Emma Reid

449 total citations
8 papers, 340 citations indexed

About

Emma Reid is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Emma Reid has authored 8 papers receiving a total of 340 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Clinical Biochemistry and 2 papers in Rheumatology. Recurrent topics in Emma Reid's work include Metabolism and Genetic Disorders (3 papers), Genomics and Rare Diseases (2 papers) and Mitochondrial Function and Pathology (2 papers). Emma Reid is often cited by papers focused on Metabolism and Genetic Disorders (3 papers), Genomics and Rare Diseases (2 papers) and Mitochondrial Function and Pathology (2 papers). Emma Reid collaborates with scholars based in United Kingdom, Italy and United States. Emma Reid's co-authors include Philippa B. Mills, Peter T. Clayton, Emma Footitt, Elio Scarpini, Simon Heales, Wendy Heywood, Elisa Oppici, Ross W. Paterson, Amanda Heslegrave and Ernestas Sirka and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and The American Journal of Human Genetics.

In The Last Decade

Emma Reid

7 papers receiving 338 citations

Peers

Emma Reid

MB

CB

PHYSI

GENET

PMH

Birthe Roos Netherlands

Ángela Arias Spain

Pascale Delonlay France

María Teresa García‐Silva Spain

Nicole Lesko Sweden

Irene De Biase United States

A. E. M. Stroomer Netherlands

Amanda Lam United Kingdom

Emma Footitt United Kingdom

Annette S. Feigenbaum Canada

Birthe Roos Netherlands

Emma Reid

187 ×1.1

MB

178 ×1.7

CB

99 ×1.2

PHYSI

31 ×0.5

GENET

11 ×0.2

PMH

Citations per year, relative to Emma Reid Emma Reid (= 1×) peers Birthe Roos

Countries citing papers authored by Emma Reid

Since Specialization

Citations

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

Fields of papers citing papers by Emma Reid

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emma Reid

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

All Works

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8 of 8 papers shown

1.

Solem, Michele, et al.. (2025). Absence of hippocampal pathology persists in the Q175DN mouse model of Huntington's disease despite elevated HTT aggregation. Journal of Huntington s Disease. 14(1). 59–84.

2.

Ryan, David, et al.. (2023). A rare case of KILT syndrome in Ireland: A case report. SHILAP Revista de lepidopterología. 10. 100131–100131. 1 indexed citations

3.

Reid, Emma, Hywel Williams, Glenn Anderson, et al.. (2017). Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delay. Journal of Inherited Metabolic Disease. 40(3). 385–394. 15 indexed citations

4.

Reid, Emma, Apostolos Papandreou, Suzanne Drury, et al.. (2016). Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. Brain. 139(11). 2844–2854. 27 indexed citations

5.

Darín, Niklas, Emma Reid, Laurence Prunetti, et al.. (2016). Mutations in PROSC Disrupt Cellular Pyridoxal Phosphate Homeostasis and Cause Vitamin-B6-Dependent Epilepsy. The American Journal of Human Genetics. 99(6). 1325–1337. 106 indexed citations

6.

Heywood, Wendy, Daniela Galimberti, Ernestas Sirka, et al.. (2015). Identification of novel CSF biomarkers for neurodegeneration and their validation by a high-throughput multiplexed targeted proteomic assay. Molecular Neurodegeneration. 10(1). 20–20. 124 indexed citations

7.

Oppici, Elisa, Sonia Fargue, Emma Reid, et al.. (2015). Pyridoxamine and pyridoxal are more effective than pyridoxine in rescuing folding-defective variants of human alanine:glyoxylate aminotransferase causing primary hyperoxaluria type I. Human Molecular Genetics. 24(19). 5500–5511. 48 indexed citations

8.

Reid, Emma, Hywel Williams, Polona Le Quesne Stabej, et al.. (2015). Seizures Due to a KCNQ2 Mutation: Treatment with Vitamin B6. JIMD Reports. 27. 79–84. 19 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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