Matthew B Johnson (Elisa De Franco)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 21

Top Venues

The Journal of experimental medicine

Journal of clinical immunology

Diabetologia

Diabetes

University of Exeter Medical School

University of Exeter Medical School (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Exeter Medical School Aug 01 2019

United Kingdom

Independent Research Fellow :: Institute of Biomedical and Clinical Science

University of Exeter Medical School Sep 23 2017 - Jul 31 2019

United Kingdom

Postdoctoral Research Associate :: Institute of Biomedical and Clinical Science

Royal Devon and Exeter NHS Foundation Trust Apr 01 2013 - Sep 22 2014

United Kingdom

Genetic Technologist :: Molecular Genetics

Education History

University of Exeter Medical School Sep 22 2014

United Kingdom

PHD :: Institute of Biomedical and Clinical Science

University of Birmingham Sep 01 2008 - Jul 01 2011

United Kingdom

BSC :: Biosciences

Publications

Matthew B Johnson, Masato Ogishi, Clara Domingo-Vila, Elisa De Franco, Matthew N Wakeling, Zineb Imane, Brittany Resnick, Evangelia Williams, Rui Pedro Galao, Richard C Caswell, James Russ-Silsby, Yoann Seeleuthner, Darawan Rinchai, Iris Fagniez, Basilin Benson, Matthew J Dufort, Cate Speake, Megan E Smithmyer, Michelle Hudson, Rebecca Dobbs, null null, Zoe Quandt, Andrew T Hattersley, Peng Zhang, Stéphanie Boisson-Dupuis, Mark S Anderson, Jean Laurent Casanova, Timothy I M Tree, Richard D Oram
Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency. The Journal of experimental medicine 221 (6) (2024)
Matthew B Johnson, Masato Ogishi, Clara Domingo-Vila, Elisa De Franco, Matthew N Wakeling, Zineb Imane, Brittany Resnick, Evangelia Williams, Rui Pedro Galao, Richard C Caswell, James Russ-Silsby, Yoann Seeleuthner, Darawan Rinchai, Iris Fagniez, Basilin Benson, Matthew J Dufort, Cate Speake, Megan E Smithmyer, Michelle Hudson, Rebecca Dobbs, null null, Zoe Quandt, Andrew T Hattersley, Peng Zhang, Stéphanie Boisson-Dupuis, Mark S Anderson, Jean Laurent Casanova, Timothy I M Tree, Richard D Oram
Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency. The Journal of experimental medicine 221 (6) (2024)
Matthew B Johnson, Masato Ogishi, Clara Domingo-Vila, Elisa De Franco, Matthew N Wakeling, Zineb Imane, Brittany Resnick, Evangelia Williams, Rui Pedro Galao, Richard C Caswell, James Russ-Silsby, Yoann Seeleuthner, Darawan Rinchai, Iris Fagniez, Basilin Benson, Matthew J Dufort, Cate Speake, Megan E Smithmyer, Michelle Hudson, Rebecca Dobbs, null null, Zoe Quandt, Andrew T Hattersley, Peng Zhang, Stéphanie Boisson-Dupuis, Mark S Anderson, Jean Laurent Casanova, Timothy I M Tree, Richard D Oram
Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency. The Journal of experimental medicine 221 (6) (2024)
Matthew B Johnson, Masato Ogishi, Clara Domingo-Vila, Elisa De Franco, Matthew N Wakeling, Zineb Imane, Brittany Resnick, Evangelia Williams, Rui Pedro Galao, Richard C Caswell, James Russ-Silsby, Yoann Seeleuthner, Darawan Rinchai, Iris Fagniez, Basilin Benson, Matthew J Dufort, Cate Speake, Megan E Smithmyer, Michelle Hudson, Rebecca Dobbs, null null, Zoe Quandt, Andrew T Hattersley, Peng Zhang, Stéphanie Boisson-Dupuis, Mark S Anderson, Jean Laurent Casanova, Timothy I M Tree, Richard D Oram
Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency. The Journal of experimental medicine 221 (6) (2024)
