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Danoy, Patrick, Sonoda, Eiichiro, Lathrop, Mark, Takeda, Shunichi and Matsuda, Fumihiko (2007) A naturally occurring genetic variant of human XRCC2 (R188H) confers increased resistance to cisplatin-induced DNA damage. Biochemical and Biophysical Research Communications, 352 3: 763-768. doi:10.1016/j.bbrc.2006.11.083 55   21 Cited 21 times in Scopus21 0
Revez, J. A., Bain, L., Chapman, B., Powell, J. E., Jansen, R., Duffy, D. L., Tung, J. Y., AAGC Collaborators, Penninx, B. W., Visscher, P. M., De Geus, E. J. C., Boomsma, D. I., Hinds, D. A., Martin, N. G., Montgomery, G. W., Ferreira, M. A. R., Danoy, Patrick and Brown, Matthew A. (2013) A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk. Genes and Immunity, 14 7: 441-446. doi:10.1038/gene.2013.38 63 1 4 Cited 5 times in Scopus5 6
Anderson, Robert P., Henry, Margaret J., Taylor, Roberta, Duncan, Emma L., Danoy, Patrick, Costa, Marylia J., Addison, Kathryn, Tye-Din, Jason A., Kotowicz, Mark A., Knight, Ross E., Pollock, Wendy, Nicholson, Geoffrey C., Toh, Ban-Hock, Brown, Matthew A. and Pasco, Julie A. (2013) A novel serogenetic approach determines the community prevalence of celiac disease and informs improved diagnostic pathways. BMC Medicine, 11 1: 188.1-188.13. doi:10.1186/1741-7015-11-188 33   11 Cited 8 times in Scopus8 41
Field, Judith, Browning, Sharon R., Johnson, Laura J., Danoy, Patrick, Varney, Michael D., Tait, Brian D., Gandhi, Kaushal S., Charlesworth Jac C., Heard, Robert N., Stewart, Graeme J., Kilpatrick, Trevor J., Foote, Simon J., Bahlo, Melanie, Butzkueven, Helmut, Wiley, James, Booth, David R., Taylor, Bruce V., Brown, Matthew A., Rubio, Justin P. and Stankovich, Jim (2010) A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis. PLoS One, 5 10: e13454.1-e13454.7. doi:10.1371/journal.pone.0013454 116 2 15 Cited 18 times in Scopus18 0
Davidson, Stuart, Wu, Xin, Liu, Yu, Wei, Meng, Danoy, Patrick, Thomas, Gethin, Cai, Qing, Sun, Linyun, Duncan, Emma, Wang, Niansong, Yu, Qinghong, Xu, Anlong, Fu, Yonggui, Brown, Matthew and Xu, Huji (2009) Association of ERAP1, but not IL23R, with ankylosing spondylitis in a Han Chinese population. Arthritis & Rheumatism, 60 11: 3263-3268. doi:10.1002/art.24933 70   62 Cited 55 times in Scopus55 0
Sharma, Shiwani, Burdon, Kathryn P., Chidlow, Glyn, Klebe, Sonja, Crawford, April, Dimasi, David P., Dave, Alpana, Martin, Sarah, Javadiyan, Shahrbanou, Wood, John P. M., Casson, Robert, Danoy, Patrick, Griggs, Kim, Hewitt, Alex W., Landers, John, Mitchell, Paul, Mackey, David A. and Craig, Jamie E. (2012) Association of genetic variants in the TMCO1 gene with clinical parameters related to glaucoma and characterization of the protein in the eye. Investigative Ophthalmology and Visual Science, 53 8: 4917-4925. doi:10.1167/iovs.11-9047 62   9 Cited 9 times in Scopus9 0
Davidson, Stuart I., Liu, Yu, Danoy, Patrick A., Wu, Xin, Thomas, Gethin P., Jiang, Lei, Sun, Linyun, Wang, Niansong, Han, Jun, Han, Huanxing, Visscher, Peter M., Brown, Matthew A. and Xu, Huji (2011) Association of STAT3 and TNFRSF1A with ankylosing spondylitis in Han Chinese. Annals of the Rheumatic Diseases, 70 2: 289-292. doi:10.1136/ard.2010.133322 95 1 30 Cited 30 times in Scopus30 0
