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Škalamera, Dubravka, Ranall, Max V., Wilson, Benjamin M., Leo, Paul, Purdon, Amy S., Hyde, Carolyn, Nourbakhsh, Ehsan, Grimmond, Sean M., Barry, Simon C., Gabrielli, Brian and Gonda, Thomas J. (2011) A high-throughput platform for lentiviral overexpression screening of the human ORFeome. PLoS One, 6 5: e20057.1-e20057.14. doi:10.1371/journal.pone.0020057 132 81 19 Cited 19 times in Scopus19 0
Zochling, Jane, Newell, Felicity, Charlesworth, Jac C., Leo, Paul, Stankovich, Jim, Cortes, Adrian, Zhou, Yuan, Stevens, Wendy, Sahhar, Joanne, Roddy, Janet, Nash, Peter, Tymms, Kathleen, Rischmueller, Maureen, Lester, Sue, Proudman, Susanna and Brown, Matthew A. (2014) An immunochip-based interrogation of scleroderma susceptibility variants identifies a novel association at DNASE1L3. Arthritis Research & Therapy, 16 5: 1-7. doi:10.1186/s13075-014-0438-8 50   0 0
Robinson, Philip, Cortes, Adrian, Leo, Paul, Evans, David and Brown, Matthew A. (2012). Ankylosing spondylitis is associated with single nucleotide polymorphisms in loci implicating four aminopeptidases. In: Abstracts of the American College of Rheumatology & Association of Rheumatology Health Professionals, Annual Scientific Meeting. Annual Scientific Meeting of the American-College-of-Rheumatology (ACR) and Association-of-Rheumatology-Health-Professionals (ARHP), Washington, DC, United States, (S688-S689). 9-14 November 2012. doi:10.1002/art.37735 61   0 0
Brooks, K., Oakes, V., Edwards, B., Ranall, M., Leo, P., Pavey, S., Pinder, A., Beamish, H., Mukhopadhyay, P., Lambie, D. and Gabrielli, B. (2013) A potent Chk1 inhibitor is selectively cytotoxic in melanomas with high levels of replicative stress. Oncogene, 32 6: 788-796. doi:10.1038/onc.2012.72 109   9 Cited 13 times in Scopus13 0
Sparrow, Duncan B., McInerney-Leo, Aideen, Gucev, Zoran S., Gardiner, Brooke, Marshall, Mhairi, Leo, Paul J., Chapman, Deborah L., Tasic, Velibor, Shishko, Abduhadi, Brown, Matthew A., Duncan, Emma L. and Dunwoodie, Sally L. (2013) Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6. Human Molecular Genetics, 22 8: 1625-1631. doi:10.1093/hmg/ddt012 59   9 Cited 10 times in Scopus10 0
Poth, Kim J., Guminski, Alexander D., Thomas, Gethin P., Leo, Paul J., Jabbar, Ibtissam A. and Saunders, Nicholas A. (2010) Cisplatin treatment induces a transient increase in tumorigenic potential associated with high interleukin-6 expression in head and neck squamous cell carcinoma. Molecular Cancer Therapeutics, 9 8: 2430-2439. doi:10.1158/1535-7163.MCT-10-0258 97   15 Cited 14 times in Scopus14 0
McInerney-Leo, A. M., Duncan, E. L., Leo, P. J., Gardiner, B., Bradbury, L. A., Harris, J. E., Clark, G. R., Brown, M. A. and Zankl, A. (2014) COL1A1 C-propeptide cleavage site mutation causes high bone mass, bone fragility and jaw lesions: a new cause of gnathodiaphyseal dysplasia?. Clinical Genetics, 1-7. doi:10.1111/cge.12440 19   Cited 0 times in Scopus0 0
Leo, PJ, Julienne, PS, Mies, FH and Williams, CJ (2001) Collisional frequency shifts in Cs-133 fountain clocks. Physical Review Letters, 86 17: 3743-3746. doi:10.1103/PhysRevLett.86.3743 76   48 Cited 52 times in Scopus52 0
