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Number of items: 80.

Kurtyka, Magdalena, Wessely, Frank, Bau, Sarah, Ifie, Eseoghene, He, Liqun, de Wit, Nienke M., Pedersen, Alberte Bay Villekjær, Keller, Maximilian, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674, de Vries, Helga E., Ansorge, Olaf, Betsholtz, Christer, De Bock, Marijke, Chaves, Catarina, Brodin, Birger, Nielsen, Morten S., Neuhaus, Winfried, Bell, Robert D., Letoha, Tamás, Meyer, Axel H., Leparc, Germán, Lenter, Martin, Lesuisse, Dominique, Cader, Zameel M., Buckley, Stephen T., Loryan, Irena and Pietrzik, Claus U. 2024. The solute carrier SLC7A1 may act as a protein transporter at the blood-brain barrier. European Journal of Cell Biology 103 (2) , 151406. 10.1016/j.ejcb.2024.151406
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Tsartsalis, Stergios, Sleven, Hannah, Fancy, Nurun, Wessely, Frank, Smith, Amy M., Willumsen, Nanet, Cheung, To Ka Dorcas, Rokicki, Michal J., Chau, Vicky, Ifie, Eseoghene, Khozoie, Combiz, Ansorge, Olaf, Yang, Xin, Jenkyns, Marion H., Davey, Karen, McGarry, Aisling, Muirhead, Robert C. J., Debette, Stephanie, Jackson, Johanna S., Montagne, Axel, Owen, David R., Miners, J. Scott, Love, Seth, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674, Cader, M. Zameel and Matthews, Paul M. 2024. A single nuclear transcriptomic characterisation of mechanisms responsible for impaired angiogenesis and blood-brain barrier function in Alzheimer’s disease. Nature Communications 15 , 2243. 10.1038/s41467-024-46630-z
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Li, Zongze ORCID: https://orcid.org/0000-0002-9923-7205, Fernandez Cardo, Lucia, Rokicki, Michal, Monzon Sandoval, Jimena, Volpato, Viola, Wessely, Frank, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 and Li, Meng ORCID: https://orcid.org/0000-0002-4803-4643 2024. Differential growth and transcriptomic profile of stem cell-derived midbrain astrocytes. eLife
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Fernandez Cardo, Lucia, Monzón Sandoval, Jimena, Li, Zongze ORCID: https://orcid.org/0000-0002-9923-7205, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 and Li, Meng ORCID: https://orcid.org/0000-0002-4803-4643 2023. Single-cell transcriptomics and In vitro lineage tracing reveals differential susceptibility of human iPSC-derived midbrain dopaminergic neurons in a cellular model of Parkinson's Disease. Cells 12 (24) , 2860. 10.3390/cells12242860
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Sri, Sarmi, Greenstein, Adam, Granata, Alessandra, Collcutt, Alex, Jochems, Angela C C, McColl, Barry W, Castro, Blanca Díaz, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674, Reyes, Carmen Arteaga, Hall, Catherine, Lawrence, Catherine B, Hawkes, Cheryl, Pegasiou-Davies, Chrysia-Maria, Gibson, Claire, Crawford, Colin L, Smith, Colin, Vivien, Denis, McLean, Fiona H, Wiseman, Frances, Brezzo, Gaia, Lalli, Giovanna, Pritchard, Harry A T, Markus, Hugh S, Bravo-Ferrer, Isabel, Taylor, Jade, Leiper, James, Berwick, Jason, Gan, Jian, Gallacher, John, Moss, Jonathan, Goense, Jozien, McMullan, Letitia, Work, Lorraine, Evans, Lowri, Stringer, Michael S, Ashford, MLJ, Abulfadl, Mohamed, Conlon, Nina, Malhotra, Paresh, Bath, Philip, Canter, Rebecca, Brown, Rosalind, Ince, Selvi, Anderle, Silvia, Young, Simon, Quick, Sophie, Szymkowiak, Stefan, Hill, Steven, Allan, Stuart, Wang, Tao, Quinn, Terry, Procter, Tessa, Farr, Tracy D, Zhao, Xiangjun, Yang, Zhiyuan, Hainsworth, Atticus H and Wardlaw, Joanna M 2023. A multi-disciplinary commentary on preclinical research to investigate vascular contributions to dementia. Cerebral Circulation - Cognition & Behavior 5 , 100189. 10.1016/j.cccb.2023.100189
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Keefe, Francesca, Monzon Sandoval, Jimena, Rosser, Anne E. ORCID: https://orcid.org/0000-0002-4716-4753, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 and Li, Meng ORCID: https://orcid.org/0000-0002-4803-4643 2023. Single-cell transcriptomics reveals conserved regulatory networks in human and mouse interneuron development. International Journal of Molecular Sciences 24 (9) , 8122. 10.3390/ijms24098122
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Cameron, Darren, Mi, Da, Vinh, Ngoc-Nga, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674, Li, Meng ORCID: https://orcid.org/0000-0002-4803-4643, Marin, Oscar, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Bray, Nicholas ORCID: https://orcid.org/0000-0002-4357-574X 2023. Single nuclei RNA sequencing of 5 regions of the human prenatal brain implicates developing neuron populations in genetic risk for schizophrenia. Biological Psychiatry 93 , pp. 157-166. 10.1016/j.biopsych.2022.06.033
