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Evangelou, Evangelos, Kerkhos, Hanneke J., Styrkarsdottir, Unnur, Ntzani, Evangelia E., Bos, Steffan D., Esko, Tonu, Evans, Daniel S., Metrustry, Sarah, Panoutsopoulou, Kalliope, Ramos, Yolande F. M., Thorleifsson, Gudmar, Tsilides, Konstantinos K., arcOGEN Consortium, Arden, Nigel, Aslam, Nadim, Bellamy, Nicholas, Birrell, Fraser, Blanco, Francisco J., Carr, Andrew, Chapman, Kay, Day-Williams, Aaron G., Deloukas, Panos, Doherty, Michael, Engstrom, Gunnar, Helgadottir, Hafdis T., Hoffman, Albert, Ingvarsson, Thorvaldur, Jonsson, Helgi, Keis, Aime, Keurentjes, J. Christiaan, Kloppenburg, Margreet, Lind, Penelope A., McCaskie, Andrew, Martin, Nicholas G., Milani, Lili, Montgomery, Grant W., Nelissen, Rob G. H. H., Nevitt, Michael C., Nilsson, Peter M., Ollier, William E. R., Parimi, Netta, Rai, Ashok, Ralston, Stuart H., Reed, Mike R., Riancho, Jose A., Rivadeneira, Fernando, Rodriquez-Fontenla, Christina, Southam, Lorraine, Thorsteinsdottir, Unnar, Tsezou, Aspasia, Wallis, Gillian A., Wilkinson, J. Mark, Gonzales, Antonio, Lane, Nancy E., Lohmander, L. Stefan, Loughlin, John, Metspalu, Andres, Uitterlinden, Andre G., Jonsdottir, Ingileif, Steffansson, Karl, Slagboom, P. Eline, Zeggini, Eleftheria, Meulenbelt, Ingrid, Ioannidis, John P. A., Spector, Tim D., van Meurs, Joyce B. J. and Valdes, Anna M. (2013) A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip. Annals of the Rheumatic Diseases, Online First 1-7. doi:10.1136/annrheumdis-2012-203114 78   Cited 7 times in Scopus7 8
Hocking, Lynne J., Lucas, Gavin J. A., Daroszewska, Anna, Mangion, Jon, Olavesen, Mark, Cundy, Tim, Nicholson, Geoff C., Ward, Lynley, Bennett, Simon T., Wuyts, Wim, Van Hul, Wim and Ralston, Stuart H. (2002) Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease. Human Molecular Genetics, 11 22: 2735-2739. doi:10.1093/hmg/11.22.2735 37   165 Cited 186 times in Scopus186 0
Lucas, Gavin J. A., Mehta, Sarju G., Hocking, Lynne J., Stewart, Tracey L., Cundy, Tim, Nicholson, Geoffrey C., Walsh, John P., Fraser, William D., Watts, Giles D. J., Ralston, Stuart H. and Kimonis, Virginia E. (2006) Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone. Bone, 38 2: 280-285. doi:10.1016/j.bone.2005.07.014 41   20 Cited 25 times in Scopus25 3
Albagha, Ommar M. E., Wani, Sachin E., Visconti, Micaela R., Alonso, Nerea, Goodman, Kirsteen, Brandi, Maria Luisa, Cundy, Tim, Chung, Pui Yan Jenny, Dargie, Rosemary, Devogelaer, Jean-Pierre, Falchetti, Alberto, Fraser, William D., Gennari, Luigi, Gianfrancesco, Fernando, Hooper, Michael J., Van Hul, Wim, Isaia, Gianluca, Nicholson, Geoff C., Nuti, Ranuccio, Papapoulos, Socrates, Montes, Javier del Pino, Ratajczak, Thomas, Rea, Sarah L., Rendina, Domenico, Gonzalez-Sarmiento, Rogelio, Di Stefano, Marco, Ward, Lynley C., Walsh, John P., Ralston, Stuart H. and Genetic Determinants of Paget's Disease (GDPD) Consortium (2011) Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. Nature Genetics, 43 7: 685-689. doi:10.1038/ng.845 72   35 Cited 41 times in Scopus41 2