McInerney-Leo, Aideen, Sparrow, Duncan B., Harris, Jessica, Gardiner, Brooke, Marshall, Mhairi, O'Reilly, Victoria C., Shi, Hongjun, Brown, Matthew A., Leo, Paul, Zankl, Andreas, Dunwoodie, Sally L. and Duncan, Emma (2015) Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects. Human Molecular Genetics, 24 5: 1234-1242. doi:10.1093/hmg/ddu534 12   Cited 0 times in Scopus0 0
Halbritter, Jan, Bizet, Albane A., Schmidts, Miriam, Porath, Jonathan D., Braun, Daniela A., Gee, Heon Yung, McInerney-Leo, Aideen M., Krug, Pauline, Filhol, Emilie, Davis, Erica E., Airik, Rannar, Czarnecki, Peter G., Lehman, Anna M., Trnka, Peter, Nitschke, Patrick, Bole-Feysot, Christine, Schueler, Markus, Knebelmann, Bertrand, Burtey, Stephane, Szabo, Attila J., Tory, Kalman, Leo, Paul J., Gardiner, Brooke, McKenzie, Fiona A., Zankl, Andreas, Brown, Matthew A., Hartley, Jane L., Maher, Eamonn R., Li, Chunmei, Leroux, Michel R., Scambler, Peter J., Zhan, Shing H., Jones, Steven J., Kayserili, Hulya, Tuysuz, Beyhan, Moorani, Khemchand N., Constantinescu, Alexandru, Krantz, Ian D., Kaplan, Bernard S., Shah, Jagesh V., Hurd, Toby W., Doherty, Dan, Katsanis, Nicholas, Duncan, Emma L., Otto, Edgar A., Beales, Philip L., Mitchison, Hannah M., Saunier, Sophie and Hildebrandt, Friedhelm (2013) Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans. American Journal of Human Genetics, 93 5: 915-925. doi:10.1016/j.ajhg.2013.09.012 36   11 Cited 13 times in Scopus13 6
Kerman, AJ, Chin, C, Vuletic, V, Chu, S, Leo, PJ, Williams, CJ and Julienne, PS (2001) Determination of Cs-Cs interaction parameters using Feshbach spectroscopy. Comptes Rendus De L Academie Des Sciences Serie Iv Physique Astrophysique, 2 4: 633-639. doi:10.1016/S1296-2147(01)01196-9 71   15 Cited 17 times in Scopus17 0
Gonda, Thomas J., Leo, Paul and Ramsay, Robert G. (2008) Estrogen and MYB in breast cancer: Potential for new therapies. Expert Opinion On Biological Therapy, 8 6: 713-717. doi:10.1517/14712598.8.6.713 67   18 Cited 20 times in Scopus20 0
Antonellis, A, Lee-Lin, SQ, Wasterlain, A, Leo, P, Quezado, M, Goldfarb, LG, Myung, K, Burgess, S, Fischbeck, KH and Green, ED (2006) Functional analyses of glycyl-tRNA synthetase mutations suggest a key role for tRNA-charging enzymes in peripheral axons. Journal of Neuroscience, 26 41: 10397-10406. doi:10.1523/JNEUROSCI.1671-06.2006 45   52 Cited 59 times in Scopus59 0
Duan, Ran, Leo, Paul, Bradbury, Linda, Brown, Matthew and Thomas, Gethin (2010) Gene expression profiling reveals a down-regulation in immune-associated genes in AS patients. Annals of the Rheumatic Diseases, 69 9: 1724-1729. doi:10.1136/ard.2009.111690 70   15 Cited 16 times in Scopus16 0
Robinson, Philip, Claushuis, Dorith, Leo, Paul, Mukhopadhyay, Pamela, Wordsworth, P., Weisman, Michael H., Maksymowych, Walter P., Rahman, Proton, Inman, Robert, Hewitt, Alex, Martin, Tammy M., Rosenbaum, James T., Wakefield, Dennis, Reveille, John D. and Brown, Matthew A. (2013). Genetic Associations In Anterior Uveitis Implicate T-Cell Co-Stimulation and Other Immune Pathways. In: 77th Annual Meeting of the American-College-of-Rheumatology / 48th Annual Meeting of the Association-of-Rheumatology-Health-Professionals, San Diego Ca, (S722-S723). Oct 25-30, 2013. doi:10.1002/art.38216 68   0 0
