Andrew T. Hattersley

126.5k total citations · 9 hit papers
634 papers, 38.9k citations indexed

About

Andrew T. Hattersley is a scholar working on Surgery, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Andrew T. Hattersley has authored 634 papers receiving a total of 38.9k indexed citations (citations by other indexed papers that have themselves been cited), including 389 papers in Surgery, 335 papers in Genetics and 288 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Andrew T. Hattersley's work include Pancreatic function and diabetes (377 papers), Diabetes and associated disorders (227 papers) and Diabetes Management and Research (161 papers). Andrew T. Hattersley is often cited by papers focused on Pancreatic function and diabetes (377 papers), Diabetes and associated disorders (227 papers) and Diabetes Management and Research (161 papers). Andrew T. Hattersley collaborates with scholars based in United Kingdom, United States and Australia. Andrew T. Hattersley's co-authors include Sian Ellard, Beverley M. Shields, Mark I. McCarthy, Timothy M. Frayling, Ewan R. Pearson, Maggie Shepherd, Sarah E. Flanagan, Angus G. Jones, Michael N. Weedon and Anna L. Gloyn and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Andrew T. Hattersley

621 papers receiving 37.9k citations

Hit Papers

5 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Switching from Insulin to Oral Sulfonylureas in Patients with Diabetes Due to Kir6.2 Mutations

2006 685 citations Ewan R. Pearson, Pål R. Njølstad et al. profile →
The fetal insulin hypothesis: an alternative explanation of the association of low bir thweight with diabetes and vascular disease

1999 657 citations Andrew T. Hattersley et al. profile →
Large-Scale Association Studies of Variants in Genes Encoding the Pancreatic β-Cell KATP Channel Subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) Confirm That the KCNJ11 E23K Variant Is Associated With Type 2 Diabetes

2003 538 citations Anna L. Gloyn, Michael N. Weedon et al. Diabetes profile →
Maturity-onset diabetes of the young (MODY): how many cases are we missing?

2010 493 citations Beverley M. Shields, Maggie Shepherd et al. Diabetologia profile →
Excess mortality and cardiovascular disease in young adults with type 1 diabetes in relation to age at onset: a nationwide, register-based cohort study

2018 473 citations Naveed Sattar, Andrew T. Hattersley et al. profile →
The clinical utility of C‐peptide measurement in the care of patients with diabetes

2013 439 citations Angus G. Jones, Andrew T. Hattersley Diabetic Medicine profile →
Disease progression and treatment response in data-driven subgroups of type 2 diabetes compared with models based on simple clinical features: an analysis using clinical trial data

2019 282 citations John Dennis, Beverley M. Shields et al. profile →
Frequency and phenotype of type 1 diabetes in the first six decades of life: a cross-sectional, genetically stratified survival analysis from UK Biobank

2017 280 citations Nicholas J. Thomas, Michael N. Weedon et al. profile →
Precision Medicine in Diabetes: A Consensus Report From the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD)

2020 224 citations Andrew T. Hattersley, Mark I. McCarthy et al. Diabetes Care profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Andrew T. Hattersley United Kingdom	107	22.6k	20.8k	16.8k	13.3k	3.6k	634	38.9k
Leif Groop Sweden	90	10.1k 0.4×	10.4k 0.5×	14.8k 0.9×	12.4k 0.9×	2.0k 0.6×	555	36.8k
David B. Dunger United Kingdom	95	7.4k 0.3×	9.0k 0.4×	14.2k 0.8×	5.2k 0.4×	8.4k 2.3×	597	32.2k
Philippe Froguel France	93	10.0k 0.4×	11.8k 0.6×	7.2k 0.4×	13.2k 1.0×	1.6k 0.4×	529	37.3k
Åke Lernmark United States	80	14.7k 0.7×	17.2k 0.8×	13.4k 0.8×	4.1k 0.3×	605 0.2×	710	26.1k
Huibert A. P. Pols Netherlands	90	7.0k 0.3×	4.3k 0.2×	6.5k 0.4×	6.9k 0.5×	1.3k 0.4×	238	31.6k
Henning Beck‐Nielsen Denmark	83	4.6k 0.2×	2.7k 0.1×	8.3k 0.5×	8.3k 0.6×	2.1k 0.6×	447	23.2k
Allan Vaag Denmark	73	3.9k 0.2×	2.9k 0.1×	6.5k 0.4×	7.7k 0.6×	4.1k 1.1×	419	20.7k
Peter H. Bennett United States	88	5.4k 0.2×	4.4k 0.2×	15.0k 0.9×	5.7k 0.4×	4.7k 1.3×	290	35.7k
Paul M. Stewart United Kingdom	89	5.2k 0.2×	2.4k 0.1×	19.1k 1.1×	4.5k 0.3×	2.1k 0.6×	374	27.6k
Per‐Henrik Groop Finland	74	4.3k 0.2×	4.1k 0.2×	9.8k 0.6×	5.8k 0.4×	956 0.3×	522	23.0k

Countries citing papers authored by Andrew T. Hattersley

Since Specialization

Citations

This map shows the geographic impact of Andrew T. Hattersley'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 Andrew T. Hattersley with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrew T. Hattersley more than expected).

Fields of papers citing papers by Andrew T. Hattersley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew T. Hattersley. 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 Andrew T. Hattersley. The network helps show where Andrew T. Hattersley may publish in the future.

Co-authorship network of co-authors of Andrew T. Hattersley

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

All Works

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20 of 20 papers shown

Wakeling, Matthew N., Andrew T. Hattersley, Michael N. Weedon, et al.. (2025). Rare Variants in NEUROD1 and PDX1 Are Low-Penetrance Causes of MODY, Whereas Those in APPL1 and WFS1 Are Not Associated With MODY. Diabetes. 74(11). 2123–2131.

