Browse By Person: Sutherland, Heidi

Gyimesi, Martina, Oikari, Lotta E., Yu, Chieh, Sutherland, Heidi G., Nyholt, Dale R., Griffiths, Lyn R., Van Wijnen, Andre J., Okolicsanyi, Rachel K., & Haupt, Larisa M. (2024) CpG methylation changes in human mesenchymal and neural stem cells in response to in vitro niche modifications. Biochimie, 223, pp. 147-157.

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.

Sutherland, Heidi G., Jenkins, Bronwyn, & Griffiths, Lyn R. (2024) Genetics of migraine: complexity, implications, and potential clinical applications. The Lancet Neurology, 23(4), pp. 429-446.

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Alfayyadh, Mohammed M., Maksemous, Neven, Sutherland, Heidi G., Lea, Rod A., & Griffiths, Lyn R. (2024) Unravelling the Genetic Landscape of Hemiplegic Migraine: Exploring Innovative Strategies and Emerging Approaches. Genes, 15(4), Article number: 443.

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.

Avgan, Nesli, Sutherland, Heidi G., Lea, Rod A., Haupt, Larisa M., Shum, David H.K., & Griffiths, Lyn R. (2024) Association Study of a Comprehensive Panel of Neuropeptide-Related Polymorphisms Suggest Potential Roles in Verbal Learning and Memory. Genes, 15(1), Article number: 30.

Mehta, Divya, de Boer, Irene, Sutherland, Heidi G., Pijpers, Judith A., Bron, Charlene, Bainomugisa, Charlotte, Haupt, Larisa M., van den Maagdenberg, Arn M.J.M., Griffiths, Lyn R., Nyholt, Dale R., & Terwindt, Gisela M. (2023) Alterations in DNA methylation associate with reduced migraine and headache days after medication withdrawal treatment in chronic migraine patients: a longitudinal study. Clinical Epigenetics, 15, Article number: 190.

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Cao, Thao Van, Sutherland, Heidi G., Benton, Miles C., Haupt, Larisa M., Lea, Rodney A., & Griffiths, Lyn R. (2023) Exploring the Functional Basis of Epigenetic Aging in Relation to Body Fat Phenotypes in the Norfolk Island Cohort. Current Issues in Molecular Biology, 45(10), pp. 7862-7877.

Theron, Danelda, Hopkins, Lloyd N., Sutherland, Heidi G., Griffiths, Lyn R., & Fernandez, Francesca (2023) Can Genetic Markers Predict the Sporadic Form of Alzheimer's Disease? An Updated Review on Genetic Peripheral Markers. International Journal of Molecular Sciences, 24(17), Article number: 13480.

Dunn, Paul J., Lea, Rodney A., Maksemous, Neven, Smith, Robert A., Sutherland, Heidi G., Haupt, Larisa M., & Griffiths, Lyn R. (2023) Exonic mutations in cell-cell adhesion may contribute to CADASIL-related CSVD pathology. Human Genetics, 142(9), pp. 1361-1373.

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Maksemous, Neven, Harder, Aster V.E., Ibrahim, Omar, Vijfhuizen, Lisanne S., Sutherland, Heidi, Pelzer, Nadine, de Boer, Irene, Terwindt, Gisela M., Lea, Rodney A., van den Maagdenberg, Arn M.J.M., & Griffiths, Lyn R. (2023) Whole Exome Sequencing of Hemiplegic Migraine Patients Shows an Increased Burden of Missense Variants in CACNA1H and CACNA1I Genes. Molecular Neurobiology, 60(6), pp. 3034-3043.

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Sutherland, Heidi G. & Griffiths, Lyn R. (2023) Circadian Factors in Cluster Headache and Migraine: It's All About the Timing. Neurology, 100(22), pp. 1035-1036.

Ghaiyed, A. P., Sutherland, H., Lea, R. A., Gardam, T., Chaseling, J., James, K., Bernie, A., Haupt, L. M., Christie, J., Griffiths, L. R., & Wright, K. M. (2023) Evaluation of an ancestry prediction strategy for historical military remains using a World War II-era sample and pedigrees with family-level admixture. Australian Journal of Forensic Sciences, 55(4), pp. 456-473.

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.

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Connell, J. R., Benton, M. C., Lea, R. A., Sutherland, H. G., Chaseling, J., Haupt, L. M., Wright, K. M., & Griffiths, L. R. (2022) Pedigree derived mutation rate across the entire mitochondrial genome of the Norfolk Island population. Scientific Reports, 12, Article number: 6827.

