Ann‐Marie Patch

39.1k citations

40 papers · 2.8k · h-index 21

Impact in

Endocrinology, Diabetes and Metabolism top 2%
- Diabetes Management and Research
- Hyperglycemia and glycemic control in critically ill and hospitalized patients
Surgery top 1%
- Pancreatic function and diabetes

Papers in

Surgery 14
- Pancreatic function and diabetes 14
Molecular Biology 14

Co-authors: Sian Ellard (17 shared papers)Sarah E. Flanagan (15 shared papers)Andrew T. Hattersley (14 shared papers)Emma L. Edghill (7 shared papers)Khalid Hussain (5 shared papers)Donald F. Steiner (2 shared papers)Julie Støy (2 shared papers)Louis H. Philipson (2 shared papers)
Journals: Cancers (3 papers)Blood (2 papers)Proceedings of the National Academy of Sciences (2 papers)Diabetes (2 papers)The Journal of Clinical Endocrinology & Metabolism (2 papers)
Partner nations: Australia United Kingdom United States

In The Last Decade

Ann‐Marie Patch

39 papers receiving 2.7k citations

Peers

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-authors

The 25 scholars most cited alongside Ann‐Marie Patch, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Ann‐Marie Patch Line = papers co-authored together Ann‐Marie Patch links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 40 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Insulin gene mutations as a cause of permanent neonatal diabetes Proceedings of the National Academy of Sciences ·Julie Støy, Emma L. Edghill, Sarah E. Flanagan, Honggang Ye, Veronica Paz, Anna Pluzhnikov, Jennifer E. Below, M. Geoffrey Hayes, Nancy J. Cox, Gregory M. Lipkind, Rebecca B. Lipton, Siri Atma W. Greeley, Ann‐Marie Patch, Sian Ellard, Donald F. Steiner, Andrew T. Hattersley, Louis H. Philipson, Graeme I. Bell, (unknown)	2007	425
2	A2AR Adenosine Signaling Suppresses Natural Killer Cell Maturation in the Tumor Microenvironment Cancer Research ·Arabella Young, Shin Foong Ngiow, Yulong Gao, Ann‐Marie Patch, Deborah S. Barkauskas, Meriem Messaoudene, Gene Lin, Jérôme D. Coudert, Kimberley Stannard, Laurence Zitvogel, Mariapia A. Degli‐Esposti, Éric Vivier, Nicola Waddell, Joel Linden, Nicholas D. Huntington, Fernando Souza-Fonseca-Guimarães, Mark J. Smyth	2017	308
3	Using SIFT and PolyPhen to Predict Loss-of-Function and Gain-of-Function Mutations Genetic Testing and Molecular Biomarkers ·Sarah E. Flanagan, Ann‐Marie Patch, Sian Ellard	2010	299
4	Insulin Mutation Screening in 1,044 Patients With Diabetes Diabetes ·Emma L. Edghill, Sarah E. Flanagan, Ann‐Marie Patch, Chris Boustred, Andrew Parrish, Beverley Shields, Maggie Shepherd, Khalid Hussain, Ritika R. Kapoor, Maciej T. Małecki, Michael J. MacDonald, Julie Støy, Donald F. Steiner, Louis H. Philipson, Graeme I. Bell, (unknown), Andrew T. Hattersley, Sian Ellard	2007	293
5	Mutations in ATP-Sensitive K+ Channel Genes Cause Transient Neonatal Diabetes and Permanent Diabetes in Childhood or Adulthood Diabetes ·Sarah E. Flanagan, Ann‐Marie Patch, Deborah Mackay, Emma L. Edghill, Anna L. Gloyn, David Robinson, Julian Hamilton‐Shield, I. Karen Temple, Sian Ellard, Andrew T. Hattersley	2007	261
