Lucy Raymond

2.1k total citations
10 papers, 215 citations indexed

About

Lucy Raymond is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Lucy Raymond has authored 10 papers receiving a total of 215 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Molecular Biology and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in Lucy Raymond's work include Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (3 papers) and RNA modifications and cancer (2 papers). Lucy Raymond is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (3 papers) and RNA modifications and cancer (2 papers). Lucy Raymond collaborates with scholars based in United Kingdom, United States and Australia. Lucy Raymond's co-authors include Alba Sanchis‐Juan, Harry Joe, Andrew J. Wallace, Adrian L. Jones, Adam Shaw, Dorothy Halliday, Jan M. Friedman, Andrew T. King, D. Gareth Evans and Rupert Obholzer and has published in prestigious journals such as Nucleic Acids Research, Scientific Reports and Human Molecular Genetics.

In The Last Decade

Lucy Raymond

10 papers receiving 212 citations

Peers

Lucy Raymond

MB

GENET

NEURO

EPIDE

CN

Eda Ütine Türkiye

Juliette Piard France

Arjan PM de Brouwer Netherlands

Lorraine Gaunt United Kingdom

Joseph Bursztyn France

Dhanya Lakshmi Narayanan India

Marisol Mirabelli-Badenier Italy

Mengmeng Shi China

Chloe Stutterd Australia

Helle Lybæk Norway

Eda Ütine Türkiye

Lucy Raymond

96 ×0.8

MB

99 ×1.0

GENET

21 ×0.3

NEURO

12 ×0.3

EPIDE

18 ×0.8

CN

Citations per year, relative to Lucy Raymond Lucy Raymond (= 1×) peers Eda Ütine

Countries citing papers authored by Lucy Raymond

Since Specialization

Citations

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

Fields of papers citing papers by Lucy Raymond

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lucy Raymond

This figure shows the co-authorship network connecting the top 25 collaborators of Lucy Raymond. A scholar is included among the top collaborators of Lucy Raymond 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 Lucy Raymond. Lucy Raymond 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

1.

Ratnaike, Thiloka, Daniel Greene, Wei Wei, et al.. (2021). MitoPhen database: a human phenotype ontology-based approach to identify mitochondrial DNA diseases. Nucleic Acids Research. 49(17). 9686–9695. 22 indexed citations

2.

Thompson, Kyle, Emanuele Bellacchio, Courtney E. French, et al.. (2021). Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease. Human Molecular Genetics. 31(4). 523–534. 13 indexed citations

3.

Vandeweyer, Geert, Ellen Elinck, Alba Sanchis‐Juan, et al.. (2021). Abundancy of polymorphic CGG repeats in the human genome suggest a broad involvement in neurological disease. Scientific Reports. 11(1). 2515–2515. 18 indexed citations

4.

Recchia, Gabriel, et al.. (2019). Creating genetic reports that are understood by nonspecialists: a case study. Genetics in Medicine. 22(2). 353–361. 14 indexed citations

5.

Niranjan, Tejasvi, Melanie May, Patrick Tarpey, et al.. (2019). Dysregulations of sonic hedgehog signaling in MED12‐related X‐linked intellectual disability disorders. Molecular Genetics & Genomic Medicine. 7(4). e00569–e00569. 10 indexed citations

6.

Raymond, Lucy, et al.. (2019). A Novel ATRX Mutation Presenting with Intellectual Disability and Severe Kyphoscoliosis. Fetal and Pediatric Pathology. 39(6). 539–543. 2 indexed citations

7.

Borooah, Shyamanga, Chloë M. Stanton, Joseph A. Marsh, et al.. (2018). Whole genome sequencing reveals novel mutations causing autosomal dominant inherited macular degeneration. Ophthalmic Genetics. 39(6). 763–770. 12 indexed citations

8.

Smogavec, Mateja, Juliane Hoyer, Damien Lederer, et al.. (2016). Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum. Journal of Medical Genetics. 53(12). 820–827. 41 indexed citations

9.

Jones, Adrian L., Harry Joe, Miriam J. Smith, et al.. (2015). Clinical and molecular predictors of mortality in neurofibromatosis 2: a UK national analysis of 1192 patients. Journal of Medical Genetics. 52(10). 699–705. 63 indexed citations

10.

Bianciardi, Laura, Marco Fichera, Pinella Failla, et al.. (2015). MECP2 missense mutations outside the canonical MBD and TRD domains in males with intellectual disability. Journal of Human Genetics. 61(2). 95–101. 20 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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