Browse by Schools (by year)

, Allen, Nicholas

, Morgan, Paul

, Seshadri, Sudha, Schellenberg, Gerard, Amouvel, Philippe, Williams, Julie

and Escott-Price, Valentina

2019. Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer’s disease. PLoS ONE 14 (7) , e0218111. 10.1371/journal.pone.0218111

Barker, Roger A., Farrell, K., Guzman, N., He, X., Lazic, S., Moore, S., Morris, R., Tyers, P., Wijeyekoon, R., Daft, D., Hewitt, S., Dayal, V., Foltynie, T., Kefalopoulou, Z., Mahlknecht, P., Lao-Kaim, N., Piccini, P., Bjartmarz, H., Björklund, A., Lindvall, O., Nelander-Wahlestedt, J., Parmar, M., Paul, G., Widner, H., Church, A., Dunnett, S.

, Peall, K.

, Rosser, A.

, Gurruchaga, J., Palfi, S., Piroth, T. and Winkler, C. 2019. Designing stem-cell-based dopamine cell replacement trials for Parkinson's disease. Nature Medicine 25 (7) , pp. 1045-1053. 10.1038/s41591-019-0507-2

Benn, Caroline, Davis, John, Dawson, Lee, Dawson, Gerry, Evans, Alison, Fox, Nick, Gallacher, John, Hutton, Mike, Isaac, John, Jones, Declan, Jones, Lesley

, Libri, Vincenzo, Lovestone, Simon, Mauricio, Rui, Moody, Catherine, Noble, Wendy, Perry, Hugh, Pickett, James, Reynolds, David, Ritche, Craig, Rohrer, John, Routledge, Carol, Rowe, James, Snyder, Heather, Spires-Jones, Tara, Swartz, Jina, Truyen, Luc and Whiting, Paul 2019. Tackling gaps in developing life-changing treatments for dementia. Alzheimer's & Dementia: Translational Research & Clinical Interventions 5 , pp. 241-253. 10.1016/j.trci.2019.05.001

Bergen, Sarah E., Ploner, Alexander, Howrigan, Daniel, O'Donovan, Michael C.

, Smoller, Jordan W., Sullivan, Patrick F., Sebat, Jonathan, Neale, Benjamin and Kendler, Kenneth S. 2019. Joint contributions of rare copy number variants and common SNPs to risk for schizophrenia. American Journal of Psychiatry 176 (1) , pp. 29-35. 10.1176/appi.ajp.2018.17040467

Bertolini, Federico, Robertson, Lindsay, Ostuzzi, Giovanni, Meader, Nicholas, Bisson, Jonathan I.

, Churchill, Rachel and Barbui, Corrado 2019. Early pharmacological interventions for preventing post-traumatic stress disorder (PTSD): a network meta-analysis. Cochrane Library 10.1002/14651858.CD013443

Bhargava, Raghav, Daughters, Katie L

and Rees, D. Aled

2019. Oxytocin therapy in hypopituitarism: challenges and opportunities. Clinical Endocrinology 90 (2) , pp. 257-264. 10.1111/cen.13909

Bisson, Jonathan I

2019. Stress related disorders and physical health. BMJ 367 , 16036. 10.1136/bmj.l6036

Bondjiers, Krustina, Hyland, Philip, Roberts, Neil, Bisson, Jonathan

, Willebrand, Mimmie and Arnberg, Filip 2019. Validation of a clinician-administered diagnostic measure of ICD-11 PTSD and Complex PTSD: The International Trauma Interview in a Swedish sample. European Journal of Psychotraumatology 10 (1) , 1665617.

