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Number of items: 54.

Davies, William 2019. An analysis of Cellular Communication Network (CCN) proteins as candidate mediators of postpartum psychosis risk. Frontiers in Psychiatry 10 , 876. 10.3389/fpsyt.2019.00876

O'Brien, Heath, Hannon, Eilis, Jeffries, Aaron R., Davies, William, Hill, Matthew J., Anney, Richard, O'Donovan, Michael, Mill, Jonathan and Bray, Nicholas 2019. Sex differences in gene expression in the human fetal brain. bioRxiv , -. 10.1101/483636

Cavenagh, Alice, Chatterjee, Sohini and Davies, William 2019. Behavioural and psychiatric phenotypes in female carriers of genetic mutations associated with X-linked ichthyosis. PLoS ONE 14 (2) , e0212330. 10.1371/journal.pone.0212330

Davies, William and Wilkinson, Lawrence 2019. Editorial overview: special issue on epigenetics and genomic imprinting. Current Opinion in Behavioral Sciences 25 , iii-v. 10.1016/j.cobeha.2018.12.006
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Humby, Trevor and Davies, William 2019. Brain gene expression in a novel mouse model of postpartum mood disorder. Translational Neuroscience 10 (1) , pp. 168-174. 10.1515/tnsci-2019-0030

Dazzan, Paola, Fusté, Montserrat and Davies, William 2018. Do defective immune system-mediated myelination processes increase postpartum psychosis risk? Trends in Molecular Medicine 24 (11) , pp. 942-949. 10.1016/j.molmed.2018.09.002

Davies, William 2018. The steroid sulfate axis and its relationship to maternal behavior and mental health. Journal of Molecular Endocrinology 61 , T199-T210. 10.1530/JME-17-0219

Richards, Gareth, Davies, William, Stewart-Williams, Steve, Bellin, Wynford and Reed, Phil 2018. 2D:4D digit ratio and religiosity in university student and general population samples. Transpersonal Psychology Review 20 (1) , pp. 23-36.

Malik, Amna, Amer, Ahmed Bait, Salama, Mohammed, Haddad, Bander, Alrifai, Muhammed T, Balwi, Mohammed Al, Davies, William and Eyaid, Wafaa 2017. X-linked ichthyosis associated with psychosis and behavioral abnormalities: a case report. Journal of Medical Case Reports 11 , 267. 10.1186/s13256-017-1420-2

Richards, Gareth, Bellin, Wynford and Davies, William 2017. Familial digit ratio (2D:4D) associations in a general population sample from Wales. Early Human Development 112 , pp. 14-19. 10.1016/j.earlhumdev.2017.06.006

Green, Tamar, Naylor, Paige and Davies, William 2017. Attention Deficit Hyperactivity Disorder (ADHD) in phenotypically-similar neurogenetic conditions: Turner syndrome and the RASopathies. Journal of Neurodevelopmental Disorders 9 (25) , pp. 794-802. 10.1186/s11689-017-9205-x

Davies, William 2017. Understanding the pathophysiology of postpartum psychosis: challenges and new approaches. World Journal of Psychiatry 7 (2) , pp. 77-88. 10.5498/wjp.v7.i2.77

Humby, Trevor, Fisher, Amelia, Allen, Christopher, Reynolds, Meghann, Hartman, Annette, Giegling, Ina, Rujescu, Dan and Davies, William 2017. A genetic variant within STS previously associated with inattention in boys with Attention Deficit Hyperactivity Disorder is associated with enhanced cognition in healthy adult males. Brain and Behavior 7 (3) , e00646. 10.1002/brb3.646

Humby, Trevor, Cross, Ellen S., Messer, Lauren, Guerrero, Silvia and Davies, William 2016. A pharmacological mouse model suggests a novel risk pathway for postpartum psychosis. Psychoneuroendocrinology 74 , pp. 363-370. 10.1016/j.psyneuen.2016.09.019

Davies, William 2016. Insights into rare diseases from social media surveys. Orphanet Journal of Rare Diseases 11 , 151. 10.1186/s13023-016-0532-x

