![Kimberley Marie Kendall](https://profiles-cardiff.imgix.net/attachments/6953?w=200&h=200&auto=format&crop=faces&fit=crop&q=90")
Trosolwyg
Rwy'n seiciatrydd academaidd sy'n angerddol am ddefnyddio dulliau data genetig a mawr i wella gofal cleifion. Mae fy ymchwil yn canolbwyntio ar ffactorau genetig a'u dylanwad ar ganlyniadau salwch mewn salwch meddwl difrifol. Credaf ym mhwysigrwydd cyfieithu canfyddiadau ymchwil i ofal cleifion, ac rwy'n ymfalchïo mewn bod yn rhan o'r tîm y tu ôl i Wasanaeth Genomeg Seiciatrig Cymru Gyfan, clinig genomeg seiciatrig pwrpasol cyntaf y DU.
Cwblheais hyfforddiant seiciatreg uwch mewn Seiciatreg Oedolion Cyffredinol yn Ne-ddwyrain Cymru, gyda chymeradwyaeth is-arbenigedd mewn Seiciatreg Adsefydlu.
Cyhoeddiad
2024
- Kendall, K., Duffin, D., Doherty, J., Irving, R., Procter, A. and Walters, J. 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., Fenner, E., Kendall, K., Bailey, G., Sandor, C., Rees, E. and Peall, K. J. 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., Van Assche, E., Andlauer, T. F. M., Choi, K. W., Luykx, J. J., Schulte, E. C. and Lu, Y. 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), article number: 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. The phenotypic expression of neuropsychiatric copy number variants. PhD Thesis, Cardiff University.
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), article number: e139. (10.1192/bjo.2020.42)
- Brcic, L., Underwood, J., Kendall, K., Caseras, X., Kirov, G. and Davies, W. 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., Brcic, L., Underwood, J., Kendall, K., Caseras, X., Kirov, G. and Davies, W. 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., Kendall, K. M., Rees, E., Kirov, G. and Caseras, X. 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., Kendall, K., Berrett, J., Lewis, C., Anney, R., Van den Bree, M. and Hall, J. 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., Kendall, K., Berrett, J., Anney, R., Bree, M. V. D. and Hall, J. 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(5), 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), article number: 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)
- McMillan, K. and Kendall, K. 2017. Basic genetics. Royal College of Psychiatrists. - teaching_resource
- Kendall, K. 2017. Clinical genetics. Royal College of Psychiatrists. - teaching_resource
- 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., Thomas, R., Corkill, R. G. and Robertson, N. 2012. A neurological presentation of intravascular B-cell lymphoma. Case Reports (10.1136/bcr-2012-006439)
2009
- Carroll, L. S., Kendall, K., O'Donovan, M. C., Owen, M. J. and Williams, N. M. 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)
Articles
- Kendall, K., Duffin, D., Doherty, J., Irving, R., Procter, A. and Walters, J. 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., Fenner, E., Kendall, K., Bailey, G., Sandor, C., Rees, E. and Peall, K. J. 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., Van Assche, E., Andlauer, T. F. M., Choi, K. W., Luykx, J. J., Schulte, E. C. and Lu, Y. 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), article number: 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), article number: e139. (10.1192/bjo.2020.42)
- Brcic, L., Underwood, J., Kendall, K., Caseras, X., Kirov, G. and Davies, W. 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., Brcic, L., Underwood, J., Kendall, K., Caseras, X., Kirov, G. and Davies, W. 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., Kendall, K. M., Rees, E., Kirov, G. and Caseras, X. 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., Kendall, K., Berrett, J., Lewis, C., Anney, R., Van den Bree, M. and Hall, J. 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., Kendall, K., Berrett, J., Anney, R., Bree, M. V. D. and Hall, J. 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(5), 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), article number: 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., Thomas, R., Corkill, R. G. and Robertson, N. 2012. A neurological presentation of intravascular B-cell lymphoma. Case Reports (10.1136/bcr-2012-006439)
- Carroll, L. S., Kendall, K., O'Donovan, M. C., Owen, M. J. and Williams, N. M. 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)
Book sections
- 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
Thesis
- Kendall, K. 2021. The phenotypic expression of neuropsychiatric copy number variants. PhD Thesis, Cardiff University.
teaching_resource
- McMillan, K. and Kendall, K. 2017. Basic genetics. Royal College of Psychiatrists. - teaching_resource
- Kendall, K. 2017. Clinical genetics. Royal College of Psychiatrists. - teaching_resource
Ymchwil
Mae fy ymchwil yn canolbwyntio ar ffactorau genetig a'u dylanwad ar ganlyniadau salwch mewn salwch meddwl difrifol. Credaf ym mhwysigrwydd cyfieithu canfyddiadau ymchwil i ofal cleifion, ac rwy'n ymfalchïo mewn bod yn rhan o'r tîm y tu ôl i Wasanaeth Genomeg Seiciatrig Cymru Gyfan, clinig genomeg seiciatrig pwrpasol cyntaf y DU.
