Evaluation of a three-dimensional MR acoustic radiation force imaging pulse sequence using a novel unbalanced bipolar motion encoding gradient von de Bever, Joshua T., Odéen, Henrik, Todd, Nick, Farrer, Alexis I., Parker, Dennis L.

Volltext

Phase aberration simulation study of MRgFUS breast treatments von Farrer, Alexis I., Almquist, Scott, Dillon, Christopher R., Neumayer, Leigh A., Parker, Dennis L., Christensen, Douglas A., Payne, Allison

Volltext

Characterization and evaluation of tissue-mimicking gelatin phantoms for use with MRgFUS von Farrer, Alexis I, Odéen, Henrik, de Bever, Joshua, Coats, Brittany, Parker, Dennis L, Payne, Allison, Christensen, Douglas A

Volltext

DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study von Trinh, Joanne, BSc, Gustavsson, Emil K, MSc, Vilariño-Güell, Carles, PhD, Bortnick, Stephanie, BSc, Latourelle, Jeanne, PhD, McKenzie, Marna B, BSc, Tu, Chelsea Szu, MSc, Nosova, Ekaterina, PhD, Khinda, Jaskaran, BSc, Milnerwood, Austen, PhD, Lesage, Suzanne, PhD, Brice, Alexis, MD, Tazir, Meriem, MD, Aasly, Jan O, MD, Parkkinen, Laura, PhD, Haytural, Hazal, MSc, Foroud, Tatiana, PhD, Myers, Richard H, PhD, Sassi, Samia Ben, MD, Hentati, Emna, MD, Nabli, Fatma, MD, Farhat, Emna, MD, Amouri, Rim, PhD, Hentati, Fayçal, MD, Farrer, Matthew J, Dr

Volltext

A Meta-Analysis of α-Synuclein Multiplication in Familial Parkinsonism von Book, Adam, Guella, Ilaria, Candido, Tara, Brice, Alexis, Hattori, Nobutaka, Jeon, Beomseok, Farrer, Matthew J

Volltext

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database von Lill, Christina M, Roehr, Johannes T, McQueen, Matthew B, Kavvoura, Fotini K, Bagade, Sachin, Schjeide, Brit-Maren M, Schjeide, Leif M, Meissner, Esther, Zauft, Ute, Allen, Nicole C, Liu, Tian, Schilling, Marcel, Anderson, Kari J, Beecham, Gary, Berg, Daniela, Biernacka, Joanna M, Brice, Alexis, DeStefano, Anita L, Do, Chuong B, Eriksson, Nicholas, Factor, Stewart A, Farrer, Matthew J, Foroud, Tatiana, Gasser, Thomas, Hamza, Taye, Hardy, John A, Heutink, Peter, Hill-Burns, Erin M, Klein, Christine, Latourelle, Jeanne C, Maraganore, Demetrius M, Martin, Eden R, Martinez, Maria, Myers, Richard H, Nalls, Michael A, Pankratz, Nathan, Payami, Haydeh, Satake, Wataru, Scott, William K, Sharma, Manu, Singleton, Andrew B, Stefansson, Kari, Toda, Tatsushi, Tung, Joyce Y, Vance, Jeffery, Wood, Nick W, Zabetian, Cyrus P, Young, Peter, Tanzi, Rudolph E, Khoury, Muin J, Zipp, Frauke, Lehrach, Hans, Ioannidis, John P A, Bertram, Lars

Volltext

RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses von Gustavsson, Emil K, Follett, Jordan, Trinh, Joanne, Barodia, Sandeep K, Real, Raquel, Liu, Zhiyong, Grant-Peters, Melissa, Fox, Jesse D, Appel-Cresswell, Silke, Stoessl, A Jon, Rajput, Alex, Rajput, Ali H, Auer, Roland, Tilney, Russel, Sturm, Marc, Haack, Tobias B, Lesage, Suzanne, Tesson, Christelle, Brice, Alexis, Vilariño-Güell, Carles, Ryten, Mina, Goldberg, Matthew S, West, Andrew B, Hu, Michele T, Morris, Huw R, Sharma, Manu, Gan-Or, Ziv, Samanci, Bedia, Lis, Pawel, Periñan, Maria Teresa, Amouri, Rim, Ben Sassi, Samia, Hentati, Faycel, Tonelli, Francesca, Alessi, Dario R, Farrer, Matthew J

