Konrad Platzer

3.4k total citations
27 papers, 498 citations indexed

About

Konrad Platzer is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Konrad Platzer has authored 27 papers receiving a total of 498 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 13 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Konrad Platzer's work include Genomics and Rare Diseases (14 papers), Genetics and Neurodevelopmental Disorders (13 papers) and Genomic variations and chromosomal abnormalities (6 papers). Konrad Platzer is often cited by papers focused on Genomics and Rare Diseases (14 papers), Genetics and Neurodevelopmental Disorders (13 papers) and Genomic variations and chromosomal abnormalities (6 papers). Konrad Platzer collaborates with scholars based in Germany, United States and Switzerland. Konrad Platzer's co-authors include Johannes R. Lemke, Sarah Weckhuysen, Friedrich C. Luft, Saskia Biskup, Susanne Ruf, Isabelle Steiner, Sigmar Stricker, Mary B. Goldring, Bodo Laube and Sylvia Bähring and has published in prestigious journals such as Journal of Clinical Investigation, Bioinformatics and Molecular and Cellular Biology.

In The Last Decade

Konrad Platzer

25 papers receiving 494 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 Platzer Germany 10 293 284 116 80 78 27 498
Christopher M. LaCoursiere United States 6 324 1.1× 315 1.1× 142 1.2× 93 1.2× 42 0.5× 7 584
Nadia Boutry‐Kryza France 10 301 1.0× 194 0.7× 139 1.2× 91 1.1× 32 0.4× 16 479
William H. Roden United States 8 158 0.5× 239 0.8× 99 0.9× 119 1.5× 29 0.4× 12 440
Kelly D. Farwell Hagman United States 12 475 1.6× 218 0.8× 85 0.7× 55 0.7× 51 0.7× 20 630
Amanda Lindy United States 8 328 1.1× 225 0.8× 146 1.3× 65 0.8× 21 0.3× 13 517
Greta Gillies Australia 9 216 0.7× 302 1.1× 114 1.0× 56 0.7× 27 0.3× 13 481
Sonya A. Gunter United States 4 166 0.6× 237 0.8× 67 0.6× 54 0.7× 31 0.4× 4 400
Théo Ribierre France 5 216 0.7× 245 0.9× 146 1.3× 90 1.1× 33 0.4× 7 471
Pierre Cacciagli France 15 391 1.3× 410 1.4× 104 0.9× 100 1.3× 19 0.2× 25 739
C. Nicole Sunnen United States 7 127 0.4× 272 1.0× 76 0.7× 112 1.4× 20 0.3× 7 430

Countries citing papers authored by Konrad Platzer

Since Specialization
Citations

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

Fields of papers citing papers by Konrad Platzer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Konrad Platzer