Chatterjee, Sohini, Humby, Trevor and Davies, William 2016. Behavioural and psychiatric phenotypes in men and boys with X-linked ichthyosis: evidence from a worldwide online survey. Plos One 11 (10) , e0164417. 10.1371/journal.pone.0164417

Hinton, Robert, Opoka, Amy, Ojarikre, Obah A., Wilkinson, Lawrence Stephen and Davies, William 2015. Preliminary evidence for aortopathy and an x-linked parent-of-origin effect on aortic valve malformation in a mouse model of Turner syndrome. Journal of Cardiovascular Development and Disease 2 (3) , pp. 190-199. 10.3390/jcdd2030190

Davies, William and Duncan, Laramie 2015. Editorial overview: Behavioral genetics. Current Opinion in Behavioral Sciences 2 , v-vii. 10.1016/j.cobeha.2014.12.002

Davies, William, Humby, Trevor, Trent, Simon, Eddy, Jessica B., Ojarikre, Obah A. and Wilkinson, Lawrence Stephen 2014. Genetic and pharmacological modulation of the steroid sulfatase axis improves response control; comparison to drugs used in ADHD. Neuropsychopharmacology 39 (11) , pp. 2622-2632. 10.1038/npp.2014.115

Davies, William 2014. Sex differences in Attention Deficit Hyperactivity Disorder: Candidate genetic and endocrine mechanisms. Frontiers in Neuroendocrinology 35 (3) , pp. 331-346. 10.1016/j.yfrne.2014.03.003

Trent, Simon, Fry, Jonathan P., Ojarikre, Obah A. and Davies, William 2014. Altered brain gene expression but not steroid biochemistry in a genetic mouse model of neurodevelopmental disorder. Molecular Autism 5 (1) , 21. 10.1186/2040-2392-5-21

van den Bos, Ruud, Davies, William, Dellu-Hagedorn, Francoise, Goudriaan, Anna E., Granon, Sylvie, Homberg, Judith, Rivalan, Marion, Swendsen, Joel and Adriani, Walter 2013. Cross-species approaches to pathological gambling: A review targeting sex differences, adolescent vulnerability and ecological validity of research tools. Neuroscience & Biobehavioral Reviews 37 (10.2) , pp. 2454-2471. 10.1016/j.neubiorev.2013.07.005

Kopsida, Eleni, Lynn, Phoebe M., Humby, Trevor, Wilkinson, Lawrence Stephen and Davies, William 2013. Dissociable effects of sry and sex chromosome complement on activity, feeding and anxiety-related behaviours in mice. PLoS ONE 8 (8) , e73699. 10.1371/journal.pone.0073699

Trent, Simon, Dean, Rachel, Veit, Bonnie, Cassano, Tommaso, Bedse, Gaurav, Ojarikre, Obah A., Humby, Trevor and Davies, William 2013. Biological mechanisms associated with increased perseveration and hyperactivity in a genetic mouse model of neurodevelopmental disorder. Psychoneuroendocrinology 38 (8) , pp. 1370-1380. 10.1016/j.psyneuen.2012.12.002

Trent, Simon and Davies, William 2013. Cognitive, behavioural and psychiatric phenotypes associated with steroid sulfatase deficiency. World Journal of Translational Medicine 2 (1) , pp. 1-12. 10.5528/wjtm.v2.i1.1

Davies, William 2013. Using mouse models to investigate sex-linked genetic effects on brain, behaviour and vulnerability to neuropsychiatric disorders. Brain Research Bulletin 92 , pp. 12-20. 10.1016/j.brainresbull.2011.06.018

Trent, Simon, Cassano, Tommaso, Bedse, Gaurav, Ojarikre, Obah A, Humby, Trevor and Davies, William 2012. Altered serotonergic function may partially account for behavioral endophenotypes in steroid sulfatase-deficient mice. Neuropsychopharmacology 37 (5) , pp. 1267-1274. 10.1038/npp.2011.314