Moayyeri, Alireza, Hsu, Yi-Hsiang, Karasik, David, Estrada, Karol, Xiao, Su-Mei, Nielson, Carrie, Srikanth, Priya, Giroux, Sylvie, Wilson, Scott G., Zheng, Hou-Feng, Smith, Albert V., Pye, Stephen R., Leo, Paul J., Teumer, Alexander, Hwang, Joo-Yeon, Ohlsson, Claes, McGuigan, Fiona, Minster, Ryan L., Hayward, Caroline, Olmos, Jose M., Lyytikainen, Leo-Pekka, Lewis, Joshua R., Swart, Karin M. A., Masi, Laura, Oldmeadow, Chris, Holliday, Elizabeth G., Cheng, Sulin, van Schoor, Natasja M., Harvey, Nicholas C., Kruk, Marcin, del Greco M, Fabiola, Igl, Wilmar, Trummer, Olivia, Grigoriou, Efi, Luben, Robert, Liu, Ching-Ti, Zhou, Yanhua, Oei, Ling, Medina-Gomez, Carolina, Zmuda, Joseph, Tranah, Greg, Brown, Suzanne J., Williams, Frances M., Soranzo, Nicole, Jakobsdottir, Johanna, Siggeirsdottir, Kristin, Holliday, Kate L., Hannemann, Anke, Go, Min Jin, Garcia, Melissa, Polasek, Ozren, Laaksonen, Marika, Zhu, Kun, Enneman, Anke W., McEvoy, Mark, Peel, Roseanne, Sham, Pak Chung, Jaworski, Maciej, Johansson, Asa, Hicks, Andrew A., Pludowski, Pawel, Scott, Rodney, Dhonukshe-Rutten, Rosalie A. M., van der Velde, Nathalie V., Kaohonen, Mika, Viikari, Jorma S., Sievaonen, Harri, Raitakari, Olli T., Gonzalez-Macias, Jesus, Hernandez, Jose L., Mellstrom, Dan, Ljunggren, Osten, Cho, Yoon Shin, Volker, Uwe, Nauck, Matthias, Homuth, Georg, Volzke, Henry, Haring, Robin, Brown, Matthew A., McCloskey, Eugene, Nicholson, Geoffrey C., Eastell, Richard, Eisman, John A., Jones, Graeme, Reid, Ian R., Dennison, Elaine M., Wark, John, Boonen, Steven, Vanderschueren, Dirk, Wu, Frederick C. W., Aspelund, Thor, Richards, J. Brent, Bauer, Doug, Hofman, Albert, Khaw, Kay-Tee, Dedoussis, George, Obermayer-Pietsch, Barbara, Gyllensten, Ulf, Pramstaller, Peter P., Lorenc, Roman S., Cooper, Cyrus, Kung, Annie Wai Chee, Lips, Paul, Alen, Markku, Attia, John, Brandi, Maria Luisa, de Groot, Lisette C. P. G. M., Lehtimaki, Terho, Riancho, Jose A., Campbell, Harry, Liu, Yongmei, Harris, Tamara B., Akesson, Kristina, Karlsson, Magnus, Lee, Jong-Young, Wallaschofski, Henri, Duncan, Emma L., O'Neill, Terence W., Gudnason, Vilmundur, Spector, Timothy D., Rousseau, Francois, Orwoll, Eric, Cummings, Steven R., Wareham, Nick J., Rivadeneira, Fernando, Uitterlinden, Andre G., Prince, Richard L., Kiel, Douglas P., Reeve, Jonathan and Kaptoge, Stephen K. (2014) Genetic determinants of heel bone properties: Genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium. Human Molecular Genetics, 23 11: 3054-3068. doi:10.1093/hmg/ddt675 36   2 Cited 2 times in Scopus2 1