Volltext

Urinary LRRK2 phosphorylation predicts parkinsonian phenotypes in G2019S LRRK2 carriers von Fraser, Kyle B, Moehle, Mark S, Alcalay, Roy N, West, Andrew B

Volltext

Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease von Lai, Dongbing, Alipanahi, Babak, Fontanillas, Pierre, Schwantes‐An, Tae‐Hwi, Aasly, Jan, Alcalay, Roy N., Beecham, Gary W., Berg, Daniela, Bressman, Susan, Brice, Alexis, Brockman, Kathrin, Clark, Lorraine, Cookson, Mark, Das, Sayantan, Van Deerlin, Vivianna, Follett, Jordan, Farrer, Matthew J., Trinh, Joanne, Gasser, Thomas, Goldwurm, Stefano, Gustavsson, Emil, Klein, Christine, Lang, Anthony E., Langston, J. William, Latourelle, Jeanne, Lynch, Timothy, Marder, Karen, Marras, Connie, Martin, Eden R., McLean, Cory Y., Mejia‐Santana, Helen, Molho, Eric, Myers, Richard H., Nuytemans, Karen, Ozelius, Laurie, Payami, Haydeh, Raymond, Deborah, Rogaeva, Ekaterina, Rogers, Michael P., Ross, Owen A., Samii, Ali, Saunders‐Pullman, Rachel, Schüle, Birgitt, Schulte, Claudia, Scott, William K., Tanner, Caroline, Tolosa, Eduardo, Tomkins, James E., Vilas, Dolores, Trojanowski, John Q., Uitti, Ryan, Vance, Jeffery M., Visanji, Naomi P., Wszolek, Zbigniew K., Zabetian, Cyrus P., Mirelman, Anat, Giladi, Nir, Orr Urtreger, Avi, Cannon, Paul, Fiske, Brian, Foroud, Tatiana

Volltext

A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants von Fritsche, Lars G, Igl, Wilmar, Grassmann, Felix, Sengupta, Sebanti, Bragg-Gresham, Jennifer L, Burdon, Kathryn P, Hebbring, Scott J, Wen, Cindy, Zack, Donald, Souied, Eric, Scholl, Hendrik P N, Bala, Elisa, Lee, Kristine E, Hunter, David J, Sardell, Rebecca J, Cipriani, Valentina, Hoffman, Joshua D, Schick, Tina, Guymer, Robyn H, Johnson, Matthew P, Jiang, Yingda, Buitendijk, Gabriëlle H S, Zhan, Xiaowei, Kwong, Alan M, Brooks, Matthew, Branham, Kari E, Foerster, Johanna R, Souzeau, Emmanuelle, McAllister, Ian L, Isaacs, Timothy, Hall, Janette, Lake, Stewart, Mackey, David A, Constable, Ian J, Craig, Jamie E, Yang, Zhenglin, Su, Zhiguang, Luo, Hongrong, Chen, Daniel, Ouyang, Hong, Mao, Guanping, Ferreyra, Henry, Stark, Klaus, Brandl, Caroline, Morrison, Margaux A, Morgan, Denise J, Park, Kyu Hyung, Farrer, Lindsay A, Li, Mingyao, Curcio, Christine A, Mohand-Saïd, Saddek, Benchaboune, Mustapha, Cree, Angela J, Rennie, Christina A, Goverdhan, Srinivas V, Grunin, Michelle, Campochiaro, Peter, Katsanis, Nicholas, Blanché, Hélène, Igo, Robert P, Truitt, Barbara, Peachey, Neal S, Klein, Ronald, Postel, Eric A, Courtenay, Monique D, Schwartz, Stephen G, Liew, Gerald, Tan, Ava G, Gopinath, Bamini, Merriam, John C, Smith, R Theodore, Shahid, Humma, Moore, Anthony T, McGrath, J Allie, Brantley, Milam A, Agarwal, Anita, Saksens, Nicole T M, de Jong, Eiko K, Cain, Melinda S, Richardson, Andrea J, Martin, Tammy M, Doheny, Kimberly F, Romm, Jane, Hayward, Caroline, Klein, Michael L, Baird, Paul N, Fauser, Sascha, Yates, John R W, Allikmets, Rando, Schaumberg, Debra A, Klein, Barbara E K, Hagstrom, Stephanie A, Lotery, Andrew J, Léveillard, Thierry, Hewitt, Alex W, Swaroop, Anand, Chew, Emily Y, Pericak-Vance, Margaret A, DeAngelis, Margaret, Heid, Iris M

