Yr Athro Anthony Isles
(e/fe)

PhD, FRSB

: Sylwebydd y cyfryngau
: Ar gael fel goruchwyliwr ôl-raddedig

Timau a rolau for Anthony Isles

Athro, Is-adran Meddygaeth Seicolegol a Niwrowyddorau Clinigol
Yr Ysgol Meddygaeth

I am a molecular and behavioural neuroscientist interested in the contribution of epigenetic mechanisms to brain and behaviour. In particular, we are investigating an intriguing family of genes, the imprinted genes, which are subject to epigenetic control acquired during development resulting in expression from one parental copy (allele) only. The research is focused on addressing what these imprinted genes are doing in the brain and how they may contribute to neurodevelopmental disorders.

Date
Type

2025

Clifton, N. E. et al. 2025. Setd1a loss-of-function disrupts epigenetic regulation of ribosomal genes via altered DNA methylation. Schizophrenia Bulletin: The Journal of Psychoses and Related Disorders (10.1093/schbul/sbaf091)

2024

Tyson, H. R., Harrison, D. J., Higgs, M. J., Isles, A. R. and John, R. M. 2024. Deficiency of the paternally-expressed imprinted Peg3 gene in mice has sexually dimorphic consequences for offspring communication and social behaviour. Frontiers in Neuroscience 18, article number: 1374781. (10.3389/fnins.2024.1374781)
Sansom, O. et al. 2024. Better translation via collaboration: The MRC National Mouse Genetics Network. Cell Genomics 4(2), article number: 100483. (10.1016/j.xgen.2023.100483)
Bosworth, M. L., Isles, A. R., Wilkinson, L. S. and Humby, T. 2024. Sex-dependent effects of Setd1a haploinsufficiency on development and adult behaviour. PLoS ONE (10.1371/journal.pone.0298717)

2023

John, R., Higgs, M. J. and Isles, A. R. 2023. Imprinted genes and the manipulation of parenting in mammals. Nature Reviews Genetics 24 (10.1038/s41576-023-00644-3)
Higgs, M., Webberley, A., Allan, A., Talat, M., John, R. and Isles, A. 2023. The parenting hub of the hypothalamus is a focus of imprinted gene action. PLoS Genetics 19(10), article number: e1010961. (10.1371/journal.pgen.1010961)

2022

Higgs, M., Hill, M., John, R. and Isles, A. 2022. Systematic investigation of imprinted gene expression and enrichment in the mouse brain explored at single-cell resolution. BMC Genomics 23, article number: 754. (10.1186/s12864-022-08986-8)
Alsaqati, M. et al. 2022. NRSF/REST lies at the intersection between epigenetic regulation, miRNA-mediated gene control and neurodevelopmental pathways associated with Intellectual disability (ID) and Schizophrenia. Translational Psychiatry 12, article number: 438. (10.1038/s41398-022-02199-z)
Clifton, N. et al. 2022. Developmental disruption to the cortical transcriptome and synaptosome in a model of SETD1A loss-of-function. Human Molecular Genetics 31(18), pp. 3095-3106. (10.1093/hmg/ddac105)
Isles, A. R. 2022. The contribution of imprinted genes to neurodevelopmental and neuropsychiatric disorders. Translational Psychiatry 12, article number: 210. (10.1038/s41398-022-01972-4)
Pregnolato, S., Sabir, H., Luyt, K., Rienecker, K. D. A., Isles, A. R. and Chakkarapani, E. 2022. Regulation of glutamate transport and neuroinflammation in a term newborn rat model of hypoxic–ischaemic brain injury. Brain and Neuroscience Advances 6, pp. 1-13. (10.1177/23982128221097568)