Brown, J. William L., Coles, Alasdair, Horakova, Dana, Havrdova, Eva, Izquierdo, Guillermo, Prat, Alexandre, Girard, Marc, Duquette, Pierre, Trojano, Maria, Lugaresi, Alessandra, Bergamaschi, Roberto, Grammond, Pierre, Alroughani, Raed, Hupperts, Raymond, McCombe, Pamela, Van Pesch, Vincent, Sola, Patrizia, Ferraro, Diana, Grand'Maison, Francois, Terzi, Murat, Lechner-Scott, Jeannette, Flechter, Schlomo, Slee, Mark, Shaygannejad, Vahid, Pucci, Eugenio, Granella, Franco, Jokubaitis, Vilija, Willis, Mark

, Rice, Claire, Scolding, Neil, Wilkins, Alastair, Pearson, Owen R, Ziemssen, Tjalf, Hutchinson, Michael, Harding, Katharine, Jones, Joanne, McGuigan, Christopher, Butzkueven, Helmut, Kalincik, Tomas and Robertson, Neil

2019. Association of initial disease-modifying therapy with later conversion to secondary progressive multiple sclerosis. Journal of the American Medical Association 321 (2) , pp. 175-187. 10.1001/jama.2018.20588

C

Calabrese, Massimiliano, Gasperini, Claudio, Tortorella, Carla, Schiavi, Gianmarco, Frisullo, Giovanni, Ragonese, Paolo, Fantozzi, Roberta, Prosperini, Luca, Annovazzi, Pietro, Cordioli, Cinzia, Di Filippo, Massimiliano, Ferraro, Diana, Gajofatto, Alberto, Malucchi, Simona, Lo Fermo, Salvatore, De Luca, Giovanna, Stromillo, Maria L., Cocco, Eleonora, Gallo, Antonio, Paolicelli, Damiano, Lanzillo, Roberta, Tomassini, Valentina

, Pesci, Ilaria, Rodegher, Maria E. and Solaro, Claudio 2019. "Better explanations" in multiple sclerosis diagnostic workup: a 3-year longitudinal study. Neurology 92 (22) , e2527. 10.1212/WNL.0000000000007573

Cameron, Darren, Blake, Derek J.

, Bray, Nicholas J.

and Hill, Matthew J.

2019. Transcriptional changes following cellular knockdown of the schizophrenia risk gene SETD1A are enriched for common variant association with the disorder. Molecular Neuropsychiatry 5 (2) , pp. 109-114. 10.1159/000497181

Castle, Dan and Robertson, Neil P.

2019. Alternatives to intravenous immunoglobulin treatment in chronic inflammatory demyelinating polyradiculoneuropathy. Journal of Neurology 266 (9) , pp. 2338-2340. 10.1007/s00415-019-09485-9

Castle, Daniel and Robertson, Neil P.

2019. Treatment of progressive multifocal leukoencephalopathy. Journal of Neurology 266 (10) , pp. 2587-2589. 10.1007/s00415-019-09501-y

Castle, Daniel, Wynford-Thomas, Ray, Loveless, Sam

, Bentley, Emily, Howell, Owain W and Tallantyre, Emma C

2019. Using biomarkers to predict clinical outcomes in multiple sclerosis. Practical Neurology 19 (4) , pp. 342-349. 10.1136/practneurol-2018-002000

Cavenagh, Alice, Chatterjee, Sohini and Davies, William

2019. Behavioural and psychiatric phenotypes in female carriers of genetic mutations associated with X-linked ichthyosis. PLoS ONE 14 (2) , e0212330. 10.1371/journal.pone.0212330

Chapman, Ria M, Tinsley, Caroline L, Hill, Matthew J

, Forrest, Marc P, Tansey, Katherine E, Pardinas, Antonio F.

, Doyle, A. Michelle, Wilkinson, Lawrence S.

, O'Donovan, Michael

and Blake, Derek J.

