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Number of items: 64.

Mencacci, Niccolò, Reynolds, Regina, Garcia Ruiz, Sonia, Vandrovcova, Jana, Forabosco, Paola, Sánchez-Ferrer, Alvaro, Volpato, Viola, Weale, Michael E., Bhatia, Kailash P., Webber, Caleb, Hardy, John, Botía, Juan and Ryten, Mina 2020. Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders. Brain 143 (9) , pp. 2771-2787. 10.1093/brain/awaa217
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Agarwal, Devika, Sandor, Cynthia, Volpato, Viola, Caffrey, Tara M., Monzon-Sandoval, Jimena, Bowden, Rory, Alegre-Abarrategui, Javier, Wade-Martins, Richard and Webber, Caleb 2020. A single-cell atlas of the human substantia nigra reveals cell-specific pathways associated with neurological disorders. Nature Communications 11 (1) , 4183. 10.1038/s41467-020-17876-0
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Hedegaard, Anne, Monzón-Sandoval, Jimena, Newey, Sarah E., Whiteley, Emma S., Webber, Caleb and Akerman, Colin J. 2020. Pro-maturational effects of human iPSC-derived cortical astrocytes upon iPSC-derived cortical neurons. Stem Cell Reports 15 , pp. 1-14. 10.1016/j.stemcr.2020.05.003
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Monzón‐Sandoval, Jimena, Poggiolini, Ilaria, Ilmer, Tobias, Wade-Martins, Richard, Webber, Caleb and Parkkinen, Laura 2020. Human‐specific transcriptome of ventral and dorsal midbrain dopamine neurons. Annals of Neurology 87 (6) , pp. 853-868. 10.1002/ana.25719
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Williams, Nigel M., Hubbard, Leon, Sandor, Cynthia, Webber, Caleb, Hendry, Hannah, Lawton, Michael, Carroll, Camille, Chaudhuri, K. Ray, Morris, Huw, Hu, Michele T., Grosset, Donald G., Kobylecki, Christopher and Silverdale, Monty 2020. Genome‐wide association study of pain in Parkinson's disease implicates TRPM8 as a risk factor. Movement Disorders 35 (4) , pp. 705-707. 10.1002/mds.28001
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Carling, Phillippa J, Mortiboys, Heather, Green, Claire, Mihaylov, Simeon, Sandor, Cynthia, Schwartzentruber, Aurelie, Taylor, Rosie, Wei, Wenbin, Hastings, Chris, Wong, Siew, Lo, Christine, Evetts, Samuel, Clemmens, Hannah, Wyles, Matthew, Willcox, Sam, Payne, Thomas, Hughes, Rachel, Ferraiuolo, Laura, Webber, Caleb, Hide, Winston, Wade-Martins, Richard, Talbot, Kevin, Hu, Michele T. and Bandmann, Oliver 2020. Deep phenotyping of peripheral tissue facilitates mechanistic disease stratification in sporadic Parkinson's disease. Progress in Neurobiology 187 , 101772. 10.1016/j.pneurobio.2020.101772
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Volpato, Viola and Webber, Caleb 2020. Addressing variability in iPSC-derived models of human disease: guidelines to promote reproducibility. Disease Models and Mechanisms 13 (1) , dmm042317. 10.1242/dmm.042317
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Mancuso, Renzo, Fryatt, Gemma, Cleal, Madeleine, Obst, Juliane, Pipi, Elena, Monzón-Sandoval, Jimena, Ribe, Elena, Winchester, Laura, Webber, Caleb, Nevado, Alejo, Jacobs, Tom, Austin, Nigel, Theunis, Clara, Grauwen, Karolien, Ruiz, Eva Daniela, Mudher, Amrit, Vicente-Rodriguez, Marta, Parker, Christine A., Simmons, Camilla, Cash, Diana, Richardson, Jill, Bullmore, Edward T., Bhatti, Junaid, Chamberlain, Samuel J., Correia, Marta M., Crofts, Anna L., Dickinson, Amber, Foster, Andrew C., Kitzbichler, Manfred G., Knight, Clare, Lynall, Mary-Ellen, Maurice, Christina, O'Donnell, Ciara, Pointon, Linda J., Hyslop, Peter St. George, Turner, Lorinda, Vertes, Petra, Widmer, Barry, Williams, Guy B., Morgan, B. Paul, Leckey, Claire A., Morgan, Angharad R., O'Hagan, Caroline, Touchard, Samuel, Cavanagh, Jonathan, Deith, Catherine, Farmer, Scott, McClean, John, McColl, Alison, McPherson, Andrew, Scouller, Paul, Sutherland, Murray, Boddeke, H. W. G. M. (Erik), Richardson, Jill C., Khan, Shahid, Murphy, Phil, Parker, Christine A., Patel, Jai, Jones, Declan, de Boer, Peter, Kemp, John, Drevets, Wayne C., Nye, Jeffrey S., Wittenberg, Gayle, Isaac, John, Bhattacharya, Anindya, Carruthers, Nick, Kolb, Hartmuth, Pariante, Carmine M., Turkheimer, Federico, Barker, Gareth J., Byrom, Heidi, Cash, Diana, Cattaneo, Annamaria, Gee, Antony, Hastings, Caitlin, Mariani, Nicole, McLaughlin, Anna, Mondelli, Valeria, Nettis, Maria, Nikkheslat, Naghmeh, Randall, Karen, Sheridan, Hannah, Simmons, Camilla, Singh, Nisha, VAn Loo, Victoria, Vicente-Rodriguez, Marta, Wood, Tobias C, Worrell, Courtney, Zajkowska, Zuzanna, Plath, Niels, Egebjerg, Jan, Eriksson, Hans, Gastambide, Francois, Adams, Karen Husted, Jeggo, Ross, Thomsen, Christian, Pederson, Jan Torleif, Campbell, Brian, Möller, Thomas, Nelson, Bob, Zorn, Stevin, O'Connor, Jason, Attenburrow, Mary Jane, Baird, Alison, Benjamin, Jithen, Clare, Stuart, Cowen, Philip, Huang, I-Shu (Dante), Hurley, Samuel, Jones, Helen, Lovestone, Simon, Mada, Francisca, Nevado-Holgado, Alejo, Oladejo, Akintayo, Ribe, Elena, Smith, Katy, Vyas, Anviti, Hughes, Zoe, Balice-Gordon, Rita, Duerr, James, Piro, Justin R, Sporn, Jonathan, Perry (PI), V Hugh, Cleal, Madeleine, Fryatt, Gemma, Gomez-Nicola, Diego, Mancuso, Renzo, Reynolds, Richard, Harrison, Neil A., Cercignani, Mara, Clarke, Charlotte L, Hoskins, Elizabeth, Kohn, Charmaine, Murray, Rosemary, Wilcock, Lauren, Wlazly, Dominika, Mount, Howard, Jones, Declan N. C., Lovestone, Simon and ., . 2019. CSF1R inhibitor JNJ-40346527 attenuates microglial proliferation and neurodegeneration in P301S mice. Brain 142 (10) , pp. 3243-3264. 10.1093/brain/awz241
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Booth, Heather D.E., Wessely, Frank, Connor-Robson, Natalie, Rinaldi, Federica, Vowles, Jane, Browne, Cathy, Evetts, Samuel G., Hu, Michele T., Cowley, Sally A., Webber, Caleb and Wade-Martins, Richard 2019. RNA sequencing reveals MMP2 and TGFB1 downregulation in LRRK2 G2019S Parkinson's iPSC-derived astrocytes. Neurobiology of Disease 129 , pp. 56-66. 10.1016/j.nbd.2019.05.006
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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
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Ward, Joey, Tunbridge, Elizabeth M., Sandor, Cynthia, Lyall, Laura M., Ferguson, Amy, Strawbridge, Rona J., Lyall, Donald M., Cullen, Breda, Graham, Nicholas, Johnston, Keira J. A., Webber, Caleb, Escott-Price, Valentina, O'Donovan, Michael, Pell, Jill P., Bailey, Mark E. S., Harrison, Paul J. and Smith, Daniel J. 2019. The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function. Molecular Psychiatry 10.1038/s41380-019-0439-8
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Lang, Charmaine, Campbell, Kieran R., Ryan, Brent J., Carling, Phillippa, Attar, Moustafa, Vowles, Jane, Perestenko, Olga V., Bowden, Rory, Baig, Fahd, Kasten, Meike, Hu, Michele T., Cowley, Sally A., Webber, Caleb and Wade-Martins, Richard 2019. Single-cell sequencing of iPSC-Dopamine neurons reconstructs disease progression and identifies HDAC4 as a regulator of Parkinson cell phenotypes. Cell Stem Cell 24 (1) , pp. 93-106. 10.1016/j.stem.2018.10.023
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Eddowes, Lucy A., Al-Hourani, Kinda, Ramamurthy, Narayan, Frankish, Jamie, Baddock, Hannah T, Sandor, Cynthia, Ryan, John D., Fusco, Dahlene N., Arezes, João, Giannoulatou, Eleni, Boninsegna, Sara, Chevaliez, Stephane, Owens, Benjamin M. J., Sun, Chia Chi, Fabris, Paolo, Giordani, Maria Teresa, Martines, Diego, Vukicevic, Slobodan, Crowe, John, Lin, Herbert Y., Rehwinkel, Jan, McHugh, Peter J., Binder, Marco, Babitt, Jodie L., Chung, Raymond T., Lawless, Matthew W., Armitage, Andrew E., Webber, Caleb, Klenerman, Paul and Drakesmith, Hal 2018. Antiviral activity of bone morphogenetic proteins and activins. Nature Microbiology 4 , pp. 339-351. 10.1038/s41564-018-0301-9
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Volpato, Viola, Smith, James, Sandor, Cynthia, Ried, Janina S., Baud, Anna, Handel, Adam, Newey, Sarah E., Wessely, Frank, Attar, Moustafa, Whiteley, Emma, Chintawar, Satyan, Verheyen, An, Barta, Thomas, Lako, Majlinda, Armstrong, Lyle, Muschet, Caroline, Artati, Aanna, Cusulin, Carlo, Christensen, Klaus, Patsch, Christoph, Sharma, Eshita, Nicod, Jerome, Brownjohn, Philip, Stubbs, Victoria, Heywood, Wendy E., Gissen, Paul, De Filippis, Roberta, Janssen, Katharina, Reinhardt, Peter, Adamski, Jerzy, Royaux, Ines, Peeters, Pieter J., Terstappen, Georg C., Graf, Martin, Livesey, Frederick J., Akerman, Colin J., Mills, Kevin, Bowden, Rory, Nicholson, George, Webber, Caleb, Cader, M. Zameel and Lakics, Viktor 2018. Reproducibility of molecular phenotypes after long-term differentiation to uuman iPSC-derived neurons: a multi-site omics study. Stem Cell Reports 11 (4) , pp. 897-911. 10.1016/j.stemcr.2018.08.013
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Yang, Yuanhao, Zhao, Huiying, Boomsma, Dorret I., Ligthart, Lannie, Belin, Andrea C., Smith, George Davey, Esko, Tonu, Freilinger, Tobias M., Hansen, Thomas Folkmann, Ikram, M. Arfan, Kallela, Mikko, Kubisch, Christian, Paraskevi, Christofidou, Strachan, David P., Wessman, Maija, Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S., Palta, Priit, Esko, Tonu, Pers, Tune H., Farh, Kai-How, Cuenca-Leon, Ester, Muona, Mikko, Furlotte, Nicholas A., Kurth, Tobais, Ingason, Andres, McMahon, George, Ligthart, Lannie, Terwindt, Gisela M., Kallela, Mikko, Freilinger, Tobais M., Ran, Caroline, Gordon, Scott G., Stam, Anine H., Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H. H., Lehtimaki, Terho, Sarin, Antti-Pekka, Wedenoja, Juho, Hinds, David A., Buring, Julie E., Schürks, Markus, Ridker, Paul M., Hrafnsdottir, Maria Gudlaug, Stefansson, Hreinn, Ring, Susan M., Hottenga, Jouke-Jan, Penninx, Brenda W. J. H., Färkkilä, Markus, Artto, Ville, Kaunisto, Mari, Vepsäläinen, Salli, Malik, Rainer, Heath, Andrew C., Madden, Pamela A. F., Martin, Nicholas G., Montgomery, Grant W., Kurki, Mitja I., Kals, Mart, Mägi, Reedik, Pärn, Kalle, Hämäläinen, Eija, Huang, Hailiang, Byrnes, Andrea E., Franke, Lude, Huang, Jie, Stergiakouli, Evie, Lee, Phil H., Sandor, Cynthia, Webber, Caleb, Cader, Zameel, Muller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Eriksson, Johan G., Salomaa, Veikko, Heikkilä, Kauko, Loehrer, Elizabeth, Uitterlinden, Andre G., Hofman, Albert, van Duijn, Cornelia M., Cherkas, Lynn, Pedersen, Linda M., Stubhaug, Audun, Nielsen, Christopher, Männikkö, Minna, Mihailov, Evelin, Milani, Lili, Göbel, Hartmut, Esserlind, Ann-Louise, Christensen, Anne Francke, Hansen, Thomas Folkmann, Werge, Thomas, Kaprio, Jaakko, Aromaa, Arpo J., Olli, Raitakari, Ikram, M. Arfan, van den Maagdenberg, Arn M. J. M., Terwindt, Gisela M. and Nyholt, Dale R. 2018. Molecular genetic overlap between migraine and major depressive disorder. European Journal of Human Genetics 26 (8) , pp. 1202-1216. 10.1038/s41431-018-0150-2