2021

Harrison, D. J. et al. 2021. Placental endocrine insufficiency programs anxiety, deficits in cognition and atypical social behaviour in offspring. Human Molecular Genetics 30(19), pp. 1863-1880., article number: ddab154. (10.1093/hmg/ddab154)
Zahova, S., Humby, T., Davies, J., Morgan, J. E. and Isles, A. 2021. Comparison of mouse models reveals a molecular distinction between psychotic illness in PWS and schizophrenia. Translational Psychiatry 11, article number: 433. (10.1038/s41398-021-01561-x)
Clift, J., Cooke, A., Isles, A. R., Dalley, J. W. and Henson, R. N. 2021. Lifting the lid on impact and peer review. Brain and Neuroscience Advances 5, pp. 1-7. (10.1177/23982128211006574)

2020

Dent, C. L., Rienecker, K. D. A., Ward, A., Wilkins, J. F., Humby, T. and Isles, A. R. 2020. Mice lacking paternal expression of imprinted 1 Grb10 are risk-takers. Genes, Brain and Behavior 19(7), article number: e12679. (10.1111/gbb.12679)
Davis, B., David, F., O’Regan, C., Adam, M., Harwood, A., Crunelli, V. and Isles, A. 2020. Impairments in sensory-motor gating and information processing in a mouse model of Ehmt1 haploinsufficiency. Brain and Neuroscience Advances 4 (10.1177/2398212820928647)
Harrison, D. J. et al. 2020. Unified behavioral scoring for preclinical models. Frontiers in Neuroscience 14, article number: 313. (10.3389/fnins.2020.00313)
Rienecker, K., Chavasse, A., Moorwood, K., Ward, A. and Isles, A. 2020. Detailed analysis of paternal knockout Grb10 mice suggests effects on stability of social behavior, rather than social dominance. Genes, Brain and Behavior 19(1), article number: e12571. (10.1111/gbb.12571)

2019

Davies, J. R., Wilkinson, L. S., Isles, A. R. and Humby, T. 2019. Prader-Willi syndrome imprinting centre deletion mice have impaired baseline and 5-HT2CR-mediated response inhibition. Human Molecular Genetics 28(18), pp. 3013-3023. (10.1093/hmg/ddz100)
Pregnolato, S., Chakkarapani, E., Isles, A. R. and Luyt, K. 2019. Glutamate Transport and Preterm Brain Injury. Frontiers in Physiology 10, article number: 417. (10.3389/fphys.2019.00417)
Creeth, H. D. J., McNamara, G. I., Isles, A. R. and John, R. M. 2019. Imprinted genes influencing the quality of maternal care. Frontiers in Neuroendocrinology 53, article number: 100732. (10.1016/j.yfrne.2018.12.003)
Tucci, V. et al. 2019. Genomic imprinting and physiological processes in mammals. Cell 176(5), pp. 952-965. (10.1016/j.cell.2019.01.043)
Isles, A. R., Winstanley, C. A. and Humby, T. 2019. Risk taking and impulsive behaviour: fundamental discoveries, theoretical perspectives and clinical implications. Philosophical Transactions B: Biological Sciences 374(1766), pp. -., article number: 128. (10.1098/rstb.2018.0128)
Isles, A. R. and John, R. M. 2019. Genomic imprinting and neurobehavioral programming by adverse early life environments: evidence from studying Cdkn1c. Current Opinion in Behavioral Sciences 25, pp. 31-35. (10.1016/j.cobeha.2018.06.008)

2015

Escott-Price, V., Kirov, G., Rees, E., Isles, A. R., Owen, M. J. and O'Donovan, M. C. 2015. No evidence for enrichment in schizophrenia for common allelic associations at imprinted loci. PLoS ONE 10(12), pp. -., article number: e0144172. (10.1371/journal.pone.0144172)
Creeth, H., McNamara, G., Tunster, S., Eddy, J., Isles, A. R. and John, R. 2015. Programming of maternal behaviour by the placenta: A novel animal model. Psychoneuroendocrinology 61, pp. 4., article number: PS1.1.3. (10.1016/j.psyneuen.2015.07.397)
Davies, J. R. et al. 2015. Calorie seeking, but not hedonic response, contributes to hyperphagia in a mouse model for Prader-Willi syndrome. European Journal of Neuroscience 42(4), pp. 2105-2113. (10.1111/ejn.12972)
Isles, A. R. 2015. 15q maternal duplication and neurodevelopmental disorders; UBE3A is the key. Human Mutation 36(7), pp. iii. (10.1002/humu.22656)
Davies, J. R., Dent, C., McNamara, G. and Isles, A. R. 2015. Behavioural effects of imprinted genes. Current Opinion in Behavioral Sciences 2, pp. 28-33. (10.1016/j.cobeha.2014.07.008)
Isles, A. R. 2015. Neural and behavioral epigenetics; what it is, and what is hype. Genes, Brain and Behavior 14(1), pp. 64-72. (10.1111/gbb.12184)

