Frances Elmslie

2.2k total citations
16 papers, 291 citations indexed

About

Frances Elmslie is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Frances Elmslie has authored 16 papers receiving a total of 291 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Frances Elmslie's work include Genomics and Rare Diseases (2 papers), BRCA gene mutations in cancer (2 papers) and Neuroscience and Neuropharmacology Research (2 papers). Frances Elmslie is often cited by papers focused on Genomics and Rare Diseases (2 papers), BRCA gene mutations in cancer (2 papers) and Neuroscience and Neuropharmacology Research (2 papers). Frances Elmslie collaborates with scholars based in United Kingdom, France and United States. Frances Elmslie's co-authors include Sahar Mansour, Ian Walpole, Nicola Foulds, Sonia Bertrand, Elaine Hughes, Daniel Bertrand, Thomas Sander, Ortrud K. Steinlein, J R Trounce and Mark Gardiner and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and Human Molecular Genetics.

In The Last Decade

Frances Elmslie

15 papers receiving 287 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Frances Elmslie United Kingdom 10 117 99 67 50 43 16 291
Muhammad Talal Alrifai Saudi Arabia 12 157 1.3× 82 0.8× 47 0.7× 13 0.3× 53 1.2× 28 444
Oddveig Røsby Norway 10 131 1.1× 114 1.2× 28 0.4× 21 0.4× 29 0.7× 13 262
Carlos E. Speck‐Martins Brazil 11 137 1.2× 58 0.6× 63 0.9× 7 0.1× 48 1.1× 23 314
Jessica Connor United States 9 80 0.7× 59 0.6× 24 0.4× 18 0.4× 25 0.6× 13 293
Anna Wedell Sweden 11 321 2.7× 142 1.4× 30 0.4× 132 2.6× 36 0.8× 28 498
Andrea Guerin Canada 8 99 0.8× 103 1.0× 33 0.5× 36 0.7× 69 1.6× 30 336
Patrick A. Lundquist United States 8 130 1.1× 55 0.6× 36 0.5× 7 0.1× 48 1.1× 16 440
Christèle du Souich Canada 13 141 1.2× 251 2.5× 29 0.4× 41 0.8× 54 1.3× 25 459
Kerith‐Rae Dias Australia 5 240 2.1× 165 1.7× 19 0.3× 46 0.9× 32 0.7× 7 364
H. G. Dörr Germany 10 100 0.9× 112 1.1× 47 0.7× 84 1.7× 89 2.1× 19 302

Countries citing papers authored by Frances Elmslie

Since Specialization
Citations

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

Fields of papers citing papers by Frances Elmslie

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frances Elmslie

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

All Works

16 of 16 papers shown
1.
Maharaj, Avinaash, Miho Ishida, Anna Rybak, et al.. (2024). QSOX2 Deficiency-induced short stature, gastrointestinal dysmotility and immune dysfunction. Nature Communications. 15(1). 8420–8420. 2 indexed citations
2.
Monahan, Kevin, Adam Shaw, Laura Monje‐Garcia, et al.. (2023). P293 Finding the missing 95%: the English national lynch syndrome transformation project. Poster presentations. A204.2–A204. 3 indexed citations
3.
Monahan, Kevin, Neil Ryan, Laura Monje‐Garcia, et al.. (2023). The English National Lynch Syndrome transformation project: an NHS Genomic Medicine Service Alliance (GMSA) programme. SHILAP Revista de lepidopterología. 2(1). e000124–e000124. 9 indexed citations
4.
Middleton, Anna, Nicola V. Taverner, Catherine Houghton, et al.. (2022). Scope of professional roles for genetic counsellors and clinical geneticists in the United Kingdom. European Journal of Human Genetics. 31(1). 9–12. 13 indexed citations
5.
Titheradge, Hannah, Nicola Cooper, Frances Elmslie, et al.. (2020). Expanding the genotype–phenotype correlation ofde novoheterozygous missense variants inYWHAGas a cause of developmental and epileptic encephalopathy. American Journal of Medical Genetics Part A. 182(4). 713–720. 14 indexed citations
6.
Haworth, A., Eva Serra, Janna Kenny, et al.. (2020). A report on the impact of rapid prenatal exome sequencing on the clinical management of 52 ongoing pregnancies: a retrospective review. BJOG An International Journal of Obstetrics & Gynaecology. 128(6). 1012–1019. 29 indexed citations
7.
8.
Cox, Helen, Julie Vogt, Jenny Morton, et al.. (2019). Deep phenotyping of 14 new patients with IQSEC2 variants, including monozygotic twins of discordant phenotype. Clinical Genetics. 95(4). 496–506. 21 indexed citations
9.
Titheradge, Hannah, Nicola Cooper, Frances Elmslie, et al.. (2019). De novo, heterozygous missense variants in YWHAG as a novel cause of developmental and epileptic encephalopathy. White Rose Research Online (University of Leeds, The University of Sheffield, University of York). 1 indexed citations
10.
Hacohen, Yael, et al.. (2018). GLUT-1 deficiency presenting with seizures and reversible leukoencephalopathy on MRI imaging. European Journal of Paediatric Neurology. 22(6). 1161–1164. 14 indexed citations
11.
Alcantara, Diana, Frances Elmslie, Martine Tétreault, et al.. (2017). SHORT syndrome due to a novel de novo mutation in PRKCE (Protein Kinase Cɛ) impairing TORC2-dependent AKT activation. Human Molecular Genetics. 26(19). 3713–3721. 17 indexed citations
12.
Vandersteen, Anthony M., Neeti Ghali, Philip Sawle, et al.. (2015). Clinical, structural, biochemical and X‐ray crystallographic correlates of pathogenicity for variants in the C‐propeptide region of the COL3A1 gene. American Journal of Medical Genetics Part A. 167(8). 1763–1772. 7 indexed citations
13.
14.
Bertrand, Daniel, Frances Elmslie, Elaine Hughes, et al.. (2005). The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits. Neurobiology of Disease. 20(3). 799–804. 76 indexed citations
15.
Foulds, Nicola, Ian Walpole, Frances Elmslie, & Sahar Mansour. (2004). Carbimazole embryopathy: An emerging phenotype. American Journal of Medical Genetics Part A. 132A(2). 130–135. 70 indexed citations
16.
Elmslie, Frances & Mark Gardiner. (1995). Genetics of the epilepsies. Current Opinion in Neurology. 8(2). 126–130. 11 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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