Genetic screening of South African families with Parkinson’s disease by Braun, Abigail, van Coller, Riaan, Amod, Ferzana Hassan, Carr, Jonathan, Moosa, Shahida, Bardien, Soraya

Get full text

Identification of a common founder couple for 40 South African Afrikaner families with Parkinson's disease by Geldenhuys, Gerhard, Glanzmann, Brigitte, Lombard, Debbie, Boolay, Sihaam, Carr, Jonathan, Bardien, Soraya

Get full text

Inherited retinal disorders in South Africa and the clinical impact of evolving technologies by Roberts, L, Goliath, R, Rebello, G, Bardien, S, September, A V, Bartmann, L, Loubser, F, Greenberg, L J, Ramesar, R S

Get full text

Direct-to-consumer genetic testing: to test or not to test, that is the question by Dandara, Collet, Greenberg, Jacqui, Lambie, Lindsay, Lombard, Zane, Naicker, Thirona, Ramesar, Raj, Ramsay, Michele, Roberts, Lisa, Theron, Magda, Venter, Phillip, Bardien-Kruger, Soraya

Get full text

Factors influencing the development of early- or late-onset Parkinson's disease in a cohort of South African patients by DER MERWE, C. Van, HAYLETT, W, HARVEY, J, LOMBARD, D, BARDIEN, S, CARR, J

Get full text

A South African family with the mitochondrial A1555G mutation on haplogroup L0d by Human, H., Lombard, D., de Jong, G., Bardien, S.

Get full text

Underrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future Directions by Schumacher‐Schuh, Artur Francisco, Bieger, Andrei, Okunoye, Olaitan, Mok, Kin Ying, Lim, Shen‐Yang, Bardien, Soraya, Ahmad‐Annuar, Azlina, Santos‐Lobato, Bruno Lopes, Strelow, Matheus Zschornack, Salama, Mohamed, Rao, Shilpa C., Zewde, Yared Zenebe, Dindayal, Saiesha, Azar, Jihan, Prashanth, Lingappa Kukkle, Rajan, Roopa, Noyce, Alastair J., Okubadejo, Njideka, Rizig, Mie, Lesage, Suzanne, Mata, Ignacio Fernandez

Get full text

Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort by Vollstedt, Eva‐Juliane, Padmanabhan, Shalini, Brice, Alexis, Tesson, Christelle, Vidailhet, Marie, Hentati, Faycel, Mirelman, Anat, Fahn, Stanley, Brüggemann, Norbert, Foroud, Tatiana, Tolosa, Eduardo, Garrido, Alicia, Annesi, Grazia, Correia Guedes, Leonor, Petrucci, Simona, Fedotova, Ekaterina Y., Alvarez, Victoria, Menéndez‐González, Manuel, Gómez‐Garre, Pilar, Mir, Pablo, Belin, Andrea Carmine, Jankovic, Joseph, Nishioka, Kenya, Funayama, Manabu, Clarimon, Jordi, Williams‐Gray, Caroline H., Camacho, Marta, Puschmann, Andreas, Carr, Jonathan, Ferese, Rosangela, Gambardella, Stefano, Chase, Bruce, Markopoulou, Katerina, Toda, Tatsushi, Lynch, Timothy, Carvalho Aguiar, Patricia, Saunders‐Pullman, Rachel, Skorvanek, Matej, Garraux, Gaetan, Chung, Sun Ju, Klivényi, Péter, Kostic, Vladimir S., Borges, Vanderci, Spitz, Mariana, Riess, Olaf, Valente, Enza Maria, Corvol, Jean‐Christophe, Klein, Christine, Aasly, Jan O., Abramycheva, Natalya Y., Al‐Mubarak, Bashayer, Ferraz, Henrique Ballalai, Barrett, Matthew J., Başak, A. Nazlı, Boon, Agnita J. W., Borges, Vanderci, Borngräber, Friederike, Bozi, Maria, Bressman, Susan, Brice, Alexis, Belin, Andrea Carmine, Cornejo‐Olivas, Mario, Chung, Sun Ju, Crosiers, David, Carvalho Aguiar, Patricia, Fahn, Stanley, Fedotova, Ekaterina Y., Foroud, Tatiana, Giladi, Nir, Gómez‐Garre, Pilar, Hattori, Nobutaka, Hertz, Jens Michael, Illarioshkin, Sergey N., Kievit, Anneke A., Koziorowski, Dariusz, Krüger, Rejko, Kühn, Andrea A., Kuhlenbäumer, Gregor, Lim, Jia Lun, Lin, Chin‐Hsien, Markopoulou, Katerina, Menéndez‐González, Manuel, Mirelman, Anat, Morris, Huw, Pachchek, Sinthuja, Puschmann, Andreas, Rossi, Malco, Sammler, Esther M., Satake, Wataru, Stefanis, Leonidas, Soto‐Beasley, Alexandra I., Spitz, Mariana, Suchowersky, Oksana, Tan, Eng‐King, Tesson, Christelle, Toda, Tatsushi, Torres‐Ramirez, Luis, Tumas, Vitor, Uyguner, Oya, Wu, Yih‐Ru

