Dunn P - Search Results

1

Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes.

Dunn P, Albury CL, Maksemous N, Benton MC, Sutherland HG, Smith RA, Haupt LM, Griffiths LR. Dunn P, et al. Front Genet. 2018 Feb 7;9:20. doi: 10.3389/fgene.2018.00020. eCollection 2018. Front Genet. 2018. PMID: 29467791 Free PMC article. Review.

2

Variant Call Format-Diagnostic Annotation and Reporting Tool: A Customizable Analysis Pipeline for Identification of Clinically Relevant Genetic Variants in Next-Generation Sequencing Data.

Benton MC, Smith RA, Haupt LM, Sutherland HG, Dunn PJ, Albury CL, Maksemous N, Lea R, Griffiths L. Benton MC, et al. J Mol Diagn. 2019 Nov;21(6):951-960. doi: 10.1016/j.jmoldx.2019.07.001. Epub 2019 Aug 20. J Mol Diagn. 2019. PMID: 31442673 Free article.

3

Genetic variants associated with exercise performance in both moderately trained and highly trained individuals.

Harvey NR, Voisin S, Dunn PJ, Sutherland H, Yan X, Jacques M, Papadimitriou ID, Haseler LJ, Ashton KJ, Haupt LM, Eynon N, Griffiths LR. Harvey NR, et al. Among authors: dunn pj. Mol Genet Genomics. 2020 Mar;295(2):515-523. doi: 10.1007/s00438-019-01639-8. Epub 2020 Jan 2. Mol Genet Genomics. 2020. PMID: 31897802

4

Investigating diagnostic sequencing techniques for CADASIL diagnosis.

Dunn PJ, Maksemous N, Smith RA, Sutherland HG, Haupt LM, Griffiths LR. Dunn PJ, et al. Hum Genomics. 2020 Jan 8;14(1):2. doi: 10.1186/s40246-019-0255-x. Hum Genomics. 2020. PMID: 31915071 Free PMC article.

5

Tiered analysis of whole-exome sequencing for epilepsy diagnosis.

Dunn PJ, Maher BH, Albury CL, Stuart S, Sutherland HG, Maksemous N, Benton MC, Smith RA, Haupt LM, Griffiths LR. Dunn PJ, et al. Mol Genet Genomics. 2020 May;295(3):751-763. doi: 10.1007/s00438-020-01657-x. Epub 2020 Mar 7. Mol Genet Genomics. 2020. PMID: 32146541

6

The MinION as a cost-effective technology for diagnostic screening of the SCN1A gene in epilepsy patients.

Ngo TTD, Lea RA, Maksemous N, Eccles DA, Smith RA, Dunn PJ, Thao VC, Ha TMT, Bùi CB, Haupt LM, Scott R, Griffiths LR. Ngo TTD, et al. Epilepsy Res. 2021 May;172:106593. doi: 10.1016/j.eplepsyres.2021.106593. Epub 2021 Feb 27. Epilepsy Res. 2021. PMID: 33721710

7

Investigation of Mitochondrial Related Variants in a Cerebral Small Vessel Disease Cohort.

Dunn PJ, Harvey NR, Maksemous N, Smith RA, Sutherland HG, Haupt LM, Griffiths LR. Dunn PJ, et al. Mol Neurobiol. 2022 Sep;59(9):5366-5378. doi: 10.1007/s12035-022-02914-3. Epub 2022 Jun 14. Mol Neurobiol. 2022. PMID: 35699875 Free PMC article.

8

Investigating a Genetic Link Between Alzheimer's Disease and CADASIL-Related Cerebral Small Vessel Disease.

Dunn PJ, Lea RA, Maksemous N, Smith RA, Sutherland HG, Haupt LM, Griffiths LR. Dunn PJ, et al. Mol Neurobiol. 2022 Dec;59(12):7293-7302. doi: 10.1007/s12035-022-03039-3. Epub 2022 Sep 29. Mol Neurobiol. 2022. PMID: 36175824 Free PMC article.

9

GSTM1 and GSTT1 polymorphisms associated with pain in a chemotherapy-induced peripheral neuropathy cohort.

Dunn PJ, Griffiths LR, Yates P, Haupt LM, Alexander KE. Dunn PJ, et al. J Cancer Res Clin Oncol. 2023 Aug;149(10):7405-7412. doi: 10.1007/s00432-023-04677-3. Epub 2023 Mar 20. J Cancer Res Clin Oncol. 2023. PMID: 36939926 Free PMC article.

10

Exonic mutations in cell-cell adhesion may contribute to CADASIL-related CSVD pathology.

Dunn PJ, Lea RA, Maksemous N, Smith RA, Sutherland HG, Haupt LM, Griffiths LR. Dunn PJ, et al. Hum Genet. 2023 Sep;142(9):1361-1373. doi: 10.1007/s00439-023-02584-8. Epub 2023 Jul 8. Hum Genet. 2023. PMID: 37422595 Free PMC article.

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