Trent, Simon, Dennehy, Alison, Richardson, Heather, Ojarikre, Obah A., Burgoyne, Paul S., Humby, Trevor and Davies, William 2012. Steroid sulfatase-deficient mice exhibit endophenotypes relevant to Attention Deficit Hyperactivity Disorder. Psychoneuroendocrinology 37 (2) , pp. 221-229. 10.1016/j.psyneuen.2011.06.006

Davies, William 2012. Does steroid sulfatase deficiency influence postpartum psychosis risk? Trends in Molecular Medicine 18 (5) , pp. 256-262. 10.1016/j.molmed.2012.03.001

Stergiakouli, Evangelia, Langley, Kate, Williams, Hywel, Walters, James Tynan Rhys, Williams, Nigel Melville, Suren, S., Giegling, I., Wilkinson, Lawrence, Owen, Michael John, O'Donovan, Michael Conlon, Rujescu, D., Thapar, Anita and Davies, William 2011. Steroid sulfatase is a potential modifier of cognition in attention deficit hyperactivity disorder. Genes Brain and Behavior 10 (3) , pp. 334-344. 10.1111/j.1601-183x.2010.00672.x

Kopsida, Eleni, Mikaelsson, Mikael Allan and Davies, William 2011. The role of imprinted genes in mediating susceptibility to neuropsychiatric disorders. Hormones and Behavior 59 (3) , pp. 375-382. 10.1016/j.yhbeh.2010.04.005

Davies, William 2011. Functional themes from psychiatric genome-wide screens. Frontiers in Genetics 2 , 89. 10.3389/fgene.2011.00089

Trent, Simon and Davies, William 2011. The influence of sex-linked genetic mechanisms on attention and impulsivity. Biological Psychology 89 (1) , pp. 1-13. 10.1016/j.biopsycho.2011.09.011

Lynn, Phoebe Mei-Ying, Stergiakouli, Evangelia and Davies, William 2011. The genomics of Turner syndrome and sex-biased neuropsychiatric disorders. In: Clelland, James D. ed. Genomics, proteomics, and the nervous system, Advances in neurobiology, vol. 2. Springer, pp. 3-20.

Davies, William 2010. Genomic imprinting on the X chromosome: implications for brain and behavioral phenotypes. Annals of the New York Academy of Sciences 1204 (s1) , pp. 14-19. 10.1111/j.1749-6632.2010.05567.x

Davies, William, Humby, Trevor, Kong, Wendy, Otter, Tamara Leonie, Burgoyne, Paul S. and Wilkinson, Lawrence Stephen 2009. Converging pharmacological and genetic evidence indicates a role for steroid sulfatase in attention. Biological Psychiatry 66 (4) , pp. 360-367. 10.1016/j.biopsych.2009.01.001

Kopsida, E., Stergiakouli, E., Lynn, P. E., Wilkinson, Lawrence and Davies, William 2009. The Role of the Y Chromosome in Brain Function. The Open Neuroendocrinology Journal 2 , pp. 20-30.

Kopsida, Eleni, Stergiakouli, Evangelia, Lynn, Phoebe Mei-Ying, Wilkinson, Lawrence Stephen and Davies, William 2009. The Role of the Y Chromosome in Brain Function. Open Neuroendocrinology Journal 2 (1) , pp. 20-30. 10.2174/1876528900902010020

Davies, William, Lynn, P. M. Y., Relkovic, D. and Wilkinson, Lawrence Stephen 2008. Imprinted genes and neuroendocrine function. Frontiers in Neuroendocrinology 29 (3) , pp. 413-427. 10.1016/j.yfrne.2007.12.001

Davies, William and Isles, Anthony Roger 2008. Genomic imprinting and disorders of the social brain; shades of grey rather than black and white. Behavioral and Brain Sciences 31 (3) , pp. 265-266. 10.1017/S0140525X08004263

Davies, William, Isles, Anthony Roger, Humby, Trevor and Wilkinson, Lawrence Stephen 2008. What are imprinted genes doing in the brain? In: Wilkins, Jon F. ed. Genomic Imprinting, Advances in experimental medicine and biology, vol. 626. Berlin: Springer, pp. 62-70. (10.1007/978-0-387-77576-0_5)