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Connell, Jasmine R., Benton, Miles C., Lea, Rodney A., Sutherland, Heidi G., Haupt, Larisa M., Wright, Kirsty M., & Griffiths, Lyn R. (2022) Evaluating the suitability of current mitochondrial DNA interpretation guidelines for multigenerational whole mitochondrial genome comparisons. Journal of Forensic Sciences, 67(5), pp. 1766-1775.

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Dunn, P. J., Harvey, N. R., Maksemous, N., Smith, R. A., Sutherland, H. G., Haupt, L. M., & Griffiths, L. R. (2022) Investigation of Mitochondrial Related Variants in a Cerebral Small Vessel Disease Cohort. Molecular Neurobiology, 59(9), pp. 5366-5378.

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Maksemous, Neven, Blayney, Claire D, Sutherland, Heidi, Smith, Robert, Lea, Rodney, Tran, Kim Ngan, Abdelrahman, Omar, McArthur, Jeffrey R., Haupt, Larisa, Cader, M. Zameel, Finol-Urdaneta, Rocio K., Adams, David J., & Griffiths, Lyn (2022) Investigation of CACNA1I Cav3.3 Dysfunction in Hemiplegic Migraine. Frontiers in Molecular Neuroscience, 15, Article number: 892820.

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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.

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Ibrahim, Omar, Sutherland, Heidi G., Lea, Rodney A., Nasrallah, Fatima, Maksemous, Neven, Smith, Robert A., Haupt, Larisa M., & Griffiths, Lyn R. (2022) Discriminating head trauma outcomes using machine learning and genomics. Journal of Molecular Medicine, 100(2), pp. 303-312.

Dunn, Paul J., Lea, Rodney A., Maksemous, Neven, Smith, Robert A., Sutherland, Heidi G., Haupt, Larisa M., & Griffiths, Lyn R. (2022) Investigating a Genetic Link Between Alzheimer's Disease and CADASIL-Related Cerebral Small Vessel Disease. Molecular Neurobiology, 59(12), pp. 7293-7302.

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Elliott, Esther K., Hopkins, Lloyd N., Hensen, Robert, Sutherland, Heidi G., Haupt, Larisa M., & Griffiths, Lyn R. (2021) Epigenetic Regulation of miR-92a and TET2 and Their Association in Non-Hodgkin Lymphoma. Frontiers in Genetics, 12, Article number: 768913.

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Tran, Ngan K., Lea, Rodney A., Holland, Samuel, Nguyen, Quan, Raghubar, Arti M., Sutherland, Heidi G., Benton, Miles C., Haupt, Larisa M., Blackburn, Nicholas B., Curran, Joanne E., Blangero, John, Mallett, Andrew J., & Griffiths, Lyn R. (2021) Multi-phenotype genome-wide association studies of the Norfolk Island isolate implicate pleiotropic loci involved in chronic kidney disease. Scientific Reports, 11(1), Article number: 19425.

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Bainomugisa, Charlotte K., Sutherland, Heidi G., Parker, Richard, Mcrae, Allan F., Haupt, Larisa M., Griffiths, Lyn R., Heath, Andrew, Nelson, Elliot C., Wright, Margaret J., Hickie, Ian B., Martin, Nicholas G., Nyholt, Dale R., & Mehta, Divya (2021) Using Monozygotic Twins to Dissect Common Genes in Posttraumatic Stress Disorder and Migraine. Frontiers in Neuroscience, 15, Article number: 678350.

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Cao, Van T., Lea, Rodney A., Sutherland, Heidi G., Benton, Miles C., Pishva, Reza S., Haupt, Larisa M., & Griffiths, Lyn R. (2021) A genome-wide methylation study of body fat traits in the Norfolk Island isolate. Nutrition, Metabolism and Cardiovascular Diseases, 31(5), pp. 1556-1563.

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Bron, Charlene, Sutherland, Heidi G., & Griffiths, Lyn R. (2021) Exploring the hereditary nature of migraine. Neuropsychiatric Disease and Treatment, 17, pp. 1183-1194.

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Groh, Isabel Anna Maria, Riva, Alessandra, Braun, Dominik, Sutherland, Heidi G., Williams, Owen, Bakuradze, Tamara, Pahlke, Gudrun, Richling, Elke, Haupt, Larisa M., Griffiths, Lyn R., Berry, David, & Marko, Doris (2021) Long-term consumption of anthocyanin-rich fruit juice: impact on gut microbiota and antioxidant markers in lymphocytes of healthy males. Antioxidants, 10(1), Article number: 27.