6	Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis Nature Genetics ·Michael N. Weedon, Inês Cebola, Ann‐Marie Patch, Sarah E. Flanagan, Elisa De Franco, Richard Caswell, Santiago A. Rodríguez‐Seguí, Charles Shaw‐Smith, Candy H.-H. Cho, Hana Lango Allen, Jayne Houghton, Christian L. Roth, Rongrong Chen, Khalid Hussain, Phil Marsh, Ludovic Vallier, Anna Murray, Sian Ellard, Jorge Ferrer, Andrew T. Hattersley	2013	194
7	Permanent Neonatal Diabetes Caused by Dominant, Recessive, or Compound Heterozygous SUR1 Mutations with Opposite Functional Effects The American Journal of Human Genetics ·Sian Ellard, Sarah E. Flanagan, Christophe A. Girard, Ann‐Marie Patch, Lorna W. Harries, Andrew Parrish, Emma L. Edghill, Deborah Mackay, Peter Proks, Kenju Shimomura, Holger Haberland, D. J. Carson, Julian Hamilton‐Shield, Andrew T. Hattersley, Frances M. Ashcroft	2007	160
8	Wolcott-Rallison Syndrome Is the Most Common Genetic Cause of Permanent Neonatal Diabetes in Consanguineous Families The Journal of Clinical Endocrinology & Metabolism ·Oscar Rubio‐Cabezas, Ann‐Marie Patch, Jayne A.L. Minton, Sarah E. Flanagan, Emma L. Edghill, Khalid Hussain, A. Balafrej, Asma Deeb, Charles Buchanan, I G Jefferson, Angham Al Mutair, Andrew T. Hattersley, Sian Ellard, (unknown)	2009	104
9	Analysis of Transcription Factors Key for Mouse Pancreatic Development Establishes NKX2-2 and MNX1 Mutations as Causes of Neonatal Diabetes in Man Cell Metabolism ·Sarah E. Flanagan, Elisa De Franco, Hana Lango Allen, Michele Zerah, Majedah Abdul-Rasoul, Julie Edge, Helen Stewart, Elham Alamiri, Khalid Hussain, S Wallis, (unknown), Oscar Rubio‐Cabezas, Jayne Houghton, Emma L. Edghill, Ann‐Marie Patch, Sian Ellard, Andrew T. Hattersley	2014	100
10	Novel GLIS3 mutations demonstrate an extended multisystem phenotype European Journal of Endocrinology ·Paul Dimitri, J T Warner, Jayne A.L. Minton, Ann‐Marie Patch, Sian Ellard, Andrew T. Hattersley, Sybil Barr, Davida Hawkes, J K Wales, John W. Gregory	2010	72
11	Mutations in the ABCC8 gene encoding the SUR1 subunit of the K _ATP channel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes diagnosed outside the neonatal period Diabetes Obesity and Metabolism ·Ann‐Marie Patch, Sarah E. Flanagan, Chris Boustred, Andrew T. Hattersley, Sian Ellard	2007	65
12	TRbase: a database relating tandem repeats to disease genes for the human genome Bioinformatics ·T. Boby, Ann‐Marie Patch, Stephen J. Aves	2004	42
13	Genome-Wide Homozygosity Analysis Reveals HADH Mutations as a Common Cause of Diazoxide-Responsive Hyperinsulinemic-Hypoglycemia in Consanguineous Pedigrees The Journal of Clinical Endocrinology & Metabolism ·Sarah E. Flanagan, Ann‐Marie Patch, Jonathan M. Locke, Teoman Akçay, Enver Şimşek, Mohammadreza Alaei, Zeinab Yekta, Meena Desai, Ritika R. Kapoor, Khalid Hussain, Sian Ellard	2011	41
14	Increased ATPase activity produced by mutations at arginine-1380 in nucleotide-binding domain 2 of ABCC8 causes neonatal diabetes Proceedings of the National Academy of Sciences ·Heidi de Wet, Mathew G. Rees, Kenju Shimomura, Jussi Aittoniemi, Ann‐Marie Patch, Sarah E. Flanagan, Sian Ellard, Andrew T. Hattersley, Mark S.P. Sansom, Frances M. Ashcroft	2007	40
15	Intratumoural Heterogeneity Underlies Distinct Therapy Responses and Treatment Resistance in Glioblastoma Cancers ·Seçkin Akgül, Ann‐Marie Patch, Rochelle C. J. D’Souza, Pamela Mukhopadhyay, Kátia Nones, Sarah Kempe, Stephen H. Kazakoff, Rosalind L. Jeffree, Brett W. Stringer, John V. Pearson, Nicola Waddell, Bryan W. Day	2019	37