Anttila, Verneri, Bulik-Sullivan, Brendan, Finucane, Hilary K., Walters, Raymond K., Bras, Jose, Duncan, Laramie, Escott-Price, Valentina, Falcone, Guido J., Gormley, Padhraig, Malik, Rainer, Patsopoulos, Nikolaos A., Ripke, Stephan, Wei, Zhi, Yu, Dongmei, Lee, Phil H., Turley, Patrick, Grenier-Boley, Benjamin, Chouraki, Vincent, Kamatani, Yoichiro, Berr, Claudine, Letenneur, Luc, Hannequin, Didier, Amouyel, Philippe, Boland, Anne, Deleuze, Jean-François, Duron, Emmanuelle, Vardarajan, Badri N., Reitz, Christiane, Goate, Alison M., Huentelman, Matthew J., Kamboh, M. Ilyas, Larson, Eric B., Rogaeva, Ekaterina, St George-Hyslop, Peter, Hakonarson, Hakon, Kukull, Walter A., Farrer, Lindsay A., Barnes, Lisa L., Beach, Thomas G., Demirci, F. Yesim, Head, Elizabeth, Hulette, Christine M., Jicha, Gregory A., Kauwe, John S.K., Kaye, Jeffrey A., Leverenz, James B., Levey, Allan I., Lieberman, Andrew P., Pankratz, Vernon S., Poon, Wayne W., Quinn, Joseph F., Saykin, Andrew J., Schneider, Lon S., Smith, Amanda G., Sonnen, Joshua A., Stern, Robert A., Van Deerlin, Vivianna M., Van Eldik, Linda J., Harold, Denise, Russo, Giancarlo, Rubinsztein, David C., Bayer, Antony, Tsolaki, Magda, Proitsi, Petra, Fox, Nick C., Hampel, Harald, Owen, Michael J., Mead, Simon, Passmore, Peter, Morgan, Kevin, Nöthen, Markus M., Rossor, Martin, Lupton, Michelle K., Hoffmann, Per, Kornhuber, Johannes, Lawlor, Brian, McQuillin, Andrew, Al-Chalabi, Ammar, Bis, Joshua C, Ruiz, Agustin, Boada, Mercè, Seshadri, Sudha, Beiser, Alexa, Rice, Kenneth, van der Lee, Sven J., De Jager, Philip L., Geschwind, Daniel H., Riemenschneider, Matthias, Riedel-Heller, Steffi, Rotter, Jerome I, Ransmayr, Gerhard, Hyman, Bradley T., Cruchaga, Carlos, Alegret, Montserrat, Winsvold, Bendik, Palta, Priit, Farh, Kai-How, Cuenca-Leon, Ester, Furlotte, Nicholas, Kurth, Tobias, Ligthart, Lannie, Terwindt, Gisela M., Freilinger, Tobias, Ran, Caroline, Gordon, Scott D., Borck, Guntram, Adams, Hieab H.H., Lehtimäki, Terho, Wedenoja, Juho, Buring, Julie E., Schürks, Markus, Hrafnsdottir, Maria, Hottenga, Jouke-Jan, Penninx, Brenda, Artto, Ville, Kaunisto, Mari, Vepsäläinen, Salli, Martin, Nicholas G., Montgomery, Grant W., Kurki, Mitja I., Hämäläinen, Eija, Huang, Hailiang, Huang, Jie, Sandor, Cynthia, Webber, Caleb, Muller-Myhsok, Bertram, Schreiber, Stefan, Salomaa, Veikko, Loehrer, Elizabeth, Göbel, Hartmut, Macaya, Alfons, Pozo-Rosich, Patricia, Hansen, Thomas, Werge, Thomas, Kaprio, Jaakko, Metspalu, Andres, Kubisch, Christian, Ferrari, Michel D., Belin, Andrea C., van den Maagdenberg, Arn M.J.M., Zwart, John-Anker, Boomsma, Dorret, Eriksson, Nicholas, Olesen, Jes, Chasman, Daniel I., Nyholt, Dale R., Avbersek, Andreja, Baum, Larry, Berkovic, Samuel, Bradfield, Jonathan, Buono, Russell, Catarino, Claudia B., Cossette, Patrick, De Jonghe, Peter, Depondt, Chantal, Dlugos, Dennis, Ferraro, Thomas N., French, Jacqueline, Hjalgrim, Helle, Jamnadas-Khoda, Jennifer, Kälviäinen, Reetta, Kunz, Wolfram S., Lerche, Holger, Leu, Costin, Lindhout, Dick, Lo, Warren, Lowenstein, Daniel, McCormack, Mark, Møller, Rikke S., Molloy, Anne, Ng, Ping-Wing, Oliver, Karen, Privitera, Michael, Radtke, Rodney, Ruppert, Ann-Kathrin, Sander, Thomas, Schachter, Steven, Schankin, Christoph, Scheffer, Ingrid, Schoch, Susanne, Sisodiya, Sanjay M., Smith, Philip, Sperling, Michael, Striano, Pasquale, Surges, Rainer, Thomas, G. Neil, Visscher, Frank, Whelan, Christopher D., Zara, Federico, Heinzen, Erin L., Marson, Anthony, Becker, Felicitas, Stroink, Hans, Zimprich, Fritz, Gasser, Thomas, Gibbs, Raphael, Heutink, Peter, Martinez, Maria, Morris, Huw R., Sharma, Manu, Ryten, Mina, Mok, Kin Y., Pulit, Sara, Bevan, Steve, Holliday, Elizabeth, Attia, John, Battey, Thomas, Boncoraglio, Giorgio, Thijs, Vincent, Chen, Wei-Min, Mitchell, Braxton, Rothwell, Peter, Sharma, Pankaj, Sudlow, Cathie, Vicente, Astrid, Markus, Hugh, Kourkoulis, Christina, Pera, Joana, Raffeld, Miriam, Silliman, Scott, Boraska Perica, Vesna, Thornton, Laura M., Huckins, Laura M., Rayner, N. William, Lewis, Cathryn M., Gratacos, Monica, Rybakowski, Filip, Keski-Rahkonen, Anna, Raevuori, Anu, Hudson, James I., Reichborn-Kjennerud, Ted, Monteleone, Palmiero, Karwautz, Andreas, Mannik, Katrin, Baker, Jessica H., O'Toole, Julie K., Trace, Sara E., Davis, Oliver S. P., Helder, Sietske G., Ehrlich, Stefan, Herpertz-Dahlmann, Beate, Danner, Unna N., van Elburg, Annemarie A., Clementi, Maurizio, Forzan, Monica, Docampo, Elisa, Lissowska, Jolanta, Hauser, Joanna, Tortorella, Alfonso, Maj, Mario, Gonidakis, Fragiskos, Tziouvas, Konstantinos, Papezova, Hana, Yilmaz, Zeynep, Wagner, Gudrun, Cohen-Woods, Sarah, Herms, Stefan, Julià, Antonio, Rabionet, Raquel, Dick, Danielle M., Ripatti, Samuli, Andreassen, Ole A., Espeseth, Thomas, Lundervold, Astri J., Steen, Vidar M., Pinto, Dalila, Scherer, Stephen W., Aschauer, Harald, Schosser, Alexandra, Alfredsson, Lars, Padyukov, Leonid, Halmi, Katherine A., Mitchell, James, Strober, Michael, Bergen, Andrew W., Kaye, Walter, Szatkiewicz, Jin Peng, Cormand, Bru, Ramos-Quiroga, Josep Antoni, Sánchez-Mora, Cristina, Ribasés, Marta, Casas, Miguel, Hervas, Amaia, Arranz, Maria Jesús, Haavik, Jan, Zayats, Tetyana, Johansson, Stefan, Williams, Nigel, Dempfle, Astrid, Rothenberger, Aribert, Kuntsi, Jonna, Oades, Robert D., Banaschewski, Tobias, Franke, Barbara, Buitelaar, Jan K., Arias Vasquez, Alejandro, Doyle, Alysa E., Reif, Andreas, Lesch, Klaus-Peter, Freitag, Christine, Rivero, Olga, Palmason, Haukur, Romanos, Marcel, Langley, Kate, Rietschel, Marcella, Witt, Stephanie