Get full text

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study by 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

Get full text

Clinical findings and genetic screening for copy number variation mutations in a cohort of South African patients with Parkinson's disease : research by Bardien, S., Mahne, A.C., Carr, J.A., Schutte, C-M

Get full text

Clinical findings and genetic screening for copy number variation mutations in a cohort of South African patients with Parkinson's disease : research by Mahne, A.C., Schutte, C-M, Carr, J.A., Bardien, S.

Get full text

Aminoglycoside-induced hearing loss in HIV-positive and HIV-negative multidrug-resistant tuberculosis patients by Harris, Tashneem, Bardien, Soraya, Schaaf, H Simon, Petersen, Lucretia, De Jong, Greetje, Fagan, Johannes J

Get full text

Clinical findings and genetic screening for copy number variation mutations in a cohort of South African patients with Parkinson's disease by Mahne, Anna Cecelia, Carr, Jonathan A, Bardien, Soraya, Schutte, Clara Maria

Get full text

Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors by 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

Get full text

Using global team science to identify genetic parkinson's disease worldwide by Vollstedt, Eva‐Juliane, Klein, Christine, Ahmad‐Annuar, Azlina, Al‐Mubarak, Bashayer, Annesi, Grazia, Barber, Thomas R., Bardien, Soraya, Başak, A. Nazlı, Bhatia, Kailash, Binkofski, Ferdinand, Bozi, Maria, Brice, Alexis, Brighina, Laura, Brockmann, Kathrin, Brücke, Thomas, Chen‐Plotkin, Alice, Ju Chung, Sun, Clark, Lorraine, Corvol, Jean‐Christophe, Cosentino, Carlos, Cras, Patrick, Crosiers, David, De Michele, Giuseppe, De Rosa, Anna, Erer, Sevda, Ertan, Sibel, Farrer, Matthew, Fiala, Ondrej, Foroud, Tatiana, Friedman, Andrzej, Frigerio, Roberta, Garraux, Gaetan, Gomez‐Esteban, Juan Carlos, Hardy, John, Hassan, Anhar, Hedera, Peter, Hentati, Faycal, Inca‐Martinez, Miguel, Infante, Jon, Jankovic, Joseph, Jesús, Silvia, Kasten, Meike, Kataoka, Hiroshi, Kim, Yun Joong, Koziorowski, Dariusz, Krüger, Rejko, Krygowska‐Wajs, Anna, Kulisevsky, Jaime, Lai, Dongbing, Lang, Anthony, LeDoux, Mark, Lesage, Suzanne, Lim, Shen‐Yang, Lin, Chin‐Hsien, Lopera, Francisco, Lopez, Grisel, Lu, Chin‐Song, Lynch, Tim, Maraganore, Demetrius, Marder, Karen, Mazzetti, Pilar, Mirelman, Anat, Morris, Huw, Naito, Anna, Ozelius, Laurie J., Padmanabhan, Shalini, Paisán‐Ruiz, Coro, Petkovic, Sonja, Petrucci, Simona, Pimentel, Márcia, Pirker, Walter, Pulkes, Teeratorn, Puschmann, Andreas, Quattrone, Aldo, Sammler, Esther, Sazci, Ali, Schrag, Anette, Sharma, Manu, Sidransky, Ellen, Petersen, Maria Skaalum, Sue, Carolyn M., Swan, Matthew, Swanberg, Maria, Taba, Pille, Tan, Manuela, Tan, Ai Huey, Tan, Eng‐King, Tayebi, Nahid, Thaler, Avner, Thomas, Astrid, Toda, Tatsushi, Torres, Luis, Valente, Enza Maria, Van Broeckhoven, Christine, Wood, Nicholas W., Wszolek, Zbigniew K., Wu, Ruey‐Meei, Yoshino, Hiroyo, Zhang, Baorong, Zimprich, Alexander

