Vera Beyer

674 citations
15 papers · 318 · h-index 9

Impact in

    • Hearing, Cochlea, Tinnitus, Genetics
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
    • Genetic Syndromes and Imprinting

Papers in

    • Genomic variations and chromosomal abnormalities 7
    • Genetics and Neurodevelopmental Disorders 4
    • DNA Repair Mechanisms 2
    • Congenital heart defects research 2

Vera Beyer

15 papers receiving 308 citations

Peers

Vera Beyer
Comparison fields: 5 of 56
  • Sensory Systems 36
  • Genetics 168
  • Cognitive Neuroscience 61
  • Molecular Biology 181
  • Otorhinolaryngology 10
Replace Matthew F. Hunter with:
Matthew F. Hunter Australia
Tiia Reimand Estonia
Teresa Palladino Italy
Jiale Xiang China
Dinah Yaeger United States
Dean Phelan Australia
Jennifer McCallum United States
Sarah Williams United States
Clemer Abad United States
Jolanda Gyftodimou Greece
Vera Beyer relative to Matthew F. Hunter Australia Matthew F. Hunter's profile →
Citations per field
00.5×1.5×
Matthew F. Hunter · 1×
Citations per year

Countries citing papers authored by Vera Beyer

Since Specialization
Citations

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

Fields of papers citing papers by Vera Beyer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

15 of 15 papers shown
#Work
1 200996
2 200845
3 200739
4 201235
5 200322
6 200917
7 200813
8 20009
9 20109
10 20117
11 20077
12 20207
13 20135
14 20124
15 20093

About Vera Beyer

Vera Beyer is a scholar working on Genetics, Molecular Biology, Plant Science, Oncology and Surgery, having authored 15 papers that have together received 318 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (4 papers), Chromosomal and Genetic Variations (3 papers), DNA Repair Mechanisms (2 papers), Congenital heart defects research (2 papers), Acute Myeloid Leukemia Research (1 paper), Autism Spectrum Disorder Research (1 paper) and Plant Virus Research Studies (1 paper). The work is most often cited by research in Sensory Systems (36 citations), Genetics (168 citations), Cognitive Neuroscience (61 citations), Molecular Biology (181 citations) and Otorhinolaryngology (10 citations). Vera Beyer has collaborated with scholars based in Germany, Netherlands and United States. Frequent co-authors include Thomas Haaf, Martin Poot, Ruben van’t Slot, Sue Holder, Ira Schwaab, Oliver Bartsch, Ulrich Zechner, Nicolai Kohlschmidt, Martin Schüler and Rainer Wiewrodt. Their work appears in journals such as European Journal of Medical Genetics, Cytogenetic and Genome Research, Gene, Neurogenetics and Human Molecular Genetics.

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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