Browse by all authors Browse By Author Name - Hocking,+Lynne+J.

Browse Results (9 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
Marioni, Riccardo E., Batty, G. David, Hayward, Caroline, Kerr, Shona M., Campbell, Archie, Hocking, Lynne J., Porteous, David J., Visscher, Peter M. and Deary, Ian J. (2014) Common genetic variants explain the majority of the correlation between height and intelligence: The generation scotland study. Behavior Genetics, 44 2: 91-96. doi:10.1007/s10519-014-9644-z 16   0 Cited 0 times in Scopus0 79
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 35   160 Cited 183 times in Scopus183 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 40   19 Cited 25 times in Scopus25 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 287   160 Cited 163 times in Scopus163 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 34   69 Cited 83 times in Scopus83 0
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   21 Cited 25 times in Scopus25 0
Marioni, Riccardo E., Davies, Gail, Hayward, Caroline, Liewald, Dave, Kerr, Shona M., Campbell, Archie, Luciano, Michelle, Smith, Blair H., Padmanabhan, Sandosh, Hocking, Lynne J., Hastie, Nicholas D., Wright, Alan F., Porteous, David J., Visscher, Peter M. and Deary, Ian J. (2014) Molecular genetic contributions to socioeconomic status and intelligence. Intelligence (Kidlington), 44 1: 26-32. doi:10.1016/j.intell.2014.02.006 18   3 Cited 5 times in Scopus5 22
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   90 Cited 107 times in Scopus107 0
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   29 Cited 35 times in Scopus35 0