Robinson P.C., Claushuis T.A.M., Cortes A., Martin T.M., Evans D.M., Leo P., Mukhopadhyay P., Bradbury L.A., Cremin K., Harris J., Maksymowych W.P., Inman R.D., Rahman P., Haroon N., Gensler L., Powell J.E., Van Der Horst-Bruinsma I.E., Hewitt A.W., Craig J.E., Lim L.L., Wakefield D., McCluskey P., Voigt V., Fleming P., Degli-Esposti M., Pointon J.J., Weisman M.H., Wordsworth B.P., Reveille J.D., Rosenbaum J.T. and Brown M.A. (2015) Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis. Arthritis and Rheumatology, 67 1: 140-151. doi:10.1002/art.38873 7   0 Cited 0 times in Scopus0 6
Hysi, Pirro G., Cheng, Ching-Yu, Springelkamp, Henriet, Macgregor, Stuart, Bailey, Jessica N. Cooke, Wojciechowski, Robert, Vitart, Veronique, Nag, Abhishek, Hewitt, Alex W., Hohn, Rene, Venturini, Cristina, Mirshahi, Alireza, Ramdas, Wishal D., Thorleifsson, Gudmar, Vithana, Eranga, Khor, Chiea-Chuen, Stefansson, Arni B., Liao, Jiemin, Haines, Jonathan L., Amin, Najaf, Wang, Ya Xing, Wild, Philipp S., Ozel, Ayse B., Li, Jun Z., Fleck, Brian W., Zeller, Tanja, Staffieri, Sandra E., Teo, Yik-Ying, Cuellar-Partida, Gabriel, Luo, Xiaoyan, Allingham, R. Rand, Richards, Julia E., Senft, Andrea, Karssen, Lennart C., Zheng, Yingfeng, Bellenguez, Celine, Xu, Liang, Iglesias, Adriana I., Wilson, James F., Kang, Jae H., van Leeuwen, Elisabeth M., Jonsson, Vesteinn, Thorsteinsdottir, Unnur, Despriet, Dominiek D. G., Ennis, Sarah, Moroi, Sayoko E., Martin, Nicholas G., Jansonius, Nomdo M., Yazar, Seyhan, Tai, E-Shyong, Amouyel, Philippe, Kirwan, James, van Koolwijk, Leonieke M. E., Hauser, Michael A., Jonasson, Fridbert, Leo, Paul, Loomis, Stephanie J., Fogarty, Rhys, Rivadeneira, Fernando, Kearns, Lisa, Lackner, Karl J., de Jong, Paulus T. V. M., Simpson, Claire L., Pennell, Craig E., Oostra, Ben A., Uitterlinden, Andre G., Saw, Seang-Mei, Lotery, Andrew J., Bailey-Wilson, Joan E., Hofman, Albert, Vingerling, Johannes R., Maubaret, Cecilia, Pfeiffer, Norbert, Wolfs, Roger C. W., Lemij, Hans G., Young, Terri L., Pasquale, Louis R., Delcourt, Cecile, Spector, Timothy D., Klaver, Caroline C. W., Small, Kerrin S., Burdon, Kathryn P., Stefansson, Kari, Wong, Tien-Yin, Viswanathan, Ananth, Mackey, David A., Craig, Jamie E., Wiggs, Janey L., van Duijn, Cornelia M., Hammond, Christopher J. and Aung, Tin (2014) Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma. Nature Genetics, 46 10: 1126-1130. doi:10.1038/ng.3087 16   2 Cited 2 times in Scopus2 83
Burdon, Kathryn P., Macgregor, Stuart, Hewitt, Alex W., Sharma, Shiwani, Chidlow, Glyn, Mills, Richard A., Danoy, Patrick, Casson, Robert, Viswanathan, Ananth C., Liu, Jimmy Z., Landers, John, Henders, Anjali K., Wood, John, Souzeau, Emmanuelle, Crawford, April, Leo, Paul, Wang, Jie Jin, Rochtchina, Elena, Nyholt, Dale R., Martin, Nicholas G., Montgomery, Grant W., Mitchell, Paul, Brown, Matthew A., Mackey, David A. and Craig, Jamie E. (2011) Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1. Nature Genetics, 43 6: 574-578. doi:10.1038/ng.824 97   105 Cited 103 times in Scopus103 1
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.513 198   189 Cited 195 times in Scopus195 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 142 34 62 Cited 65 times in Scopus65 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 292   182 Cited 178 times in Scopus178 9
