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Kruger, Rejko, Sharma, Manu, Riess, Olaf, Gasser, Thomas, Van Broeckhoven, Christine, Theuns, Jessie, Aasly, Jan, Annesi, Grazia, Bentivoglio, Anna Rita, Brice, Alexis, Djarmati, Ana, Elbaz, Alexis, Farrer, Matthew, Ferrarese, Carlo, Gibson, J. Mark, Hadjigeorgiou, Georgios M., Hattori, Nobutaka, Ioannidis, John P.A., Jasinska-Myga, Barbara, Klein, Christine, Lambert, Jean-Charles, Lesage, Suzanne, Lin, Juei-Jueng, Lynch, Timothy, Mellick, George D., de Nigris, Francesa, Opala, Grzegorz, Prigione, Alessandro, Quattrone, Aldo, Ross, Owen A., Satake, Wataru, Silburn, Peter A., Tan, Eng King, Toda, Tatsushi, Tomiyama, Hiroyuki, Wirdefeldt, Karin, Wszolek, Z., Xiromerisiou, Georgia and Maraganore, Demetrius M. (2011) A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease. Neurobiology of Aging, 32 3: 548.e9-548.e18. doi:10.1016/j.neurobiolaging.2009.11.021 163   9 Cited 16 times in Scopus16 0
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 73   Cited 6 times in Scopus6 8
Sharma, Manu, Ioannidis, John P. A., Aasly, Jan O., Annesi, Grazia, Brice, Alexis, Bertram, Lars, Bozi, Maria, Barcikowska, Maria, Crosiers, David, Clarke, Carl E., Facheris, Maurizio F., Farrer, Matthew, Garraux, Gaetan, Gispert, Suzana, Auburger, Georg, Vilarino-Guell, Carles, Hadjigeorgiou, Georgios M., Hicks, Andrew A., Hattori, Nobutaka, Jeon, Beom S., Jamrozik, Zygmunt, Krygowska-Wajs, Anna, Lesage, Suzanne, Lill, Christina M., Lin, Juei-Jueng, Lynch, Timothy, Lichtner, Peter, Lang, Anthony E., Libioulle, Cecile, Murata, Miho, Mok, Vincent, Jasinska-Myga, Barbara, Mellick, George D., Morrison, Karen E., Meitnger, Thomas, Zimprich, Alexander, Opala, Grzegorz, Pramstaller, Peter P., Pichler, Irene, Park, Sung Sup, Quattrone, Aldo, Rogaeva, Ekaterina, Ross, Owen A., Stefanis, Leonidas, Stockton, Joanne D., Satake, Wataru, Silburn, Peter A., Strom, Tim M., Theuns, Jessie, Tan, Eng-King, Toda, Tatsushi, Tomiyama, Hiroyuki, Uitti, Ryan J., Van Broeckhoven, Christine, Wirdefeldt, Karin, Wszolek, Zbigniew, Xiromerisiou, Georgia, Yomono, Harumi S., Yueh, Kuo-Chu, Zhao, Yi, Gasser, Thomas, Maraganore, Demetrius, Krueger, Rejko and GEOPD consortium (2012) A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. Journal of Medical Genetics, 49 11: 721-726. doi:10.1136/jmedgenet-2012-101155 74   16 Cited 17 times in Scopus17 1
Ross, Owen, A., Soto-Ortolaza, AIexandra I., Heckman, Michael, G., Aasly, Jan, O., Abahuni, Nadine, Annesi, Grazia, Bacon, Justin, A., Bardien, Soraya, Bozi, Maria, Brice, Alexis, Brighina, Laura, Van Broeckhoven, Christine, Carr, Jonathan, Chartier-Harlin, Marie-Christine, Dardiotis, Efthimios, Dickson, Dennis, W., Diehl, Nancy, N., Elbaz, Alexis, Ferrarese, Carlo, Ferraris, Alessandro, Fiske, Brian, Gibson, J. Mark, Gibson, Rachel, Hadjigeorgiou, Georgios, M., Hattori, Nobutaka, Ioannidis, John, P. A., Jasinska-Myga, Barbara, Jeon, Beom, S., Kim, Yun Joong, Klein, Christine, Kruger, Rejko, Kyratzi, Elli, Lesage, Suzanne, Lin, Chin-Hsien, Lynch, Timothy, Maraganore, Demetruis M., Mellick, George D., Mutez, Eugenie, Nilsson, Christer, Opala, Grzegorz, Park, Sung Sup, Puschmann, Andreas, Quattrone, Aldo, Sharma, Manu, Silburn, Peter