Danoy, P, Pryce, K, Hadler, J, Bradbury, LA, Farrar, C, Pointon, J, Ward, M, Weisman, M, Reveille, JD, Wordsworth, BP, Stone, MA, Maksymowych, WP, Rahman, P, Gladman, D, Inman, RD, Brown, MA, Australo-Anglo-Amer and Spondyloarthrit Res Consortium (2010) Association of variants at 1q32 and STAT3 with ankylosing spondylitis suggests genetic overlap with Crohn's disease. PLoS Genetics, 6 12: e1001195-1-e1001195-5. doi:10.1371/journal.pgen.1001195 88   68 Cited 78 times in Scopus78 1
Danoy, Patrick, Wei, Meng, Hadler, Johanna, Jiang, Lei, He, Dongyi, Sun, Linyun, Zeng, Xiaofeng, Visscher, Peter M., Brown, Matthew A. and Xu, Huji (2011) Association of variants in MMEL1 and CTLA4 with rheumatoid arthritis in the Han Chinese population. Annals of the Rheumatic Diseases, 70 10: 1793-1797. doi:10.1136/ard.2010.144576 80 3 8 Cited 6 times in Scopus6 0
Lill, Christina M., Liu, Tian, Schjeide, Brit-Marem, Roehr, Johannes T., Akkad, Denis A., Damotte, Vincent, Alcina, Antonio, Ortiz, Migual A., Arroyo, Rafa, Lopez de Lapuente, Aitzkoa, Blaschke, Paul, Winkelmann, Alexander, Gerdes, Lisa-Ann, Luessi, Felix, Fernadez, Oscar, Izquierdo, Guillermo, Antiguedad, Alfredo, Hoffjan, Sabine, Cournu-Reibeix, Isabelle, Gromoller, Silvana, Faber, Hans, Liebsch, Maria, Meissner, Esther, Chanvillard, Coralie, Touze, Emmanuel, Pico, Fernando, Corcia, Philippe, 19ANZgene Consortium, Bahlo, Melanie, Booth, David R., Broadley, Simon A., Brown, Matthew A., Browning, Brian L., Browning, Sharon R., Butzkueven, Helmut, Carroll, William M., Cox, Mathew B., Chapman, Caron, Clarke, Glynnis, Danoy, Patrick, Drysdale, Karen, Field, Judith, Foote, Simon J., Greer, Judith M., Griffiths, Lyn R., Hadler, Johanna, Jensen, Cathy J., Johnson, Laura J., Kermode, Allan G., Heard, Rober N., Kilpatrick, Trevor J., Lechner-Scott, Jeanette, Marriott, Mark, Mason, Deborah, Moscato, Pablo, Pender, Michael P., Perreau, Victoria M., Rubio, Justin P., Scott, Rodney J., Slee, Mark, Stankovich, Jim, Stewart, Graeme J., Tajouri, Lotfi, Taylor, Bruce V., Wiley, James, Wilkins, Ella J., Dorner, Thomas, Steinhagen-Thiessen, Elisabeth, Baeckman, Lars, Heekeren, Hauke R., Li, Shu-Chen, Lindenberger, Ulman, Chan, Andrew, Hartung, Hans-Peter, Aktas, Orhan, Lohse, Peter, Kumpfel, Tania, Kubisch, Christian, Epplen, Joerg T., Zettl, Uwe K., Fontaine, Bertrand, Vandenbroeck, Koen, Matesanz, Fuencisla, Urcelay, Elena, Bertram, Lars and Zipp, Frauke (2012) Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects. Journal of Medical Genetics, 49 9: 558-562. doi:10.1136/jmedgenet-2012-101175 125   7 Cited 4 times in Scopus4 1
Bis, Joshua C., DeCarli, Charles, Smith, Albert Vernon, van der Lijn, Fedde, Crivello, Fabrice, Fornage, Myriam, Debette, Stephanie, Shulman, Joshua M., Schmidt, Helena, Srikanth, Velandai, Schuur, Maaike, Yu, Lei, Choi, Seung-Hoan, Sigurdsson, Sigurdur, Verhaaren, Benjamin F. J., DeStefano, Anita L., Lambert, Jean-Charles, Jack, Clifford R., Struchalin, Maksim, Stankovich, Jim, Ibrahim-Verbaas, Carla A., Fleischman, Debta, Zijdenbos, Alex, den Heijer, Tom, Mazoyer, Bernard, Coker, Laura