Oei, Ling, Estrada, Karol, Duncan, Emma L., Christiansen, Claus, Liu, Ching-Ti, Langdahl, Bente L., Obermayer-Pietsch, Barbara, Riancho, José A., Prince, Richard L., van Schoor, Natasja M., McCloskey, Eugene, Hsu, Yi-Hsiang, Evangelou, Evangelos, Ntzani, Evangelia, Evans, David M., Alonso, Nerea, Husted, Lise B., Valero, Carmen, Hernandez, Jose L., Lewis, Joshua R., Kaptoge, Stephen K., Zhu, Kun, Cupples, L. Adrienne, Medina-Gómez, Carolina, Vandenput, Liesbeth, Kim, Ghi Su, Lee, Seung Hun, Castaño-Betancourt, Martha C., Oei, Edwin H. G., Martinez, Josefina, Daroszewska, Anna, van der Klift, Marjolein, Mellström, Dan, Herrera, Lizbeth, Karlsson, Magnus K., Hofman, Albert, Ljunggren, Östen, Pols, Huibert A. P., Stolk, Lisette, van Meurs, Joyce B. J., Ioannidis, John P. A., Zillikens, M. Carola, Lips, Paul, Karasik, David, Uitterlinden, André G., Styrkarsdottir, Unnur, Brown, Matthew A., Koh, Jung-Min, Richards, J. Brent, Reeve, Jonathan, Ohlsson, Claes, Ralston, Stuart H., Kiel, Douglas P. and Rivadeneira, Fernando (2014) Genome-wide association study for radiographic vertebral fractures: a potential role for the 16q24 BMD locus. Bone, 59 20-27. doi:10.1016/j.bone.2013.10.015 37   3 Cited 3 times in Scopus3 1
Albagha, Omar M. E., Visconti, Micaela R., Alonso, Nerea, Langston, Anne L., Cundy, Tim, Dargie, Rosemary, Dunlop, Malcolm G., Fraser, William D., Hooper, Michael J., Isaia, Gianluca, Nicholson, Geoff C., del Pino Montes, Javier, Gonzalez-Sarmiento, Rogelio, di Stefano, Marco, Tenesa, Albert, Walsh, John P. and Ralston, Stuart H. (2010) Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone. Nature Genetics, 42 6: 520-525. doi:10.1038/ng.562 62   79 Cited 88 times in Scopus88 10
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 297   186 Cited 187 times in Scopus187 9
Hocking, Lynne J., Herbert, Craig A., Nicholls, Rosie K., Williams, Fiona, Bennett, Simon T., Cundy, Tim, Nicholson, Geoff C., Wuyts, Wim, Van Hul, Wim Van and Ralston, Stuart H. (2001) Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35. American Journal of Human Genetics, 69 5: 1055-1061. doi:10.1086/323798 39   70 Cited 84 times in Scopus84 0
Morrison, Nigel A., Stephens, Alexandre A., Osato, Motomi, Polly, Patsie, Tan, Timothy C., Yamashita, Namiko, Doecke, James D., Pasco, Julie, Fozzard, Nicolette, Jones, Graeme, Ralston, Stuart H., Sambrook, Philip N., Prince, Richard L. and Nicholson, Geoff C. (2012) Glutamine repeat variants in human RUNX2 associated with decreased femoral neck BMD, broadband ultrasound attenuation and target gene transactivation. PloS One, 7 8: . doi:10.1371/journal.pone.0042617 60   4 Cited 5 times in Scopus5 2
Lucas, Gavin J. A., Riches, Phillip L., Hocking, Lynne J., Cundy, Tim, Nicholson, Geoffrey C., Walsh, John P. and Ralston, Stuart H. (2008) Identification of a major locus for Paget's disease on chromosome 10p13 in families of British descent. Journal of Bone And Mineral Research, 23 1: 58-63. doi:10.1359/JBMR.071004 39   22 Cited 25 times in Scopus25 0