2014

Dent, C. L. and Isles, A. R. 2014. An Overview of measuring impulsive behavior in mice. Current Protocols in Mouse Biology 4(2), pp. 35-45. (10.1002/9780470942390.mo140015)
Davis, B. A. and Isles, A. R. 2014. Modelling the genetic contribution to mental illness: a timely end for the psychiatric rodent?. European Journal of Neuroscience 39(11), pp. 1933-1942. (10.1111/ejn.12607)
Rees, E. et al. 2014. Analysis of copy number variations at 15 schizophrenia-associated loci. British Journal of Psychiatry 204(2), pp. 108-114. (10.1192/bjp.bp.113.131052)
Dent, C., Isles, A. R. and Humby, T. 2014. Measuring risk-taking in mice: balancing the risk between seeking reward and danger. European Journal of Neuroscience 39(4), pp. 520-530. (10.1111/ejn.12430)
Dent, C. and Isles, A. R. 2014. Brain-expressed imprinted genes and adult behaviour: the example of Nesp and Grb10. Mammalian Genome 25(1-2), pp. 87-93. (10.1007/s00335-013-9472-0)
McNamara, G. and Isles, A. R. 2014. Influencing the social group: the role of imprinted genes. Advances in Genetics 86, pp. 107-134. (10.1016/B978-0-12-800222-3.00006-1)
Cowley, M. et al. 2014. Developmental programming mediated by complementary roles of imprinted Grb10 in mother and pup. PLoS Biology 12(2), pp. e1001799. (10.1371/journal.pbio.1001799)

2013

Relkovic, D. and Isles, A. R. 2013. Behavioural and cognitive profiles of mouse models for Prader-Willi syndrome. Brain Research Bulletin 92, pp. 41-48. (10.1016/j.brainresbull.2011.09.009)
McNamara, G. I. and Isles, A. R. 2013. Dosage-sensitivity of imprinted genes expressed in the brain: 15q11–q13 and neuropsychiatric illness. Biochemical Society Transactions 41(3), pp. 721-726. (10.1042/BST20130008)

2012

Relkovic, D., Humby, T., Hagan, J. J., Wilkinson, L. S. and Isles, A. R. 2012. Enhanced appetitive learning and reversal learning in a mouse model for Prader-Willi syndrome. Behavioral Neuroscience 126(3), pp. 488-492. (10.1037/a0028155)

2011

Isles, A. R. 2011. Genomic imprinting; the cost of mother's care. Bioessays 33(12), pp. 924-926. (10.1002/bies.201100115)
Ingason, A. et al. 2011. Maternally derived microduplications at 15q11-q13: Implication of imprinted genes in psychotic illness. American Journal of Psychiatry 168(4), pp. 408-417. (10.1176/appi.ajp.2010.09111660)
Garfield, A. S. et al. 2011. Distinct physiological and behavioural functions for parental alleles of imprinted Grb10. Nature 469(7331), pp. 534-538. (10.1038/nature09651)

2010

Hinton, E. C., Isles, A. R., Williams, N. M. and Parkinson, J. A. 2010. Excessive appetitive arousal in Prader–Willi syndrome. Appetite 54(1), pp. 225-228. (10.1016/j.appet.2009.12.002)
Relkovic, D. et al. 2010. Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader–Willi syndrome. European Journal of Neuroscience 31(1), pp. 156-164. (10.1111/j.1460-9568.2009.07048.x)

