Ulla Werlauff

842 citations
41 papers · 381 · h-index 12

Impact in

Papers in

    • Neurogenetic and Muscular Disorders Research 19
    • Muscle Physiology and Disorders 15
    • Mitochondrial Function and Pathology 4

Ulla Werlauff

35 papers receiving 375 citations

Peers

Ulla Werlauff
Comparison fields: 5 of 55
  • Genetics 185
  • Psychiatry and Mental health 54
  • Neurology 46
  • Cardiology and Cardiovascular Medicine 68
  • Speech and Hearing 19
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Citations per year

Countries citing papers authored by Ulla Werlauff

Since Specialization
Citations

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

Fields of papers citing papers by Ulla Werlauff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 41 papers — load more, or switch the sort, to bring in the rest.

#Work
1 200053
2 201334
3 201633
4 201730
5 201226
6 200917
7 201917
8 201517
9 201415
10 200114
11 202113
12 201411
13 201811
14 201810
15 20159
16 20089
17 20228
18 20228
19 20237
20 20215

About Ulla Werlauff

Ulla Werlauff is a scholar working on Genetics, Molecular Biology, Neurology, Psychiatry and Mental health and Surgery, having authored 41 papers that have together received 381 indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (19 papers), Muscle Physiology and Disorders (15 papers), Genetic Neurodegenerative Diseases (6 papers), Parkinson's Disease Mechanisms and Treatments (5 papers), Cardiomyopathy and Myosin Studies (5 papers), Congenital Anomalies and Fetal Surgery (5 papers), Family and Disability Support Research (4 papers) and Mitochondrial Function and Pathology (4 papers). The work is most often cited by research in Genetics (185 citations), Psychiatry and Mental health (54 citations), Neurology (46 citations), Cardiology and Cardiovascular Medicine (68 citations) and Speech and Hearing (19 citations). Ulla Werlauff has collaborated with scholars based in Denmark, South Korea and Sweden. Frequent co-authors include Birgit F. Steffensen, John Vissing, Nanna Witting, Morten Dunø, Charlotte Handberg, Mogens Erlandsen, Anna‐Karin Kroksmark, Jes Rahbek, Thomas Sejersen and Ulrika Kreicbergs. Their work appears in journals such as Neuromuscular Disorders, Journal of Neuromuscular Diseases, Disability and Rehabilitation, Journal of Evaluation in Clinical Practice and Muscle & Nerve.

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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