Matthew N. Wakeling

2.0k total citations
28 papers, 790 citations indexed

About

Matthew N. Wakeling is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Matthew N. Wakeling has authored 28 papers receiving a total of 790 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 15 papers in Molecular Biology and 11 papers in Surgery. Recurrent topics in Matthew N. Wakeling's work include Pancreatic function and diabetes (10 papers), Genomics and Rare Diseases (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Matthew N. Wakeling is often cited by papers focused on Pancreatic function and diabetes (10 papers), Genomics and Rare Diseases (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Matthew N. Wakeling collaborates with scholars based in United Kingdom, Finland and United States. Matthew N. Wakeling's co-authors include Anthony Stellon, Richard Smith, Xavier Watkins, Rachel Lyne, Gos Micklem, Julie Sullivan, Kim Rutherford, Sian Ellard, Wenyan Ji and Mark Woodbridge and has published in prestigious journals such as SHILAP Revista de lepidopterología, Bioinformatics and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Matthew N. Wakeling

25 papers receiving 780 citations

Peers

Countries citing papers authored by Matthew N. Wakeling

Since Specialization

Citations

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

Fields of papers citing papers by Matthew N. Wakeling

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew N. Wakeling. 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 Matthew N. Wakeling. The network helps show where Matthew N. Wakeling may publish in the future.

Co-authorship network of co-authors of Matthew N. Wakeling

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew N. Wakeling. A scholar is included among the top collaborators of Matthew N. Wakeling 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 Matthew N. Wakeling. Matthew N. Wakeling 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