2019. Convergent evidence that ZNF804A is a regulator of pre-messenger RNA processing and gene expression. Schizophrenia Bulletin 45 (6) , pp. 1267-1278. 10.1093/schbul/sby183

Charney, Alexander W., Stahl, Eli A., Green, Elaine K., Chen, Chia-Yen, Moran, Jennifer L., Chambert, Kimberly, Belliveau, Richard A., Forty, Liz, Gordon-Smith, Katherine, Lee, Phil H., Bromet, Evelyn J., Buckley, Peter F., Escamilla, Michael A., Fanous, Ayman H., Fochtmann, Laura J., Lehrer, Douglas S., Malaspina, Dolores, Marder, Stephen R., Morley, Christopher P., Nicolini, Humberto, Perkins, Diana O., Rakofsky, Jeffrey J., Rapaport, Mark H., Medeiros, Helena, Sobell, Janet L., Backlund, Lena, Bergen, Sarah E., Juréus, Anders, Schalling, Martin, Lichtenstein, Paul, Knowles, James A., Burdick, Katherine E., Jones, Ian

, Jones, Lisa A., Hultman, Christina M., Perlis, Roy, Purcell, Shaun M., McCarroll, Steven A., Pato, Carlos N., Pato, Michele T., Di Florio, Arianna

, Craddock, Nick

, Landén, Mikael, Smoller, Jordan W., Ruderfer, Douglas M. and Sklar, Pamela 2019. Contribution of rare copy number variants to bipolar disorder risk Is limited to schizoaffective cases. Biological Psychiatry 86 (2) , pp. 110-119. 10.1016/j.biopsych.2018.12.009

Chu, Alexander L., Stochl, Jan, Lewis, Glyn, Zammit, Stanley

, Jones, Peter B. and Khandaker, Golam M. 2019. Longitudinal association between inflammatory markers and specific symptoms of depression in a prospective birth cohort. Brain, Behavior, and Immunity 76 , pp. 74-81. 10.1016/j.bbi.2018.11.007

Cinesi, Cinzia, Yang, Bin and Dion, Vincent

2019. GFP reporters to monitor instability and expression of expanded CAG/CTG repeats. Richard, Guy-Franck, ed. Trinucleotide Repeats: Methods and Protocols, Vol. 2056. Methods in Molecular Biology, Humana Press, pp. 255-268. (10.1007/978-1-4939-9784-8_16)

Ciosi, Marc, Maxwell, Alastair, Cumming, Sarah, Hensman Moss, Davina, Alshammari, Asma, Flower, Michael, Durr, Alexandra, Leavitt, Blair, Roos, Raymund, Holmans, Peter

, Jones, Lesley

, Langbehn, Douglas, Kwak, Seung, Tabrizi, Sarah and Monckton, Darren 2019. A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes. EBioMedicine 48 , pp. 568-580. 10.1016/j.ebiom.2019.09.020

Clifton, Nicholas E.

, Hannon, Eilis

, Harwood, Janet C., Di Florio, Arianna

, Thomas, Kerrie L.

, Holmans, Peter A.

, Walters, James T. R.

, O'Donovan, Michael

, Pocklington, Andrew J.

and Hall, Jeremy

2019. Dynamic expression of genes associated with schizophrenia and bipolar disorder across development. Translational Psychiatry 9 , 74. 10.1038/s41398-019-0405-x

Collins, Stephan C., Mikhaleva, Anna, Vrcelj, Katarina, Vancollie, Valerie E., Wagner, Christel, Demeure, Nestor, Whitley, Helen, Kannan, Meghna, Balz, Rebecca, Anthony, Lauren F. E., Edwards, Andrew, Moine, Hervé, White, Jacqueline K., Adams, David J., Reymond, Alexandre, Lelliott, Christopher J., Webber, Caleb

and Yalcin, Binnaz 2019. Large-scale neuroanatomical study uncovers 198 gene associations in mouse brain morphogenesis. Nature Communications 10 (1) , 3465. 10.1038/s41467-019-11431-2

Collishaw, Stephan

, Furzer, Emma, Thapar, Ajay K.

and Sellers, Ruth 2019. Brief report: a comparison of child mental health inequalities in three UK population cohorts. European Child and Adolescent Psychiatry 28 (11) , pp. 1547-1549. 10.1007/s00787-019-01305-9

Crawford, Karen, Bracher-Smith, Matthew, Owen, David

, Kendall, Kimberley M.

