Gene Uncovered by Multiplex Ligation-Dependent Probe Amplification 2007 ·Journal of Molecular Diagnostics ·Constanze Pagenstecher,Dorothea Gadzicki,Dietlinde Stienen,Siegfried Uhlhaas,Elisabeth Mangold,Nils Rahner,Mine Arslan‐Kirchner,Peter Propping,Waltraut Friedl,Stefan Aretz	7
11	High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome 2005 ·Human Mutation ·Stefan Aretz,Dietlinde Stienen,Siegfried Uhlhaas,Steffan Loff,Walter Back,Constanze Pagenstecher,D. Ross McLeod,Gail E. Graham,Elisabeth Mangold,René Santer,Peter Propping,Waltraut Friedl	174

About Dietlinde Stienen

Dietlinde Stienen is a scholar working on Pathology and Forensic Medicine, Urology and Cancer Research, having authored 11 papers that have together received 715 indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (7 papers), Cancer Genomics and Diagnostics (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Pathology and Forensic Medicine (514 citations), Cancer Research (189 citations) and Oncology (230 citations). Dietlinde Stienen has collaborated with scholars based in Germany, Netherlands and Denmark. Frequent co-authors include Stefan Aretz, Siegfried Uhlhaas, Peter Propping, Waltraut Friedl, Steffan Loff, Walter Back, Stefanie Vogt, Elke Holinski‐Feder, Elisabeth Mangold and D. Ross McLeod. Their work appears in journals such as International Journal of Cancer, Journal of Medical Genetics and Human Mutation.

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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