Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study
Noyce, Alastair J, Kia, Demis A, Hemani, Gibran, Nicolas, Aude, Price, T Ryan, De Pablo-Fernandez, Eduardo, Haycock, Philip C, Lewis, Patrick A, Foltynie, Thomas, Davey Smith, George, Schrag, Anette, Lees, Andrew J, Hardy, John, Singleton, Andrew, Nalls, Mike A, Pearce, Neil, Lawlor, Debbie A, Wood, Nicholas W
Published in PLoS medicine (13.06.2017)
Published in PLoS medicine (13.06.2017)
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Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study
Nalls, Mike A, PhD, McLean, Cory Y, PhD, Rick, Jacqueline, PhD, Eberly, Shirley, MS, Hutten, Samantha J, PhD, Gwinn, Katrina, MD, Sutherland, Margaret, PhD, Martinez, Maria, PhD, Heutink, Peter, PhD, Williams, Nigel M, PhD, Hardy, John, PhD, Gasser, Thomas, MD, Brice, Alexis, MD, Price, T Ryan, MS, Nicolas, Aude, PhD, Keller, Margaux F, PhD, Molony, Cliona, PhD, Gibbs, J Raphael, MS, Chen-Plotkin, Alice, MD, Suh, Eunran, PhD, Letson, Christopher, BS, Fiandaca, Massimo S, MD, Mapstone, Mark, PhD, Federoff, Howard J, MD, Noyce, Alastair J, MRCP, Morris, Huw, MD, Van Deerlin, Vivianna M, MD, Weintraub, Daniel, MD, Zabetian, Cyrus, MD, Hernandez, Dena G, MS, Lesage, Suzanne, PhD, Mullins, Meghan, BA, Conley, Emily Drabant, PhD, Northover, Carrie A M, PhD, Frasier, Mark, PhD, Marek, Ken, MD, Day-Williams, Aaron G, PhD, Stone, David J, PhD, Ioannidis, John P A, Prof, Singleton, Andrew B, Dr
Published in Lancet neurology (01.10.2015)
Published in Lancet neurology (01.10.2015)
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CADPS functional mutations in patients with bipolar disorder increase the sensitivity to stress
Sitbon, Jérémy, Nestvogel, Dennis, Kappeler, Caroline, Nicolas, Aude, Maciuba, Stephanie, Henrion, Annabelle, Troudet, Réjane, Courtois, Elisa, Grannec, Gaël, Latapie, Violaine, Barau, Caroline, Le Corvoisier, Philippe, Pietrancosta, Nicolas, Henry, Chantal, Leboyer, Marion, Etain, Bruno, Nosten-Bertrand, Marika, Martin, Thomas F. J., Rhee, JeongSeop, Jamain, Stéphane
Published in Molecular psychiatry (01.02.2022)
Published in Molecular psychiatry (01.02.2022)
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Common and rare variant analysis in early-onset bipolar disorder vulnerability
Jamain, Stéphane, Cichon, Sven, Etain, Bruno, Mühleisen, Thomas W, Georgi, Alexander, Zidane, Nora, Chevallier, Lucie, Deshommes, Jasmine, Nicolas, Aude, Henrion, Annabelle, Degenhardt, Franziska, Mattheisen, Manuel, Priebe, Lutz, Mathieu, Flavie, Kahn, Jean-Pierre, Henry, Chantal, Boland, Anne, Zelenika, Diana, Gut, Ivo, Heath, Simon, Lathrop, Mark, Maier, Wolfgang, Albus, Margot, Rietschel, Marcella, Schulze, Thomas G, McMahon, Francis J, Kelsoe, John R, Hamshere, Marian, Craddock, Nicholas, Nöthen, Markus M, Bellivier, Frank, Leboyer, Marion
Published in PloS one (11.08.2014)
Published in PloS one (11.08.2014)
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Genetic discovery and risk characterization in type 2 diabetes across diverse populations
Polfus, Linda M., Darst, Burcu F., Highland, Heather, Sheng, Xin, Ng, Maggie C.Y., Below, Jennifer E., Petty, Lauren, Bien, Stephanie, Sim, Xueling, Wang, Wei, Fontanillas, Pierre, Patel, Yesha, Preuss, Michael, Schurmann, Claudia, Du, Zhaohui, Lu, Yingchang, Rhie, Suhn K., Mercader, Joseph M., Tusie-Luna, Teresa, González-Villalpando, Clicerio, Orozco, Lorena, Spracklen, Cassandra N., Cade, Brian E., Jensen, Richard A., Sun, Meng, Joo, Yoonjung Yoonie, An, Ping, Yanek, Lisa R., Bielak, Lawrence F., Tajuddin, Salman, Nicolas, Aude, Chen, Guanjie, Raffield, Laura, Guo, Xiuqing, Chen, Wei-Min, Nadkarni, Girish N., Graff, Mariaelisa, Tao, Ran, Pankow, James S., Daviglus, Martha, Qi, Qibin, Boerwinkle, Eric A., Liu, Simin, Phillips, Lawrence S., Peters, Ulrike, Carlson, Chris, Wikens, Lynne R., Le Marchand, Loic, North, Kari E., Buyske, Steven, Kooperberg, Charles, Loos, Ruth J.F., Stram, Daniel O., Haiman, Christopher A.