H., Enzinger, Christian, Danoy, Patrick, Amin, Najaf, Arfanakis, Konstantinos, van Buchem, Mark, de Bruijn, Renée F.A.G., Beiser, Alexa, Dufouil, Carole, Huang, Juebin, Cavalieri, Margherita, Thomson, Russell, Niessen, Wiro J., Chibnik, Lori B., Gislason, Gauti K., Hofman, Albert, Pikula, Aleksandra, Amouyel, Philippe, Freeman, Kevin B., Phan, Thanh G., Oostra, Ben A., Stein, Jason L., Medland, Sarah E., Vasquez, Alejandro Arias, Hibar, Derrek P., Wright, Margaret J., Franke, Barbara, Martin, Nicholas G., Thompson, Paul M., Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) Consortium, Nalls, Michael A., Uitterlinden, Andre G., Au, Rhoda, Elbaz, Alexis, Beare, Richard J., van Swieten, John C., Lopez, Oscar L., Harris, Tamara B., Chouraki, Vincent, Breteler, Monique M.B., De Jager, Philip L., Becker, James T., Vernooij, Meike W., Knopman, David, Fazekas, Franz, Wolf, Philip A., van der Lugt, Aad, Gudnason, Vilmundur, Longstreth Jr, W.T., Brown, Matthew A., Bennett, David A., van Duijn, Cornelia M., Mosley, Thomas H., Schmidt, Reinhold, Tzourio, Christophe, Launer, Lenore J., Ikram, M. Arfan, Seshadri, Sudha and Cohorts Heart Aging Res Genomic Ep (2012) Common variants at 12q14 and 12q24 are associated with hippocampal volume. Nature Genetics, 44 5: 545-551. doi:10.1038/ng.2237 93   46 Cited 51 times in Scopus51 44
Ritchie, Matthew E., Liu, Ruijie, Carvalho, Benilton S., The Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZgene), Irizarry, Rafael A., Brown, Matthew A., Csurhes, Peter A., Danoy, Patrick, Greer, Judith M., Hadler, Johanna, Pryce, Karena and Pender, Michael P. (2011) Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips. BMC Bioinformatics, 12 68.1-68.12. doi:10.1186/1471-2105-12-68 75 9 11 Cited 13 times in Scopus13 1
Jiang, Lei, Willner, Dana, Danoy, Patrick, Xu, Huji and Brown, Matthew A. (2013) Comparison of the performance of two commercial genome-wide association study genotyping platforms in Han Chinese samples. G3-Genes Genomes Genetics, 3 1: 23-29. doi:10.1534/g3.112.004069 46   5 Cited 5 times in Scopus5 0
Karaderi, T., Pointon, J. J., Wordsworth, T. W. H., Harvey, D., Appleton, L. H., Cohen, C. J., Farrar, C., Harin, A., Brown, M. A., Wordsworth, B. P., The Australo-Anglo-American Spondyloarthritis Consortium, Kenna, Tony J., Gethin, Thomas P., Bradbury, Linda A. and Danoy, Patrick (2012) Evidence of genetic association between TNFRSF1A encoding the p55 tumour necrosis factor receptor, and ankylosing spondylitis in UK Caucasians. Clinical and Experimental Rheumatology, 30 1: 110-113. 107 15 4 Cited 4 times in Scopus4
Terwisscha van Scheltinga, Afke F., Bakker, Steven C., van Haren, Neeltje E. M., Derks, Eske M., Buizer-Voskamp, Jacobine E., Boos, Heleen B. M., Cahn, Wiepke, Pol, Hilleke E. Hulshoff, Ripke, Stephan, Ophoff, Roel A., Kahn, Rene S., Psychiatric Genome-wide Association Study Consortium, Mowry, Bryan J., McGrath, John J ., Nertney, Deborah A ., Brown, Matthew A., Danoy, Patrick A. and Catts, Stanley V. (2013) Genetic schizophrenia risk variants jointly modulate total brain and white matter volume. Biological Psychiatry, 73 6: 525-531. doi:10.1016/j.biopsych.2012.08.017 74   16 Cited 16 times in Scopus16 0