2009

Doe, C. M. et al. 2009. Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviour. Human Molecular Genetics 18(12), pp. 2140-2148. (10.1093/hmg/ddp137)
Isles, A. R. 2009. Evolution of genomic imprinting in humans: Does bipedalism have a role?. Trends in Genetics 25(11), pp. 495-500. (10.1016/j.tig.2009.09.010)

2008

Doe, C., Garfield, A., Humby, T., Relkovic, D., Wilkinson, L. S. and Isles, A. R. 2008. 5-HT2CR pre-RNA editing, alternate splicing and function in a mouse model of Prader-Willi syndrome. Fundamental & Clinical Pharmacology 22(s2), pp. 125. (10.1111/j.1472-8206.2008.00601.x)
Davies, W. and Isles, A. R. 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, W., Isles, A. R., Humby, T. and Wilkinson, L. S. 2008. What are imprinted genes doing in the brain?. In: Wilkins, J. 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)
Isles, A. R. 2008. Feel the heat: epigenetic coding of thermotolerance in the chick (Commentary on Yossifoffet al.). European Journal of Neuroscience 28(11), pp. 2266. (10.1111/j.1460-9568.2008.06544.x)
Isles, A. R. and Wilkinson, L. S. 2008. Epigenetics: what is it and why is it important to mental disease?. British Medical Bulletin 85(1), pp. 35-45. (10.1093/bmb/ldn004)

2007

Wilkinson, L. S., Davies, W. and Isles, A. R. 2007. Genomic imprinting effects on brain development and function. Nature Reviews Neuroscience 8(11), pp. 832-843. (10.1038/nrn2235)
Lambourne, S. L., Humby, T., Isles, A. R., Emson, P. C., Spillantini, M. G. and Wilkinson, L. S. 2007. Impairments in impulse control in animal models transgenic for the human FTPD-17 tauV337M mutation are exacerbated by age. Human Molecular Genetics 16(14), pp. 1708-1719. (10.1093/hmg/ddm119)
Davies, W., Humby, T., Isles, A. R., Burgoyne, P. S. and Wilkinson, L. S. 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)
Davies, W., Isles, A. R., Humby, T. and Wilkinson, L. S. 2007. What are imprinted genes doing in the brain? [Review]. Epigenetics 2(4), pp. 201-206. (10.4161/epi.2.4.5379)

2006

Isles, A. R., Davies, W. and Wilkinson, L. S. 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, W., Isles, A. R., Burgoyne, P. S. and Wilkinson, L. S. 2006. X-linked imprinting: effects on brain and behaviour. Bioessays 28(1), pp. 35-44. (10.1002/bies.20341)
Isles, A. R. and Humby, T. 2006. Modes of imprinted gene action in learning disability. Journal of Intellectual Disability Research 50(5), pp. 318-325. (10.1111/j.1365-2788.2006.00843.x)

2005

Isles, A. R., Hathway, G. J., Humby, T., de la Riva, C., Kendrick, K. M. and Wilkinson, L. S. 2005. An mTph2 SNP gives rise to alterations in extracellular 5-HT levels, but not in performance on a delayed-reinforcement task. European Journal of Neuroscience 22(4), pp. 997-1000. (10.1111/j.1460-9568.2005.04265.x)
Davies, W. et al. 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, W., Isles, A. R. and Wilkinson, L. S. 2005. Imprinted gene expression in the brain. Neuroscience & Biobehavioral Reviews 29(3), pp. 421-430. (10.1016/j.neubiorev.2004.11.007)
Plagge, A. et al. 2005. Imprinted Nesp55 influences behavioral reactivity to novel environments. Molecular and Cellular Biology 25(8), pp. 3019-3026. (10.1128/MCB.25.8.3019-3026.2005)
Isles, A. R. and Holland, A. J. 2005. Imprinted genes and mother-offspring interactions. Early Human Development 81(1), pp. 73-77.

