Browse by Current Cardiff authors

Hou, Jiahui, Hess, Jonathan L., Zhang, Chunling, van Rooij, Jeroen G. J., Hearn, Gentry C., Fan, Chun Chieh, Faraone, Stephen V., Fennema‐Notestine, Christine, Lin, Shu‐Ju, Escott‐Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Seshadri, Sudha, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Tsuang, Ming T., Kremen, William S., Gaiteri, Chris and Glatt, Stephen J. 2024. Meta‐analysis of transcriptomic studies of blood and six brain regions identifies a consensus of 15 cross‐tissue mechanisms in Alzheimer's disease and suggests an origin of cross‐study heterogeneity. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 10.1002/ajmg.b.33019

Cardno, Alastair G, Allardyce, Judith ORCID: https://orcid.org/0000-0003-4094-552X, Bakker, Steven C, Toulopoulou, Timothea, Kravariti, Eugenia, Picchioni, Marco M, Kane, Fergus, Rijsdijk, Frühling V, Mahmood, Tariq, Nasser El Din, Soumaya, du Toit, Deline, Jones, Lisa A, Quattrone, Diego, Walters, James T R ORCID: https://orcid.org/0000-0002-6980-4053, Legge, Sophie E, Holmans, Peter A ORCID: https://orcid.org/0000-0003-0870-9412, Murray, Robin M and Vassos, Evangelos 2024. Associations of psychotic symptom dimensions with clinical and developmental variables in twin and general clinical samples. The British Journal of Psychiatry , pp. 1-8. 10.1192/bjp.2024.129

Tume, Claire E., Chick, Sophie L., Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Cameron, Darren and Bray, Nicholas J. ORCID: https://orcid.org/0000-0002-4357-574X 2024. Genetic implication of specific glutamatergic neurons of the prefrontal cortex in the pathophysiology of schizophrenia. Biological Psychiatry 4 (5) , 100345. 10.1016/j.bpsgos.2024.100345

Benger, Lauren, LINC Consortium, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Mon-Williams, Mark, Katzourou, Ioanna and Van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2024. Adverse childhood experiences and multimorbidity of internalising and cardiometabolic conditions in an older-age population. Presented at: International Population Data Linkage Conference, Chicago, USA, 15-18 September 2025. Conference Proceedings for International Population Data Linkage Conference. International Journal of Population Data Science. , vol.9 (5) Swansea University, p. 133. 10.23889/ijpds.v9i5.2617

Legge, Sophie E., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Woolway, Grace, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Cardno, Alastair G., Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael J. ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2024. Genetic and phenotypic features of Schizophrenia in the UK Biobank. JAMA Psychiatry 81 , pp. 681-690. 10.1001/jamapsychiatry.2024.0200

Trastulla, Lucia, Dolgalev, Georgii, Moser, Sylvain, Jiménez-Barrón, Laura, Andlauer, Till, von Scheidt, Moritz, Schizophrenia Working Group of the Psychiatric Genomics Consorti, Budde, Monika, Heilbronner, Urs, Papiol, Sergei, Teumer, Alexander, Homouth, Georg, Falkai, Peter, Volzke, Henry, Dorr, Marcus, Schulze, Thomas, Gagneur, Julien, Iorio, Francesco, Müller-Myhsok, Bertram, Schunkert, Heribert, Ziller, Michael, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Georgieva, Lyudmila, Hamshere, Marian L. ORCID: https://orcid.org/0000-0002-8990-0958, Kavanagh, David, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Legge, Sophie, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Richards, Alexander L., Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Williams, Nigel M. ORCID: https://orcid.org/0000-0003-1177-6931 and Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412 2024. Distinct genetic liability profiles define clinically relevant patient strata across common diseases. Nature Communications 15 , 5534. 10.1038/s41467-024-49338-2

Uzochukwu, Emeka C., Harding, Katherine E., Hrastelj, James ORCID: https://orcid.org/0000-0002-7991-5259, Kreft, Karim L., Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Robertson, Neil P. ORCID: https://orcid.org/0000-0002-5409-4909, Tallantyre, Emma C. ORCID: https://orcid.org/0000-0002-3760-6634 and Lawton, Michael 2024. Modelling disease progression of Multiple Sclerosis in a South Wales cohort. Neuroepidemiology 58 (3) , pp. 218-226. 10.1159/000536427

Hall, Jessica H., Chawner, Samuel J. R. A., Wolstencroft, Jeanne, Skuse, David, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2024. Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs). Translational Psychiatry 14 (1) , 259. 10.1038/s41398-024-02975-z

Kim, Kyung-Hee, Hong, Eun Pyo, Lee, Yukyeong, McLean, Zachariah, Elezi, Emanuela, Lee, Ramee, Kwak, Seung, McAllister, Branduff, Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131, Lobanov, Sergey, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Orth, Michael, Ciosi, Marc, Monckton, Darren, Long, Jeffrey, Lucente, Diane, Wheeler, Vanessa, MacDonald, Marcy, Gusella, James and Lee, Jong-Min 2024. Posttranscriptional regulation of FAN1 by miR-124-3p at rs3512 underlies onset-delaying genetic modification in Huntington's disease. Proceedings of the National Academy of Sciences 121 (16) , e2322924121. 10.1073/pnas.2322924121

Hess, Jonathan L., Mattheisen, Manuel, Greenwood, Tiffany A., Tsuang, Ming T., Edenberg, Howard J., Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Faraone, Stephen V. and Glatt, Stephen J. 2024. A polygenic resilience score moderates the genetic risk for schizophrenia: Replication in 18,090 cases and 28,114 controls from the Psychiatric Genomics Consortium. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 195 (2) , e32957. 10.1002/ajmg.b.32957

Kreft, Karim L., Uzochukwu, Emeka, Loveless, Sam ORCID: https://orcid.org/0000-0002-5124-4115, Willis, Mark ORCID: https://orcid.org/0000-0003-3024-6063, Wynford-Thomas, Ray, Harding, Katharine E., Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Lawton, Michael, Tallantyre, Emma C. ORCID: https://orcid.org/0000-0002-3760-6634 and Robertson, Neil P. ORCID: https://orcid.org/0000-0002-5409-4909 2024. Relevance of multiple sclerosis severity genotype in predicting disease course: A real-world cohort. Annals of Neurology 95 (3) , pp. 459-470. 10.1002/ana.26831

Hong, Eun Pyo, Ramos, Eliana Marisa, Aziz, N. Ahmad, Massey, Thomas H. ORCID: https://orcid.org/0000-0002-9804-2131, McAllister, Branduff, Lobanov, Sergey ORCID: https://orcid.org/0000-0002-3126-1903, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Kwak, Seung, Orth, Michael, Ciosi, Marc, Lomeikaite, Vilija, Monckton, Darren G., Long, Jeffrey D., Lucente, Diane, Wheeler, Vanessa C., Gillis, Tammy, MacDonald, Marcy E., Sequeiros, Jorge, Gusella, James F. and Lee, Jong-Min 2024. Modification of Huntington's disease by short tandem repeats. Brain Communications 6 (2) , fcae016. 10.1093/braincomms/fcae016

O'Connell, Kevin, Koromina, Maria, van der Veen, Tracey, Boltz, Toni, David, Friederike, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412 and Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889 2024. Genomics yields biological and phenotypic insights into bipolar disorder. Biological Psychiatry Item availability restricted.

