Siegfried Uhlhaas

2.3k total citations
37 papers, 1.4k citations indexed

About

Siegfried Uhlhaas is a scholar working on Pathology and Forensic Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Siegfried Uhlhaas has authored 37 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Pathology and Forensic Medicine, 12 papers in Molecular Biology and 12 papers in Genetics. Recurrent topics in Siegfried Uhlhaas's work include Genetic factors in colorectal cancer (17 papers), Metabolism and Genetic Disorders (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Siegfried Uhlhaas is often cited by papers focused on Genetic factors in colorectal cancer (17 papers), Metabolism and Genetic Disorders (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Siegfried Uhlhaas collaborates with scholars based in Germany, China and Netherlands. Siegfried Uhlhaas's co-authors include Peter Propping, Waltraut Friedl, Stefan Aretz, Elisabeth Mangold, Constanze Pagenstecher, Dietlinde Stienen, Walter Back, Reiner Caspari, Steffan Loff and Karsten Schulmann and has published in prestigious journals such as Nucleic Acids Research, International Journal of Cancer and Clinica Chimica Acta.

In The Last Decade

Siegfried Uhlhaas

37 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Siegfried Uhlhaas Germany 17 886 471 428 326 293 37 1.4k
Jan Osinga Netherlands 23 225 0.3× 342 0.7× 754 1.8× 365 1.1× 384 1.3× 34 1.5k
Michael O. Woods Canada 20 525 0.6× 418 0.9× 535 1.3× 557 1.7× 119 0.4× 37 1.3k
Yvonne Hendriks Netherlands 14 705 0.8× 550 1.2× 246 0.6× 195 0.6× 162 0.6× 22 1.1k
Kristina Lagerstedt‐Robinson Sweden 24 777 0.9× 617 1.3× 589 1.4× 445 1.4× 268 0.9× 74 1.8k
Antti Ylikorkala Finland 9 506 0.6× 300 0.6× 564 1.3× 123 0.4× 161 0.5× 9 1.1k
Claudia Miranda Italy 22 147 0.2× 410 0.9× 776 1.8× 172 0.5× 203 0.7× 33 1.5k
Elena Arighi Italy 17 143 0.2× 682 1.4× 1.2k 2.7× 326 1.0× 326 1.1× 19 1.9k
Ezra Y. Rosen United States 10 159 0.2× 381 0.8× 299 0.7× 177 0.5× 102 0.3× 32 924
Yukihiro Takagi Japan 9 250 0.3× 469 1.0× 370 0.9× 45 0.1× 152 0.5× 11 847
Alexa Kidd New Zealand 14 122 0.1× 177 0.4× 663 1.5× 327 1.0× 58 0.2× 24 1.1k

Countries citing papers authored by Siegfried Uhlhaas

Since Specialization
Citations

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

Fields of papers citing papers by Siegfried Uhlhaas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Siegfried Uhlhaas

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

All Works

20 of 20 papers shown
1.
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
2.
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
3.
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
4.
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
5.
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
6.
Liu, Xiaorong, Waltraut Friedl, Siegfried Uhlhaas, et al.. (2006). May the APC gene somatic mutations in tumor tissues influence the clinical features of Chinese sporadic colorectal cancers?. Acta Oncologica. 46(6). 757–762. 7 indexed citations
7.
Aretz, Stefan, Arend Koch, Siegfried Uhlhaas, et al.. (2005). Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations?. Pediatric Blood & Cancer. 47(6). 811–818. 72 indexed citations
8.
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
9.
Aretz, Stefan, Siegfried Uhlhaas, Yuli Sun, et al.. (2004). Familial adenomatous polyposis: Aberrant splicing due to missense or silent mutations in theAPCgene. Human Mutation. 24(5). 370–380. 89 indexed citations
10.
Aretz, Stefan, Siegfried Uhlhaas, Reiner Caspari, et al.. (2003). Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis. European Journal of Human Genetics. 12(1). 52–58. 103 indexed citations
11.
Friedl, Waltraut, Siegfried Uhlhaas, Karsten Schulmann, et al.. (2002). Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriers. Human Genetics. 111(1). 108–111. 123 indexed citations
12.
Propping, Peter, Waltraut Friedl, Thomas F. Wienker, Siegfried Uhlhaas, & Klaus Zerres. (2000). Adult syndrome allelic to limb mammary syndrome (LMS)?. American Journal of Medical Genetics. 90(2). 179–179. 3 indexed citations
13.
Caspari, Reiner, Siegfried Uhlhaas, Waltraut Friedl, Michael Knapp, & Peter Propping. (2000). Mapping of a gene for nonspecific X-linked mental retardation (MRX 75) to Xq24-q26. American Journal of Medical Genetics. 93(4). 290–293. 4 indexed citations
14.
Propping, Peter, et al.. (2000). Adult syndrome allelic to limb mammary syndrome (LMS)?. American Journal of Medical Genetics. 90(2). 179–182. 23 indexed citations
15.
Friedl, Waltraut, Roland Kruse, Siegfried Uhlhaas, et al.. (1999). Frequent 4‐bp deletion in exon 9 of the SMAD4MADH4 gene in familial juvenile polyposis patients. Genes Chromosomes and Cancer. 25(4). 403–406. 5 indexed citations
16.
Friedl, Waltraut, Roland Kruse, Siegfried Uhlhaas, et al.. (1999). Frequent 4-bp deletion in exon 9 of theSMAD4/MADH4 gene in familial juvenile polyposis patients. Genes Chromosomes and Cancer. 25(4). 403–406. 63 indexed citations
17.
Zhu, Shengtao, Markus M. Nöthen, Siegfried Uhlhaas, et al.. (1996). Apolipoprotein E genotype distribution in schizophrenia. Psychiatric Genetics. 6(2). 75–80. 23 indexed citations
18.
Rietschel, Marcella, Waltraut Friedl, Siegfried Uhlhaas, et al.. (1991). MASA syndrome: Clinical variability and linkage analysis. American Journal of Medical Genetics. 41(1). 10–14. 13 indexed citations
19.
Körner, Judith, Siegfried Uhlhaas, Jacques Mallet, Peter Propping, & A. Gal. (1988). Further RFLPs at the human tyrosine hydroxylase locus. Nucleic Acids Research. 16(18). 9078–9078. 2 indexed citations
20.
Propping, Peter, et al.. (1987). Genetic influences on CNS diseases secondary to alcoholism.. PubMed. 241. 97–105. 1 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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