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Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052, Millin, Stephanie, Dahl, Andrew, Schalkamp, Ann-Kathrin, Lawton, Michael, Hubbard, Leon, Rahman, Nabila, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Ben-Shlomo, Yoav, Grosset, Donald G., Hu, Michele T., Marchini, Jonathan and Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 2022. Universal clinical Parkinson’s disease axes identify a major influence of neuroinflammation. Genome Medicine 14 , 129. 10.1186/s13073-022-01132-9
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Monzón-Sandoval, Jimena, Burlacu, Elena, Agarwal, Devika, Handel, Adam E., Wei, Liting, Davis, John, Cowley, Sally A., Cader, M. Zameel and Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 2022. Lipopolysaccharide distinctively alters human microglia transcriptomes to resemble microglia from Alzheimer's disease mouse models. Disease Models and Mechanisms 15 (10) , dmm049349. 10.1242/dmm.049349
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Pokhilko, Alexandra, Handel, Adam, Curion, Fabiola, Volpato, Viola, Whiteley, Emma, Bostrand, Sunniva, Newey, Sarah, Akerman, Colin, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674, Clark, Michael, Bowden, Rory and Cader, M. Zameel 2022. Targeted single-cell RNA sequencing of transcription factors facilitates biological insights from human cell experimental models. Genome Research 31 , pp. 1069-1081. 10.1101/gr.273961.120
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Monzon-Sandoval, Jimena, Burlacu, Elena, Agarwal, Devika, Handel, Adam, Wei, Liting, Davis, John, Cowley, Sally, Cader, Zameel and Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 2022. LPS distinctively alters iPSC-microglia transcriptomes to resemble Alzheimer’s disease genetic mouse model microglia. Disease Models and Mechanisms
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Meijboom, Katharina, Volpato, Viola, Monzón-Sandoval, Jimena, Hoolachan, Joseph, Hammond, Suzan, Abendroth, Frank, deJong, Olivier, Hazell, Gareth, Ahlskog, Nina, Wood, Matthew, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 and Bowerman, Melissa 2021. Combining multi-omics and drug perturbation profiles to identify muscle-specific treatments for spinal muscular atrophy. JCI Insight 6 (13) , e149446. 10.1172/jci.insight.149446
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Ward, Joey, Tunbridge, Elizabeth M., Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052, Lyall, Laura M., Ferguson, Amy, Strawbridge, Rona J., Lyall, Donald M., Cullen, Breda, Graham, Nicholas, Johnston, Keira J. A., Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Pell, Jill P., Bailey, Mark E. S., Harrison, Paul J. and Smith, Daniel J. 2020. 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 25 , pp. 3091-3099. 10.1038/s41380-019-0439-8
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Mencacci, Niccolò, Reynolds, Regina, Garcia Ruiz, Sonia, Vandrovcova, Jana, Forabosco, Paola, Sánchez-Ferrer, Alvaro, Volpato, Viola, Weale, Michael E., Bhatia, Kailash P., Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0002-8905-1052, Volpato, Viola, Caffrey, Tara M., Monzon Sandoval, Jimena, Bowden, Rory, Alegre-Abarrategui, Javier, Wade-Martins, Richard and Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674 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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Carling, Phillippa J, Mortiboys, Heather, Green, Claire, Mihaylov, Simeon, Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052, 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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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Williams, Nigel M. ORCID: https://orcid.org/0000-0003-1177-6931, Hubbard, Leon, Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674, 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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Volpato, Viola and Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0003-4075-7676, Leckey, Claire A., Morgan, Angharad R. ORCID: https://orcid.org/0000-0003-4075-7676, 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. ORCID: https://orcid.org/0000-0002-9584-3769, Cercignani, Mara ORCID: https://orcid.org/0000-0002-4550-2456, Clarke, Charlotte L, Hoskins, Elizabeth, Kohn, Charmaine, Murray, Rosemary, Wilcock, Lauren, Wlazly, Dominika, Mount, Howard, Jones, Declan N. C., Lovestone, Simon, Gomez-Nicola, Diego and Perry, V. Hugh 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 ORCID: https://orcid.org/0000-0001-8350-6928, Rinaldi, Federica, Vowles, Jane, Browne, Cathy, Evetts, Samuel G., Hu, Michele T., Cowley, Sally A., Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674 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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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 ORCID: https://orcid.org/0000-0001-8063-7674 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) , 93-106.e6. 