Esther Gill

436 total citations
13 papers, 224 citations indexed

About

Esther Gill is a scholar working on Molecular Biology, Physiology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Esther Gill has authored 13 papers receiving a total of 224 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Physiology and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Esther Gill's work include Muscle Physiology and Disorders (3 papers), Hereditary Neurological Disorders (3 papers) and RNA regulation and disease (2 papers). Esther Gill is often cited by papers focused on Muscle Physiology and Disorders (3 papers), Hereditary Neurological Disorders (3 papers) and RNA regulation and disease (2 papers). Esther Gill collaborates with scholars based in Germany, Netherlands and United States. Esther Gill's co-authors include Markus Schuelke, Werner Stenzel, Susanne Morales-Gonzalez, Franziska Seifert, Ellen Knierim, Arpad von Moers, Gudrun Schottmann, Mina Petkova, Dominik Seelow and Sathya D. Unudurthi and has published in prestigious journals such as Neurology, Movement Disorders and Journal of Medical Genetics.

In The Last Decade

Esther Gill

13 papers receiving 223 citations

Peers

Esther Gill

CMN

GENET

PHYSI

Hannah E. Steele United Kingdom

Marie‐France Rioux Canada

Gudrun Schottmann Germany

Shinobu Fukumura Japan

Fabrizia Stregapede Italy

Devon Lamb Thrush United States

Mathieu Lachance Canada

Maartje Pennings Netherlands

Ivan Litvinenko Bulgaria

Elena I. Ilina Germany

Hannah E. Steele United Kingdom

Esther Gill

180 ×1.2

77 ×1.2

CMN

30 ×0.6

GENET

27 ×0.6

GENET

32 ×0.8

PHYSI

Citations per year, relative to Esther Gill Esther Gill (= 1×) peers Hannah E. Steele

Countries citing papers authored by Esther Gill

Since Specialization

Citations

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

Fields of papers citing papers by Esther Gill

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Esther Gill

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

All Works

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13 of 13 papers shown

Morales-Gonzalez, Susanne, et al.. (2018). Muscle Weakness, Cardiomyopathy, and L-2-Hydroxyglutaric Aciduria Associated with a Novel Recessive SLC25A4 Mutation. JIMD Reports. 43. 27–35. 8 indexed citations

Radke, Josefine, Randi Koll, Esther Gill, et al.. (2018). Autophagic vacuolar myopathy is a common feature of CLN3 disease. Annals of Clinical and Translational Neurology. 5(11). 1385–1393. 11 indexed citations

Gill, Esther, et al.. (2018). P 328. Novel Homozygous Variants Confirm SPTBN4-Related Congenital Myopathy and Expand the Clinical Phenotype. Neuropediatrics. 1 indexed citations

Schottmann, Gudrun, Jana Marie Schwarz, Esther Gill, et al.. (2017). Recessive mutation in EXOSC3 associates with mitochondrial dysfunction and pontocerebellar hypoplasia. Mitochondrion. 37. 46–54. 15 indexed citations

Knierim, Ellen, Esther Gill, Franziska Seifert, et al.. (2017). A recessive mutation in beta-IV-spectrin (SPTBN4) associates with congenital myopathy, neuropathy, and central deafness. Human Genetics. 136(7). 903–910. 35 indexed citations

Hu, Hao, Christoph Hübner, Zoltán Lukács, et al.. (2016). Klüver–Bucy syndrome associated with a recessive variant in HGSNAT in two siblings with Mucopolysaccharidosis type IIIC (Sanfilippo C). European Journal of Human Genetics. 25(2). 253–256. 2 indexed citations

Petkova, Mina, Susanne Morales-Gonzalez, Karima Relizani, et al.. (2016). Characterization of a Dmd EGFP reporter mouse as a tool to investigate dystrophin expression. Skeletal Muscle. 6(1). 25–25. 15 indexed citations

Schottmann, Gudrun, Carmen Lorenz, Natalie Weinhold, et al.. (2016). A movement disorder with dystonia and ataxia caused by a mutation in the HIBCH gene. Movement Disorders. 31(11). 1733–1739. 23 indexed citations

Schottmann, Gudrun, Heinz Jungbluth, Ulrike Schara, et al.. (2015). Recessive truncating IGHMBP2 mutations presenting as axonal sensorimotor neuropathy. Neurology. 84(5). 523–531. 27 indexed citations

10.

Schottmann, Gudrun, Dominik Seelow, Franziska Seifert, et al.. (2015). Recessive REEP1 mutation is associated with congenital axonal neuropathy and diaphragmatic palsy. Neurology Genetics. 1(4). e32–e32. 20 indexed citations

11.

Rajab, Anna, Markus Schuelke, Esther Gill, et al.. (2015). Recessive DEAF1 mutation associates with autism, intellectual disability, basal ganglia dysfunction and epilepsy. Journal of Medical Genetics. 52(9). 607–611. 17 indexed citations

12.

Knierim, Ellen, Dominik Seelow, Esther Gill, Arpad von Moers, & Markus Schuelke. (2014). Clinical application of whole exome sequencing reveals a novel compound heterozygous TK2-mutation in two brothers with rapidly progressive combined muscle-brain atrophy, axonal neuropathy, and status epilepticus. Mitochondrion. 20. 1–6. 13 indexed citations

13.

Petkova, Mina, Susanne Lützkendorf, Esther Gill, et al.. (2014). POMK mutation in a family with congenital muscular dystrophy with merosin deficiency, hypomyelination, mild hearing deficit and intellectual disability. Journal of Medical Genetics. 51(4). 275–282. 37 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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