H., Dalsgaard, Soeren, Børglum, Anders D., Waldman, Irwin, Wilmot, Beth, Molly, Nikolas, Bau, Claiton H.D., Crosbie, Jennifer, Schachar, Russell, Loo, Sandra K., McGough, James J., Grevet, Eugenio H., Medland, Sarah E., Robinson, Elise, Weiss, Lauren A., Bacchelli, Elena, Bailey, Anthony, Bal, Vanessa, Battaglia, Agatino, Betancur, Catalina, Bolton, Patrick, Cantor, Rita, Celestino-Soper, Patrícia, Dawson, Geraldine, De Rubeis, Silvia, Duque, Frederico, Green, Andrew, Klauck, Sabine M., Leboyer, Marion, Levitt, Pat, Maestrini, Elena, Mane, Shrikant, De-Luca, Daniel Moreno-, Parr, Jeremy, Regan, Regina, Reichenberg, Abraham, Sandin, Sven, Vorstman, Jacob, Wassink, Thomas, Wijsman, Ellen, Cook, Edwin, Santangelo, Susan, Delorme, Richard, Rogé, Bernadette, Magalhaes, Tiago, Arking, Dan, Schulze, Thomas G., Thompson, Robert C., Strohmaier, Jana, Matthews, Keith, Melle, Ingrid, Morris, Derek, Blackwood, Douglas, McIntosh, Andrew, Bergen, Sarah E, Schalling, Martin, Jamain, Stéphane, Maaser, Anna, Fischer, Sascha B., Reinbold, Céline S., Fullerton, Janice M., Guzman-Parra, José, Mayoral, Fermin, Schofield, Peter R., Cichon, Sven, Mühleisen, Thomas W., Degenhardt, Franziska, Schumacher, Johannes, Bauer, Michael, Mitchell, Philip B., Gershon, Elliot S., Rice, John, Potash, James B., Zandi, Peter P., Craddock, Nicholas, Ferrier, I. Nicol, Alda, Martin, Rouleau, Guy A., Turecki, Gustavo, Ophoff, Roel, Pato, Carlos, Anjorin, Adebayo, Stahl, Eli, Leber, Markus, Czerski, Piotr M., Cruceanu, Cristiana, Jones, Ian, Posthuma, Danielle, Andlauer, Till F.M., Forstner, Andreas J., Streit, Fabian, Baune, Bernhard T., Air, Tracy, Sinnamon, Grant, Wray, Naomi R., MacIntyre, Donald J., Porteous, David, Homuth, Georg, Rivera, Margarita, Grove, Jakob, Middeldorp, Christel M., Hickie, Ian, Pergadia, Michele, Mehta, Divya, Smit, Johannes H., Jansen, Rick, de Geus, Eco, Dunn, Erin, Li, Qingqin S., Nauck, Matthias, Schoevers, Robert A., Beekman, Aartjan TF, Knowles, James A., Viktorin, Alexander, Arnold, Paul, Barr, Cathy L., Bedoya-Berrio, Gabriel, Bienvenu, O. Joseph, Brentani, Helena, Burton, Christie, Camarena, Beatriz, Cappi, Carolina, Cath, Danielle, Cavallini, Maria, Cusi, Daniele, Darrow, Sabrina, Denys, Damiaan, Derks, Eske M., Dietrich, Andrea, Fernandez, Thomas, Figee, Martijn, Freimer, Nelson, Gerber, Gloria, Grados, Marco, Greenberg, Erica, Hanna, Gregory L., Hartmann, Andreas, Hirschtritt, Matthew E., Hoekstra, Pieter J., Huang, Alden, Huyser, Chaim, Illmann, Cornelia, Jenike, Michael, Kuperman, Samuel, Leventhal, Bennett, Lochner, Christine, Lyon, Gholson J., Macciardi, Fabio, Madruga-Garrido, Marcos, Malaty, Irene A., Maras, Athanasios, McGrath, Lauren, Miguel, Eurípedes C., Mir, Pablo, Nestadt, Gerald, Nicolini, Humberto, Okun, Michael S., Pakstis, Andrew, Paschou, Peristera, Piacentini, John, Pittenger, Christopher, Plessen, Kerstin, Ramensky, Vasily, Ramos, Eliana M., Reus, Victor, Richter, Margaret A., Riddle, Mark A., Robertson, Mary M., Roessner, Veit, Rosário, Maria, Samuels, Jack F., Sandor, Paul, Stein, Dan J., Tsetsos, Fotis, Van Nieuwerburgh, Filip, Weatherall, Sarah, Wendland, Jens R., Wolanczyk, Tomasz, Worbe, Yulia, Zai, Gwyneth, Goes, Fernando S., McLaughlin, Nicole, Nestadt, Paul S., Grabe, Hans-Jorgen, Depienne, Christel, Konkashbaev, Anuar, Lanzagorta, Nuria, Valencia-Duarte, Ana, Bramon, Elvira, Buccola, Nancy, Cahn, Wiepke, Cairns, Murray, Chong, Siow A., Cohen, David, Crespo-Facorro, Benedicto, Crowley, James, Davidson, Michael, DeLisi, Lynn, Dinan, Timothy, Donohoe, Gary, Drapeau, Elodie, Duan, Jubao, Haan, Lieuwe, Hougaard, David, Karachanak-Yankova, Sena, Khrunin, Andrey, Klovins, Janis, Ku?inskas, Vaidutis, Lee Chee Keong, Jimmy, Limborska, Svetlana, Loughland, Carmel, Lönnqvist, Jouko, Maher, Brion, Mattheisen, Manuel, McDonald, Colm, Murphy, Kieran C., Nenadic, Igor, van Os, Jim, Pantelis, Christos, Pato, Michele, Petryshen, Tracey, Quested, Digby, Roussos, Panos, Sanders, Alan R., Schall, Ulrich, Schwab, Sibylle G., Sim, Kang, So, Hon-Cheong, Stögmann, Elisabeth, Subramaniam, Mythily, Toncheva, Draga, Waddington, John, Walters, James, Weiser, Mark, Cheng, Wei, Cloninger, Robert, Curtis, David, Gejman, Pablo V., Henskens, Frans, Mattingsdal, Morten, Oh, Sang-Yun, Scott, Rodney, Webb, Bradley, Breen, Gerome, Churchhouse, Claire, Bulik, Cynthia M., Daly, Mark, Dichgans, Martin, Faraone, Stephen V., Guerreiro, Rita, Holmans, Peter, Kendler, Kenneth S., Koeleman, Bobby, Mathews, Carol A., Price, Alkes, Scharf, Jeremiah, Sklar, Pamela, Williams, Julie, Wood, Nicholas W., Cotsapas, Chris, Palotie, Aarno, Smoller, Jordan W., Sullivan, Patrick, Rosand, Jonathan, Corvin, Aiden, Neale, Benjamin M. and Anney, Richard 2018. Analysis of shared heritability in common disorders of the brain. Science 360 (6395) , eaap8757. 10.1126/science.aap8757
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Nash, Anthony, Holgado, Alejo J. Nevado, Lovestone, Simon, Cader, M. Zameel and Webber, Caleb 2018. Headache and type 2 diabetes association: a US national ambulatory case-control study. bioRxiv 10.1101/336586
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Sandor, Cynthia, Beer, Nicola L. and Webber, Caleb 2017. Diverse type 2 diabetes genetic risk factors functionally converge in a phenotype-focused gene network. PLoS Computational Biology 13 (10) , e1005816. 10.1371/journal.pcbi.1005816
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Webber, Caleb 2017. Epistasis in neuropsychiatric disorders. Trends in Genetics 33 (4) , pp. 256-265. 10.1016/j.tig.2017.01.009

