Konrad Oexle

7.8k total citations
63 papers, 1.3k citations indexed

About

Konrad Oexle is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Konrad Oexle has authored 63 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 21 papers in Genetics and 11 papers in Neurology. Recurrent topics in Konrad Oexle's work include Muscle Physiology and Disorders (8 papers), Restless Legs Syndrome Research (8 papers) and Metabolism and Genetic Disorders (7 papers). Konrad Oexle is often cited by papers focused on Muscle Physiology and Disorders (8 papers), Restless Legs Syndrome Research (8 papers) and Metabolism and Genetic Disorders (7 papers). Konrad Oexle collaborates with scholars based in Germany, Switzerland and Austria. Konrad Oexle's co-authors include Rémy Bruggmann, Janine Meienberg, Gábor Mátyás, Angelika Zwirner, James R. Connor, Stephanie M. Patton, Richard P. Allen, Alfried Kohlschütter, Christoph Hübner and Thomas Meitinger and has published in prestigious journals such as Nature Communications, The Journal of Immunology and Diabetes Care.

In The Last Decade

Konrad Oexle

57 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Konrad Oexle Germany 20 609 312 192 186 175 63 1.3k
Göknur Haliloğlu Türkiye 23 922 1.5× 259 0.8× 210 1.1× 110 0.6× 189 1.1× 116 1.7k
Paola Pichiule United States 14 707 1.2× 282 0.9× 151 0.8× 100 0.5× 332 1.9× 16 1.5k
Esther Leshinsky‐Silver Israel 25 928 1.5× 522 1.7× 132 0.7× 171 0.9× 103 0.6× 76 1.7k
Vincenzo Salpietro Italy 22 481 0.8× 387 1.2× 245 1.3× 89 0.5× 73 0.4× 89 1.2k
Charles Marques Lourenço Brazil 23 883 1.4× 309 1.0× 179 0.9× 187 1.0× 667 3.8× 106 1.9k
Elisabeth Rosser United Kingdom 17 657 1.1× 347 1.1× 173 0.9× 52 0.3× 84 0.5× 35 1.1k
Jean‐Baptiste Rivière Canada 18 591 1.0× 575 1.8× 98 0.5× 85 0.5× 79 0.5× 36 1.2k
Chiara Fiorillo Italy 22 836 1.4× 134 0.4× 200 1.0× 130 0.7× 180 1.0× 93 1.4k
Guy M. Lenk United States 23 616 1.0× 191 0.6× 220 1.1× 287 1.5× 241 1.4× 38 1.7k