Ferreira, Manuel A. R., Matheson, Melanie C., Tang, Clara S., Granell, Raquel, Ang, Wei., Hui, Jennie, Kiefer, Amy K., Duffy, David L., Baltic, Svetlana, Danoy, Patrick, Bui, Minh, Price, Loren, Sly, Peter D., Eriksson, Nicholas, Madden, Pamela A., Abraham, Michael J. A., Holt, Patrick G., Heath, p Andrew C., Hunter, Michael, Musk, Bill, Robertson, Colin F., Le Souef, Peter, Montgomery, Grant W., Henderson, A. John, Tung, Joyce Y., Dharmage, Shyamali C., Brown, Matthew A., James, Alan, Thompson, Philip J., Pennell, Craig, Martin, Nicholas G., Evans, David M., Hinds, David A., Hopper, John L. and Australian Asthma Genetics Consortium Collaborators (2013) Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype. Journal of Allergy And Clinical Immunology, 133 6: 1564-1571. doi:10.1016/j.jaci.2013.10.030 58   6 Cited 8 times in Scopus8 50
Danoy, Patrick and Brown, Matthew A. (2008) Genome-wide association studies and musculoskeletal diseases. International Journal of Clinical Rheumatology, 3 6: 537-542. doi:10.2217/17460816.3.6.537 50   Cited 0 times in Scopus0 0
Ripke, Stephan, Sanders, Alan R., Kedler, Kenneth S., Levinson, Douglas F., Sklar, Pamela, Holmans, Peter A., Lin, Dan-Yu, Duan, Jubao, Ophoff, Roel A., Andreassen, Ole A., Scolnick, Edward, Cichon, Sven, St. Clair, David, Corvin, Aiden, Gurling, Hugh, Werge, Thomas, Rujescu, Dan, Blackwood, Douglas H. R., Pato, Carlos N., Malhotra, Anil K., Purcell, Shaun, Dudbridge, Frank, Neale, Benjamin M., Rossin, Lizzy, Visscher, Peter M., Posthuma, Danielle, Ruderfer, Douglas M., Fanous, Ayman, Hreinn, Stefansson, Steinberg, Stacy, Mowry, Bryan J., Golimbet, Vera, De Hert, Marc, Jonsson, Erik G., Bitter, Istvan, Pietilainen, Olli P., Collier, David A., Tosato, Sarah, Agartz, Ingrid, Albus, Margot, Alexander, Madeline, Amdur, Richard L., Amin, Farooq, Bass, Nicholas, Bergen, Sarah E., Black, Donald W., Borglum, Anders D., Brown, Matthew A., Bruggeman, Richard, Buccola, Nancy G., Byerley, William F., Cahn, Wiepke, Cantor, Rita M., Carr, Vaughan J., Catts, Stanley V., Choudhury, Khalid, Cloninger, C. Robert, Cormican, Paul, Craddock, Nicholas, Danoy, Patrick A., Datta, Susmita, de Haan, Lieuwe, Demontis, Ditte, Dikeos, Dimitris, Djurovic, Srdjan, Donnelly, Peter, Donohoe, Gary, Linh, Duong, Dwyer, Sarah, Fink-Jensen, Anders, Freedman, Robert, Freimer, Nelson B., Friedle, Marion, Georgieva, Lyudmila, Giegling, Ina, Gill, Michael, Clenthoj, Birte, Godard, Stephanie, Hamshere, Marian, Hansen, Mark, Hansen, Thomas, Hartmann, Annette M., Henskens, Frans A., Hougaard, David M., Hultman, Christina M., Ingason, Andres, Jablensky, Assen V., Jakobsen, Klaus D., Jay, Maurice, Jurgens, Gesche, Kahn, Rene S., Keller, Matthew C., Kenis, Gunter, Kenny, Elaine, Kim, Yunjung, Kirov, George K., Konnerth, Heike, Konte, Bettina, Krabbendam, Lydia, Krasucki, Robert, Lasseter, Virginia K., Laurent, Claudine, Lawrence, Jacob, Lencz, Todd, Lerer, F. Bernhard, Liang, Kung-Yee, Lichtenstein, Paul, Liebermann, Jeffrey A., Linszen, Don H., Lonnqvist, Jouko, Loughland, Carmel M., Maclean, Alan W., Maher, Brion S., Maier, Wolfgang, Mallet, Jacques, Malloy, Pat, Mattheisen, Manuel, Mattingsdal, Morten, McGhee, Kevin A., McGrath, John