Bivariate genome-wide association analysis strengthens the role of bitter receptor clusters on chromosomes 7 and 12 in human bitter taste

por Hwang, Liang-Dar, Gharahkhani, Puya, Breslin, Paul A. S., Gordon, Scott D., Zhu, Gu, Martin, Nicholas G., Reed, Danielle R., Wright, Margaret J.
Publicado 2018

The Association of Genetic Predisposition to Depressive Symptoms with Non-suicidal and Suicidal Self-Injuries

por Maciejewski, Dominique F., Renteria, Miguel E., Abdellaoui, Abdel, Medland, Sarah E., Few, Lauren R., Gordon, Scott D., Madden, Pamela A.F., Montgomery, Grant, Trull, Timothy J., Heath, Andrew C., Statham, Dixie J., Martin, Nicholas G., Zietsch, Brendan P., Verweij, Karin J.H.
Publicado 2016

First all-in-one diagnostic tool for DNA intelligence: genome-wide inference of biogeographic ancestry, appearance, relatedness, and sex with the Identitas v1 Forensic Chip

por Keating, Brendan, Bansal, Aruna T., Walsh, Susan, Millman, Jonathan, Newman, Jonathan, Kidd, Kenneth, Budowle, Bruce, Eisenberg, Arthur, Donfack, Joseph, Gasparini, Paolo, Budimlija, Zoran, Henders, Anjali K., Chandrupatla, Hareesh, Duffy, David L., Gordon, Scott D., Hysi, Pirro, Liu, Fan, Medland, Sarah E., Rubin, Laurence, Martin, Nicholas G., Spector, Timothy D., Kayser, Manfred
Publicado 2012

Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis

por Painter, Jodie N., Anderson, Carl A., Nyholt, Dale R., Macgregor, Stuart, Lin, Jianghai, Lee, Sang Hong, Lambert, Ann, Zhao, Zhen Z., Roseman, Fenella, Guo, Qun, Gordon, Scott D., Wallace, Leanne, Henders, Anjali K., Visscher, Peter M., Kraft, Peter, Martin, Nicholas G., Morris, Andrew P., Treloar, Susan A., Kennedy, Stephen H., Missmer, Stacey A., Montgomery, Grant W., Zondervan, Krina T.
Publicado 2010

Associations between the CADM2 gene, substance use, risky sexual behavior, and self‐control: A phenome‐wide association study

por Arends, Rachel M., Pasman, Joëlle A., Verweij, Karin J.H., Derks, Eske M., Gordon, Scott D., Hickie, Ian, Thomas, Nathaniel S., Aliev, Fazil, Zietsch, Brendan P., van der Zee, Matthijs D., Mitchell, Brittany L., Martin, Nicholas G., Dick, Danielle M., Gillespie, Nathan A., de Geus, Eco J.C., Boomsma, Dorret I., Schellekens, Arnt F.A., Vink, Jacqueline M.
Publicado 2021

Higher polygenic risk for melanoma is associated with improved survival in a high ultraviolet radiation setting

por Seviiri, Mathias, Scolyer, Richard A., Bishop, D. Timothy, Newton-Bishop, Julia A., Iles, Mark M., Lo, Serigne N., Stretch, Johnathan R., Saw, Robyn P. M., Nieweg, Omgo E., Shannon, Kerwin F., Spillane, Andrew J., Gordon, Scott D., Olsen, Catherine M., Whiteman, David C., Landi, Maria Teresa, Thompson, John F., Long, Georgina V., MacGregor, Stuart, Law, Matthew H.
Publicado 2022

Uncovering the complex relationship between balding, testosterone and skin cancers in men

por Ong, Jue-Sheng, Seviiri, Mathias, Dusingize, Jean Claude, Wu, Yeda, Han, Xikun, Shi, Jianxin, Olsen, Catherine M., Neale, Rachel E., Thompson, John F., Saw, Robyn P. M., Shannon, Kerwin F., Mann, Graham J., Martin, Nicholas G., Medland, Sarah E., Gordon, Scott D., Scolyer, Richard A., Long, Georgina V., Iles, Mark M., Landi, Maria Teresa, Whiteman, David C., MacGregor, Stuart, Law, Matthew H.
Publicado 2023

Genome-wide association meta-analysis identifies new endometriosis risk loci

por Nyholt, Dale R., Low, Siew-Kee, Anderson, Carl A., Painter, Jodie N., Uno, Satoko, Morris, Andrew P., MacGregor, Stuart, Gordon, Scott D., Henders, Anjali K., Martin, Nicholas G., Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Kennedy, Stephen H., Treloar, Susan A., Missmer, Stacey A., Adachi, Sosuke, Tanaka, Kenichi, Nakamura, Yusuke, Zondervan, Krina T., Zembutsu, Hitoshi, Montgomery, Grant W.
Publicado 2012