2004

Isles, A. R., Humby, T., Walters, E. and Wilkinson, L. S. 2004. Common genetic effects on variation in impulsivity and activity in mice. Journal of Neuroscience 24(30), pp. 6733-6740. (10.1523/JNEUROSCI.1650-04.2004)
Isles, A. R., Davies, W., Burrmann, D., Burgoyne, P. S. and Wilkinson, L. S. 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)

2003

Isles, A. R., Humby, T. and Wilkinson, L. S. 2003. Measuring impulsivity in mice using a novel operant delayed reinforcement task: effects of behavioural manipulations and d-amphetamine. Psychopharmacology 170(4), pp. 376-382. (10.1007/s00213-003-1551-6)
Davies, W., Isles, A. R., Burgoyne, P. S., Ward, B. O., Humby, T., de la Riva, C. and Wilkinson, L. S. 2003. Evidence for X-linked imprinted gene functioning on cognition in mice; a possible neurochemical basis, and implications for cognitive sexual dimorphism [Abstract]. Journal of Psychopharmacology 17(S), pp. A70.

2002

Isles, A. R. and Wilkinson, L. S. 2002. Neuroendocrinology Briefings 16: Genomic Imprinting, Hormones and Behaviour. Journal of Neuroendocrinology 14(5), pp. 425-426. (10.1046/j.1365-2826.2002.00445.x)
Isles, A. R. and Wilkinson, L. S. 2002. Genomic imprinting, hormones and behaviour. Journal of Neuroendocrinology 14(5), pp. 425-426.
Isles, A. R., Baum, M. J., Ma, D., Szeto, A., Keverne, E. B. and Allen, N. D. 2002. A possible role for imprinted genes in inbreeding avoidance and dispersal from the natal area in mice. Proceedings of the Royal Society B: Biological Sciences 269(1492), pp. 665-670. (10.1098/rspb.2001.1911)

2001

Isles, A. R. 2001. Reversible regulation of mouse genes. Trends Genet 17(8), pp. 441-441.
Isles, A. R. 2001. When is a clone not a clone?. Trends Genet 17(8), pp. 441-441.
Isles, A. R., Baum, M. J., Ma, D., Keverne, E. B. and Allen, N. D. 2001. Genetic imprinting: urinary odour preferences in mice. Nature 409(6822), pp. 783-784. (10.1038/35057323)
Isles, A. R. et al. 2001. Conditional ablation of neurones in transgenic mice. Journal of Neurobiology 47(3), pp. 183-193. (10.1002/neu.1026)
Davies, W., Isles, A. R. and Wilkinson, L. S. 2001. Imprinted genes and mental dysfunction. Annals of Medicine 33(6), pp. 428-436. (10.3109/07853890108995956)

2000

Isles, A. R. and Wilkinson, L. S. 2000. Imprinted genes, cognition and behaviour. Trends in Cognitive Sciences 4(8), pp. 309-318. (10.1016/S1364-6613(00)01504-7)

Mae gan fy ngrŵp ddiddordeb mewn cyfraniad mecanweithiau epigenetig i'r ymennydd ac ymddygiad. Yn benodol, rydym yn ymchwilio i deulu diddorol o enynnau, y genynnau wedi'u hargraffu, sy'n destun rheolaeth epigenetig a gafwyd yn ystod y datblygiad gan arwain at fynegiant o un copi rhiant (alel) yn unig. Mae'r ymchwil yn canolbwyntio ar fynd i'r afael â'r hyn y mae'r genynnau hyn yn ei wneud yn yr ymennydd a sut y gallant gyfrannu at anhwylderau niwroddatblygiadol. Mae ymchwil ddiweddar mewn cydweithrediad â'r Athro Rosalind John (Prifysgol Caerdydd) yn ymchwilio i a all newidiadau ym mynegiant brych genynnau wedi'u hargraffu ddylanwadu ar ymddygiad mamol a chanlyniadau disgynyddion diweddarach.

Mae gen i ddiddordeb hefyd mewn datblygu a defnyddio modelau cyn-glinigol ar gyfer anhwylderau niwro-ddatblygiadol a niwroseiciatrig, ac ar hyn o bryd rwy'n arwain clwstwr MURIDAE o fewn Rhwydwaith Genetig Llygoden Cenedlaethol UKRI:MRC.

