Publications by authors named "Miles Thompson"

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E
Evidence demands action: An invitation to share the burden of proof.
Danielle M Andrade, Anne T Berg, Arunan Selvarajah, Andrea Sabo, Carolina Gorodetsky, Miles Thompson

Epilepsia· October 2025

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Exploring Participant-Generated Examples of Social Change: A Two-Stage, Mixed Methods, Delphi Study.
Miles Thompson, Ben Rosser, Eleanor Stone, Holly Parker, Eleanor Harrison-Wolff

J Community Psychol· July 2025

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Dravet syndrome: From neurodevelopmental to neurodegenerative disease?
Arunan Selvarajah, Andrea Sabo, Carolina Gorodetsky, Paula T Marques, Ilakkiah Chandran, Miles Thompson

Epilepsia· June 2025

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Genetic variants of accessory proteins and G proteins in human genetic disease.
Miles D Thompson, Peter Chidiac, Pedro A Jose, Alexander S Hauser, Caroline M Gorvin

Crit Rev Clin Lab Sci· March 2025

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G protein-coupled receptor (GPCR) pharmacogenomics.
Miles D Thompson, David Reiner-Link, Alessandro Berghella, Brinda K Rana, G Enrico Rovati

Crit Rev Clin Lab Sci· December 2024

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G protein-coupled receptor (GPCR) gene variants and human genetic disease.
Miles D Thompson, Maire E Percy, David E C Cole, Daniel G Bichet, Alexander S Hauser

Crit Rev Clin Lab Sci· August 2024

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Rare Genetic Developmental Disabilities: Mabry Syndrome (MIM 239300) Index Cases and Glycophosphatidylinositol (GPI) Disorders.
Miles D Thompson, Alexej Knaus

Genes (Basel)· May 2024

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Innovations in Phenotyping and Diagnostics Create Opportunities for Improved Treatment and Genetic Counseling for Rare Diseases.
Miles D Thompson

Genes (Basel)· May 2024

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Health professionals' perspectives on psychological distress and meeting patients' support needs in rheumatology care settings: A qualitative study.
Christine Silverthorne, Jo Daniels, Miles Thompson, Joanna C Robson, Mwidimi Ndosi

Musculoskeletal Care· June 2023

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Excluding Digenic Inheritance of and Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3).
Miles D Thompson, Xueying Li, Michele Spencer-Manzon, Danielle M Andrade, Yoshiko Murakami

Genes (Basel)· January 2023

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UK clinical and community psychology: Exploring personal and professional connections.
Miles Thompson, Jenny Stuart, Rose E Vincent, Louise Goodbody

J Community Psychol· September 2022

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Student mental health in higher education: the contextual influence of "cuts, competition & comparison".
Miles Thompson, Chris Pawson, Arianna Delfino, Alex Saunders, Holly Parker

Br J Educ Psychol· June 2022

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Antiseizure effects of the cannabinoids in the amygdala-kindling model.
Merrick S Fallah, Lukasz Dlugosz, Brian W Scott, Miles D Thompson, W McIntyre Burnham

Epilepsia· September 2021

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50 Years Ago in TheJournal ofPediatrics: Familial Hyperphosphatasia with Mental Retardation, Seizures, and Neurologic Deficits.
Miles D Thompson, David E Cole, C Charlton Mabry

J Pediatr· July 2020

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A post glycosylphosphatidylinositol (GPI) attachment to proteins, type 2 (PGAP2) variant identified in Mabry syndrome index cases: Molecular genetics of the prototypical inherited GPI disorder.
Miles D Thompson, Alexej A Knaus, Bruce A Barshop, Almuth Caliebe, Hiltrud Muhle

Eur J Med Genet· April 2020

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Significantly different clinical phenotypes associated with mutations in synthesis and transamidase+remodeling glycosylphosphatidylinositol (GPI)-anchor biosynthesis genes.
Leigh C Carmody, Hannah Blau, Daniel Danis, Xingman A Zhang, Jean-Philippe Gourdine, Miles D Thompson

Orphanet J Rare Dis· February 2020

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Mutations in PIGS, Encoding a GPI Transamidase, Cause a Neurological Syndrome Ranging from Fetal Akinesia to Epileptic Encephalopathy.
Thi Tuyet Mai Nguyen, Yoshiko Murakami, Kristen M Wigby, Nissan V Baratang, Justine Rousseau, Miles Thompson

Am J Hum Genet· October 2018

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Orexin Receptor Multimerization versus Functional Interactions: Neuropharmacological Implications for Opioid and Cannabinoid Signalling and Pharmacogenetics.
Miles D Thompson, Takeshi Sakurai, Innocenzo Rainero, Mary C Maj, Jyrki P Kukkonen

Pharmaceuticals (Basel)· October 2017

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Cysteinyl Leukotrienes Pathway Genes, Atopic Asthma and Drug Response: From Population Isolates to Large Genome-Wide Association Studies.
Miles D Thompson, Valerie Capra, Mark T Clunes, G E Rovati, Jana Stankova

Front Pharmacol· December 2016

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Rare Noncoding Mutations Extend the Mutational Spectrum in the PGAP3 Subtype of Hyperphosphatasia with Mental Retardation Syndrome.
Alexej Knaus, Tomonari Awaya, Ingo Helbig, Zaid Afawi, Manuela Pendziwiat, Miles D Thompson

Hum Mutat· August 2016

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Recessive PIGN Mutations in Fryns Syndrome: Evidence for Genetic Heterogeneity.
Miles D Thompson, David E Cole

Hum Mutat· July 2016

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Variation in the Serotonin Transporter Gene and Alcoholism: Risk and Response to Pharmacotherapy.
Miles D Thompson, George A Kenna

Alcohol Alcohol· March 2016

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Cellular signalling of cysteinyl leukotriene type 1 receptor variants CysLT₁-G300S and CysLT₁-I206S.
Louiza Yaddaden, Steeve Véronneau, Miles D Thompson, Marek Rola-Pleszczynski, Jana Stankova

Prostaglandins Leukot Essent Fatty Acids· February 2016

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Neurogenetic Aspects of Hyperphosphatasia in Mabry Syndrome.
David E C Cole, Miles D Thompson

Subcell Biochem· January 2016

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Pharmacogenetics of the G protein-coupled receptors.
Miles D Thompson, David E C Cole, Valerie Capra, Katherine A Siminovitch, G Enrico Rovati

Methods Mol Biol· May 2015

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