Corinna Hartmann

825 total citations
7 papers, 106 citations indexed

About

Corinna Hartmann is a scholar working on Genetics, Neurology and Surgery. According to data from OpenAlex, Corinna Hartmann has authored 7 papers receiving a total of 106 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 2 papers in Neurology and 1 paper in Surgery. Recurrent topics in Corinna Hartmann's work include Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomic variations and chromosomal abnormalities (2 papers). Corinna Hartmann is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomic variations and chromosomal abnormalities (2 papers). Corinna Hartmann collaborates with scholars based in Germany, United States and Belgium. Corinna Hartmann's co-authors include Katja Lohmann, Heather C. Mefford, Christine Klein, Katherine L. Helbig, Tobias Bäumer, Alexander Münchau, Connie Marras, Lars Bertram, Aloysius Domingo and Arndt Rolfs and has published in prestigious journals such as Hepatology, Epilepsia and Movement Disorders.

In The Last Decade

Corinna Hartmann

7 papers receiving 104 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Corinna Hartmann Germany	5	53	45	36	27	14	7	106
Chelsea Chambers United States	6	44 0.8×	26 0.6×	40 1.1×	12 0.4×	16 1.1×	10	98
Hormos Salimi Dafsari Germany	8	55 1.0×	40 0.9×	70 1.9×	28 1.0×	10 0.7×	18	173
Amy Crunk United States	6	59 1.1×	24 0.5×	58 1.6×	16 0.6×	23 1.6×	10	131
Daniela Bernardo Italy	6	14 0.3×	68 1.5×	72 2.0×	47 1.7×	10 0.7×	13	146
Linn Öijerstedt Sweden	5	26 0.5×	53 1.2×	42 1.2×	13 0.5×	14 1.0×	14	124
Alexandre D. Laporte Canada	5	40 0.8×	14 0.3×	52 1.4×	16 0.6×	21 1.5×	5	99
Raffaella Minardi Italy	7	80 1.5×	18 0.4×	45 1.3×	25 0.9×	55 3.9×	21	134
Sanna Puusepp Estonia	6	77 1.5×	15 0.3×	84 2.3×	36 1.3×	14 1.0×	8	149
Elena Alonso Spain	4	26 0.5×	20 0.4×	40 1.1×	6 0.2×	15 1.1×	10	89
Christine Strippel Germany	7	18 0.3×	76 1.7×	20 0.6×	24 0.9×	18 1.3×	17	113

Countries citing papers authored by Corinna Hartmann

Since Specialization

Citations

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

Fields of papers citing papers by Corinna Hartmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Corinna Hartmann

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

All Works

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7 of 7 papers shown

1.

Hartmann, Corinna. (2020). La moda del coaching. 16–22. 1 indexed citations

2.

Tunç, Sinem, Norbert Brüggemann, Corinna Hartmann, et al.. (2017). Facial twitches in ADCY5 -associated disease - Myokymia or myoclonus? An electromyography study. Parkinsonism & Related Disorders. 40. 73–75. 14 indexed citations

3.

Lill, Christina M., Corinna Hartmann, Katja Lohmann, et al.. (2016). Launching the movement disorders society genetic mutation database (MDSGene). Movement Disorders. 31(5). 607–609. 32 indexed citations

4.

Lohmann, Katja, Aloysius Domingo, Arndt Rolfs, et al.. (2016). Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability. Neurology Genetics. 2(5). e106–e106. 30 indexed citations

5.

Hartmann, Corinna, Sarah von Spiczak, Arvid Suls, et al.. (2015). Investigating the genetic basis of fever‐associated syndromic epilepsies using copy number variation analysis. Epilepsia. 56(3). e26–32. 14 indexed citations

6.

Helbig, Katherine L., Corinna Hartmann, & Heather C. Mefford. (2013). The unexpected role of copy number variations in juvenile myoclonic epilepsy. Epilepsy & Behavior. 28. S66–S68. 14 indexed citations

7.

Hartmann, Corinna, et al.. (1982). Micro tubule dependent biliary secretion of micelle forming bile acids. Hepatology. 2(5). 715. 1 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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