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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
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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
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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
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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
Item availability restricted. |
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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
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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
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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 |
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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. |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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Davies, William
2016.
Insights into rare diseases from social media surveys.
Orphanet Journal of Rare Diseases
11
, 151.
10.1186/s13023-016-0532-x
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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
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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Davies, William 2011. Functional themes from psychiatric genome-wide screens. Frontiers in Genetics 2 , 89. 10.3389/fgene.2011.00089 |
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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 |
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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. |
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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 |
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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 |
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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. |
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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 |
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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 |
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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 |
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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) |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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