, Pardinas, Antonio F., Einon, Mark

, Escott-Price, Valentina

, Walters, James T. R.

and Kirov, George

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

Cunningham, Adam, Hill, Liam, Mon-Williams, Mark, Peall, Kathryn

, Linden, David, Hall, Jeremy

, Owen, Michael

and van den Bree, Marianne

2019. Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion Syndrome. Journal of Neurodevelopmental Disorders 11 , 8. 10.1186/s11689-019-9271-3

Czamara, Darina, Eraslan, Gökçen, Page, Christian M., Lahti, Jari, Lahti-Pulkkinen, Marius, Hämäläinen, Esa, Kajantie, Eero, Laivuori, Hannele, Villa, Pia M., Reynolds, Rebecca M., Nystad, Wenche, Håberg, Siri E., London, Stephanie J., O'Donnell, Kieran J., Garg, Elika, Meaney, Michael J., Entringer, Sonja, Wadhwa, Pathik D., Buss, Claudia, Jones, Meaghan J., Lin, David T. S., MacIsaac, Julie L., Kobor, Michael S., Koen, Nastassja, Zar, Heather J., Koenen, Karestan C., Dalvie, Shareefa, Stein, Dan J., Kondofersky, Ivan, Müller, Nikola S., Theis, Fabian J., Räikkönen, Katri, Binder, Elisabeth B., Craddock, Nick

, Escott-Price, Valentina

2019. Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. Nature Communications 10 , 2548. 10.1038/s41467-019-10461-0

D

D'Ambrosio, Enrico, Dahoun, Tarik, Pardinas, Antonio F.

, Veronese, Mattia, Bloomfield, Michael A.P., Jauhar, Sameer, Bonoldi, Ilaria, Rogdaki, Maria, Froudist-Walsh, Sean, Walters, James T. R.

and Howes, Oliver D. 2019. The effect of a genetic variant at the schizophrenia associated AS3MT/BORCS7 locus on striatal dopamine function: A PET imaging study. Psychiatry Research: Neuroimaging 291 , pp. 34-41. 10.1016/j.pscychresns.2019.07.005

Davda, Nikunj, Tallantyre, Emma

and Robertson, Neil P.

2019. Early MRI predictors of prognosis in multiple sclerosis. Journal of Neurology 266 (12) , pp. 3171-3173. 10.1007/s00415-019-09589-2

Davies, Jennifer R.

, Wilkinson, Lawrence S.

, Isles, Anthony R.

and Humby, Trevor

2019. Prader-Willi syndrome imprinting centre deletion mice have impaired baseline and 5-HT2CR-mediated response inhibition. Human Molecular Genetics 28 (18) , pp. 3013-3023. 10.1093/hmg/ddz100

Davies, Molly R., Kalsi, Gursharan, Armour, Chérie, Jones, Ian R.

, McIntosh, Andrew M., Smith, Daniel J., Walters, James T.R.

, Bradley, John R., Kingston, Nathalie, Ashford, Sofie, Beange, Ioana, Brailean, Anamaria, Cleare, Anthony J., Coleman, Jonathan R.I., Curtis, Charles J., Curzons, Susannah C.B., Davis, Katrina A.S., Dowey, Le Roy C., Gault, Victor A., Goldsmith, Kimberley A., Bennett, Megan Hammond, Hirose, Yoriko, Hotopf, Matthew, Hübel, Christopher, Kanz, Carola, Leng, Jennifer, Lyall, Donald M., Mason, Bethany D., McAtarsney-Kovacs, Monika, Monssen, Dina, Moulton, Alexei, Ovington, Nigel, Palaiologou, Elisavet, Pariante, Carmine M., Parikh, Shivani, Peel, Alicia J., Price, Ruth K., Rimes, Katharine A., Rogers, Henry C., Sambrook, Jennifer, Skelton, Megan, Spaul, Anna, Suarez, Eddy L.A., Sykes, Bronte L., Thomas, Keith G., Young, Allan H., Vassos, Evangelos, Veale, David, White, Katie M., Wingrove, Janet, Eley, Thalia C. and Breen, Gerome 2019. The Genetic Links to Anxiety and Depression (GLAD) study: online recruitment into the largest recontactable study of depression and anxiety. Behaviour Research and Therapy 123 , 103503. 10.1016/j.brat.2019.103503