A., Sohn, Young Ho, Stefanis, Leonidas, Tadic, Vera, Theuns, Jessie, Tomiyama, Hiroyuki, Uitti, Ryan J., Valente, Enza Maria, van de Loo, Simone, Vassilatis, Demetrios K., Vilarino-Guell, Carles, White, Linda R., Wirdefeldt, Karin, Wszolek, Zbigniew K., Wu, Ruey-Meei, Farrer, Matthew J. and on behalf of the Genetic Epidemiology Of Parkinson's Disease (GEO-PD) Consortium (2011) Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: A case-control study. Lancet Neurology, 10 10: 898-908. doi:10.1016/S1474-4422(11)70175-2 101   65 Cited 62 times in Scopus62 1
Elliott, Katherine S., Zeggini, Eleftheria, McCarthy, Mark I., Gudmundsson, Julius, Sulem, Patrick, Stacey, Simon N., Thorlacius, Steinunn, Amundadottir, Laufey, Gronberg, Henrik, Xu, Jianfeng, Gaborieau, Valerie, Eeles, Rosalind A., Neal, David E., Donovan, Jenny L., Hamdy, Freddie C., Muir, Kenneth, Hwang, Shih-Jen, Spitz, Margaret R., Zanke, Brent, Carvajal-Carmona, Luis, Brown, Kevin M., Hayward, Nicholas K., Macgregor, Stuart, Tomlinson, Ian P. M., Lemire, Mathieu, Amos, Christopher I., Murabito, Joanne M., Isaacs, William B., Easton, Douglas F., Brennan, Paul, Barkardottir, Rosa B., Gudbjartsson, Daniel F., Rafnar, Thorunn, Hunter, David J., Chanock, Stephen J., Stefansson, Kari and Ioannidis, John P. A. (2010) Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studies. PLoS One, 5 5: e10858-e10864. doi:10.1371/journal.pone.0010858 69 2 16 Cited 15 times in Scopus15 0
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 33   2 Cited 2 times in Scopus2 1
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   163 Cited 164 times in Scopus164 9
Elbaz, Alexis, Ross, Owen A., Ioannidis, John P. A., Soto-Ortolaza, Alexandra I., Moisan, Frédéric, Aasly, Jan, Annesi, Grazia, Bozi, Maria, Brighina, Laura, Chartier-Harlin, Marie-Christine, Destée, Alain, Ferrarese, Carlo, Ferraris, Alessandro, Gibson, J. Mark, Gispert, Suzana, Hadjigeorgiou, Georgios M., Jasinska-Myga, Barbara, Klein, Christine, Krüger, Rejko, Lambert, Jean-Charles, Lohmann, Katja, van de Loo, Simone, Loriot, Marie-Anne, Lynch, Timothy, Mellick, George D., Mutez, Eugénie, Nilsson, Christer, Opala, Grzegorz, Puschmann, Andreas, Quattrone, Aldo, Sharma, Manu, Silburn, Peter A., Stefanis, Leonidas, Uitti, Ryan J., Valente, Enza Maria, Vilariño-Güell, Carles, Wirdefeldt, Karin, Wszolek, Zbigniew K., Xiromerisiou, Georgia, Maraganore, Demetrius M., Farrer, Matthew J. and on behalf of the Genetic Epidemiology of Parkinson’s Disease (GEO-PD) consortium (2011) Independent and joint effects of the MAPT and SNCA genes in Parkinson Disease. Annals of Neurology, 69 5: 778-792. doi:10.1002/ana.22321 61   36 Cited 35 times in Scopus35 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.2007.11.007 105   37 Cited 52 times in Scopus52 0
