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Dr Kimberley Marie Kendall
Timau a rolau for Kimberley Marie Kendall
Darlithydd Clinigol
Uwch Gymrawd Clinigol
Trosolwyg
Rwy'n seiciatrydd academaidd clinigol sy'n arbenigo mewn sail genomig salwch meddwl difrifol ac mewn cyfieithu darganfyddiadau biolegol i ymarfer clinigol. Mae fy ymchwil yn canolbwyntio ar sut mae risg genetig yn siapio canlyniadau salwch a sut y gall mecanweithiau moleciwlaidd lywio ymyriadau o fewn gwasanaethau clinigol yn y byd go iawn.
Rwy'n gyd-ymchwilydd ar raglen Mental Health Goals Omics Psychosis, menter fawr yn y DU sy'n anelu at recriwtio carfan fawr o unigolion â seicosis ac integreiddio eu data aml-omig â ffenoteipio clinigol dwfn. Rwy'n arwain recriwtio yng Nghymru ar gyfer y rhaglen hon ac astudiaeth CONNECT, ac rwy'n gwasanaethu fel Arweinydd Arbenigedd Ymchwil Iechyd a Gofal Cymru ar gyfer Iechyd Meddwl. Yn glinigol, rwy'n gweithio yng Ngwasanaeth Genomeg Seiciatrig Cymru Gyfan, clinig genomeg seiciatrig pwrpasol cyntaf y DU, gan ddarparu cwnsela a phrofion genomig seiciatrig i unigolion â chyflyrau seiciatrig a'u teuluoedd, yn ogystal ag unigolion y nodwyd eu bod yn cario amrywiadau risg genetig seiciatrig.
Cyhoeddiad
2026
- Musliner, K. L. et al., 2026. Potential for genomics to help guide preventive strategies in psychiatry. JAMA Psychiatry (10.1001/jamapsychiatry.2026.2583)
- Eisner, E. et al., 2026. Using passive sensing to predict psychosis relapse: an in-depth qualitative study exploring perspectives of people with psychosis. Schizophrenia Bulletin: The Journal of Psychoses and Related Disorders 52 (4) sbaf126. (10.1093/schbul/sbaf126)
- Quinn, A. et al., 2026. Severe Mental Illness Longitudinal Evaluation (SMILE): protocol for establishing a cohort and bioresource for UK-based patients with psychosis. BMJ Open 16 (7) e116077. (10.1136/bmjopen-2025-116077)
- Bladon, S. et al., 2026. Evaluating wearable devices for remote monitoring in psychosis: Pilot study nested within the CONNECT cohort study. JMIR Formative Research 10 e86049. (10.2196/86049)
- Eisner, E. et al., 2026. Views of people with psychosis about algorithm-based relapse prediction and data sharing: qualitative study. Journal of Medical Internet Research 28 e86753. (10.2196/86753)
- Brah, H. S. et al., 2026. Clinical genetic testing in schizophrenia: a systematic review and meta-analysis. Biological psychiatry 99 (7), pp.541-549. (10.1016/j.biopsych.2025.09.010)
- Ball, H. et al., 2026. Mental health professionals’ perspectives on digital remote monitoring in services for people with psychosis. Schizophrenia Bulletin: The Journal of Psychoses and Related Disorders 52 (1) sbaf043. (10.1093/schbul/sbaf043)
- Kendall, K. M. et al. 2026. The relationship between schizophrenia polygenic scores, blood-based proteins and psychosis diagnosis in the UK Biobank. Schizophrenia 12 24. (10.1038/s41537-025-00725-8)
2025
- Rammos, A. et al., 2025. Copy number variants and their implications for developmental and behavioural problems in cleft lip and/or palate. Human Molecular Genetics 34 (18), pp.1563-1574. (10.1093/hmg/ddaf115)
2024
- Kendall, K. et al. 2024. The translation of psychiatric genetics findings to the clinic. Schizophrenia Research 267 , pp.470-472. (10.1016/j.schres.2023.10.024)
2022
- Wadon, M. et al. 2022. Clinical and genotypic analysis in determining dystonia non-motor phenotypic heterogeneity: a UK Biobank study. Journal of Neurology 269 , pp.6436-6451. (10.1007/s00415-022-11307-4)
2021
- Kendall, K. M. et al. 2021. The genetic basis of major depression. Psychological Medicine 51 (13), pp.2217-2230. (10.1017/S0033291721000441)
- Martin, J. et al. 2021. Examining sex differences in neurodevelopmental and psychiatric genetic risk in anxiety and depression. PLoS ONE 16 (9) e0248254. (10.1371/journal.pone.0248254)
- Silva, A. I. et al. 2021. Analysis of diffusion tensor imaging data from the UK Biobank confirms dosage effect of 15q11.2 copy number variation on white matter and shows association with cognition. Biological Psychiatry 90 (5), pp.307-316. (10.1016/j.biopsych.2021.02.969)
- Caseras, X. et al. 2021. Effects of genomic copy number variants penetrant for schizophrenia on cortical thickness and surface area in healthy individuals: analysis of the UK Biobank. British Journal of Psychiatry 218 (2), pp.104-111. (10.1192/bjp.2020.139)
- Kendall, K. 2021. Clinical genetics [TrOn learning module]. [Online].Royal College of Psychiatrists. Available at: https://elearninghub.rcpsych.ac.uk/products/TrOn_Clinical_genetics.
