Copy number variations in neurodevelopmental disorders
Grayton, Hannah M, Fernandes, Cathy, Rujescu, Dan, Collier, David A
Published in Progress in neurobiology (01.10.2012)
Published in Progress in neurobiology (01.10.2012)
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An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation
Hannon, Eilis, Dempster, Emma, Viana, Joana, Burrage, Joe, Smith, Adam R, Macdonald, Ruby, St Clair, David, Mustard, Colette, Breen, Gerome, Therman, Sebastian, Kaprio, Jaakko, Toulopoulou, Timothea, Hulshoff Pol, Hilleke E, Bohlken, Marc M, Kahn, Rene S, Nenadic, Igor, Hultman, Christina M, Murray, Robin M, Collier, David A, Bass, Nick, Gurling, Hugh, McQuillin, Andrew, Schalkwyk, Leonard, Mill, Jonathan
Published in Genome Biology (30.08.2016)
Published in Genome Biology (30.08.2016)
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Benchmarking causal reasoning algorithms for gene expression-based compound mechanism of action analysis
Hosseini-Gerami, Layla, Higgins, Ixavier Alonzo, Collier, David A, Laing, Emma, Evans, David, Broughton, Howard, Bender, Andreas
Published in BMC bioinformatics (18.04.2023)
Published in BMC bioinformatics (18.04.2023)
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Galectin-3 activates spinal microglia to induce inflammatory nociception in wild type but not in mice modelling Alzheimer’s disease
Sideris-Lampretsas, George, Oggero, Silvia, Zeboudj, Lynda, Silva, Rita, Bajpai, Archana, Dharmalingam, Gopuraja, Collier, David A., Malcangio, Marzia
Published in Nature communications (22.06.2023)
Published in Nature communications (22.06.2023)
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Full-length transcript sequencing of human and mouse cerebral cortex identifies widespread isoform diversity and alternative splicing
Leung, Szi Kay, Jeffries, Aaron R., Castanho, Isabel, Jordan, Ben T., Moore, Karen, Davies, Jonathan P., Dempster, Emma L., Bray, Nicholas J., O’Neill, Paul, Tseng, Elizabeth, Ahmed, Zeshan, Collier, David A., Jeffery, Erin D., Prabhakar, Shyam, Schalkwyk, Leonard, Jops, Connor, Gandal, Michael J., Sheynkman, Gloria M., Hannon, Eilis, Mill, Jonathan
Published in Cell reports (Cambridge) (16.11.2021)
Published in Cell reports (Cambridge) (16.11.2021)
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Expression-based drug screening of neural progenitor cells from individuals with schizophrenia
Readhead, Benjamin, Hartley, Brigham J., Eastwood, Brian J., Collier, David A., Evans, David, Farias, Richard, He, Ching, Hoffman, Gabriel, Sklar, Pamela, Dudley, Joel T., Schadt, Eric E., Savić, Radoslav, Brennand, Kristen J.
Published in Nature communications (24.10.2018)
Published in Nature communications (24.10.2018)
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A genome-wide association study in individuals of African ancestry reveals the importance of the Duffy-null genotype in the assessment of clozapine-related neutropenia
Legge, Sophie E., Pardiñas, Antonio F., Helthuis, Marinka, Jansen, John A., Jollie, Karel, Knapper, Steven, MacCabe, James H., Rujescu, Dan, Collier, David A., O’Donovan, Michael C., Owen, Michael J, Walters, James T. R.
