Leigh Demain

521 total citations
12 papers, 209 citations indexed

About

Leigh Demain is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Leigh Demain has authored 12 papers receiving a total of 209 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 2 papers in Clinical Biochemistry and 2 papers in Genetics. Recurrent topics in Leigh Demain's work include Mitochondrial Function and Pathology (5 papers), RNA regulation and disease (4 papers) and RNA modifications and cancer (3 papers). Leigh Demain is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), RNA regulation and disease (4 papers) and RNA modifications and cancer (3 papers). Leigh Demain collaborates with scholars based in United Kingdom, United States and Netherlands. Leigh Demain's co-authors include William G. Newman, Gerard S. Conway, James O’Sullivan, Jill Urquhart, Rabia Faridi, Saima Riazuddin, Emma M. Jenkinson, Muhammad Zaman Khan Assir, Thomas B. Friedman and Simon H. S. Pearce and has published in prestigious journals such as Annals of Oncology, European Journal of Human Genetics and Reproductive BioMedicine Online.

In The Last Decade

Leigh Demain

9 papers receiving 207 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Leigh Demain United Kingdom 7 134 59 48 37 35 12 209
Faezeh Mojahedi Iran 6 82 0.6× 38 0.6× 64 1.3× 51 1.4× 4 0.1× 8 160
Xiaozhen Liu China 10 187 1.4× 52 0.9× 57 1.2× 37 1.0× 2 0.1× 29 275
Samantha L.P. Schilit United States 6 89 0.7× 27 0.5× 64 1.3× 44 1.2× 2 0.1× 13 151
Keith Masterson United States 5 252 1.9× 99 1.7× 46 1.0× 42 1.1× 115 3.3× 8 318
Alexis Ceecee Britten‐Jones Australia 10 124 0.9× 116 2.0× 34 0.7× 2 0.1× 10 0.3× 34 314
Nuria Martí‐Gutiérrez United States 4 114 0.9× 66 1.1× 28 0.6× 4 0.1× 21 0.6× 6 131
Flavia Amanda Costa‐Barbosa Brazil 8 113 0.8× 13 0.2× 96 2.0× 100 2.7× 14 0.4× 13 225
Anita Shanmugham United States 4 82 0.6× 48 0.8× 275 5.7× 13 0.4× 15 0.4× 4 357
Tammy Kammin United Kingdom 5 58 0.4× 21 0.4× 54 1.1× 38 1.0× 1 0.0× 5 115
R. J. E. Jongbloed Netherlands 11 309 2.3× 15 0.3× 167 3.5× 22 0.6× 45 1.3× 15 480

Countries citing papers authored by Leigh Demain

Since Specialization
Citations

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

Fields of papers citing papers by Leigh Demain

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Leigh Demain

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

All Works

12 of 12 papers shown
1.
Campbell, Christopher, Leigh Demain, Sarah Jenkinson, et al.. (2025). Evaluating DNA methylation episignatures as a first-tier diagnostic test in individuals with suspected genetic disorders. European Journal of Human Genetics. 34(2). 296–299.
2.
Kershaw, Christopher J., Leigh Demain, George J. Burghel, et al.. (2025). Whole Genome Sequencing to Identify Novel Germline Fumarate Hydratase Mutation in Child With Bilateral Renal Cell Carcinoma. Clinical Genetics. 107(6). 702–704.
3.
4.
Demain, Leigh, et al.. (2022). Homozygous missense variants in BMPR15 can result in primary ovarian insufficiency. Reproductive BioMedicine Online. 45(4). 727–729. 4 indexed citations
5.
McDermott, John, Peter Woolf, Jamie M. Ellingford, et al.. (2021). A Nonadaptive Combinatorial Group Testing Strategy to Facilitate Health Care Worker Screening during the Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) Outbreak. Journal of Molecular Diagnostics. 23(5). 532–540. 5 indexed citations
6.
Demain, Leigh, Emma Miles, Cheryl T. Fitzgerald, et al.. (2021). Biallelic loss of function variants in STAG3 result in primary ovarian insufficiency. Reproductive BioMedicine Online. 43(5). 899–902. 7 indexed citations
7.
Demain, Leigh, et al.. (2019). A recurrent missense variant in HARS2 results in variable sensorineural hearing loss in three unrelated families. Journal of Human Genetics. 65(3). 305–311. 9 indexed citations
8.
McDermott, John, Iain Bruce, Ajit Mahaveer, et al.. (2019). Diagnosing and Preventing Hearing Loss in the Genomic Age. Trends in Hearing. 23. 2760890695–2760890695. 17 indexed citations
9.
Demain, Leigh, Imane Cherkaoui Jaouad, Ilham Ratbi, et al.. (2017). Marfanoid habitus is a nonspecific feature of Perrault syndrome. Clinical Dysmorphology. 26(4). 200–204. 9 indexed citations
10.
Demain, Leigh, Gerard S. Conway, & William G. Newman. (2016). Genetics of mitochondrial dysfunction and infertility. Clinical Genetics. 91(2). 199–207. 61 indexed citations
11.
Demain, Leigh, Jill Urquhart, James O’Sullivan, et al.. (2016). Expanding the genotypic spectrum of Perrault syndrome. Clinical Genetics. 91(2). 302–312. 62 indexed citations
12.
Faridi, Rabia, Atteeq U. Rehman, Robert J. Morell, et al.. (2016). Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome. Clinical Genetics. 91(2). 328–332. 35 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

Breakdown of academic impact, for papers by Faezeh Mojahedi Breakdown of academic impact, for papers by Xiaozhen Liu Breakdown of academic impact, for papers by Samantha L.P. Schilit Breakdown of academic impact, for papers by Keith Masterson Breakdown of academic impact, for papers by Alexis Ceecee Britten‐Jones Breakdown of academic impact, for papers by Nuria Martí‐Gutiérrez Breakdown of academic impact, for papers by Flavia Amanda Costa‐Barbosa Breakdown of academic impact, for papers by Anita Shanmugham Breakdown of academic impact, for papers by Tammy Kammin Breakdown of academic impact, for papers by R. J. E. Jongbloed
Rankless by CCL
2026