Cortes, Adrian, Hadler, Johanna, Pointon, Jenny P., Robinson, Philip C., Karaderi, Tugce, Leo, Paul, Cremin, Katie, Pryce, Karena, Harris, Jessica, Lee, Seunghun, Joo, Kyung Bin, Shim, Seung-Cheol, Weisman, Michael, Ward, Michael, Zhou, Xiaodong, Garchon, Henri-Jean, Chiocchia, Gilles, Nossent, Johannes, Lie, Benedicte A., Førre, Øystein, Tuomilehto, Jaakko, Laiho, Kari, Jiang, Lei, Liu, Yu, Wu, Xin, Bradbury, Linda A., Elewaut, Dirk, Burgos-Vargas, Ruben, Stebbings, Simon, Appleton, Louise, Farrah, Claire, Lau, Jonathan, Kenna, Tony J., Haroon, Nigil, Ferreira, Manuel A., Yang, Jian, Mulero, Juan, Fernandez-Sueiro, Jose Luis, Gonzalez-Gay, Miguel A., Lopez-Larrea, Carlos, Deloukas, Panos, Donnelly, Peter, Bowness, Paul, Gafney, Karl, Gaston, Hill, Gladman, Dafna D., Rahman, Proton, Maksymowych, Walter P., Xu, Huji, Crusius, J. Bart A., van der Horst-Bruinsma, Irene E., Chou, Chung-Tei, Valle-Oñate, Raphael, Romero-Sánchez, Consuelo, Hansen, Inger Myrnes, Pimentel-Santos, Fernando M., Inman, Robert D., Videm, Vibeke, Martin, Javier, Breban, Maxime, Reveille, John D., Evans, David M., Kim, Tae-Hwan, Wordsworth, Bryan Paul, Brown, Matthew A., Australo-Anglo-American Spondyloarthritis Consortium (TASC), Groupe Française d?Etude Génétique des Spondylarthrites (GFEGS), Nord-Trøndelag Health Study (HUNT), Spondyloarthritis Research Consortium of Canada (SPARCC) and Wellcome Trust Case Control Consortium 2 (WTCCC2) (2013) Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci. Nature Genetics, 45 7: 730-740. doi:10.1038/ng.2667 140   52 Cited 57 times in Scopus57 17
Zhao, Liang, Glazov, Evgeny, Diwakar Ram Pattabiraman, Al-Owaidi, Faisal, Ping Zhang, Brown, Matthew A., Paul Leo and Gonda, Thomas J. (2011) Integrated genome-wide chromatin occupancy and expression analyses identify key myeloid pro-differentiation transcription factors repressed by Myb. Nucleic Acids Research, 39 11: 4664-4679. doi:10.1093/nar/gkr024 132 52 23 Cited 23 times in Scopus23 0
Zheng, Hou-Feng, Duncan, Emma L., Yerges-Armstrong, Laura M., Eriksson, Joel, Bergström, Ulrica, Leo, Paul J., Leslie, William D., Goltzman, David, Blangero, John, Hanley, David A., Carless, Melanie A., Streeten, Elizabeth A., Lorentzon, Mattias, Brown, Matthew A., Spector, Tim D., Pettersson-Kymmer, Ulrika, Ohlsson, Claes, Mitchell, Braxton D. and Richards, J. Brent (2013) Meta-analysis of genome-wide studies identifies MEF2C SNPs associated with bone mineral density at forearm. Journal of Medical Genetics, 50 7: 473-478. doi:10.1136/jmedgenet-2012-101287 43 35 2 Cited 1 times in Scopus1 6
Damask, JN, Gray, G, Leo, P, Simer, G, Rochford, K and Veasey, D (2003) Method to measure and estimate total outage probability for PMD-impaired systems. Ieee Photonics Technology Letters, 15 1: 48-50. doi:10.1109/LPT.2002.805861 73   11 Cited 13 times in Scopus13 0
Cole, Nelson B., DiEuliis, Diane, Leo, Paul, Mitchell, Drake C. and Nussbaum, Robert L. (2008) Mitochondrial translocation of alpha-synuclein is promoted by intracellular acidification. Experimental Cell Research, 314 10: 2076-2089. doi:10.1016/j.yexcr.2008.03.012 48   62 Cited 65 times in Scopus65 0
