Stefanie Beck‐Wödl

1.0k total citations
27 papers, 401 citations indexed

About

Stefanie Beck‐Wödl is a scholar working on Physiology, Molecular Biology and Cell Biology. According to data from OpenAlex, Stefanie Beck‐Wödl has authored 27 papers receiving a total of 401 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Physiology, 8 papers in Molecular Biology and 7 papers in Cell Biology. Recurrent topics in Stefanie Beck‐Wödl's work include Lysosomal Storage Disorders Research (16 papers), Cellular transport and secretion (6 papers) and Carbohydrate Chemistry and Synthesis (5 papers). Stefanie Beck‐Wödl is often cited by papers focused on Lysosomal Storage Disorders Research (16 papers), Cellular transport and secretion (6 papers) and Carbohydrate Chemistry and Synthesis (5 papers). Stefanie Beck‐Wödl collaborates with scholars based in Germany, Switzerland and Netherlands. Stefanie Beck‐Wödl's co-authors include Lüdger Schöls, Ingeborg Krägeloh‐Mann, Peter Bauer, Samuel Groeschel, Christiane Kehrer, K. Harzer, Judith Böhringer, Tobias B. Haack, Matthis Synofzik and Jennifer Müller vom Hagen and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and International Journal of Molecular Sciences.

In The Last Decade

Stefanie Beck‐Wödl

25 papers receiving 396 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stefanie Beck‐Wödl Germany	13	178	155	102	76	55	27	401
Marie-Louise Bondeson Sweden	15	372 2.1×	76 0.5×	133 1.3×	44 0.6×	60 1.1×	26	711
Carlos Eduardo Steiner Brazil	15	157 0.9×	145 0.9×	203 2.0×	67 0.9×	65 1.2×	58	586
Maria Chiara Malaguti Italy	7	118 0.7×	112 0.7×	60 0.6×	31 0.4×	26 0.5×	18	303
Rebecca E.H. Whiting United States	12	194 1.1×	296 1.9×	52 0.5×	60 0.8×	135 2.5×	19	421
Ji‐Yoen Kim United States	9	288 1.6×	86 0.6×	142 1.4×	38 0.5×	38 0.7×	9	508
Gerarda Cappuccio Italy	15	348 2.0×	53 0.3×	287 2.8×	33 0.4×	47 0.9×	59	611
Deborah Barbouth United States	11	285 1.6×	118 0.8×	412 4.0×	54 0.7×	43 0.8×	32	678
Helen McDermott United Kingdom	11	457 2.6×	138 0.9×	117 1.1×	50 0.7×	137 2.5×	22	807
Catharine E. Krebs United States	11	160 0.9×	68 0.4×	91 0.9×	34 0.4×	132 2.4×	17	454
C. Ortez Spain	15	422 2.4×	44 0.3×	118 1.2×	37 0.5×	78 1.4×	76	691

Countries citing papers authored by Stefanie Beck‐Wödl

Since Specialization

Citations

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

Fields of papers citing papers by Stefanie Beck‐Wödl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stefanie Beck‐Wödl. 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 Stefanie Beck‐Wödl. The network helps show where Stefanie Beck‐Wödl may publish in the future.

Co-authorship network of co-authors of Stefanie Beck‐Wödl

This figure shows the co-authorship network connecting the top 25 collaborators of Stefanie Beck‐Wödl. A scholar is included among the top collaborators of Stefanie Beck‐Wödl 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 Stefanie Beck‐Wödl. Stefanie Beck‐Wödl 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

Kern, Jan Marco, Judith Böhringer, Dagmar Timmann, et al.. (2023). Clinical, Imaging, Genetic, and Disease Course Characteristics in Patients With GM2 Gangliosidosis. Neurology. 102(1). e207898–e207898. 2 indexed citations

Kuechler, Alma, Tabib Dabir, Stephanie Spranger, et al.. (2023). Novel Variants of SOX4 in Patients with Intellectual Disability. International Journal of Molecular Sciences. 24(4). 3519–3519. 2 indexed citations

Groeschel, Samuel, K. Harzer, Christiane Kehrer, et al.. (2022). Predicting clinical phenotypes of metachromatic leukodystrophy based on the arylsulfatase A activity and the ARSA genotype? – Chances and challenges. Molecular Genetics and Metabolism. 137(3). 273–282. 15 indexed citations

Grünert, Sarah C., Luciana Hannibal, Anke Schumann, et al.. (2021). Identification and Characterization of a Novel Splice Site Mutation Associated with Glycogen Storage Disease Type VI in Two Unrelated Turkish Families. Diagnostics. 11(3). 500–500. 2 indexed citations

