Heidi R Fuller

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 11

Top Venues

Cells

Biomolecules

Neuroscience insights

Human molecular genetics

Keele University School of Medicine

University of Wales (PHD)

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

Affiliation History

Keele University School of Medicine

United Kingdom

Senior Lecturer in Medical Science

Education History

University of Wales

United Kingdom

PHD

Publications

Ena Španić Popovački, Dora Vogrinc, Heidi R Fuller, Lea Langer Horvat, Davor Mayer, Janja Kopić, Klara Pintarić, Mirjana Babić Leko, Mihaela Pravica, Željka Krsnik, Darko Marčinko, Marina Šagud, Patrick R Hof, Mihovil Mladinov, Goran Šimić
Increased NLRP1 mRNA and Protein Expression Suggests Inflammasome Activation in the Dorsolateral Prefrontal and Medial Orbitofrontal Cortex in Schizophrenia. Biomolecules 14 (3) (2024)
Ena Španić Popovački, Dora Vogrinc, Heidi R Fuller, Lea Langer Horvat, Davor Mayer, Janja Kopić, Klara Pintarić, Mirjana Babić Leko, Mihaela Pravica, Željka Krsnik, Darko Marčinko, Marina Šagud, Patrick R Hof, Mihovil Mladinov, Goran Šimić
Increased NLRP1 mRNA and Protein Expression Suggests Inflammasome Activation in the Dorsolateral Prefrontal and Medial Orbitofrontal Cortex in Schizophrenia. Biomolecules 14 (3) (2024)
Ena Španić Popovački, Dora Vogrinc, Heidi R Fuller, Lea Langer Horvat, Davor Mayer, Janja Kopić, Klara Pintarić, Mirjana Babić Leko, Mihaela Pravica, Željka Krsnik, Darko Marčinko, Marina Šagud, Patrick R Hof, Mihovil Mladinov, Goran Šimić
Increased NLRP1 mRNA and Protein Expression Suggests Inflammasome Activation in the Dorsolateral Prefrontal and Medial Orbitofrontal Cortex in Schizophrenia. Biomolecules 14 (3) (2024)
Sharon J Brown, Darija Šoltić, Silvia A Synowsky, Sally L Shirran, Ellie Chilcott, Hannah K Shorrock, Thomas Henry Gillingwater, Rafael J Yáñez-Muñoz, Bernard Schneider, Melissa Bowerman, Heidi R Fuller
AAV9-mediated SMN gene therapy rescues cardiac desmin but not Lamin a/C and elastin dysregulation in Smn 2B/- spinal muscular atrophy mice. Human molecular genetics (2023)
Emily C Storey, Heidi R Fuller
Genotype-Phenotype Correlations in Human Diseases Caused by Mutations of LINC Complex-Associated Genes: A Systematic Review and Meta-Summary. Cells 11 (24) (2022)
Emily C Storey, Heidi R Fuller
Genotype-Phenotype Correlations in Human Diseases Caused by Mutations of LINC Complex-Associated Genes: A Systematic Review and Meta-Summary. Cells 11 (24) (2022)
Emily C Storey, Heidi R Fuller
Genotype-Phenotype Correlations in Human Diseases Caused by Mutations of LINC Complex-Associated Genes: A Systematic Review and Meta-Summary. Cells 11 (24) (2022)
Sharon J Brown, Rachel A Kline, Silvia A Synowsky, Sally L Shirran, Ian Holt, Kelly A Sillence, Peter Claus, Brunhilde Wirth, Thomas M Wishart, Heidi R Fuller
The Proteome Signatures of Fibroblasts from Patients with Severe, Intermediate and Mild Spinal Muscular Atrophy Show Limited Overlap. Cells 11 (17) (2022)
Emily C Storey, Heidi R Fuller
Genotype-Phenotype Correlations in Human Diseases Caused by Mutations of LINC Complex-Associated Genes: A Systematic Review and Meta-Summary. Cells 11 (24) (2022)
Darija Šoltić, Heidi R Fuller
Molecular Crosstalk Between Non-SMN-Related and SMN-Related Spinal Muscular Atrophy. Neuroscience insights 15 (2020)
Yolanda Gómez-Gálvez, Heidi R Fuller, Silvia Synowsky, Sally L Shirran, Monte A Gates
Quantitative proteomic profiling of the rat substantia nigra places glial fibrillary acidic protein at the hub of proteins dysregulated during aging: Implications for idiopathic Parkinson's disease. Journal of neuroscience research 98 (7) (2020)

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Publication Activity (10 Years)

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Heidi R Fuller