- Kendall, K. 2021. The phenotypic expression of neuropsychiatric copy number variants. PhD Thesis , Cardiff University.
- McMillan, K. and Kendall, K. 2021. Basic genetics [TrOn learning module]. [Online].Royal College of Psychiatrists. Available at: https://elearninghub.rcpsych.ac.uk/products/TrOn_Basic_genetics.
2020
- Kendall, K. M. et al. 2020. Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: a data linkage study. BJPsych Open 6 (6) e139. (10.1192/bjo.2020.42)
- Brcic, L. et al. 2020. Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank. Journal of Medical Genetics 57 (10), pp.692-698. (10.1136/jmedgenet-2019-106676)
- Gubb, S. et al. 2020. Medical and neurobehavioural phenotypes in male and female carriers of Xp22.31 duplications in the UK Biobank. Human Molecular Genetics 29 (17), pp.2872-2881. (10.1093/hmg/ddaa174)
- Warland, A. et al. 2020. Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank. Molecular Psychiatry 25 (4), pp.854-862. (10.1038/s41380-019-0355-y)
2019
- Legge, S. E. et al. 2019. Association of genetic liability to psychotic experiences with neuropsychotic disorders and traits. JAMA Psychiatry 76 (12), pp.1256-1265. (10.1001/jamapsychiatry.2019.2508)
- Escott-Price, V. et al. 2019. Polygenic risk for schizophrenia and season of birth within the UK Biobank cohort. Psychological Medicine 49 (15), pp.2499-2504. (10.1017/S0033291718000454)
- Underwood, J. et al. 2019. Autism spectrum disorder diagnosis in adults: phenotype and genotype findings from a clinically derived cohort. British Journal of Psychiatry 215 (5), pp.647-653. (10.1192/bjp.2019.30)
- Underwood, J. et al. 2019. SA20COPY Number variants and polygenic risk scores in adults with autism spectrum disorder (ASD): results from the NCMH adult ASD cohort. European Neuropsychopharmacology 29 (S4), pp.S1198-S1199. (10.1016/j.euroneuro.2018.08.242)
- Kendall, K. M. et al. 2019. Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank. British Journal of Psychiatry 214 (05), pp.297-304. (10.1192/bjp.2018.301)
- Kendall, K. M. et al. 2019. Association of rare copy number variants with risk of depression. JAMA Psychiatry 76 (8), pp.818-825. (10.1001/jamapsychiatry.2019.0566)
- Crawford, K. et al. 2019. Medical consequences of pathogenic CNVs in adults: Analysis of the UK Biobank. Journal of Medical Genetics 56 , pp.131-138. (10.1136/jmedgenet-2018-105477)
2018
- Owen, D. et al. 2018. Effects of pathogenic CNVs on physical traits in participants of the UK Biobank. BMC Genomics 19 (1) 867. (10.1186/s12864-018-5292-7)
2017
- Cosgrove, D. et al., 2017. Cognitive characterization of schizophrenia risk variants involved in synaptic transmission: evidence of CACNA1C's role in working memory. Neuropsychopharmacology 42 , pp.2612-2622. (10.1038/npp.2017.123)
- Keynejad, R. C. et al., 2017. Docbate: a National Medical Student Debate. Academic Psychiatry 41 (6), pp.839-841. (10.1007/s40596-017-0697-1)
- Kendall, K. M. et al. 2017. Cognitive performance among carriers of pathogenic copy number variants: analysis of 152,000 UK Biobank subjects. Biological Psychiatry 82 (2), pp.P103-110. (10.1016/j.biopsych.2016.08.014)
- Kendall, K. , Kirov, G. and Owen, M. 2017. Schizophrenia Genetics. In: Benjamin, S. , Virginia, S. and Pedro, R. eds. Kaplan and Sadock?s Comprehensive Textbook of Psychiatry. Wolters Kluwer
2016
- Whitton, L. et al., 2016. Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 171 (8), pp.1170-1179. (10.1002/ajmg.b.32503)
- Rees, E. et al. 2016. Analysis of intellectual disability copy number variants for association with schizophrenia. JAMA Psychiatry 73 (9), pp.963-969. (10.1001/jamapsychiatry.2016.1831)
2015
- Kendall, K. and Owen, M. J. 2015. Intellectual disability and psychiatric comorbidity: challenges and clinical issues. Psychiatric Times 32 (5)
2012