Published in Molecular psychiatry (01.03.2019)
Published in Molecular psychiatry (01.03.2019)
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Transcriptional Signatures of Tau and Amyloid Neuropathology
Castanho, Isabel, Murray, Tracey K., Hannon, Eilis, Jeffries, Aaron, Walker, Emma, Laing, Emma, Baulf, Hedley, Harvey, Joshua, Bradshaw, Lauren, Randall, Andrew, Moore, Karen, O’Neill, Paul, Lunnon, Katie, Collier, David A., Ahmed, Zeshan, O’Neill, Michael J., Mill, Jonathan
Published in Cell reports (Cambridge) (11.02.2020)
Published in Cell reports (Cambridge) (11.02.2020)
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Rare Deletions at the Neurexin 3 Locus in Autism Spectrum Disorder
Vaags, Andrea K., Lionel, Anath C., Sato, Daisuke, Goodenberger, McKinsey, Stein, Quinn P., Curran, Sarah, Ogilvie, Caroline, Ahn, Joo Wook, Drmic, Irene, Senman, Lili, Chrysler, Christina, Thompson, Ann, Russell, Carolyn, Prasad, Aparna, Walker, Susan, Pinto, Dalila, Marshall, Christian R., Stavropoulos, Dimitri J., Zwaigenbaum, Lonnie, Fernandez, Bridget A., Fombonne, Eric, Bolton, Patrick F., Collier, David A., Hodge, Jennelle C., Roberts, Wendy, Szatmari, Peter, Scherer, Stephen W.
Published in American journal of human genetics (13.01.2012)
Published in American journal of human genetics (13.01.2012)
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Common variants on 8p12 and 1q24.2 confer risk of schizophrenia
Shi, Yongyong, Li, Zhiqiang, Xu, Qi, Wang, Ti, Li, Tao, Shen, Jiawei, Zhang, Fengyu, Chen, Jianhua, Zhou, Guoquan, Ji, Weidong, Li, Baojie, Xu, Yifeng, Liu, Dengtang, Wang, Peng, Yang, Ping, Liu, Benxiu, Sun, Wensheng, Wan, Chunling, Qin, Shengying, He, Guang, Steinberg, Stacy, Cichon, Sven, Werge, Thomas, Sigurdsson, Engilbert, Tosato, Sarah, Palotie, Aarno, Nöthen, Markus M, Rietschel, Marcella, Ophoff, Roel A, Collier, David A, Rujescu, Dan, Clair, David St, Stefansson, Hreinn, Stefansson, Kari, Ji, Jue, Wang, Qingzhong, Li, Wenjin, Zheng, Linqing, Zhang, Hairong, Feng, Guoyin, He, Lin
Published in Nature genetics (01.12.2011)
Published in Nature genetics (01.12.2011)
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Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders
Tropeano, Maria, Ahn, Joo Wook, Dobson, Richard J B, Breen, Gerome, Rucker, James, Dixit, Abhishek, Pal, Deb K, McGuffin, Peter, Farmer, Anne, White, Peter S, Andrieux, Joris, Vassos, Evangelos, Ogilvie, Caroline Mackie, Curran, Sarah, Collier, David A
Published in PloS one (18.04.2013)
Published in PloS one (18.04.2013)
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Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women
Shifman, Sagiv, Johannesson, Martina, Bronstein, Michal, Chen, Sam X, Collier, David A, Craddock, Nicholas J, Kendler, Kenneth S, Li, Tao, O'Donovan, Michael, O'Neill, F Anthony, Owen, Michael J, Walsh, Dermot, Weinberger, Daniel R, Sun, Cuie, Flint, Jonathan, Darvasi, Ariel
Published in PLoS genetics (01.02.2008)
Published in PLoS genetics (01.02.2008)
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BrainSeq: Neurogenomics to Drive Novel Target Discovery for Neuropsychiatric Disorders
Schubert, Christian R., O’Donnell, Patricio, Quan, Jie, Wendland, Jens R., Xi, Hualin S., Winslow, Ashley R., Domenici, Enrico, Essioux, Laurent, Kam-Thong, Tony, Airey, David C., Calley, John N., Collier, David A., Wang, Hong, Eastwood, Brian, Ebert, Philip, Liu, Yushi, Nisenbaum, Laura, Ruble, Cara, Scherschel, James E., Smith, Ryan Matthew, Qian, Hui-Rong, Merchant, Kalpana, Didriksen, Michael, Matsumoto, Mitsuyuki, Saito, Takeshi, Brandon, Nicholas J., Cross, Alan J., Wang, Qi, Manji, Husseini, Kolb, Hartmuth, Furey, Maura, Drevets, Wayne C., Shin, Joo Heon, Jaffe, Andrew E., Jia, Yankai, Straub, Richard E., Deep-Soboslay, Amy, Hyde, Thomas M., Kleinman, Joel E., Weinberger, Daniel R.