Wilkinson, Lawrence Stephen, Davies, William and Isles, Anthony Roger 2007. Genomic imprinting effects on brain development and function. Nature Reviews Neuroscience 8 (11) , pp. 832-843. 10.1038/nrn2235

Davies, William, Humby, Trevor, Isles, Anthony Roger, Burgoyne, Paul S. and Wilkinson, Lawrence Stephen 2007. X-monosomy effects on visuospatial attention in mice: a candidate gene and implications for Turner syndrome and attention deficit hyperactivity disorder. Biological psychiatry 61 (12) , pp. 1351-1360. 10.1016/j.biopsych.2006.08.011

Lynn, Phoebe Mei-Ying and Davies, William 2007. The 39,XO mouse as a model for the neurobiology of Turner syndrome and sex-biased neuropsychiatric disorders. Behavioural Brain Research 179 (2) , pp. 173-182. 10.1016/j.bbr.2007.02.013

Davies, William, Isles, Anthony Roger, Humby, Trevor and Wilkinson, Lawrence Stephen 2007. What are imprinted genes doing in the brain? [Review]. Epigenetics 2 (4) , pp. 201-206. 10.4161/epi.2.4.5379

Davies, William and Wilkinson, Lawrence Stephen 2006. It is not all hormones: Alternative explanations for sexual differentiation of the brain. Brain Research 1126 (1) , pp. 36-45. 10.1016/j.brainres.2006.09.105

Isles, Anthony Roger, Davies, William and Wilkinson, Lawrence Stephen 2006. Genomic imprinting and the social brain. Philosophical Transactions of the Royal Society of London Series B - Biological Sciences 361 (1476) , pp. 2229-2237. 10.1098/rstb.2006.1942

Davies, William, Isles, Anthony Roger, Burgoyne, Paul S. and Wilkinson, Lawrence Stephen 2006. X-linked imprinting: effects on brain and behaviour. Bioessays 28 (1) , pp. 35-44. 10.1002/bies.20341

Davies, William, Isles, Anthony Roger, Smith, Rachel, Karunadasa, Delicia, Burrmann, Doreen, Humby, Trevor, Ojarikre, Obah, Biggin, Carol, Skuse, David, Burgoyne, Paul S. and Wilkinson, Lawrence Stephen 2005. Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice. Nature Genetics 37 (6) , pp. 625-629. 10.1038/ng1577

Davies, William, Isles, Anthony Roger and Wilkinson, Lawrence Stephen 2005. Imprinted gene expression in the brain. Neuroscience & Biobehavioral Reviews 29 (3) , pp. 421-430. 10.1016/j.neubiorev.2004.11.007

Davies, William, Smith, Rachel J., Kelsey, Gavin and Wilkinson, Lawrence Stephen 2004. Expression patterns of the novel imprinted genes Nap1l5 and Peg13 and their non-imprinted host genes in the adult mouse brain. Gene Expression Patterns 4 (6) , pp. 741-747. 10.1016/j.modgep.2004.03.008

Isles, Anthony Roger, Davies, William, Burrmann, Doreen, Burgoyne, Paul S. and Wilkinson, Lawrence Stephen 2004. Effects on fear reactivity in XO mice are due to haploinsufficiency of a non-PAR X gene: implications for emotional function in Turner's syndrome. Human Molecular Genetics 13 (17) , pp. 1849-1855. 10.1093/hmg/ddh203

Davies, William, Isles, Anthony Roger and Wilkinson, Lawrence Stephen 2001. Imprinted genes and mental dysfunction. Annals of Medicine 33 (6) , pp. 428-436. 10.3109/07853890108995956

Humby, Trevor, Laird, Fiona M., Davies, William and Wilkinson, Lawrence Stephen 1999. Visuospatial attentional functioning in mice: interactions between cholinergic manipulations and genotype. European Journal of Neuroscience 11 (8) , pp. 2813-2823. 10.1046/j.1460-9568.1999.00701.x

This list was generated on Sun Dec 15 05:33:02 2019 GMT.

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