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 ORCID: https://orcid.org/0000-0002-8905-1052, 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0002-8905-1052, 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0002-8905-1052, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0003-1784-5483, 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 ORCID: https://orcid.org/0000-0001-5195-0143, Russo, Giancarlo, Rubinsztein, David C., Bayer, Antony ORCID: https://orcid.org/0000-0002-7514-248X, Tsolaki, Magda, Proitsi, Petra, Fox, Nick C., Hampel, Harald, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, 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 ORCID: https://orcid.org/0000-0002-8905-1052, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0002-3491-4519, 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 ORCID: https://orcid.org/0000-0003-1177-6931, 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 ORCID: https://orcid.org/0000-0002-2033-2657, 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 ORCID: https://orcid.org/0000-0003-2171-0610, 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 ORCID: https://orcid.org/0000-0002-1682-9134, 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 ORCID: https://orcid.org/0000-0002-6980-4053, 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 ORCID: https://orcid.org/0000-0003-0870-9412, Kendler, Kenneth S., Koeleman, Bobby, Mathews, Carol A., Price, Alkes, Scharf, Jeremiah, Sklar, Pamela, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Wood, Nicholas W., Cotsapas, Chris, Palotie, Aarno, Smoller, Jordan W., Sullivan, Patrick, Rosand, Jonathan, Corvin, Aiden, Neale, Benjamin M. and Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X 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 ORCID: https://orcid.org/0000-0001-8063-7674 2018. Headache and type 2 diabetes association: a US national ambulatory case-control study. [Online]. bioRxiv. Available at: https://doi.org/10.1101/336586
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Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052, Beer, Nicola L. and Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0002-8905-1052, 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 ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0002-8905-1052, 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0002-8905-1052, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0002-8905-1052, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0002-6083-407X, 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0001-8063-7674, 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 ORCID: https://orcid.org/0000-0001-8063-7674 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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Mikkelsen, Tarjei S., Wakefield, Mattew J., Aken, Bronwen, Amemiya, Chris T., Chang, Jean L., Duke, Sahannon, Garber, Manuel, Gentles, Andrew J., Goodstadt, Leo, Heger, Andreas, Jurka, Jerzy, Kamal, Michael, Mauceli, Evan, Searle, Stephen M. J., Sharpe, Ted, Baker, Michelle L., Batzer, Mark A., Benos, Panayiotis, Belov, Katherine, Clamp, Michele, Cook, April, Cuff, James, Das, Radhika, Davidow, Lance, Deakin, Janine E., Fazzari, Melissa J., Glass, Jacob L., Grabherr, Manfred, Greally, John M., Gu, Wanjun, Hore, Timothy A., Huttley, Gavin A., Kleber, Michael, Jirtle, Randy L., Koina, Edda, Lee, Jeannie T., Mahony, Shaun, Marra, Marco A., Miller, Robert D., Nicholls, Robert D., Oda, Mayumi, Papenfuss, Anthony T., Parra, Zuly E., Pollock, David D., Ray, David A., Schein, Jacqueline E., Speed, Terence P., Thompson, Katherine, VandeBerg, John L., Wade, Claire M., Walker, Jerilyn A., Waters, Paul D., Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674, Weidman, Jennifer R., Xie, Xiaohui, Zody, Michael C., Broad Institute Genome Sequencing Platform, Broad Institute Whole Genome Assembly Team, Marshall Graves, Jennier A., Ponting, Chris P., Breen, Matthew, Samollow, Paul B., Lander, Eric S. and Lindbald-Toh, Kerstin 2007. Genome of the marsupial Monodelphis domestica reveals innovation in non-coding sequences. Nature 447 (7141) , pp. 167-177. 10.1038/nature05805