Clifton, Nicholas ORCID: https://orcid.org/0000-0003-2597-5253, Schulmann, Anton, Schizophrenia Working Group of the Psychiatric Genomics Consorti, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Vawter, Marquis 2023. The relationship between case-control differential gene expression from brain tissue and genetic associations in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 192 (5-6) , pp. 85-92. 10.1002/ajmg.b.32931

Harrison, Judith R. ORCID: https://orcid.org/0000-0002-5775-2524, Foley, Sonya F. ORCID: https://orcid.org/0000-0002-8390-2709, Baker, Emily, Bracher-Smith, Matthew, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Stergiakouli, Evie, Linden, David E.J. ORCID: https://orcid.org/0000-0002-5638-9292, Caseras, Xavier ORCID: https://orcid.org/0000-0002-8490-6891, Jones, Derek K. ORCID: https://orcid.org/0000-0003-4409-8049 and Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 2023. Pathway-specific polygenic scores for Alzheimer's disease are associated with changes in brain structure in younger and older adults. Brain Communications 5 (5) , fcad229. 10.1093/braincomms/fcad229

Le Guen, Yann, Luo, Guo, Ambati, Aditya, Damotte, Vincent, Jansen, Iris, Yu, Eric, Nicolas, Aude, de Rojas, Itziar, Peixoto Leal, Thiago, Miyashita, Akinori, Bellenguez, Céline, Lian, Michelle Mulan, Parveen, Kayenat, Morizono, Takashi, Park, Hyeonseul, Grenier-Boley, Benjamin, Naito, Tatsuhiko, Küçükali, Fahri, Talyansky, Seth D., Yogeshwar, Selina Maria, Sempere, Vicente, Satake, Wataru, Alvarez, Victoria, Arosio, Beatrice, Belloy, Michael E., Benussi, Luisa, Boland, Anne, Borroni, Barbara, Bullido, María J., Caffarra, Paolo, Clarimon, Jordi, Daniele, Antonio, Darling, Daniel, Debette, Stéphanie, Deleuze, Jean-François, Dichgans, Martin, Dufouil, Carole, During, Emmanuel, Düzel, Emrah, Galimberti, Daniela, Garcia-Ribas, Guillermo, García-Alberca, José María, García-González, Pablo, Giedraitis, Vilmantas, Goldhardt, Oliver, Graff, Caroline, Grünblatt, Edna, Hanon, Olivier, Hausner, Lucrezia, Heilmann-Heimbach, Stefanie, Holstege, Henne, Hort, Jakub, Jung, Yoo Jin, Jürgen, Deckert, Kern, Silke, Kuulasmaa, Teemu, Lee, Kun Ho, Lin, Ling, Masullo, Carlo, Mecocci, Patrizia, Mehrabian, Shima, de Mendonça, Alexandre, Boada, Mercè, Mir, Pablo, Moebus, Susanne, Moreno, Fermin, Nacmias, Benedetta, Nicolas, Gael, Niida, Shumpei, Nordestgaard, Børge G., Papenberg, Goran, Papma, Janne, Parnetti, Lucilla, Pasquier, Florence, Pastor, Pau, Peters, Oliver, Pijnenburg, Yolande A. L., Piñol-Ripoll, Gerard, Popp, Julius, Porcel, Laura Molina, Puerta, Raquel, Pérez-Tur, Jordi, Rainero, Innocenzo, Ramakers, Inez, Real, Luis M., Riedel-Heller, Steffi, Rodriguez-Rodriguez, Eloy, Ross, Owen A., Luís Royo, Jose, Rujescu, Dan, Scarmeas, Nikolaos, Scheltens, Philip, Scherbaum, Norbert, Schneider, Anja, Seripa, Davide, Skoog, Ingmar, Solfrizzi, Vincenzo, Spalletta, Gianfranco, Squassina, Alessio, van Swieten, John, Sánchez-Valle, Raquel, Tan, Eng-King, Tegos, Thomas, Teunissen, Charlotte, Thomassen, Jesper Qvist, Tremolizzo, Lucio, Vyhnalek, Martin, Verhey, Frans, Waern, Margda, Wiltfang, Jens, Zhang, Jing, Zetterberg, Henrik, Blennow, Kaj, He, Zihuai, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Amouyel, Philippe, Jessen, Frank, Kehoe, Patrick G., Andreassen, Ole A., Van Duin, Cornelia, Tsolaki, Magda, Sánchez-Juan, Pascual, Frikke-Schmidt, Ruth, Sleegers, Kristel, Toda, Tatsushi, Zettergren, Anna, Ingelsson, Martin, Okada, Yukinori, Rossi, Giacomina, Hiltunen, Mikko, Gim, Jungsoo, Ozaki, Kouichi, Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Foo, Jia Nee, van der Flier, Wiesje, Ikeuchi, Takeshi, Ramirez, Alfredo, Mata, Ignacio, Ruiz, Agustín, Gan-Or, Ziv, Lambert, Jean-Charles, Greicius, Michael D., Mignot, Emmanuel, Bellenguez, Céline, Küçükali, Fahri, Jansen, Iris, Andrade, Victor, Moreno-Grau, Sonia, Amin, Najaf, Grenier-Boley, Benjamin, Campos-Martin, Rafael, Holmans, Peter A., Boland, Anne, Kleineidam, Luca, Damotte, Vincent, van der Lee, Sven J., Kuulasmaa, Teemu, de Rojas, Itziar, Yaqub, Amber, Prokic, Ivana, Costa, Marcos R, Chapuis, Julien, Ahmad, Shahzad, Giedraitis, Vilmantas, Aarsland, Dag, Garcia-Gonzalez, Pablo, Abdelnour, Carla, Alarcón-Martín, Emilio, Alcolea, Daniel, Alegret, Montserrat, Alvarez, Ignacio, Álvarez, Victoria, Armstrong, Nicola J., Anthoula, Tsolaki, Appollonio, Ildebrando, Arcaro, Marina, Archetti, Silvana, Arias Pastor, Alfonso, Arosio, Beatrice, Athanasiu, Lavinia, Bailly, Henri, Banaj, Nerisa, Baquero, Miquel, Belén Pastor, Ana, Benussi, Luisa, Berr, Claudine, Besse, Céline, Bessi, Valentina, Binetti, Giuliano, Bizarro, Alessandra, Blesa, Rafael, Boada, Mercè, Borroni, Barbara, Boschi, Silvia, Bossù, Paola, Bråthen, Geir, Bresner, Catherine, Brodaty, Henry, Brookes, Keeley J., Ignacio Brusco, Luis, Buiza-Rueda, Dolores, BÛrger, Katharina, Burholt, Vanessa, Calero, Miguel, Chene, Geneviève, Carracedo, Ángel, Cecchetti, Roberta, Cervera-Carles, Laura, Charbonnier, Camille, Chillotti, Caterina, Ciccone, Simona, Claassen, Jurgen A.H.R., Clarimon, Jordi, Clark, Christopher, Conti, Elisa, Corma-Gómez, Anaïs, Costantini, Emanuele, Custodero, Carlo, Daian, Delphine, Dalmasso, Maria Carolina, Daniele, Antonio, Dardiotis, Efthimios, Dartigues, Jean-François, de Deyn, Peter Paul, Debette, Stéphanie, Deckert, Jürgen, del