Addysgu
I teach psychiatry on the Cardiff University Medicine MBBCh course, including small group teaching on suicide and self harm and communication skills. I also examine formative and summative psychiatry ISCE examinations. I am an academic mentor to 3 students on the course and have been involved in peer reviewing a psychiatry exam question book published by the Royal College of Psychiatrists. I have also authored/co-authored two genetics modules for Trainees Online, Royal College of Psychiatrists.
Bywgraffiad
Uwch Gymrawd Clinigol, Cenhadaeth Iechyd Meddwl, Prifysgol Caerdydd
Medi 2024 – presennol
Ffrwd Waith Seicosis Cynnar, Cenhadaeth Iechyd Meddwl
- Rwy'n gweithio gydag aelodau ffrwd waith i ddatblygu ein protocolau astudio, gan gysoni'r rhain ag astudiaethau cysylltiedig.
- Rwy'n cysylltu â'r Genhadaeth Iechyd Meddwl ehangach, gan gynnwys cyflwyno i bartneriaid y diwydiant
- Rwy'n mentora dau feddyg F3 a gyflogir gan y ffrwd waith, gan eu helpu i ddatblygu eu nodau gyrfa a'u sgiliau arwain.
Treial Llwyfan Aml-fraich Seicosis Cynnar, Aml-gam (PUMA)
- Rwy'n aelod o Weithgor Seilwaith PUMA ac ar hyn o bryd rwy'n gweithio gydag aelodau PUMA i gynnal adolygiad systematig.
Astudiaeth CONNECT o Dechnoleg Gwisgadwy mewn Psychosis, Ymddiriedolaeth Wellcome
- Rwy'n cyd-arwain recriwtio Cymru ar gyfer tri bwrdd iechyd ar gyfer yr astudiaeth hon ledled y DU.
- Rwy'n rheoli ein Cydlynydd Ymchwil CONNECT.
Gwasanaeth Genomeg Seiciatrig Cymru Gyfan
- Rwy'n gweithio ochr yn ochr â genetegydd clinigol, cwnselydd genetig, a chyd-seiciatryddion i redeg y gwasanaeth hwn, sy'n cynnwys apwyntiadau cleifion, gwaith allgymorth clinigol, a gwerthusiadau gwasanaeth.
2021 - 2024, Seiciatreg Oedolion Hyfforddiant Uwch, Trac Academaidd Clinigol Cymru
- ST6, Tîm Ymyrraeth Gynnar mewn Seicosis, Bwrdd Iechyd Prifysgol Caerdydd a'r Fro.
- ST5, Merthyr Tudful CMHT, Bwrdd Iechyd Prifysgol Cwm Taf Morgannwg.
- ST4, Tîm Allgymorth ac Adferiad Gogledd / Uned Adsefydlu Tŷ Pinewood, Bwrdd Iechyd Prifysgol Cwm Taf Morgannwg.
2020 - 2021, Hyfforddiant Seiciatreg Craidd, Trac Academaidd Clinigol Cymru
- CT3, Bwrdd Iechyd Prifysgol Cwm Taf Morgannwg.
2017 - 2020, Cymrawd Ymchwil Glinigol Ymddiriedolaeth Wellcome, Canolfan MRC ar gyfer Geneteg a Genomeg Niwroseiciatrig, Prifysgol Caerdydd.
2013 - 2017, Hyfforddiant Seiciatreg Craidd, Trac Academaidd Clinigol Cymru
- CT1 - 2, Bwrdd Iechyd Prifysgol Caerdydd a'r Fro.
2011 - 2013, Hyfforddiant Meddygol Craidd, Bwrdd Iechyd Prifysgol Cwm Taf a Chaerdydd a'r Fro.
2009 - 2011, Rhaglen Sylfaen, Aneurin Bevan a Bwrdd Iechyd Prifysgol Caerdydd a'r Fro.
Anrhydeddau a dyfarniadau
2024, Ymchwilydd Gyrfa Gynnar y Flwyddyn Coleg Brenhinol y Seiciatryddion - ar y rhestr fer (roedd y canlyniad yn aros ym mis Tachwedd 2024).
2024, Uwch Gymrodoriaeth Glinigol (£140,000), Cenhadaeth Iechyd Meddwl.
2024, bwrsariaeth Cyngres Ryngwladol RCPsych, Bwrsariaeth RCPsych Cymru.
2024, Ffi presenoldeb cyrsiau hyfforddi, Gwobr Ymchwil Arweinwyr y Dyfodol mewn Seicosis.
2022, Dychwelyd canlyniadau CNV pathogenig i gyfranogwyr NCMH, Gwobr Deori Iechyd Meddwl - Categori effaith gynnar.
