Matthew B. Johnson

2.8k total citations
66 papers, 1.2k citations indexed

About

Matthew B. Johnson is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Matthew B. Johnson has authored 66 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 24 papers in Surgery and 13 papers in Molecular Biology. Recurrent topics in Matthew B. Johnson's work include Diabetes and associated disorders (17 papers), Pancreatic function and diabetes (17 papers) and Hyperglycemia and glycemic control in critically ill and hospitalized patients (8 papers). Matthew B. Johnson is often cited by papers focused on Diabetes and associated disorders (17 papers), Pancreatic function and diabetes (17 papers) and Hyperglycemia and glycemic control in critically ill and hospitalized patients (8 papers). Matthew B. Johnson collaborates with scholars based in United Kingdom, United States and Finland. Matthew B. Johnson's co-authors include Sarah E. Flanagan, Sian Ellard, Andrew T. Hattersley, Richard Caswell, Thomas W. Laver, Elisa De Franco, Zvonimir Krajcer, Michael Bacharach, Hana Lango Allen and David Williams and has published in prestigious journals such as Nature Communications, The Journal of Clinical Endocrinology & Metabolism and Diabetes.

In The Last Decade

Matthew B. Johnson

62 papers receiving 1.1k citations

Peers

Countries citing papers authored by Matthew B. Johnson

Since Specialization

Citations

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

Fields of papers citing papers by Matthew B. Johnson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthew B. Johnson