Ser, Teodoro, Denning, Nicola, Dichgans, Martin, Diehl-Schmid, Janine, Diez-Fairen, Mónica, Dionigi Rossi, Paolo, Djurovic, Srdjan, Duron, Emmanuelle, Düzel, Emrah, Dufouil, Carole, Escott-Price, Valentina, Espinosa, Ana, Ewers, Michael, Fernández-Fuertes, Marta, Ferreira, Catarina B, Ferri, Evelyn, Fin, Bertrand, Fischer, Peter, Fladby, Tormod, Fließbach, Klaus, Fortea, Juan, Fostinelli, Silvia, Fox, Nick C., Franco-Macías, Emlio, Bullido, María J., Frank-García, Ana, Froelich, Lutz, Galimberti, Daniela, Maria García-Alberca, Jose, García-González, Pablo, Garcia-Madrona, Sebastian, Garcia-Ribas, Guillermo, Ghidoni, Roberta, Giegling, Ina, Giorgio, Giaccone, Goldhardt, Oliver, González-Pérez, Antonio, Graff, Caroline, Grande, Giulia, Green, Emma, Grimmer, Timo, Grünblatt, Edna, Guetta-Baranes, Tamar, Haapasalo, Annakaisa, Hadjigeorgiou, Georgios, Hampel, Harald, Hanon, Olivier, Hardy, John, Hartmann, Annette M., Hausner, Lucrezia, Harwood, Janet, Heilmann-Heimbach, Stefanie, Helisalmi, Seppo, Heneka, Michael T., Hernández, Isabel, Herrmann, Martin J., Hoffmann, Per, Holmes, Clive, Holstege, Henne, Huerto Vilas, Raquel, Hulsman, Marc, Johansson, Charlotte, Kilander, Lena, Kinhult Ståhlbom, Anne, Kivipelto, Miia, Koivisto, Anne, Kornhuber, Johannes, Kosmidis, Mary H., Lage, Carmen, Laukka, Erika J, Lauria, Alessandra, Lehtisalo, Jenni, Lerch, Ondrej, Lleó, Alberto, de Munain, Adolfo Lopez, Löwemark, Malin, Luckcuck, Lauren, Macías, Juan, MacLeod, Catherine A., Maier, Wolfgang, Mangialasche, Francesca, Marco, Spallazzi, Marquié, Marta, Marshall, Rachel, Martín Montes, Angel, Martínez Rodríguez, Carmen, Masullo, Carlo, Mead, Simon, Mecocci, Patrizia, Medina, Miguel, Meggy, Alun, Mehrabian, Shima, Mendoza, Silvia, Menéndez-González, Manuel, Mir, Pablo, Moebus, Susanne, Mol, Merel, Molina-Porcel, Laura, Montrreal, Laura, Morelli, Laura, Moreno, Fermin, Morgan, Kevin, Möthen, Markus M, Muchnik, Carolina, Nacmias, Benedetta, Ngandu, Tiia, Nicolas, Gael, Nordestgaard, Børge G., Olaso, Robert, Orellana, Adelina, Orsini, Michela, Ortega, Gemma, Padovani, Alessandro, Paolo, Caffarra, Papenberg, Goran, Parnetti, Lucilla, Pastor, Pau, Pérez-Cordón, Alba, Pérez-Tur, Jordi, Pericard, Pierre, Peters, Oliver, Pijnenburg, Yolande A.L., Pineda, Juan A., Piñol-Ripoll, Gerard, Pisanu, Claudia, Polak, Thomas, Popp, Julius, Posthuma, Danielle, Priller, Josef, Puerta, Raquel, Quenez, Olivier, Quintela, Inés, Qvist Thomassen, Jesper, Rábano, Alberto, Rainero, Innocenzo, Ramakers, Inez, Real, Luis M., Reinders, Marcel J.T., Riedel-Heller, Steffi, Riederer, Peter, Roberto, Natalia, Rodriguez-Rodriguez, Eloy, Rongve, Arvid, Rosas Allende, Irene, Rosende-Roca, Maitée, Luis Royo, Jose, Rubino, Elisa, Rujescu, Dan, Eugenia Sáez, María, Sakka, Paraskevi, Saltvedt, Ingvild, Sanabria, Ángela, Sánchez-Arjona, María Bernal, Sanchez-Garcia, Florentino, Sánchez Juan, Pascual, Sánchez-Valle, Raquel, Sando, Sigrid B., Scamosci, Michela, Scarmeas, Nikolaos, Scarpini, Elio, Scheltens, Philip, Scherbaum, Norbert, Scherer, Martin, Schmid, Matthias, Schneider, Anja, Schott, Jonathan M., Selbæk, Geir, Seripa, Davide, Shadrin, Alexey A., Skrobot, Olivia, Soininen, Hilkka, Solfrizzi, Vincenzo, Solomon, Alina, Sorbi, Sandro, Sotolongo-Grau, Oscar, Spalletta, Gianfranco, Spottke, Annika, Squassina, Alessio, Stordal, Eystein, Pablo Tartan, Juan, Tárraga, Lluís, Tesí, Niccolo, Thalamuthu, Anbupalam, Thomas, Tegos, Traykov, Latchezar, Tremolizzo, Lucio, Tybjærg-Hansen, Anne, Uitterlinden, Andre, Ullgren, Abbe, Ulstein, Ingun, Valero, Sergi, van der Lugt, Aad, Van Dongen, Jasper, van Rooij, Jeroen, van Swieten, John, Vandenberghe, Rik, Verhey, Frans, Vidal, Jean-Sébastien, Vogelgsang, Jonathan, Vyhnalek, Martin, Wagner, Michael, Wallon, David, Weinhold, Leonie, Wiltfang, Jens, Windle, Gill, Woods, Bob, Yannakoulia, Mary, Zulaica, Miren, Laczo, Jan, Matoska, Vaclav, Serpente, Maria, Assogna, Francesca, Piras, Fabrizio, Piras, Federica, Ciullo, Valentina, Shofany, Jacob, Ferrarese, Carlo, Andreoni, Simona, Sala, Gessica, Paola Zoia, Chiara, Del Zompo, Maria, Benussi, Alberto, Bastiani, Patrizia, Takalo, Mari, Natunen, Teemu, Laatikainen, Tiina, Tuomilehto, Jaakko, Antikainen, Riitta, Strandberg, Timo, Lindström, Jaana, Peltonen, Markku, Abraham, Richard, Al-Chalabi, Ammar, Bass, Nicholas J., Brayne, Carol, Brown, Kristelle S., Collinge, John, Craig, David, Deloukas, Pangiotis, Fox, Nick, Gerrish, Amy, Gill, Michael, Gwilliam, Rhian, Hardy, John, Harold, Denise, Hollingworth, Paul, Johnston, Jarret A., Jones, Lesley, Lawlor, Brian, Livingston, Gill, Lovestone, Simon, Lupton, Michelle, Lynch, Aoibhinn, Mann, David, McGuinness, Bernadette, McQuillin, Andrew, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Passmore, Peter, Powell, John F., Proitsi, Petra, Rossor, Martin, Shaw, Christopher E., David Smith, A., Gurling, Hugh, Todd, Stephen, Mummery, Catherine, Ryan, Nathalie, Lacidogna, Giordano, Adarmes-Gómez, Ad, Mauleón, Ana, Pancho, Ana, Gailhajenet, Anna, Lafuente, Asunción, Macias-García, D., Martín, Elvira, Pelejà, Esther, Carrillo, F., Sastre Merlín, Isabel, Garrote-Espina, L., Vargas, Liliana, Carrion-Claro, M., Marín, M., Labrador, Ma, Buendia, Mar, Dolores