Baud, Anna, Wessely, Frank, Mazzacuva, Francesca, McCormick, James, Camuzeaux, Stephane, Heywood, Wendy E., Little, Daniel, Vowles, Jane, Tuefferd, Marianne, Mosaku, Olukunbi, Lako, Majlinda, Armstrong, Lyle, Webber, Caleb, Cader, M. Zameel, Peeters, Pieter, Gissen, Paul, Cowley, Sally A. and Mills, Kevin 2017. Multiplex high-throughput targeted proteomic assay to identify induced pluripotent stem cells. Analytical Chemistry 89 (4) , pp. 2440-2448. 10.1021/acs.analchem.6b04368

Sandor, Cynthia, Robertson, Paul, Lang, Charmaine, Heger, Andreas, Booth, Heather, Vowles, Jane, Witty, Lorna, Bowden, Rory, Hu, Michele, Cowley, Sally A., Wade-Martins, Richard and Webber, Caleb 2017. Transcriptomic profiling of purified patient-derived dopamine neurons identifies convergent perturbations and therapeutics for Parkinson's disease. Human Molecular Genetics 26 (3) , pp. 552-566. 10.1093/hmg/ddw412
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Sandor, Cynthia, Honti, Frantisek, Haerty, Wilfried, Szewczyk-Krolikowski, Konrad, Tomlinson, Paul, Evetts, Sam, Millin, Stephanie, Keane, Thomas, McCarthy, Shane A., Durbin, Richard, Talbot, Kevin, Hu, Michele, Webber, Caleb, Ponting, Chris P. and Wade-Martins, Richard 2017. Whole-exome sequencing of 228 patients with sporadic Parkinson's disease. Scientific Reports 7 , 41188. 10.1038/srep41188
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Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S., Palta, Proot, Esko, Tonu, Pers, Tune H., Farh, Kai-How, Cuenca-Leon, Ester, Muona, Mikko, Furlotte, Nicholas A., Kurth, Tobias, Ingason, Andres, McMahon, George, Ligthart, Lannie, Terwindt, Gisela M., Kallela, Mikko, Freilinger, Tobias M., Ran, Caroline, Gordon, Scott G., Stam, Annie H., Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H. H., Lehtimäki, Terho, Sarin, Antti-Pekka, Wedenoja, Juho, Hinds, David A., Buring, Julie E., Schürks, Markus, Ridker, Paul M., Gudlaug Hrafnsdottir, Maria, Stefansson, Hreinn, Ring, Susan M., Hottenga, Jouke-Jan, Penninx, Brenda W. J. H., Färkkilä, Markus, Artto, Ville, Kaunisto, Mari, Vepsäläinen, Salli, Malik, Rainer, Heath, Andrew C., Madden, Pamela A. F., Martin, Nicholas G., Montgomery, Grant W., Kurki, Mitja I., Kals, Mart, Mägi, Reedik, Pärn, Kalle, Hämäläinen, Eija, Huang, Hailiang, Byrnes, Andrea E., Franke, Lude, Huang, Jie, Stergiakouli, Evie, Lee, Phil H., Sandor, Cynthia, Webber, Caleb, Cader, Zameel, Mullter-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Eriksson, Johan G., Salomaa, Veikko, Heikkilä, Kauko, Loehrer, Elizabeth, Uitterlinden, Andre, Hofman, Albert, van Duijn, Cornelia M., Cherkas, Lynn, Pedersen, Linda M., Stubhaug, Audun, Nielsen, Christopher S., Männikkö, Minna, Mihailov, Evelin, Milani, Liki, Göbel, Hartmut, Esserlind, Ann-Louise, Christensen, Anne Francke, Hansen, Thomas Folkmann, Werge, Thomas, International Headache Genetics Consortium, , Kaprio, Jaakko, Aromaa, Arpo J., Raitakari, Olli, Ikram, M. Arfan, Spector, Tim, Järvelin, Marjo-Riitta, Metspalu, Andres, Kubisch, Christian, Strachan, David P., Ferrari, Michel D., Belin, Andrea C., Dichgans, Martin, Wessman, Jaiha, van den Maagdenberg, Arn M. J. M., Zwart, John-Anker, Boomsma, Dorret I., Smith, George Davey, Stefansson, Kari, Eriksson, Nicholas, Daly, Mark J., Neale, Benjamin M., Olesen, Jes, Chasman, Daniel I., Nyholt, Dale R. and Palotie, Aarno 2016. Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics 48 (10) , p. 1296. 10.1038/ng1016-1296c

Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S., Palta, Priit, Esko, Tonu, Pers, Tune H., Farh, Kai-How, Cuenca-Leon, Ester, Muona, Mikko, Furlotte, Nicholas A., Kurth, Tobais, Ingason, Andres, McMahon, George, Ligthart, Lannie, Terwindt, Gisela M., Kallela, Mikko, Freilinger, Tobias M., Ran, Caroline, Gordon, Scott G., Stam, Anine H., Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H. H., Lehtimäki, Terho, Sarin, Anti-Pekka, Wedenoja, Juho, Hinds, David A., Buring, Julie E., Schürks, Markus, Ridker, Paul M., Hrafnsdottir, Maria Gudlaug, Stefansson, Hreinn, Ring, Susan M., Hottenga, Jouke-Jan, Penninx, Brenda W. J. H., Färkkilä, Markus, Artto, Ville, Mari, Kaunisto, Vepsäläinen, Salli, Malik, Rainer, Heath, Andrew C., Madden, Pamela A. F., Martin, Nicholas G., Montgomery, Grant W., Kurki, Mitja I., Kals, Mart, Mägi, Reedik, Pärn, Kalle, Hämäläinen, Eija, Huang, Hailiang, Byrnes, Andrea E., Franke, Lude, Huang, Jie, Stergiakouli, Evie, Lee, Phil H., Sandor, Cynthia, Webber, Caleb, Cader, Zameel, Muller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Eriksson, Johan G., Salomaa, Veikko, Heikkilä, Kauko, Loehrer, Elizabeth, Uitterlinden, Andre G., Hofman, Albert, van Duijn, Cornelia M., Cherkas, Lynn, Pedersen, Linda, Stubhaug, Audun, Nielsen, Christopher S., Männikkö, Minna, Mihailov, Evelin, Milani, Liki, Göbel, Hartmut, Esserlind, Ann-Louise, Christensen, Anne Francke, Hansen, Thomas Folkmann, Wege, Thomas, International Headache Genetics Consortium, , Kaprio, Jaakko, Aromaa, Arpo J., Raitakari, Olli, Ikram, M. Arfan, Spector, Tim, Järvelin, Marjo-Riitta, Metspalu, Andres, Kubisch, Christian, Strachan, David P., Ferrari, Michel D., Belin, Andrea C., Dichgans, Martin, Wessman, Maija, van den Maagdenberg, Arn M. J. M., Zwart, John-Anker, Boomsma, Dorret I., Smith, George Davey, Stefansson, Kari, Eriksson, Nicholas, Daly, Mark J., Neale, Benjamin M., Olesen, Jes, Chasman, Daniel I., Nyhol, Dale R. and Palotie, Aarno 2016. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics 48 (8) , pp. 856-866. 10.1038/ng.3598

