Annelies Rotthier

1.0k total citations
10 papers, 736 citations indexed

About

Annelies Rotthier is a scholar working on Cell Biology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Annelies Rotthier has authored 10 papers receiving a total of 736 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Cell Biology, 4 papers in Molecular Biology and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Annelies Rotthier's work include Endoplasmic Reticulum Stress and Disease (5 papers), Hereditary Neurological Disorders (4 papers) and Sphingolipid Metabolism and Signaling (3 papers). Annelies Rotthier is often cited by papers focused on Endoplasmic Reticulum Stress and Disease (5 papers), Hereditary Neurological Disorders (4 papers) and Sphingolipid Metabolism and Signaling (3 papers). Annelies Rotthier collaborates with scholars based in Belgium, Switzerland and Germany. Annelies Rotthier's co-authors include Vincent Timmerman, Jonathan Baets, Katrien Janssens, Peter De Jonghe, Michaela Auer‐Grumbach, Els De Vriendt, Albena Jordanova, Thorsten Hornemann, Anke Penno and Haluk Topaloğlu and has published in prestigious journals such as Nature Genetics, Brain and Kidney International.

In The Last Decade

Annelies Rotthier

10 papers receiving 732 citations

Peers

Annelies Rotthier

CMN

PHYSI

NEURO

Joseph Ochaba United States

Laura Cassina Italy

Julián Esteve-Rudd United States

Sarah M. Carpanini United Kingdom

Annabelle Chaussenot France

Gianluca Figlia Germany

Juliet Rashidian Canada

Benjamin L.L. Clayton United States

Anja W. Fjorback Denmark

Joseph Ochaba United States

Annelies Rotthier

347 ×0.9

288 ×1.0

CMN

90 ×0.4

76 ×0.5

PHYSI

96 ×1.1

NEURO

Citations per year, relative to Annelies Rotthier Annelies Rotthier (= 1×) peers Joseph Ochaba

Countries citing papers authored by Annelies Rotthier

Since Specialization

Citations

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

Fields of papers citing papers by Annelies Rotthier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annelies Rotthier

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

All Works

Sort: Min cites: Since: Top N: Style:

10 of 10 papers shown

Hureaux, Marguerite, Emma Ashton, Karin Dahan, et al.. (2019). High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults. Kidney International. 96(6). 1408–1416. 32 indexed citations

Ashton, Emma, Anne Debost‐Legrand, Valérie Benoît, et al.. (2018). Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies. Kidney International. 93(4). 961–967. 67 indexed citations

Saenen, Johan, Geert Vandeweyer, Annelies Rotthier, et al.. (2017). Targeted Next-Generation Sequencing of 51 Genes Involved in Primary Electrical Disease. Journal of Molecular Diagnostics. 19(3). 445–459. 15 indexed citations

Rotthier, Annelies, Jonathan Baets, Vincent Timmerman, & Katrien Janssens. (2012). Mechanisms of disease in hereditary sensory and autonomic neuropathies. Nature Reviews Neurology. 8(2). 73–85. 117 indexed citations

Rotthier, Annelies, Anke Penno, Bernd Rautenstrauß, et al.. (2011). Characterization of two mutations in the SPTLC1 subunit of serine palmitoyltransferase associated with hereditary sensory and autonomic neuropathy type I. Human Mutation. 32(6). E2211–E2225. 32 indexed citations

Rotthier, Annelies, Michaela Auer‐Grumbach, Katrien Janssens, et al.. (2010). Mutations in the SPTLC2 Subunit of Serine Palmitoyltransferase Cause Hereditary Sensory and Autonomic Neuropathy Type I. The American Journal of Human Genetics. 87(4). 513–522. 134 indexed citations

Kurth, Ingo, J. Christopher Hennings, Antje K. Huebner, et al.. (2009). Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy. Nature Genetics. 41(11). 1179–1181. 184 indexed citations

Rotthier, Annelies, Jonathan Baets, Els De Vriendt, et al.. (2009). Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation. Brain. 132(10). 2699–2711. 116 indexed citations

Hornemann, Thorsten, Anke Penno, Richard J. Kahnoski, et al.. (2009). A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associated. Neurogenetics. 10(2). 135–143. 22 indexed citations

10.

Kılıç, Sara Şebnem, et al.. (2008). Humoral immunodeficiency in congenital insensitivity to pain with anhidrosis. Neurogenetics. 10(2). 161–165. 17 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.

Explore authors with similar magnitude of impact