Green, Harry, Ji Chen, Jonathan P Evans, et al.. (2024). Hyperglycaemia is a causal risk factor for upper limb pathologies. International Journal of Epidemiology. 53(1). 2 indexed citations

Wyatt, Rebecca C., Sven Olek, Elisa De Franco, et al.. (2023). FOXP3 TSDR Measurement Could Assist Variant Classification and Diagnosis of IPEX Syndrome. Journal of Clinical Immunology. 43(3). 662–669. 8 indexed citations

Perera, Luke A., Andrew T. Hattersley, Heather P. Harding, et al.. (2023). Infancy‐onset diabetes caused by de‐regulated AMPylation of the human endoplasmic reticulum chaperone BiP. EMBO Molecular Medicine. 15(3). e16491–e16491. 15 indexed citations

Young, Katherine, Andrew McGovern, Inês Barroso, et al.. (2022). The impact of population-level HbA1c screening on reducing diabetes diagnostic delay in middle-aged adults: a UK Biobank analysis. Diabetologia. 66(2). 300–309. 4 indexed citations

Thompson, William, Robin N. Beaumont, Alan Kuang, et al.. (2021). Fetal alleles predisposing to metabolically favorable adiposity are associated with higher birth weight. Human Molecular Genetics. 31(11). 1762–1775. 3 indexed citations

Hughes, Alice E., Elisa De Franco, Evgenia Globa, et al.. (2021). Identification of GCK‐ maturity‐onset diabetes of the young in cases of neonatal hyperglycemia: A case series and review of clinical features. Pediatric Diabetes. 22(6). 876–881. 9 indexed citations

Thompson, William, Jessica Tyrrell, Maria Carolina Borges, et al.. (2019). Association of maternal circulating 25(OH)D and calcium with birth weight: A mendelian randomisation analysis. PLoS Medicine. 16(6). e1002828–e1002828. 32 indexed citations

Dennis, John, Beverley M. Shields, Anita Hill, et al.. (2018). Precision Medicine in Type 2 Diabetes: Clinical Markers of Insulin Resistance Are Associated With Altered Short- and Long-term Glycemic Response to DPP-4 Inhibitor Therapy. Diabetes Care. 41(4). 705–712. 59 indexed citations

10.

Day, Jacob, Sarah E. Flanagan, Maggie Shepherd, et al.. (2017). Hyperglycaemia‐related complications at the time of diagnosis can cause permanent neurological disability in children with neonatal diabetes. Diabetic Medicine. 34(7). 1000–1004. 7 indexed citations

11.

Edghill, Emma L., Karen Stals, Richard A. Oram, et al.. (2012). HNF1B deletions in patients with young‐onset diabetes but no known renal disease. Diabetic Medicine. 30(1). 114–117. 32 indexed citations

12.

Ellard, Sian, et al.. (2010). 肝細胞核因子1β(HNF1B)遺伝子の変異は子宮と腎の合併奇形では一般的であるが,孤立性子宮奇形では認められない. American Journal of Obstetrics and Gynecology. 203(4). 1–364. 9 indexed citations

13.

Oram, Richard A., Emma L. Edghill, Sarah E. Flanagan, et al.. (2010). Mutations in the hepatocyte nuclear factor-1β (HNF1B) gene are common with combined uterine and renal malformations but are not found with isolated uterine malformations. American Journal of Obstetrics and Gynecology. 203(4). 364.e1–364.e5. 47 indexed citations

14.

Bell, Christopher G., Sarah Finer, Cecilia M. Lindgren, et al.. (2010). Integrated Genetic and Epigenetic Analysis Identifies Haplotype-Specific Methylation in the FTO Type 2 Diabetes and Obesity Susceptibility Locus. PLoS ONE. 5(11). e14040–e14040. 185 indexed citations

15.

Panicker, Vijay, Ponnusamy Saravanan, Bijay Vaidya, et al.. (2009). Common Variation in the DIO2 Gene Predicts Baseline Psychological Well-Being and Response to Combination Thyroxine Plus Triiodothyronine Therapy in Hypothyroid Patients. The Journal of Clinical Endocrinology & Metabolism. 94(5). 1623–1629. 238 indexed citations

16.

Shields, Beverley M., Rachel M. Freathy, Bridget Knight, et al.. (2009). Phosphodiesterase 8B Gene Polymorphism Is Associated with Subclinical Hypothyroidism in Pregnancy. The Journal of Clinical Endocrinology & Metabolism. 94(11). 4608–4612. 23 indexed citations

17.

Hattersley, Andrew T., Jan Bruining, Julian Hamilton‐Shield, Pål R. Njølstad, & Kim C. Donaghue. (2006). ISPAD Clinical Practice Consensus Guidelines 2006?2007 The diagnosis and management of monogenic diabetes in children. Pediatric Diabetes. 7(6). 352–360. 91 indexed citations

18.

Singh, Rinki, Ewan R. Pearson, Peter Avery, et al.. (2006). Reduced beta cell function in offspring of mothers with young-onset type 2 diabetes. Diabetologia. 49(8). 1876–1880. 26 indexed citations

19.

Proks, Peter, Jennifer F. Antcliff, Anna L. Gloyn, Andrew T. Hattersley, & F M Ashcroft. (2005). Molecular basis of Kir6.2 mutations causing neonatal diabetes and neonatal diabetes with neurological features. Biophysical Journal. 88.

20.

Dobson, Lee, Christopher Sheldon, & Andrew T. Hattersley. (2004). Conventional measures underestimate glycaemia in cystic fibrosis patients. Diabetic Medicine. 21(7). 691–696. 95 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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