Yorck Hellenbroich

2.8k total citations
44 papers, 952 citations indexed

About

Yorck Hellenbroich is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Yorck Hellenbroich has authored 44 papers receiving a total of 952 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 26 papers in Cellular and Molecular Neuroscience and 10 papers in Neurology. Recurrent topics in Yorck Hellenbroich's work include Genetic Neurodegenerative Diseases (21 papers), Mitochondrial Function and Pathology (19 papers) and Neurological disorders and treatments (6 papers). Yorck Hellenbroich is often cited by papers focused on Genetic Neurodegenerative Diseases (21 papers), Mitochondrial Function and Pathology (19 papers) and Neurological disorders and treatments (6 papers). Yorck Hellenbroich collaborates with scholars based in Germany, Poland and United Kingdom. Yorck Hellenbroich's co-authors include Christine Zühlke, E. Schwinger, Andreas Dalski, Katrin Bürk, Christine Klein, Johann Hagenah, P. Vieregge, S. Bubel, J. Dichgans and Gabriele Gillessen‐Kaesbach and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Neurology.

In The Last Decade

Yorck Hellenbroich

40 papers receiving 927 citations

Peers

Yorck Hellenbroich

CMN

GENET

NEURO

Elisabeth Rosser United Kingdom

V. Volpini Spain

Barbara Leube Germany

Olga Calabrese Italy

Laura Davis Keppen United States

Tine Deconinck Belgium

Sabina Barresi Italy

Shelley Kennedy Canada

Yoshio Morimatsu Japan

Hanna Mierzewska Poland

Elisabeth Rosser United Kingdom

Yorck Hellenbroich

657 ×1.0

301 ×0.6

CMN

347 ×1.3

GENET

173 ×0.7

NEURO

170 ×2.0

NEURO

Citations per year, relative to Yorck Hellenbroich Yorck Hellenbroich (= 1×) peers Elisabeth Rosser

Countries citing papers authored by Yorck Hellenbroich

Since Specialization

Citations

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

Fields of papers citing papers by Yorck Hellenbroich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yorck Hellenbroich

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

Young, Natalie, Christoph S. Clemen, Rolf Schröder, et al.. (2024). An Intronic Heterozygous SYNE2 Splice Site Mutation: A Rare Cause for Myalgia and hyperCKemia?. SHILAP Revista de lepidopterología. 3(1). 100–109.

Dalski, Andreas, Martje G. Pauly, Henner Hanssen, et al.. (2024). Repeat length in spinocerebellar ataxia type 4 (SCA4) predicts age at onset and disease severity. Journal of Neurology. 271(9). 6289–6300. 1 indexed citations

Spielmann, Malte, Julia Schmidt, Christina M. Lill, et al.. (2023). Phenotypic specificity in patients with neurodevelopmental delay does not correlate with diagnostic yield of trio-exome sequencing. European Journal of Medical Genetics. 66(7). 104774–104774. 2 indexed citations

Hellenbroich, Yorck, et al.. (2021). Lymphangioma of the fetal neck within the PIK3CA‐related‐overgrowth spectrum (PROS): A case report. SHILAP Revista de lepidopterología. 9(7). e04527–e04527. 4 indexed citations

Recke, Andreas, Uta Jappe, Lars Steinmüller‐Magin, et al.. (2019). Identification of the recently described plasminogen gene mutation p.Lys330Glu in a family from Northern Germany with hereditary angioedema. Clinical and Translational Allergy. 9(1). 9–9. 24 indexed citations

Hotz, Alrun, Yorck Hellenbroich, Jürgen Sperner, et al.. (2013). Microdeletion 5q14.3 and anomalies of brain development. American Journal of Medical Genetics Part A. 161(9). 2124–2133. 25 indexed citations

Brüggemann, Norbert, Juliane Spiegler, Yorck Hellenbroich, et al.. (2012). Beneficial Prenatal Levodopa Therapy in Autosomal Recessive Guanosine Triphosphate Cyclohydrolase 1 Deficiency. Archives of Neurology. 69(8). 1071–1071. 19 indexed citations

Bernard, Veronica, et al.. (2011). Two dominantly inherited ataxias linked to chromosome 16q22.1: SCA4 and SCA31 are not allelic. Journal of Neurology. 258(7). 1223–1227. 7 indexed citations

Dafinger, Claudia, Max C. Liebau, Solaf M. Elsayed, et al.. (2011). Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamics. Journal of Clinical Investigation. 121(7). 2662–2667. 141 indexed citations

10.

Caliebe, Almuth, Hester Y. Kroes, Jasper J. van der Smagt, et al.. (2010). Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene. European Journal of Medical Genetics. 53(4). 179–185. 54 indexed citations

11.

Zühlke, Christine, Elizabeth Roeder, Sabine Purmann, et al.. (2007). Homozygous myotonic dystrophy: Clinical findings in two patients and review of the literature. American Journal of Medical Genetics Part A. 143A(17). 2058–2061. 4 indexed citations

12.

Hellenbroich, Yorck, K. Gierga, E. Reusche, et al.. (2005). Spinocerebellar ataxia type 4 (SCA4): Initial pathoanatomical study reveals widespread cerebellar and brainstem degeneration. Journal of Neural Transmission. 113(7). 829–843. 27 indexed citations

13.

Hellenbroich, Yorck, et al.. (2005). Spinocerebellar ataxia type 4. Journal of Neurology. 252(12). 1472–1475. 13 indexed citations

14.

Zühlke, Christine, Andreas Dalski, Korinna Straube, et al.. (2004). Extension of the mutation spectrum in Friedreich's ataxia: detection of an exon deletion and novel missense mutations. European Journal of Human Genetics. 12(11). 979–982. 33 indexed citations

15.

Dalski, Andreas, et al.. (2004). Mutation analysis in the fibroblast growth factor 14 gene: frameshift mutation and polymorphisms in patients with inherited ataxias. European Journal of Human Genetics. 13(1). 118–120. 70 indexed citations

16.

Zühlke, Christine, et al.. (2003). Phenotypical variability of expanded alleles in the TATA-binding protein gene. Journal of Neurology. 250(2). 161–163. 42 indexed citations

17.

Hellenbroich, Yorck, S. Bubel, Heike Pawlack, et al.. (2003). Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region. Journal of Neurology. 250(6). 668–671. 36 indexed citations

18.

Hagenah, Johann, Christine Zühlke, Yorck Hellenbroich, Wolfgang Heide, & Christine Klein. (2003). Focal dystonia as a presenting sign of spinocerebellar ataxia 17. Movement Disorders. 19(2). 217–220. 48 indexed citations

19.

Zühlke, Christine, Yorck Hellenbroich, Andreas Dalski, et al.. (2001). Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxia. European Journal of Human Genetics. 9(3). 160–164. 89 indexed citations

20.

Hellenbroich, Yorck, et al.. (2001). R124C Mutation of the βIGH3 Gene Leads to Remarkable Phenotypic Variability in a Greek Four-Generation Family with Lattice Corneal Dystrophy Type 1. Ophthalmologica. 215(6). 444–447. 6 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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