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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.

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Ibrahim, Omar, Sutherland, Heidi G., Maksemous, Neven, Smith, Robert, Haupt, Larisa M., & Griffiths, Lyn R. (2020) Exploring neuronal vulnerability to head trauma using a whole exome approach. Journal of Neurotrauma, 37(17), pp. 1870-1879.

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Maksemous, Neven, Sutherland, Heidi G., Smith, Robert A., Haupt, Larisa M., & Griffiths, Lyn R. (2020) Comprehensive exonic sequencing of known ataxia genes in episodic ataxia. Biomedicines, 8(5), Article number: 134.

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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.

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Harvey, N. R., Voisin, Sarah, Dunn, Paul J., Sutherland, H., Yan, Xu, Jacques, Macsue, Papadimitriou, Ioannis D., Haseler, Luke J., Ashton, Kevin J., Haupt, L. M., Eynon, Nir, & Griffiths, Lyn R. (2020) Genetic variants associated with exercise performance in both moderately trained and highly trained individuals. Molecular Genetics and Genomics, 295(2), pp. 515-523.

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Abdelrahman, Omar, Sutherland, Heidi, Haupt, Larisa, & Griffiths, Lyn (2020) Saliva as a comparable-quality source of DNA for Whole Exome Sequencing on Ion platforms. Genomics, 112(2), pp. 1437-1443.

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Dunn, P. J., Maksemous, N., Sutherland, H. G., Haupt, L. M., & Griffiths, L. R. (2020) Investigating diagnostic sequencing techniques for CADASIL diagnosis. Human Genomics, 14, Article number: 2.

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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.

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Benton, Miles C., Lea, Rodney A., MacArtney-Coxson, Donia, Sutherland, Heidi G., White, Nicole, Kennedy, Daniel, Mengersen, Kerry, Haupt, Larisa M., & Griffiths, Lyn R. (2019) Genome-wide allele-specific methylation is enriched at gene regulatory regions in a multi-generation pedigree from the Norfolk Island isolate. Epigenetics and Chromatin, 12, Article number: 60.

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

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Bradshaw, Gabrielle, Haupt, Larisa, Aquino, Eunise, Lea, Rodney, Sutherland, Heidi, & Griffiths, Lyn (2019) Single nucleotide polymorphisms in MIR143 contribute to protection against non-Hodgkin lymphoma (NHL) in Caucasian populations. Genes, 10(3), Article number: 185 1-20.

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Maksemous, Neven, Smith, Robert, Sutherland, Heidi, Maher, Bridget, Abdelrahman, Omar, Nicholson, Garth A., Carpenter, Elisabeth, Lea, Rodney, Cader, Zameel M., & Griffiths, Lyn (2019) Targeted next generation sequencing identifies a genetic spectrum of DNA variants in patients with hemiplegic migraine. Cephalalgia Reports, 2, pp. 1-9.

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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.

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Aquino, Eunise, Benton, Miles, Haupt, Larisa, Sutherland, Heidi, Griffiths, Lyn, & Lea, Rodney (2018) Current understanding of DNA methylation and age-related disease. OBM Genetics, 2(2), Article number: 016 1-17.

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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.

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Abdelrahman, Omar, Sutherland, Heidi, Avgan, Nesli, Spriggens, Lauren, Lea, Rodney, Haupt, Larisa, Shum, David, & Griffiths, Lyn (2018) Investigation of the CADM2 polymorphism rs17518584 in memory and executive functions measures in a cohort of young healthy individuals. Neurobiology of Learning and Memory, 155, pp. 330-336.

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Pollock, Charmaine, Sutherland, Heidi, Maher, Bridget, Lea, Rodney, Haupt, Larisa, Frith, Alison, MacGregor, E. Anne, & Griffiths, Lyn (2018) The NRP1 migraine risk variant shows evidence of association with menstrual migraine. Journal of Headache and Pain, 19, Article number: 31 1-7.

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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.

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Maksemous, Neven, Smith, Robert, Sutherland, Heidi, Sampaio, Hugo, & Griffiths, Lyn (2018) Whole-exome sequencing implicates SCN2A in episodic ataxia, but multiple ion channel variants may contribute to phenotypic complexity. International Journal of Molecular Sciences, 19(10), Article number: 3113 1-9.

