Sylvia Stöckler

4.4k total citations
81 papers, 2.4k citations indexed

About

Sylvia Stöckler is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, Sylvia Stöckler has authored 81 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Clinical Biochemistry, 30 papers in Molecular Biology and 22 papers in Physiology. Recurrent topics in Sylvia Stöckler's work include Metabolism and Genetic Disorders (38 papers), Muscle metabolism and nutrition (12 papers) and Biochemical and Molecular Research (11 papers). Sylvia Stöckler is often cited by papers focused on Metabolism and Genetic Disorders (38 papers), Muscle metabolism and nutrition (12 papers) and Biochemical and Molecular Research (11 papers). Sylvia Stöckler collaborates with scholars based in Canada, Austria and Germany. Sylvia Stöckler's co-authors include F. Hanefeld, Clara van Karnebeek, Jens Frahm, Gajja S. Salomons, Barbara Plecko, Peter W. Schütz, Gunther Helms, Iris Marquardt, U. Holzbach and Wolfgang Hänicke and has published in prestigious journals such as The Lancet, PLoS ONE and Brain.

In The Last Decade

Sylvia Stöckler

74 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sylvia Stöckler Canada	22	1.2k	1.0k	622	465	388	81	2.4k
Sylvia Stöckler‐Ipsiroglu Canada	30	1.3k 1.1×	954 0.9×	762 1.2×	522 1.1×	477 1.2×	103	2.5k
Jaume Campistol Spain	29	1.3k 1.0×	1.2k 1.2×	146 0.2×	484 1.0×	356 0.9×	99	2.4k
Barbara Garavaglia Italy	36	1.4k 1.2×	2.0k 2.0×	211 0.3×	501 1.1×	373 1.0×	152	4.0k
Robert Surtees United Kingdom	23	757 0.6×	848 0.8×	141 0.2×	246 0.5×	259 0.7×	45	2.2k
Hiroshi Mitsubuchi Japan	23	687 0.6×	775 0.8×	144 0.2×	390 0.8×	188 0.5×	92	2.0k
Aída Ormazábal Spain	28	865 0.7×	729 0.7×	96 0.2×	207 0.4×	422 1.1×	86	1.8k
R. Surtees United Kingdom	24	922 0.8×	994 1.0×	98 0.2×	425 0.9×	549 1.4×	45	2.2k
Κ. Hyland United States	30	995 0.8×	789 0.8×	101 0.2×	289 0.6×	581 1.5×	69	2.5k
Thierry Billette de Villemeur France	27	320 0.3×	1.0k 1.0×	452 0.7×	954 2.1×	125 0.3×	111	2.4k
N. G. G. M. Abeling Netherlands	25	566 0.5×	943 0.9×	96 0.2×	297 0.6×	228 0.6×	84	2.0k

Countries citing papers authored by Sylvia Stöckler

Since Specialization

Citations

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

Fields of papers citing papers by Sylvia Stöckler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sylvia Stöckler

This figure shows the co-authorship network connecting the top 25 collaborators of Sylvia Stöckler. A scholar is included among the top collaborators of Sylvia Stöckler 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 Sylvia Stöckler. Sylvia Stöckler 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

Ipsiroglu, O., Oliviero Bruni, James R. Connor, et al.. (2024). The iron deficiency conundrum – limitations of existing clinical practice guidelines and next steps. Sleep Medicine. 115. S315–S315.

Yeganeh, Mehdi, Catherine Jones, Gloria Y. F. Ho, et al.. (2023). Use of dexamethasone in acute rhabdomyolysis in LPIN1 deficiency. Molecular Genetics and Metabolism Reports. 35. 100961–100961. 1 indexed citations

Stöckler, Sylvia, et al.. (2022). Iron deficiency and common neurodevelopmental disorders—A scoping review. PLoS ONE. 17(9). e0273819–e0273819. 26 indexed citations

Ipsiroglu, O., et al.. (2018). Prenatal alcohol exposure and sleep-wake behaviors: exploratory and naturalistic observations in the clinical setting and in an animal model. Sleep Medicine. 54. 101–112. 17 indexed citations

