Sumaya Alkanderi

483 total citations
10 papers, 322 citations indexed

About

Sumaya Alkanderi is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Sumaya Alkanderi has authored 10 papers receiving a total of 322 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Sumaya Alkanderi's work include Genetic and Kidney Cyst Diseases (5 papers), Fetal and Pediatric Neurological Disorders (3 papers) and Adrenal Hormones and Disorders (3 papers). Sumaya Alkanderi is often cited by papers focused on Genetic and Kidney Cyst Diseases (5 papers), Fetal and Pediatric Neurological Disorders (3 papers) and Adrenal Hormones and Disorders (3 papers). Sumaya Alkanderi collaborates with scholars based in United Kingdom, France and United States. Sumaya Alkanderi's co-authors include John A. Sayer, Colin G. Miles, Shalabh Srivastava, Elisa Molinari, Simon A. Ramsbottom, Kathryn White, Sophie Saunier, C. Henry, Laura Yates and Sally Johnson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Scientific Reports and Journal of the American Society of Nephrology.

In The Last Decade

Sumaya Alkanderi

9 papers receiving 321 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sumaya Alkanderi United Kingdom 9 242 183 69 64 37 10 322
Amali Mallawaarachchi Australia 13 300 1.2× 217 1.2× 124 1.8× 50 0.8× 32 0.9× 28 457
Shakila Abdul-Majeed United States 9 196 0.8× 215 1.2× 15 0.2× 33 0.5× 32 0.9× 10 347
Ryan J. Russo United States 10 386 1.6× 374 2.0× 42 0.6× 45 0.7× 104 2.8× 10 506
Régine Perrichot France 8 359 1.5× 412 2.3× 115 1.7× 72 1.1× 82 2.2× 14 508
Sharon Mulroy United Kingdom 5 244 1.0× 275 1.5× 30 0.4× 26 0.4× 79 2.1× 6 353
Caroline Bénech France 8 132 0.5× 196 1.1× 13 0.2× 41 0.6× 16 0.4× 14 278
Gundula Povysil United States 9 131 0.5× 141 0.8× 29 0.4× 8 0.1× 16 0.4× 18 314
Cherie Stayner New Zealand 12 225 0.9× 169 0.9× 8 0.1× 47 0.7× 34 0.9× 19 314
M. JOYCE CRUMLEY Canada 6 245 1.0× 45 0.2× 48 0.7× 12 0.2× 20 0.5× 8 307
Julie Kaylor United States 9 103 0.4× 104 0.6× 21 0.3× 35 0.5× 11 0.3× 11 206

Countries citing papers authored by Sumaya Alkanderi

Since Specialization
Citations

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

Fields of papers citing papers by Sumaya Alkanderi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sumaya Alkanderi

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

All Works

10 of 10 papers shown
1.
Elston, Marianne S., et al.. (2020). Variable Phenotypes Seen with a Homozygous CYP24A1 Mutation: Case Report. SN Comprehensive Clinical Medicine. 2(7). 995–1002.
2.
Griffin, Tomás P., Caroline Joyce, Sumaya Alkanderi, et al.. (2020). Biallelic CYP24A1 variants presenting during pregnancy: clinical and biochemical phenotypes. Endocrine Connections. 9(6). 530–541. 10 indexed citations
3.
Hyšpler, Radomı́r, et al.. (2019). Novel <b><i>CYP24A1</i></b> Mutation in a Young Male Patient with Nephrolithiasis: Case Report. Kidney & Blood Pressure Research. 44(4). 870–877. 11 indexed citations
4.
Molinari, Elisa, Simon A. Ramsbottom, Shalabh Srivastava, et al.. (2019). Targeted exon skipping rescues ciliary protein composition defects in Joubert syndrome patient fibroblasts. Scientific Reports. 9(1). 10828–10828. 19 indexed citations
5.
Molinari, Elisa, Eva L. Decker, Holly Mabillard, et al.. (2018). Human urine-derived renal epithelial cells provide insights into kidney-specific alternate splicing variants. European Journal of Human Genetics. 26(12). 1791–1796. 18 indexed citations
6.
Alkanderi, Sumaya, Elisa Molinari, Ranad Shaheen, et al.. (2018). ARL3 Mutations Cause Joubert Syndrome by Disrupting Ciliary Protein Composition. The American Journal of Human Genetics. 103(4). 612–620. 59 indexed citations
7.
Molinari, Elisa, Shalabh Srivastava, C. Henry, et al.. (2018). Targeted exon skipping of a CEP290 mutation rescues Joubert syndrome phenotypes in vitro and in a murine model. Proceedings of the National Academy of Sciences. 115(49). 12489–12494. 51 indexed citations
8.
Enerbäck, Sven, Daniel Nilsson, Noel Edwards, et al.. (2017). Acidosis and Deafness in Patients with Recessive Mutations in FOXI1. Journal of the American Society of Nephrology. 29(3). 1041–1048. 72 indexed citations
9.
Alkanderi, Sumaya, Laura Yates, Sally Johnson, & John A. Sayer. (2017). Lessons learned from a multidisciplinary renal genetics clinic. QJM. 110(7). 453–457. 30 indexed citations
10.
Srivastava, Shalabh, Simon A. Ramsbottom, Elisa Molinari, et al.. (2017). A human patient-derived cellular model of Joubert syndrome reveals ciliary defects which can be rescued with targeted therapies. Human Molecular Genetics. 26(23). 4657–4667. 52 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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