Matthew B Johnson, Masato Ogishi, Clara Domingo-Vila, Elisa De Franco, Matthew N Wakeling, Zineb Imane, Brittany Resnick, Evangelia Williams, Rui Pedro Galao, Richard C Caswell, James Russ-Silsby, Yoann Seeleuthner, Darawan Rinchai, Iris Fagniez, Basilin Benson, Matthew J Dufort, Cate Speake, Megan E Smithmyer, Michelle Hudson, Rebecca Dobbs, null null, Zoe Quandt, Andrew T Hattersley, Peng Zhang, Stéphanie Boisson-Dupuis, Mark S Anderson, Jean Laurent Casanova, Timothy I M Tree, Richard D Oram
Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency. The Journal of experimental medicine 221 (6) (2024)
Matthew B Johnson, Masato Ogishi, Clara Domingo-Vila, Elisa De Franco, Matthew N Wakeling, Zineb Imane, Brittany Resnick, Evangelia Williams, Rui Pedro Galao, Richard C Caswell, James Russ-Silsby, Yoann Seeleuthner, Darawan Rinchai, Iris Fagniez, Basilin Benson, Matthew J Dufort, Cate Speake, Megan E Smithmyer, Michelle Hudson, Rebecca Dobbs, null null, Zoe Quandt, Andrew T Hattersley, Peng Zhang, Stéphanie Boisson-Dupuis, Mark S Anderson, Jean Laurent Casanova, Timothy I M Tree, Richard D Oram
Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency. The Journal of experimental medicine 221 (6) (2024)
Matthew B Johnson, Masato Ogishi, Clara Domingo-Vila, Elisa De Franco, Matthew N Wakeling, Zineb Imane, Brittany Resnick, Evangelia Williams, Rui Pedro Galao, Richard C Caswell, James Russ-Silsby, Yoann Seeleuthner, Darawan Rinchai, Iris Fagniez, Basilin Benson, Matthew J Dufort, Cate Speake, Megan E Smithmyer, Michelle Hudson, Rebecca Dobbs, null null, Zoe Quandt, Andrew T Hattersley, Peng Zhang, Stéphanie Boisson-Dupuis, Mark S Anderson, Jean Laurent Casanova, Timothy I M Tree, Richard D Oram
Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency. The Journal of experimental medicine 221 (6) (2024)
Matthew B Johnson, Masato Ogishi, Clara Domingo-Vila, Elisa De Franco, Matthew N Wakeling, Zineb Imane, Brittany Resnick, Evangelia Williams, Rui Pedro Galao, Richard C Caswell, James Russ-Silsby, Yoann Seeleuthner, Darawan Rinchai, Iris Fagniez, Basilin Benson, Matthew J Dufort, Cate Speake, Megan E Smithmyer, Michelle Hudson, Rebecca Dobbs, null null, Zoe Quandt, Andrew T Hattersley, Peng Zhang, Stéphanie Boisson-Dupuis, Mark S Anderson, Jean Laurent Casanova, Timothy I M Tree, Richard D Oram
Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency. The Journal of experimental medicine 221 (6) (2024)
Rebecca C Wyatt, Sven Olek, Elisa De Franco, Bjoern Samans, Kashyap Patel, Jayne Houghton, Steffi Walter, Janika Schulze, Rosa Bacchetta, Andrew T Hattersley, Sarah E Flanagan, Matthew B Johnson
FOXP3 TSDR Measurement Could Assist Variant Classification and Diagnosis of IPEX Syndrome. Journal of clinical immunology 43 (3) (2023)
Rebecca C Wyatt, Sven Olek, Elisa De Franco, Bjoern Samans, Kashyap Patel, Jayne Houghton, Steffi Walter, Janika Schulze, Rosa Bacchetta, Andrew T Hattersley, Sarah E Flanagan, Matthew B Johnson
FOXP3 TSDR Measurement Could Assist Variant Classification and Diagnosis of IPEX Syndrome. Journal of clinical immunology 43 (3) (2023)
Rebecca C Wyatt, Sven Olek, Elisa De Franco, Bjoern Samans, Kashyap Patel, Jayne Houghton, Steffi Walter, Janika Schulze, Rosa Bacchetta, Andrew T Hattersley, Sarah E Flanagan, Matthew B Johnson
FOXP3 TSDR Measurement Could Assist Variant Classification and Diagnosis of IPEX Syndrome. Journal of clinical immunology 43 (3) (2023)
Rebecca C Wyatt, Sven Olek, Elisa De Franco, Bjoern Samans, Kashyap Patel, Jayne Houghton, Steffi Walter, Janika Schulze, Rosa Bacchetta, Andrew T Hattersley, Sarah E Flanagan, Matthew B Johnson