Mae ein gwaith yn gofyn am ddull amlddisgyblaethol er mwyn archwilio agweddau ar ymddygiad, niwrobioleg a geneteg foleciwlaidd. Rydym yn archwilio ffenoteipiau ymddygiadol mewn modelau cnofilod yn bennaf ac yn defnyddio technegau moleciwlaidd ar gyfer mynd i'r afael â mynegiant genynnau a rheoleiddio epigenetig y genom (addasu histon a methylation DNA).

Meysydd prosiect ymchwil cyfredol

Genynnau, ymennydd ac ymddygiad wedi'u hargraffu
Cydlynu canlyniadau placenta, ymennydd mamol, a phlant
Datblygiad ymennydd ac ymddygiad mewn modelau llygoden genetig ar gyfer sgitsoffrenia

Cyllid Ymchwil

Gwobr Iechyd Meddwl Wellcome (2025-2030) - "Y glud sy'n dal y darnau gyda'i gilydd: datgloi iechyd gwybyddol mewn anhwylderau seicotig"

UKRI:Cyngor Ymchwil Feddygol (2022-2027) - "MURIDAE: Dulliau ar gyfer Deall, Cofnodi ac Integreiddio Data ar draws Bywyd Cynnar"

Ymddiriedolaeth Leverhulme, grant prosiect (2022-2026) - "Cyfraniad genynnau wedi'u mynegi gan famau i ymddygiad rhieni"

Goruchwyliwr adolygu llenyddiaeth SCC Blwyddyn 1

Darlithydd ar Genomeg Clefydau Etifeddol Cyffredin a Phrin (MET 950)

Modiwl Pscyhology Intercalated 'Sail wyddonol meddygaeth seicolegol' (ME3085)

Tiwtor personol i fyfyrwyr sy'n dilyn rhaglen MBBCh

Biowybodeg ac Epidemioleg Genetig MSc - Goruchwyliwr prosiect data; Goruchwyliwr prosiect traethawd hir

Education and qualifications

2000: PhD (Zoology) University of Cambridge, Cambridge, UK
1994: BSc Zoology & Genetics, University of Sheffield, UK

Career overview

2006 - present: Professor, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK
2003 - 2008 Beebe Ttrust Research Fellow, Department of Psychiatry, University of Cambridge, Cambridge, UK
1999 - 2003 Post-doctoral researcher, The Babraham Institute, Cambridge, UK
1994 - 1995 ESF Trainee technician, Department of Genetics, Leicester University, UK

Anrhydeddau a dyfarniadau

Cymrawd y Royal Scoiety of Biology

Safleoedd academaidd blaenorol

2006 - presennol: Athro, Canolfan MRC ar gyfer Geneteg a Genomeg Niwroseiciatrig, Prifysgol Caerdydd, Caerdydd, y DU
2003 - 2008 Cymrawd Ymchwil Ymddiriedolaeth Beebe, Adran Seiciatreg, Prifysgol Caergrawnt, Caergrawnt, DU
1999 - 2003 Ymchwilydd ôl-ddoethurol, Sefydliad Babraham , Caergrawnt, UK
1994 - 1995 ESF Technegydd dan hyfforddiant, Adran Geneteg, Prifysgol Caerlŷr, UK

Pwyllgorau ac adolygu

Mewnol

Cynrychiolydd MEDIC, DENTL & PHRMY ar y Pwyllgor Safonau Biolegol (2022-presennol)
Arweinydd, Thema Niwrowyddoniaeth ac Iechyd Meddwl, rhaglen hyfforddiant doethurol GW4 MRC BioMed (2015-2022)
Cyfarwyddwr rhaglen PhD Niwrowyddoniaeth Integreiddiol Ymddiriedolaeth Wellcome (2014-2024)