Alonso, María, Guitart, Marina, Moreno, Mariona, Ibarria, Marta, Periñán, Mt, Aguilera, Nuria, Gómez-Garre, P., Cañabate, Pilar, Escuela, R., Pineda-Sánchez, R., Vigo-Ortega, R., Jesús, S., Preckler, Silvia, Rodrigo-Herrero, Silvia, Diego, Susana, Vacca, Alessandro, Roveta, Fausto, Salvadori, Nicola, Chipi, Elena, Boecker, Henning, Laske, Christoph, Perneczky, Robert, Anastasiou, Costas, Janowitz, Daniel, Malik, Rainer, Anastasiou, Anna, Parveen, Kayenat, Lage, Carmen, López-García, Sara, Antonell, Anna, Yonkova Mihova, Kalina, Belezhanska, Diyana, Weber, Heike, Kochen, Silvia, Solis, Patricia, Medel, Nancy, Lisso, Julieta, Sevillano, Zulma, Politis, Daniel G., Cores, Valeria, Cuesta, Carolina, Ortiz, Cecilia, Ignacio Bacha, Juan, Rios, Mario, Saenz, Aldo, Sanchez Abalos, Mariana, Kohler, Eduardo, Lis Palacio, Dana, Etchepareborda, Ignacio, Kohler, Matias, Novack, Gisela, Ariel Prestia, Federico, Galeano, Pablo, Castaño, Eduardo M., Germani, Sandra, Reyes Toso, Carlos, Rojo, Matias, Ingino, Carlos, Mangone, Carlos, Engelborghs, Sebastiaan, Fabrizio, Tagliavini, Fallgaard Nielsen, Sune, Farotti, Lucia, Fenoglio, Chiara, Jan Biessels, Geert, Love, Seth, Kehoe, Patrick G., Pasquier, Florence, Van Broeckhoven, Christine, Rubinsztein, David C., Teipel, Stefan, Fievet, Nathalie, Deramecourt, Vincent, Forsell, Charlotte, Thonberg, Håkan, Bjerke, Maria, De Roeck, Ellen, Teresa Martínez-Larrad, María, Olivar, Natividad, Ghanbari, Mohsen, Sachdev, Perminder, Mather, Karen, Jessen, Frank, Arfan Ikram, M., de Mendonça, Alexandre, Hort, Jakub, Magda, Tsolaki, Amouyel, Philippe, Williams, Julie, Frikke-Schmidt, Ruth, Clarimon, Jordi, Deleuze, Jean-François, Rossi, Giacomina, Andreassen, Ole A., Ingelsson, Martin, Hiltunen, Mikko, Sleegers, Kristel, van Duijn, Cornelia M., Sims, Rebecca, van der Flier, Wiesje M., Ruiz, Agustín, Ramirez, Alfredo, Lambert, Jean-Charles, Aguilera, N., Alarcon, E., Alegret, M., Boada, M., Buendia, M., Cano, A., Cañabate, P., Carracedo, A., Corbatón-Anchuelo, A., de Rojas, I., Diego, S., Espinosa, A., Gailhajenet, A., García-González, P., Guitart, M., González-Péerez, A., Ibarria, M., Lafuente, A., Macias, J., Maroñas, O., Martín, E., Martínez, M.T., Marquié, M., Montrreal, L., Moreno-Grau, S., Moreno, M., Nuñez-Llaves, R., Olivé, C., Orellana, A., Ortega, G., Pancho, A., Pelejà, E., Pérez-Cordon, A., Pineda, J.A., Puerta, R., Preckler, S., Quintela, I., Real, L.M., Rosende-Roca, M., Ruiz, A., Sáez, M.E., Sanabria, 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ORCID: https://orcid.org/0000-0003-0870-9412, Boland, Anne, Damotte, Vincent, van der Lee, Sven J., Costa, Marcos R., Kuulasmaa, Teemu, Yang, Qiong, de Rojas, Itziar, Bis, Joshua C., Yaqub, Amber, Prokic, Ivana, Chapuis, Julien, Ahmad, Shahzad, Giedraitis, Vilmantas, Aarsland, Dag, Garcia-Gonzalez, Pablo, Abdelnour, Carla, Alarcón-Martín, Emilio, Alcolea, Daniel, Alegret, Montserrat, Alvarez, Ignacio, Álvarez, Victoria, Armstrong, Nicola J., Tsolaki, Anthoula, Antúnez, Carmen, Appollonio, Ildebrando, Arcaro, Marina, Archetti, Silvana, Pastor, Alfonso Arias, Arosio, Beatrice, Athanasiu, Lavinia, Bailly, Henri, Banaj, Nerisa, Baquero, Miquel, Barral, Sandra, Beiser, Alexa, Pastor, Ana Belén, Below, Jennifer E., Benchek, Penelope, Benussi, Luisa, Berr, Claudine, Besse, Céline, Bessi, Valentina, Binetti, Giuliano, Bizarro, Alessandra, Blesa, Rafael, Boada, Mercè, Boerwinkle, Eric, Borroni, Barbara, Boschi, Silvia, Bossù, Paola, Bråthen, Geir, Bressler, Jan, Bresner, Catherine ORCID: https://orcid.org/0000-0003-2673-9762, Brodaty, Henry, Brookes, Keeley J., Brusco, Luis Ignacio, Buiza-Rueda, Dolores, Bûrger, Katharina, Burholt, Vanessa, Bush, William S., Calero, Miguel, Cantwell, Laura B., Chene, Geneviève, Chung, Jaeyoon, Cuccaro, Michael L., Carracedo, Ángel, Cecchetti, Roberta, Cervera-Carles, Laura, Charbonnier, Camille, Chen, Hung-Hsin, Chillotti, Caterina, Ciccone, Simona, Claassen, Jurgen A. H. 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Legge, S. E., Hamshere, M. L. ORCID: https://orcid.org/0000-0002-8990-0958, Ripke, S., Pardinas, A. F. ORCID: https://orcid.org/0000-0001-6845-7590, Goldstein, J. I., Rees, E. ORCID: https://orcid.org/0000-0002-6168-9222, Richards, A. L., Leonenko, G. ORCID: https://orcid.org/0000-0001-8025-661X, Jorskog, L. F., Goldstein, J. I., Jarskog, L. F., Hilliard, C., Alfirevic, A., Duncan, L., Fourches, D., Huang, H., Lek, M., Neale, B. M., Ripke, S., Shianna, K., Szatkiewicz, J. P., Tropsha, A., van den Oord, E. J. C. G., Cascorbi, I., Dettling, M., Gazit, E., Goff, D. C., Holden, A. L., Kelly, D. L., Malhotra, A. K, Nielsen, J., Pirmohamed, M., Rujescu, D., Werge, T., Levy, D. L., Josiassen, R. C., Kennedy, J. L., Lieberman, J. A., Daly, M. J., Sullivan, P. F., Chambert, K. D., Collier, D. A., Genovese, G., Giegling, I., Holmans, P. ORCID: https://orcid.org/0000-0003-0870-9412, Jonasdottir, A., Kirov, G. ORCID: https://orcid.org/0000-0002-3427-3950, McCarroll, S. A., MacCabe, J. H., Mantripragada, K ORCID: https://orcid.org/0000-0003-2070-8105, Moran, J. L., Neale, B. M., Stefansson, H., Rujescu, D., Daly, M. J., Sullivan, P. F., Owen, M. J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, M. C. ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, J.T. R ORCID: https://orcid.org/0000-0002-6980-4053 2017. Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia. Molecular Psychiatry 22 , pp. 1502-1508. 10.1038/mp.2016.97