Nguyen, Duc-Quang, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 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 ORCID: https://orcid.org/0000-0001-8063-7674 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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Lindblad-Toh, Kerstin, Wade, Claire M., Mikkelsen, Tarjei S., Karlsson, Elinor K., Jaffe, David B., Kamal, Michael, Clamp, Michele, Chang, Jean L., Kulbokas III, Edward J., Zody, Michael C., Mauceli, Evan, Xie, Xiaohui, Breen, Matthew, Wayne, Robert K., Ostrander, Elaine A., Ponting, Chris P., Galibert, Francis, Smith, Douglas R., DeJong, Pieter J., Kirkness, Ewen, Alvarez, Pablo, Biagi, Tara, Brockman, William, Butler, Jonathan, Chin, Chee-Wye, Cook, April, Cuff, James, Daly, Mark J., DeCaprio, David, Gnerre, Sante, Grabherr, Manfred, Kellis, Manolis, Kleber, Michael, Bardeleben, Carolyne, Goodstadt, Leo, Heger, Andreas, Hitte, Christophe, Kim, Lisa, Koepfli, Klaus-Peter, Parker, Heidi G., Pollinger, John P., Searle, Stephen M. J., Sutter, Nathan B., Thomas, Rachael, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 and Lander, Eric S. Lander 2005. Genome sequence, comparative analysis and haplotype structure of the domestic dog. Nature 438 (7069) , pp. 803-819. 10.1038/nature04338