Kochinke, Korinna, Zweier, Christiane, Nijhof, Bonnie, Fenckova, Michaela, Cizek, Pavel, Honti, Frank, Keerthikumar, Shivakumar, Oortveld, Merel A. W., Kleefstra, Tjitske, Kramer, Jamie M., Webber, Caleb, Huynen, Martijn A. and Schenck, Annette 2016. Systematic phenomics analysis deconvolutes genes mutated in intellectual disability into biologically coherent modules. American Journal of Human Genetics 98 (1) , pp. 149-164. 10.1016/j.ajhg.2015.11.024

Tan, Jennifer Y., Sirey, Tamara, Honti, Frantisek, Graham, Bryony, Piovesan, Allison, Merkenschlager, Matthias, Webber, Caleb, Ponting, Chris P. and Marques, Ana C. 2015. Corrigendum: Extensive microRNA-mediated crosstalk between lncRNAs and mRNAs in mouse embryonic stem cells. Genome Research 25 (9) , 1410.1. 10.1101/gr.196568.115
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Steinberg, Julia, Honti, Frantisek, Meader, Stephen and Webber, Caleb 2015. Haploinsufficiency predictions without study bias. Nucleic Acids Research 43 (15) , e101. 10.1093/nar/gkv474
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Andrews, Tallulah, Honti, Frantisek, Pfundt, Rolph, De Leeuw, Nicole, Hehir-Kwa, Jayne, Silfhout, Anneke Vulto-cvan, De Vries, Bert and Webber, Caleb 2015. The clustering of functionally related genes contributes to CNV-mediated disease. Genome Research 25 (6) , pp. 802-813. 10.1101/gr.184325.114
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Tan, Jennifer Y., Sirey, Tamara, Honti, Frantisek, Graham, Byrony, Piovesan, Allison, Merkenschlager, Matthias, Webber, Caleb, Ponting, Chris P. and Marques, Ana C. 2015. Extensive microRNA-mediated crosstalk between lncRNAs and mRNAs in mouse embryonic stem cells. Genome Research 25 (5) , pp. 655-666. 10.1101/gr.181974.114
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Grice, Stuart J., Liu, Ji-Long and Webber, Caleb 2015. Synergistic interactions between Drosophila orthologues of genes spanned by De Novo human CNVs support multiple-hit models of autism. PLoS Genetics 11 (3) , e1004998. 10.1371/journal.pgen.1004998
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Andrews, Tallulah, Meader, Stephen, Vulto-van Silfhout, Anneke, Taylor, Avigail, Steinberg, Juila, Hehir-Kwa, Jayne, Pfundt, Rolph, de Leeuw, Nicole, de Vries, Bert B.A. and Webber, Caleb 2015. Gene networks underlying convergent and pleiotropic phenotypes in a large and systematically-phenotyped cohort with heterogeneous developmental disorders. PLoS Genetics 11 (3) , e1005012. 10.1371/journal.pgen.1005012
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Taylor, Avigail, Steinberg, Julia and Webber, Caleb 2015. Duplications in ADHD patients harbour neurobehavioural genes that are co-expressed with genes associated with hyperactivity in the mouse. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 168 (2) , pp. 97-107. 10.1002/ajmg.b.32285
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Taylor, Avigail, Steinberg, Julia, Andrews, Tallulah S. and Webber, Caleb 2015. GeneNet toolbox for MATLAB: a flexible platform for the analysis of gene connectivity in biological networks. Bioinformatics 31 (3) , pp. 442-444. 10.1093/bioinformatics/btu669
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Honti, Frantisek, Meader, Stephen and Webber, Caleb 2014. Unbiased functional clustering of gene variants with a phenotypic-linkage network. PLoS Computational Biology 10 (8) , e1003815. 10.1371/journal.pcbi.1003815
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Ferry, Quentin, Steinberg, Julia, Webber, Caleb, FitzPatrick, David R., Ponting, Chris P., Zisserman, Andrew and Nell?ker, Christoffer 2014. Diagnostically relevant facial gestalt information from ordinary photos. eLife 2014 (3) , e02020. 10.7554/eLife.02020.001
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Robinson, Peter N. and Webber, Caleb 2014. Phenotype ontologies and cross-species analysis for translational research. PLoS Genetics 10 (4) , e1004268. 10.1371/journal.pgen.1004268
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Vulto-van Silfhout, Anneke T., Hehir-Kwa, Jayne Y., van Bon, Bregje W. M., Schuurs-Hoeijmakers, Janneke H M., Meader, Stephen, Hellebrekers, Claudia J. M., Thoonen, Ilse J. M., de Brouwer, Arjan P. M., Brunner, Han G., Webber, Caleb, Pfundt, Rolph, de Leeuw, Nicole and De Vries, Bert B. A. 2013. Clinical significance of de novo and inherited copy-number variation. Human Mutation 34 (12) , pp. 1679-1687. 10.1002/humu.22442

Steinberg, Julia and Webber, Caleb 2013. The roles of FMRP-regulated genes in autism spectrum disorder: single- and multiple-hit genetic etiologies. American Journal of Human Genetics 93 (5) , pp. 825-839. 10.1016/j.ajhg.2013.09.013
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Brandler, William M., Morris, Andrew P., Evans, David M., Scerri, Thomas S., Kemp, John P., Timpson, Nicholas J., St Pourcain, Beate, Smith, George Davey, Ring, Susan M., Stein, John, Monaco, Anthony P., Talcott, Joel B., Fisher, Simon E., Webber, Caleb and Paracchini, Silvia 2013. Common variants in left/right asymmetry genes and pathways are associated with relative hand skill. PLoS Genetics 9 (9) , e1003751. 10.1371/journal.pgen.1003751
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Heger, Andreas, Webber, Caleb, Goodson, Martin, Ponting, Chris P. and Lunter, Gerton 2013. GAT: A simulation framework for testing the association of genomic intervals. Bioinformatics 29 (16) , pp. 2046-2048. 10.1093/bioinformatics/btt343
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Noh, Hyun Ji, Ponting, Chris P., Boulding, Hannah C., Meader, Stephen, Betancur, Catalina, Buxbaum, Joseph D., Pinto, Dalila, Marshall, Christian R., Lionel, Anath C., Scherer, Stephen W. and Webber, Caleb 2013. Network topologies and convergent aetiologies arising from deletions and duplications observed in individuals with autism. PLoS Genetics 9 (6) , e1003523. 10.1371/journal.pgen.1003523
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Hoerder-Suabedissen, Anna, Oeschger, Franziska M., Krishnan, Michelle L., Belgard, T. Grant, Wang, Wei Zhi, Lee, Sheena, Webber, Caleb, Petretto, Enrico, Edwards, A. David and Molnár, Zoltán 2013. Expression profiling of mouse subplate reveals a dynamic gene network and disease association with autism and schizophrenia. Proceedings of the National Academy of Sciences 110 (9) , pp. 3555-3560. 10.1073/pnas.1218510110