- Kendall, K. and Robertson, N. 2012. Neuroimaging. Journal of Neurology 259 (9), pp.2009-2011. (10.1007/s00415-012-6652-x)
- Kendall, K. et al. 2012. A neurological presentation of intravascular B-cell lymphoma. Case Reports (10.1136/bcr-2012-006439)
2009
- Carroll, L. S. et al. 2009. Evidence that putative ADHD low risk alleles atSNAP25may increase the risk of schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (7), pp.893-899. (10.1002/ajmg.b.30915)
Adrannau llyfrau
- Kendall, K. , Kirov, G. and Owen, M. 2017. Schizophrenia Genetics. In: Benjamin, S. , Virginia, S. and Pedro, R. eds. Kaplan and Sadock?s Comprehensive Textbook of Psychiatry. Wolters Kluwer
Erthyglau
- Musliner, K. L. et al., 2026. Potential for genomics to help guide preventive strategies in psychiatry. JAMA Psychiatry (10.1001/jamapsychiatry.2026.2583)
- Eisner, E. et al., 2026. Using passive sensing to predict psychosis relapse: an in-depth qualitative study exploring perspectives of people with psychosis. Schizophrenia Bulletin: The Journal of Psychoses and Related Disorders 52 (4) sbaf126. (10.1093/schbul/sbaf126)
- Quinn, A. et al., 2026. Severe Mental Illness Longitudinal Evaluation (SMILE): protocol for establishing a cohort and bioresource for UK-based patients with psychosis. BMJ Open 16 (7) e116077. (10.1136/bmjopen-2025-116077)
- Bladon, S. et al., 2026. Evaluating wearable devices for remote monitoring in psychosis: Pilot study nested within the CONNECT cohort study. JMIR Formative Research 10 e86049. (10.2196/86049)
- Eisner, E. et al., 2026. Views of people with psychosis about algorithm-based relapse prediction and data sharing: qualitative study. Journal of Medical Internet Research 28 e86753. (10.2196/86753)
- Brah, H. S. et al., 2026. Clinical genetic testing in schizophrenia: a systematic review and meta-analysis. Biological psychiatry 99 (7), pp.541-549. (10.1016/j.biopsych.2025.09.010)
- Ball, H. et al., 2026. Mental health professionals’ perspectives on digital remote monitoring in services for people with psychosis. Schizophrenia Bulletin: The Journal of Psychoses and Related Disorders 52 (1) sbaf043. (10.1093/schbul/sbaf043)
- Kendall, K. M. et al. 2026. The relationship between schizophrenia polygenic scores, blood-based proteins and psychosis diagnosis in the UK Biobank. Schizophrenia 12 24. (10.1038/s41537-025-00725-8)
- Rammos, A. et al., 2025. Copy number variants and their implications for developmental and behavioural problems in cleft lip and/or palate. Human Molecular Genetics 34 (18), pp.1563-1574. (10.1093/hmg/ddaf115)
- Kendall, K. et al. 2024. The translation of psychiatric genetics findings to the clinic. Schizophrenia Research 267 , pp.470-472. (10.1016/j.schres.2023.10.024)
- Wadon, M. et al. 2022. Clinical and genotypic analysis in determining dystonia non-motor phenotypic heterogeneity: a UK Biobank study. Journal of Neurology 269 , pp.6436-6451. (10.1007/s00415-022-11307-4)
- Kendall, K. M. et al. 2021. The genetic basis of major depression. Psychological Medicine 51 (13), pp.2217-2230. (10.1017/S0033291721000441)
- Martin, J. et al. 2021. Examining sex differences in neurodevelopmental and psychiatric genetic risk in anxiety and depression. PLoS ONE 16 (9) e0248254. (10.1371/journal.pone.0248254)
- Silva, A. I. et al. 2021. Analysis of diffusion tensor imaging data from the UK Biobank confirms dosage effect of 15q11.2 copy number variation on white matter and shows association with cognition. Biological Psychiatry 90 (5), pp.307-316. (10.1016/j.biopsych.2021.02.969)
- Caseras, X. et al. 2021. Effects of genomic copy number variants penetrant for schizophrenia on cortical thickness and surface area in healthy individuals: analysis of the UK Biobank. British Journal of Psychiatry 218 (2), pp.104-111. (10.1192/bjp.2020.139)
