| Next generation sequencing methods for diagnosis of epilepsy syndromes P Dunn, CL Albury, N Maksemous, MC Benton, HG Sutherland, RA Smith, ... Frontiers in genetics 9, 314696, 2018 | 149 | 2018 |
| Investigating diagnostic sequencing techniques for CADASIL diagnosis PJ Dunn, N Maksemous, RA Smith, HG Sutherland, LM Haupt, LR Griffiths Human Genomics 14, 1-10, 2020 | 18 | 2020 |
| Tiered analysis of whole-exome sequencing for epilepsy diagnosis PJ Dunn, BH Maher, CL Albury, S Stuart, HG Sutherland, N Maksemous, ... Molecular Genetics and Genomics 295, 751-763, 2020 | 18 | 2020 |
| Genetic variants associated with exercise performance in both moderately trained and highly trained individuals NR Harvey, S Voisin, PJ Dunn, H Sutherland, X Yan, M Jacques, ... Molecular Genetics and Genomics 295 (2), 515-523, 2020 | 18 | 2020 |
| Variant call format–diagnostic annotation and reporting tool: A customizable analysis pipeline for identification of clinically relevant genetic variants in next-generation … MC Benton, RA Smith, LM Haupt, HG Sutherland, PJ Dunn, CL Albury, ... The Journal of Molecular Diagnostics 21 (6), 951-960, 2019 | 10 | 2019 |
| Next generation sequencing methods for diagnosis of epilepsy syndromes. Front Genet. 2018; 9: 20 P Dunn, CL Albury, N Maksemous, MC Benton, HG Sutherland, RA Smith, ... | 8 | 2018 |
| Investigation of mitochondrial related variants in a cerebral small vessel disease cohort PJ Dunn, NR Harvey, N Maksemous, RA Smith, HG Sutherland, LM Haupt, ... Molecular Neurobiology 59 (9), 5366-5378, 2022 | 5 | 2022 |
| The MinION as a cost-effective technology for diagnostic screening of the SCN1A gene in epilepsy patients TTD Ngo, RA Lea, N Maksemous, DA Eccles, RA Smith, PJ Dunn, ... Epilepsy Research 172, 106593, 2021 | 2 | 2021 |
| Investigating a genetic link between alzheimer’s disease and CADASIL-related cerebral small vessel disease PJ Dunn, RA Lea, N Maksemous, RA Smith, HG Sutherland, LM Haupt, ... Molecular Neurobiology 59 (12), 7293-7302, 2022 | 1 | 2022 |
| Targeted exonic sequencing identifies novel causes of disease in a cerebral small vessel disease cohort P Dunn, N Maksemous, R Smith, H Sutherland, L Haupt, L Griffiths | 1 | 2022 |
| Exonic mutations in cell–cell adhesion may contribute to CADASIL-related CSVD pathology PJ Dunn, RA Lea, N Maksemous, RA Smith, HG Sutherland, LM Haupt, ... Human Genetics 142 (9), 1361-1373, 2023 | | 2023 |
| GSTM1 and GSTT1 polymorphisms associated with pain in a chemotherapy-induced peripheral neuropathy cohort PJ Dunn, LR Griffiths, P Yates, LM Haupt, KE Alexander Journal of Cancer Research and Clinical Oncology 149 (10), 7405-7412, 2023 | | 2023 |
| Identifying new genes and genetic factors causative of CADASIL and related stroke and dementia disorders PJ Dunn Queensland University of Technology, 2022 | | 2022 |
