Elisabeth Dietschi

634 total citations
15 papers, 323 citations indexed

About

Elisabeth Dietschi is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Elisabeth Dietschi has authored 15 papers receiving a total of 323 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 2 papers in Surgery. Recurrent topics in Elisabeth Dietschi's work include Genetics and Neurodevelopmental Disorders (4 papers), Neurological diseases and metabolism (2 papers) and Platelet Disorders and Treatments (2 papers). Elisabeth Dietschi is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Neurological diseases and metabolism (2 papers) and Platelet Disorders and Treatments (2 papers). Elisabeth Dietschi collaborates with scholars based in Switzerland, Germany and United States. Elisabeth Dietschi's co-authors include Tosso Leeb, Vidhya Jagannathan, Cord Drögemüller, Frank Steffen, Hannes Lohi, Mirjam Frischknecht, Peter Schawalder, Kerstin Lindblad‐Toh, Jennifer J. Rilstone and Berge A. Minassian and has published in prestigious journals such as PLoS ONE, PLoS Genetics and Haematologica.

In The Last Decade

Elisabeth Dietschi

15 papers receiving 317 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elisabeth Dietschi Switzerland	10	147	137	56	52	45	15	323
Katie M. Minor United States	12	143 1.0×	263 1.9×	81 1.4×	67 1.3×	99 2.2×	44	464
Meharji Arumilli Finland	12	127 0.9×	214 1.6×	37 0.7×	26 0.5×	37 0.8×	24	332
Catharine E. Krebs United States	11	91 0.6×	160 1.2×	128 2.3×	62 1.2×	132 2.9×	17	454
Joan Kalnitsky United States	9	20 0.1×	203 1.5×	30 0.5×	211 4.1×	25 0.6×	11	554
Izabella Baranowska Körberg Sweden	8	85 0.6×	112 0.8×	17 0.3×	20 0.4×	34 0.8×	12	272
Sachi Okabayashi Japan	11	21 0.1×	99 0.7×	39 0.7×	52 1.0×	76 1.7×	23	316
Jeffrey Sommer United States	11	210 1.4×	363 2.6×	116 2.1×	10 0.2×	26 0.6×	27	506
Rebecca E.H. Whiting United States	12	52 0.4×	194 1.4×	28 0.5×	36 0.7×	135 3.0×	19	421
Martin Heinrichs Germany	7	42 0.3×	89 0.6×	70 1.3×	23 0.4×	26 0.6×	14	300
Justyna Augustyniak Poland	11	37 0.3×	199 1.5×	31 0.6×	16 0.3×	10 0.2×	19	317

Countries citing papers authored by Elisabeth Dietschi

Since Specialization

Citations

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

Fields of papers citing papers by Elisabeth Dietschi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisabeth Dietschi

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

All Works

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15 of 15 papers shown

Risio, Luisa De, Elisabeth Dietschi, Tosso Leeb, et al.. (2024). A preliminary genome‐wide association study of paroxysmal dyskinesia in the Norwich Terrier. Animal Genetics. 55(6). 914–917. 1 indexed citations

Gurtner, Corinne, Miriam Kleiter, Kernt Köhler, et al.. (2020). YARS2 Missense Variant in Belgian Shepherd Dogs with Cardiomyopathy and Juvenile Mortality. Genes. 11(3). 313–313. 4 indexed citations

Letko, Anna, Elisabeth Dietschi, Vidhya Jagannathan, et al.. (2019). A Missense Variant in SCN8A in Alpine Dachsbracke Dogs Affected by Spinocerebellar Ataxia. Genes. 10(5). 362–362. 9 indexed citations

Dietschi, Elisabeth, Ulrich Rytz, Peter Schawalder, et al.. (2019). An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome. PLoS Genetics. 15(5). e1008102–e1008102. 15 indexed citations

Brenig, Bertram, et al.. (2019). Christmas disease in a Hovawart family resembling human hemophilia B Leyden is caused by a single nucleotide deletion in a highly conserved transcription factor binding site of the F9 gene promoter. Haematologica. 104(11). 2307–2313. 5 indexed citations

Galichet, Arnaud, Vidhya Jagannathan, Dominique J. Wiener, et al.. (2017). A de novo variant in the ASPRV1 gene in a dog with ichthyosis. PLoS Genetics. 13(3). e1006651–e1006651. 34 indexed citations

Kleiter, Miriam, Michael Leschnik, Sandra Högler, et al.. (2017). A Missense Variant inKCNJ10in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA1). G3 Genes Genomes Genetics. 7(2). 663–669. 22 indexed citations

Kleiter, Miriam, Elisabeth Dietschi, Michael Leschnik, et al.. (2017). A SINE Insertion inATP1B2in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA2). G3 Genes Genomes Genetics. 7(8). 2729–2737. 19 indexed citations

Drögemüller, Michaela, Anne Schänzer, Vidhya Jagannathan, et al.. (2016). Neuronal ceroid lipofuscinosis (NCL) is caused by the entire deletion of CLN8 in the Alpenländische Dachsbracke dog. Molecular Genetics and Metabolism. 120(3). 269–277. 21 indexed citations

10.

Frischknecht, Mirjam, Vidhya Jagannathan, Philippe Plattet, et al.. (2015). A Non-Synonymous HMGA2 Variant Decreases Height in Shetland Ponies and Other Small Horses. PLoS ONE. 10(10). e0140749–e0140749. 47 indexed citations

11.

Bianchi, Matteo, Stina S. Dahlgren, Jonathan Massey, et al.. (2015). A Multi-Breed Genome-Wide Association Analysis for Canine Hypothyroidism Identifies a Shared Major Risk Locus on CFA12. PLoS ONE. 10(8). e0134720–e0134720. 14 indexed citations

12.

Frischknecht, Mirjam, Vidhya Jagannathan, Marta Owczarek‐Lipska, et al.. (2013). A COL11A2 Mutation in Labrador Retrievers with Mild Disproportionate Dwarfism. PLoS ONE. 8(3). e60149–e60149. 34 indexed citations

13.

Seppälä, Eija H., Tarja S. Jokinen, Masaki Fukata, et al.. (2011). LGI2 Truncation Causes a Remitting Focal Epilepsy in Dogs. PLoS Genetics. 7(7). e1002194–e1002194. 79 indexed citations

14.

Dietschi, Elisabeth, Peter Schawalder, & Charlotte Gaillard. (2003). Estimation of genetic parameters for canine hip dysplasia in the Swiss Newfoundland population. Journal of Animal Breeding and Genetics. 120(3). 150–161. 12 indexed citations

15.

Schawalder, Peter, David Spreng, Elisabeth Dietschi, G. Dolf, & Charlotte Gaillard. (1996). Die Hüftgelenksdysplasie im Umfeld von sekundären Einflüssen und ektopischen Ursachen. Bern Open Repository and Information System (University of Bern). 7 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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