Published in HGG advances (08.04.2021)
Published in HGG advances (08.04.2021)
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Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets
Kia, Demis A, Zhang, David, Guelfi, Sebastian, Manzoni, Claudia, Hubbard, Leon, Reynolds, Regina H, Botía, Juan, Ryten, Mina, Ferrari, Raffaele, Lewis, Patrick A, Williams, Nigel, Trabzuni, Daniah, Hardy, John, Wood, Nicholas W
Published in Archives of neurology (Chicago) (01.04.2021)
Published in Archives of neurology (Chicago) (01.04.2021)
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Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
Lesage, Suzanne, Deramecourt, Vincent, Jacoupy, Maxime, Hassoun, Sidi Mohamed, Pujol, Claire, Maurage, Claude-Alain, Sahbatou, Mourad, Liebau, Stefan, Bilgic, Basar, Emre, Murat, Erginel-Unaltuna, Nihan, Guven, Gamze, Tison, François, Tranchant, Christine, Corvol, Jean-Christophe, Krack, Paul, Hernandez, Dena G., Gibbs, J. Raphael, Hardy, John, Wood, Nicholas W., Durr, Alexandra, Deleuze, Jean-François, Tazir, Meriem, Destée, Alain, Lohmann, Ebba, Corti, Olga, Brice, Alexis, Lesage, Suzanne, Tison, François, Vidailhet, Marie, Corvol, Jean-Christophe, Agid, Yves, Anheim, Mathieu, Bonnet, Anne-Marie, Borg, Michel, Broussolle, Emmanuel, Durif, Franck, Krack, Paul, Klebe, Stephan, Lohmann, Ebba, Vérin, Marc, Viallet, François, Brice, Alexis, Majounie, Elisa, Corvol, Jean Christophe, Ben-Shlomo, Yoav, Berg, Daniela, Bhatia, Kailash, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M., Brockmann, Kathrin, Burn, David J., Chen, Honglei, Clarke, Carl E., Cookson, Mark R., Counsell, Carl, van Dijk, Karin D., Dong, Jing, Escott-Price, Valentina, Evans, Jonathan R., Gray, Emma, Guerreiro, Rita, van Hilten, Jacobus J., Hollenbeck, Albert, Holmans, Peter, Hu, Michèle, Hudson, Gavin, Hunt, Sarah E., Kilarski, Laura L., Jansen, Iris E., Langford, Cordelia, Lees, Andrew, Lorenz, Delia, Lubbe, Steven, Lungu, Codrin, Martinez, María, Mätzler, Walter, McNeill, Alisdair, Moorby, Catriona, O’Sullivan, Sean S., Pearson, Justin, Ravina, Bernard, Rivadeneira, Fernando, Ryten, Mina, Schapira, Anthony, Sharma, Manu, Sheerin, Una-Marie, Sidransky, Ellen, Spencer, Chris C.A., Stefánsson, Kári, Strange, Amy, Talbot, Kevin, Trabzuni, Daniah, Uitterlinden, André G., van de Warrenburg, Bart, Williams-Gray, Caroline H., Winder-Rhodes, Sophie, Hardy, John, Wood, Nicholas W.
