Dr Kimberley Kendall
WCAT Fellow, Division of Psychological Medicine and Clinical Neurosciences
- kendallkm@cardiff.ac.uk
- +44 (0)29 2068 8418
- 2.01 - Desk 36, Adeilad Hadyn Ellis, Heol Maendy, Caerdydd, CF24 4HQ
Trosolwg
I am a psychiatrist doing my PhD on copy number variation in adult psychiatric disorders funded by a Wellcome Trust Clinical Research Fellowship.
Bywgraffiad
Education and Qualifications
Member of the Royal College of Psychiatrists (MRCPsych)
Medicine MBBCh, Cardiff University
Medical Genetics BSc - First Class Honours, Cardiff University
Anrhydeddau a Dyfarniadau
2017 Wellcome Trust Clinical Research Training Fellowship
2012 Cardiff MRC Centre Clinical Academic Mentorship Scheme
2007 Wellcome Trust Vacation Scholarship
Aelodaethau proffesiynol
Member of the Royal College of Psychiatrists (MRCPsych)
Registered with the General Medical Council (7047089)
Safleoedd academaidd blaenorol
2017 - present Wellcome Trust Clinical Research Fellow, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University
2013 - present Wales Clinical Academic Track Fellow, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University
Pwyllgorau ac adolygu
2017 - present Athena SWAN Self Assessment Team, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University
Cyhoeddiadau
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)
- 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
- Kendall, K. 2017. Clinical genetics. Royal College of Psychiatrists. - teaching_resource
- McMillan, K. and Kendall, K. 2017. Basic genetics. Royal College of Psychiatrists. - teaching_resource
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)
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.
My research is on copy number variants (CNVs) in major psychiatric disorders that affect adults. I am particularly interested in the phenotypic expression of neuropsychiatric CNVs.