#	Work	Indexed citations
1	Rare Variants in NEUROD1 and PDX1 Are Low-Penetrance Causes of MODY, Whereas Those in APPL1 and WFS1 Are Not Associated With MODY 2025 ·Diabetes ·(unknown), Matthew N. Wakeling, Andrew T. Hattersley, Michael N. Weedon, Kevin Colclough, Thomas W. Laver, Kashyap Patel	0
2	Large copy number variants are an important cause of congenital hyperinsulinism that should be screened for during routine testing 2025 ·Frontiers in Endocrinology ·Sarah E. Flanagan, (unknown), Jonna M. E. Männistö, James T. Bennett, (unknown), Matthew B. Johnson, Matthew N. Wakeling, Jayne Houghton, Thomas W. Laver	0
3	Widening the phenotypic spectrum caused by pathogenic PDX1 variants in individuals with neonatal diabetes 2024 ·BMJ Open Diabetes Research & Care ·Nicola Jeffery, (unknown), Jayne Houghton, Evgenia Globa, Matthew N. Wakeling, Sarah E. Flanagan, Andrew T. Hattersley, Kashyap Patel, Elisa De Franco	1
4	Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements 2024 ·European Journal of Human Genetics ·Thomas W. Laver, Matthew N. Wakeling, Richard Caswell, (unknown), Daphne Yau, Jonna M. E. Männistö, Jayne Houghton, (unknown), Michael N. Weedon, Vrinda Saraff, Melanie Kershaw, Engela Honey, Nuala Murphy, Dinesh Giri, (unknown), (unknown), Indraneel Banerjee, (unknown), Nick Owens, Sarah E. Flanagan	2
5	The Role of ONECUT1 Variants in Monogenic and Type 2 Diabetes Mellitus 2023 ·Diabetes ·(unknown), Kashyap Patel, Thomas W. Laver, (unknown), Matthew B. Johnson, Matthew N. Wakeling, (unknown), Andrew T. Hattersley, Sarah E. Flanagan, Michael N. Weedon, Elisa De Franco	8
6	Paediatric diabetes subtypes in a consanguineous population: a single-centre cohort study from Kurdistan, Iraq 2023 ·Diabetologia ·(unknown), (unknown), (unknown), (unknown), Petra Dušátková, Matthew N. Wakeling, Elisa De Franco, Štěpánka Průhová, Jan Lebl	1
7	Infancy‐onset diabetes caused by de‐regulated AMPylation of the human endoplasmic reticulum chaperone BiP 2023 ·EMBO Molecular Medicine ·Luke A. Perera, Andrew T. Hattersley, Heather P. Harding, Matthew N. Wakeling, Sarah E. Flanagan, (unknown), Jamal Raza, Alice Gardham, David Ron, Elisa De Franco	15
8	REVEL Is Better at Predicting Pathogenicity of Loss-of-Function than Gain-of-Function Variants 2023 ·Human Mutation ·(unknown), Matthew N. Wakeling, Matthew B. Johnson, Sarah E. Flanagan, Thomas W. Laver	6
9	Refinements and considerations for trio whole-genome sequence analysis when investigating Mendelian diseases presenting in early childhood 2022 ·Human Genetics and Genomics Advances ·Courtney E. French, Helen Dolling, Karyn Mégy, Alba Sanchis-Juan, Ajay Kumar, Isabelle Delon, Matthew N. Wakeling, (unknown), Shruti Agrawal, Topun Austin, (unknown), Soo‐Mi Park, Alasdair Parker, Chinthika Piyasena, (unknown), Sian Ellard, David H. Rowitch, F. Lucy Raymond	10
10	Evaluation of Evidence for Pathogenicity Demonstrates That BLK , KLF11 , and PAX4 Should Not Be Included in Diagnostic Testing for MODY 2022 ·Diabetes ·Thomas W. Laver, Matthew N. Wakeling, Olivia Knox, Kevin Colclough, Caroline F. Wright, Sian Ellard, Andrew T. Hattersley, Michael N. Weedon, Kashyap Patel	35
11	SavvyCNV: Genome-wide CNV calling from off-target reads 2022 ·PLoS Computational Biology ·Thomas W. Laver, Elisa De Franco, Matthew B. Johnson, Kashyap Patel, Sian Ellard, Michael N. Weedon, Sarah E. Flanagan, Matthew N. Wakeling	12
12	Loss of MANF Causes Childhood-Onset Syndromic Diabetes Due to Increased Endoplasmic Reticulum Stress 2021 ·Diabetes ·Hossam Montaser, Kashyap Patel, Diego Balboa, Hazem Ibrahim, Väinö Lithovius, Anna Näätänen, Vikash Chandra, Korcan Demir, Sezer Acar, Tawfeg Ben‐Omran, Kevin Colclough, Jonathan M. Locke, Matthew N. Wakeling, Maria Lindahl, Andrew T. Hattersley, Jonna Saarimäki‐Vire, Timo Otonkoski	46
13	Annotating high-impact 5′untranslated region variants with the UTRannotator 2020 ·Bioinformatics ·Xiaolei Zhang, Matthew N. Wakeling, James S. Ware, Nicola Whiffin	31
14	Missense substitutions at a conserved 14-3-3 binding site in HDAC4 cause a novel intellectual disability syndrome 2020 ·SHILAP Revista de lepidopterología ·Emma Wakeling, Meriel McEntagart, (unknown), Charles Shaw‐Smith, Karen Stals, Matthew N. Wakeling, Angela Barnicoat, Clare Beesley, Andrea Hanson‐Kahn, Mary K. Kukolich, David A. Stevenson, Philippe M. Campeau, Sian Ellard, Sarah H. Elsea, Xiang-Jiao Yang, Richard Caswell	11
15	Comprehensive screening shows that mutations in the known syndromic genes are rare in infants presenting with hyperinsulinaemic hypoglycaemia 2018 ·Clinical Endocrinology ·Thomas W. Laver, Matthew N. Wakeling, (unknown), Jayne Houghton, Khalid Hussain, Sian Ellard, Sarah E. Flanagan	7
16	Phenotype of CNTNAP1: a study of patients demonstrating a specific severe congenital hypomyelinating neuropathy with survival beyond infancy 2018 ·European Journal of Human Genetics ·Karen Low, Karen Stals, Richard Caswell, Matthew N. Wakeling, Jill Clayton‐Smith, Alan Donaldson, Nicola Foulds, Andrew Norman, Miranda Splitt, (unknown), K. Vijayakumar, Anirban Majumdar, (unknown), Sian Ellard, (unknown)	18
17	Homozygosity mapping provides supporting evidence of pathogenicity in recessive Mendelian disease 2018 ·Genetics in Medicine ·Matthew N. Wakeling, Thomas W. Laver, Caroline F. Wright, Elisa De Franco, Karen Stals, Ann‐Marie Patch, Andrew T. Hattersley, Sarah E. Flanagan, Sian Ellard	23
18	Assimilation of vertical motion from simulated cloudy satellite imagery in an idealized single column model 2014 ·Quarterly Journal of the Royal Meteorological Society ·Matthew N. Wakeling, J. R. Eyre, Susan Hughes, Ian Roulstone	1
19	InterMine: a flexible data warehouse system for the integration and analysis of heterogeneous biological data 2012 ·Bioinformatics ·Richard Smith, J. Aleksić, Daniela Butano, Adrian R. Carr, Sergio Contrino, Fengyuan Hu, Mike Lyne, Rachel Lyne, (unknown), Kim Rutherford, Radek Štěpán, Julie Sullivan, Matthew N. Wakeling, Xavier Watkins, Gos Micklem	164
20	Hidradenitis suppurativa associated with use of oral contraceptives. 1989 ·BMJ ·Anthony Stellon, Matthew N. Wakeling	57

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