Get full text

The commercial genetic testing landscape for Parkinson's disease by Cook, Lola, Schulze, Jeanine, Verbrugge, Jennifer, Beck, James C., Marder, Karen S., Saunders-Pullman, Rachel, Klein, Christine, Naito, Anna, Alcalay, Roy N., Brice, Alexis, Kumeh, Amasi, West, Andrew B., Singleton, Andrew, Naito, Anna, Schüle, Birgitt, Fiske, Brian, Gabbert, Carolin, Marras, Connie, Blauwendraat, Cornelis, Thaxton, Courtney, Alessi, Dario, Craig, David, Fon, Edward A., Forbes, Emily, Valente, Enza Maria, Sammler, Esther, Chao, Gill, Riboldi, Giulietta, Elloumi, Houda Zghal, Mata, Ignacio, Beck, James C., Fong, Jamie C., Corvol, Jean-Christophe, Schulze, Jeanine, Verbrugge, Jennifer, Shulman, Joshua, Peterschmitt, Judith, Marder, Karen, Lohmann, Katja, Nudelman, Kelly, Lange, Lara, Cook, Lola, Cookson, Mark R., Nance, Martha, Farrer, Matthew, Grigorian, Melina, Schwarzschild, Michael A., Mencacci, Niccolo, Ross, Owen, Mistry, Pramod, Hodges, Priscila, Blake, Rachel, Saunders-Pullman, Rachel, Alcalay, Roy N., Sardi, S. Pablo, Farhan, Sali, Strom, Samuel, Padmanabhan, Shalini, Mohan, Shruthi, Longerich, Simonne, Schneider, Susanne, Lesage, Suzanne, Bardakjian, Tanya, Foroud, Tatiana, Courtin, Thomas, Tropea, Thomas, Liu, Yunlong, Gan-Or, Ziv, Shalash, Ali S., Hall, Anne, Thaler, Avner, Sue, Carolyn M., Mascalzoni, Deborah, Raymond, Deborah, Gatto, Emilia Mabel, Pal, Gian D., König, Inke, Novakovic, Ivana, Merello, Marcelo, Salari, Mehri, Mencacci, Niccolo Emanuele, Hattori, Nobutaka, Suchowersky, Oksana, Bardien, Soraya, Chung, Sun Ju, Simuni, Tatyana, Lynch, Timothy, Bonifati, Vincenzo

Get full text

eVOC: a controlled vocabulary for unifying gene expression data by Kelso, Janet, Visagie, Johann, Theiler, Gregory, Christoffels, Alan, Bardien, Soraya, Smedley, Damian, Otgaar, Darren, Greyling, Gary, Jongeneel, C Victor, McCarthy, Mark I, Hide, Tania, Hide, Winston

Get full text

Apoptosis-Inducing Signal Sequence Mutation in Carbonic Anhydrase IV Identified in Patients with the RP17 Form of Retinitis Pigmentosa by Rebello, George, Ramesar, Rajkumar, Vorster, Alvera, Roberts, Lisa, Ehrenreich, Liezle, Oppon, Ekow, Gama, Dumisani, Bardien, Soraya, Greenberg, Jacquie, Bonapace, Giuseppe, Waheed, Abdul, Shah, Gul N., Sly, William S.

Get full text

Inherited retinal disorders in South Africa and the clinical impact of evolving technologies : how human genetics came to SA by Bardien, S., Loubser, F., Bartmann, L., Rebello, G., Roberts, L., Ramesar, R.S., September, A.V., Bardien, S., Greenberg, L.J., Goliath, R.

Get full text

An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17q by Bardienb, Soraya, Ebenezer, Neil, Greenberg, Jacquie, Inglehearn, Chris F., Bartmann, Lecia, Goliath, Rene, Beighton, Peter, Ramesar, Rajkumar, Bhattacharya, Shomi S.

Get full text