U Friedrich

2.3k total citations
66 papers, 1.5k citations indexed

About

U Friedrich is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, U Friedrich has authored 66 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 26 papers in Genetics and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in U Friedrich's work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (11 papers) and Retinal Development and Disorders (11 papers). U Friedrich is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (11 papers) and Retinal Development and Disorders (11 papers). U Friedrich collaborates with scholars based in Germany, Denmark and Poland. U Friedrich's co-authors include Bernhard H. F. Weber, Philip Coffino, Jørgen Nielsen, H. B�nisch, Peter Gerner‐Smidt, U. Zimmermann, Takayuki Tsuboi, J. Dippon, Thorsten Walles and Godehard Friedel and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Biomaterials.

In The Last Decade

U Friedrich

64 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
U Friedrich Germany 21 706 459 243 170 151 66 1.5k
Mi‐Ryoung Song South Korea 27 1.2k 1.7× 492 1.1× 149 0.6× 40 0.2× 42 0.3× 68 2.3k
Florian Kreppel Germany 29 1.5k 2.2× 1.2k 2.5× 59 0.2× 100 0.6× 101 0.7× 79 3.5k
Juehua Yu China 22 1.4k 1.9× 249 0.5× 286 1.2× 47 0.3× 69 0.5× 69 2.2k
Sergio M. Gloor Switzerland 26 1.4k 2.0× 178 0.4× 201 0.8× 20 0.1× 42 0.3× 43 2.5k
M. Lalande United States 31 1.9k 2.7× 1.8k 4.0× 174 0.7× 45 0.3× 47 0.3× 62 3.2k
Ran Wei China 23 745 1.1× 173 0.4× 83 0.3× 30 0.2× 76 0.5× 108 1.7k
Catherine R. O’Riordan United States 25 2.0k 2.8× 1.2k 2.6× 84 0.3× 33 0.2× 59 0.4× 41 3.5k
Bernard Pessac France 27 1.2k 1.7× 377 0.8× 35 0.1× 69 0.4× 52 0.3× 76 2.7k
J. Timothy Stout United States 27 1.6k 2.3× 425 0.9× 25 0.1× 718 4.2× 450 3.0× 76 2.7k
Mohammad A. Rafi United States 30 1.2k 1.7× 242 0.5× 134 0.6× 18 0.1× 92 0.6× 66 2.6k

Countries citing papers authored by U Friedrich

Since Specialization
Citations

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

Fields of papers citing papers by U Friedrich

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of U Friedrich

This figure shows the co-authorship network connecting the top 25 collaborators of U Friedrich. A scholar is included among the top collaborators of U Friedrich 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 U Friedrich. U Friedrich 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.
Strunz, Tobias, et al.. (2022). Vitronectin and Its Interaction with PAI-1 Suggests a Functional Link to Vascular Changes in AMD Pathobiology. Cells. 11(11). 1766–1766. 9 indexed citations
2.
Straub, Kristina, et al.. (2019). Identification of the retinoschisin-binding site on the retinal Na/K-ATPase. PLoS ONE. 14(5). e0216320–e0216320. 14 indexed citations
3.
Friedrich, U, J. Backhaus, Stephan König, et al.. (2019). Validation and educational impact study of the NANEP high-fidelity simulation model for open preperitoneal mesh repair of umbilical hernia. Hernia. 24(4). 873–881. 9 indexed citations
4.
Straub, Kristina, et al.. (2018). Pathomechanism of mutated and secreted retinoschisin in X-linked juvenile retinoschisis. Experimental Eye Research. 177. 23–34. 17 indexed citations
5.
Friedrich, U, Thomas Schubert, Magdalena Schneider, et al.. (2015). Synonymous variants in HTRA1 implicated in AMD susceptibility impair its capacity to regulate TGF-β signaling. Human Molecular Genetics. 24(22). 6361–6373. 39 indexed citations
6.
Apaolaza, Paola S., Ana del Pozo‐Rodríguez, Alicia Rodríguez‐Gascón, et al.. (2015). Solid lipid nanoparticle-based vectors intended for the treatment of X-linked juvenile retinoschisis by gene therapy: In vivo approaches in Rs1h-deficient mouse model. Journal of Controlled Release. 217. 273–283. 48 indexed citations
7.
Friedrich, U, Connie A. Myers, Lars G. Fritsche, et al.. (2011). Risk- and non-risk-associated variants at the 10q26 AMD locus influence ARMS2 mRNA expression but exclude pathogenic effects due to protein deficiency. Human Molecular Genetics. 20(7). 1387–1399. 56 indexed citations
8.
Ehmann, Rainer, et al.. (2011). Canine scent detection in the diagnosis of lung cancer: revisiting a puzzling phenomenon. European Respiratory Journal. 39(3). 669–676. 145 indexed citations
9.
Friedrich, U, et al.. (2005). Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: Cytogenetic and molecular analysis with delineation of the phenotype. American Journal of Medical Genetics Part A. 136A(3). 259–264. 8 indexed citations
10.
Veit, Michael, et al.. (1997). Fre2, a proviral integration site of Friend murine leukemia virus that is closely linked to Fv2. Leukemia. 11(5). 619–623. 1 indexed citations
11.
Friedrich, U, et al.. (1997). Experimental and Clinical Experience with New Pyeloureteral Stents in Pediatric Urology. Journal of Endourology. 11(6). 431–439. 2 indexed citations
12.
Hasle, Henrik, Jørgen H. Olsen, Jørgen Nielsen, et al.. (1996). Occurrence of cancer in women with Turner syndrome. British Journal of Cancer. 73(9). 1156–1159. 82 indexed citations
13.
Winnefeld, K, et al.. (1995). Selenium in serum and whole blood in patients with surgical interventions. Biological Trace Element Research. 50(2). 149–155. 16 indexed citations
14.
Friedrich, U, et al.. (1994). Quantitative Investigations of Acetylcholinesterase Activities in Colorectal Malformations*. European Journal of Pediatric Surgery. 4(6). 352–357. 1 indexed citations
15.
Gravholt, Claus Højbjerg, et al.. (1994). Fluorescence in situ hybridization reveals a break in the ?-satellite DNA of chromosome 1 in a family with a balanced whole-arm translocation. Human Genetics. 94(5). 504–8. 6 indexed citations
16.
DeLisi, L. E., U Friedrich, Justin T. Wahlstrom, et al.. (1994). Schizophrenia and Sex Chromosome Anomalies. Schizophrenia Bulletin. 20(3). 495–505. 134 indexed citations
17.
Friedrich, U, Torben Bjerregaard Larsen, & J. Nielsen. (1991). Diagnostic reliability of the cytogenetic centromere heteromorphism in the human X chromosome. Clinical Genetics. 40(6). 465–466. 1 indexed citations
18.
Gerner‐Smidt, Peter & U Friedrich. (1978). The mutagenic effect of benzene, toluene and xylene studied by the SCE technique. Mutation Research/Genetic Toxicology. 58(2-3). 313–316. 53 indexed citations
19.
Nielsen, Jørgen, U Friedrich, & Takayuki Tsuboi. (1969). Chromosome Abnormalities in Patients Treated with Chlorpromazine, Perphenazine, and Lysergide. BMJ. 3(5671). 634–636. 42 indexed citations
20.
Nielsen, Jørgen, U Friedrich, E. Jacobsen, & Takayuki Tsuboi. (1968). Lysergide and chromosome abnormalities.. BMJ. 2(5608). 801–803. 20 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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