Ann‐Marie Patch

38.4k total citations
40 papers, 2.7k citations indexed

About

Ann‐Marie Patch is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Ann‐Marie Patch has authored 40 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 14 papers in Surgery and 13 papers in Genetics. Recurrent topics in Ann‐Marie Patch's work include Pancreatic function and diabetes (14 papers), Diabetes and associated disorders (8 papers) and Hyperglycemia and glycemic control in critically ill and hospitalized patients (7 papers). Ann‐Marie Patch is often cited by papers focused on Pancreatic function and diabetes (14 papers), Diabetes and associated disorders (8 papers) and Hyperglycemia and glycemic control in critically ill and hospitalized patients (7 papers). Ann‐Marie Patch collaborates with scholars based in Australia, United Kingdom and United States. Ann‐Marie Patch's co-authors include Sian Ellard, Sarah E. Flanagan, Andrew T. Hattersley, Emma L. Edghill, Khalid Hussain, Julie Støy, Louis H. Philipson, Donald F. Steiner, Graeme I. Bell and Julian Hamilton‐Shield and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Genetics.

In The Last Decade

Ann‐Marie Patch

39 papers receiving 2.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ann‐Marie Patch Australia 21 1.5k 1.2k 1.0k 856 295 40 2.7k
Christophe A. Girard United Kingdom 28 1.2k 0.8× 704 0.6× 1.4k 1.4× 843 1.0× 128 0.4× 36 2.9k
Jarkko Ustinov Finland 26 1.5k 1.0× 767 0.6× 896 0.9× 599 0.7× 125 0.4× 65 2.5k
Tilo Moede Sweden 20 1.2k 0.8× 610 0.5× 990 1.0× 585 0.7× 78 0.3× 33 2.0k
Patrick Jacquemin Belgium 31 2.0k 1.3× 868 0.7× 2.1k 2.0× 318 0.4× 413 1.4× 64 3.9k
Myra A. Lipes United States 19 808 0.5× 658 0.5× 1.1k 1.0× 682 0.8× 202 0.7× 24 2.3k
Joan‐Marc Servitja Spain 22 644 0.4× 389 0.3× 1.0k 1.0× 205 0.2× 269 0.9× 42 1.9k
Maria Nesterova United States 30 703 0.5× 214 0.2× 1.5k 1.4× 632 0.7× 669 2.3× 71 2.8k
Anne‐Marie Madec France 23 620 0.4× 551 0.4× 516 0.5× 694 0.8× 73 0.2× 49 1.7k
Ziliang Ao Canada 24 2.0k 1.3× 992 0.8× 683 0.7× 1.1k 1.3× 147 0.5× 49 2.5k
Maki Moritani Japan 22 435 0.3× 440 0.4× 804 0.8× 310 0.4× 246 0.8× 58 1.5k

Countries citing papers authored by Ann‐Marie Patch

Since Specialization
Citations

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

Fields of papers citing papers by Ann‐Marie Patch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ann‐Marie Patch. 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 Ann‐Marie Patch. The network helps show where Ann‐Marie Patch may publish in the future.

