Browse By Person: Albury, Cassie

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Number of items: 14.

Contribution to Journal

Albury, Cassie L., Sutherland, Heidi G., Lam, Alexis W.Y., Tran, Ngan K., Lea, Rod A., Haupt, Larisa M., & Griffiths, Lyn R. (2024) Identification of Polymorphisms in EAAT1 Glutamate Transporter Gene SLC1A3 Associated with Reduced Migraine Risk. Genes, 15(6), Article number: 797.

Haupt, Larisa M., Haywood, Alison, Sutherland, Heidi G., Yu, Chieh, Albury, Cassie L., Pharasi, Anushka, Zunk, Mathew, George, Rani, Griffiths, Lyn R., Good, Phillip, & Hardy, Janet (2024) The effects of OPRM1 118A>G on methadone response in pain management in advanced cancer at end of life. Scientific Reports, 14(1), Article number: 3411.

Ozberk, Deniz, Haywood, Alison, Sutherland, Heidi G., Yu, Chieh, Albury, Cassie L., Zunk, Mathew, George, Rani, Good, Phillip, Griffiths, Lyn R., Hardy, Janet, & Haupt, Larisa M. (2022) Association of KCNJ6 rs2070995 and methadone response for pain management in advanced cancer at end-of-life. Scientific Reports, 12, Article number: 17422.

Number of full-text downloads

26

Number of citations in Scopus

1

Ozberk, Deniz, Haywood, Alison, Sutherland, Heidi G., Yu, Chieh, Albury, Cassie L., Zunk, Mathew, George, Rani, Good, Phillip, Griffiths, Lyn R., Hardy, Janet, & Haupt, Larisa M. (2022) Association of polymorphisms in ARRB2 and clinical response to methadone for pain in advanced cancer. Pharmacogenomics, 23(5), pp. 281-289.

Number of full-text downloads

33

Number of citations in Scopus

2

Number of citations in Web of Science®

1

Sutherland, Heidi G., Maksemous, Neven, Albury, Cassie L., Ibrahim, Omar, Smith, Robert A., Lea, Rod A., Haupt, Larisa M., Jenkins, Bronwyn, Tsang, Benjamin, & Griffiths, Lyn R. (2020) Comprehensive Exonic Sequencing of Hemiplegic Migraine-Related Genes in a Cohort of Suspected Probands Identifies Known and Potential Pathogenic Variants. Cells, 9(11), Article number: 2368 1-16.

Number of full-text downloads

111

Number of citations in Scopus

14

Number of citations in Web of Science®

10

Dunn, Paul J., Maher, Bridget H., Albury, Cassie L., Stuart, Shani, Sutherland, Heidi G., Maksemous, Neven, Benton, Miles C., Smith, Robert A., Haupt, Larisa M., & Griffiths, Lyn R. (2020) Tiered analysis of whole-exome sequencing for epilepsy diagnosis. Molecular Genetics and Genomics, 295(3), pp. 751-763.

Number of citations in Scopus

14

Number of citations in Web of Science®

7

Harvey, N. R., Albury, C.L., Stuart, S., Benton, M. C., Eccles, D. A., Connell, Jasmine, Sutherland, H. G., Allcock, R. J.N., Lea, R. A., Haupt, L. M., & Griffiths, L. R. (2019) Ion torrent high throughput mitochondrial genome sequencing (HTMGS). PLoS One, 14(11), Article number: e0224847.

Number of full-text downloads

112

Number of citations in Scopus

10

Number of citations in Web of Science®

9

Sutherland, Heidi G., Albury, Cassie L., & Griffiths, Lyn R. (2019) Advances in genetics of migraine. Journal of Headache and Pain, 20, Article number: 72.

Number of full-text downloads

146

Number of citations in Scopus

113

Number of citations in Web of Science®

82

Benton, Miles, Smith, Robert, Haupt, Larisa, Sutherland, Heidi, Dunn, Paul, Albury, Cassie, Maksemous, Neven, Lea, Rodney, & Griffiths, Lyn (2019) Variant Call Format (VCF)-Diagnostic Annotation and Reporting Tool (VCF-DART) A Customizable Analysis Pipeline for Identification of Clinically Relevant Genetic Variants in Next-Generation Sequencing Data. Journal of Molecular Diagnostics, 21(6), pp. 951-960.

Number of citations in Scopus

5

Number of citations in Web of Science®

4

Bradshaw, Gabrielle, Lualhati, Robbie, Albury, Cassie, Maksemous, Neven, Roos-Araujo, Deidre, Smith, Robert, Benton, Miles, Eccles, David, Lea, Rodney, Sutherland, Heidi, Haupt, Larisa, & Griffiths, Lyn (2018) Exome sequencing diagnoses x-linked moesin-associated immunodeficiency in a primary immunodeficiency case. Frontiers in Immunology, 9, Article number: 420 1-9.

Number of full-text downloads

220

Number of citations in Scopus

24

Number of citations in Web of Science®

19

Dunn, Paul, Albury, Cassie, Maksemous, Neven, Benton, Miles, Sutherland, Heidi, Smith, Robert, Haupt, Larisa, & Griffiths, Lyn (2018) Next generation sequencing methods for diagnosis of epilepsy syndromes. Frontiers in Genetics, 9, Article number: 20 1-11.

Number of full-text downloads

192

Number of citations in Scopus

99

Number of citations in Web of Science®

74

Albury, Cassie, Stuart, Shani, Haupt, Larisa, & Griffiths, Lyn (2017) Ion channelopathies and migraine pathogenesis. Molecular Genetics and Genomics, 292(4), pp. 729-739.

Number of full-text downloads

228

Number of citations in Scopus

20

Number of citations in Web of Science®

17

Albury, Cassie, Gerring, Zac, Griffiths, Lyn, Nyholt, Dale, & Rodriguez-Acevedo, Astrid (2017) RE: Six novel rare non-synonymous mutations for migraine without aura identified by exome sequencing (Letter to the Editor). Journal of Neurogenetics, 31(4), pp. 320-321.

Number of full-text downloads

126

Number of citations in Scopus

1

Number of citations in Web of Science®

2

QUT Thesis

Albury, Cassie Louise (2018) Using whole exome sequencing and genetic association studies to investigate common and complex migraine. PhD thesis, Queensland University of Technology.

Number of full-text downloads

490

This list was generated on Sun Aug 4 09:23:33 2024 AEST.