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Abdelrahman, Omar, Sutherland, Heidi, Haupt, Larisa, & Griffiths, Lyn (2018) An emerging role for epigenetic factors in relation to executive function. Briefings in Functional Genomics, 17(3), pp. 170-180.

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Avgan, Nesli, Sutherland, Heidi, Spriggens, Lauren, Yu, Chieh, Abdelrahman, Omar Ezzeldin Ibrahim, Bellis, Claire, Haupt, Larisa, Shum, David, & Griffiths, Lyn (2017) BDNF variants may modulate long-term visual memory performance in a healthy cohort. International Journal of Molecular Sciences, 18(3), Article number: 655 1-14.

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Avgan, Nesli, Sutherland, Heidi, Lea, Rodney, Spriggens, Lauren, Haupt, Larisa, Shum, David, & Griffiths, Lyn (2017) A CREB1 gene polymorphism (rs2253206) is associated with prospective memory in a healthy cohort. Frontiers in Behavioral Neuroscience, 11, Article number: 86 1-9.

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Stuart, Shani, Benton, Miles, Eccles, David, Sutherland, Heidi, Haupt, Larisa, Lea, Rodney, & Griffiths, Lyn (2017) Gene-centric analysis implicates nuclear encoded mitochondrial protein gene variants in migraine susceptibility. Molecular Genetics and Genomic Medicine, 5(2), pp. 157-163.

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Sutherland, Heidi & Griffiths, Lyn (2017) Genetics of migraine: Insights into the molecular basis of migraine disorders. Headache, 57(4), pp. 537-569.

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Sutherland, Heidi, Champion, Morgane, Plays, Amelie, Stuart, Shani, Haupt, Larisa, Frith, Alison, MacGregor, E. Anne, & Griffiths, Lyn (2017) Investigation of polymorphisms in genes involved in estrogen metabolism in menstrual migraine. Gene, 607, pp. 36-40.

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Benton, Miles, Sutherland, Heidi, Macartney-Coxson, Donia, Haupt, Larisa, Lea, Rodney, & Griffiths, Lyn (2017) Methylome-wide association study of whole blood DNA in the Norfolk Island isolate identifies robust loci associated with age. Aging, 9(3), pp. 753-768.

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Bradshaw, Gabrielle, Sutherland, Heidi, Haupt, Larisa, & Griffiths, Lyn (2016) Dysregulated microRNA expression profiles and potential cellular, circulating and polymorphic biomarkers in non-Hodgkin Lymphoma. Genes, 7(12), Article number: 130 1-19.

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Loo, Keat Wei, Sutherland, Heidi, Au, Anthony, Camilleri, Emily, Haupt, Larisa, Gan, Siew Hua, & Griffiths, Lyn (2016) Methylenetetrahydrofolate reductase CpG islands: Epigenotyping. Journal of Clinical Laboratory Analysis, 30(4), pp. 335-344.

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Gasparini, Claudia, Sutherland, Heidi, Maher, Bridget, Rodriguez Acevedo, Astrid Jannet, Khlifi, Elhame, Haupt, Larisa, & Griffiths, Lyn (2015) Case-control study of ADARB1 and ADARB2 gene variants in migraine. Journal of Headache and Pain, 16, Article number: 31 1-8.

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Menon, Saras, Lea, Rodney, Ingle, Sarah, Sutherland, Heidi, Wee, Shirley, Haupt, Larisa, Palmer, Michelle, & Griffiths, Lyn (2015) Effects of dietary folate intake on migraine disability and frequency. Headache, 55(2), pp. 301-309.

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Bradshaw, Gabrielle, Sutherland, Heidi, Camilleri, Emily, Lea, Rodney, Haupt, Larisa, & Griffiths, Lyn (2015) Genetic and epigenetic variants in the MTHFR gene are not associated with non-Hodgkin lymphoma. Meta Gene, 6, pp. 91-95.

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Loo, Keat Wei, Sutherland, Heidi, Au, Anthony, Camilleri, Emily, Haupt, Larisa, Gan, Siew Hua, & Griffiths, Lyn (2015) A potential epigenetic marker mediating serum folate and vitamin B12 levels contributes to the risk of ischemic stroke. BioMed Research International, 2015, Article number: 167976 1-4.

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Sutherland, Heidi, Hermile, Heloise, Sanche, Rebecca, Menon, Saras, Lea, Rodney, Haupt, Larisa, & Griffiths, Lyn (2014) Association study of MTHFD1 coding polymorphisms R134K and R653Q with migraine susceptibility. Headache, 54(9), pp. 1506-1514.