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O'Dushlaine, C, Kenny, E, Heron, E, Donohoe, G, Gill, M, Morris, D, Corvin, A, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Georgieva, Lyudmila and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2011. Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility. Molecular Psychiatry 16 (3) , pp. 286-292. 10.1038/mp.2010.7

Peterson, Roseann E., Maes, Hermine H., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Sanders, Alan R., Levinson, Douglas F., Shi, Jianxin, Kendler, Kenneth S., Gejman, Pablo V. and Webb, Bradley T. 2011. Genetic risk sum score comprised of common polygenic variation is associated with body mass index. Human Genetics 129 (2) , pp. 221-230. 10.1007/s00439-010-0917-1

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Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Russo, Giancarlo, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Dwyer, Sarah Lynne, Smith, Rhodri L., Green, Elaine Karen, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2011. Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries. Human Molecular Genetics 20 (2) , pp. 387-391. 10.1093/hmg/ddq471

Bridges, Michael, Heron, Elizabeth A., O'Dushlaine, Colm, Segurado, Ricardo, Morris, Derek, Corvin, Aiden, Gill, Michael, Pinto, Carlos, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Georgieva, Lyudmila, Nikolov, Ivan, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Toncheva, Draga, Milanova, Vihra and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2011. Genetic classification of populations using supervised learning. PLoS ONE 6 (5) , e14802. 10.1371/journal.pone.0014802

Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Jones, L., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Green, Elaine Karen, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Bass, N., McQuillin, A., Gurling, H., St Clair, D., Young, A. H., Ferrier, I. N., Farmer, Anne, McGuffin, Peter, Sklar, P., Purcell, S., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2011. Polygenic dissection of the bipolar phenotype. British Journal of Psychiatry 198 (4) , pp. 284-288. 10.1192/bjp.bp.110.087866

Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Dwyer, Sarah Lynne, Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Gerrish, Amy, Hollingworth, Paul, Chapman, Jade Alice, Denning, Nicola, Abraham, Richard Alun, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Pahwa, Jaspreet Singh, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Dowzell, Kimberley Frances, Thomas, Charlene, Stretton, Alexandra, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K., Brayne, Carol, Rubinsztein, David C., Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle S., Passmore, Peter A., Craig, David, McGuiness, Bernadette, Todd, Stephen, Johnston, Janet A., Holmes, Clive, Mann, David, Smith, A. David, Love, Seth, Kehoe, Patrick G., Hardy, John, Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2011. No evidence that extended tracts of homozygosity are associated with Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (7) , pp. 764-771. 10.1002/ajmg.b.31216

Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, McCarthy, Geraldine, Jones, Lisa, Murphy, Kieran C., Sanders, Robert D., Gray, Marion Y., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, McGuffin, Peter, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Cardno, Alastair G. 2011. Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (8) , pp. 929-940. 10.1002/ajmg.b.31240

Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, O'Dushlaine, Colm, Purcell, Shaun, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2011. Evaluation of an approximation method for assessment of overall significance of multiple-dependent tests in a genomewide association study. Genetic Epidemiology 35 (8) , pp. 861-866. 10.1002/gepi.20636

Dudbridge, Frank, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 and Wilson, Scott G. 2011. A flexible model for association analysis in sibships with missing genotype data. Annals of Human Genetics 75 (3) , pp. 428-438. 10.1111/j.1469-1809.2010.00636.x

Kendler, Kenneth S., Kalsi, Gursharan, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Sanders, Alan R., Aggen, Steven H., Dick, Danielle M., Aliev, Fazil, Shi, Jianxin, Levinson, Douglas F. and Gejman, Pablo V. 2011. Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample. Alcoholism-Clinical and Experimental Research 35 (5) , pp. 963-975. 10.1111/j.1530-0277.2010.01427.x

Levinson, D. F., Duan, J., Oh, S., Wang, K., Sanders, A. R., Shi, J., Zhang, N., Mowry, B. J., Olincy, A., Amin, F., Cloninger, C. R., Silverman, J. M., Buccola, N. G., Byerley, W. F., Black, D. W., Kendler, K. S., Freedman, R., Dudbridge, F., Pe'er, I., Hakonarson, H., Bergen, S. E., Fanous, A. H., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 and Gejman, P. V. 2011. Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications. American Journal of Psychiatry 168 (3) , pp. 302-316. 10.1176/appi.ajp.2010.10060876

Lips, E. S., Cornelisse, L. N., Toonen, R. F., Min, J. L., Hultman, C. M., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Purcell, S. M., Smit, A. B., Verhage, M, Sullivan, P. F., Visscher, P. M. and Posthuma, D 2011. Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia. Molecular Psychiatry , pp. 1-11. 10.1038/mp.2011.117

Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Agha, Sharifah Shameem ORCID: https://orcid.org/0000-0001-9541-6786, Davies, Charlotte, Stergiakouli, Evangelia, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2011. Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants. British Journal of Psychiatry 199 (5) , pp. 398-403.

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Allison, David B., Raychaudhuri, Soumya, Korn, Joshua M., McCarroll, Steven A., Altshuler, David, Sklar, Pamela, Purcell, Shaun, Daly, Mark J., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Georgieva, Lyudmila and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2010. Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. PLoS Genetics 6 (9) , e1001097. 10.1371/journal.pgen.1001097

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Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, H., Cardno, Alastair G., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, L. A., Murphy, K. C., Sanders, Rebecca, McCarthy, G., Gray, M. Y., Jones, G., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2006. Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes. Journal of Medical Genetics 43 (7) , pp. 563-567. 10.1136/jmg.2005.035345

Macgregor, Stuart, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 2006. Use of phenotypic covariates in association analysis by sequential addition of cases. European Journal of Human Genetics 14 (5) , pp. 529-534. 10.1038/sj.ejhg.5201604

Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, MacGregor, S., Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Nikolov, I. N. and Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 2005. Covariate linkage analysis of GAW14 simulated data incorporating subclinical phenotype, sex, population, parent-of-origin, and interaction. BMC Genetics 6 (1) , S45. 10.1186/1471-2156-6-S1-S45

Levinson, D. F. and Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 2005. The effect of linkage disequilibrium on linkage analysis of incomplete pedigrees. BMC Genetics 6 (1) , S6-S6. 10.1186/1471-2156-6-S1-S6

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Hughes, G. P., Brooks, Simon P. ORCID: https://orcid.org/0000-0001-9853-6177, Hodges, A. H., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Thomas, J. M., Goldstein, D., Dunnett, Stephen Bruce ORCID: https://orcid.org/0000-0003-1826-1578 and Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612 2005. Integrating behaviour and brain gene expression in Huntington's disease transgenic mouse models. Journal of Neurology, Neurosurgery and Psychiatry 76 , A41-A41.