- Kendall, K. M. et al. 2020. Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: a data linkage study. BJPsych Open 6 (6) e139. (10.1192/bjo.2020.42)
- Brcic, L. et al. 2020. Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank. Journal of Medical Genetics 57 (10), pp.692-698. (10.1136/jmedgenet-2019-106676)
- Gubb, S. et al. 2020. Medical and neurobehavioural phenotypes in male and female carriers of Xp22.31 duplications in the UK Biobank. Human Molecular Genetics 29 (17), pp.2872-2881. (10.1093/hmg/ddaa174)
- Warland, A. et al. 2020. Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank. Molecular Psychiatry 25 (4), pp.854-862. (10.1038/s41380-019-0355-y)
- Legge, S. E. et al. 2019. Association of genetic liability to psychotic experiences with neuropsychotic disorders and traits. JAMA Psychiatry 76 (12), pp.1256-1265. (10.1001/jamapsychiatry.2019.2508)
- Escott-Price, V. et al. 2019. Polygenic risk for schizophrenia and season of birth within the UK Biobank cohort. Psychological Medicine 49 (15), pp.2499-2504. (10.1017/S0033291718000454)
- Underwood, J. et al. 2019. Autism spectrum disorder diagnosis in adults: phenotype and genotype findings from a clinically derived cohort. British Journal of Psychiatry 215 (5), pp.647-653. (10.1192/bjp.2019.30)
- Underwood, J. et al. 2019. SA20COPY Number variants and polygenic risk scores in adults with autism spectrum disorder (ASD): results from the NCMH adult ASD cohort. European Neuropsychopharmacology 29 (S4), pp.S1198-S1199. (10.1016/j.euroneuro.2018.08.242)
- Kendall, K. M. et al. 2019. Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank. British Journal of Psychiatry 214 (05), pp.297-304. (10.1192/bjp.2018.301)
- Kendall, K. M. et al. 2019. Association of rare copy number variants with risk of depression. JAMA Psychiatry 76 (8), pp.818-825. (10.1001/jamapsychiatry.2019.0566)
- Crawford, K. et al. 2019. Medical consequences of pathogenic CNVs in adults: Analysis of the UK Biobank. Journal of Medical Genetics 56 , pp.131-138. (10.1136/jmedgenet-2018-105477)
- Owen, D. et al. 2018. Effects of pathogenic CNVs on physical traits in participants of the UK Biobank. BMC Genomics 19 (1) 867. (10.1186/s12864-018-5292-7)
- Cosgrove, D. et al., 2017. Cognitive characterization of schizophrenia risk variants involved in synaptic transmission: evidence of CACNA1C's role in working memory. Neuropsychopharmacology 42 , pp.2612-2622. (10.1038/npp.2017.123)
- Keynejad, R. C. et al., 2017. Docbate: a National Medical Student Debate. Academic Psychiatry 41 (6), pp.839-841. (10.1007/s40596-017-0697-1)
- Kendall, K. M. et al. 2017. Cognitive performance among carriers of pathogenic copy number variants: analysis of 152,000 UK Biobank subjects. Biological Psychiatry 82 (2), pp.P103-110. (10.1016/j.biopsych.2016.08.014)
- Whitton, L. et al., 2016. Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 171 (8), pp.1170-1179. (10.1002/ajmg.b.32503)
- Rees, E. et al. 2016. Analysis of intellectual disability copy number variants for association with schizophrenia. JAMA Psychiatry 73 (9), pp.963-969. (10.1001/jamapsychiatry.2016.1831)
- Kendall, K. and Owen, M. J. 2015. Intellectual disability and psychiatric comorbidity: challenges and clinical issues. Psychiatric Times 32 (5)
- Kendall, K. and Robertson, N. 2012. Neuroimaging. Journal of Neurology 259 (9), pp.2009-2011. (10.1007/s00415-012-6652-x)
- Kendall, K. et al. 2012. A neurological presentation of intravascular B-cell lymphoma. Case Reports (10.1136/bcr-2012-006439)
- Carroll, L. S. et al. 2009. Evidence that putative ADHD low risk alleles atSNAP25may increase the risk of schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (7), pp.893-899. (10.1002/ajmg.b.30915)
Gosodiad
- Kendall, K. 2021. The phenotypic expression of neuropsychiatric copy number variants. PhD Thesis , Cardiff University.