Sharma, Manu, Ioannidis, John P. A., Aasly, Jan O., Annesi, Grazia, Brice, Alexis, Van Broeckhoven, Christine, Bertram, Lars, Bozi, Maria, Crosiers, David, Clarke, Carl, Facheris, Maurizio, Farrer, Matthew, Garraux, Gaetan, Gispert, Suzana, Auburger, Georg, Vilarino-Gueell, Carles, Hadjigeorgiou, Georgios M., Hicks, Andrew A., Hattori, Nobutaka, Jeon, Beom, Lesage, Suzanne, Lill, Christina M., Lin, Juei-Jueng, Lynch, Timothy, Lichtner, Peter, Lang, Anthony E., Mok, Vincent, Jasinska-Myga, Barbara, Mellick, George D., Morrison, Karen E., Opala, Grzegorz, Pramstaller, Peter P., Pichler, Irene, Park, Sung Sup, Quattrone, Aldo, Rogaeva, Ekaterina, Ross, Owen A., Stefanis, Leonidas, Stockton, Joanne D., Satake, Wataru, Silburn, Peter A., Theuns, Jessie, Tan, Eng-King, Toda, Tatsushi, Tomiyama, Hiroyuki, Uitti, Ryan J., Wirdefeldt, Karin, Wszolek, Zbigniew, Xiromerisiou, Georgia, Yueh, Kuo-Chu, Zhao, Yi, Gasser, Thomas, Maraganore, Demetrius, Krueger, Rejko and On behalf of the GEO-PD Consortium (2012) Large-scale replication and heterogeneity in Parkinson disease genetic loci. Neurology, 79 7: 659-667. doi:10.1212/WNL.0b013e318264e353 86 1 37 Cited 38 times in Scopus38 4
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 89   104 Cited 112 times in Scopus112 0
Heckman, Michael G., Soto-Ortolaza, Alexandra I., Aasly, Jan O., Abahuni, Nadine, Annesi, Grazia, Bacon, Justin A., Bardien, Soraya, Bozi, Maria, Brice, Alexis, Brighina, Laura, Carr, Jonathan, Chartier-Harlin, Marie-Christine, Dardiotis, Efthimios, Dickson, Dennis W., Diehl, Nancy N., Elbaz, Alexis, Ferrarese, Carlo, Fiske, Brian, Gibson, J. Mark, Gibson, Rachel, Hadjigeorgiou, Georgios M., Hattori, Nobutaka, Ioannidis, John P. A., Boczarska-Jedynak, Magdalena, Jasinska-Myga, Barbara, Jeon, Beom S., Kim, Yun Joong, Klein, Christine, Kruger, Rejko, Kyratzi, Elli, Lesage, Suzanne, Lin, Chin-Hsien, Lynch, Timothy, Maraganore, Demetrius M., Mellick, George D., Mutez, Eugenie, Nilsson, Christer, Opala, Grzegorz, Park, Sung Sup, Petrucci, Simona, Puschmann, Andreas, Quattrone, Aldo, Sharma, Manu, Silburn, Peter A., Sohn, Young Ho, Stefanis, Leonidas, Tadic, Vera, Theuns, Jessie, Tomiyama, Hiroyuki, Uitti, Ryan J., Valente, Enza Maria, Van Broeckhoven, Christine, van de Loo, Simone, Vassilatis, Demetrios K., Vilarino-Gueell, Carles, White, Linda R., Wirdefeldt, Karin, Wszolek, Zbigniew K., Wu, Ruey-Meei, Hentati, Faycal, Farrer, Matthew J. and Ross, Owen A. (2013) Population-specific Frequencies for LRRK2 Susceptibility Variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium. Movement Disorders, 28 12: 1740-1744. doi:10.1002/mds.25600 25   0 Cited 0 times in Scopus0 1
Matheson, Gordon O., Kluegl, Martin, Engebretsen, Lars, Bendiksen, Fredrik, Blair, Steven N., Borjesson, Mats, Budgett, Richard, Derman, Wayne, Erdener, Ugur, Ioannidis, John P. A., Khan, Karim M., Martinez, Rodrigo, van Mechelen, Willem, Mountjoy, Margo, Sallis, Robert E., Schwellnus, Martin, Shultz, Rebecca, Soligard, Torbjorn, Steffen, Kathrin, Sundberg, Carl Johan, Weiler, Richard and Ljungqvist, Arne (2013) Prevention and management of non-communicable disease: the IOC consensus statement, Lausanne 2013. British Journal of Sports Medicine, 47 16: 1003-1011. doi:10.1136/bjsports-2013-093034 22   8 Cited 10 times in Scopus10 18
Matheson, Gordon O., Kluegl, Martin, Engebretsen, Lars, Bendiksen, Fredrik, Blair, Steven N., Borjesson, Mats, Budgett, Richard, Derman, Wayne, Erdener, Ugur, Ioannidis, John P. A., Khan, Karim M., Martinez, Rodrigo, van Mechelen, Willem, Mountjoy, Margo, Sallis, Robert E., Schwellnus, Martin, Shultz, Rebecca, Soligard, Torbjorn, Steffen, Kathrin, Sundberg, Carl Johan, Weiler, Richard and Ljungqvist, Arne (2013) Prevention and management of non-communicable disease: The IOC consensus statement, Lausanne 2013. Sports Medicine, 43 11: 1075-1088. doi:10.1007/s40279-013-0104-3 25   3 Cited 3 times in Scopus3 11