Allanol

Aelod o Grŵp Cynghori Darganfod Gwyddorau Hymennydd ac Ymddygiad Wellcome (2023-presennol)
Aelod o Fwrdd Golygyddol, Trafodion Athronyddol y Gymdeithas Frenhinol B (2020-2025)
Golygydd Cyswllt, Frontiers in Developmental Epigenetics (2017-2024)
Aelod o'r Bwrdd Golygyddol, Genes Brain and Behavior (2017-presennol)
Aelod o'r Bwrdd Golygyddol, Brain and Neuroscience Advances (2017-presennol)
Ymddiriedolwr, Cymdeithas Niwrowyddoniaeth Prydain (2017-2022)
Aelod o banel GEMM y Cyngor Ymchwil Feddygol (2016-2022)
Golygydd Cyswllt, Cyfnodolyn Niwrowyddorau Ewropeaidd (2008-2020)

Goruchwyliaeth gyfredol

Isadora Sinha

Prosiectau'r gorffennol

Myfyrwyr PhD diweddar (goruchwyliwr arweiniol)

Dr Matthew Higgs; Traethawd ymchwil PhD Dull Lefel Systemau i Ganfod a dilysu genynnau sydd wedi'u hargraffu sy'n ymwneud â gofal rhieni a'r cylchedwaith niwral cysylltiedig; Enillydd Gwobr Bruce Cattanach Cymdeithas Geneteg 2024
Dr Simona Zahova; Traethawd PhD Archwilio rôl syndrom Prader-Willi cyfwng critigol mewn salwch a gwybyddiaeth seiciatrig
Dr Matthew Bosworth; PhD thesis Canlyniadau swyddogaethol haploinsufficiency Set1da; o ystumio i ymddygiad
Dr Manal Adam; Traethawd PhD Epigeneteg ac anhwylderau niwroddatblygiadol: nodweddu moleciwlaidd ac ymddygiadol llygoden knockout Ehmt1 / Glp
Dr Kira Rienecker; Traethawd PhD Paternal Grb10 mewn ymennydd ac ymddygiad

Mae'n hanfodol bod gwyddonwyr yn ceisio esbonio eu maes ymchwil i leygoedd cynulleidfaoedd, ac yn wir, lle bo hynny'n bosibl, bod ein hymchwil yn cael ei lywio gan ein rhyngweithio â'r cyhoedd yn gyffredinol. Rwy'n ymgymryd â gweithgareddau ymgysylltu'n rheolaidd ac wedi siarad mewn digwyddiadau fel Pint of Science, Caffi Athroniaeth Caerdydd, a dathliadau Canmlwyddiant MRC yn BayArt.

Rwyf hefyd yn awyddus i hyrwyddo niwrowyddoniaeth ac roeddwn yn Ymddiriedolwr Cymdeithas Niwroscaince Prydain o 2017-2022, lle glanheais eu cylchgrawn cymdeithas, helpu gyda phrosiectau BNA Credible Neuroscience a fi oedd y prif siaradwr mewn sesiwn weminar o'r enw 'Gyrfaoedd mewn niwrowyddoniaeth (a thu hwnt!) ' a fynychwyd gan ymchwilwyr gyrfa gynnar o bob cwr o'r byd.

Yn ychwanegol, rwyf wedi trafod fy ymchwil gyda rhieni a gofalwyr unigolion â syndrom Prader-Willi mewn digwyddiadau fel Arweinyddiaeth IPWSO ECHO®, ac wedi recordio podlediadau ar gyfer Natur a'r Gymdeithas Biocemegol yn egluro fy ymchwil. Mae ein gwaith hefyd wedi cael sylw mewn erthyglau newyddion yn y Smithsonian, Scientific American a hyd yn oed y Daily Mail.

Contact Details

IslesAR1@caerdydd.ac.uk
+44 29206 88467
Adeilad Hadyn Ellis, Ystafell 2.48, Heol Maendy, Caerdydd, CF24 4HQ

Themâu ymchwil

Arbenigeddau

Niwrowyddoniaeth ymddygiadol
Bioleg foleciwlaidd
Niwroddatblygiad

Genynnau wedi’u hargraffu yng ‘nghanolbwynt magu plant’ yr ymennydd yn pennu a ydy llygod yn rhieni da ai peidio

25 October 2023

Yr Athro Anthony Isles (e/fe) PhD, FRSB