Jonas Denecke

6.0k total citations
82 papers, 2.1k citations indexed

About

Jonas Denecke is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Jonas Denecke has authored 82 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 20 papers in Genetics and 17 papers in Genetics. Recurrent topics in Jonas Denecke's work include Neurogenetic and Muscular Disorders Research (17 papers), Glycosylation and Glycoproteins Research (12 papers) and Metabolism and Genetic Disorders (11 papers). Jonas Denecke is often cited by papers focused on Neurogenetic and Muscular Disorders Research (17 papers), Glycosylation and Glycoproteins Research (12 papers) and Metabolism and Genetic Disorders (11 papers). Jonas Denecke collaborates with scholars based in Germany, United States and Netherlands. Jonas Denecke's co-authors include Thorsten Marquardt, Christian Kranz, J. Weglage, Reinhold Feldmann, Hans-Georg Koch, Jessika Johannsen, Erik Harms, Kurt Ullrich, Michael Pietsch and Maja Hempel and has published in prestigious journals such as Journal of Clinical Investigation, Blood and Brain.

In The Last Decade

Jonas Denecke

75 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jonas Denecke Germany 27 1.3k 460 361 320 252 82 2.1k
Donna M. Krasnewich United States 28 1.3k 1.0× 671 1.5× 362 1.0× 119 0.4× 134 0.5× 59 2.4k
Maja Di Rocco Italy 34 1.5k 1.1× 1.2k 2.6× 860 2.4× 254 0.8× 203 0.8× 147 3.6k
Agata Fiumara Italy 27 1.1k 0.8× 1.0k 2.3× 474 1.3× 210 0.7× 65 0.3× 131 2.4k
Jolanta Sykut‐Cegielska Poland 24 998 0.7× 282 0.6× 336 0.9× 503 1.6× 47 0.2× 77 1.7k
Robert Steinfeld Germany 29 1.6k 1.2× 820 1.8× 279 0.8× 418 1.3× 73 0.3× 56 2.8k
Georg Christoph Korenke Germany 25 914 0.7× 410 0.9× 381 1.1× 404 1.3× 63 0.3× 57 1.7k
Philippe Latour France 28 733 0.5× 559 1.2× 137 0.4× 99 0.3× 118 0.5× 103 2.5k
Ronen Spiegel Israel 26 884 0.7× 314 0.7× 335 0.9× 338 1.1× 62 0.2× 97 1.9k
Federica Deodato Italy 23 801 0.6× 640 1.4× 144 0.4× 608 1.9× 90 0.4× 55 1.7k
Majid Alfadhel Saudi Arabia 28 1.4k 1.0× 232 0.5× 920 2.5× 625 2.0× 83 0.3× 157 2.5k

Countries citing papers authored by Jonas Denecke

Since Specialization
Citations

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

Fields of papers citing papers by Jonas Denecke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jonas Denecke