Nowotny, P., Hinrichs, A. L., Smemo, S., Kauwe, J. S., Maxwell, T., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Turic, D., Jehu, L., Hollingworth, P., Moore, P., Bryden, L., Myers, A., Doil, L. M., Tacey, K. M., Gibson, A. M., McKeith, I. G., Perry, R. H., Morris, C. M., Thal, L., Morris, J. C., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Lovestone, S. and Grupe, A. 2005. Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 136B (1) , pp. 62-68. 10.1002/ajmg.b.30186

Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Hollingworth, P., Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Tunstall, N., Jones, S., Moore, P., Wavrant DeVrieze, F., Myers, A., Crook, R., Compton, D., Marshall, H., Meyer, D., Shears, S., Booth, J., Ramic, D., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, N., Abraham, R., Kehoe, P., Williams, H., Rudrasingham, V., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Hardy, J., Goate, A., Lovestone, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2005. Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 135B (1) , pp. 24-32. 10.1002/ajmg.b.30114

Lambert, D., Middle, F., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Segurado, Ricardo, Raybould, Rachel, Corvin, A., Green, Elaine Karen, O'Mahony, E., Nikolov, Ivan, Mulcahy, T., Haque, S., Bort, S., Bennett, P., Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Lendon, C., Jones, Lisa Anne, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Gill, M. and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2005. Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22. Molecular psychiatry 10 (9) , pp. 831-841. 10.1038/sj.mp.4001684

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Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. Streamlined analysis of pooled genotype data in SNP-based association studies. Genetic Epidemiology 28 (3) , pp. 273-282. 10.1002/gepi.20062

Li, Y., Hollingworth, P., Moore, P., Foy, C., Archer, N., Powell, J., Nowotny, P., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Tacey, K., Doil, L., van Luchene, R., Garcia, V., Rowland, V., Lau, K., Cantanese, J., Sninsky, J., Hardy, J., Thal, L., Morris, J. C., Goate, A., Lovestone, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Grupe, A. 2005. Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease. Human Mutation 25 (3) , pp. 270-277. 10.1002/humu.20138

Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Schmidt, Karl Michael ORCID: https://orcid.org/0000-0002-0227-3024 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2005. Design of Case-controls Studies with Unscreened Controls. Annals of Human Genetics 69 (5) , pp. 566-576. 10.1111/j.1529-8817.2005.00175.x

Seaman, S. R. and Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 2005. Effect of genotyping error on type-I error rate of affected sib pair studies with genotyped parents. Human Heredity 59 (3) , pp. 157-164. 10.1159/000085939

Li, Yonghong, Nowotny, Petra, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Smemo, Scott, Kauwe, John S. K., Hinrichs, Anthony L., Tacey, Kristina, Doil, Lisa, Luchene, Ryan van, Garcia, Veronica, Rowland, Charles, Schrodi, Steve, Leong, Diane, Gogic, Goran, Chan, Joanne, Cravchik, Anibal, Ross, David, Lau, Kit, Kwok, Shirley, Chang, Sheng-Yung, Catanese, Joseph, Sninsky, John, White, Thomas J., Hardy, John, Powell, John, Lovestone, Simon, Morris, John C., Thal, Leon, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Goate, Alison and Grupe, Andrew 2004. Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family. Proceedings of the National Academy of Sciences 101 (44) , pp. 15688-15693. 10.1073/pnas.0403535101

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Mowry, B J, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Pulver, A E, Gejman, P V, Riley, B, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Laurent, C, Schwab, S G, Wildenauer, D B, Bauché, S, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Wormley, B, Sanders, A R, Nestadt, G, Liang, K Y, Duan, J, Ribble, R, Norton, N, Soubigou, S, Maier, W, Ewen-White, K R, deMarchi, N, Carpenter, B, Walsh, D, Williams, H, Jay, M, Albus, M, Nertney, D A, Papadimitriou, G, O'Neill, A, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Deleuze, J-F, Lerer, F B, Dikeos, D, Kendler, K S, Mallet, J, Silverman, J M, Crowe, R R and Levinson, D F 2004. Multicenter linkage study of schizophrenia loci on chromosome 22q. Molecular Psychiatry 9 (8) , pp. 784-795. 10.1038/sj.mp.4001481

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Bernardinelli, L., Berzuini, C., Seaman, S. and Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 2004. Bayesian trio models for association in the presence of genotyping errors. Genetic Epidemiology 26 (1) , pp. 70-80. 10.1002/gepi.10291

Myers, Amanda J., Marshall, Helen, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Compton, Danielle, Crook, Richard J.P., Mander, Adrian P., Nowotny, Petra, Smemo, Scott, Dunstan, Melanie ORCID: https://orcid.org/0000-0003-3817-2142, Jehu, Luke, Wang, Jen C., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Morris, John C., Norton, Joanne, Chakraventy, Sumi, Tunstall, Nigel, Lovestone, Simon, Petersen, Ronald, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Hardy, John and Goate, Alison 2004. Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD. American Journal of Medical Genetics 124B (1) , pp. 29-37. 10.1002/ajmg.b.20036

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Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Ekholm, B., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Lindblom, Y., Chowdari, K. V., Cardno, Alastair George, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, Lisa Anne, Murphy, Kieran Christopher, Sanders, Robert David, McCarthy, Geraldine MaryTeresa, Gray, Marion Yvonne, Jones, G., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Nimgaonkar, V., Adolfson, R., Osby, U., Terenius, L., Sedvall, G., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2003. A systematic genomewide linkage study in 353 sib pairs with schizophrenia. The American journal of human genetics 73 (6) , pp. 1355-1367. 10.1086/380206

Hensiek, A.E., Roxburgh, R., Smilie, B., Coraddu, F., Åkesson, E., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Sawcer, S.J. and Compston, D.A.S. 2003. Updated results of the United Kingdom linkage-based genome screen in multiple sclerosis. Journal of Neuroimmunology 143 (1-2) , pp. 25-30. 10.1016/j.jneuroim.2003.08.007

Levinson, Douglas F., Zubenko, George S., Crowe, Raymond R., DePaulo, Raymond J., Scheftner, William S., Weissman, Myrna M., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Zubenko, Wendy N., Boutelle, Sandra, Murphy-Eberenz, Kathleen, MacKinnon, Dean, McInnis, Melvin G., Marta, Diana H., Adams, Philip, Sassoon, Stephanie, Knowles, James A., Thomas, Jo and Chellis, Jennifer 2003. Genetics of recurrent early-onset depression (GenRED): Design and preliminary clinical characteristics of a repository sample for genetic linkage studies. American Journal of Medical Genetics 119B (1) , pp. 118-130. 10.1002/ajmg.b.20009