Waddell, N., Stein, S. R., Wagner, S. A., Bennett, I., Djougarian, A., Melana, S., Jaffer, S., Holland, J. F., Pogo, B. G. T., Gonda, T. J., Brown, M. A., Leo, P., Saunders, N. A., McMillan, N. A., Cocciardi, S., Vargas, A. C., Lakhani, S. R., Chenevix-Trench, G., Newman, B. and Francis, G. D. (2012) Morphological and molecular analysis of a breast cancer cluster at the ABC Studio in Toowong. Pathology, 44 5: 469-472. doi:10.1097/PAT.0b013e3283559e67 139 2 0 Cited 0 times in Scopus0 3
Andreas Zankl, Duncan, Emma L., Leo, Paul J., Clark, Graeme R., Glazov, Evgeny A., Addor, Marie-Claude, Herlin, Troels, Kim, Chong Ae, Leheup, Bruno P., McGill, Jim, McTaggart, Steven, Mittas, Stephan, Mitche, Anna L., Mortier, Geert R., Robertson, Stephen P., Schroeder, Marie, Terha, Paulien and Brown, Matthew A. (2012) Multicentric carpotarsal osteolysis is caused by mutations clustering in the amino-terminal transcriptional activation domain of MAFB. American Journal of Human Genetics, 90 3: 494-501. doi:10.1016/j.ajhg.2012.01.003 129 11 17 Cited 17 times in Scopus17 5
Zhang, Lei, Li, Jian, Pei, Yu-Fang, Lin, Yong, Shen, Hui, Estrada, Karol, Rivadeneira, Fernando, Guitterlinden, Andre, Shin, Chan Soo, Choi, Hyung Jin, Duncan, Emma L., Leo, Paul J., Brown, Matthew A., Liu, Yao-Zhong, Liu, Yongjun, Zhang, Ji-Gang, Tian, Qing, Wang, Yu-Ping, Zhu, Xue-Zhen, Wu, Shuyan, Papasian, Christopher J. and Deng, Hong-Wen (2012). Multi-stage genome-wide association meta-analyses identified gender-specific loci associated with bone mineral density. In: Abstracts from the NIH Office of Research on Women's Health Ninth Annual Interdisciplinary Women's Health Research Symposium. Ninth Annual NIH Interdisciplinary Women’s Health Research Symposium, Bethesda, MD, United States, (1009-1010). 15 November 2012. doi:10.1089/jwh.2012.ab02 73   0 0
Zhang, Lei, Choi, Hyung Jin, Estrada, Karol, Leo, Paul J., Li, Jian, Pei, Yu-Fang, Zhang, Yinping, Lin, Yong, Shen, Hui, Liu, Yao-Zhong, Liu, Yongjun, Zhao, Yingchun, Zhang, Ji-Gang, Tian, Qing, Wang, Yu-ping, Han, Yingying, Ran, Shu, Hai, Rong, Zhu, Xue-Zhen, Wu, Shuyan, Yan, Han, Liu, Xiaogang, Yang, Tie-Lin, Guo, Yan, Zhang, Feng, Guo, Yan-fang, Chen, Yuan, Chen, Xiangding, Tan, Lijun, Zhang, Lishu, Deng, Fei-Yan, Deng, Hongyi, Rivadeneira, Fernando, Duncan, Emma L., Lee, Jong Young, Han, Bok Ghee, Cho, Nam H., Nicholson, Geoffrey C., McColskey, Eugene, Eastell, Richard, Prince, Richard L., Eisman, John A., Jones, Graeme, Reid, Ian R., Sambrook, Philip N., Dennison, Elaine M., Danoy, Patrick, Yerges-Armstrong, Laura M., Streeten, Elizabeth A., Hu, Tian, Xiang, Shuanglin, Papasian, Christopher J., Brown, Matthew A., Shin, Chan Soo, Uitterlinden, André G. and Deng, Hong-Wen (2014) Multi-stage genome-wide association meta-analyses identified two new loci for bone mineral density. Human Molecular Genetics, 23 7: 1923-1933. doi:10.1093/hmg/ddt575 62   7 Cited 10 times in Scopus10 2