Davies, William

2019. An analysis of Cellular Communication Network (CCN) proteins as candidate mediators of postpartum psychosis risk. Frontiers in Psychiatry 10 , 876. 10.3389/fpsyt.2019.00876

Davies, William

and Wilkinson, Lawrence

2019. Editorial overview: special issue on epigenetics and genomic imprinting. Current Opinion in Behavioral Sciences 25 , iii-v. 10.1016/j.cobeha.2018.12.006

Di Florio, Arianna

, Gordon-Smith, Katherine, Forty, Liz, Kosorok, Michael R., Fraser, Christine, Perry, Amy, Bethell, Andrew, Craddock, Nick

, Jones, Lisa and Jones, Ian R.

2019. Stratification of the risk of bipolar disorder recurrences in pregnancy and postpartum. British Journal of Psychiatry 213 (3) , pp. 542-547. 10.1192/bjp.2018.92

Dimitriadis, Stavros I.

, Simos, Panagiotis G., Fletcher, Jack M. and Papanicolaou, Andrew C. 2019. Typical and aberrant functional brain flexibility: lifespan development and aberrant organization in traumatic brain injury and dyslexia. Brain Sciences 9 (12) , 380. 10.3390/brainsci9120380

Douglas, Katie, Groves, Samantha, Porter, Richard, Jorden, Jenny, Wilson, Lynere, Melzer, Tracy, Wise, Richard

, Bisson, Jonathan

and Bell, Caroline 2019. Traumatic imagery following glucocorticoid administration in earthquake-related post-traumatic stress disorder: A preliminary functional magnetic resonance imaging study. Australian and New Zealand Journal of Psychiatry 53 (12) , pp. 1167-1178. 10.1177/0004867419851860

Drakesmith, Mark

, Parker, Greg D., Smith, Jacqueline, Linden, Stefanie C., Rees, Elliott

, Williams, Nigel

, van den Bree, Marianne

, Jones, Derek K.

and Linden, David E. J. 2019. Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white-matter structures. Translational Psychiatry 9 (1) , 102. 10.1038/s41398-019-0440-7

Duarte, Rodrigo R.R., Bachtel, Nathaniel D., Côtel, Marie-Caroline, Lee, Sang H., Selvackadunco, Sashika, Watson, Iain A., Hovsepian, Gary A., Troakes, Claire, Breen, Gerome D., Nixon, Douglas F., Murray, Robin M., Bray, Nicholas J.

, Eleftherianos, Ioannis, Vernon, Anthony C., Powell, Timothy R. and Srivastava, Deepak P. 2019. The psychiatric risk gene NT5C2 regulates adenosine monophosphate-activated protein kinase signaling and protein translation in human neural progenitor cells. Biological Psychiatry 86 (2) , pp. 120-130. 10.1016/j.biopsych.2019.03.977

E

Eaton, C. B.

, Thomas, R. H.

, Hamandi, K. H., Payne, G. C., Kerr, M. P., Linden, D. E. J.

, Owen, M. J.

, Cunningham, A. C., Bartsch, U. B., Struik, S. S. and van den Bree, M. B. M.

