Esther Meyer

6.6k total citations
51 papers, 2.6k citations indexed

About

Esther Meyer is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Esther Meyer has authored 51 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 23 papers in Molecular Biology and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Esther Meyer's work include Genetic Syndromes and Imprinting (12 papers), Prenatal Screening and Diagnostics (12 papers) and Epigenetics and DNA Methylation (10 papers). Esther Meyer is often cited by papers focused on Genetic Syndromes and Imprinting (12 papers), Prenatal Screening and Diagnostics (12 papers) and Epigenetics and DNA Methylation (10 papers). Esther Meyer collaborates with scholars based in United Kingdom, Germany and United States. Esther Meyer's co-authors include Marc Kachelrieß, Rainer Raupach, Michael Lell, Bernhard Schmidt, Manju A. Kurian, Eamonn R. Maher, Shanaz Pasha, Louise Tee, Daniel Prell and Thomas Eggermann and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Brain.

In The Last Decade

Esther Meyer

49 papers receiving 2.5k citations

Peers

Countries citing papers authored by Esther Meyer

Since Specialization

Citations

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

Fields of papers citing papers by Esther Meyer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Esther Meyer

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Clinical and Molecular Genetic Characterization of Landau Kleffner Syndrome: An Observational Cohort and Experimental Study 2025 ·Annals of Neurology ·Adeline Ngoh, (unknown), (unknown), Xiumin Chen, Kimberley M. Reid, (unknown), Esther Meyer, Dale Moulding, Natalie Trump, J. Helen Cross, (unknown), (unknown), Dimitri M. Kullmann, Joseph W. Lynch, Victoria L. Harvey, Manju A. Kurian	0
2	Review of the phenotype of early-onset generalised progressive dystonia due to mutations in KMT2B 2017 ·European Journal of Paediatric Neurology ·Kathleen M. Gorman, Esther Meyer, Manju A. Kurian	28
3	Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis 2016 ·Journal of Medical Genetics ·Natalie Trump, Amy McTague, Helen Brittain, Apostolos Papandreou, Esther Meyer, Adeline Ngoh, Rodger Palmer, Deborah Morrogh, C. R. Boustred, Jane A. Hurst, Lucy Jenkins, Manju A. Kurian, Richard H. Scott	147
4	The clinical and genetic heterogeneity of paroxysmal dyskinesias 2015 ·Brain ·A. Gardiner, Fatima Jaffer, Russell C. Dale, Robyn Labrum, Roberto Erro, Esther Meyer, Georgia Xiromerisiou, María Stamelou, Matthew C. Walker, Dimitri M. Kullmann, Thomas T. Warner, Paul Jarman, Michael G. Hanna, Manju A. Kurian, Kailash P. Bhatia, Henry Houlden	101
5	PLA2G6-associated neurodegeneration (PLAN): Further expansion of the clinical, radiological and mutation spectrum associated with infantile and atypical childhood-onset disease 2014 ·Molecular Genetics and Metabolism ·Marjorie Illingworth, Esther Meyer, W.K. Chong, Adnan Y. Manzur, Lucinda Carr, R. T. Younis, C Hardy, Fiona McDonald, Anne Marie Childs, Bruce H. Stewart, Daniel Warren, Rachel Kneen, Marissa King, Susan J. Hayflick, Manju A. Kurian	69
6	Comparison of 3D turbo spin-echo SPACE sequences with conventional 2D MRI sequences to assess the shoulder joint 2014 ·European Journal of Radiology ·(unknown), (unknown), Michael Akbar, Esther Meyer, Dominik Paul, (unknown), Marc‐André Weber	24
7	Clinical evaluation of the normalized metal artefact reduction algorithm caused by dental fillings in CT 2013 ·Dentomaxillofacial Radiology ·Xianzu Gong, Esther Meyer, Xianjun Yu, (unknown), (unknown), Kuo‐How Huang, Runze Wu	20
8	Frequency split metal artifact reduction (FSMAR) in computed tomography 2012 ·Medical Physics ·Esther Meyer, Rainer Raupach, Michael Lell, Bernhard Schmidt, Marc Kachelrieß	207