Co-authorship network of co-authors of Ann‐Marie Patch

This figure shows the co-authorship network connecting the top 25 collaborators of Ann‐Marie Patch. A scholar is included among the top collaborators of Ann‐Marie Patch 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 Ann‐Marie Patch. Ann‐Marie Patch 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.
Lakis, Vanessa, Ruth J. Lyons, Tam Nguyen, et al.. (2025). Spatial Transcriptomics Reveals Novel Mechanisms Involved in Perineural Invasion in Pancreatic Ductal Adenocarcinomas. Cancers. 17(5). 852–852. 4 indexed citations
2.
Straube, Jasmin, Therese Vu, Björn von Eyß, et al.. (2023). Cre recombinase expression cooperates with homozygous FLT3 internal tandem duplication knockin mouse model to induce acute myeloid leukemia. Leukemia. 37(4). 741–750. 1 indexed citations
3.
Dumenil, Troy, Thuy T. Le, Andrii Slonchak, et al.. (2021). Injection site vaccinology of a recombinant vaccinia-based vector reveals diverse innate immune signatures. PLoS Pathogens. 17(1). e1009215–e1009215. 14 indexed citations
4.
Patch, Ann‐Marie, Cameron Snell, Deborah S. Smith, et al.. (2020). FGFR2c Mesenchymal Isoform Expression Is Associated with Poor Prognosis and Further Refines Risk Stratification within Endometrial Cancer Molecular Subtypes. Clinical Cancer Research. 26(17). 4569–4580. 14 indexed citations
5.
Fennell, Lochlan, Jennifer Borowsky, Diane McKeone, et al.. (2020). Alterations in signaling pathways that accompany spontaneous transition to malignancy in a mouse model of BRAF mutant microsatellite stable colorectal cancer. Neoplasia. 22(2). 120–128. 11 indexed citations
6.
Dick, Ian M., Gary Lee, Arthur W. Musk, et al.. (2018). Malignant cells from pleural fluids in malignant mesothelioma patients reveal novel mutations. Lung Cancer. 119. 64–70. 20 indexed citations
7.
Wakeling, Matthew N., Thomas W. Laver, Caroline F. Wright, et al.. (2018). Homozygosity mapping provides supporting evidence of pathogenicity in recessive Mendelian disease. Genetics in Medicine. 21(4). 982–986. 23 indexed citations
8.
Young, Arabella, Shin Foong Ngiow, Ann‐Marie Patch, et al.. (2017). A2AR Adenosine Signaling Suppresses Natural Killer Cell Maturation in the Tumor Microenvironment. Cancer Research. 78(4). 1003–1016. 296 indexed citations
9.
Patch, Ann‐Marie, Ian M. Dick, Stephen H. Kazakoff, et al.. (2017). Whole exome sequencing of an asbestos-induced wild-type murine model of malignant mesothelioma. BMC Cancer. 17(1). 396–396. 24 indexed citations
10.
Flanagan, Sarah E., Elisa De Franco, Hana Lango Allen, et al.. (2014). Analysis of Transcription Factors Key for Mouse Pancreatic Development Establishes NKX2-2 and MNX1 Mutations as Causes of Neonatal Diabetes in Man. Cell Metabolism. 19(1). 146–154. 99 indexed citations
11.
Weedon, Michael N., Inês Cebola, Ann‐Marie Patch, et al.. (2013). Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis. Nature Genetics. 46(1). 61–64. 191 indexed citations
12.
Dimitri, Paul, Jayne A.L. Minton, Ann‐Marie Patch, et al.. (2010). Novel GLIS3 mutations demonstrate an extended multisystem phenotype. European Journal of Endocrinology. 164(3). 437–443. 71 indexed citations
13.
Flanagan, Sarah E., Ann‐Marie Patch, & Sian Ellard. (2010). Using SIFT and PolyPhen to Predict Loss-of-Function and Gain-of-Function Mutations. Genetic Testing and Molecular Biomarkers. 14(4). 533–537. 295 indexed citations
14.
Hanley, Karen Piper, Tom Hearn, Andrew Berry, et al.. (2010). In vitro expression of NGN3 identifies RAB3B as the predominant Ras-associated GTP-binding protein 3 family member in human islets. Journal of Endocrinology. 207(2). 151–161. 19 indexed citations
15.
Patch, Ann‐Marie, et al.. (2009). Neonatal diabetes mellitus due to pancreas agenesis: a new case report and review of the literature. Pediatric Diabetes. 10(7). 487–491. 7 indexed citations
16.
Locke, Jonathan M., Sarah E. Flanagan, Ann‐Marie Patch, et al.. (2008). Recessive mutations in the INS gene; a novel common cause of permanent neonatal diabetes in consanguineous pedigrees. Queensland's institutional digital repository (The University of Queensland). 2 indexed citations
17.
Klupa, Tomasz, Irina Kowalska, Krystyna Wyka, et al.. (2008). Mutations in the ABCC8 (SUR1 subunit of the KATP channel) gene are associated with a variable clinical phenotype. Clinical Endocrinology. 71(3). 358–362. 30 indexed citations
18.
Ellard, Sian, Sarah E. Flanagan, Christophe A. Girard, et al.. (2007). Permanent Neonatal Diabetes Caused by Dominant, Recessive, or Compound Heterozygous SUR1 Mutations with Opposite Functional Effects. The American Journal of Human Genetics. 81(2). 375–382. 158 indexed citations
19.
Patch, Ann‐Marie & Stephen J. Aves. (2007). Fingerprinting fission yeast: polymorphic markers for molecular genetic analysis of Schizosaccharomyces pombe strains. Microbiology. 153(3). 887–897. 5 indexed citations
20.
Støy, Julie, Emma L. Edghill, Sarah E. Flanagan, et al.. (2007). Insulin gene mutations as a cause of permanent neonatal diabetes. Proceedings of the National Academy of Sciences. 104(38). 15040–15044. 426 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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