Barbara Utermann

649 citations
18 papers · 413 · h-index 13

Impact in

    • Hearing, Cochlea, Tinnitus, Genetics
  • Genetics top 10%
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders

Papers in

    • Genomic variations and chromosomal abnormalities 9
    • Genetics and Neurodevelopmental Disorders 2
    • Hedgehog Signaling Pathway Studies 3
    • DNA Repair Mechanisms 1

Barbara Utermann

18 papers receiving 318 citations

Peers

Barbara Utermann
Comparison fields: 5 of 49
  • Sensory Systems 59
  • Genetics 207
  • Pediatrics, Perinatology and Child Health 122
  • Developmental Biology 7
  • Cellular and Molecular Neuroscience 50
Replace Jolanda Gyftodimou with:
Jolanda Gyftodimou Greece
Jennifer McCallum United States
Alisha Wilkens United States
Damina Balmer Switzerland
Leanne Moynihan United Kingdom
Rita Teek Estonia
Greta Gillies Australia
Noah R. Druckenbrod United States
W. J. Kimberling United States
Beatriz R. Versiani Brazil
Barbara Utermann relative to Jolanda Gyftodimou Greece Jolanda Gyftodimou's profile →
Citations per field
00.5×7.2×
Jolanda Gyftodimou · 1×
Citations per year

Countries citing papers authored by Barbara Utermann

Since Specialization
Citations

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

Fields of papers citing papers by Barbara Utermann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

18 of 18 papers shown
#Work
1 200262
2 200641
3 200237
4 200632
5 199732
6 200429
7 200829
8 199729
9 199728
10 199019
11 200417
12 200414
13 199813
14 200412
15 19966
16 20136
17 20004
18 20123

About Barbara Utermann

Barbara Utermann is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Pathology and Forensic Medicine and Cellular and Molecular Neuroscience, having authored 18 papers that have together received 413 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (6 papers), Hedgehog Signaling Pathway Studies (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Fetal and Pediatric Neurological Disorders (2 papers), Chromosomal and Genetic Variations (2 papers), Biomedical Research and Pathophysiology (1 paper) and DNA Repair Mechanisms (1 paper). The work is most often cited by research in Sensory Systems (59 citations), Genetics (207 citations), Pediatrics, Perinatology and Child Health (122 citations), Developmental Biology (7 citations) and Cellular and Molecular Neuroscience (50 citations). Barbara Utermann has collaborated with scholars based in Austria, Germany and Switzerland. Frequent co-authors include Gerd Utermann, Martin Erdel, Hans‐Christoph Duba, Andreas Janecke, Judith Löffler, Helga Weirich‐Schwaiger, Dieter Kotzot, Christine Fauth, Doris Nekahm-Heis and Barbara Günther. Their work appears in journals such as Human Genetics, The Journal of Pediatrics, European Journal of Human Genetics, Movement Disorders and Archives of Dermatological Research.

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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