Krägeloh‐Mann, Ingeborg, Samuel Groeschel, Stefanie Beck‐Wödl, et al.. (2020). Natural history of Krabbe disease – a nationwide study in Germany using clinical and MRI data. Orphanet Journal of Rare Diseases. 15(1). 243–243. 19 indexed citations

Beck‐Wödl, Stefanie, Christiane Kehrer, K. Harzer, et al.. (2020). Long‐term disease course of two patients with multiple sulfatase deficiency differs from metachromatic leukodystrophy in a broad cohort. JIMD Reports. 58(1). 80–88. 5 indexed citations

Elgizouli, Magdeldin, Jasmin Beygo, Florian Erger, et al.. (2020). The adult phenotype of Schaaf-Yang syndrome. Orphanet Journal of Rare Diseases. 15(1). 294–294. 19 indexed citations

Grünert, Sarah C., Anke Schumann, Peter Freisinger, et al.. (2020). Citrin deficiency mimicking mitochondrial depletion syndrome. BMC Pediatrics. 20(1). 518–518. 7 indexed citations

Laugwitz, Lucia, Rebecca Buchert, Samuel Groeschel, et al.. (2020). Pontocerebellar hypoplasia type 11: Does the genetic defect determine timing of cerebellar pathology?. European Journal of Medical Genetics. 63(7). 103938–103938. 5 indexed citations

10.

Kehrer, Christiane, Judith Böhringer, Stefanie Beck‐Wödl, et al.. (2019). Phenotypic variation between siblings with Metachromatic Leukodystrophy. Orphanet Journal of Rare Diseases. 14(1). 136–136. 25 indexed citations

11.

Kuechler, Alma, Mona Grimmel, Jessica Becker, et al.. (2018). De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies. Human Genetics. 137(5). 401–411. 16 indexed citations

12.

Beck‐Wödl, Stefanie, K. Harzer, Marc Sturm, et al.. (2018). Homozygous TBC1 domain-containing kinase (TBCK) mutation causes a novel lysosomal storage disease – a new type of neuronal ceroid lipofuscinosis (CLN15)?. Acta Neuropathologica Communications. 6(1). 145–145. 31 indexed citations

13.

Gieldon, Laura, Luisa Mackenroth, Andreas Rump, et al.. (2017). Skewed X‐inactivation in a family with DLG3‐associated X‐linked intellectual disability. American Journal of Medical Genetics Part A. 173(9). 2545–2550. 12 indexed citations

14.

Krägeloh-Mann, Inge, K. Harzer, Kevin Rostásy, et al.. (2017). Late onset Krabbe disease due to the new GALC p.Ala543Pro mutation, with intriguingly high residual GALC activity in vitro. European Journal of Paediatric Neurology. 21(3). 522–529. 5 indexed citations

15.

Soehn, Anne S., Tim W. Rattay, Stefanie Beck‐Wödl, et al.. (2016). Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H /SPG35 in 4 families. Neurology. 87(2). 186–191. 21 indexed citations

16.

Reuter, Miriam S., Angelika Rieß, Ute Moog, et al.. (2016). FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum. Journal of Medical Genetics. 54(1). 64–72. 56 indexed citations

17.

Synofzik, Matthis, Jennifer Müller vom Hagen, Tobias B. Haack, et al.. (2014). X-linked Charcot-Marie-Tooth disease, Arts syndrome, and prelingual non-syndromic deafness form a disease continuum: evidence from a family with a novel PRPS1 mutation. Orphanet Journal of Rare Diseases. 9(1). 24–24. 42 indexed citations

18.

Schicks, Julia, Jennifer Müller vom Hagen, Peter Bauer, et al.. (2013). Niemann-Pick type C is frequent in adult ataxia with cognitive decline and vertical gaze palsy. Neurology. 80(12). 1169–1170. 24 indexed citations

19.

Harzer, K., Stefanie Beck‐Wödl, & Peter Bauer. (2013). Niemann-Pick Disease Type C: New Aspects in a Long Published Family – Partial Manifestations in Heterozygotes. JIMD Reports. 12. 25–29. 16 indexed citations

20.

Lemke, Johannes R., Stefanie Beck‐Wödl, Andreas Zankl, et al.. (2009). Juvenile myoclonic epilepsy with photosensitivity in a female with Velocardiofacial syndrome (del(22)(q11.2))—Causal relationship or coincidence?. Seizure. 18(9). 660–663. 8 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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