2020, Rôl amrywiadau rhif copi niwroddatblygiadol mewn iselder, Gwobr Ymchwil Cymdeithas Seiciatrig Ewrop.
2018, Dau grynodeb yn yr 20 cais gorau, Cystadleuaeth Ymchwilydd Gyrfa Cynnar y Flwyddyn Biobank y DU.
2016, cymrodoriaeth PhD (£202,982.66), Cymrodoriaeth Hyfforddiant Ymchwil Glinigol Ymddiriedolaeth Wellcome.
Aelodaethau proffesiynol
Tystysgrif Cwblhau Hyfforddiant Arbenigol - Seiciatreg Oedolion Cyffredinol, Cymeradwyaeth mewn Seiciatreg Adsefydlu.
Aelod o Goleg Brenhinol y Seiciatryddion (MRCPsych)
Cofrestrwyd gyda'r Cyngor Meddygol Cyffredinol (7047089)
Ymrwymiadau siarad cyhoeddus
- Cyfieithiad clinigol o ganfyddiadau genetig seiciatrig, Cymdeithas Niwrowyddoniaeth Prydain a'r Senedd (2024).
- Gwasanaeth Genomeg Seiciatrig Cymru Gyfan, Ymddiriedolaeth GIG Sefydliad Dwyrain Llundain (2024).
- Amrywiadau rhif copi mewn seiciatreg oedolion cyffredinol a'u cyfieithu i'r clinig, Canolfan SGDP, King's College Llundain (2023).
- Amrywiadau rhif copi mewn seiciatreg oedolion cyffredinol a'u cyfieithu i'r clinig, American Academy of Child and Adolescent Psychiatry Meeting (2022).
- Copïo amrywiad rhif a'u rhyngweithio â sgoriau risg polygenig mewn anhwylderau seiciatrig, Cyngres Geneteg Seiciatrig y Byd, Florence (2022).
- Trefnydd a chadeirydd, British Journal of Psychiatry Journal Club Cymru (2022).
- Amrywiadau rhif copi mewn seiciatreg oedolion cyffredinol, Adran Seiciatreg, Prifysgol Caergrawnt (2022).
- Archwilio'r rôl mae atebolrwydd genetig i sgitsoffrenia yn ei chwarae mewn salwch corfforol, trwy gysylltu â chofnodion y GIG; Caffi genomeg – rôl CNVs prin mewn anhwylderau seiciatrig, Arddangosfa Genomeg Cymru Gyfan (2021).
- Dychweliad canlyniadau CNV niwroddatblygiadol i gyfranogwyr ymchwil – materion moesegol a datblygu protocol, Cyngres Geneteg Seiciatrig y Byd (2020).
- Geneteg iechyd meddwl – CNVs prin, Gweminar Cymdeithas Frenhinol Meddygaeth (2020).
- Cyflwyniad i'r ffenomena iselder a'i epidemioleg - cyflwyniad tîm, Labordy Worldwide Consortiwm Genomeg Seiciatrig ( 2020).
- Mynegiant ffenoteipig CNVs niwroseiciatrig, Canolfan SGDP, Coleg y Brenin Llundain (2020).
Pwyllgorau ac adolygu
2024 – presennol, Aelod o Fwrdd Golygyddol Darganfod Iechyd Meddwl.
2022 - presennol, Arholwr PhD
- Prifysgol Caerdydd (arholwr mewnol).
- King's College Llundain (arholwr allanol).
- Prifysgol Montreal (arholwr allanol).
2021 - presennol, Mentor, Cynllun Mentora Cymdeithas Menywod mewn Gofal Iechyd, Barts ac Ysgol Feddygol Llundain.
2022 - presennol, Aelod o'r Pwyllgor
- Pwyllgor Aelodaeth, Cymdeithas Ryngwladol Geneteg Seiciatrig.
2018 - 2024, Ymgysylltu Allgymorth, Grŵp Schizophrenia, Consortiwm Genomeg Seiciatrig.
Parhaus, Gweithgaredd adolygu cymheiriaid
- PLoS One, Journal of Psychiatric Research, Journal of Affective Disorders, Meddygaeth Seicolegol, British Journal of Psychiatry, Seiciatreg Fiolegol, Adroddiadau Gwyddonol, Seiciatreg Moleciwlaidd, Seiciatreg JAMATRY, Geneteg Glinigol.
2015 - 2022, mentor academaidd, cwrs MBBCh Meddygaeth, Prifysgol Caerdydd.
Contact Details
KendallKM@caerdydd.ac.uk
+44 29206 88418
Adeilad Hadyn Ellis, Ystafell 2.01, Heol Maendy, Caerdydd, CF24 4HQ
+44 29206 88418
Adeilad Hadyn Ellis, Ystafell 2.01, Heol Maendy, Caerdydd, CF24 4HQ
Themâu ymchwil
Arbenigeddau
- Geneteg Seiciatrig
- Cyfieithiad Clinigol