FOXP3 TSDR Measurement Could Assist Variant Classification and Diagnosis of IPEX Syndrome. Journal of clinical immunology 43 (3) (2023)
Rebecca C Wyatt, Sven Olek, Elisa De Franco, Bjoern Samans, Kashyap Patel, Jayne Houghton, Steffi Walter, Janika Schulze, Rosa Bacchetta, Andrew T Hattersley, Sarah E Flanagan, Matthew B Johnson
FOXP3 TSDR Measurement Could Assist Variant Classification and Diagnosis of IPEX Syndrome. Journal of clinical immunology (2023)
Rebecca C Wyatt, Sven Olek, Elisa De Franco, Bjoern Samans, Kashyap Patel, Jayne Houghton, Steffi Walter, Janika Schulze, Rosa Bacchetta, Andrew T Hattersley, Sarah E Flanagan, Matthew B Johnson
FOXP3 TSDR Measurement Could Assist Variant Classification and Diagnosis of IPEX Syndrome. Journal of clinical immunology 43 (3) (2023)
Rebecca C Wyatt, Sven Olek, Elisa De Franco, Bjoern Samans, Kashyap Patel, Jayne Houghton, Steffi Walter, Janika Schulze, Rosa Bacchetta, Andrew T Hattersley, Sarah E Flanagan, Matthew B Johnson
FOXP3 TSDR Measurement Could Assist Variant Classification and Diagnosis of IPEX Syndrome. Journal of clinical immunology 43 (3) (2023)
Thomas W Laver, Elisa De Franco, Matthew B Johnson, Kashyap Amratlal Patel, Sian Ellard, Michael N Weedon, Sarah E. Flanagan, Matthew N Wakeling
SavvyCNV: Genome-wide CNV calling from off-target reads. PLoS computational biology 18 (3) (2022)
Rebecca C Wyatt, William A Hagopian, Bart O Roep, Kashyap A Patel, Brittany Resnick, Rebecca Dobbs, Michelle Hudson, null null, Elisa De Franco, Sian Ellard, Sarah E Flanagan, Andrew T Hattersley, Richard D Oram, Matthew B Johnson
Congenital beta cell defects are not associated with markers of islet autoimmunity, even in the context of high genetic risk for type 1 diabetes. Diabetologia 65 (7) (2022)
Jasmin J Hopkins, Alexandra J Childs, Jayne A L Houghton, Thomas I Hewat, Navoda Atapattu, Matthew B Johnson, Kashyap Amratlal Patel, Thomas W Laver, Sarah E. Flanagan
Hyperinsulinaemic hypoglycaemia diagnosed in childhood can be monogenic. The Journal of clinical endocrinology and metabolism (2022)
Matthew B Johnson, Kashyap A Patel, Elisa De Franco, William Hagopian, Michael Killian, Timothy James McDonald, Timothy I M Tree, Clara Domingo-Vila, Michelle Hudson, Suzanne Hammersley, Rebecca Dobbs, null null, Sian Ellard, Sarah E. Flanagan, Andrew T Hattersley, Richard D Oram
Type 1 diabetes can present before the age of 6 months and is characterised by autoimmunity and rapid loss of beta cells. Diabetologia 63 (12) (2020)
Kashyap A Patel, Jarno L T Kettunen, Markku Laakso, Alena Stančáková Yaluri, Thomas W Laver, Kevin Colclough, Matthew B Johnson, Marc Abramowicz, Leif Groop, Päivi J Miettinen, Maggie H Shepherd, Sarah E Flanagan, Sian Ellard, Nobuya Inagaki, Andrew T Hattersley, Tiinamaija Tuomi, Miriam Cnop, Michael N Weedon
Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance. Nature communications 8 (1) (2017)
Matthew B Johnson, Matthew B Johnson, Hana Lango Allen, Aisha Al Senani, Nancy Elbarbary, Zeynep Siklar, Merih Berberoglu, Zineb Imane, Alireza Haghighi, Zahra Razavi, Irfan Ullah, Saif Alyaarubi, Daphne Gardner, Sian Ellard, Andrew T Hattersley, Sarah E Flanagan
Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes. Diabetes 66 (8) (2017)

Matthew B Johnson.css-eqlu8i{font-size:small;padding-left:4px;} (Elisa De Franco)

Publication Activity (10 Years)

Top Topics

Top Venues

Matthew B Johnson (Elisa De Franco)