Gwefannau
- Kendall, K. 2021. Clinical genetics [TrOn learning module]. [Online].Royal College of Psychiatrists. Available at: https://elearninghub.rcpsych.ac.uk/products/TrOn_Clinical_genetics.
- McMillan, K. and Kendall, K. 2021. Basic genetics [TrOn learning module]. [Online].Royal College of Psychiatrists. Available at: https://elearninghub.rcpsych.ac.uk/products/TrOn_Basic_genetics.
Ymchwil
Mae fy ymchwil yn archwilio sut mae ffactorau risg genomig ar gyfer salwch meddwl difrifol yn siapio bioleg a nodweddion clinigol, gan gynnwys diagnosis, difrifoldeb symptomau a comorbidity. Rwy'n defnyddio dulliau aml-omig i ymchwilio i'r mecanweithiau sy'n cysylltu risg genetig â biofarcwyr sy'n seiliedig ar waed a chanlyniadau salwch. Rwyf hefyd yn arwain gwaith cyfieithu drwy Wasanaeth Genomeg Seiciatrig Cymru Gyfan, gan ganolbwyntio ar hyn o bryd ar sut mae cleifion yn profi cwnsela genetig seiciatrig a phrofion mewn gofal arferol. Fy nod hirdymor yw integreiddio data aml-omig â ffenoteipio clinigol manwl i lywio strategaethau triniaeth wedi'u personoli ac yn y pen draw gwella canlyniadau i bobl sy'n byw gyda salwch meddwl difrifol.
Addysgu
Addysgu
Rwy'n darparu addysgu israddedig ac ôl-raddedig mewn seiciatreg, genomeg seiciatrig a sgiliau cyfathrebu ym Mhrifysgol Caerdydd. Mae fy addysgu yn cwmpasu seiciatreg glinigol craidd, cymhwyso genomeg mewn iechyd meddwl, a'r heriau moesegol a chyfathrebu sy'n gysylltiedig â thrafod risg genetig gyda chleifion a theuluoedd. Rwy'n cyfrannu at addysgu grŵp bach, darlithoedd grŵp mawr a gweithdai sy'n seiliedig ar sgiliau, ac rwy'n cefnogi datblygiad cwricwlwm ynghylch meddygaeth genomig a salwch meddwl difrifol.
Goruchwylio a Mentora
Rwyf wedi bod yn brif neu gyd-oruchwyliwr ar gyfer nifer o fyfyrwyr meddygol, seicoleg ac MSc, gan gynnwys prosiectau sydd wedi arwain at gyflwyniadau cynhadledd a gwaith arobryn. Mae goruchwyliaeth ddiweddar wedi cynnwys prosiectau ar genomeg seiciatrig, seicosis ac iechyd corfforol, a gwerthuso gwasanaethau clinigol newydd fel Gwasanaeth Genomeg Seiciatrig Cymru Gyfan. Rwy'n ymrwymedig i ddatblygu ymchwilwyr a chlinigwyr gyrfa gynnar sydd â sgiliau cryf mewn arfarniad beirniadol, dulliau ymchwil a seiciatreg drosiannol.
Cysylltiadau Academaidd a Hyfforddiant
Rwy'n seiciatrydd academaidd clinigol sydd wedi'i leoli yn y Ganolfan Geneteg a Genomeg Niwroseiciatrig, Prifysgol Caerdydd, ac yn gweithio ar ryngwyneb genomeg seiciatrig a gofal clinigol. Mae fy hyfforddiant yn cynnwys PhD mewn Meddygaeth, hyfforddiant arbenigol uwch mewn Seiciatreg Oedolion Cyffredinol gyda chymeradwyaeth mewn Seiciatreg Adsefydlu, a BSc mewn Geneteg Feddygol. Rwyf hefyd wedi ymgymryd â hyfforddiant arweinyddiaeth a rheoli ffurfiol, gan gefnogi fy rolau mewn arweinyddiaeth rhaglenni, goruchwylio a datblygiad addysgol.