Hiller, LaDeana W., International Chicken Genome Sequencing Consortium and Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 2004. Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution. Nature 432 , pp. 659-716. 10.1038/nature03154

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 ORCID: https://orcid.org/0000-0001-8063-7674, 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

Abdellah, Zahra, International Human Genome Sequencing Consortium and Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 2004. Finishing the euchromatic sequence of the human genome. Nature 431 , pp. 931-945. 10.1038/nature03001

Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 and Ponting, Chris P. 2004. Genes and homology. Current Biology 14 (9) , R332-R333. 10.1016/j.cub.2004.04.016

Gibbs, Richard A., Weinstock, George M., Metzker, Michael L., Muzny, Donna M., Sodergren, Erica J., Scherer, Steven, Scott, Graham, Steffen, David, Worley, Kim C., Burch, Paula E., Okwuonu, Geoffrey, Hines, Sandra, Lewis, Lora, DeRamo, Christine, Delgado, Oliver, Dugan-Rocha, Shannon, Miner, George, Morgan, Margaret, Hawes, Alicia, Gill, Rachel, Celera, A., Holt, Robert A., Adams, Mark D., Amanatides, Peter G., Baden-Tillson, Holly, Barnstead, Mary, Chin, Soo, Evans, Cheryl A., Ferriera, Steve, Fosler, Carl, Glodek, Anna, Gu, Zhiping, Jennings, Don, Kraft, Cheryl L., Nguyen, Trixie, Pfannkoch, Cynthia M., Sitter, Cynthia, Sutton, Granger G., Venter, J. Craig, Woodage, Trevor, Smith, Douglas, Lee, Hong-Mei, Gustafson, Erik, Cahill, Patrick, Kana, Arnold, Doucette-Stamm, Lynn, Weinstock, Keith, Fechtel, Kim, Weiss, Robert B., Dunn, Diane M., Green, Eric D., Blakesley, Robert W., Bouffard, Gerard G., de Jong, Pieter J., Osoegawa, Kazutoyo, Zhu, Baoli, Marra, Marco, Schein, Jacqueline, Bosdet, Ian, Fjell, Chris, Jones, Steven, Krzywinski, Martin, Mathewson, Carrie, Siddiqui, Asim, Wye, Natasja, McPherson, John, Zhao, Shaying, Fraser, Claire M., Shetty, Jyoti, Shatsman, Sofiya, Geer, Keita, Chen, Yixin, Abramzon, Sofyia, Nierman, William C., Gibbs, Richard A., Weinstock, George M., Havlak, Paul H., Chen, Rui, James Durbin, K., Egan, Amy, Ren, Yanru, Song, Xing-Zhi, Li, Bingshan, Liu, Yue, Qin, Xiang, Cawley, Simon, Weinstock, George M., Worley, Kim C., Cooney, A. J., Gibbs, Richard A., D'Souza, Lisa M., Martin, Kirt, Qian Wu, Jia, Gonzalez-Garay, Manuel L., Jackson, Andrew R., Kalafus, Kenneth J., McLeod, Michael P., Milosavljevic, Aleksandar, Virk, Davinder, Volkov, Andrei, Wheeler, David A., Zhang, Zhengdong, Bailey, Jeffrey A., Eichler, Evan E., Tuzun, Eray, Birney, Ewan, Mongin, Emmanuel, Ureta-Vidal, Abel, Woodwark, Cara, Zdobnov, Evgeny, Bork, Peer, Suyama, Mikita, Torrents, David, Alexandersson, Marina, Trask, Barbara J., Young, Janet M., Smith, Douglas, Huang, Hui, Fechtel, Kim, Wang, Huajun, Xing, Heming, Weinstock, Keith, Daniels, Sue, Gietzen, Darryl, Schmidt, Jeanette, Stevens, Kristian, Vitt, Ursula, Wingrove, Jim, Camara, Francisco, Mar Albà, M., Abril, Josep F., Guigo, Roderic, Smit, Arian, Dubchak, Inna, Rubin, Edward M., Couronne, Olivier, Poliakov, Alexander, Hübner, Norbert, Ganten, Detlev, Goesele, Claudia, Hummel, Oliver, Kreitler, Thomas, Lee, Young-Ae, Monti, Jan, Schulz, Herbert, Zimdahl, Heike, Himmelbauer, Heinz, Lehrach, Hans, Jacob, Howard J., Bromberg, Susan, Gullings-Handley, Jo, Jensen-Seaman, Michael I., Kwitek, Anne E., Lazar, Jozef, Pasko, Dean, Tonellato, Peter J., Twigger, Simon, Ponting, Chris P., Duarte, Jose M., Rice, Stephen, Goodstadt, Leo, Beatson, Scott A., Emes, Richard D., Winter, Eitan E., Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674, Brandt, Petra, Nyakatura, Gerald, Adetobi, Margaret, Chiaromonte, Francesca, Elnitski, Laura, Eswara, Pallavi, Hardison, Ross C., Hou, Minmei, Kolbe, Diana, Makova, Kateryna, Miller, Webb, Nekrutenko, Anton, Riemer, Cathy, Schwartz, Scott, Taylor, James, Yang, Shan, Zhang, Yi, Lindpaintner, Klaus, Andrews, T. Dan, Caccamo, Mario, Clamp, Michele, Clarke, Laura, Curwen, Valerie, Durbin, Richard, Eyras, Eduardo, Searle, Stephen M., Cooper, Gregory M., Batzoglou, Serafim, Brudno, Michael, Sidow, Arend, Stone, Eric A., Craig Venter, J., Payseur, Bret A., Bourque, Guillaume, López-Otín, Carlos, Puente, Xose S., Chakrabarti, Kushal, Chatterji, Sourav, Dewey, Colin, Pachter, Lior, Bray, Nicolas, Yap, Von Bing, Caspi, Anat, Tesler, Glenn, Pevzner, Pavel A., Haussler, David, Roskin, Krishna M., Baertsch, Robert, Clawson, Hiram, Furey, Terrence S., Hinrichs, Angie S., Karolchik, Donna, Kent, William J., Rosenbloom, Kate R., Trumbower, Heather, Weirauch, Matt, Cooper, David Neil ORCID: https://orcid.org/0000-0002-8943-8484, Stenson, Peter, Ma, Bin, Brent, Michael, Arumugam, Manimozhiyan, Shteynberg, David, Copley, Richard R., Taylor, Martin S., Riethman, Harold, Mudunuri, Uma, Peterson, Jane, Guyer, Mark, Felsenfeld, Adam, Old, Susan, Mockrin, Stephen and Collins, Francis 2004. Genome sequence of the Brown Norway rat yields insights into mammalian evolution. Nature 428 (6982) , pp. 493-521. 10.1038/nature02426

Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 and Barton, Geoffrey J. 2003. Increased coverage obtained by combination of methods for protein sequence database searching. Bioinformatics 19 (11) , pp. 1397-1403. 10.1093/bioinformatics/btg156

Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 and Barton, Geoffrey J. 2001. Estimation of p-values for global alignments of protein sequences. Bioinformatics 17 (12) , pp. 1158-1167. 10.1093/bioinformatics/17.12.1158

McCarthy, Linda C., Bihoreau, Marie-Therese, Kiguwa, Susanna L., Browne, Julie, Watanabe, Takeshi K., Hishigaki, Haretsugu, Tsuji, Atsushi, Kiel, Susanne, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674, Davis, Maria E., Knights, Catherine, Smith, Angela, Critcher, Ricky, Huxtall, Patrick, Hudson Jr., James R., Ono, Toshihide, Hayashi, Hiroumi, Takagi, Toshihisa, Nakamura, Yusuke, Tanigami, Akira, Goodfellow, Peter N., Lathrop, G. Mark and James, Michael R. 2000. A whole-genome radiation hybrid panel and framework map of the rat genome. Mammalian Genome 11 (9) , pp. 791-795. 10.1007/s003350010132

Watanabe, Takeshi K., Bihoreau, Marie-Therese, McCarthy, Linda C., Kiguwa, Susanna L., Hishigaki, Haretsugu, Tsuji, Atsushi, Browne, Julie, Yamasaki, Yuki, Mizoguchi-Miyakita, Ayako, Oga, Keiko, Ono, Toshihide, Okuno, Shiro, Kanemoto, Naohide, Takahashi, Ei-ichi, Tomita, Kazuhiro, Hayashi, Hiromi, Adachi, Masakazu, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674, Davis, Marie, Kiel, Susanne, Knights, Catherine, Smith, Angela, Critcher, Ricky, Miller, Jonathan, Thangarajah, Thiru, Day, Philip J. R., Hudson Jr., James R., Irie, Yasuo, Takagi, Toshihisa, Nakamura, Yusuke, Goodfellow, Peter N., Lathrop, G. Mark, Tanigami, Akira and James, Michael R. 1999. A radiation hybrid map of the rat genome containing 5,255 markers. Nature Genetics 22 , pp. 27-36. 10.1038/8737

Deloukas, P., Schuler, G. D., Gyapay, G., Beasley, E. M., Soderlund, C., Rodriguez-Tomé, P., Hui, L., Matise, T. C., McKusick, K. B., Beckmann, J. S., Bentolilia, S., Bihoreau, M. -T., Birren, B. B., Browne, J., Butler, A., Caslte, A. B., Chiannilkulchai, N., Clee, C., Day, P. J. R., Dehejia, A., Dibling, T., Drouot, N., Duprat, S., Fizames, C., Fox, S., Gelling, S., Green, L., Harrison, P., Hocking, R., Holloway, E., Hunt, S., Keil, S., Lijnzaad, P., Louis-Dit-Sully, C., Ma, J., Mendis, A., Miller, J., Morissette, J., Muselet, D., Nusbaum, H. C., Peck, A., Rozen, S., Simon, D., Slonim, D. K., Staples, R., Stein, L. D., Stewart, E. A., Suchard, M. A., Thangarajah, T., Vega-Czarny, N., Webber, C. ORCID: https://orcid.org/0000-0001-8063-7674, Wu, X., Hudson, J., Auffray, C., Nomura, N., Sikela, J. M., Polymeropoulos, M. H., James, M. R., Lander, E. S., Hudson, T. J., Myers, R. M., Cox, D. R., Weissenback, J., Bogusky, M. S. and Bentley, D. R. 1998. A physical map of 30,000 human genes. Science 282 (5389) , pp. 744-746. 10.1126/science.282.5389.744

This list was generated on Fri Apr 19 04:21:21 2024 BST.