Boulding, Hannah and Webber, Caleb 2012. Large-scale objective association of mouse phenotypes with human symptoms through structural variation identified in patients with developmental disorders. Human Mutation 33 (5) , pp. 874-883. 10.1002/humu.22069

Webber, Caleb 2011. Functional enrichment analysis with structural variants: pitfalls and strategies. Cytogenetic and Genome Research 135 (3-4) , pp. 277-285. 10.1159/000331670

Mills, Ryan E., Pittard, W. Stephen, Mullaney, Julienne M., Farooq, Umar, Creasy, Todd H., Mahurkar, Anup A., Kemeza, David M., Strassler, Daniel S., Ponting, Chris P., Webber, Caleb and Devine, Scott E. 2011. Natural genetic variation caused by small insertions and deletions in the human genome. Genome Research 21 (6) , pp. 830-839. 10.1101/gr.115907.110
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Shaikh, Tamim H., Haldeman-Englert, Chad, Geiger, Elizabeth A., Ponting, Chris P. and Webber, Caleb 2011. Genes and biological processes commonly disrupted in rare and heterogeneous developmental delay syndromes. Human Molecular Genetics 20 (5) , pp. 880-893. 10.1093/hmg/ddq527

Agam, Avigail, Yalcin, Binnaz, Bhomra, Amarjit, Cubin, Matthew, Webber, Caleb, Holmes, Christopher, Flint, Jonathan and Mott, Richard 2010. Elusive copy number variation in the mouse genome. PLoS ONE 5 (9) , pp. 1-13. 10.1371/journal.pone.0012839
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Pinto, Dalila, Pagnamenta, Alistair T., Klei, Lambertus, Anney, Richard, Merico, Daniele, Regan, Regina, Conroy, Judith, Magalhaes, Tiago R., Correia, Catarina, Abrahams, Brett S., Almeida, Joana, Bacchelli, Elena, Bader, Gary D., Bailey, Anthony J., Baird, Gillian, Battaglia, Agatino, Berney, Tom, Bolshakova, Nadia, Boelte, Sven, Bolton, Patrick F., Bourgeron, Thomas, Brennan, Sean, Brian, Jessica, Bryson, Susan E., Carson, Andrew R., Casallo, Guillermo, Casey, Jillian, Chung, Brian H. Y., Cochrane, Lynne, Corsello, Christina, Crawford, Emily L., Crossett, Andrew, Cytrynbaum, Cheryl, Dawson, Geraldine, de Jonge, Maretha, Delorme, Richard, Drmic, Irene, Duketis, Eftichia, Duque, Frederico, Estes, Annette, Farrar, Penny, Fernandez, Bridget A., Folstein, Susan E., Fombonne, Eric, Freitag, Christine M., Gilbert, John, Gillberg, Christopher, Glessner, Joseph T., Goldberg, Jeremy, Green, Andrew, Green, Jonathan, Guter, Stephen J., Hakonarson, Hakon, Heron, Elizabeth A., Hill, Matthew, Holt, Richard, Howe, Jennifer L., Hughes, Gillian, Hus, Vanessa, Igliozzi, Roberta, Kim, Cecilia, Klauck, Sabine M., Kolevzon, Alexander, Korvatska, Olena, Kustanovich, Vlad, Lajonchere, Clara M., Lamb, Janine A., Laskawiec, Magdalena, Leboyer, Marion, Le Couteur, Ann, Leventhal, Bennett L., Lionel, Anath C., Liu, Xiao-Qing, Lord, Catherine, Lotspeich, Linda, Lund, Sabata C., Maestrini, Elena, Mahoney, William, Mantoulan, Carine, Marshall, Christian R., McConachie, Helen, McDougle, Christopher J., McGrath, Jane, McMahon, William M., Merikangas, Alison, Migita, Ohsuke, Minshew, Nancy J., Mirza, Ghazala K., Munson, Jeff, Nelson, Stanley F., Noakes, Carolyn, Noor, Abdul, Nygren, Gudrun, Oliveira, Guiomar, Papanikolaou, Katerina, Parr, Jeremy R., Parrini, Barbara, Paton, Tara, Pickles, Andrew, Pilorge, Marion, Piven, Joseph, Ponting, Chris P., Posey, David J., Poustka, Annemarie, Poustka, Fritz, Prasad, Aparna, Ragoussis, Jiannis, Renshaw, Katy, Rickaby, Jessica, Roberts, Wendy, Roeder, Kathryn, Roge, Bernadette, Rutter, Michael L., Bierut, Laura J., Rice, John P., Salt, Jeff, Sansom, Katherine, Sato, Daisuke, Segurado, Ricardo, Sequeira, Ana F., Senman, Lili, Shah, Naisha, Sheffield, Val C., Soorya, Latha, Sousa, Ines, Stein, Olaf, Sykes, Nuala, Stoppioni, Vera, Strawbridge, Christina, Tancredi, Raffaella, Tansey, Katherine E., Thiruvahindrapduram, Bhooma, Thompson, Ann P., Thomson, Susanne, Tryfon, Ana, Tsiantis, John, Van Engeland, Herman, Vincent, John B., Volkmar, Fred, Wallace, Simon, Wang, Kai, Wang, Zhouzhi, Wassink, Thomas H., Webber, Caleb, Weksberg, Rosanna, Wing, Kirsty, Wittemeyer, Kerstin, Wood, Shawn, Wu, Jing, Yaspan, Brian L., Zurawiecki, Danielle, Zwaigenbaum, Lonnie, Buxbaum, Joseph D., Cantor, Rita M., Cook, Edwin H., Coon, Hilary, Cuccaro, Michael L., Devlin, Bernie, Ennis, Sean, Gallagher, Louise, Geschwind, Daniel H., Gill, Michael, Haines, Jonathan L., Hallmayer, Joachim, Miller, Judith, Monaco, Anthony P., Nurnberger, John I., Paterson, Andrew D., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Szatmari, Peter, Vicente, Astrid M., Vieland, Veronica J., Wijsman, Ellen M., Scherer, Stephen W., Sutcliffe, James S. and Betancur, Catalina 2010. Functional impact of global rare copy number variation in autism spectrum disorders. Nature 466 (7304) , pp. 368-372. 10.1038/nature09146