16	Unexpected UVR and non-UVR mutation burden in some acral and cutaneous melanomas Laboratory Investigation ·Robert V. Rawson, Peter A. Johansson, Nicholas K. Hayward, Nicola Waddell, Ann‐Marie Patch, Serigne Lo, John V. Pearson, John F. Thompson, Graham J. Mann, Richard A. Scolyer, James S. Wilmott	2017	34
17	APC Mutation Marks an Aggressive Subtype of BRAF Mutant Colorectal Cancers Cancers ·Lochlan J. Fennell, Alexandra Kane, Cheng Liu, Diane McKeone, Winnie Fernando, Chang Su, Catherine Bond, Saara Jamieson, Troy Dumenil, Ann‐Marie Patch, Stephen H. Kazakoff, John V. Pearson, Nicola Waddell, Barbara Leggett, Vicki Whitehall	2020	32
18	Mutations in the ABCC8 (SUR1 subunit of the K_ATP channel) gene are associated with a variable clinical phenotype Clinical Endocrinology ·Tomasz Klupa, Irina Kowalska, Krystyna Wyka, Jan Skupień, Ann‐Marie Patch, Sarah E. Flanagan, Anna Noczyńska, Małgorzata Arciszewska, Sian Ellard, Andrew T. Hattersley, Jacek Sieradzki, Wojciech Młynarski, Maciej T. Małecki	2008	30
19	Telomere sequence content can be used to determine ALT activity in tumours Nucleic Acids Research ·Michael Lee, Erdahl Teber, Oliver Holmes, Kátia Nones, Ann‐Marie Patch, Rebecca A. Dagg, Loretta M. S. Lau, Joyce H. Y. Lee, Christine E. Napier, Jonathan W. Arthur, Sean M. Grimmond, Nicholas K. Hayward, Peter A. Johansson, Graham J. Mann, Richard A. Scolyer, James S. Wilmott, Roger R. Reddel, John V. Pearson, Nicola Waddell, Hilda A. Pickett	2018	27
20	Whole exome sequencing of an asbestos-induced wild-type murine model of malignant mesothelioma BMC Cancer ·Sophie Sneddon, Ann‐Marie Patch, Ian M. Dick, Stephen H. Kazakoff, John V. Pearson, Nicola Waddell, Richard J. N. Allcock, Robert A. Holt, Bruce Robinson, Jenette Creaney	2017	26

About Ann‐Marie Patch

Ann‐Marie Patch is a scholar working on Surgery, Molecular Biology, Genetics, Endocrinology, Diabetes and Metabolism and Oncology, having authored 40 papers that have together received 2.8k indexed citations. Recurring topics across this work include Pancreatic function and diabetes (14 papers), Hyperglycemia and glycemic control in critically ill and hospitalized patients (5 papers), Diabetes and associated disorders (5 papers), Cancer Genomics and Diagnostics (4 papers), Diabetes Management and Research (3 papers), Cutaneous Melanoma Detection and Management (3 papers), Immune Cell Function and Interaction (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (638 citations), Surgery (1.4k citations), Genetics (955 citations), Physiology (138 citations) and Cell Biology (236 citations). Ann‐Marie Patch has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include Sian Ellard, Sarah E. Flanagan, Andrew T. Hattersley, Emma L. Edghill, Khalid Hussain, Donald F. Steiner, Julie Støy, Louis H. Philipson, Graeme I. Bell and Julian Hamilton‐Shield. Their work appears in journals such as Cancers, Blood, Proceedings of the National Academy of Sciences, Diabetes and The Journal of Clinical Endocrinology & Metabolism.

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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Ann‐Marie Patch

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Ann‐Marie Patch

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