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

All Works

20 of 20 papers shown
1.
Weiss, Deike, Anna Perez, P. Weber, et al.. (2024). Cognitive function in SMA patients with 2 or 3 SMN2 copies treated with SMN-modifying or gene addition therapy during the first year of life. European Journal of Paediatric Neurology. 51. 17–23. 12 indexed citations
2.
Loos, Sebastian, Jonas Denecke, Ellen Knierim, et al.. (2024). Immunoadsorption is equally effective as plasma exchange in paediatric neuroimmunological disorders - A retrospective multicentre study. European Journal of Paediatric Neurology. 54. 58–63.
3.
Dulz, Simon, et al.. (2024). Overview of Neuro-Ophthalmic Findings in Leukodystrophies. Journal of Clinical Medicine. 13(17). 5114–5114.
4.
Witt, Stefanie, Jessika Johannsen, Deike Weiss, et al.. (2024). DySMA – an Instrument to Monitor Swallowing Function in Children with Spinal Muscular Atrophy ages 0 to 24 Months: Development, Consensus, and Pilot Testing. Journal of Neuromuscular Diseases. 11(2). 473–483. 2 indexed citations
5.
Kreienkamp, Hans‐Jürgen, Matias Wagner, Heike Weigand, et al.. (2021). Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in males. Human Genetics. 141(2). 257–272. 13 indexed citations
6.
Kloth, Katja, Bernarda Lozić, Mariëtte J.V. Hoffer, et al.. (2021). ANK3 related neurodevelopmental disorders: expanding the spectrum of heterozygous loss-of-function variants. Neurogenetics. 22(4). 263–269. 14 indexed citations
7.
Ven, Amelie T. van der, Jessika Johannsen, Fanny Kortüm, et al.. (2021). Prevalence and clinical prediction of mitochondrial disorders in a large neuropediatric cohort. Clinical Genetics. 100(6). 766–770. 8 indexed citations
8.
Schob, Claudia, Maja Hempel, Dana Šafka Brožková, et al.. (2021). Dominant KPNA3 Mutations Cause Infantile‐Onset Hereditary Spastic Paraplegia. Annals of Neurology. 90(5). 738–750. 6 indexed citations
9.
10.
Johannsen, Jessika, Fanny Kortüm, Georg Rosenberger, et al.. (2018). A novel missense variant in the SDR domain of the WWOX gene leads to complete loss of WWOX protein with early-onset epileptic encephalopathy and severe developmental delay. Neurogenetics. 19(3). 151–156. 18 indexed citations
11.
Pechmann, Astrid, Thorsten Langer, David Schorling, et al.. (2018). Evaluation of Children with SMA Type 1 Under Treatment with Nusinersen within the Expanded Access Program in Germany. Journal of Neuromuscular Diseases. 5(2). 135–143. 104 indexed citations
12.
Said, Edith, Jessica X. Chong, Maja Hempel, et al.. (2017). Survival beyond the perinatal period expands the phenotypes caused by mutations in GLE1. American Journal of Medical Genetics Part A. 173(11). 3098–3103. 8 indexed citations
13.
Schulz, Angela, Jonas Denecke, & Alfried Kohlschütter. (2015). Epilepsy in neuronal ceroid lipofuscinoses. 3(4). 199–206. 6 indexed citations
14.
Omran, Heymut, et al.. (2009). Novel ALG8 mutations expand the clinical spectrum of congenital disorder of glycosylation type Ih. Molecular Genetics and Metabolism. 98(3). 305–309. 19 indexed citations
15.
Denecke, Jonas & Thorsten Marquardt. (2008). Congenital dyserythropoietic anemia type II (CDAII/HEMPAS): Where are we now?. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1792(9). 915–920. 18 indexed citations
16.
Kranz, Christian, Jonas Denecke, Volker Debus, et al.. (2007). A Defect in Dolichol Phosphate Biosynthesis Causes a New Inherited Disorder with Death in Early Infancy. The American Journal of Human Genetics. 80(3). 433–440. 72 indexed citations
17.
Denecke, Jonas, Christian Kranz, Dirk Kemming, Hans-Georg Koch, & Thorsten Marquardt. (2004). An activated 5? cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id). Human Mutation. 23(5). 477–486. 48 indexed citations
18.
Kranz, Christian, Jonas Denecke, Ludwig Lehle, et al.. (2004). Congenital Disorder of Glycosylation Type Ik (CDG-Ik): A Defect of Mannosyltransferase I. The American Journal of Human Genetics. 74(3). 545–551. 62 indexed citations
19.
Feldmann, Reinhold, et al.. (2002). Phenylketonuria: No Specific Frontal Lobe-Dependent Neuropsychological Deficits of Early-Treated Patients in Comparison with Diabetics. Pediatric Research. 51(6). 761–765. 29 indexed citations
20.
Kranz, Christian, Jonas Denecke, Mark A. Lehrman, et al.. (2001). A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If). Journal of Clinical Investigation. 108(11). 1613–1619. 104 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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