Genome-wide association identifies ATOH7 as a major gene determining human optic disc size

por Macgregor, Stuart, Hewitt, Alex W., Hysi, Pirro G., Ruddle, Jonathan B., Medland, Sarah E., Henders, Anjali K., Gordon, Scott D., Andrew, Toby, McEvoy, Brian, Sanfilippo, Paul G., Carbonaro, Francis, Tah, Vikas, Li, Yi Ju, Bennett, Sonya L., Craig, Jamie E., Montgomery, Grant W., Tran-Viet, Khanh-Nhat, Brown, Nadean L., Spector, Timothy D., Martin, Nicholas G., Young, Terri L., Hammond, Christopher J., Mackey, David A.
Publicado 2010

A prospective cohort study of prodromal Alzheimer’s disease: Prospective Imaging Study of Ageing: Genes, Brain and Behaviour (PISA)

por Lupton, Michelle K., Robinson, Gail A., Adam, Robert J., Rose, Stephen, Byrne, Gerard J., Salvado, Olivier, Pachana, Nancy A., Almeida, Osvaldo P., McAloney, Kerrie, Gordon, Scott D, Raniga, Parnesh, Fazlollahi, Amir, Xia, Ying, Ceslis, Amelia, Sonkusare, Saurabh, Zhang, Qing, Kholghi, Mahnoosh, Karunanithi, Mohan, Mosley, Philip E, Lv, Jinglei, Borne, Léonie, Adsett, Jessica, Garden, Natalie, Fripp, Jurgen, Martin, Nicholas G., Guo, Christine C, Breakspear, Michael
Publicado 2020

Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia

por Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D., Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Pourcain, Beate St, Francks, Clyde, Marioni, Riccardo E., Zhao, Jingjing, Paracchini, Silvia, Talcott, Joel B., Monaco, Anthony P., Stein, John F., Gruen, Jeffrey R., Olson, Richard K., Willcutt, Erik G., DeFries, John C., Pennington, Bruce F., Smith, Shelley D., Wright, Margaret J., Martin, Nicholas G., Auton, Adam, Bates, Timothy C., Fisher, Simon E., Luciano, Michelle
Publicado 2023

Discovery of 42 genome-wide significant loci associated with dyslexia

por Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D., Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Pourcain, Beate St, Francks, Clyde, Marioni, Riccardo E., Zhao, Jingjing, Paracchini, Silvia, Talcott, Joel B., Monaco, Anthony P., Stein, John F., Gruen, Jeffrey R., Olson, Richard K., Willcutt, Erik G., DeFries, John C., Pennington, Bruce F., Smith, Shelley D., Wright, Margaret J., Martin, Nicholas G., Auton, Adam, Bates, Timothy C., Fisher, Simon E., Luciano, Michelle
Publicado 2022

Genetic meta-analysis of twin birth weight shows high genetic correlation with singleton birth weight

por Beck, Jeffrey J, Pool, René, van de Weijer, Margot, Chen, Xu, Krapohl, Eva, Gordon, Scott D, Nygaard, Marianne, Debrabant, Birgit, Palviainen, Teemu, van der Zee, Matthijs D, Baselmans, Bart, Finnicum, Casey T, Yi, Lu, Lundström, Sebastian, van Beijsterveldt, Toos, Christiansen, Lene, Heikkilä, Kauko, Kittelsrud, Julie, Loukola, Anu, Ollikainen, Miina, Christensen, Kaare, Martin, Nicholas G, Plomin, Robert, Nivard, Michel, Bartels, Meike, Dolan, Conor, Willemsen, Gonneke, de Geus, Eco, Almqvist, Catarina, Magnusson, Patrik K E, Mbarek, Hamdi, Ehli, Erik A, Boomsma, Dorret I, Hottenga, Jouke-Jan
Publicado 2021

Identical twins carry a persistent epigenetic signature of early genome programming

por van Dongen, Jenny, Gordon, Scott D., McRae, Allan F., Odintsova, Veronika V., Mbarek, Hamdi, Breeze, Charles E., Sugden, Karen, Lundgren, Sara, Castillo-Fernandez, Juan E., Hannon, Eilis, Moffitt, Terrie E., Hagenbeek, Fiona A., van Beijsterveldt, Catharina E. M., Jan Hottenga, Jouke, Tsai, Pei-Chien, Min, Josine L., Hemani, Gibran, Ehli, Erik A., Paul, Franziska, Stern, Claudio D., Heijmans, Bastiaan T., Slagboom, P. Eline, Daxinger, Lucia, van der Maarel, Silvère M., de Geus, Eco J. C., Willemsen, Gonneke, Montgomery, Grant W., Reversade, Bruno, Ollikainen, Miina, Kaprio, Jaakko, Spector, Tim D., Bell, Jordana T., Mill, Jonathan, Caspi, Avshalom, Martin, Nicholas G., Boomsma, Dorret I.
Publicado 2021

Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability

por Hysi, Pirro G., Valdes, Ana, Liu, Fan, Furlotte, Nicholas A., Evans, David M., Bataille, Veronique, Visconti, Alessia, Hemani, Gibran, McMahon, George, Ring, Susan M., Davey Smith, George, Duffy, David L., Zhu, Gu, Gordon, Scott D., Medland, Sarah E., Lin, Bochao D., Willemsen, Gonneke, Hottenga, JoukeJan, Vuckovic, Dragana, Girotto, Giorgia, Gandin, Ilaria, Sala, Cinzia, Concas, Maria Pina, Brumat, Marco, Gasparini, Paolo, Toniolo, Daniela, Cocca, Massimiliano, Robino, Antonietta, Yazar, Seyhan, Hewitt, Alex W., Chen, Yan, Zeng, Changqing, Uitterlinden, Andre G., Ikram, M. Arfan, Hamer, Merel A., van Duijn, Cornelia M., Nijsten, Tamar, Mackey, David A., Falchi, Mario, Boomsma, Dorret I., Martin, Nicholas G., Hinds, David A., Kayser, Manfred, Spector, Timothy D.
Publicado 2018

Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color

por Simcoe, Mark, Valdes, Ana, Liu, Fan, Furlotte, Nicholas A., Evans, David M., Hemani, Gibran, Ring, Susan M., Smith, George Davey, Duffy, David L., Zhu, Gu, Gordon, Scott D., Medland, Sarah E., Vuckovic, Dragana, Girotto, Giorgia, Sala, Cinzia, Catamo, Eulalia, Concas, Maria Pina, Brumat, Marco, Gasparini, Paolo, Toniolo, Daniela, Cocca, Massimiliano, Robino, Antonietta, Yazar, Seyhan, Hewitt, Alex, Wu, Wenting, Kraft, Peter, Hammond, Christopher J., Shi, Yuan, Chen, Yan, Zeng, Changqing, Klaver, Caroline C. W., Uitterlinden, Andre G., Ikram, M. Arfan, Hamer, Merel A., van Duijn, Cornelia M., Nijsten, Tamar, Han, Jiali, Mackey, David A., Martin, Nicholas G., Cheng, Ching-Yu, Hinds, David A., Spector, Timothy D., Kayser, Manfred, Hysi, Pirro G.
Publicado 2021

Genomewide Association for Major Depressive Disorder: A possible role for the presynaptic protein Piccolo

por Sullivan, Patrick F., de Geus, Eco J.C., Willemsen, Gonneke, James, Michael R., Smit, Jan H., Zandbelt, Tim, Arolt, Volker, Baune, Bernhard T., Blackwood, Douglas, Cichon, Sven, Coventry, William L., Domschke, Katharina, Farmer, Anne, Fava, Maurizio, Gordon, Scott D., He, Qianchuan, Heath, Andrew, Heutink, Peter, Holsboer, Florian, Hoogendijk, Witte J., Hottenga, Jouke Jan, Hu, Yijuan, Kohli, Martin, Lin, Danyu, Lucae, Suzanne, MacIntyre, Donald J., Maier, Wolfgang, McGhee, Kevin A., McGuffin, Peter, Montgomery, Grant, Muir, Walter J., Nolen, Willem, Nöthen, Markus M., Perlis, Roy H., Pirlo, Katrina, Posthuma, Danielle, Rietschel, Marcella, Rizzu, Patizia, Schosser, Alexandra, Smit, August B., Smoller, Jordan W., Tzeng, Jung-Ying, van Dyck, Richard, Verhage, Matthijs, Zitman, Frans G., Martin, Nicholas G., Wray, Naomi R., Boomsma, Dorret I., Penninx, Brenda W.J.H.
Publicado 2008