J., McIntosh, Andrew, McLean, Duncan E., McQuillin, Andrew, Melle, Ingrid, Michie, Patricia T., Milanova, Vihra, Morris, Derek W., Mors, Ole, Mortensen, Preben B., Moskvina, Valentina, Muglia, Pierandrea, Myin-Germeys, Inez, Nertney, Deborah A., Nestadt, Gerald, Nielsen, Jimmi, Nikolov, Ivan, Nordentoft, Merete, Norton, Nadine, Nothen, Markus M., O'Dushlaine, Colm T., Olincy, Ann, Olsen, Line, O'Neill, F. Anthony, Orntoft, Torben F., Owen, Michael J., Pantelis, Christos, Papadimitriou, George, Pato, Michele T., Peltonen, Leena, Petursson, Hannes, Pickard, Ben, Pimm, Jonathan, Pulver, Ann E., Puri, Vinay, Quested, Digby, Quinn, Emma M., Rasmussen, Henrik B., Rethelyi, Janos M., Ribble, Robert, Rietschel, Marcella, Riley, Brien P., Ruggeri, Mirella, Schall, Ulrich, Schulze, Thomas G., Schwab, Sibylle G., Scott, Rodney J., Shi, Jianxin, Sigurdson, Engilbert, Silverman, Jeremy M., Spencer, Chris C. A., Stefansson, Kari, Strange, Amy, Strengman, Eric, Stroup, T. Scott, Suvisaari, Jaana, Terenius, Lars, Thirumalai, Srinivasa, Thygesen, Johan H., Timm, Sally, Toncheva, Draga, van den Oord, Edwin, van Os, Jim, van Winkel, Ruud, Veldink, Jan, Walsh, Dermot, Wang, August G., Wiesrma, Durk, Wildenauer, Dieter B., Williams, Hywel J., Williams, Nigel M., Wormley, Brandon, Zammitt, Stan, Sullivan, Patrick F., O'Donovan, Micahel C., Daly, Mark J. and Gejman, Pablo V. (2011) Genome-wide association study identifies five new schizophrenia loci. Nature Genetics, 43 10: 969-976. doi:10.1038/ng.940 632   354 Cited 546 times in Scopus546 49
Bahlo, Melanie, Booth, David R., Broadley, Simon A., Brown, Matthew A., Foote, Simon J., Griffiths, Lyn R., Kilpatrick, Trevour J., Lechner-Scott, Jeanette, Moscato, Pablo, Perreau, Victoria M., Rubio, Justin P., Scott, Rodney J., Stankovich, Jim, Stewart, Graeme J., Taylor, Bruce V., Wiley, James, Clarke, Glynnis, Cox, Mathew B., Csurhes, Peter A., Danoy, Patrick, Drysdale, Karen, Field, Judith, Foote, Simon J., Greer, Judith M., Griffiths, Lyn R, Hadler, Johanna, McMorran, Brendan J., Jensen, Cathy J., Johnson, Laura J., McCallum, Ruth, Merriman, Marilyn, Merriman, Tony, Pryce, Karena, Tajouri, Lotfi, Wilkins, Ella J., Browning, Brian L., Browning, Sharon R., Perera, Devindri, Butzkueven, Helmut, Carroll, William M., Chapman, Caron, Kermode, Allan G., Marriott, Mark, Mason, Deborah, Heard, Robert N., Pender, Michael P., Slee, Mark, Tubridy, Niall and Willoughby, Ernest (2009) Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. Nature Genetics, 41 7: 824-828. doi:10.1038/ng.396 238   214 Cited 255 times in Scopus255 4
Reveille, John D., Sims, Anne-Marie, Danoy, Patrick, Evans, David M., Leo, Paul, Pointon, Jennifer J., Jin, Rui, Zhou, Xiaodong, Bradbury, Linda A., Appleton, Louise H., Davis, John C., Diekman, Laura, Doan, Tracey, Dowling, Alison, Duan, Ran, Duncan, Emma L., Farrar, Claire, Hadler, Johanna, Harvey, David, Karaderi, Tugce, Mogg, Rebecca, Pomeroy, Emma, Pryce, Karena, Taylor, Jacqueline, Savage, Laurie, Deloukas, Panos, Kumanduri, Vasudev, Peltonen, Leena, Ring, Sue M., Whittaker, Pamela, Glazov, Evgeny, Thomas, Gethin P., Maksymowych, Walter P., Inman, Robert D., Ward, Michael M., Stone, Millicent A., Weisman, Michael H., Wordsworth, B. Paul and Brown, Mathew A. (2010) Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. Nature Genetics, 42 2: 123-127. doi:10.1038/ng.513 196   186 Cited 192 times in Scopus192 9
