Comparison of Risk-Prediction Instruments in Frail Older Patients Diagnosed with COVID-19

por O’Caoimh, Rónán, O’Donovan, M., McGrath, K., Moloney, E.
Publicado 2021

The relative contribution of common and rare genetic variants to ADHD

por Martin, J, O'Donovan, M C, Thapar, A, Langley, K, Williams, N
Publicado 2015

Clinical Indicators of Symptom Dimensions and Cognitive Ability in Schizophrenia

por Farakish, L., Legge, S., Owen, M., O’Donovan, M., Walters, J., Cardno, A.
Publicado 2022

Real-world implementation of non-endoscopic triage testing for Barrett’s oesophagus during COVID-19

por Landy, R, Killcoyne, S, Tang, C, Juniat, S, O’Donovan, M, Goel, N, Gehrung, M, Fitzgerald, R C
Publicado 2023

The dynamic interplay between sleep and mood: an intensive longitudinal study of individuals with bipolar disorder

por Lewis, K. J. S., Tilling, K., Gordon-Smith, K., Saunders, K. E. A., Di Florio, A., Jones, L., Jones, I., O'Donovan, M. C., Heron, J.
Publicado 2023

Investigating the genetic underpinnings of early-life irritability

por Riglin, L, Eyre, O, Cooper, M, Collishaw, S, Martin, J, Langley, K, Leibenluft, E, Stringaris, A, Thapar, A K, Maughan, B, O'Donovan, M C, Thapar, A
Publicado 2017

Steroid sulfatase is a potential modifier of cognition in attention deficit hyperactivity disorder

por Stergiakouli, E, Langley, K, Williams, H, Walters, J, Williams, N M, Suren, S, Giegling, I, Wilkinson, L S, Owen, M J, O'Donovan, M C, Rujescu, D, Thapar, A, Davies, W
Publicado 2011

Schizophrenia copy number variants and associative learning

por Clifton, N E, Pocklington, A J, Scholz, B, Rees, E, Walters, J T R, Kirov, G, O'Donovan, M C, Owen, M J, Wilkinson, L S, Thomas, K L, Hall, J
Publicado 2017

Genetic risk for schizophrenia is associated with altered visually-induced gamma band activity: evidence from a population sample stratified polygenic risk

por Dimitriadis, S. I., Perry, G., Foley, S. F., Tansey, K. E., Jones, D. K., Holmans, P., Zammit, S., Hall, J., O’Donovan, M. C., Owen, M. J., Singh, K. D., Linden, D. E.
Publicado 2021

Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia

por Ingason, A, Giegling, I, Hartmann, A M, Genius, J, Konte, B, Friedl, M, Ripke, S, Sullivan, P F, St. Clair, D, Collier, D A, O'Donovan, M C, Mirnics, K, Rujescu, D
Publicado 2015

Common alleles contribute to schizophrenia in CNV carriers

por Tansey, K E, Rees, E, Linden, D E, Ripke, S, Chambert, K D, Moran, J L, McCarroll, S A, Holmans, P, Kirov, G, Walters, J, Owen, M J, O'Donovan, M C
Publicado 2016

Erratum: Common alleles contribute to schizophrenia in CNV carriers

por Tansey, K E, Rees, E, Linden, D E, Ripke, S, Chambert, K D, Moran, J L, McCarroll, S A, Holmans, P, Kirov, G, Walters, J, Owen, M J, O'Donovan, M C
Publicado 2015

Genetic risk for schizophrenia is associated with increased proportion of indirect connections in brain networks revealed by a semi-metric analysis: evidence from population sample...

por Dimitriadis, S I, Perry, G, Lancaster, T M, Tansey, K E, Singh, K D, Holmans, P, Pocklington, A, Davey Smith, G, Zammit, S, Hall, J, O’Donovan, M C, Owen, M J, Jones, D K, Linden, D E
Publicado 2022

Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia

por Lips, E S, Cornelisse, L N, Toonen, R F, Min, J L, Hultman, C M, Holmans, P A, O'Donovan, M C, Purcell, S M, Smit, A B, Verhage, M, Sullivan, P F, Visscher, P M, Posthuma, D
Publicado 2012

MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls

por Cosgrove, D, Harold, D, Mothersill, O, Anney, R, Hill, M J, Bray, N J, Blokland, G, Petryshen, T, Richards, A, Mantripragada, K, Owen, M, O'Donovan, M C, Gill, M, Corvin, A, Morris, D W, Donohoe, G
Publicado 2017

Pilot study of cytological testing for oesophageal squamous cell dysplasia in a high-risk area in Northern Iran

por Roshandel, G, Merat, S, Sotoudeh, M, Khoshnia, M, Poustchi, H, Lao-Sirieix, P, Malhotra, S, O'Donovan, M, Etemadi, A, Nickmanesh, A, Pourshams, A, Norouzi, A, Debiram, I, Semnani, S, Abnet, C C, Dawsey, S M, Fitzgerald, R C, Malekzadeh, R
Publicado 2014

Psychiatric gene discoveries shape evidence on ADHD's biology

por Thapar, A, Martin, J, Mick, E, Arias Vásquez, A, Langley, K, Scherer, S W, Schachar, R, Crosbie, J, Williams, N, Franke, B, Elia, J, Glessner, J, Hakonarson, H, Owen, M J, Faraone, S V, O'Donovan, M C, Holmans, P
Publicado 2016

Integrated Care Models for Managing and Preventing Frailty: A Systematic Review for the European Joint Action on Frailty Prevention (ADVANTAGE JA)

por Hendry, A, Vanhecke, E, Carriazo, AM, López-Samaniego, L, Espinosa, JM, Sezgin, D, O’Donovan, M, Hammar, T, Ferry, P, Vella, A, Bacaicoa, OA, Braga, M, Ciutan, M, Velivasi, A, Lamprini Koula, M, Van der Heyden, J, Liew, A, O’Caoimh, R
Publicado 2019

Multi-omic cross-sectional cohort study of pre-malignant Barrett’s esophagus reveals early structural variation and retrotransposon activity

por Katz-Summercorn, A. C., Jammula, S., Frangou, A., Peneva, I., O’Donovan, M., Tripathi, M., Malhotra, S., di Pietro, M., Abbas, S., Devonshire, G., Januszewicz, W., Blasko, A., Nowicki-Osuch, K., MacRae, S., Northrop, A., Redmond, A. M., Wedge, D. C., Fitzgerald, R. C.
Publicado 2022

Exome arrays capture polygenic rare variant contributions to schizophrenia

por Richards, A. L., Leonenko, G., Walters, J. T., Kavanagh, D. H., Rees, E. G., Evans, A., Chambert, K. D., Moran, J. L., Goldstein, J., Neale, B. M., McCarroll, S. A., Pocklington, A. J., Holmans, P. A., Owen, M. J., O'Donovan, M. C.
Publicado 2016