Treena Cranston

3.3k citations

45 papers · 1.8k indexed · h-index 22

Nephrology top 1%
Molecular Biology
Oncology top 10%
Genetics top 5%
Surgery top 10%

Co-authors: Rajesh V. Thakker Fadil Hannan M. Andrew Nesbit Michael R. Bowl Nigel Rust Sarah Howles Paul Newey Kimberly Gilmour
Topics: Parathyroid Disorders and Treatments (11 papers)Erythrocyte Function and Pathophysiology (6 papers)Immunodeficiency and Autoimmune Disorders (6 papers)
Cited by: Nephrology Oncology Genetics
Journals: New England Journal of Medicine Nature Genetics Journal of Clinical Oncology
Partner nations: United Kingdom United States Italy

In The Last Decade

Treena Cranston

44 papers receiving 1.7k citations

Peers

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	EMQN best practice guidelines for analysis and reporting of microsatellite instability in solid tumours 2025 ·European Journal of Human Genetics ·Richard Gallon,Liam McCormick,Angelica A. Saetta,Cristina Albuquerque,(unknown),Treena Cranston,(unknown),(unknown),(unknown),(unknown),(unknown),George J. Burghel	0
2	A randomized controlled trial of a self-guided mobile app targeting repetitive negative thought to prevent depression in university students: study protocol of the Nurture-U Reducing Worry prevention trial 2024 ·BMC Psychiatry ·(unknown),Deborah Phillips,Treena Cranston,(unknown),Michelle Newton,Helen Cook,Gordon Taylor	1
3	GNA11 Variants Identified in Patients with Hypercalcemia or Hypocalcemia 2020 ·Journal of Bone and Mineral Research ·Sarah Howles,Caroline M. Gorvin,Treena Cranston,Angela Rogers,(unknown),(unknown),Kate Gibson,Mushtaqur Rahman,Allen W. Root,M. Andrew Nesbit,Fadil Hannan,Rajesh V. Thakker	8
4	Pachydermoperiostosis Masquerading as Acromegaly 2017 ·Journal of the Endocrine Society ·(unknown),(unknown),(unknown),Márta Korbonits,Treena Cranston,Ashley Grossman	9
5	Do patients with incidentally discovered bilateral adrenal nodules represent an early form of ARMC5-mediated bilateral macronodular hyperplasia? 2016 ·Endocrine ·(unknown),(unknown),Treena Cranston,Stylianos Tsagarakis,Ashley Grossman	11
6	SDHC Mutations are Associated with Cardiac Paragangliomas: A Case Report of a Patient With a Dopamine-Secreting Tumor and Review of the Literature 2015 ·AACE Clinical Case Reports ·(unknown),(unknown),Treena Cranston,Colin Forfar,Niki Karavitaki,Ashley Grossman	1
7	Mutations Affecting G-Protein Subunit α₁₁in Hypercalcemia and Hypocalcemia 2013 ·New England Journal of Medicine ·M. Andrew Nesbit,Fadil Hannan,Sarah Howles,Valerie Babinsky,Rosie Head,Treena Cranston,Nigel Rust,Maurine R. Hobbs,Hunter Heath,Rajesh V. Thakker	240
8	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 2012 ·Fadil Hannan,M. Andrew Nesbit,Treena Cranston,Rajesh V. Thakker	3
9	A complex endocrine conundrum 2012 ·Familial Cancer ·Gul Bano,(unknown),(unknown),Patricia D. Wilson,Treena Cranston,Shirley Hodgson	1
10	Cell division cycle protein 73 homolog (CDC73) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors 2010 ·Human Mutation ·Paul Newey,Michael R. Bowl,Treena Cranston,Rajesh V. Thakker	130
11	Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidism 2010 ·Human Molecular Genetics ·Michael R. Bowl,Samantha Mirczuk,I. V. Grigorieva,Siân E. Piret,Treena Cranston,Lorraine Southam,Jeremy Allgrove,S. Bahl,Caroline Brain,John Loughlin,Zulf Mughal,(unknown),N. Shaw,(unknown),Dov Tiosano,M. Andrew Nesbit,Rajesh V. Thakker	26
