Stephanie Karch

458 total citations
8 papers, 146 citations indexed

About

Stephanie Karch is a scholar working on Molecular Biology, Genetics and Nutrition and Dietetics. According to data from OpenAlex, Stephanie Karch has authored 8 papers receiving a total of 146 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Nutrition and Dietetics. Recurrent topics in Stephanie Karch's work include RNA regulation and disease (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and RNA modifications and cancer (2 papers). Stephanie Karch is often cited by papers focused on RNA regulation and disease (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and RNA modifications and cancer (2 papers). Stephanie Karch collaborates with scholars based in Germany, United States and Netherlands. Stephanie Karch's co-authors include Ute Moog, Martin Granzow, Katrin Hinderhofer, Angelika Seitz, Nagarajan Paramasivam, Nicola Dikow, Christina Evers, Claus R. Bartram, Roland Eils and Nicole I. Wolf and has published in prestigious journals such as American Journal of Neuroradiology, American Journal of Medical Genetics Part A and Clinical Epigenetics.

In The Last Decade

Stephanie Karch

8 papers receiving 143 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stephanie Karch Germany	8	101	50	27	23	14	8	146
Matthew Zemel United States	5	89 0.9×	63 1.3×	21 0.8×	32 1.4×	32 2.3×	6	160
Amy Crunk United States	6	58 0.6×	59 1.2×	11 0.4×	16 0.7×	5 0.4×	10	131
Nathalie Roeckel-Trévisiol France	4	56 0.6×	31 0.6×	22 0.8×	56 2.4×	6 0.4×	5	126
Dana Marafi United States	8	88 0.9×	70 1.4×	5 0.2×	22 1.0×	6 0.4×	24	171
Kirill Shkura United Kingdom	5	127 1.3×	58 1.2×	6 0.2×	39 1.7×	9 0.6×	5	212
Clara D. van Karnebeek Netherlands	9	97 1.0×	60 1.2×	5 0.2×	18 0.8×	53 3.8×	23	174
Adele Guglielmi Italy	5	72 0.7×	9 0.2×	43 1.6×	49 2.1×	19 1.4×	10	135
A. T. Pagnamenta United Kingdom	3	142 1.4×	81 1.6×	7 0.3×	33 1.4×	50 3.6×	3	215
Ilona Krey Germany	8	77 0.8×	116 2.3×	12 0.4×	53 2.3×	16 1.1×	21	203
Laura C. Murphy United Kingdom	8	116 1.1×	64 1.3×	5 0.2×	17 0.7×	7 0.5×	14	197

Countries citing papers authored by Stephanie Karch

Since Specialization

Citations

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

Fields of papers citing papers by Stephanie Karch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephanie Karch

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

All Works

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8 of 8 papers shown

Harting, Inga, Ingeborg Krägeloh‐Mann, Annette Bley, et al.. (2020). POLR3A variants with striatal involvement and extrapyramidal movement disorder. Neurogenetics. 21(2). 121–133. 26 indexed citations

Karch, Stephanie, Ute Moog, György Fekete, et al.. (2020). Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome. Clinical Epigenetics. 12(1). 63–63. 9 indexed citations

Harting, Inga, Stephanie Karch, Ute Moog, et al.. (2019). Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement. American Journal of Neuroradiology. 40(5). 903–907. 10 indexed citations

Dikow, Nicola, Ute Moog, Stephanie Karch, et al.. (2019). What do parents expect from a genetic diagnosis of their child with intellectual disability?. Journal of Applied Research in Intellectual Disabilities. 32(5). 1129–1137. 8 indexed citations

Dikow, Nicola, Martin Granzow, Luitgard Graul‐Neumann, et al.. (2017). DDX3X mutations in two girls with a phenotype overlapping Toriello–Carey syndrome. American Journal of Medical Genetics Part A. 173(5). 1369–1373. 27 indexed citations

Evers, Christina, Angelika Seitz, Birgit Assmann, et al.. (2017). Diagnosis of CoPAN by whole exome sequencing: Waking up a sleeping tiger's eye. American Journal of Medical Genetics Part A. 173(7). 1878–1886. 25 indexed citations

Evers, Christina, Lilian Kaufmann, Angelika Seitz, et al.. (2016). Exome sequencing reveals a novel CWF19L1 mutation associated with intellectual disability and cerebellar atrophy. American Journal of Medical Genetics Part A. 170(6). 1502–1509. 12 indexed citations

Dikow, Nicola, Stephanie Karch, Martin Granzow, et al.. (2014). 3p25.3 microdeletion of GABA transporters SLC6A1 and SLC6A11 results in intellectual disability, epilepsy and stereotypic behavior. American Journal of Medical Genetics Part A. 164(12). 3061–3068. 29 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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