Countries citing papers authored by Konrad Oexle

Since Specialization
Citations

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

Fields of papers citing papers by Konrad Oexle

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Konrad Oexle

This figure shows the co-authorship network connecting the top 25 collaborators of Konrad Oexle. A scholar is included among the top collaborators of Konrad Oexle 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 Konrad Oexle. Konrad Oexle 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.
Eising, Else, Arianna Vino, Juliane Winkelmann, et al.. (2025). De novo protein-coding gene variants in developmental stuttering. Molecular Psychiatry. 31(1). 104–115.
2.
Hoffstaedter, Felix, Federico Raimondo, Simon B. Eickhoff, et al.. (2025). Beyond volume: Unraveling the genetics of human brain geometry. Science Advances. 11(24). eadr1644–eadr1644.
3.
Sindermann, Lisa, Federico Raimondo, Konrad Oexle, et al.. (2025). Neurobiological correlates of schizophrenia-specific and highly pleiotropic genetic risk scores for neuropsychiatric disorders. Translational Psychiatry. 15(1). 230–230.
4.
Zhao, Chen, Daniel D. Lam, Wojciech Krężel, et al.. (2024). RLS-associated MEIS transcription factors control distinct processes in human neural stem cells. Scientific Reports. 14(1). 28986–28986. 1 indexed citations
5.
Othman, Alaa, Kimberly Begemann, Sonja Binder, et al.. (2024). The reactive pyruvate metabolite dimethylglyoxal mediates neurological consequences of diabetes. Nature Communications. 15(1). 5745–5745. 5 indexed citations
6.
Witzel, Simon, Matias Wagner, Chen Zhao, et al.. (2022). Fast versus slow disease progression in amyotrophic lateral sclerosis–clinical and genetic factors at the edges of the survival spectrum. Neurobiology of Aging. 119. 117–126. 6 indexed citations
7.
Schormair, Barbara, Chen Zhao, Aaro V. Salminen, Konrad Oexle, & Juliane Winkelmann. (2022). Reassessment of candidate gene studies for idiopathic restless legs syndrome in a large genome-wide association study dataset of European ancestry. SLEEP. 45(8). 5 indexed citations
8.
Lam, Daniel D., Ana Nikolić, Chen Zhao, et al.. (2021). Intronic elements associated with insomnia and restless legs syndrome exhibit cell-type-specific epigenetic features contributing to MEIS1 regulation. Human Molecular Genetics. 31(11). 1733–1746. 5 indexed citations
9.
Wagner, Matias, Sarah L. Stenton, Tim M. Strom, et al.. (2020). Lifetime risk of autosomal recessive mitochondrial disorders calculated from genetic databases. EBioMedicine. 54. 102730–102730. 39 indexed citations
10.
Salminen, Aaro V., et al.. (2020). Therapeutic effectiveness of thalidomide in a patient with treatment-resistant restless legs syndrome. Journal of Clinical Sleep Medicine. 16(10). 1815–1817. 2 indexed citations
11.
Hackmann, Karl, Andreas Rump, Stefan A. Haas, et al.. (2015). Tentative clinical diagnosis of Lujan‐Fryns syndrome—A conglomeration of different genetic entities?. American Journal of Medical Genetics Part A. 170(1). 94–102. 8 indexed citations
12.
Diehl‐Schmid, Janine & Konrad Oexle. (2015). Genetik der Demenzen. Der Nervenarzt. 86(7). 891–902. 2 indexed citations
13.
Huth, Cornelia, Astrid Zierer, Margit Heier, et al.. (2015). Biomarkers of iron metabolism are independently associated with impaired glucose metabolism and type 2 diabetes: the KORA F4 study. European Journal of Endocrinology. 173(5). 643–653. 55 indexed citations
14.
Hackmann, Karl, Jens Schallner, Evelin Schröck, et al.. (2013). Severe intellectual disability, West syndrome, Dandy–Walker malformation, and syndactyly in a patient with partial tetrasomy 17q25.3. American Journal of Medical Genetics Part A. 161(12). 3144–3149. 13 indexed citations
15.
Oexle, Konrad & Thomas Meitinger. (2011). Sampling GWAS subjects from risk populations. Genetic Epidemiology. 35(3). 148–153. 3 indexed citations
16.
Oexle, Konrad. (2010). A remark on rare variants. Journal of Human Genetics. 55(4). 219–226. 5 indexed citations
17.
Oexle, Konrad, Barbara Finckh, Alfried Kohlschütter, et al.. (2009). Islet cell antibodies in diabetes mellitus associated with a mitochondrial tRNALeu(UUR) gene mutation. Experimental and Clinical Endocrinology & Diabetes. 104(3). 212–217. 5 indexed citations
18.
Oexle, Konrad, Luisa Bonafé, & Beat Steinmann. (2002). Remark on utility and error rates of the allopurinol test in detecting mild ornithine transcarbamylase deficiency. Molecular Genetics and Metabolism. 76(1). 71–75. 4 indexed citations
19.
Young, Peter, Florian Stögbauer, Peter De Jonghe, et al.. (2000). PMP22 Thr118Met is not a clinically relevant CMT1 marker. Journal of Neurology. 247(9). 696–700. 11 indexed citations
20.
Oexle, Konrad, R. Herrmann, Catherine Dodé, et al.. (1996). Neurosensory Hearing Loss in Secondary Adhalinopathy. Neuropediatrics. 27(1). 32–36. 10 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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