U Friedrich

2.3k citations
66 papers · 1.5k · h-index 21

Impact in

    • Retinal Diseases and Treatments
  • Genetics top 5%
    • Genomic variations and chromosomal abnormalities
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genetics and Neurodevelopmental Disorders

Papers in

    • Retinal Development and Disorders 11
    • Sexual Differentiation and Disorders 5
    • Genomic variations and chromosomal abnormalities 12
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7

U Friedrich

64 papers receiving 1.4k citations

Peers

U Friedrich
Comparison fields: 5 of 127
  • Ophthalmology 170
  • Genetics 459
  • Sensory Systems 70
  • Biotechnology 104
  • Molecular Biology 706
Replace Mi‐Ryoung Song with:
Mi‐Ryoung Song South Korea
Wolfgang Jagla Germany
Günter Giese Germany
Florian Kreppel Germany
J. Timothy Stout United States
Bernard Pessac France
Brian A. Donahue United States
Lawrence J. Rizzolo United States
Catherine R. O’Riordan United States
Takeshi Matsui Japan
U Friedrich relative to Mi‐Ryoung Song South Korea Mi‐Ryoung Song's profile →
Citations per field
00.5×4.3×
Mi‐Ryoung Song · 1×
Citations per year

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-authors

The 25 scholars most cited alongside U Friedrich, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with U Friedrich Line = papers co-authored together U Friedrich links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 66 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2011145
2 1994134
3 2000101
4 199682
5 201678
6 197776
7 198661
8 201156
9 197853
10 201548
11 199848
12 196942
13 201539
14 201038
15 197032
16 201728
17
Inverted tandem duplication of the short arm of chromosome 8: a non-random de novo structural aberration in man. Localization of the gene for glutathione reductase in subband 8p21.1.
198225
18 198425
19 201623
20 196820

About U Friedrich

U Friedrich is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 66 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Retinal Development and Disorders (11 papers), Prenatal Screening and Diagnostics (11 papers), Chromosomal and Genetic Variations (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Sexual Differentiation and Disorders (5 papers), Cellular transport and secretion (4 papers) and Photoreceptor and optogenetics research (4 papers). The work is most often cited by research in Ophthalmology (170 citations), Genetics (459 citations), Sensory Systems (70 citations), Biotechnology (104 citations) and Molecular Biology (706 citations). U Friedrich has collaborated with scholars based in Germany, Denmark and Poland. Frequent co-authors include Bernhard H. F. Weber, Philip Coffino, Jørgen Nielsen, H. B�nisch, Peter Gerner‐Smidt, U. Zimmermann, Takayuki Tsuboi, Rainer Ehmann, J. Dippon and Godehard Friedel. Their work appears in journals such as Clinical Genetics, Human Molecular Genetics, Prenatal Diagnosis, Annals of Human Genetics and Investigative Ophthalmology & Visual Science.

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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