Juliane Winkelmann

630 total citations
11 papers, 273 citations indexed

About

Juliane Winkelmann is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Juliane Winkelmann has authored 11 papers receiving a total of 273 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Juliane Winkelmann's work include Genomics and Rare Diseases (9 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Congenital heart defects research (3 papers). Juliane Winkelmann is often cited by papers focused on Genomics and Rare Diseases (9 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Congenital heart defects research (3 papers). Juliane Winkelmann collaborates with scholars based in Germany, Austria and Czechia. Juliane Winkelmann's co-authors include Michael Zech, Sylvia Boesch, Bernhard Haslinger, Werner Poewe, Andrés Ceballos-Baumann, Daniel D. Lam, Riccardo Berutti, Katharina Vill, Tim M. Strom and Tim M. Strom and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Gene.

In The Last Decade

Juliane Winkelmann

10 papers receiving 273 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Juliane Winkelmann Germany 7 138 136 92 86 35 11 273
Karen Grütz Germany 10 140 1.0× 61 0.4× 95 1.0× 61 0.7× 12 0.3× 15 224
Claire Guissart France 12 65 0.5× 73 0.5× 76 0.8× 174 2.0× 40 1.1× 22 301
Jiaxi Yu China 8 99 0.7× 55 0.4× 170 1.8× 182 2.1× 17 0.5× 20 269
Marisol Mirabelli-Badenier Italy 10 44 0.3× 100 0.7× 29 0.3× 104 1.2× 17 0.5× 13 238
Maartje Pennings Netherlands 10 48 0.3× 76 0.6× 112 1.2× 134 1.6× 31 0.9× 21 272
Satya R. Vemula United States 10 229 1.7× 61 0.4× 181 2.0× 113 1.3× 7 0.2× 13 344
Valerija Dobričić Serbia 11 165 1.2× 45 0.3× 163 1.8× 124 1.4× 19 0.5× 21 296
Fabrizia Stregapede Italy 9 43 0.3× 47 0.3× 90 1.0× 83 1.0× 38 1.1× 17 205
Mathilde Cohen-Tannoudji France 5 88 0.6× 84 0.6× 36 0.4× 150 1.7× 100 2.9× 6 256
D. G. Hernandez United Kingdom 3 126 0.9× 43 0.3× 45 0.5× 67 0.8× 57 1.6× 3 216

Countries citing papers authored by Juliane Winkelmann

Since Specialization
Citations

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

Fields of papers citing papers by Juliane Winkelmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Juliane Winkelmann

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

All Works

11 of 11 papers shown
1.
Brügger, Melanie, Matias Wagner, Elisabeth Graf, et al.. (2024). Genome Sequencing for Cases Unsolved by Exome Sequencing: Identifying a Single-Exon Deletion in TBCK in a Case from 30 Years Ago. Neuropediatrics. 55(4). 260–264. 1 indexed citations
2.
Brunet, Theresa, Elisabeth Graf, Marjon Arens, et al.. (2024). Variants that get straight to your heart – Cardiogenetic secondary findings in exome sequencing. Gene. 935. 149063–149063.
3.
Pavelekova, Petra, Ján Necpál, Robert Jech, et al.. (2023). Predictors of whole exome sequencing in dystonic cerebral palsy and cerebral palsy-like disorders. Parkinsonism & Related Disorders. 111. 105352–105352. 2 indexed citations
4.
Garavaglia, Barbara, Sadeq Vallian, Luigi Romito, et al.. (2022). AOPEP variants as a novel cause of recessive dystonia: Generalized dystonia and dystonia-parkinsonism. Parkinsonism & Related Disorders. 97. 52–56. 6 indexed citations
5.
Škorvánek, Matěj, Petra Pavelekova, Chen Zhao, et al.. (2021). Variant recurrence confirms the existence of a FBXO31‐related spastic‐dystonic cerebral palsy syndrome. Annals of Clinical and Translational Neurology. 8(4). 951–955. 7 indexed citations
6.
Zech, Michael, Daniel D. Lam, & Juliane Winkelmann. (2019). Update on KMT2B-Related Dystonia. Current Neurology and Neuroscience Reports. 19(11). 92–92. 31 indexed citations
7.
Germain, Pierre‐Luc, Michael Zech, Sina Atashpaz, et al.. (2018). KMT2B Is Selectively Required for Neuronal Transdifferentiation, and Its Loss Exposes Dystonia Candidate Genes. Cell Reports. 25(4). 988–1001. 26 indexed citations
8.
Zech, Michael, Sylvia Boesch, Riccardo Berutti, et al.. (2017). SOX5-Null Heterozygous Mutation in a Family with Adult-Onset Hyperkinesia and Behavioral Abnormalities. SHILAP Revista de lepidopterología. 2017. 1–6. 3 indexed citations
9.
Zech, Michael, Robert Jech, Petra Havránková, et al.. (2017). KMT2B rare missense variants in generalized dystonia. Movement Disorders. 32(7). 1087–1091. 27 indexed citations
10.
Zech, Michael, Sylvia Boesch, Esther M. Maier, et al.. (2016). Haploinsufficiency of KMT2B, Encoding the Lysine-Specific Histone Methyltransferase 2B, Results in Early-Onset Generalized Dystonia. The American Journal of Human Genetics. 99(6). 1377–1387. 99 indexed citations
11.
Zech, Michael, Sylvia Boesch, Angela Jochim, et al.. (2016). Clinical exome sequencing in early‐onset generalized dystonia and large‐scale resequencing follow‐up. Movement Disorders. 32(4). 549–559. 71 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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2026