2019. Prevalence and aetiology of epileptic seizures in young people with 22Q11.2 Deletion syndrome and relationships with other neurodevelopmental disorders. Presented at: SSBP 22nd Educational Day and Research Symposium 2019, Birmingham, England, 4-6 September 2019. Journal of Intellectual Disability Research. , vol.63 (9) Wiley, p. 1080. 10.1111/jir.12676

Eggink, Hendriekje, Coenen, Maraike A., de Jong, Ronald, Toonen, Rivka F., Eissens, Melanie H., Veenstra, Wencke S., Peall, Kathryn J.

, Sival, Deborah A., Elema, Agnes and Tijssen, Marina AJ. 2019. Motor and non-motor determinants of health-related quality of life in young dystonia patients. Parkinsonism & Related Disorders 58 , pp. 50-55. 10.1016/j.parkreldis.2018.08.008

Egmond, Martje E., Contarino, Maria Fiorella, Lugtenberg, Coen H.A., Peall, Kathryn J.

, Brouwer, Oebele F., Fung, Victor S.C., Roze, Emmanuel, Stewart, Roy E., Willemsen, Michel A., Wolf, Nicole I., Koning, Tom J. and Tijssen, Marina A. 2019. Variable interpretation of the dystonia consensus classification items compromises its solidity. Movement Disorders 34 (3) , pp. 317-320. 10.1002/mds.27627

Ellis, Colin A., Berkovic, Samuel F., Epstein, Michael P., Ottman, Ruth, Epi4K Consortium, Smith, Phil E. M.

and Thomas, Rhy H. 2019. The “maternal effect” on epilepsy risk: analysis of familial epilepsies and reassessment of prior evidence. Annals of Neurology 87 (1) , pp. 132-138. 10.1002/ana.25625

Ellis, Natalie, Grubb, Carla-Marie, Mustoe, Sophie, Watkins, Eleanor, Codling, David, Fitch, Sarah, Stirland, Lucy, Quraishy, Munzir, Jenkinson, Josie and Harrison, Judith

2019. Venous thromboembolism risk in psychiatric in-patients: a multicentre cross-sectional study. BJPsych Bulletin 43 (6) , pp. 255-259. 10.1192/bjb.2019.25

Escott-Price, Valentina

, Baker, Emily, Shoai, Maryam, Leonenko, Ganna

, Myers, Amanda J., Huentelman, Matt and Hardy, John 2019. Genetic analysis suggests high misassignment rates in clinical Alzheimer's cases and controls. Neurobiology of Aging 77 , pp. 178-182. 10.1016/j.neurobiolaging.2018.12.002

Escott-Price, Valentina

, Bracher-Smith, Matthew, Menzies, Georgina

, Walters, James

2019. Genetic liability to schizophrenia is negatively associated with educational attainment in UK Biobank. Journal of Molecular Psychiatry , -. 10.1038/s41380-018-0328-6
Item availability restricted.

Escott-Price, Valentina

, Pardinas, Antonio F.

, Santiago, Enrique, Walters, James

2019. The relationship between common variant schizophrenia liability and number of offspring in the UK Biobank. American Journal of Psychiatry 176 (8) , pp. 661-666. 10.1176/appi.ajp.2018.18020140

Escott-Price, Valentina

, Smith, Daniel J., Kendall, Kimberley

, Ward, Joey, Kirov, George

, Walters, James

2019. Polygenic risk for schizophrenia and season of birth within the UK Biobank cohort. Psychological Medicine 49 (15) , pp. 2499-2504. 10.1017/S0033291718000454

F

Favre, Pauline, Pauling, Melissa, Stout, Jacques, Hozer, Franz, Sarrazin, Samuel, Abé, Christoph, Alda, Martin, Alloza, Clara, Alonso-Lana, Silvia, Andreassen, Ole A., Baune, Bernhard T., Benedetti, Francesco, Busatto, Geraldo F., Canales-Rodríguez, Erick J., Caseras, Xavier

, Chaim-Avancini, Tiffany Moukbel, Ching, Christopher R. K., Dannlowski, Udo, Deppe, Michael, Eyler, Lisa T., Fatjo-Vilas, Mar, Foley, Sonya F.

