Search Results - "GRIFFITHS, Lyn R."

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    Advances in genetics of migraine by Sutherland, Heidi G., Albury, Cassie L., Griffiths, Lyn R.

    Published in Journal of headache and pain (21-06-2019)
    “…Background Migraine is a complex neurovascular disorder with a strong genetic component. There are rare monogenic forms of migraine, as well as more common…”
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    Journal Article
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    The impact of APOA5, APOB, APOC3 and ABCA1 gene polymorphisms on ischemic stroke: Evidence from a meta-analysis by Au, Anthony, Griffiths, Lyn R., Irene, Looi, Kooi, Cheah Wee, Wei, Loo Keat

    Published in Atherosclerosis (01-10-2017)
    “…Genetic studies have been reported on the association between APOA5, APOB, APOC3 and ABCA1 gene polymorphisms and ischemic stroke, but results remain…”
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    Journal Article
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    Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes by Dunn, Paul, Albury, Cassie L, Maksemous, Neven, Benton, Miles C, Sutherland, Heidi G, Smith, Robert A, Haupt, Larisa M, Griffiths, Lyn R

    Published in Frontiers in genetics (07-02-2018)
    “…Epilepsy is a neurological disorder characterized by an increased predisposition for seizures. Although this definition suggests that it is a single disorder,…”
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    Human Mesenchymal Stem Cells Retain Multilineage Differentiation Capacity Including Neural Marker Expression after Extended In Vitro Expansion by Okolicsanyi, Rachel K, Camilleri, Emily T, Oikari, Lotta E, Yu, Chieh, Cool, Simon M, van Wijnen, Andre J, Griffiths, Lyn R, Haupt, Larisa M

    Published in PloS one (10-09-2015)
    “…The suitability of human mesenchymal stem cells (hMSCs) in regenerative medicine relies on retention of their proliferative expansion potential in conjunction…”
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    Evaluation of a 7-Gene Genetic Profile for Athletic Endurance Phenotype in Ironman Championship Triathletes by Grealy, Rebecca, Herruer, Jasper, Smith, Carl L E, Hiller, Doug, Haseler, Luke J, Griffiths, Lyn R

    Published in PloS one (30-12-2015)
    “…Polygenic profiling has been proposed for elite endurance performance, using an additive model determining the proportion of optimal alleles in endurance…”
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    A causal role for TRESK loss of function in migraine mechanisms by Pettingill, Philippa, Weir, Greg A, Wei, Tina, Wu, Yukyee, Flower, Grace, Lalic, Tatjana, Handel, Adam, Duggal, Galbha, Chintawar, Satyan, Cheung, Jonathan, Arunasalam, Kanisa, Couper, Elizabeth, Haupt, Larisa M, Griffiths, Lyn R, Bassett, Andrew, Cowley, Sally A, Cader, M Zameel

    Published in Brain (London, England : 1878) (01-12-2019)
    “…The two-pore potassium channel, TRESK has been implicated in nociception and pain disorders. We have for the first time investigated TRESK function in human…”
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    Can Genetic Markers Predict the Sporadic Form of Alzheimer’s Disease? An Updated Review on Genetic Peripheral Markers by Theron, Danelda, Hopkins, Lloyd N, Sutherland, Heidi G, Griffiths, Lyn R, Fernandez, Francesca

    “…Alzheimer’s disease (AD) is the most common form of dementia that affects millions of individuals worldwide. Although the research over the last decades has…”
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    Review: Alternative Splicing (AS) of Genes As An Approach for Generating Protein Complexity by Roy, Bishakha, Haupt, Larisa M, Griffiths, Lyn R

    Published in Current genomics (01-05-2013)
    “…Prior to the completion of the human genome project, the human genome was thought to have a greater number of genes as it seemed structurally and functionally…”
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    Exploiting Heparan Sulfate Proteoglycans in Human Neurogenesis-Controlling Lineage Specification and Fate by Yu, Chieh, Griffiths, Lyn R, Haupt, Larisa M

    Published in Frontiers in integrative neuroscience (17-10-2017)
    “…Unspecialized, self-renewing stem cells have extraordinary application to regenerative medicine due to their multilineage differentiation potential. Stem cell…”
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    Exonic mutations in cell–cell adhesion may contribute to CADASIL-related CSVD pathology by Dunn, Paul J., Lea, Rodney A., Maksemous, Neven, Smith, Robert A., Sutherland, Heidi G., Haupt, Larisa M., Griffiths, Lyn R.

    Published in Human genetics (01-09-2023)
    “…Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a condition caused by mutations in NOTCH3 and results…”
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    The gene SMART study: method, study design, and preliminary findings by Yan, Xu, Eynon, Nir, Papadimitriou, Ioannis D, Kuang, Jujiao, Munson, Fiona, Tirosh, Oren, O'Keefe, Lannie, Griffiths, Lyn R, Ashton, Kevin J, Byrne, Nuala, Pitsiladis, Yannis P, Bishop, David J

    Published in BMC genomics (14-11-2017)
    “…The gene SMART (genes and the Skeletal Muscle Adaptive Response to Training) Study aims to identify genetic variants that predict the response to both a single…”
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    The effects of OPRM1 118A>G on methadone response in pain management in advanced cancer at end of life by 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

    Published in Scientific reports (10-02-2024)
    “…Cancer pain is the most feared symptom at end of life. Methadone has advantages over other opioids but is associated with significant variability in clinical…”
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    Shared Molecular Genetic Mechanisms Underlie Endometriosis and Migraine Comorbidity by Adewuyi, Emmanuel O, Sapkota, Yadav, International Endogene Consortium Iec, andMe Research Team, International Headache Genetics Consortium Ihgc, Auta, Asa, Yoshihara, Kosuke, Nyegaard, Mette, Griffiths, Lyn R, Montgomery, Grant W, Chasman, Daniel I, Nyholt, Dale R

    Published in Genes (29-02-2020)
    “…Observational epidemiological studies indicate that endometriosis and migraine co-occur within individuals more than expected by chance. However, the aetiology…”
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    Associations between Cerebrovascular Function and the Expression of Genes Related to Endothelial Function in Hormonal Migraine by Dzator, Jemima S A, Smith, Robert A, Coupland, Kirsten G, Howe, Peter R C, Griffiths, Lyn R

    “…There is evidence to suggest that hormonal migraine is associated with altered cerebrovascular function. We aimed to investigate whether the expression of…”
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    GSTM1 and GSTT1 polymorphisms associated with pain in a chemotherapy-induced peripheral neuropathy cohort by Dunn, Paul J., Griffiths, Lyn R., Yates, Patsy, Haupt, Larisa M., Alexander, Kim E.

    “…Purpose Chemotherapy induced peripheral neuropathy (CIPN) is a debilitating condition that is a direct consequence of receiving cancer treatment. The molecular…”
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    Association of KCNJ6 rs2070995 and methadone response for pain management in advanced cancer at end-of-life by 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.

    Published in Scientific reports (19-10-2022)
    “…Opioids are the therapeutic agents of choice to manage moderate to severe pain in patients with advanced cancer, however the unpredictable inter-individual…”
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    Saliva as a comparable-quality source of DNA for Whole Exome Sequencing on Ion platforms by Ibrahim, Omar, Sutherland, Heidi G., Haupt, Larisa M., Griffiths, Lyn R.

    Published in Genomics (San Diego, Calif.) (01-03-2020)
    “…Whole Exome Sequencing (WES) utilises overlapping fragments prone to sequencing artefacts. Saliva, a non-invasive source of DNA, has been successfully used in…”
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