The genetic architecture of sporadic and multiple consecutive miscarriage

por Laisk, Triin, Soares, Ana Luiza G., Ferreira, Teresa, Painter, Jodie N., Censin, Jenny C., Laber, Samantha, Bacelis, Jonas, Chen, Chia-Yen, Lepamets, Maarja, Lin, Kuang, Liu, Siyang, Millwood, Iona Y., Ramu, Avinash, Southcombe, Jennifer, Andersen, Marianne S., Yang, Ling, Becker, Christian M., Børglum, Anders D., Gordon, Scott D., Bybjerg-Grauholm, Jonas, Helgeland, Øyvind, Hougaard, David M., Jin, Xin, Johansson, Stefan, Juodakis, Julius, Kartsonaki, Christiana, Kukushkina, Viktorija, Lind, Penelope A., Metspalu, Andres, Montgomery, Grant W., Morris, Andrew P., Mors, Ole, Mortensen, Preben B., Njølstad, Pål R., Nordentoft, Merete, Nyholt, Dale R., Lippincott, Margaret, Seminara, Stephanie, Salumets, Andres, Snieder, Harold, Zondervan, Krina, Werge, Thomas, Chen, Zhengming, Conrad, Donald F., Jacobsson, Bo, Li, Liming, Martin, Nicholas G., Neale, Benjamin M., Nielsen, Rasmus, Walters, Robin G., Granne, Ingrid, Medland, Sarah E., Mägi, Reedik, Lawlor, Deborah A., Lindgren, Cecilia M.
Publicado 2020

Identification of shared risk loci and pathways for bipolar disorder and schizophrenia

por Forstner, Andreas J., Hecker, Julian, Hofmann, Andrea, Maaser, Anna, Reinbold, Céline S., Mühleisen, Thomas W., Leber, Markus, Strohmaier, Jana, Degenhardt, Franziska, Treutlein, Jens, Mattheisen, Manuel, Schumacher, Johannes, Streit, Fabian, Meier, Sandra, Herms, Stefan, Hoffmann, Per, Lacour, André, Witt, Stephanie H., Reif, Andreas, Müller-Myhsok, Bertram, Lucae, Susanne, Maier, Wolfgang, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Pfennig, Andrea, Bauer, Michael, Hautzinger, Martin, Moebus, Susanne, Schenk, Lorena M., Fischer, Sascha B., Sivalingam, Sugirthan, Czerski, Piotr M., Hauser, Joanna, Lissowska, Jolanta, Szeszenia-Dabrowska, Neonila, Brennan, Paul, McKay, James D., Wright, Adam, Mitchell, Philip B., Fullerton, Janice M., Schofield, Peter R., Montgomery, Grant W., Medland, Sarah E., Gordon, Scott D., Martin, Nicholas G., Krasnov, Valery, Chuchalin, Alexander, Babadjanova, Gulja, Pantelejeva, Galina, Abramova, Lilia I., Tiganov, Alexander S., Polonikov, Alexey, Khusnutdinova, Elza, Alda, Martin, Cruceanu, Cristiana, Rouleau, Guy A., Turecki, Gustavo, Laprise, Catherine, Rivas, Fabio, Mayoral, Fermin, Kogevinas, Manolis, Grigoroiu-Serbanescu, Maria, Becker, Tim, Schulze, Thomas G., Rietschel, Marcella, Cichon, Sven, Fier, Heide, Nöthen, Markus M.
Publicado 2017

Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium()

por Power, Robert A., Tansey, Katherine E., Buttenschøn, Henriette Nørmølle, Cohen-Woods, Sarah, Bigdeli, Tim, Hall, Lynsey S., Kutalik, Zoltán, Lee, S. Hong, Ripke, Stephan, Steinberg, Stacy, Teumer, Alexander, Viktorin, Alexander, Wray, Naomi R., Arolt, Volker, Baune, Bernard T., Boomsma, Dorret I., Børglum, Anders D., Byrne, Enda M., Castelao, Enrique, Craddock, Nick, Craig, Ian W., Dannlowski, Udo, Deary, Ian J., Degenhardt, Franziska, Forstner, Andreas J., Gordon, Scott D., Grabe, Hans J., Grove, Jakob, Hamilton, Steven P., Hayward, Caroline, Heath, Andrew C., Hocking, Lynne J., Homuth, Georg, Hottenga, Jouke J., Kloiber, Stefan, Krogh, Jesper, Landén, Mikael, Lang, Maren, Levinson, Douglas F., Lichtenstein, Paul, Lucae, Susanne, MacIntyre, Donald J., Madden, Pamela, Magnusson, Patrik K.E., Martin, Nicholas G., McIntosh, Andrew M., Middeldorp, Christel M., Milaneschi, Yuri, Montgomery, Grant W., Mors, Ole, Müller-Myhsok, Bertram, Nyholt, Dale R., Oskarsson, Hogni, Owen, Michael J., Padmanabhan, Sandosh, Penninx, Brenda W.J.H., Pergadia, Michele L., Porteous, David J., Potash, James B., Preisig, Martin, Rivera, Margarita, Shi, Jianxin, Shyn, Stanley I., Sigurdsson, Engilbert, Smit, Johannes H., Smith, Blair H., Stefansson, Hreinn, Stefansson, Kari, Strohmaier, Jana, Sullivan, Patrick F., Thomson, Pippa, Thorgeirsson, Thorgeir E., Van der Auwera, Sandra, Weissman, Myrna M., Breen, Gerome, Lewis, Cathryn M.
Publicado 2017