, Grotegerd, Dominik, Hajek, Tomas, Haukvik, Unn K., Howells, Fleur M., Jahanshad, Neda, Kugel, Harald, Lagerberg, Trine V., Lawrie, Stephen M., Linke, Julia O., McIntosh, Andrew, Melloni, Elisa M. T., Mitchell, Philip B., Polosan, Mircea, Pomarol-Clotet, Edith, Repple, Jonathan, Roberts, Gloria, Roos, Annerine, Rosa, Pedro G. P., Salvador, Raymond, Sarró, Salvador, Schofield, Peter R., Serpa, Mauricio H., Sim, Kang, Stein, Dan J., Sussmann, Jess E., Temmingh, Henk S., Thompson, Paul M., Verdolini, Norma, Vieta, Eduard, Wessa, Michele, Whalley, Heather C., Zanetti, Marcus V., Leboyer, Marion, Mangin, Jean-François, Henry, Chantal, Duchesnay, Edouard and Houenou, Josselin 2019. Widespread white matter microstructural abnormalities in bipolar disorder: evidence from mega- and meta-analyses across 3033 individuals. Neuropsychopharmacology 44 , pp. 2285-2293. 10.1038/s41386-019-0485-6

Flower, Michael, Lomeilkaite, Vilila, Ciosi, Marc, Cumming, Sarah, Morales, Fernando, Lo, Kitty, Hensman Moss, Davina, Jones, Lesley

, Monckton, Darren G., Tabrizi, Sarah J., Kraus, Peter, Hoffman, Rainer, Tobin, Alan, Borowsky, Beth, Keenan, S., Whitlock, Kathryn B., Queller, Sarah, Campbell, Colin, Wang, Chiachi, Langbehn, Doug, Axelson, Eric, Johnson, Hans, Acharya, Tanka, Cash, Dave M., Frost, Chris, Jones, Rebecca

, Jurgens, Caroline, ‘t Hart, Ellen P., van der Grond, Jeroen, Witjes- Ane, Marie-Noelle N., Roos, Raymund A. C., Dumas, Eve M., van den Bogaard, Simon J. A., Stopford, Cheryl, Craufurd, David, Callaghan, Jenny, Arran, Natalie, Rosas, Diana D., Lee, S., Monaco, W., O’Regan, Alison, Milchman, Cassie, Frajman, E., Labuschagne, Izelle, Stout, Julie, Campbell, Melissa, Andrews, Sophie C., Bechtel, Natalie, Reilmann, Ralf, Bohlen, Stefan, Kennard, Chris, Berna, Claire, Hicks, Stephen, Durr, Alexandra, Pourchot, C., Bardinet, Eric, Nigaud, Kevin, Valabre`gue, Romain, Lehericy, Stephane, Marelli, Cecilia, Jauffret, Celine, Justo, Damian, Leavitt, Blair, Decolongon, Joji, Sturrock, Aaron, Coleman, Alison, Dar Santos, Rachelle, Patel, A., Gibbard, Claire, Whitehead, Daisy, Wild, Ed, Owen, Gail, Crawford, Helen, Malone, Ian, Lahiri, Nayana, Fox, Nick C., Hobbs, Nicola Z., Scahill, Rachael I., Ordidge, Roger, Pepple, Tracey, Read, Joy, Say, Miranda J., Landwehrmeyer, Bernhard, Daidj, Ferroudja, Bassez, Guillaume, Lignier, Baptiste, Couppey, Florence, Delmas, Stéphanie, Deux, Jean-François, Hankiewicz, Karolina, Dogan, Celine, Minier, Lisa, Chevalier, Pascale, Hamadouche, Amira, Catt, Michael, van Hees, Vincent, Catt, Sharon, Schwalber, Ameli, Dittrich, Juliane, Kierkegaard, Marie, Wenninger, Stephan, Schoser, Benedikt, Schüller, Angela, Stahl, Kristina, Künzel, Heike, Wolff, Martin, Jellinek, Anna, Moreno, Cecilia Jimenez, Gorman, Grainne, Lochmüller, Hanns, Trenell, Michael, van Laar, Sandra, Wood, Libby, Cassidy, Sophie, Newman, Jane, Charman, Sarah, Steffaneti, Renae, Taylor, Louise, Brownrigg, Allan, Day, Sharon, Atalaia, Antonio, Raaphorst, Joost, Okkersen, Kees, Engelen, Baziel van, Nikolaus, Stephanie, Cornelissen, Yvonne, van Nimwegen, Marlies, Maas, Daphne, Klerks, Ellen, Bouman, Sacha, Knoop, Hans, Heskamp, Linda, Heerschap, Arend, Rahmadi, Ridho, Groot, Perry, Heskes, Tom, Kapusta, Katarzyna, Glennon, Jeffrey, Abghari, Shaghayegh, Aschrafi, Armaz, Poelmans, Geert, Treweek, Shaun, Hogarth, Fiona, Littleford, Roberta, Donnan, Peter, Hapca, Adrian, Hannah, Michael, McKenzie, Emma, Rauchhaus, Petra, Cumming, Sarah A., Adam, Berit, Faber, Catharina, Merkies, Ingemar, TRACK-HD Investigators and OPTIMISTIC Consortium 2019. MSH3 modifies somatic instability and disease severity in Huntington’s and myotonic dystrophy type 1. Brain 142 (7) , pp. 1876-1886. 10.1093/brain/awz115