Hehir-Kwa, Jayne Y., Wieskamp, Nienke, Webber, Caleb, Pfundt, Rolph, Brunner, Han G., Gilissen, Christian, de Vries, Bert B. A., Ponting, Chris P. and Veltman, Joris A. 2010. Accurate distinction of pathogenic from benign CNVs in mental retardation. PLoS Computational Biology 6 (4) , e1000752. 10.1371/journal.pcbi.1000752
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Webber, Caleb, Hehir-Kwa, Jayne Y., Nguyen, Duc-Quang, De Vries, Bert B. A., Veltman, Joris A. and Ponting, Chris P. 2009. Forging links between human mental retardation-associated CNVs and mouse gene knockout models. PLoS Genetics 5 (6) , e1000531. 10.1371/journal.pgen.1000531
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Nguyen, Duc-Quang, Webber, Caleb, Hehir-Kwa, Jayne, Pfundt, Rolph, Veltman, Joris and Ponting, Chris P. 2008. Reduced purifying selection prevails over positive selection in human copy number variant evolution. Genome Research 18 (11) , pp. 1711-1723. 10.1101/gr.077289.108
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Walsh, Thomas P., Webber, Caleb, Searle, Stephen, Sturrock, Shane S. and Barton, Geoffrey J. 2008. SCANPS: a web server for iterative protein sequence database searching by dynamic programing, with display in a hierarchical SCOP browser. Nucleic Acids Research 36 (Supple) , W25-W29. 10.1093/nar/gkn320
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Warren, Wesley C., Hillier, LaDeana W., Marshall Graves, Jennifer A., Birney, Ewan, Ponting, Chris P., Grützner, Frank, Belov, Katherine, Miller, Webb, Clarke, Laura, Chinwalla, Asif T., Yang, Shiaw-Pyng, Heger, Andreas, Locke, Devin P., Miethke, Pat, Waters, Paul D., Veyrunes, Frédéric, Fulton, Lucinda, Fulton, Bob, Graves, Tina, Wallis, John, Puente, Xose S., López-Otín, Carlos, Ordóñez, Gonzalo R., Eichler, Evan E., Chen, Lin, Cheng, Ze, Deakin, Jenine E., Aslop, Amber, Thompson, Katherine, Kirby, Patrick, Papenfuss, Anthony T., Wakefield, Matthew J., Olender, Tsviya, Lancet, Doron, Huttley, Gavin A., Smit, Arian F. A., Pask, Andrew, Temple-Smith, Peter, Batzer, Mark A., Walker, Jerilyn A., Konkel, Miriam K., Harris, Robert S., Whittington, Camilla M., Wong, Emily S. W., Gemmell, Neil J., Buschiazzo, Emmanuel, Vargas Jentzsch, Iris M., Merkel, Angelika, Schmitz, Juergen, Zemann, Anja, Churakov, Gennady, Kriegs, Jan Ole, Brosius, Juergen, Murchison, Elizabeth P., Sachidanandam, Ravi, Smith, Carly, Hannon, Gregory J., Tsend-Ayush, Enkhjargal, McMillan, Daniel, Attenborough, Rosalind, Rens, Willem, Ferguson-Smith, Malcolm, Lefèvre, Christophe M., Sharp, Julie A., Nicholas, Kevin R., Ray, David A., Kube, Michael, Reinhardt, Richard, Pringle, Thomas H., Taylor, James, Jones, Russell C., Nixon, Brett, Dacheux, Jean-Louis, Niwa, Hitoshi, Sekita, Yoko, Huang, Xiaoqiu, Stark, Alexander, Kheradpour, Pouya, Kellis, Manolis, Flicek, Paul, Chen, Yuan, Webber, Caleb, Hardison, Ross, Nelson, Joanne, Hallsworth-Pepin, Kym, Delehaunty, Kim, Markovic, Chris, Minx, Pat, Feng, Yucheng, Kremitzki, Colin, Mitreva, Makedonka, Glasscock, Jarret, Wylie, Todd, Wohldmann, Patricia, Thiru, Prathapan, Nhan, Michael N., Pohl, Craig S., Smith, Scott M., Hour, Shungfeng, renfree, Marilyn B., Mardis, Elaine R. and Wilson, Richard K. 2008. Genome analysis of the platypus reveals unique signatures of evolution. Nature 453 , pp. 175-183. 10.1038/nature06936
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Goodstadt, Leo, Heger, Andreas, Webber, Caleb and Ponting, Chris P. 2007. An analysis of the gene complement of a marsupial, Monodelphis domestica: evolution of lineage-specific genes and giant chromosomes. Genome Research 17 (7) , pp. 969-981. 10.1101/gr.6093907
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Nguyen, Duc-Quang, Webber, Caleb and Ponting, Chris P. 2006. Bias of selection on human copy-number variants. PLoS Genetics 2 (2) , e20. 10.1371/journal.pgen.0020020
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Webber, Caleb and Ponting, Chris P. 2005. Hotspots of mutation and breakage in dog and human chromosomes. Genome Research 15 (12) , pp. 1787-1797. 10.1101/gr.3896805
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Wong, Gane Ka-Shu, Liu, Bin, Wang, Jun, Zhang, Yong, Yang, Xu, Zhang, Zengjin, Meng, Qingshun, Zhou, Jun, Li, Dawei, Zhang, Jingjing, Ni, Peixiang, Li, Songgang, Ran, Longhua, Li, Heng, Zhang, Jianguo, Li, Ruiqiang, Li, Shengting, Zheng, Hongkun, Lin, Wei, Li, Guangyun, Wang, Xioaling, Zhao, Wenming, Li, Jun, Ye, Chen, Dai, Mmingtao, Ruan, Jue, Zhou, Yan, Li, Yuanzhe, He, Ximiao, Zhang, Yunze, Wang, Jing, Huang, Xingang, Tong, Wei, Chen, Jie, Ye, Jia, Chen, Chen, Wei, Ning, Li, Guoqing, Dong, Le, Lan, Fengdi, Sun, Yongqiao, Zhang, Zhenpeng, Yang, Zheng, Yu, Yingpu, Huang, Yanqing, He, Dandan, Xi, Yan, Wei, Dong, Qi, Qiuhui, Li, Wenjie, Shi, Jianping, Wang, Miaoheng, Xie, Fei, Wang, Jianjun, Zhang, Xiaowei, Wang, Pei, Zhao, Yiqiang, Li, Ning, Yang, Ning, Dong, Wei, Hu, Songnian, Zeng, Changqing, Zheng, Weimou, Hao, Bailin, Hillier, LaDeana W., Yang, Shuaw-Pyng, Warren, Wesley C., Wilson, Richard K., Brandström, Mikael, Ellegren, Hans, Crooijmans, Richard P. M. A., van der Poel, Jan J., Bovenhuis, Henk, Groenen, Martien A. M., Ovcharenko, Ivan, Gordon, Laurie, Stubbs, Lisa, Lucas, Susan, Glavina, Tijana, Aerts, Andrea, Kaiser, Pete, Rothwell, Lisa, Young, John R., Rogers, Sally, Walker, Brian A., van Hateren, Andy, Kaufman, Jim, Bumstead, Nat, Lamont, Susan J., Zhou, Huaijun, Hocking, Paul M., Morrice, Dvaid, de Koning, Dirk-Jan, Law, Andy, Bartley, Neil, Burt, David W., Hunt, Henry, Cheng, Hans H., Gunnarsson, Ulrika, Wahlberg, Per, Andersson, Leif, Kindlund, Ellen, Tammi, Martti T., Andersson, Björn, Webber, Caleb, Ponting, Chris P., Overton, Ian M., Boardman, Paul E., Tang, Haizhou, Hubbard, Simon J., Wilson, Stuart A., Yu, Jun, Wang, Jian and Yang, HuanMing 2004. A genetic variation map for chicken with 2.8 million single-nucleotide polymorphisms. Nature 432 (7018) , pp. 717-722. 10.1038/nature03156

Webber, Caleb and Ponting, Chris P. 2004. Genes and homology. Current Biology 14 (9) , R332-R333. 10.1016/j.cub.2004.04.016

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This list was generated on Fri Oct 30 06:23:38 2020 GMT.