Uschi Lindert

1.1k total citations
12 papers, 617 citations indexed

About

Uschi Lindert is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Uschi Lindert has authored 12 papers receiving a total of 617 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Rheumatology. Recurrent topics in Uschi Lindert's work include Connective tissue disorders research (8 papers), Bone and Dental Protein Studies (4 papers) and Trace Elements in Health (3 papers). Uschi Lindert is often cited by papers focused on Connective tissue disorders research (8 papers), Bone and Dental Protein Studies (4 papers) and Trace Elements in Health (3 papers). Uschi Lindert collaborates with scholars based in Switzerland, Germany and United States. Uschi Lindert's co-authors include Walter Schaffner, Viola Günther, Cecilia Giunta, Marianne Rohrbach, David R. Eyre, Jair Tenorio, Pablo Lapunzina, José A. Caparrós‐Martín, Víctor L. Ruiz‐Pérez and Víctor Martínez‐Glez and has published in prestigious journals such as Journal of Biological Chemistry, Molecular and Cellular Biology and Journal of Virology.

In The Last Decade

Uschi Lindert

12 papers receiving 608 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Uschi Lindert Switzerland 9 232 229 195 160 139 12 617
Lampros A. Mavrogiannis United Kingdom 7 152 0.7× 160 0.7× 254 1.3× 71 0.4× 27 0.2× 15 508
Herbert M. Espinoza United States 14 105 0.5× 32 0.1× 505 2.6× 119 0.7× 35 0.3× 16 731
Stephen Pelsue United States 11 68 0.3× 56 0.2× 160 0.8× 149 0.9× 13 0.1× 20 506
Elsa J. Brochmann Murray United States 15 74 0.3× 70 0.3× 352 1.8× 19 0.1× 62 0.4× 30 582
Luchuan Liang United States 10 38 0.2× 212 0.9× 244 1.3× 170 1.1× 12 0.1× 11 786
R. Stallings United States 5 90 0.4× 139 0.6× 351 1.8× 92 0.6× 8 0.1× 7 594
Jane R. Dunlevy United States 16 33 0.1× 52 0.2× 289 1.5× 72 0.5× 27 0.2× 30 652
Anjali Nandal United States 7 84 0.4× 196 0.9× 253 1.3× 9 0.1× 40 0.3× 9 607
Lilit Atanesyan Netherlands 10 45 0.2× 56 0.2× 147 0.8× 44 0.3× 56 0.4× 16 313
I.M. Shapiro United States 15 42 0.2× 49 0.2× 213 1.1× 130 0.8× 88 0.6× 32 606

Countries citing papers authored by Uschi Lindert

Since Specialization
Citations

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

Fields of papers citing papers by Uschi Lindert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Uschi Lindert

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

All Works

12 of 12 papers shown
1.
Lim, Pei Jin, Uschi Lindert, Lennart Opitz, et al.. (2021). Omics Profiling of S2P Mutant Fibroblasts as a Mean to Unravel the Pathomechanism and Molecular Signatures of X-Linked MBTPS2 Osteogenesis Imperfecta. Frontiers in Genetics. 12. 662751–662751. 4 indexed citations
2.
Lim, Pei Jin, Uschi Lindert, Lennart Opitz, et al.. (2019). Transcriptome Profiling of Primary Skin Fibroblasts Reveal Distinct Molecular Features Between PLOD1- and FKBP14-Kyphoscoliotic Ehlers–Danlos Syndrome. Genes. 10(7). 517–517. 13 indexed citations
3.
Lindert, Uschi, Maria Gnoli, Maria Francesca Bedeschi, et al.. (2017). Insight into the Pathology of a COL1A1 Signal Peptide Heterozygous Mutation Leading to Severe Osteogenesis Imperfecta. Calcified Tissue International. 102(3). 373–379. 12 indexed citations
4.
Damme, Tim Van, Alain Colige, Delfien Syx, et al.. (2016). Expanding the clinical and mutational spectrum of the Ehlers–Danlos syndrome, dermatosparaxis type. Genetics in Medicine. 18(9). 882–891. 34 indexed citations
5.
Lindert, Uschi, Marius Kraenzlin, Belinda Campos‐Xavier, et al.. (2015). Urinary pyridinoline cross-links as biomarkers of osteogenesis imperfecta. Orphanet Journal of Rare Diseases. 10(1). 104–104. 6 indexed citations
6.
Lindert, Uschi, Mary Ann Weis, Jyoti Rai, et al.. (2015). Molecular Consequences of the SERPINH1/HSP47 Mutation in the Dachshund Natural Model of Osteogenesis Imperfecta. Journal of Biological Chemistry. 290(29). 17679–17689. 36 indexed citations
7.
Balasubramanian, Meena, Michael Parker, Ann Dalton, et al.. (2013). Genotype–phenotype study in type V osteogenesis imperfecta. Clinical Dysmorphology. 22(3). 93–101. 32 indexed citations
8.
Günther, Viola, et al.. (2012). Simian Virus 40 Strains with Novel Properties Generated by Replacing the Viral Enhancer with Synthetic Oligonucleotides. Journal of Virology. 86(6). 3135–3142. 3 indexed citations
9.
Günther, Viola, Uschi Lindert, & Walter Schaffner. (2012). The taste of heavy metals: Gene regulation by MTF-1. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1823(9). 1416–1425. 274 indexed citations
10.
Martínez‐Glez, Víctor, Eulalia Valencia, José A. Caparrós‐Martín, et al.. (2011). Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta. Human Mutation. 33(2). 343–350. 155 indexed citations
11.
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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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