Gunnar Sanner

679 total citations
22 papers, 371 citations indexed

About

Gunnar Sanner is a scholar working on Molecular Biology, Psychiatry and Mental health and Neurology. According to data from OpenAlex, Gunnar Sanner has authored 22 papers receiving a total of 371 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Psychiatry and Mental health and 5 papers in Neurology. Recurrent topics in Gunnar Sanner's work include Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (5 papers) and Cerebral Palsy and Movement Disorders (5 papers). Gunnar Sanner is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (5 papers) and Cerebral Palsy and Movement Disorders (5 papers). Gunnar Sanner collaborates with scholars based in Sweden, United States and Norway. Gunnar Sanner's 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 and has published in prestigious journals such as Movement Disorders, Developmental Medicine & Child Neurology and Human Genetics.

In The Last Decade

Gunnar Sanner

22 papers receiving 351 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Gunnar Sanner Sweden	11	110	103	99	97	84	22	371
Yoshio Morimatsu Japan	11	77 0.7×	76 0.7×	114 1.2×	69 0.7×	69 0.8×	33	336
Philip Kennedy United Kingdom	8	135 1.2×	90 0.9×	56 0.6×	22 0.2×	80 1.0×	11	436
Emilio Le Piane Italy	12	227 2.1×	180 1.7×	133 1.3×	87 0.9×	59 0.7×	22	440
Zeliha Matur Türkiye	10	113 1.0×	101 1.0×	103 1.0×	38 0.4×	51 0.6×	48	350
M. Harold Fogelson United States	10	31 0.3×	111 1.1×	61 0.6×	99 1.0×	141 1.7×	18	410
De Falco Fa Italy	15	177 1.6×	103 1.0×	180 1.8×	42 0.4×	143 1.7×	42	599
Véronique Humbertclaude France	14	225 2.0×	137 1.3×	100 1.0×	75 0.8×	319 3.8×	29	631
Daniel J. Lacey United States	12	106 1.0×	99 1.0×	71 0.7×	181 1.9×	95 1.1×	21	412
Teemu Laitinen Finland	11	87 0.8×	67 0.7×	94 0.9×	75 0.8×	48 0.6×	11	386
Christopher Rittey United Kingdom	10	193 1.8×	113 1.1×	147 1.5×	74 0.8×	73 0.9×	16	498

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

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20 of 20 papers shown

Schoumans, Jacqueline, Gunnar Sanner, Magnus Nordenskjöld, & Britt‐Marie Anderlid. (2005). Detailed clinical description of four patients with 1.3 and 2.1 Mb chromosome imbalances derived from a familial t(12;17)(q24.33;q25.3). American Journal of Medical Genetics Part A. 134A(3). 254–258. 3 indexed citations

Wahlström, J., Laurie J. Ozelius, P. L. Kramer, et al.. (1994). The gene for familial dystonia with myoclonic jerks responsive to alcohol is not located on the distal end of 9q. Clinical Genetics. 45(2). 88–92. 11 indexed citations

Sanner, Gunnar, et al.. (1993). Early onset dystonia decreasing with development. Brain and Development. 15(4). 295–298. 2 indexed citations

Sanner, Gunnar, et al.. (1993). Movement patterns in children with Down's syndrome: A pilot study. Physiotherapy Theory and Practice. 9(1). 33–41. 5 indexed citations

Schuback, Deborah E., Laurie J. Ozelius, Gösta Holmgren, et al.. (1991). Dopamine beta-hydroxylase gene excluded in four subtypes of hereditary dystonia. Human Genetics. 87(3). 311–316. 6 indexed citations

Sommerfelt, Kristian, Mårten Kyllerman, & Gunnar Sanner. (1991). Hereditary spastic paraplegia with epileptic myoclonus. Acta Neurologica Scandinavica. 84(2). 157–160. 12 indexed citations

Forsgren, Lars, et al.. (1990). Alcohol‐responsive myoclonic dystonia in a large family: Dominant inheritance and phenotypic variation. Movement Disorders. 5(4). 270–279. 60 indexed citations

Hagberg, Bengt, J Rapola, Jan‐Eric Månsson, et al.. (1986). Salla Disease Variants. Neuropediatrics. 17(1). 44–47. 24 indexed citations

Sanner, Gunnar, et al.. (1985). Refractive Errors in the Fragile‐X Syndrome. Acta Paediatrica. 74(6). 974–974. 2 indexed citations

10.

Sanner, Gunnar & Björn Bergström. (1979). BENIGN PAROXYSMAL TORTICOLLIS IN INFANCY. Acta Paediatrica. 68(3). 219–223. 33 indexed citations

11.

Sanner, Gunnar. (1979). Pathogenetic and Preventive Aspects of Non‐progressive Ataxic Syndromes. Developmental Medicine & Child Neurology. 21(5). 663–671. 9 indexed citations

12.

Bille, B, Johnny Ludvigsson, & Gunnar Sanner. (1977). Prophylaxis of Migraine in Children. Headache The Journal of Head and Face Pain. 17(2). 61–63. 43 indexed citations

13.

Gustavson, K.‐H., Svante B. Ross, & Gunnar Sanner. (1977). Low serum dopamine‐β‐hydroxylase activity in the dysequilibrium syndrome. Clinical Genetics. 11(3). 270–272. 4 indexed citations

14.

Bergström, Kjell & Gunnar Sanner. (1974). PNEUMOENCEPHALOGRAPHY IN NON‐PROGRESSIVE ATAXIC SYNDROMES A Study of 26 Children and Adolescents. Acta Paediatrica. 63(5). 732–742. 6 indexed citations

15.

Sanner, Gunnar & Bengt Hagberg. (1974). 188 Cases of Non-Progressive Ataxic Syndromes in Childhood – Aspects of aetiology and classification. Neuropediatrics. 5(3). 224–235. 17 indexed citations

16.

Sanner, Gunnar. (1973). The dysequilibrium syndrome in cerebral palsy : clinical, pneumoencephalographic and genetic investigations. 1 indexed citations

17.

Sanner, Gunnar. (1973). The Dysequilibrium Syndrome – A genetic study. Neuropediatrics. 4(4). 403–413. 17 indexed citations

18.

Hagberg, Bengt, Gunnar Sanner, & Michael Steen. (1972). The dysequilibrium syndrome in cerebral palsy. Clinical aspects and treatment.. PubMed. 226. 1–63. 36 indexed citations

19.

Gustavson, K.‐H., Bengt Hagberg, & Gunnar Sanner. (1969). [Causes of cerebral palsy. 4. The CP-syndrome with genetic background].. PubMed. 66(17). 1773–9. 1 indexed citations

20.

Gustavson, K.‐H., et al.. (1969). IDENTICAL SYNDROMES OF CEREBRAL PALSY IN THE SAME FAMILY. Acta Paediatrica. 58(4). 330–340. 52 indexed citations

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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