Schmidts, Miriam, Vodopiutz, Julia, Christou-Savina, Sonia, Cortés, Claudio R., McInerney-Leo, Aideen M., Emes, Richard D., Arts, Heleen H., Tüysüz, Beyhan, D'Silva, Jason, Leo, Paul J., Giles, Tom C., Oud, Machteld M., Harris, Jessica A., Koopmans, Marije, Marshall, Mhairi, Elçioglu, Nursel, Kuechler, Alma, Bockenhauer, Detlef, Moore, Anthony T., Wilson, Louise C., Janecke, Andreas R., Hurles, Matthew E., Emmet, Warren, Gardiner, Brooke, Streubel, Berthold, Dopita, Belinda, Zankl, Andreas, Kayserili, Hülya, Scambler, Peter J., Brown, Matthew A., Beales, Philip L., Wicking, Carol, UK10K, Duncan, Emma L. and Mitchison, Hannah M. (2013) Mutations in the gene encoding IFT dynein complex component WDR34 cause Jeune asphyxiating thoracic dystrophy. American Journal of Human Genetics, 93 5: 932-944. doi:10.1016/j.ajhg.2013.10.003 56 1 6 Cited 9 times in Scopus9 2
McInerney-Leo, A., Zankl, A., Duncan, E., Clark, G., Leo, P., Glasov, E. and Brown, M. (2012). Next generation sequencing identifies mutations clustering in the amino-terminal transcriptional activation domain of Mafb in multicentric carpotarsal osteolysis. In: Australian Rheumatology Association in conjunction with Rheumatology Health Professionals 53rd Annual Scientific Meeting Conference Abstracts. Australian Rheumatology Association in conjunction with Rheumatology Health Professionals 53rd Annual Scientific Meeting, Canberra, Australia, (2-2). 12-15 May 2012. doi:10.1111/j.1445-5994.2012.02759.x 47   0 1
Peterson, Daniel L., Ward, Bryan C., Rochford, Kent B., Leo, Paul J. and Simer, Greg (2002) Polarization mode dispersion compensator field trial and field fiber characterization. Optics Express, 10 14: 614-621. 75 5 12
Chin, Cheng, Vuletic, Vladan, Kerman, Andrew J., Chu, Steven, Tiesinga, Eite, Leo, Paul J. and Williams, Carl J. (2004) Precision Feshbach spectroscopy of ultracold Cs-2. Physical Review A, 70 3: 032701-1-032701-13. doi:10.1103/PhysRevA.70.032701 60   89 Cited 88 times in Scopus88 0
Venturi, V, Leo, PJ, Tiesinga, E, Williams, CJ and Whittingham, IB (2003) Purely-long-range bound states of He(2s S-3)+He(2p P-3). Physical Review A, 68 2: . doi:10.1103/PhysRevA.68.022706 34   17 Cited 18 times in Scopus18 0
McInerney-Leo, Aideen M., Schmidts, Miriam, Cortés, Claudio R., Leo, Paul J., Gener, Blanca, Courtney, Andrew D., Gardiner, Brooke, Harris, Jessica A., Lu, Yeping, Marshall, Mhairi, Scrambler, Peter J., Beales, Philip L., Brown, Matthew A., Zankl, Andreas, Mitchison, Hannah M., Duncan, Emma L., Wicking, Carol and UK10K Consortium (2013) Short-rib polydactyly and Jeune Syndromes are caused by mutations in WDR60. American Journal of Human Genetics, 93 3: 515-523. doi:10.1016/j.ajhg.2013.06.022 61   6 Cited 9 times in Scopus9 4
Leo, PJ, Gray, GR, Simer, GJ and Rochford, KB (2003) State of polarization changes: Classification and measurement. Journal of Lightwave Technology, 21 10: 2189-2193. doi:10.1109/JLT.2003.816813 51   9 Cited 20 times in Scopus20 0
Paul Leo (2014): The University of Queensland Centre for Clinical Genomics (UQCCG) Genomic Medicine Project. The University of Queensland. Collection. 17  
