Reinhard Keimer

589 total citations
6 papers, 127 citations indexed

About

Reinhard Keimer is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Reinhard Keimer has authored 6 papers receiving a total of 127 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Reinhard Keimer's work include Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Epilepsy research and treatment (2 papers). Reinhard Keimer is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Epilepsy research and treatment (2 papers). Reinhard Keimer collaborates with scholars based in Germany, Palestinian Territory and Switzerland. Reinhard Keimer's co-authors include Jason J. LeBlanc, Andreas Schulze‐Bonhage, Christian E. Elger, M. Trippel, Peter C. Warnke, Florian von Deimling, Susanne Fauser, Joachim Spreer, Kathrin Wagner and Thomas Bast and has published in prestigious journals such as Neurology, European Journal of Human Genetics and Clinical Genetics.

In The Last Decade

Reinhard Keimer

5 papers receiving 125 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Reinhard Keimer Germany	4	79	61	50	24	23	6	127
Georg Dorfmüller France	8	161 2.0×	133 2.2×	96 1.9×	22 0.9×	33 1.4×	16	215
Jean Michel Pedespan France	6	58 0.7×	41 0.7×	28 0.6×	24 1.0×	20 0.9×	13	137
Luca Zagaroli Italy	6	111 1.4×	76 1.2×	53 1.1×	44 1.8×	11 0.5×	13	201
Leonor Cabral‐Lim Philippines	7	152 1.9×	103 1.7×	68 1.4×	27 1.1×	22 1.0×	14	239
Chen-Jui Ho Taiwan	9	69 0.9×	48 0.8×	41 0.8×	48 2.0×	22 1.0×	16	160
Biagio Orlando Italy	8	91 1.2×	62 1.0×	45 0.9×	12 0.5×	33 1.4×	19	152
Ugo Leggio Italy	5	178 2.3×	115 1.9×	104 2.1×	20 0.8×	19 0.8×	7	210
Lucia Tancredi Italy	3	36 0.5×	32 0.5×	34 0.7×	47 2.0×	11 0.5×	4	119
Joe McMenamin Ireland	7	45 0.6×	39 0.6×	27 0.5×	89 3.7×	6 0.3×	14	205
Hans Lindsten Sweden	7	185 2.3×	165 2.7×	63 1.3×	10 0.4×	50 2.2×	9	241

Countries citing papers authored by Reinhard Keimer

Since Specialization

Citations

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

Fields of papers citing papers by Reinhard Keimer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Reinhard Keimer

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

All Works

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6 of 6 papers shown

1.

Hengel, Holger, Rebecca Buchert, Marc Sturm, et al.. (2020). First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery. European Journal of Human Genetics. 28(8). 1034–1043. 20 indexed citations

2.

Hengel, Holger, et al.. (2018). A previously identified missense mutation in STYXL1 is likely benign. European Journal of Medical Genetics. 62(11). 103582–103582. 2 indexed citations

3.

Hengel, Holger, Reinhard Keimer, Angelika Rieß, et al.. (2018). GPT2 mutations cause developmental encephalopathy with microcephaly and features of complicated hereditary spastic paraplegia. Clinical Genetics. 94(3-4). 356–361. 11 indexed citations

4.

Schulze‐Bonhage, Andreas, M. Trippel, Kathrin Wagner, et al.. (2008). Outcome and predictors of interstitial radiosurgery in the treatment of gelastic epilepsy. Neurology. 71(4). 277–282. 50 indexed citations

5.

Marquard, Klaus, et al.. (2005). Giant Axonal Neuropathy – a neurodegenerative disorder – a novel mutation in the GAN-Gen. Neuropediatrics. 36(2).

6.

Schulze‐Bonhage, Andreas, M. Trippel, Reinhard Keimer, et al.. (2004). Interstitial radiosurgery in the treatment of gelastic epilepsy due to hypothalamic hamartomas. Neurology. 62(4). 644–647. 44 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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