Fonville, Leon, Drakesmith, Mark

, Zammit, Stanley

, Lewis, Glyn, Jones, Derek

and David, Anthony S 2019. MRI indices of cortical development in young people with psychotic experiences: influence of genetic risk and persistence of symptoms. Schizophrenia Bulletin 45 (1) , pp. 169-179. 10.1093/schbul/sbx195

G

Garay, Samantha M., Savory, Katrina A., Sumption, Lorna A.

, Penketh, Richard J.A., Jones, Ian R.

, Janssen, Anna B. and John, Rosalind M.

2019. Seasonal variation in salivary cortisol but not symptoms of depression and trait anxiety in pregnant women undergoing an elective caesarean section. Psychoneuroendocrinology 108 , pp. 14-19. 10.1016/j.psyneuen.2019.05.029

Germuska, Michael

, Chandler, Hannah L., Stickland, Rachael

, Foster, Catherine

, Fasano, Fabrizio, Okell, T.W., Steventon, Jessica, Tomassini, Valentina

, Murphy, Kevin

and Wise, Richard

2019. Dual-calibrated fMRI measurement of absolute cerebral metabolic rate of oxygen consumption and effective oxygen diffusivity. NeuroImage 184 , pp. 717-728. 10.1016/j.neuroimage.2018.09.035

Goold, Robert, Flower, Michael, Moss, Davina Hensman, Medway, Christopher

, Wood-Kaczmar, Alison, Andre, Ralph, Farshim, Pamela, Bates, Gill P, Holmans, Peter

, Jones, Lesley

and Tabrizi, Sarah J 2019. FAN1 modifies Huntington's disease progression by stabilising the expanded HTT CAG repeat. Human Molecular Genetics 28 (4) , pp. 650-661. 10.1093/hmg/ddy375

Gordon-Smith, Katherine, Saunders, Kate, Geddes, John R, Harrison, Paul J, Hinds, Chris, Craddock, Nick

and Jones, Lisa 2019. Large-scale roll out of electronic longitudinal mood-monitoring for research in affective disorders: Report from the UK bipolar disorder research network. Journal of Affective Disorders 246 , pp. 789-793. 10.1016/j.jad.2018.12.099

Gorman, Kathleen M., Meyer, Esther, Grozeva, Detelina

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