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Wei, Keat, Sutherland, Heidi, Camilleri, Emily, Haupt, Larisa, Griffiths, Lyn, & Gan, Siew Hua (2014) Computational epigenetic profiling of CpG islets in MTHFR. Molecular Biology Reports, 41(12), pp. 8285-8292.

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Gasparini, Claudia, Sutherland, Heidi, Haupt, Larisa, & Griffiths, Lyn (2014) Genetic analysis of GRIA2 and GRIA4 genes in migraine. Headache, 54(2), pp. 303-312.

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Rodriguez Acevedo, Astrid Jannet, Smith, Robert, Roy, Bishakha, Sutherland, Heidi, Lea, Rodney, Frith, Alison, MacGregor, Anne, & Griffiths, Lyn (2014) Genetic association and gene expression studies suggest that genetic variants in the SYNE1 and TNF genes are related to menstrual migraine. Journal of Headache and Pain, 15, Article number: 62 1-9.

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Sutherland, Heidi, Maher, Bridget, Rodriguez Acevedo, Astrid Jannet, Haupt, Larisa, & Griffiths, Lyn (2014) Investigation of brain-derived neurotrophic factor (BDNF) gene variants in migraine. Headache, 54(7), pp. 1184-1193.

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Pradeepa, Madapura, Grimes, Graeme, Taylor, Gillian, Sutherland, Heidi, & Bickmore, Wendy (2014) Psip1/Ledgf p75 restrains Hox gene expression by recruiting both trithorax and polycomb group proteins. Nucleic Acids Research, 42(14), pp. 9021-9032.

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Avgan, Nesli, Sutherland, Heidi, Spriggens, Lauren, Rodriguez-Acevedo, Astrid, Haupt, Larisa, Shum, David, & Griffiths, Lyn (2014) Variation H452Y in HTR2A gene affects immediate visual memory. Journal of Genetics and Genome Research, 1(2), pp. 1-4.

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Maher, Bridget, Taylor, Megan, Stuart, Shani, Okolicsanyi, Rachel K., Roy, Bishakha, Sutherland, Heidi, Haupt, Larisa, & Griffiths, Lyn (2013) Analysis of 3 common polymorphisms in the KCNK18 gene in an Australian Migraine Case-control cohort. Gene, 528(2), pp. 343-346.

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Sutherland, Heidi, Buteri, J., Menon, Saras, Haupt, Larisa, MacGregor, E., Lea, Rodney, & Griffiths, Lyn (2013) Association study of the calcitonin gene-related polypeptide-alpha (CALCA) and the receptor activity modifying 1 (RAMP1) genes with migraine. Gene, 515(1), pp. 187-192.

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Yogeetha, B.S., Haupt, Larisa, McKenzie, K., Sutherland, Heidi, Okolicsanyi, Rachel K., Lea, Rodney, Maher, Bridget, Chan, Raymond, Shum, David, & Griffiths, Lyn (2013) BDNF and TNF-alpha polymorphisms in memory. Molecular Biology Reports, 40(9), pp. 5483-5490.

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Stuart, Shani, Maher, Bridget, Sutherland, Heidi, Benton, Miles, Rodriguez-Acevedo, Astrid, Lea, Rodney, Haupt, Larisa, & Griffiths, Lyn (2013) Genetic variation in cytokine-related genes and migraine susceptibility. Twin Research and Human Genetics, 16(6), pp. 1076-1086.

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Gasparini, Claudia, Sutherland, Heidi, & Griffiths, Lyn (2013) Studies on the pathophysiology and genetic basis of migraine. Current Genomics, 14(5), pp. 300-315.

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Pradeepa, Madapura, Sutherland, Heidi, Ule, Jernej, Grimes, Graeme, & Bickmore, Wendy (2012) Psip1/ledgf p52 binds methylated histone H3K36 and splicing factors and contributes to the regulation of alternative splicing. PLoS Genetics, 8(5), Article number: e1002717 1-15.

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Briers, Stephanie, Crawford, Catherine, Bickmore, Wendy, & Sutherland, Heidi (2009) KRAB zinc-finger proteins localise to novel KAP1-containing foci that are adjacent to PML nuclear bodies. Journal of Cell Science, 122(7), pp. 937-946.