Volltext

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study von Ross, Owen A, Dr, Soto-Ortolaza, Alexandra I, BSc, Heckman, Michael G, MS, Aasly, Jan O, Prof, Abahuni, Nadine, MD, Annesi, Grazia, Prof, Bacon, Justin A, BSc, Bardien, Soraya, PhD, Bozi, Maria, MD, Brice, Alexis, Prof, Brighina, Laura, MD, Van Broeckhoven, Christine, Prof, Carr, Jonathan, Prof, Chartier-Harlin, Marie-Christine, Prof, Dardiotis, Efthimios, MD, Dickson, Dennis W, Prof, Diehl, Nancy N, BS, Elbaz, Alexis, Prof, Ferrarese, Carlo, Prof, Ferraris, Alessandro, MD, Fiske, Brian, PhD, Gibson, J Mark, Prof, Gibson, Rachel, PhD, Hadjigeorgiou, Georgios M, MD, Hattori, Nobutaka, Prof, Ioannidis, John PA, Prof, Jasinska-Myga, Barbara, MD, Jeon, Beom S, Prof, Kim, Yun Joong, Prof, Klein, Christine, Prof, Kruger, Rejko, MD, Kyratzi, Elli, MD, Lesage, Suzanne, PhD, Lin, Chin-Hsien, MD, Lynch, Timothy, Prof, Maraganore, Demetrius M, Prof, Mellick, George D, PhD, Mutez, Eugénie, MD, Nilsson, Christer, Prof, Opala, Grzegorz, Prof, Park, Sung Sup, Prof, Puschmann, Andreas, MD, Quattrone, Aldo, Prof, Sharma, Manu, PhD, Silburn, Peter A, Prof, Sohn, Young Ho, Prof, Stefanis, Leonidas, MD, Tadic, Vera, MD, Theuns, Jessie, PhD, Tomiyama, Hiroyuki, MD, Uitti, Ryan J, Prof, Valente, Enza Maria, Prof, van de Loo, Simone, PhD, Vassilatis, Demetrios K, PhD, Vilariño-Güell, Carles, PhD, White, Linda R, Prof, Wirdefeldt, Karin, MD, Wszolek, Zbigniew K, Prof, Wu, Ruey-Meei, Prof, Farrer, Matthew J, Prof

Volltext

Genome-wide determinants of mortality and motor progression in Parkinson’s disease von Tan, Manuela M. X., Lawton, Michael A., Pollard, Miriam I., Brown, Emmeline, Real, Raquel, Carrasco, Alejandro Martinez, Bekadar, Samir, Jabbari, Edwin, Reynolds, Regina H., Iwaki, Hirotaka, Blauwendraat, Cornelis, Kanavou, Sofia, Hubbard, Leon, Malek, Naveed, Grosset, Katherine A., Bajaj, Nin, Barker, Roger A., Burn, David J., Bresner, Catherine, Foltynie, Thomas, Wood, Nicholas W., Williams-Gray, Caroline H., Andreassen, Ole A., Toft, Mathias, Elbaz, Alexis, Artaud, Fanny, Brice, Alexis, Corvol, Jean-Christophe, Aasly, Jan, Farrer, Matthew J., Nalls, Michael A., Singleton, Andrew B., Williams, Nigel M., Ben-Shlomo, Yoav, Hardy, John, Hu, Michele T. M., Grosset, Donald G., Shoai, Maryam, Pihlstrøm, Lasse, Morris, Huw R.