This figure shows the co-authorship network connecting the top 25 collaborators of Konrad Platzer. A scholar is included among the top collaborators of Konrad Platzer 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 Platzer. Konrad Platzer 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.
Schönauer, Ria, Georgia Vasileiou, Alma Kuechler, et al.. (2024). Pathogenic PHIP Variants are Variably Associated With CAKUT. Kidney International Reports. 9(8). 2484–2497. 3 indexed citations
2.
Popp, Bernt, et al.. (2024). The MorbidGenes panel: a monthly updated list of diagnostically relevant rare disease genes derived from diverse sources. Human Genetics. 143(12). 1459–1463. 1 indexed citations
3.
Takatsu, Hiroyuki, Yusuke Kosugi, Haruo Ogawa, et al.. (2024). De Novo Missense Variations of ATP8B2 Impair Its Phosphatidylcholine Flippase Activity. Molecular and Cellular Biology. 44(11). 473–488. 1 indexed citations
4.
Pérez‐Palma, Eduardo, Tobias Brünger, Konrad Platzer, et al.. (2023). CNV-ClinViewer: enhancing the clinical interpretation of large copy-number variants online. Bioinformatics. 39(5). 8 indexed citations
5.
Chen, Siwei, Antje Garten, Saskia Biskup, et al.. (2023). Epilepsies of presumed genetic etiology show enrichment of rare variants that occur in the general population. The American Journal of Human Genetics. 110(7). 1110–1122.
6.
Platzer, Konrad, Heinrich Sticht, Caleb Bupp, et al.. (2022). De Novo Missense Variants in SLC32A1 Cause a Developmental and Epileptic Encephalopathy Due to Impaired GABAergic Neurotransmission. Annals of Neurology. 92(6). 958–973. 12 indexed citations
7.
Kumar, Ajith, Angela F. Brady, Tessa Homfray, et al.. (2022). Expanding the phenotype of TAB2 variants and literature review. American Journal of Medical Genetics Part A. 188(11). 3331–3342. 6 indexed citations
8.
Sticht, Heinrich, François Lecoquierre, Alice Goldenberg, et al.. (2022). Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy. European Journal of Human Genetics. 31(3). 345–352. 4 indexed citations
9.
Stawarski, Michał, Lenka Nosková, Martin Magner, et al.. (2022). GABBR1 monoallelic de novo variants linked to neurodevelopmental delay and epilepsy. The American Journal of Human Genetics. 109(10). 1885–1893. 14 indexed citations
10.
11.
Zacher, Pia, Tobias Bartolomaeus, Nicole Scholz, et al.. (2022). Altered gene expression profiles impair the nervous system development in individuals with 15q13.3 microdeletion. Scientific Reports. 12(1). 13507–13507. 2 indexed citations
12.
Platzer, Konrad, et al.. (2022). AutoCaSc: Prioritizing candidate genes for neurodevelopmental disorders. Human Mutation. 43(12). 1795–1807. 5 indexed citations
13.
Zacher, Pia, Tobias Bartolomaeus, Diana Le Duc, et al.. (2021). The genetic landscape of intellectual disability and epilepsy in adults and the elderly: a systematic genetic work-up of 150 individuals. Genetics in Medicine. 23(8). 1492–1497. 31 indexed citations
14.
Horn, Susanne, Bernt Popp, Konrad Platzer, et al.. (2021). Phenotype-tissue expression and exploration (PTEE) resource facilitates the choice of tissue for RNA-seq-based clinical genetics studies. BMC Genomics. 22(1). 802–802. 7 indexed citations
15.
Duc, Diana Le, Julia Hentschel, Mathias Stiller, et al.. (2020). In cis TP53 and RAD51C pathogenic variants may predispose to sebaceous gland carcinomas. European Journal of Human Genetics. 29(3). 489–494.
16.
Platzer, Konrad, Irina Hüning, Thomas Schwarzmayr, et al.. (2014). Exome sequencing identifies compound heterozygous mutations in C12orf57 in two siblings with severe intellectual disability, hypoplasia of the corpus callosum, chorioretinal coloboma, and intractable seizures. American Journal of Medical Genetics Part A. 164(8). 1976–1980. 6 indexed citations
17.
Beygo, Jasmin, Miriam Elbracht, Matthias Begemann, et al.. (2014). Novel deletions affecting the MEG3-DMR provide further evidence for a hierarchical regulation of imprinting in 14q32. European Journal of Human Genetics. 23(2). 180–188. 48 indexed citations
18.
Lemke, Johannes R., Rik Hendrickx, Bodo Laube, et al.. (2013). GRIN2B mutations in west syndrome and intellectual disability with focal epilepsy. Annals of Neurology. 75(1). 147–154. 158 indexed citations
19.
Maass, Philipp G., Andreas Rump, Herbert Schulz, et al.. (2012). A misplaced lncRNA causes brachydactyly in humans. Journal of Clinical Investigation. 122(11). 3990–4002. 88 indexed citations
20.
Bens, Susanne, Andrea Haake, Julia Richter, et al.. (2012). Frequency and characterization of DNA methylation defects in children born SGA. European Journal of Human Genetics. 21(8). 838–843. 13 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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