NEW EMBO MEMBER’S REVIEW: Addressing protein localization within the nucleus

par Bickmore, Wendy A., Sutherland, Heidi G.E.
Publié 2002

NEW EMBO MEMBER’S REVIEW: Addressing protein localization within the nucleus

par Bickmore, Wendy A., Sutherland, Heidi G.E.
Publié 2002

Exploring the Hereditary Nature of Migraine

par Bron, Charlene, Sutherland, Heidi G, Griffiths, Lyn R
Publié dans Neuropsychiatr Dis Treat (2021)

Studies on the Pathophysiology and Genetic Basis of Migraine

par Gasparini, Claudia F, Sutherland, Heidi G., Griffiths, Lyn R
Publié 2013

Advances in genetics of migraine

par Sutherland, Heidi G., Albury, Cassie L., Griffiths, Lyn R.
Publié dans J Headache Pain (2019)

KRAB zinc-finger proteins localise to novel KAP1-containing foci that are adjacent to PML nuclear bodies

par Briers, Stephanie, Crawford, Catherine, Bickmore, Wendy A., Sutherland, Heidi G.
Publié 2009

Dysregulated MicroRNA Expression Profiles and Potential Cellular, Circulating and Polymorphic Biomarkers in Non-Hodgkin Lymphoma

par Bradshaw, Gabrielle, Sutherland, Heidi G., Haupt, Larisa M., Griffiths, Lyn R.
Publié dans Genes (Basel) (2016)

Whole-Exome Sequencing Implicates SCN2A in Episodic Ataxia, but Multiple Ion Channel Variants May Contribute to Phenotypic Complexity

par Maksemous, Neven, Smith, Robert A., Sutherland, Heidi G., Sampaio, Hugo, Griffiths, Lyn R.
Publié dans Int J Mol Sci (2018)

Psip1/Ledgf p52 Binds Methylated Histone H3K36 and Splicing Factors and Contributes to the Regulation of Alternative Splicing

par Pradeepa, Madapura M., Sutherland, Heidi G., Ule, Jernej, Grimes, Graeme R., Bickmore, Wendy A.
Publié 2012

Comprehensive Exonic Sequencing of Known Ataxia Genes in Episodic Ataxia

par Maksemous, Neven, Sutherland, Heidi G., Smith, Robert A., Haupt, Larisa M., Griffiths, Lyn R.
Publié dans Biomedicines (2020)

Exploring Neuronal Vulnerability to Head Trauma Using a Whole Exome Approach

par Ibrahim, Omar, Sutherland, Heidi G., Maksemous, Neven, Smith, Robert, Haupt, Larisa M., Griffiths, Lyn R.
Publié dans J Neurotrauma (2020)

Psip1/Ledgf p75 restrains Hox gene expression by recruiting both trithorax and polycomb group proteins

par Pradeepa, Madapura M., Grimes, Graeme R., Taylor, Gillian C.A., Sutherland, Heidi G., Bickmore, Wendy A.
Publié 2014

Genetic and epigenetic variants in the MTHFR gene are not associated with non-Hodgkin lymphoma

par Bradshaw, Gabrielle, Sutherland, Heidi G., Camilleri, Emily T., Lea, Rodney A., Haupt, Larisa M., Griffiths, Lyn R.
Publié dans Meta Gene (2015)

Single Nucleotide Polymorphisms in MIR143 Contribute to Protection against Non-Hodgkin Lymphoma (NHL) in Caucasian Populations

par Bradshaw, Gabrielle, Haupt, Larisa M., Aquino, Eunise M., Lea, Rodney A., Sutherland, Heidi G., Griffiths, Lyn R.
Publié dans Genes (Basel) (2019)

Methylome-wide association study of whole blood DNA in the Norfolk Island isolate identifies robust loci associated with age

par Benton, Miles C., Sutherland, Heidi G., Macartney-Coxson, Donia, Haupt, Larisa M., Lea, Rodney A., Griffiths, Lyn R.
Publié dans Aging (Albany NY) (2017)

Disruption of Ledgf/Psip1 Results in Perinatal Mortality and Homeotic Skeletal Transformations

par Sutherland, Heidi G., Newton, Kathryn, Brownstein, David G., Holmes, Megan C., Kress, Clémence, Semple, Colin A., Bickmore, Wendy A.
Publié 2006

Case-control study of ADARB1 and ADARB2 gene variants in migraine

par Gasparini, Claudia F, Sutherland, Heidi G, Maher, Bridget, Rodriguez-Acevedo, Astrid J, Khlifi, Elhame, Haupt, Larisa M, Griffiths, Lyn R
Publié dans J Headache Pain (2015)

Gene‐centric analysis implicates nuclear encoded mitochondrial protein gene variants in migraine susceptibility

par Stuart, Shani, Benton, Miles C., Eccles, David A., Sutherland, Heidi G., Haupt, Larisa M., Lea, Rodney A., Griffiths, Lyn R.
Publié dans Mol Genet Genomic Med (2017)

G9a Histone Methyltransferase Contributes to Imprinting in the Mouse Placenta

par Wagschal, Alexandre, Sutherland, Heidi G., Woodfine, Kathryn, Henckel, Amandine, Chebli, Karim, Schulz, Reiner, Oakey, Rebecca J., Bickmore, Wendy A., Feil, Robert
Publié 2008

A CREB1 Gene Polymorphism (rs2253206) Is Associated with Prospective Memory in a Healthy Cohort

par Avgan, Nesli, Sutherland, Heidi G., Lea, Rodney A., Spriggens, Lauren K., Haupt, Larisa M., Shum, David H. K., Griffiths, Lyn R.
Publié dans Front Behav Neurosci (2017)