James Fasham

518 total citations
10 papers, 182 citations indexed

About

James Fasham is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, James Fasham has authored 10 papers receiving a total of 182 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Cell Biology. Recurrent topics in James Fasham's work include Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Genetic and Kidney Cyst Diseases (2 papers). James Fasham is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Genetic and Kidney Cyst Diseases (2 papers). James Fasham collaborates with scholars based in United Kingdom, United States and Palestinian Territory. James Fasham's co-authors include Emma L. Baple, Andrew H. Crosby, Sian Ellard, Caroline F. Wright, Adam C. Gunning, Julia S. Johansen, J. Philip Karl, Mohammed Sharif, John Kirwan and Patrick Garnero and has published in prestigious journals such as PLoS Genetics, Journal of Medical Genetics and European Journal of Human Genetics.

In The Last Decade

James Fasham

10 papers receiving 177 citations

Peers

James Fasham

MB

GENET

RHEUM

CB

SURGE

Anne‐Marie Guerrot France

Birutė Burnytė Lithuania

Minal Menezes Australia

Kristien Hoornaert Belgium

Janine Dokas Germany

Rikkert L. Snoeckx Belgium

Maria Walther Germany

Delphine Héron France

Teruyoshi Miyahara Japan

Katerina Vlahos Australia

Anne‐Marie Guerrot France

James Fasham

136 ×1.5

MB

84 ×1.0

GENET

18 ×0.4

RHEUM

23 ×1.1

CB

11 ×0.6

SURGE

Citations per year, relative to James Fasham James Fasham (= 1×) peers Anne‐Marie Guerrot

Countries citing papers authored by James Fasham

Since Specialization

Citations

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

Fields of papers citing papers by James Fasham

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of James Fasham

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

All Works

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10 of 10 papers shown

1.

Fasham, James, Adam C. Gunning, Martina Owens, et al.. (2024). TECPR2‐related hereditary sensory and autonomic neuropathy in two siblings from Palestine. American Journal of Medical Genetics Part A. 194(7). e63579–e63579. 2 indexed citations

2.

Ma, Yan, Xun Wang, Xiaodong Jiao, et al.. (2022). CLCC1 c. 75C>A Mutation in Pakistani Derived Retinitis Pigmentosa Families Likely Originated With a Single Founder Mutation 2,000–5,000 Years Ago. Frontiers in Genetics. 13. 804924–804924. 2 indexed citations

3.

Lin, Siying, James Fasham, Nouar Qutob, et al.. (2021). Consolidating biallelic SDHD variants as a cause of mitochondrial complex II deficiency. European Journal of Human Genetics. 29(10). 1570–1576. 6 indexed citations

4.

Fasham, James, David J. Evans, Thomas T. Warner, et al.. (2021). Final Exon Frameshift Biallelic PTPN23 Variants Are Associated with Microcephalic Complex Hereditary Spastic Paraplegia. Brain Sciences. 11(5). 614–614. 3 indexed citations

5.

Gunning, Adam C., James Fasham, Andrew H. Crosby, et al.. (2020). Assessing performance of pathogenicity predictors using clinically relevant variant datasets. Journal of Medical Genetics. 58(8). 547–555. 69 indexed citations

6.

Fasham, James, Jamie Harrison, Katie B. Williams, et al.. (2020). No association between SCN9A and monogenic human epilepsy disorders. PLoS Genetics. 16(11). e1009161–e1009161. 11 indexed citations

7.

Prince, Claire, James Fasham, Wasim Ahmad, et al.. (2019). Novel nonsense variants in SLURP1 and DSG1 cause palmoplantar keratoderma in Pakistani families. BMC Medical Genetics. 20(1). 145–145. 5 indexed citations

8.

Rawlins, Lettie E., Barry A. Chioza, Claire Salter, et al.. (2019). MNS1 variant associated with situs inversus and male infertility. European Journal of Human Genetics. 28(1). 50–55. 23 indexed citations

9.

Rawlins, Lettie E., Hannah Jones, Olivia Wenger, et al.. (2019). An Amish founder variant consolidates disruption of CEP55 as a cause of hydranencephaly and renal dysplasia. European Journal of Human Genetics. 27(4). 657–662. 20 indexed citations

10.

Karl, J. Philip, Raquel Granell, John Kirwan, et al.. (2007). Can biochemical markers serve as surrogates for imaging in knee osteoarthritis?. Arthritis & Rheumatism. 56(12). 4038–4047. 41 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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