Wagner, Anjuli D., et al.. (2015). Suggested clinical immobilization test (SCIT) for diagnosis of Willis–Ekbom disease in clinical practice. Sleep Medicine. 16. S205–S206. 1 indexed citations

Karnebeek, Clara van, Gabriella Horváth, Jacqueline Purtzki, et al.. (2014). Deep Brain Stimulation and Dantrolene for Secondary Dystonia in X-Linked Adrenoleukodystrophy. JIMD Reports. 15. 113–6. 16 indexed citations

Plecko, Barbara, Philippa B. Mills, Peter T. Clayton, et al.. (2014). Pyridoxine responsiveness in novel mutations of the PNPO gene. Neurology. 82(16). 1425–1433. 67 indexed citations

Horváth, Gabriella, Sandra Sirrs, Sylvia Stöckler, et al.. (2013). Three years experience with dried blood spot α-glucosidase screening for Pompe disease in British Columbia, Canada. BMC Musculoskeletal Disorders. 14(S2). 5 indexed citations

Gelinas, Jennifer N., et al.. (2012). Child Neurology: Krabbe disease. Neurology. 79(19). e170–2. 3 indexed citations

10.

Stöckler, Sylvia, et al.. (2012). Cultural aspects in the management of inborn errors of metabolism. Journal of Inherited Metabolic Disease. 35(6). 1147–1152. 18 indexed citations

11.

Karnebeek, Clara van, Hans Hartmann, Sravan Jaggumantri, et al.. (2012). Lysine restricted diet for pyridoxine-dependent epilepsy: First evidence and future trials. Molecular Genetics and Metabolism. 107(3). 335–344. 80 indexed citations

12.

Karnebeek, Clara van, et al.. (2012). The treatable intellectual disability APP www.treatable-id.org: A digital tool to enhance diagnosis & care for rare diseases. Orphanet Journal of Rare Diseases. 7(1). 47–47. 37 indexed citations

13.

Schütz, Peter W., Peter K. H. Wong, John R. OʼKusky, Sheila M. Innis, & Sylvia Stöckler. (2010). Effects of d-3-hydroxybutyrate treatment on hypoglycemic coma in rat pups. Experimental Neurology. 227(1). 180–187. 7 indexed citations

14.

Roels, Frank, Marianne Depreter, M. Girós, et al.. (2002). Differential organ involvement in peroxisomal disorders. Journal of Inherited Metabolic Disease. 25. 99–99.

15.

Stöckler, Sylvia, et al.. (1997). Guanidino compounds in guanidinoacetate methyltransferase deficiency, a new inborn error of creatine synthesis. Metabolism. 46(10). 1189–1193. 80 indexed citations

16.

Stöckler, Sylvia, et al.. (1994). Symmetric hypoplasia of the temporal cerebral lobes in an infant with glutaric aciduria type II (multiple acyl-coenzyme A dehydrogenase deficiency). The Journal of Pediatrics. 124(4). 601–604. 14 indexed citations

17.

Stöckler, Sylvia, U. Holzbach, F. Hanefeld, et al.. (1994). Creatine Deficiency in the Brain: A New, Treatable Inborn Error of Metabolism. Pediatric Research. 36(3). 409–413. 291 indexed citations

18.

Stöckler, Sylvia, et al.. (1993). Liposomal amphotericin-B (AmBisome) for treatment of cutaneous widespread candidosis in an infant with methylmalonic acidaemia. European Journal of Pediatrics. 152(12). 981–983. 5 indexed citations

19.

Stöckler, Sylvia, R. Kleinert, Franz Ebner, & Eduard Paschke. (1993). Mucopolysaccharidosis I and intracranial tumor in a patient with high-pressure hydrocephalus. Pediatric Radiology. 23(5). 353–354. 6 indexed citations

20.

Kurz, R., et al.. (1990). Factors involved in the pathogenesis of unexpected near miss events of infants (ALTE).. PubMed. 30(3-4). 435–47. 7 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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