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew B. Johnson. A scholar is included among the top collaborators of Matthew B. Johnson 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 B. Johnson. Matthew B. Johnson 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	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
2	P159 The prevalence of premalignant upper GI conditions is underestimated based on endoscopic diagnosis: interim data from a multicentre, prospective study 2024 ·Poster presentations ·Andreas V. Hadjinicolaou, Inés Modolell, (unknown), Jacobo Ortiz Fernández‐Sordo, Krashna Patel, Danielle Morris, (unknown), Matthew Banks, (unknown), Leo Alexandre, Matthew B. Johnson, Nigel Trudgill, Yeng Ang, (unknown), Massimiliano di Pietro	1
3	Type 1 diabetes genetic risk score variation across ancestries using whole genome sequencing and array-based approaches 2024 ·Scientific Reports ·(unknown), (unknown), Seth A. Sharp, Richard A. Oram, Matthew B. Johnson, (unknown), Kashyap Patel	2
4	FOXP3 TSDR Measurement Could Assist Variant Classification and Diagnosis of IPEX Syndrome 2023 ·Journal of Clinical Immunology ·Rebecca C. Wyatt, Sven Olek, Elisa De Franco, (unknown), Kashyap Patel, Jayne Houghton, Steffi Walter, (unknown), Rosa Bacchetta, Andrew T. Hattersley, Sarah E. Flanagan, Matthew B. Johnson	8
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	Effect-based monitoring of two rivers under urban and agricultural influence reveals a range of biological activities in sediment and water extracts 2023 ·Journal of Environmental Management ·Frédéric D.L. Leusch, (unknown), (unknown), (unknown), Matthew B. Johnson, Peta A. Neale, Michael Stewart, Louis A. Tremblay, (unknown), Grant L. Northcott	11
7	Increased referrals for congenital hyperinsulinism genetic testing in children with trisomy 21 reflects the high burden of non‐genetic risk factors in this group 2022 ·Pediatric Diabetes ·(unknown), Thomas W. Laver, Jayne Houghton, Jonna M. E. Männistö, (unknown), Stephen Brearey, (unknown), Antonia Dastamani, (unknown), Nuala Murphy, Birgit Rami‐Merhar, (unknown), Hanna Huopio, Indraneel Banerjee, Matthew B. Johnson, Sarah E. Flanagan	6
8	Hyperinsulinemic Hypoglycemia Diagnosed in Childhood Can Be Monogenic 2022 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), (unknown), Jayne Houghton, (unknown), Navoda Atapattu, Matthew B. Johnson, Kashyap Patel, Thomas W. Laver, Sarah E. Flanagan	7
9	Congenital beta cell defects are not associated with markers of islet autoimmunity, even in the context of high genetic risk for type 1 diabetes 2022 ·Diabetologia ·Rebecca C. Wyatt, William Hagopian, Bart O. Roep, Kashyap Patel, Brittany Resnick, (unknown), Michelle Hudson, Elisa De Franco, Sian Ellard, Sarah E. Flanagan, Andrew T. Hattersley, Richard A. Oram, Matthew B. Johnson	2
10	Fanconi Bickel syndrome: clinical phenotypes and genetics in a cohort of Sudanese children 2020 ·International Journal of Pediatric Endocrinology ·(unknown), (unknown), (unknown), Matthew B. Johnson, (unknown), (unknown), Mohamed Ahmed Abdullah	9
11	Screening of monogenic autoimmune diabetes among children with type 1 diabetes and multiple autoimmune diseases: is it worth doing? 2019 ·Journal of Pediatric Endocrinology and Metabolism ·(unknown), Lenka Elblová, Matthew B. Johnson, Petra Dušátková, Barbora Obermannová, Lenka Petruželková, Stanislava Koloušková, Marta Šnajderová, Eva Froňková, Michael Svatoň, Jan Lebl, Andrew T. Hattersley, Zdenĕk Šumnı́k, Štěpánka Průhová	6
12	Genetic Mechanisms Highlight Shared Pathways for the Pathogenesis of Polygenic Type 1 Diabetes and Monogenic Autoimmune Diabetes 2019 ·Current Diabetes Reports ·Matthew B. Johnson, Karen Cerosaletti, Sarah E. Flanagan, Jane H. Buckner	25
13	Significant Prevalence of Severe Monogenic Immune Defects Among Children with Type 1 Diabetes and Low T1D-Genetic Risk Score 2018 ·Štěpánka Průhová, (unknown), Lenka Elblová, Matthew B. Johnson, Petra Dušátková, Barbora Obermannová, Lenka Petruželková, Stanislava Koloušková, Marta Šnajderová, (unknown), Michael Svatoň, Jan Lebl, Andrew T. Hattersley, Zdenĕk Šumnı́k	1
14	Recessively InheritedLRBAMutations Cause Autoimmunity Presenting as Neonatal Diabetes 2017 ·Diabetes ·Matthew B. Johnson, Elisa De Franco, Hana Lango Allen, (unknown), Nancy Samir Elbarbary, Zeynep Şıklar, Merih Berberoğlu, (unknown), Alireza Haghighi, (unknown), Irfan Ullah, Saif Al-Yaarubi, Daphne Gardner, Ayla Güven, Sian Ellard, Andrew T. Hattersley, Sarah E. Flanagan	48
15	Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance 2017 ·Nature Communications ·Kashyap Patel, Jarno L. T. Kettunen, Markku Laakso, Alena Stančáková, Thomas W. Laver, Kevin Colclough, Matthew B. Johnson, Marc Abramowicz, Leif Groop, Päivi J. Miettinen, Maggie Shepherd, Sarah E. Flanagan, Sian Ellard, Nobuya Inagaki, Andrew T. Hattersley, (unknown), Miriam Cnop, Michael N. Weedon	87
16	Dominant ER Stress–Inducing WFS1 Mutations Underlie a Genetic Syndrome of Neonatal/Infancy-Onset Diabetes, Congenital Sensorineural Deafness, and Congenital Cataracts 2017 ·Diabetes ·Elisa De Franco, Sarah E. Flanagan, Takuya Yagi, Damien Abreu, Jana Mahadevan, Matthew B. Johnson, Garan Jones, (unknown), (unknown), Ngee Lek, (unknown), (unknown), Richard Caswell, Sian Ellard, Fumihiko Urano, Andrew T. Hattersley	75
17	Patterning of Quantum Dot Bioconjugates via Particle Lithography 2010 ·Langmuir ·(unknown), (unknown), Joel C. Keay, Matthew B. Johnson, David W. Schmidtke	8
18	Results of a Multicenter Trial for the Treatment of Traumatic Vascular Injury with a Covered Stent 2006 ·The Journal of Trauma: Injury, Infection, and Critical Care ·(unknown), Zvonimir Krajcer, Matthew B. Johnson, David Williams, Michael Bacharach, (unknown)	87
19	Carrier detection in hemophilia A: ABO blood group, multiple measurements, and application of logistic discrimination 1988 ·American Journal of Medical Genetics ·M. E. Percy, (unknown), Marie Garvey, John Freedman, Jerry Teitel, Peter G. Blake, (unknown), (unknown), Matthew B. Johnson, Martin J. Inwood, David Andrews, Penny Brasher, John M. Opitz, James F. Reynolds	2
20	Effect of bilateral adrenalectomy on diabetes mellitus. 1957 ·PubMed ·(unknown), B. J. Kennedy, Matthew B. Johnson	1

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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