Anne Hempelmann

571 total citations
8 papers, 236 citations indexed

About

Anne Hempelmann is a scholar working on Psychiatry and Mental health, Molecular Biology and Genetics. According to data from OpenAlex, Anne Hempelmann has authored 8 papers receiving a total of 236 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Psychiatry and Mental health, 4 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Anne Hempelmann's work include Epilepsy research and treatment (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Ion channel regulation and function (3 papers). Anne Hempelmann is often cited by papers focused on Epilepsy research and treatment (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Ion channel regulation and function (3 papers). Anne Hempelmann collaborates with scholars based in Germany, United States and Australia. Anne Hempelmann's co-authors include Thomas Sander, Armin Heils, Susanne Lorenz, Kirsten P. Lenzen, Andrew Escayg, Bin Tang, T. Sander, Bettina Schmitz, Falk W. Lohoff and Susanne Höfels and has published in prestigious journals such as Epilepsia, Neurobiology of Disease and Neuroscience Letters.

In The Last Decade

Anne Hempelmann

8 papers receiving 233 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anne Hempelmann Germany 8 125 124 108 74 21 8 236
Estelle Fédirko France 6 62 0.5× 74 0.6× 87 0.8× 84 1.1× 21 1.0× 6 192
Theresa Scattergood United States 5 100 0.8× 117 0.9× 85 0.8× 51 0.7× 15 0.7× 7 220
Kameryn M. Butler United States 7 92 0.7× 115 0.9× 94 0.9× 129 1.7× 21 1.0× 13 249
Melinda S. Martin United States 7 168 1.3× 153 1.2× 197 1.8× 89 1.2× 33 1.6× 10 321
Katharina Pernhorst Germany 9 116 0.9× 116 0.9× 104 1.0× 61 0.8× 14 0.7× 9 290
Fatima Jaffer United Kingdom 6 86 0.7× 138 1.1× 47 0.4× 67 0.9× 8 0.4× 12 264
Mathieu Lachance Canada 6 152 1.2× 124 1.0× 97 0.9× 143 1.9× 65 3.1× 9 330
Alexis Lupien‐Meilleur Canada 4 97 0.8× 112 0.9× 40 0.4× 88 1.2× 38 1.8× 5 217
Susanne Ruf Germany 5 74 0.6× 103 0.8× 83 0.8× 112 1.5× 27 1.3× 6 221
Dora Steel United Kingdom 9 111 0.9× 131 1.1× 105 1.0× 107 1.4× 17 0.8× 17 360

Countries citing papers authored by Anne Hempelmann

Since Specialization
Citations

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

Fields of papers citing papers by Anne Hempelmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Hempelmann

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

All Works

8 of 8 papers shown
1.
Kovel, Carolien G. F. de, Dalila Pinto, Ulrike Tauer, et al.. (2010). Whole-genome linkage scan for epilepsy-related photosensitivity: A mega-analysis. Epilepsy Research. 89(2-3). 286–294. 33 indexed citations
2.
Hempelmann, Anne, Joana Cobilanschi, Armin Heils, et al.. (2007). Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy. Epilepsy Research. 74(1). 28–32. 13 indexed citations
3.
Tang, Bin, et al.. (2007). Mutation analysis of the hyperpolarization-activated cyclic nucleotide-gated channels HCN1 and HCN2 in idiopathic generalized epilepsy. Neurobiology of Disease. 29(1). 59–70. 53 indexed citations
4.
Hempelmann, Anne, Armin Heils, & Thomas Sander. (2006). Confirmatory evidence for an association of the connexin-36 gene with juvenile myoclonic epilepsy. Epilepsy Research. 71(2-3). 223–228. 42 indexed citations
5.
Hempelmann, Anne, Santosh Kumar, Muralitharan Shanmugakonar, & Thomas Sander. (2006). Myofibrillogenesis regulator 1 gene (MR-1) mutation in an Omani family with paroxysmal nonkinesigenic dyskinesia. Neuroscience Letters. 402(1-2). 118–120. 19 indexed citations
6.
Lenzen, Kirsten P., Armin Heils, Susanne Lorenz, Anne Hempelmann, & Thomas Sander. (2005). Association analysis of the Arg220His variation of the human gene encoding the GABA δ subunit with idiopathic generalized epilepsy. Epilepsy Research. 65(1-2). 53–57. 17 indexed citations
7.
Lenzen, Kirsten P., Armin Heils, Susanne Lorenz, Anne Hempelmann, & Thomas Sander. (2005). Association Analysis of Malic Enzyme 2 Gene Polymorphisms with Idiopathic Generalized Epilepsy. Epilepsia. 46(10). 1637–1641. 10 indexed citations
8.
Lenzen, Kirsten P., Armin Heils, Susanne Lorenz, et al.. (2005). Supportive evidence for an allelic association of the human KCNJ10 potassium channel gene with idiopathic generalized epilepsy. Epilepsy Research. 63(2-3). 113–118. 49 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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