Fractional anisotropy of the uncinate fasciculus and cingulum in bipolar disorder type I, type II, unaffected siblings and healthy controls

por Foley, Sonya F., Bracher-Smith, Matthew, Tansey, Katherine E., Harrison, Judith R., Parker, Greg D., Caseras, Xavier
Publicado 2018

Copy Number Variants Increasing Risk for Schizophrenia: Shared and Distinct Effects on Brain Morphometry and Cognitive Performance

por Caseras, Xavier, Legge, Sophie E., Bracher-Smith, Matthew, Anney, Richard, Owen, Michael J., Escott-Price, Valentina, Kirov, George
Publicado 2022

Age-dependent effect of APOE and polygenic component on Alzheimer's disease

por Bellou, Eftychia, Baker, Emily, Leonenko, Ganna, Bracher-Smith, Matthew, Daunt, Paula, Menzies, Georgina, Williams, Julie, Escott-Price, Valentina
Publicado 2020

Effects of genomic copy number variants penetrant for schizophrenia on cortical thickness and surface area in healthy individuals: analysis of the UK Biobank

por Caseras, Xavier, Kirov, George, Kendall, Kimberley M., Rees, Elliott, Legge, Sophie E., Bracher-Smith, Matthew, Escott-Price, Valentina, Murphy, Kevin
Publicado 2021

Machine learning for the life-time risk prediction of Alzheimer’s disease: a systematic review

por Rowe, Thomas W, Katzourou, Ioanna K, Stevenson-Hoare, Joshua O, Bracher-Smith, Matthew R, Ivanov, Dobril K, Escott-Price, Valentina
Publicado 2021

Machine learning for prediction of schizophrenia using genetic and demographic factors in the UK biobank

por Bracher-Smith, Matthew, Rees, Elliott, Menzies, Georgina, Walters, James T.R., O'Donovan, Michael C., Owen, Michael J., Kirov, George, Escott-Price, Valentina
Publicado 2022

Whole genome analysis in APOE4 homozygotes identifies the DAB1-RELN pathway in Alzheimer's disease pathogenesis

por Bracher-Smith, Matthew, Leonenko, Ganna, Baker, Emily, Crawford, Karen, Graham, Andrew C., Salih, Dervis A., Howell, Brian W., Hardy, John, Escott-Price, Valentina
Publicado 2022

Pathway-specific polygenic scores for Alzheimer’s disease are associated with changes in brain structure in younger and older adults

por Harrison, Judith R, Foley, Sonya F, Baker, Emily, Bracher-Smith, Matthew, Holmans, Peter, Stergiakouli, Evie, Linden, David E J, Caseras, Xavier, Jones, Derek K, Escott-Price, Valentina
Publicado 2023

Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach

por Donnelly, Nicholas, Cunningham, Adam, Salas, Sergio Marco, Bracher-Smith, Matthew, Chawner, Samuel, Stochl, Jan, Ford, Tamsin, Raymond, F. Lucy, Escott-Price, Valentina, van den Bree, Marianne B. M.
Publicado 2023

Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank

por Kendall, Kimberley M., Bracher-Smith, Matthew, Fitzpatrick, Harry, Lynham, Amy, Rees, Elliott, Escott-Price, Valentina, Owen, Michael J., O'Donovan, Michael C., Walters, James T.R., Kirov, George
Publicado 2019

Predictive modeling of schizophrenia from genomic data: Comparison of polygenic risk score with kernel support vector machines approach

por Vivian‐Griffiths, Timothy, Baker, Emily, Schmidt, Karl M., Bracher‐Smith, Matthew, Walters, James, Artemiou, Andreas, Holmans, Peter, O'Donovan, Michael C., Owen, Michael J., Pocklington, Andrew, Escott‐Price, Valentina
Publicado 2018

Association of Rare Copy Number Variants With Risk of Depression

por Kendall, Kimberley Marie, Rees, Elliott, Bracher-Smith, Matthew, Legge, Sophie, Riglin, Lucy, Zammit, Stanley, O’Donovan, Michael Conlon, Owen, Michael John, Jones, Ian, Kirov, George, Walters, James Tynan Rhys
Publicado 2019

Association of genetic liability for psychiatric disorders with accelerometer-assessed physical activity in the UK Biobank

por Dennison, Charlotte A., Legge, Sophie E., Bracher-Smith, Matthew, Menzies, Georgina, Escott-Price, Valentina, Smith, Daniel J., Doherty, Aiden R., Owen, Michael J., O’Donovan, Michael C., Walters, James T. R.
Publicado 2021

Polygenic risk for schizophrenia and subcortical brain anatomy in the UK Biobank cohort

por Grama, Steluta, Willcocks, Isabella, Hubert, John J., Pardiñas, Antonio F., Legge, Sophie E., Bracher-Smith, Matthew, Menzies, Georgina E., Hall, Lynsey S., Pocklington, Andrew J., Anney, Richard J. L., Bray, Nicholas J., Escott-Price, Valentina, Caseras, Xavier
Publicado 2020

The Duffy-null genotype and risk of infection

por Legge, Sophie E, Christensen, Rune H, Petersen, Liselotte, Pardiñas, Antonio F, Bracher-Smith, Matthew, Knapper, Steven, Bybjerg-Grauholm, Jonas, Baekvad-Hansen, Marie, Hougaard, David M, Werge, Thomas, Nordentoft, Merete, Mortensen, Preben Bo, Owen, Michael J, O’Donovan, Michael C, Benros, Michael E, Walters, James T R
Publicado 2020

Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits

por Legge, Sophie E., Jones, Hannah J., Kendall, Kimberley M., Pardiñas, Antonio F., Menzies, Georgina, Bracher-Smith, Matthew, Escott-Price, Valentina, Rees, Elliott, Davis, Katrina A. S., Hotopf, Matthew, Savage, Jeanne E., Posthuma, Danielle, Holmans, Peter, Kirov, George, Owen, Michael J., O’Donovan, Michael C., Zammit, Stanley, Walters, James T. R.
Publicado 2019