Rice, K. M. and Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 2003. Allowing for Genotyping Error in Analysis of Unmatched Case-Control Studies. Annals of Human Genetics 67 (2) , pp. 165-174. 10.1046/j.1469-1809.2003.00020.x

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Myers, Amanda, Wavrant De-Vrieze, Fabienne, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Crook, Richard, Compton, Danielle, Marshall, Helen, Meyer, David, Shears, Shantia, Booth, Jeremy, Ramic, Dzanan, Knowles, Heather, Morris, John C., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine, Abraham, Richard, Kehoe, Pat, Williams, Hywel, Rudrasingham, Varuni, Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Giles, Peter ORCID: https://orcid.org/0000-0003-3143-6854, Tunstall, Nigel, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Lovestone, Simon, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Hardy, John and Goate, Alison 2002. Full genome screen for Alzheimer disease: Stage II analysis. American Journal Of Medical Genetics Part A 114 (2) , pp. 235-244. 10.1002/ajmg.10183

Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 2002. Detecting gene-gene interactions using affected sib pair analysis with covariates. Human Heredity 53 (2) , pp. 92-102. 10.1159/000057987

Bennett, P., Segurado, R., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Bort, S., McCandless, F., Lambert, D., Heron, J., Comerford, C., Middle, F., Corvin, A., Pelios, G., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Larsen, B., Mulcahy, T., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, O'Connell, R., O'Mahony, E., Payne, A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Gill, M. 2002. The Wellcome trust UK-Irish bipolar affective disorder sibling-pair genome screen: first stage report. Molecular Psychiatry 7 (2) , pp. 189-200. 10.1038/sj.mp.4000957

Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 2001. Likelihood-ratio affected sib-pair tests applied to multiply affected sibships: issues of power and type I error rate. Genetic Epidemiology 20 (1) , pp. 44-56. 10.1002/1098-2272(200101)

Myers, A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Marshall, H., Kwon, J., Meyer, D., Ramic, D., Shears, S., Booth, J., DeVrieze, F. W., Crook, R., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Abraham, R., Tunstall, N., Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Carty, S., Lillystone, S., Kehoe, P., Rudrasingham, V., Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Lovestone, S., Perez-Tur, J., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Hardy, J. and Goate, A. M. 2000. Susceptibility locus for Alzheimer's disease on chromosome 10. Science 290 (5500) , pp. 2304-2305. 10.1126/science.290.5500.2304

Levinson, D. F., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Straub, R. E., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Wildenauer, D. B., Gejman, P. V., Pulver, A. E., Laurent, C., Kendler, K. S., Walsh, D., Norton, N., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Schwab, S. G., Lerer, B., Mowry, B. J., Sanders, A. R., Antonarakis, S. E., Blouin, J. L., DeLeuze, J. F. and Mallet, J. 2000. Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III. American Journal of Human Genetics 67 (3) , pp. 652-663. 10.1086/303041

Murphy, K. C., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A. G., Jones, L. A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Thompson, P., Thonas, N., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Chromosome 22q, velo-cardio-facial syndrome (VCFS) and schizophrenia. Journal of Medical Genetics 37 , S58-S58.

Bandmann, O., Vaughan, J. R., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Marsden, C. D. and Wood, N. W. 2000. Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's disease. Movement Disorders 15 (1) , pp. 30-35. 10.1002/1531-8257(200001)15:13.0.CO;2-V

Neuman, R. J., Saccone, N. L., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Rice, J. P. and Sun, L. 2000. Clustering methods applied to allele sharing data. Genetic Epidemiology 19 (1) , pp. 57-63. 10.1002/1098-2272(2000)19:1+<::AID-GEPI9>3.0.CO;2-D

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Rees, M. I., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Norton, N., Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., McCarthy, G., Gray, M. Y., Fenton, I., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs. Human Molecular Genetics 8 (9) , pp. 1729-1739. 10.1093/hmg/8.9.1729

Wavrant-De Vrieze, F., Crook, R., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Kehoe, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Roehl, K., Laliiri, D. K., Shears, S., Booth, J., Wu, W., Goate, A., Chartier-Harlin, M. C., Hardy, J. and Perez-Tur, J. 1999. Genetic variability at the amyloid-beta precursor protein locus may contribute to the risk of late-onset Alzheimer's disease. Neuroscience Letters 269 (2) , pp. 67-70.

Hateboer, N., Lazarou, L. P., Williams, A. J., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 and Ravine, D. 1999. Familial phenotype differences in PKD11. Kidney International 56 (1) , pp. 34-40. 10.1046/j.1523-1755.1999.00541.x

Rees, M. I., Fenton, I., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Norton, N., Cardno, A., Asherson, P., Spurlock, G., Vallada, H., Dawson, E., Li, M. W., Collier, D. A., Powell, J. F., Nanko, S., Gill, M., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Autosome search for schizophrenia susceptibility genes in multiply affected families. Molecular Psychiatry 4 (4) , pp. 353-359. 10.1038/sj.mp.4000521

Wavrant-DeVrieze, F., Rudrasingham, V., Lambert, J. C., Chakraverty, S., Kehoe, P., Crook, R., Amouyel, P., Wu, W., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Perez-Tur, J., Frigard, B., Morric, J. C., Carty, S., Cottel, D., Tunstall, N., Lovestone, S., Petersen, R. C., Chartier-Harlin, M. C., Goate, A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Hardy, J. 1999. No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease. Neuroscience Letters 262 (2) , pp. 137-139. 10.1016/S0304-3940(99)00035-X

Kehoe, P., Wavrant-De Vrieze, F., Crook, R., Wu, W. S., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Fenton, I., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Lovestone, S., Perez-Tur, J., Hutton, M., Chartier-Harlin, M. C., Shears, S., Roehl, K., Booth, J., Van Voorst, W., Ramic, D., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Goate, A., Hardy, J. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. A full genome scan for late onset Alzheimer's disease. Human Molecular Genetics 8 (2) , pp. 237-245. 10.1093/hmg/8.2.237

Bandmann, O., Vaughan, J., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Marsden, C. D. and Wood, N. W. 1999. Toxins, genetics, and Parkinson's disease: the role of N-acetyltransferase 2. Advances in Neurology -New York- Raven Press- 80 , pp. 199-204.

Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 1998. Affected sib-pair methods for detecting linkage to dichotomous traits: review of the methodology. Human biology 70 (6) , pp. 1025-1040.