Duncan, Emma L., Danoy, Patrick, Kemp, John P., Leo, Paul J., McCloskey, Eugene, Nicholson, Geoffrey C., Eastell, Richard, Prince, Richard L., Eisman, John A., Jones, Graeme, Sambrook, Philip N., Reid, Ian R., Dennison, Elaine M., Wark, John, Richards, J. Brent, Uitterlinden, Andre G., Spector, Tim D., Esapa, Chris, Cox, Roger D., Brown, Steve D. M., Thakker, Rajesh V., Addison, Kathryn A., Bradbury, Linda A., Center, Jacqueline R., Cooper, Cyrus, Cremin, Catherine, Estrada, Karol, Felsenberg, Dieter, Glueer, Claus-C., Hadler, Johanna, Henry, Margaret J., Hofman, Albert, Kotowicz, Mark A., Makovey, Joanna, Nguyen, Sing C., Nguyen, Tuan V., Pasco, Julie A., Pryce, Karena, Reid, David M., Rivadeneira, Fernando, Roux, Christian, Stefansson, Kari, Styrkarsdottir, Unnur, Thorleifsson, Gudmar, Tichawangana, Rumbidzai, Evans, David M. and Brown, Matthew A. (2011) Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. PLoS Genetics, 7 4: e1001372.1-e1001372.10. doi:10.1371/journal.pgen.1001372 139 27 60 Cited 63 times in Scopus63 0
Estrada, Karol, Styrkarsdottir, Unnur, Evangelou, Evangelos, Hsu, Yi-Hsiang, Duncan, Emma L., Ntzani, Evangelia E., Oei, Ling, Albagha, Omar M. E., Amin, Najaf, Kemp, John P., Koller, Daniel L., Li, Guo, Liu, Ching-Ti, Minster, Ryan L., Moayyeri, Alireza, Vandenput, Liesbeth, Willner, Dana, Xiao, Su-Mei, Yerges-Armstrong, Laura M., Zheng, Hou-Feng, Alonso, Nerea, Eriksson, Joel, Kammerer, Candace M., Kaptoge, Stephen K., Leo, Paul J., Thorleifsson, Gudmar, Wilson, Scott G., Wilson, James F., Aalto, Ville, Alen, Markku, Aragaki, Aaron K., Aspelund, Thor, Center, Jacqueline R., Dailiana, Zoe, Duggan, David J ., Garcia, Melissa, Garcia-Giralt, Natàlia, Giroux, Sylvie, Hallmans, Göran, Hocking, Lynne J., Husted, Lise Bjerre, Jameson, Karen A., Khusainova, Rita, Kim, Ghi Su, Kooperberg, Charles, Koromila, Theodora, Kruk, Marcin, Laaksonen, Marika, Lacroix, Andrea Z., Lee, Seung Hun, Leung, Ping C., Lewis, Joshua R ., Masi, Laura, Mencej-Bedrac, Simona, Nguyen, Tuan V., Nogues, Xavier, Patel, Millan S., Prezelj, Janez, Rose, Lynda M., Scollen, Serena, Siggeirsdottir, Kristin, Smith, Albert V., Svensson, Olle, Trompet, Stella, Trummer, Olivia, van Schoor, Natasja M., Woo, Jean, Zhu, Kun, Balcells, Susana, Brandi, Maria Luisa, Buckley, Brendan M., Cheng, Sulin, Christiansen, Claus, Cooper, Cyrus, Dedoussis, George, Ford, Ian, Frost, Morten, Goltzman, David, Gonzalez-Macias, Jesús, Kahonen, Mika, Karlsson, Magnus, Khusnutdinova, Elza, Koh, Jung?Min, Kollia, Panagoula, Langdahl, Bente Lomholt, Leslie, William D., Lips, Paul, Ljunggren, Östen, Lorenc, Roman S., Marc, Janja, Mellstrom, Dan, Obermayer-Pietsch, Barbara, Olmos, José M ., Pettersson-Kymmer, Ulrika, Reid, David M., Riancho, José A., Ridker, Paul M., Rousseau, François, Slagboom, P. Eline, Tang, Nelson L.S., Urreizti, Roser, Van Hul, Wim, Viikari, Jorma, Zarrabeitia, Maria T., Aulchenko, Yurii