12	Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours 2006 ·Clinical Endocrinology ·Karin Bradley,Branca Cavaco,Michael R. Bowl,Brian Harding,Treena Cranston,Carl Fratter,G. M. Besser,(unknown),M.W.J. Davie,N.E. Dudley,Valeriano Leite,Gregory P. Sadler,A Seller,Rajesh V. Thakker	83
13	Neonatal severe hyperparathyroidism: genotype/phenotype correlation and the use of pamidronate as rescue therapy 2004 ·European Journal of Pediatrics ·Simon Waller,Tom Kurzawinski,Lewis Spitz,Rajesh V. Thakker,Treena Cranston,Simon H. S. Pearce,Tim Cheetham,William G. van’t Hoff	61
14	Psychological impact of genetic testing for familial hypercholesterolemia within a previously aware population: A randomized controlled trial 2004 ·American Journal of Medical Genetics Part A ·Theresa M. Marteau,Victoria Senior,Steve E. Humphries,Martin Bobrow,Treena Cranston,Martin Crook,Lorna Day,(unknown),Rob Horne,(unknown),(unknown),(unknown),Helen Middleton‐Price,Richard Savine,Jim Sikorski,Melanie Watson,John Weinman,Anthony S. Wierzbicki,Richard Wray	152
15	Refining the Amsterdam Criteria and Bethesda Guidelines: Testing Algorithms for the Prediction of Mismatch Repair Mutation Status in the Familial Cancer Clinic 2004 ·Journal of Clinical Oncology ·Lara Lipton,Victoria Johnson,(unknown),(unknown),Peter Risby,Amir Taher Eftekhar Sadat,Treena Cranston,Louise Izatt,Peter Sasieni,S V Hodgson,Huw Thomas,Ian Tomlinson	84
16	Rapid protein‐based assays for the diagnosis of T^–B⁺ severe combined immunodeficiency 2001 ·British Journal of Haematology ·Kimberly Gilmour,Treena Cranston,Sam Loughlin,(unknown),Tracy Lester,Teresa Español,M. Hernández,Gianfranco Savoldi,E. Graham Davies,Mario Abinun,Christine Kinnon,Alison Jones,Hubert B. Gaspar	11
17	Mutations in severe combined immune deficiency (SCID) due to JAK3 deficiency 2001 ·Human Mutation ·Luigi D. Notarangelo,Patrizia Mella,Alison Jones,Geneviève de Saint Basile,Gianfranco Savoldi,Treena Cranston,Mauno Vihinen,Richard Fabian Schumacher	82
18	Eleven novel JAK3 mutations in patients with severe combined immunodeficiency?including the first patients with mutations in the kinase domain 2001 ·Human Mutation ·Patrizia Mella,Richard Fabian Schumacher,Treena Cranston,Geneviève de Saint Basile,Gianfranco Savoldi,Luigi D. Notarangelo	26
19	X-Linked lymphoproliferative disease: three atypical cases 2001 ·Clinical & Experimental Immunology ·Kiran Nistala,Kimberly Gilmour,Treena Cranston,E. Graham Davies,David Goldblatt,H. Bobby Gaspar,Alison Jones	47
20	Diagnosis of X-linked lymphoproliferative disease by analysis of SLAM-associated protein expression 2000 ·European Journal of Immunology ·Kimberly Gilmour,Treena Cranston,Alison Jones,E. Graham Davies,David Goldblatt,Adrian J. Thrasher,Christine Kinnon,Kim E. Nichols,Hubert B. Gaspar	51

About Treena Cranston

Treena Cranston is a scholar working on Nephrology, Oncology and Endocrinology, Diabetes and Metabolism, having authored 45 papers that have together received 1.8k indexed citations. Recurring topics across this work include Parathyroid Disorders and Treatments (11 papers), Erythrocyte Function and Pathophysiology (6 papers) and Immunodeficiency and Autoimmune Disorders (6 papers). The work is most often cited by research in Nephrology (656 citations), Oncology (442 citations) and Genetics (419 citations). Treena Cranston has collaborated with scholars based in United Kingdom, United States and Italy. Frequent 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. Their work appears in journals such as New England Journal of Medicine, Nature Genetics and Journal of Clinical Oncology.

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