Volltext

Collaborative Analysis of α-Synuclein Gene Promoter Variability and Parkinson Disease von Maraganore, Demetrius M, de Andrade, Mariza, Elbaz, Alexis, Farrer, Matthew J, Ioannidis, John P, Krüger, Rejko, Rocca, Walter A, Schneider, Nicole K, Lesnick, Timothy G, Lincoln, Sarah J, Hulihan, Mary M, Aasly, Jan O, Ashizawa, Tetsuo, Chartier-Harlin, Marie-Christine, Checkoway, Harvey, Ferrarese, Carlo, Hadjigeorgiou, Georgios, Hattori, Nobutaka, Kawakami, Hideshi, Lambert, Jean-Charles, Lynch, Timothy, Mellick, George D, Papapetropoulos, Spiridon, Parsian, Abbas, Quattrone, Aldo, Riess, Olaf, Tan, Eng-King, Van Broeckhoven, Christine, Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium, for the

Volltext

Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease von Theuns, Jessie, Verstraeten, Aline, Sleegers, Kristel, Wauters, Eline, Gijselinck, Ilse, Smolders, Stefanie, Crosiers, David, Corsmit, Ellen, Elinck, Ellen, Sharma, Manu, Krüger, Rejko, Lesage, Suzanne, Brice, Alexis, Chung, Sun Ju, Kim, Mi-Jung, Kim, Young Jin, Ross, Owen A, Wszolek, Zbigniew K, Rogaeva, Ekaterina, Xi, Zhengrui, Lang, Anthony E, Klein, Christine, Weissbach, Anne, Mellick, George D, Silburn, Peter A, Hadjigeorgiou, Georgios M, Dardiotis, Efthimios, Hattori, Nobutaka, Ogaki, Kotaro, Tan, Eng-King, Zhao, Yi, Aasly, Jan, Valente, Enza Maria, Petrucci, Simona, Annesi, Grazia, Quattrone, Aldo, Ferrarese, Carlo, Brighina, Laura, Deutschländer, Angela, Puschmann, Andreas, Nilsson, Christer, Garraux, Gaëtan, LeDoux, Mark S, Pfeiffer, Ronald F, Boczarska-Jedynak, Magdalena, Opala, Grzegorz, Maraganore, Demetrius M, Engelborghs, Sebastiaan, De Deyn, Peter Paul, Cras, Patrick, Cruts, Marc, Van Broeckhoven, Christine

Volltext

Simulation of therapeutic ultrasound treatments using the hybrid angular spectrum technique von Christensen, Douglas, Almquist, Scott, Farrer, Alexis, Parker, Dennis, Payne, Allison