S., Castano-Betancourt, Martha, Grundberg, Elin, Herrera, Lizbeth, Ingvarsson, Thorvaldur, Johannsdottir, Hrefna, Kwan, Tony, Li, Rui, Luben, Robert, Medina-Gomez, Carolina, Palsson, Stefan Th, Reppe, Sjur, Rotter, Jerome I., Sigurdsson, Gunnar, van Meurs, Joyce B. J., Verlaan, Dominique, Williams, Frances M.K., Wood, Andrew R., Zhou, Yanhua, Gautvik, Kaare M., Pastinen, Tomi, Raychaudhuri, Soumya, Cauley, Jane A., Chasman, Daniel I., Clark, Graeme R., Cummings, Steven R., Danoy, Patrick, Dennison, Elaine M., Eastell, Richard, Eisman, John A., Gudnason, Vilmundur, Hofman, Albert, Jackson, Rebecca D., Jones, Graeme, Jukema, J. Wouter, Khaw, Kay?Tee, Lehtimaki, Terho, Liu, Yongmei, Lorentzon, Mattias, McCloskey, Eugene, Mitchell, Braxton D., Nandakumar, Kannabiran, Nicholson, Geoffrey C., Oostra, Ben A., Peacock, Munro, Pols, Huibert A. P., Prince, Richard L., Raitakari, Olli, Reid, Ian R., Robbins, John, Sambrook, Philip N., Sham, Pak Chung, Shuldiner, Alan R., Tylavsky, Frances A., van Duijn, Cornelia M., Wareham, Nick J., Cupples, L. Adrienne, Econs, Michael J., Evans, David M., Harris, Tamara B., Kung, Annie W. C., Psaty, Bruce M., Reeve, Jonathan, Spector, Timothy D ., Streeten, Elizabeth A., Zillikens, M. Carola, Thorsteinsdottir, Unnur, Ohlsson, Claes, Karasik, David, Richards, J. Brent, Brown, Matthew A., Stefansson, Kari, Uitterlinden, André G., Ralston, Stuart H., Ioannidis, John P. A., Kiel, Douglas P. and Rivadeneira, Fernando (2012) Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. Nature Genetics, 44 5: 491-501. doi:10.1038/ng.2249 290   172 Cited 167 times in Scopus167 9
Piret, Sian E., Danoy, Patrick, Dahan, Karin, Reed, Anita A. C., Pryce, Karena, Wong, William, Torres, Rosa J., Puig, Juan G., Müller, Thomas, Kotanko, Peter, Lhotta, Karl, Devuyst, Olivier, Brown, Matthew A. and Thakker, Rajesh V. (2011) Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21. Human Genetics, 129 1: 51-58. doi:10.1007/s00439-010-0897-1 81   11 Cited 12 times in Scopus12 0
Burdon, Kathryn P., Crawford, April, Casson, Robert J., Hewitt, Alex W., Landers, John, Danoy, Patrick, Mackey, David A., Mitchell, Paul, Healey, Paul R. and Craig, Jamie E. (2012) Glaucoma risk alleles at CDKN2B-AS1 are associated with lower intraocular pressure, normal-tension glaucoma, and advanced glaucoma. Ophthalmology, 119 8: 1539-1545. doi:10.1016/j.ophtha.2012.02.004 19   16 Cited 17 times in Scopus17 0
Chia, N. L., Bryce, M., Hickman, P. E., Potter, J. M., Glasgow, N., Koerbin, G., Danoy, P., Brown, M. A. and Cavanaugh, J. (2013) High-resolution SNP microarray investigation of copy number variations on chromosome 18 in a control cohort. Cytogenetic and Genome Research, 141 1: 16-25. doi:10.1159/000350767 27   0 Cited 0 times in Scopus0 0
Davidson, Stuart I., Jiang, Lei, Cortes, Adrian, Wu, Xin, Glazov, Evgeny A., Zheng, Yi, Danoy, Patrick A., Liu, Yi, Thomas, Gethin P., Brown, Matthew A. and Xu, Huji (2013) High-throughput sequencing of IL23R reveals a low-frequency, nonsynonymous single-nucleotide polymorphism that is associated with ankylosing spondylitis in a Han Chinese population. Arthritis and Rheumatism, 65 7: 1747-1752. doi:10.1002/art.37976 35   4 Cited 4 times in Scopus4 0
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