Lars Brichta

3.0k citations
24 papers · 2.0k · h-index 18

Impact in

Papers in

    • RNA modifications and cancer 8
    • RNA Research and Splicing 4
    • Cancer-related gene regulation 3
    • Neurogenetic and Muscular Disorders Research 10

Lars Brichta

24 papers receiving 2.0k citations

Peers

Lars Brichta
Comparison fields: 5 of 94
  • Genetics 880
  • Biological Psychiatry 65
  • Neurology 341
  • Cellular and Molecular Neuroscience 400
  • Molecular Biology 1.3k
Replace Stéphanie Millecamps with:
Stéphanie Millecamps France
Lyndsey Braun United States
Chengyong Shen United States
Elize D. Haasdijk Netherlands
Christine Haenggeli United States
Antonella Borreca Italy
Friedrich Metzger Switzerland
Smita Saxena Switzerland
Johannes Schwarz Germany
Jisook Moon South Korea
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Citations per field
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Stéphanie Millecamps · 1×
Citations per year

Countries citing papers authored by Lars Brichta

Since Specialization
Citations

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

Fields of papers citing papers by Lars Brichta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Lars Brichta, 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 Lars Brichta Line = papers co-authored together Lars Brichta links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2003310
2 2006257
3 2013171
4 2014162
5 2006126
6 2019124
7 2019121
8 2006116
9 2006104
10 2006104
11 201791
12 201583
13 201076
14 200634
15 200632
16 201929
17 200528
18 200826
19 201610
20 20187

About Lars Brichta

Lars Brichta is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Neurology and Surgery, having authored 24 papers that have together received 2.0k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (10 papers), RNA modifications and cancer (8 papers), RNA Research and Splicing (4 papers), Parkinson's Disease Mechanisms and Treatments (3 papers), Neurotransmitter Receptor Influence on Behavior (3 papers), Cancer-related gene regulation (3 papers), Neuroscience and Neuropharmacology Research (3 papers) and Vascular Malformations and Hemangiomas (2 papers). The work is most often cited by research in Genetics (880 citations), Biological Psychiatry (65 citations), Neurology (341 citations), Cellular and Molecular Neuroscience (400 citations) and Molecular Biology (1.3k citations). Lars Brichta has collaborated with scholars based in United States, Germany and Poland. Frequent co-authors include Paul Greengard, Brunhilde Wirth, Eric Hahnen, Marc Flajolet, Markus Rießland, Berthold Schrank, Raoul Heller, Irmgard Hölker, A. Baasner and Hanns Lochmüller. Their work appears in journals such as Human Genetics, Human Molecular Genetics, Nature Neuroscience, Pediatric Dermatology and Arteriosclerosis Thrombosis and Vascular Biology.

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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