9	Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy 2012 ·Epilepsia ·Annapurna Poduri, (unknown), Edward Neilan, Princess C. Elhosary, Manju A. Kurian, Esther Meyer, Brenda J. Barry, Omar Khwaja, Mustafa A. Salih, Tommy Stödberg, Ingrid E. Scheffer, Eamonn R. Maher, Mustafa Şahin, Bai‐Lin Wu, Gerard T. Berry, Christopher A. Walsh, Jonathan Picker, Sanjeev V. Kothare	68
10	Promoter mutation is a common variant in GJC2-associated Pelizaeus–Merzbacher-like disease 2011 ·Molecular Genetics and Metabolism ·Esther Meyer, Manju A. Kurian, Neil V. Morgan, A. McNeill, Shanaz Pasha, Louise Tee, (unknown), Andrew Norman, Marjo S. van der Knaap, Evangeline Wassmer, Richard C. Trembath, L A Brueton, Eamonn R. Maher	18
11	Mutations in FLVCR2 Are Associated with Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome (Fowler Syndrome) 2010 ·The American Journal of Human Genetics ·Esther Meyer, Christopher J. Ricketts, Neil V. Morgan, Mark R. Morris, Shanaz Pasha, Louise Tee, Fatimah Rahman, Anne Bazin, Bettina Bessières, Pierre Déchelotte, (unknown), Mudher Al‐Adnani, Tamás Marton, David Tannahill, Richard C. Trembath, Catherine Fallet‐Bianco, P. Cox, Denise Williams, Eamonn R. Maher	46
12	Normalized metal artifact reduction (NMAR) in computed tomography 2010 ·Medical Physics ·Esther Meyer, Rainer Raupach, Michael Lell, Bernhard Schmidt, Marc Kachelrieß	440
13	Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia 2009 ·Journal of Clinical Investigation ·Manju A. Kurian, Juan Zhen, Shuyuan Cheng, Yan Li, Santosh Mordekar, Philip Jardine, Neil V. Morgan, Esther Meyer, Louise Tee, Shanaz Pasha, Evangeline Wassmer, Simon Heales, Paul Gissen, Maarten E. A. Reith, Eamonn R. Maher	148
14	Germline Mutation in NLRP2 (NALP2) in a Familial Imprinting Disorder (Beckwith-Wiedemann Syndrome) 2009 ·PLoS Genetics ·Esther Meyer, Derek Lim, Shanaz Pasha, Louise Tee, Fatimah Rahman, John R.W. Yates, C. Geoffrey Woods, Wolf Reik, Eamonn R. Maher	183
15	Genetic and Epigenetic Analysis of Recurrent Hydatidiform Mole 2009 ·Human Mutation ·Bruce E. Hayward, Michel De Vos, (unknown), M.R. Abdollahi, Graham R. Taylor, Esther Meyer, Denise Williams, Eamonn R. Maher, (unknown), (unknown), (unknown), Hussain Jafri, Yasmin Abdul Rashid, Eamonn Sheridan, David T. Bonthron	88
16	ICR1 Epimutations in 11p15 are Restricted to Patients with Silver-Russell Syndrome Features 2008 ·Journal of Pediatric Endocrinology and Metabolism ·Thomas Eggermann, Esther Meyer, Ahmet Okay Çağlayan, Munis Dündar, Nadine Schönherr	6
17	(Epi)mutations in 11p15 significantly contribute to Silver–Russell syndrome: but are they generally involved in growth retardation? 2006 ·European Journal of Medical Genetics ·Nadine Schönherr, Esther Meyer, Katja Eggermann, Michael B. Ranke, H Wollmann, Thomas Eggermann	38
18	Mosaic tetrasomy 14pter‐q13 due to a supernumerary isodicentric derivate of proximal chromosome 14q 2005 ·American Journal of Medical Genetics Part A ·Thomas Eggermann, Ulrike Gamerdinger, Kristin Bosse, (unknown), (unknown), Esther Meyer, (unknown), Herdit M. Schüler, Eckhard Korsch, Gesa Schwanitz	7
19	Supernumerary marker chromosome 7 and maternal uniparental disomy 7 in a boy with growth retardation and triangular face 2005 ·Clinical Dysmorphology ·Thomas Eggermann, (unknown), H Wollmann, Klaus Zerres, Guang Dai, Esther Meyer, Oliver Bartsch	8
20	Searching for genomic variants in IGF2 and CDKN1C in Silver–Russell syndrome patients 2004 ·Molecular Genetics and Metabolism ·(unknown), Esther Meyer, (unknown), Jürgen Tomiuk, H Wollmann, Thomas Eggermann	16

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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