Volltext

Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors von Liu, Hui, Dehestani, Mohammad, Blauwendraat, Cornelis, Makarious, Mary B., Leonard, Hampton, Kim, Jonggeol J., Schulte, Claudia, Noyce, Alastair, Jacobs, Benjamin M., Foote, Isabelle, Sharma, Manu, Koks, Sulev, Mellick, George D, Pirker, Walter, Zimprich, Alexander, Lang, Anthony E, Rogaeva, Ekaterina, Taba, Pille, Brice, Alexis, Chartier‐Harlin, Marie‐Christine, Corvol, Jean‐Christophe, Domenighetti, Cloé, Elbaz, Alexis, Lesage, Suzanne, Mutez, Eugenie, Sugier, Pierre‐Emmanuel, Sreelatha, Ashwin Ashok Kumar, Grover, Sandeep, Brockmann, Kathrin, Deutschländer, Angela B, Gasser, Thomas, Krüger, Jens, Lichtner, Peter, Radivojkov‐Blagojevic, Milena, Schulte, Claudia, Sharma, Manu, Dardiotis, Efthimos, Hadjigeorgiou, Georges M, Simitsi, Athina Maria, Stefanis, Leonidas, Annesi, Grazia, Brighina, Laura, Ferrarese, Carlo, Petrucci, Simona, Pezzoli, Gianni, Quattrone, Andrea, Straniero, Letizia, Gagliardi, Monica, Valente, Enza Maria, Zecchinelli, Anna, Hattori, Nobutaka, Nakayama, Akiyoshi, Matsuo, Hirotaka, Nishioka, Kenya, Bobbili, Dheeraj, Kruger, Rejko, Landoulsi, Zied, May, Patrick, Pavelka, Lukas, Bloem, Bastiaan R, Warrenburg, Bart PC, Aasly, Jan, Pihlstrøm, Lasse, Toft, Mathias, Ferreira, Joaquim J, Guedes, Leonor Correia, Bardien, Soraya, Carr, Jonathan, Chung, Sun Ju, Kim, Yun Joong, Diez‐Fairen, Monica, Ezquerra, Mario, Pastor, Pau, Tolosa, Eduardo, Belin, Andrea C, Pedersen, Nancy L, Puschmann, Andreas, Ran, Caroline, Rödström, Emil Y, Wirdefeldt, Karin, Clarke, Carl E, Morrison, Karen E, Tan, Manuela, Edsall, Connor, Farrer, Matt J, Krainc, Dimitri, Singleton, Andrew B, Burbulla, Lena F, Hernandez, Dena G, Nalls, Mike, Singleton, Andrew, Gasser, Thomas, Bandres‐Ciga, Sara

Volltext

Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson’s disease von Brown, Emmeline E., Blauwendraat, Cornelis, Trinh, Joanne, Rizig, Mie, Nalls, Mike A., Leveille, Etienne, Ruskey, Jennifer A., Jonvik, Hallgeir, Tan, Manuela M.X., Bandres-Ciga, Sara, Hassin-Baer, Sharon, Brockmann, Kathrin, Infante, Jon, Tolosa, Eduardo, Ezquerra, Mario, Ben Romdhan, Sawssan, Benmahdjoub, Mustapha, Arezki, Mohamed, Mhiri, Chokri, Hardy, John, Singleton, Andrew B., Alcalay, Roy N., Gasser, Thomas, Grosset, Donald G., Williams, Nigel M., Pittman, Alan, Gan-Or, Ziv, Fernandez-Santiago, Ruben, Brice, Alexis, Lesage, Suzanne, Farrer, Matthew, Wood, Nicholas, Morris, Huw R.

Volltext

The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants von 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, Destée, 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, Eugénie, 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, Vilariño-Güell, Carles, White, Linda R, Wirdefeldt, Karin, Wszolek, Zbigniew K, Wu, Ruey-Meei, Xiromerisiou, Georgia, Maraganore, Demetrius M, Farrer, Matthew J, Ross, Owen A

Volltext

A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease von Krüger, 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, Zbigniew, Xiromerisiou, Georgia, Maraganore, Demetrius M

Volltext

Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson's disease: analysis of a large multicenter study von Wang, Lisa, Heckman, Michael G., Aasly, Jan O., Annesi, Grazia, Bozi, Maria, Chung, Sun Ju, Clarke, Carl, Crosiers, David, Eckstein, Gertrud, Garraux, Gaetan, Hadjigeorgiou, Georgios M., Hattori, Nobu, Jeon, Beom, Kim, Yun J., Kubo, Masato, Lesage, Suzanne, Lin, Juei Jueng, Lynch, Timothy, Lichtner, Peter, Mellick, George D., Mok, Vincent, Morrison, Karin E., Quattrone, Aldo, Satake, Wataru, Silburn, Peter A., Stefanis, Leonidas, Stockton, Joanne D., Tan, Eng King, Toda, Tatsushi, Brice, Alexis, Van Broeckhoven, Christine, Uitti, Ryan J., Wirdefeldt, Karin, Wszolek, Zbigniew, Xiromerisiou, Georgia, Maraganore, Demetrius M., Gasser, Thomas, Krüger, Rejko, Farrer, Matthew J., Ross, Owen A., Sharma, Manu

Volltext