Gunnar Sanner

679 citations
22 papers · 371 indexed · h-index 11
Topics
Mitochondrial Function and Pathology (5 papers)Metabolism and Genetic Disorders (5 papers)Cerebral Palsy and Movement Disorders (5 papers)

In The Last Decade

Gunnar Sanner

22 papers receiving 351 citations

Peers

Gunnar Sanner
Comparison fields: 5 of 56
  • Psychiatry and Mental health 110
  • Cellular and Molecular Neuroscience 103
  • Neurology 99
  • Pediatrics, Perinatology and Child Health 97
  • Molecular Biology 84
Replace Yoshio Morimatsu with:
Yoshio Morimatsu Japan
Véronique Humbertclaude France
De Falco Fa Italy
Emilio Le Piane Italy
M. Harold Fogelson United States
Anu Anttinen Finland
Daniel J. Lacey United States
M. Brinciotti Italy
Helen Young Australia
Anita Devlin United Kingdom
Gunnar Sanner relative to Yoshio Morimatsu Japan Yoshio Morimatsu's profile →
Citations per field
00.5×
Yoshio Morimatsu · 1×
Citations per year

Countries citing papers authored by Gunnar Sanner

Since Specialization
Citations

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

Fields of papers citing papers by Gunnar Sanner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gunnar Sanner

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

All Works

20 of 20 papers shown
#WorkIndexed citations
1 3
2 11
3 2
4 5
5 6
6 12
7 60
8 24
9 2
10 33
11 9
12 43
13 4
14 6
15 17
16
The dysequilibrium syndrome in cerebral palsy : clinical, pneumoencephalographic and genetic investigations
1
17 17
18
The dysequilibrium syndrome in cerebral palsy. Clinical aspects and treatment.
36
19
[Causes of cerebral palsy. 4. The CP-syndrome with genetic background].
1
20 52

About Gunnar Sanner

Gunnar Sanner is a scholar working on Clinical Biochemistry, Psychiatry and Mental health and Neurology, having authored 22 papers that have together received 371 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (5 papers) and Cerebral Palsy and Movement Disorders (5 papers). The work is most often cited by research in Psychiatry and Mental health (110 citations), Neurology (99 citations) and Cellular and Molecular Neuroscience (103 citations). Gunnar Sanner has collaborated with scholars based in Sweden, United States and Norway. Frequent co-authors include Bengt Hagberg, K.‐H. Gustavson, Björn Bergström, Gösta Holmgren, Johnny Ludvigsson, B Bille, Lars Forsgren, Michael Steen, J. Wahlström and Ulf Drugge. Their work appears in journals such as Movement Disorders, Developmental Medicine & Child Neurology and Human 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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