Cameron, Sarina R., Dahler, Alison L., Endo-Munoz, Liliana B., Jabbar, Ibtissam, Thomas, Gethin P., Leo, Paul J., Poth, Kim, Rickwood, Danny, Guminski, Alexander and Saunders, Nicholas A. (2010) Tumor-initiating activity and tumor morphology of HNSCC is modulated by interactions between clonal variants within the tumor. Laboratory Investigation, 90 11: 1594-1603. doi:10.1038/labinvest.2010.131 68   15 Cited 15 times in Scopus15 0
Leo, PJ, Venturi, V, Whittingham, IB and Babb, JF (2001) Ultracold collisions of metastable helium atoms. Physical Review A, 6404 4: . doi:10.1103/PhysRevA.64.042710 33   21 0
Cremin, K., Leo, P., Harris, J. E., De Smit, E., Bradbury, L., McKelvie, P., Hill, C. L., Brown, M. A. and Hewitt, A. W. (2014) Utility of temporal artery biopsy samples for genome-wide analysis of giant cell arteritis. Genes and Immunity, 15 5: 338-340. doi:10.1038/gene.2014.19 17   0 Cited 0 times in Scopus0 0
McInerney-Leo, Aideen M., Marshall, Mhairi S., Gardiner, Brooke, Benn, Diana E., McFarlane, Janelle, Robinson, Bruce G., Brown, Matthew A., Leo, Paul J., Clifton-Bligh, Roderick J. and Duncan, Emma L. (2014) Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas. Clinical Endocrinology, 80 1: 25-33. doi:10.1111/cen.12331 38   7 Cited 7 times in Scopus7 0
McInerney-Leo, Aideen, Harris, Jessica E., Leo, Paul, Marshall, Mhairi, Gardiner, Brooke, Kinning, Esther, Leong, Huey Yin, McKenzie, Fiona, Ong, PeiTee, Vodopiutz, Julia, Wicking, Carol A., Brown, Matthew A., Zanki, Andreas and Duncan, Emma (2014) Whole exome sequencing is an efficient, sensitive and specific method for determining the genetic cause of short-rib thoracic dystrophies. Clinical Genetics, . doi:10.1111/cge.12550 16   Cited 0 times in Scopus0 2
McInerney-Leo, Aideen M., Marshall, Mhairi S., Gardiner, Brooke, Coucke, Paul J., Van Laer, Lut, Loeys, Bart L., Summers, Kim M., Symoens, Sofie, West, Jennifer A., West, Malcolm J., Wordsworth, B. Paul, Zankl, Andreas, Leo, Paul J., Brown, Matthew A. and Duncan, Emma L. (2013) Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome. BoneKEy Reports, 2 456: 1-9. doi:10.1038/bonekey.2013.190 44 2 0
Zheng, Hou-Feng, Duncan, Emma, Eriksson, Joel, Bergstrom, Ulrica, Yerges-Armstrong, Laura M., Leo, Paul J., Vandenput, Liesbeth, Nicholson, Geoffrey, Ladouceur, Martin, Prince, Richard L., Leslie, William D., Eisman, John A., Goltzman, David, Jones, Graeme, Xiao, Yongjun, Liu, Jeff, Reid, Lanr, Sambrook, Philip N., Dennison, Elaine M., Danoy, Patrick, Wilson, Scott G., McCloskey, Eugene, Eastell, Richard, Spector, Tim, Mitchell, Braxton D., Streeten, Elizabeth A., Brommage, Robert, Lorentzon, Mattias, Pettersson, Ulrika, Brown, Matthew A., Ohlsson, Claes and Richards, J. Brent (2012). Wnt16 Is associated with bone mineral density, osteoporotic fracture and bone strength: a Large-Scale Meta-Analysis of Genomewide Association Studies. In: Abstracts of the IOF-ECCEO12 European Congress on Osteoporosis and Osteoarthritis and the 2nd IOF-ESCEO Pre-clinical Symposium. IOF-ECCEO European Congress on Osteoporosis and Osteoarthritis / 2nd IOF-ESCEO Pre-Clinical Symposium, Bordeaux France, (S402-S403). 21-24 March 2012. doi:10.1007/s00198-012-1924-y 73   0 0