Treena Cranston

3.3k total citations
45 papers, 1.8k citations indexed

About

Treena Cranston is a scholar working on Oncology, Molecular Biology and Nephrology. According to data from OpenAlex, Treena Cranston has authored 45 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Oncology, 12 papers in Molecular Biology and 11 papers in Nephrology. Recurrent topics in Treena Cranston's work include Parathyroid Disorders and Treatments (11 papers), Erythrocyte Function and Pathophysiology (6 papers) and Immunodeficiency and Autoimmune Disorders (6 papers). Treena Cranston is often cited by papers focused on Parathyroid Disorders and Treatments (11 papers), Erythrocyte Function and Pathophysiology (6 papers) and Immunodeficiency and Autoimmune Disorders (6 papers). Treena Cranston collaborates with scholars based in United Kingdom, United States and Italy. Treena Cranston's co-authors include Rajesh V. Thakker, Fadil Hannan, M. Andrew Nesbit, Michael R. Bowl, Nigel Rust, Sarah Howles, Paul Newey, Kimberly Gilmour, Alison Jones and Rosie Head and has published in prestigious journals such as New England Journal of Medicine, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Treena Cranston

44 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Treena Cranston United Kingdom 22 656 477 442 419 361 45 1.8k
Sonia L. Sugg United States 29 250 0.4× 833 1.7× 863 2.0× 389 0.9× 607 1.7× 88 2.7k
Geeta Lal United States 20 313 0.5× 316 0.7× 513 1.2× 256 0.6× 525 1.5× 61 1.5k
Trisha Dwight Australia 23 131 0.2× 514 1.1× 356 0.8× 217 0.5× 508 1.4× 42 1.6k
Diana Learoyd Australia 30 162 0.2× 682 1.4× 620 1.4× 497 1.2× 812 2.2× 77 2.7k
Jan Steffen Jürgensen Germany 15 115 0.2× 873 1.8× 258 0.6× 272 0.6× 179 0.5× 35 1.9k
William G. Dilley United States 21 208 0.3× 461 1.0× 636 1.4× 521 1.2× 544 1.5× 40 2.1k
Barbara K. Kinder United States 17 247 0.4× 260 0.5× 364 0.8× 120 0.3× 229 0.6× 34 970
Joan Wither Canada 28 171 0.3× 475 1.0× 291 0.7× 333 0.8× 72 0.2× 108 2.7k
J.C. Kingswood United Kingdom 21 105 0.2× 712 1.5× 714 1.6× 270 0.6× 186 0.5× 53 2.6k
Gunhild Keller Germany 21 162 0.2× 555 1.2× 357 0.8× 99 0.2× 50 0.1× 45 1.6k

Countries citing papers authored by Treena Cranston

Since Specialization
Citations

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

Fields of papers citing papers by Treena Cranston

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Treena Cranston

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

All Works

20 of 20 papers shown
1.
Gallon, Richard, Liam McCormick, Angelica A. Saetta, et al.. (2025). EMQN best practice guidelines for analysis and reporting of microsatellite instability in solid tumours. European Journal of Human Genetics. 34(1). 134–146.
2.
3.
Howles, Sarah, Caroline M. Gorvin, Treena Cranston, et al.. (2020). GNA11 Variants Identified in Patients with Hypercalcemia or Hypocalcemia. Journal of Bone and Mineral Research. 38(6). 907–917. 8 indexed citations
4.
Korbonits, Márta, et al.. (2017). Pachydermoperiostosis Masquerading as Acromegaly. Journal of the Endocrine Society. 1(2). 109–112. 9 indexed citations
5.
6.
Cranston, Treena, et al.. (2015). SDHC Mutations are Associated with Cardiac Paragangliomas: A Case Report of a Patient With a Dopamine-Secreting Tumor and Review of the Literature. AACE Clinical Case Reports. 1(4). e273–e277. 1 indexed citations
7.
Nesbit, M. Andrew, Fadil Hannan, Sarah Howles, et al.. (2013). Mutations Affecting G-Protein Subunit α11in Hypercalcemia and Hypocalcemia. New England Journal of Medicine. 368(26). 2476–2486. 240 indexed citations
8.
Hannan, Fadil, M. Andrew Nesbit, Treena Cranston, & Rajesh V. Thakker. (2012). A calcium-sensing receptor (CaSR) variant, Glu250Lys, present in familial hypocalciuric hypercalcaemia (FHH) and autosomal dominant hypocalcaemic hypercalciuria (ADHH) probands represents a functionally neutral polymorphism: lessons for CaSR mutational analysis. 28. 3 indexed citations
9.
Bano, Gul, et al.. (2012). A complex endocrine conundrum. Familial Cancer. 12(3). 577–580. 1 indexed citations
10.
Newey, Paul, Michael R. Bowl, Treena Cranston, & Rajesh V. Thakker. (2010). Cell division cycle protein 73 homolog (CDC73) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors. Human Mutation. 31(3). 295–307. 130 indexed citations
11.
Bowl, Michael R., Samantha Mirczuk, I. V. Grigorieva, et al.. (2010). Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidism. Human Molecular Genetics. 19(10). 2028–2038. 26 indexed citations
12.
Bradley, Karin, Branca Cavaco, Michael R. Bowl, et al.. (2006). Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours. Clinical Endocrinology. 64(3). 299–306. 83 indexed citations
13.
Waller, Simon, Tom Kurzawinski, Lewis Spitz, et al.. (2004). Neonatal severe hyperparathyroidism: genotype/phenotype correlation and the use of pamidronate as rescue therapy. European Journal of Pediatrics. 163(10). 589–594. 61 indexed citations
14.
Marteau, Theresa M., Victoria Senior, Steve E. Humphries, et al.. (2004). Psychological impact of genetic testing for familial hypercholesterolemia within a previously aware population: A randomized controlled trial. American Journal of Medical Genetics Part A. 128A(3). 285–293. 152 indexed citations
15.
Lipton, Lara, Victoria Johnson, Peter Risby, et al.. (2004). Refining the Amsterdam Criteria and Bethesda Guidelines: Testing Algorithms for the Prediction of Mismatch Repair Mutation Status in the Familial Cancer Clinic. Journal of Clinical Oncology. 22(24). 4934–4943. 84 indexed citations
16.
Gilmour, Kimberly, Treena Cranston, Sam Loughlin, et al.. (2001). Rapid protein‐based assays for the diagnosis of T–B+ severe combined immunodeficiency. British Journal of Haematology. 112(3). 671–676. 11 indexed citations
17.
Notarangelo, Luigi D., Patrizia Mella, Alison Jones, et al.. (2001). Mutations in severe combined immune deficiency (SCID) due to JAK3 deficiency. Human Mutation. 18(4). 255–263. 82 indexed citations
18.
Mella, Patrizia, Richard Fabian Schumacher, Treena Cranston, et al.. (2001). Eleven novel JAK3 mutations in patients with severe combined immunodeficiency?including the first patients with mutations in the kinase domain. Human Mutation. 18(4). 355–356. 26 indexed citations
19.
Nistala, Kiran, Kimberly Gilmour, Treena Cranston, et al.. (2001). X-Linked lymphoproliferative disease: three atypical cases. Clinical & Experimental Immunology. 126(1). 126–130. 47 indexed citations
20.
Gilmour, Kimberly, Treena Cranston, Alison Jones, et al.. (2000). Diagnosis of X-linked lymphoproliferative disease by analysis of SLAM-associated protein expression. European Journal of Immunology. 30(6). 1691–1697. 51 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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