Bywgraffiad
Rolau cyfredol
2024 - presennol - Uwch Gymrawd Clinigol, Prifysgol Caerdydd
2022 - presennol - Ymgynghorydd Seiciatrydd, Gwasanaeth Genomeg Seiciatrig Cymru Gyfan
2024 - presennol - Arweinydd Arbenigedd Iechyd Meddwl, Ymchwil Iechyd a Gofal Cymru
Rolau yn y gorffennol
2021 - 2024 - Hyfforddiant Uwch Seiciatreg Oedolion, Trac Academaidd Clinigol Cymru
2020 - 2021 - Hyfforddiant Seiciatreg Craidd, Trac Academaidd Clinigol Cymru
2017 - 2020 - Cymrawd Ymchwil Clinigol Wellcome Trust, Prifysgol Caerdydd
2013 - 2017 - Hyfforddiant Seiciatreg Craidd, Trac Academaidd Clinigol Cymru
2011 - 2013 - Hyfforddiant Meddygol Craidd, Deoniaeth Cymru
2009 - 2011 - Rhaglen Sylfaen, Deoniaeth Cymru
Anrhydeddau a dyfarniadau
2024 - Gwobr Ymchwil Arweinwyr y Dyfodol mewn Seicosis
2022 - Gwobr Deorydd Iechyd Meddwl - Categori effaith gynnar
2020 - Gwobr Ymchwil Cymdeithas Seiciatrig Ewrop
Aelodaethau proffesiynol
Tystysgrif Cwblhau Hyfforddiant Arbenigol - Seiciatreg Oedolion Cyffredinol, Cymeradwyaeth mewn Seiciatreg Adsefydlu
Aelod o Goleg Brenhinol y Seiciatryddion
Wedi'i gofrestru gyda'r Cyngor Meddygol Cyffredinol
Ymrwymiadau siarad cyhoeddus
2026 - Gwasanaeth Genomeg Seiciatrig Cymru Gyfan. Y Cyfarfod Llawn. Cyngres Ryngwladol Coleg Brenhinol y Seiciatryddion
2025 -Dylanwadu ar bolisi iechyd meddwl yn y Senedd. Cyngres Ryngwladol Coleg Brenhinol y Seiciatryddion
2025 - Dathlu Merthyr Tudful - Gwyddonwyr. Caffi Gwyddoniaeth, BBC Radio Wales
2024 - Cyfieithu clinigol o ganfyddiadau genetig seiciatrig, Cymdeithas Niwrowyddoniaeth Prydain a'r Senedd
2024 - Gwasanaeth Genomeg Seiciatrig Cymru Gyfan, Ymddiriedolaeth GIG Sefydliad Dwyrain Llundain
2023 - Amrywiadau rhif copïau mewn seiciatreg oedolion cyffredinol a'u cyfieithu i'r clinig, Coleg y Brenin Llundain
2022 - Amrywiad rhif copïau a'u rhyngweithio â sgoriau risg polygenig, Cyngres Geneteg Seiciatrig y Byd
2022 - Trefnydd a chadeirydd, British Journal of Psychiatry Journal Club Cymru
2022 - Amrywiadau rhif copïau mewn seiciatreg oedolion gyffredinol, Adran Seiciatreg, Prifysgol Caergrawnt
Pwyllgorau ac adolygu
Rheolau cyfredol
2022 - presennol - Arholwr PhD - Prifysgol Copenhagen (allanol), Prifysgol Caerdydd (mewnol), Coleg y Brenin Llundain (allanol), Prifysgol Montreal (allanol).
Adolygiad gan gymheiriaid - sawl cyfnodolyn gan gynnwys JAMA Psychiatry, Biological Psychiatry a Molecular Psychiatry
Rolau yn y gorffennol
2024 - 2025 - Aelod o Fwrdd Golygyddol Discover Mental Health
2022 - 2025 - Pwyllgor Aelodaeth Cymdeithas Ryngwladol Geneteg Seiciatrig
2018 - 2024 - Cymdeithas Ryngwladol Geneteg Seiciatrig Aelodaeth Pwyllgor Cyswllt Allgymorth Grŵp Sgitsoffrenia
Ymgysylltu
ArrayContact Details
Themâu ymchwil
Arbenigeddau
- Geneteg Seiciatrig
- Cyfieithiad Clinigol