Published in Neuron (Cambridge, Mass.) (16.12.2015)
Published in Neuron (Cambridge, Mass.) (16.12.2015)
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A human tau seeded neuronal cell model recapitulates molecular responses associated with Alzheimer’s disease
Ficulle, Elena, Kananathan, Sarubini, Airey, David, Gharbi, Severine I., Humphryes-Kirilov, Neil, Scherschel, James, Dunbar, Charlotte, Eastwood, Brian J., Laing, Emma, Collier, David A., Bose, Suchira
Published in Scientific reports (17.02.2022)
Published in Scientific reports (17.02.2022)
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PACAP and PAC1 receptor in brain development and behavior
Shen, Sanbing, Gehlert, Donald R, Collier, David A
Published in Neuropeptides (Edinburgh) (01.12.2013)
Published in Neuropeptides (Edinburgh) (01.12.2013)
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Genome-wide RNAseq study of the molecular mechanisms underlying microglia activation in response to pathological tau perturbation in the rTg4510 tau transgenic animal model
Wang, Hong, Li, Yupeng, Ryder, John W, Hole, Justin T, Ebert, Philip J, Airey, David C, Qian, Hui-Rong, Logsdon, Benjamin, Fisher, Alice, Ahmed, Zeshan, Murray, Tracey K, Cavallini, Annalisa, Bose, Suchira, Eastwood, Brian J, Collier, David A, Dage, Jeffrey L, Miller, Bradley B, Merchant, Kalpana M, O'Neill, Michael J, Demattos, Ronald B
Published in Molecular neurodegeneration (17.12.2018)
Published in Molecular neurodegeneration (17.12.2018)
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Journal Article
Ohnologs are overrepresented in pathogenic copy number mutations
McLysaght, Aoife, Makino, Takashi, Grayton, Hannah M., Tropeano, Maria, Mitchell, Kevin J., Vassos, Evangelos, Collier, David A.
Published in Proceedings of the National Academy of Sciences - PNAS (07.01.2014)
Published in Proceedings of the National Academy of Sciences - PNAS (07.01.2014)
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At-Risk Variant in TCF7L2 for Type II Diabetes Increases Risk of Schizophrenia
Hansen, Thomas, Ingason, Andrés, Djurovic, Srdjan, Melle, Ingrid, Fenger, Mogens, Gustafsson, Omar, Jakobsen, Klaus D, Rasmussen, Henrik B, Tosato, Sarah, Rietschel, Marcella, Frank, Josef, Owen, Mike, Bonetto, Chiara, Suvisaari, Jaana, Thygesen, Johan Hilge, Pétursson, Hannes, Lönnqvist, Jouko, Sigurdsson, Engilbert, Giegling, Ina, Craddock, Nick, O'Donovan, Michael C, Ruggeri, Mirella, Cichon, Sven, Ophoff, Roel A, Pietiläinen, Olli, Peltonen, Leena, Nöthen, Markus M, Rujescu, Dan, St. Clair, David, Collier, David A, Andreassen, Ole A, Werge, Thomas
Published in Biological psychiatry (1969) (01.07.2011)
Published in Biological psychiatry (1969) (01.07.2011)
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Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics
Giegling, Ina, Hosak, Ladislav, Mössner, Rainald, Serretti, Alessandro, Bellivier, Frank, Claes, Stephan, Collier, David A., Corrales, Alejo, DeLisi, Lynn E., Gallo, Carla, Gill, Michael, Kennedy, James L., Leboyer, Marion, Maier, Wolfgang, Marquez, Miguel, Massat, Isabelle, Mors, Ole, Muglia, Pierandrea, Nöthen, Markus M., Ospina-Duque, Jorge, Owen, Michael J., Propping, Peter, Shi, YongYong, St Clair, David, Thibaut, Florence, Cichon, Sven, Mendlewicz, Julien, O'Donovan, Michael C., Rujescu, Dan
Published in The world journal of biological psychiatry (03.10.2017)
Published in The world journal of biological psychiatry (03.10.2017)
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