Sharma, Manu, Maraganore, Demetrius M., Ioannidis, John P. A., Riess, Olaf, Aasly, Jan O., Annesi, Grazia, Abahuni, Nadine, Bentivoglio, Anna Rita, Brice, Alexis, Van Broeckhoven, Christine, Chartier-Harlin, Marie-Christine, Destee, Alain, Djarmati, Ana, Elbaz, Alexis, Farrer, Matthew, Ferrarese, Carlo, Gibson, J. Mark, Gispert, Suzana, Hattori, Nobutaka, Jasinska-Myga, Barbara, Klein, Christine, Lesage, Suzanne, Lynch, Timothy, Lichtner, Peter, Lambert, Jean-Charles, Lang, Anthony E., Mellick, George D., De Nigris, Francesca, Opala, Grzegorz, Quattrone, Aldo, Riva, Chiara, Rogaeva, Ekaterina, Ross, Owen A., Satake, Wataru, Silburn, Peter A., Theuns, Jessie, Toda, Tatsushi, Tomiyama, Hiroyuki, Uitti, Ryan J., Wirdefeldt, Karin, Wszolek, Zbigniew, Gasser, Thomas, Kruger, Rejko and for the Genetic Epidemiology of Parkinson's Disease Consortium (2011) Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease. Neurobiology of Aging, 32 11: 2108.e1-2108.e5. doi:10.1016/j.neurobiolaging.2011.05.024 64   0 Cited 6 times in Scopus6 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. 126   133 Cited 151 times in Scopus151
Heckman, Michael G., Elbaz, Alexis, Soto-Ortolaza, Alexandra I., Serie, Daniel J., Aasly, Jan O., Annesi, Grazia, Auburger, Georg, Bacon, Justin A., Boczarska-Jedynak, Magdalena, Bozi, Maria, Brighina, Laura, Chartier-Harlin, Marie-Christine, Dardiotis, Efthimios, Destee, Alain, Ferrarese, Carlo, Ferraris, Alessandro, Fiske, Brian, Gispert, Suzana, Hadjigeorgiou, Georgios M., Hattori, Nobutaka, Ioannidis, John P. A., Jasinska-Myga, Barbara, Jeon, Beom S., Kim, Yun Joong, Klein, Christine, Kruger, Rejko, Kyratzi, Elli, Lin, Chin-Hsien, Lohmann, Katja, Loriot, Marie-Anne, Lynch, Timothy, Mellick, George D., Mutez, Eugenie, Opala, Grzegorz, Park, Sung Sup, Petrucci, Simona, Quattrone, Aldo, Sharma, Manu, Silburn, Peter A., Sohn, Young Ho, Stefanis, Leonidas, Tadic, Vera, Tomiyama, Hiroyuki, Uitti, Ryan J., Valente, Enza Maria, Vassilatis, Demetrios K., Vilarino-Guell, Carles, White, Linda R., Wirdefeldt, Karin, Wszolek, Zbigniew K., Wu, Ruey-Meei, Xiromerisiou, Georgia, Maraganore, Demetrius M., Farrer, Matthew J., Ross, Owen A. and on behalf of the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium (2014) The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants. Neurobiology of Aging, 35 1: 266.e5-266.e14. doi:10.1016/j.neurobiolaging.2013.07.013 20   0 Cited 1 times in Scopus1 0
Maraganore, Demetrius M., Lesnick, Timothy G., Elbaz, Alexis, Chartier-Harlin, Marie-Christine, Gasser, Thomas, Krüger, Rejko, Hattori, Nobutaka, Mellick, George D., Quattrone, Aldo, Satoh, Jun-Ichi, Toda, Taksushi, Wang, Jian, Ioannidis, John P. A., de Andrade, Mariza, Rocca, Walter A., UCHL1 Global Genetics Consortium and Silburn, Peter A. (2004) UCHL1 is a Parkinson's disease susceptibility gene. Annals of Neurology, 55 4: 512-521. doi:10.1002/ana.20017 114   139 Cited 161 times in Scopus161 0