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Sutherland, Heidi & Bickmore, Wendy (2009) Transcription factories: gene expression in unions? Nature Reviews Genetics, 10(7), pp. 457-466.

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Wagschal, Alexandre, Sutherland, Heidi, Woodfine, Kathryn, Henckel, Amandine, Chebli, Karim, Schulz, Reiner, Oakey, Rebecca, Bickmore, Wendy, & Feil, Robert (2008) G9a histone methyltransferase contributes to imprinting in the mouse placenta. Molecular and Cellular Biology, 28(3), pp. 1104-1113.

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Michailidou, Zoi, Carter, Rod, Marshall, E., Sutherland, Heidi, Brownstein, David, Owen, E., Cockett, K., Kelly, V., Ramage, Lynne, Al-Dujaili, E.A.S., Ross, M., Maraki, Ioanna, Newton, K., Holmes, Megan, Seckl, Jonathan, Morton, Nik, Kenyon, Chris, & Chapman, Karen (2008) Glucocorticoid receptor haploinsufficiency causes hypertension and attenuates hypothalamic-pituitary-adrenal axis and blood pressure adaptions to high-fat diet. FASEB Journal, 22(11), pp. 3896-3907.

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Marshall, Heather M., Ronen, Keshet, Berry, Charles, Llano, Manuel, Sutherland, Heidi, Saenz, Dyana, Bickmore, Wendy, Poeschla, Eric, & Bushman, Frederic D. (2007) Role of PSIP 1/LEDGF/p75 in lentiviral infectivity and integration targeting. PLoS ONE, 2(12), Article number: e1340.

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Sutherland, Heidi G., Newton, Kathryn, Brownstein, David G., Holmes, Megan C., Kress, Clémence, Semple, Colin A., & Bickmore, Wendy A. (2006) Disruption of Ledgf/Psip1 results in perinatal mortality and homeotic skeletal transformations. Molecular and Cellular Biology, 26(19), pp. 7201-7210.

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Sutherland, Heidi G.E., Lam, Yun Wah, Briers, Stephanie, Lamond, Angus I., & Bickmore, Wendy A. (2004) 3D3/lyric: A novel transmembrane protein of the endoplasmic reticulum and nuclear envelope, which is also present in the nucleolus. Experimental Cell Research, 294(1), pp. 94-105.

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Gilbert, Nick, Boyle, Shelagh, Sutherland, Heidi, Las Heras, Jose de, Allan, James, Jenuwein, Thomas, & Bickmore, Wendy A. (2003) Formation of facultative heterochromatin in the absence of HP1. EMBO Journal, 22(20), pp. 5540-5550.

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Bickmore, Wendy A. & Sutherland, Heidi G.E. (2002) Erratum: Addressing protein localization within the nucleus (EMBO Journal (2002) 21 (1248-1254)). EMBO Journal, 21(10), p. 2507.

Bickmore, Wendy A. & Sutherland, Heidi G.E. (2002) Addressing protein localization within the nucleus. EMBO Journal, 21(6), pp. 1248-1254.

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Dellaire, Graham, Makarov, Evgeny M., Cowger, Jeff J.M., Longman, Dasa, Sutherland, Heidi G.E., Lührmann, Reinhard, Torchia, Joseph, & Bickmore, Wendy A. (2002) Mammalian PRP4 kinase copurifies and interacts with components of both the U5 snRNP and the N-CoR deacetylase complexes. Molecular and Cellular Biology, 22(14), pp. 5141-5156.

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Sutherland, Heidi G.E., Mumford, Gail K., Newton, Kathryn, Ford, Lisa V., Farrall, Rachel, Dellaire, Graham, Cáceres, J. F., & Bickmore, Wendy A. (2001) Large-scale identification of mammalian proteins localized to nuclear sub-compartments. Human Molecular Genetics, 10(18), pp. 1995-2011.

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Whitelaw, Emma, Sutherland, Heidi, Kearns, Margot, Morgan, Hugh, Weaving, Linda, & Garrick, David (2001) Epigenetic effects on transgene expression. In Tymms, Martin J. & Kola, Ismail (Eds.) Gene Knockout Protocols. Humana Press, Totowa, New Jersey, pp. 351-368.

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Sutherland, Heidi G.E., Kearns, Margot, Morgan, Hugh D., Headley, Alexander P., Morris, Christine, Martin, David I.K., & Whitelaw, Emma (2000) Reactivation of heritably silenced gene expression in mice. Mammalian Genome, 11(5), pp. 347-355.

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