Koay, M. Audrey, Woon, Peng Y., Zhang, Yun, Miles, Lisa J., Duncan, Emma L., Ralston, Stuart H., Compston, Juliet E., Cooper, Cyrus, Keen, Richard, Langdahl, Bente L., MacLelland, Alasdair, O'Riordan, Jeffrey, Pols, Huibert A., Reid, David M., Uitterlinden, Andre G., Wass, John A.H. and Brown, Matthew A. (2004) Influence of LRP5 polymorphisms on normal variation in BMD. Journal of Bone And Mineral Research, 19 10: 1619-1627. doi:10.1359/JBMR.040704 65   91 Cited 103 times in Scopus103 0
Langdahl, Bente L., Uitterlinden, André G., Ralston, Stuart H., Trikalinos, Thomas A., Balcells, Susanne, Brandi, Maria Luisa, Scollen, Serena, Lips, Paul, Lorenc, Roman, Obermayer-Pietsch, Barbara, Reid, David M., Armas, Jácome Bruges, Arp, Pascal P., Bassiti, Amelia, Bustamante, Mariona, Husted, Lise Bjerre, Carey, Alison H., Cano, Ramon Pérez, Dobnig, Harald, Dunning, Alison M., Fahrleitner-Pammer, Astrid, Falchetti, Alberto, Karczmarewicz, Elzbieta, Kruk, Marcin, van Leeuwen, Johannes P. T. M., Masi, Laura, van Meurs, Joyce B. J., Mangion, Jon, McGuigan, Fiona E .A., Mellibovsky, Leonardo, Mosekilde, Leif, Nogués, Xavier, Pols, Huibert A. P., Reeve, Jonathan, Renner, Wilfried, Rivadeneira, Fernando, van Schoor, Natasja M., Ioannidis, John P. A.., Duncan, Emma L., Aberdeen Prospective Osteoporosis Study (APOSS) Investigators, Danish Osteoporosis Prevention Study (DOPS) Investigators, European Prospective Osteoporosis Study (EPOS) Investigators, European Polish Osteoporosis Study (EPOLOS) Study, Familial Osteoporosis Study (FAMOS) Investigators, Longitudinal Aging Study Amsterdam (LASA) Investigators and Rotterdam Group (ERGO) Investigators (2008) Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: The GENOMOS study. Bone, 42 5: 969-981. doi:10.1016/j.bone.2007.11.007 109   40 Cited 53 times in Scopus53 0
Ralston, Stuart H., Uitterlinden, André G., Brandi, Maria Luisa, Balcells, Susana, Langdahl, Bente L., Lips, Paul, Lorenc, Roman, Obermayer-Pietsch, Barbara, Scollen, Serena, Bustamante, Mariona, Husted, Lise Bjerre, Carey, Alisoun H., Diez-Perez, Adolfo, Dunning, Alison M., Falchetti, Alberto, Karczmarewicz, Elzbieta, Kruk, Marcin, van Leeuwen, Johannes P.T.M., van Meurs, Joyce B. J., Mangion, Jon, McGuigan, Fiona E. A., Mellibovsky, Leonardo, del Monte, Francesca, Pols, Huibert A. P., Reeve, Jonathan, Reid, David M., Renner, Wilfried, Rivadeneira, Fernando, van Schoor, Natasja M., Sherlock, Rachael E., Loannidis, John P.A., GENOMOS Investigators, FAMOS Investigators and Duncan, Emma (2006) Large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes: The GENOMOS study. PLoS Medicine, 3 4: 0515-0523. doi:10.1371/journal.pmed.0030090 100   94 Cited 110 times in Scopus110 1