Kehoe, P. G., Williams, H., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Wilcock, G., Cairns, N. J., Neal, J. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. The butyrylcholinesterase K variant and susceptibility to Alzheimer's disease. Journal of Medical Genetics 35 (12) , pp. 1034-1035. 10.1136/jmg.35.12.1034

Bandmann, O., Valente, E. M., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Surtees, R. A., Walters, J. H., Wevers, R. A., Marsden, C. D. and Wood, N. W. 1998. Dopa-responsive dystonia: a clinical and molecular genetic study. Annals of Neurology 44 (4) , pp. 649-656. 10.1002/ana.410440411

Wu, W. S., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Wavrant-DeVrieze, F., Shears, S., Kehoe, P., Crook, R., Booth, J., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Perez-Tur, J., Roehl, K., Fenton, I., Chartier-Harlin, M. C., Lovestone, S., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Hutton, M., Hardy, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Goate, A. 1998. Genetic studies on chromosome 12 in late-onset Alzheimer disease. JAMA - The Journal of the American Medical Association 280 (7) , pp. 619-622. 10.1001/jama.280.7.619

Daniels, J., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Turic, D., McGuffin, P., Plomin, R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. A simple method for analyzing microsatellite allele image patterns generated from DNA pools and its application to allelic association studies. American Journal of Human Genetics 62 (5) , pp. 1189-1197. 10.1086/301816

Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Spurlock, G., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Mant, R., Murphy, K., Jones, L., Cardno, A., Asherson, P., Blackwood, D., Muir, W., Meszaros, K., Aschauer, H., Mallet, J., Laurent, C., Pekkarinen, P., Seppala, J., Stefanis, C. N., Papadimitriou, G. N., Macciardi, F., Verga, M., Pato, C., Azevedo, H., Crocq, M. A., Gurling, H. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia. Molecular Psychiatry 3 (2) , pp. 141-149.

Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1998. Efficient strategies for genome scanning with affected sib pairs - Reply. American Journal of Human Genetics 62 (1) , pp. 205-207. 10.1086/301683

Hateboer, N., Lazarou, L., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, A. J. and Ravine, D. 1998. Inter-family variability of phenotype in autosomal dominant polycystic kidney disease type 1. European Journal of Human Genetics 6 (1) , p. 71.

Murphy, K. C., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A. G., Jones, L. A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. A linkage study of chromosome 22q in SIB-pairs with schizophrenia. Schizophrenia Research 29 (1-2) , pp. 131-132. 10.1016/S0920-9964(97)88632-X

Spurlock, G., Heils, A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, J., D'Souza, U. M., Cardno, A., Murphy, K. C., Jones, L., Buckland, Paul Robert, McGuffin, P., Lesch, K. .P and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. A family based association study of T102C polymorphism in 5HT2A and schizophrenia plus identification of new polymorphisms in the promoter. Molecular Psychiatry 3 (1) , pp. 42-49. 10.1038/sj.mp.4000342

Bandmann, O., Vaughan, J., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Marsden, C. D. and Wood, N. W. 1997. Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease. The Lancet 350 (9085) , pp. 1136-1139. 10.1016/S0140-6736(97)03495-8

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Baboolal, K., Ravine, D., Daniels, J., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Coles, G. A. and Williams, J. D. 1997. Association of the angiotensin I converting enzyme gene deletion polymorphism with early onset of ESRF in PKD1 adult polycystic kidney disease. Kidney International 52 (3) , pp. 607-613. 10.1038/ki.1997.373

Hateboer, N., Dijk, M., Torra, R., Bogdanova, N., Davies, F., Lazarou, L., Breuning, M., SaggarMalik, A. K., Jeffery, S., Millan, J. L. S., Martinez, I., Walker, R., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Ravine, D. and Coles, G. A. 1997. Phenotype PKD2 vs. PKD1; results from the European concerted action. Journal of the American Society of Nephrology 8 , A1722-A1722.

Rees, M., Norton, N., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., Scourfield, J., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Moorhead, S., Feldman, E., Sadler, S., Cole, T., Redman, K., Farmer, A., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1997. Association studies of bipolar disorder at the human serotonin transporter gene (hSERT; 5HTT). Molecular Psychiatry 2 (5) , pp. 398-402. 10.1038/sj.mp.4000256

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 and McGuffin, P. 1997. Association studies in psychiatric genetics. Molecular Psychiatry 2 (4) , pp. 270-273. 10.1038/sj.mp.4000292

Daniels, J. K., Spurlock, G., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A. G., Jones, L. A., Murphy, K. C., Asherson, P., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Fenton, I., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. Linkage study of chromosome 6p in sib-pairs with schizophrenia. American Journal of Medical Genetics 74 (3) , pp. 319-323. 10.1002/(SICI)1096-8628(19970531)74:3<319::AID-AJMG14>3.0.CO;2-R

Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1997. Efficient strategies for genome scanning using maximum-likelihood affected-sib-pair analysis. American Journal of Human Genetics 60 (3) , pp. 657-666.

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Kehoe, P., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Liddell, M., Lovestone, S., Holmes, C., Powell, J., Neal, J., Wilcock, G. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Association between a PS-1 intronic polymorphism and late onset Alzheimer's disease. NeuroReport 7 (13) , pp. 2155-2158. 10.1097/00001756-199609020-00019

Asherson, P., Mant, R., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Cardno, A., Murphy, K., Jones, L., Collier, D., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Linkage, association and mutational analysis of the dopamine D3 receptor gene in schizophrenia. Molecular Psychiatry 1 (2) , pp. 125-132.

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Wood, N. W., Sawcer, S. J., Kellar-Wood, H. F., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Clayton, D., Robertson, Neil ORCID: https://orcid.org/0000-0002-5409-4909 and Compston, D. A. 1995. The T-cell receptor beta locus and susceptibility to multiple sclerosis. Neurology 45 (10) , pp. 1859-1863. 10.1212/WNL.45.10.1859

Wood, N. W., Sawcer, S. J., Kellar-Wood, H. F., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Clayton, D., Robertson, Neil ORCID: https://orcid.org/0000-0002-5409-4909 and Compston, D. A. 1995. Susceptibility to multiple sclerosis and the immunoglobulin heavy chain variable region. Journal of Neurology 242 (10) , pp. 677-682. 10.1007/BF00866919

Kellar-Wood, H. F., Wood, N. W., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Clayton, D., Robertson, Neil ORCID: https://orcid.org/0000-0002-5409-4909 and Compston, D. A. 1995. Multiple sclerosis and the HLA-D region: linkage and association studies. Journal of Neuroimmunology 58 (2) , pp. 183-190. 10.1016/0165-5728(95)00015-T

Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, McGuffin, P. and Clayton, D. 1995. Genome scan for association and linkage. Genetic Epidemiology 12 (6) , pp. 613-618. 10.1002/gepi.1370120615

Robertson, Neil ORCID: https://orcid.org/0000-0002-5409-4909, Wood, N., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Kellar-Wood, H. F., Sawcer, S. and Wood, N. W. 1995. Strategies for the identification of susceptibility genes in multiple sclerosis [Editorial]. The International Ms Journal 2 , pp. 19-28.

Wood, N. W., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Clayton, D., Robertson, Neil Patrick ORCID: https://orcid.org/0000-0002-5409-4909 and Compston, D. A. 1994. No linkage or association between multiple sclerosis and the myelin basic protein gene in affected sibling pairs. Journal of Neurology, Neurosurgery & Psychiatry 57 (10) , pp. 1191-1194. 10.1136/jnnp.57.10.1191

Eoli, M., Wood, N.W., Kellar-Wood, H.F., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Clayton, D. and Compston, D.A.S. 1994. No linkage between multiple sclerosis and the T cell receptor alpha chain locus. Journal of the Neurological Sciences 124 (1) , p. 32. 10.1016/0022-510X(94)90007-8

Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 1993. Asymptotic properties of affected-sib-pair linkage analysis. American journal of human genetics 52 (2) , pp. 362-374.