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Number of items: 23.

Schalkamp, Ann-Kathrin, Peall, Kathryn J. ORCID: https://orcid.org/0000-0003-4749-4944, Harrison, Neil A. ORCID: https://orcid.org/0000-0002-9584-3769, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Barnaghi, Payam and Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052 2025. Wearables-derived risk score for unintrusive detection of α-synuclein aggregation or dopaminergic deficit. EBioMedicine 117 , 105782. 10.1016/j.ebiom.2025.105782
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Bettencourt, Conceicao, Skene, Nathan, Bandres‐Ciga, Sara, Anderson, Emma, Winchester, Laura M., Foote, Isabelle F., Schwartzentruber, Jeremy, Botia, Juan A., Nalls, Mike, Singleton, Andrew, Schilder, Brian M., Humphrey, Jack, Marzi, Sarah J., Toomey, Christina E., Kleifat, Ahmad Al, Harshfield, Eric L., Garfield, Victoria, Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052, Keat, Samuel, Tamburin, Stefano, Frigerio, Carlo Sala, Lourida, Ilianna, the Deep Dementia Phenotyping (DEMON) Network, Ranson, Janice M. and Llewellyn, David J. 2023. Artificial intelligence for dementia genetics and omics. Alzheimer's & Dementia: The Journal of the Alzheimer's Association 19 , pp. 5905-5921. 10.1002/alz.13427
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MacIver, Claire, Bailey, Grace, Luque Laguna, Pedro, Wadon, Megan, Schalkamp, Ann-Kathrin, Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052, Jones, Derek ORCID: https://orcid.org/0000-0003-4409-8049, Tax, Chantal ORCID: https://orcid.org/0000-0002-7480-8817 and Peall, Kathryn ORCID: https://orcid.org/0000-0003-4749-4944 2023. Macro- and micro-structural Insights into primary dystonia A UK Biobank study. Journal of Neurology 10.1007/s00415-023-12086-2
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Schalkamp, Ann-Kathrin, Peall, Kathryn J. ORCID: https://orcid.org/0000-0003-4749-4944, Harrison, Neil A. ORCID: https://orcid.org/0000-0002-9584-3769 and Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052 2023. Wearable movement-tracking data identify Parkinson's disease years before clinical diagnosis. Nature Medicine 29 , pp. 2048-2056. 10.1038/s41591-023-02440-2
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Stevenson-Hoare, Joshua, Schalkamp, Ann-Kathrin, Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052, Hardy, John and Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 2023. New cases of dementia are rising in elderly populations in Wales, UK. Journal of the Neurological Sciences 451 , 120715. 10.1016/j.jns.2023.120715
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Wadon, Megan, Fenner, Eilidh, Kendall, Kimberley ORCID: https://orcid.org/0000-0002-6755-6121, Bailey, Grace, Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222 and Peall, Kathryn J. ORCID: https://orcid.org/0000-0003-4749-4944 2022. Clinical and genotypic analysis in determining dystonia non-motor phenotypic heterogeneity: a UK Biobank study. Journal of Neurology 269 , pp. 6436-6451. 10.1007/s00415-022-11307-4
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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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Schalkamp, Ann-Kathrin, Rahman, Nabila, Monzón-Sandoval, Jimena and Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052 2022. Deep phenotyping for precision medicine in Parkinson's disease. Disease Models and Mechanisms 15 (6) , dmm049376. 10.1242/dmm.049376
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Wadon, Megan E., Bailey, Grace A., Yilmaz, Zehra ORCID: https://orcid.org/0000-0003-1967-5270, Hubbard, Emily, AlSaeed, Meshari, Robinson, Amy, McLauchlan, Duncan, Barbano, Richard L., Marsh, Laura, Factor, Stewart A., Fox, Susan H., Adler, Charles H., Rodriguez, Ramon L., Comella, Cynthia L., Reich, Stephen G., Severt, William L., Goetz, Christopher G., Perlmutter, Joel S., Jinnah, Hyder A., Harding, Katharine E., Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052 and Peall, Kathryn J. 2021. Non-motor phenotypic subgroups in adult-onset idiopathic, isolated, focal cervical dystonia. Brain and Behavior 11 (8) , e2292. 10.1002/brb3.2292
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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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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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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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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, ORCID: https://orcid.org/0000-0002-8905-1052, ORCID: https://orcid.org/0000-0001-8063-7674, ORCID: https://orcid.org/0000-0002-3491-4519, , ORCID: https://orcid.org/0000-0003-1177-6931, ORCID: https://orcid.org/0000-0002-2033-2657, ORCID: https://orcid.org/0000-0003-2171-0610, ORCID: https://orcid.org/0000-0002-1682-9134, , , ORCID: https://orcid.org/0000-0002-6980-4053, ORCID: https://orcid.org/0000-0003-0870-9412, ORCID: https://orcid.org/0000-0002-4069-0259 and 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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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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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

Eyre, Steve, Bowes, John, Diogo, Dorothée, Lee, Annette, Barton, Anne, Martin, Paul, Zhernakova, Alexandra, Stahl, Eli, Viatte, Sebastien, McAllister, Kate, Amos, Christopher I, Padyukov, Leonid, Toes, Rene E M, Huizinga, Tom W J, Wijmenga, Cisca, Trynka, Gosia, Franke, Lude, Westra, Harm-Jan, Alfredsson, Lars, Hu, Xinli, Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052, de Bakker, Paul I W, Davila, Sonia, Khor, Chiea Chuen, Heng, Khai Koon, Andrews, Robert, Edkins, Sarah, Hunt, Sarah E, Langford, Cordelia, Symmons, Deborah, Concannon, Pat, Onengut-Gumuscu, Suna, Rich, Stephen S, Deloukas, Panos, Gonzalez-Gay, Miguel A, Rodriguez-Rodriguez, Luis, Ärlsetig, Lisbeth, Martin, Javier, Rantapää-Dahlqvist, Solbritt, Plenge, Robert M, Raychaudhuri, Soumya, Klareskog, Lars, Gregersen, Peter K, Worthington, Jane, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Dunajewski, Katherine, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Fraser, Christine, Green, Elaine, Grozeva, Detelina, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2012. High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Nature Genetics 44 (12) , pp. 1336-1340. 10.1038/ng.2462

This list was generated on Sun Nov 9 11:36:07 2025 GMT.


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