Browse by all authors Browse By Author Name - Van+Hul,+Wim

Browse Results (5 results found)

Subscribe to the RSS feed for this result setSubscribe to the RSS feed for this result set

  Abstract Views File Downloads Thomson Reuters Web of Science Citation Count Scopus Citation Count Altmetric Score
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 38   165 Cited 186 times in Scopus186 0
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 74   35 Cited 42 times in Scopus42 2
Albagha, Omar, Fraser, William, Gennari, Luigi, Hooper, Michael, Van Hul, Wim, Isaia, Gianluca, Nicholson, Geoff, Papapoulos, Socrates, Montes, Javier del Pino, Gonzalez-Sarmiento, Rogelio, di Stefano, Marco, Wani, Sachin, Walsh, John, Ralston, Stuart for the GDPD Consortium, Visconti, Micaela, Alonso, Nerea, Goodman, Kristeen, Brandi, Maria Luisa, Cundy, Tim, Dargie, Rosemary and Falchetti, Alberto (2011). Genome wide association study identifies seven loci that account for 86% of the population attributable risk of Paget's disease of bone. In: 1stIOF-ESCEO Pre-Clinical Symposium Oral Communication Abstracts. 1st IOF-ESCEO Pre-Clinical Symposium, Valencia, Spain, (12-12). 23-26 March 2011. doi:10.1007/s00198-011-1564-7 139   0 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 299   189 Cited 190 times in Scopus190 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