Ioannidis, John P. A., Ng, Mandy Y., Sham, Pak C., Zintzaras, Elias, Lewis, Cathryn M., Deng, Hong-Wen, Econs, Michael J., Karasik, David, Devoto, Marcella, Kammerer, Candace M., Spector, Tim, Andrew, Toby, Cupples, L. Adrienne, Duncan, Emma L,, Foroud, Tatiana, Kiel, Douglas P., Koller, Daniel, Langdahl, Bente, Mitchell, Braxton D., Peacock, Munro, Recker, Robert, Shen, Hui, Sol-Church, Katia, Spotila, Loretta D., Uitterlinden, Andre G., Wilson, Scott G., Kung, Annie W. C. and Ralston, Stuart H. (2007) Meta-analysis of genome-wide scans provides evidence for sex- and site-specific regulation of bone mass. Journal of bone and mineral research, 22 2: 173-183. doi:10.1359/JBMR.060806 92   105 Cited 113 times in Scopus113 0
Hocking, Lynne J., Lucas, Gavin J. A., Daroszewska, Anna, Cundy, Tim, Nicholson, Geoff C., Donath, Judit, Walsh, John P., Finlayson, Catriona, Cavey, James R., Ciani, Barbara, Sheppard, Paul W., Layfield, Robert and Ralston, Stuart H. (2004) Novel UBA domain mutations of SQSTM1 in Paget's disease of bone: Genotype phenotype correlation, functional analysis, and structural consequences. Journal of Bone and Mineral Research, 19 7: 1122-1127. doi:10.1359/JBMR.0403015 26   93 Cited 109 times in Scopus109 0
Vilarino-Guell, Carles, Miles, Lisa J., Duncan, Emma L., Ralston, Stuart H., Compston, Juliet E., Cooper, Cyrus, Langdahl, Bente L., MacLelland, Alasdair, Pols, Huibert A., Reid, David M., Uitterlinden, Andre G., Steer, Colin D., Tobias, Jon H., Wass, John A. and Brown, Matthew A. (2007) PTHR1 polymorphisms influence BMD variation through effects on the growing skeleton. Calcified Tissue International, 81 4: 270-278. doi:10.1007/s00223-007-9072-7 52   9 Cited 12 times in Scopus12 0
Uitterlinden, André G., Ralston, Stuart H., Brandi, Maria Luisa, Carey, Alisoun H., Grinberg, Daniel, Langdahl, Bente L., Lips, Paul, Lorenc, Roman, Obermayer-Pietsch, Barbara, Reeve, Jonathan, Reid, David M., Amedei, Antonietta, Bassiti, Amelia, Bustamante, Mariona, Husted, Lise Bjerre, Diez-Perez, Adolfo, Dobnig, Harald, Dunning, Alison, Enjuanes, Anna, Fahrleitner-Pammer, Astrid, Fang, Yue, Karczmarewicz, Elzbieta, Kruk, Marcin, van Leeuwen, Johannes P.T.M., Mavilia, Carmelo, van Meurs, Joyce B. J., Mangion, Jon, McGuigan, Fiona E. A., Pols, Huibert A. P., Renner, Wilfried, Rivadeneira, Fernando, van Schoor, Natasja M., Scollen, Serena, Sherlock, Rachael E., Ioannidis, John P.A., APOSS Investigators, EPOS Investigators, EPOLOS Investigators, FAMOS Investigators, Duncan, Emma, LASA Investigators and Rotterdam Study Investigators (2006) The Association between Common Vitamin D Receptor Gene Variations and Osteoporosis: A Participant-Level Meta-Analysis. Annals of Internal Medicine, 145 4: 255-264. 130   135 Cited 152 times in Scopus152
Lucas, Gavin J. A., Hocking, Lynne J., Daroszewska, Anna, Cundy, Tim, Nicholson, Geoff C., Walsh, John P., Fraser, William D., Meier, Christian, Hooper, Michael J. and Ralston, Stuart H. (2005) Ubiquitin-associated domain mutations of SQSTM1 in Paget's disease of bone: Evidence for a founder effect in patients of British descent. Journal of Bone And Mineral Research, 20 2: 227-231. doi:10.1359/JBMR.041106 36   30 Cited 35 times in Scopus35 0