Published in American journal of human genetics (03.03.2016)
Published in American journal of human genetics (03.03.2016)
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Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis
Noyce, Alastair J., Hemani, Gibran, Mora, Gabriele, Bartolomei, Ilaria, Benigni, Michele, Borghero, Giuseppe, Brunetti, Maura, Calvo, Andrea, Cammarosano, Stefania, Cannas, Antonino, Caponnetto, Claudia, Casale, Federico, Cavallaro, Sebastiano, Chiò, Adriano, Colletti, Tiziana, Conforti, Francesca L., Conte, Amelia, Corrado, Lucia, Costantino, Emanuela, D'Alfonso, Sandra, Femiano, Cinzia, Ferrarese, Carlo, Fini, Nicola, Floris, Gianluca, Grassano, Maurizio, Lattante, Serena, Logroscino, Giancarlo, Loi, Daniela, Mancardi, Gianluigi, Mandich, Paola, Manera, Umberto, Marinou, Kalliopi, Marrali, Giuseppe, Marrosu, Maria Giovanna, Mazzini, Letizia, Melis, Maurizio, Messina, Sonia, Mora, Gabriele, Occhineri, Patrizia, Origone, Paola, Pani, Carla, Petrucci, Antonio, Pirisi, Angelo, Restagno, Gabriella, Ricci, Claudia, Riva, Nilo, Sabatelli, Mario, Santarelli, Marialuisa, Spataro, Rossella, Tanel, Raffaella, Tremolizzo, Lucio, Volanti, Paolo, Zollino, Marcella, Arepalli, Sampath, Bowser, Robert, Broach, James, Camu, William, Chia, Ruth, Chiò, Adriano, Ding, Jinhui, Dunckley, Travis L., Eicher, John D., Faghri, Faraz, Feldman, Eva, Fratta, Pietro, Geiger, Joshua T., Gerhard, Glenn, Hardy, John, Harms, Matthew B., Heiman‐Patterson, Terry D., Kamel, Freya, MacGowan, Daniel J.L., Maragakis, Nicholas J., Murphy, Natalie A., Myllykangas, Liisa, Nalls, Mike A., Nicolas, Aude, Orrell, Richard W., Pamphlett, Roger, Pickering‐Brown, Stuart, Pioro, Erik, Pliner, Hannah A., Pulst, Stefan M., Ravits, John M., Rothstein, Jeffrey D., Salvi, Erika, Sendtner, Michael, Simmons, Zachary, Stone, David C., Sulkava, Raimo, Troncoso, Juan C., Van Damme, Philip, Van Deerlin, Vivianna M., Van Den Bosch, Ludo, Zinman, Lorne, Tienari, Pentti J., Stone, David J., Nalls, Mike A., Singleton, Andrew B., Traynor, Bryan J.
Published in Annals of neurology (01.04.2019)
Published in Annals of neurology (01.04.2019)
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Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease
Lesage, Suzanne, Bras, Jose, Cormier-Dequaire, Florence, Condroyer, Christel, Nicolas, Aude, Darwent, Lee, Guerreiro, Rita, Majounie, Elisa, Federoff, Monica, Heutink, Peter, Wood, Nicholas W, Gasser, Thomas, Hardy, John, Tison, François, Singleton, Andrew, Brice, Alexis
Published in Neurology. Genetics (01.06.2015)
Published in Neurology. Genetics (01.06.2015)
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NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases
Blauwendraat, Cornelis, Faghri, Faraz, Pihlstrom, Lasse, Geiger, Joshua T, Elbaz, Alexis, Lesage, Suzanne, Corvol, Jean-Christophe, May, Patrick, Nicolas, Aude, Abramzon, Yevgeniya, Murphy, Natalie A, Gibbs, J. Raphael, Ryten, Mina, Ferrari, Raffaele, Bras, Jose, Guerreiro, Rita, Williams, Julie, Sims, Rebecca, Lubbe, Steven, Hernandez, Dena G, Mok, Kin Y, Robak, Laurie, Campbell, Roy H, Rogaeva, Ekaterina, Traynor, Bryan J, Chia, Ruth, Chung, Sun Ju, Hardy, John A, Brice, Alexis, Wood, Nicholas W, Houlden, Henry, Shulman, Joshua M, Morris, Huw R, Gasser, Thomas, Krüger, Rejko, Heutink, Peter, Sharma, Manu, Simón-Sánchez, Javier, Nalls, Mike A, Singleton, Andrew B, Scholz, Sonja W
Published in Neurobiology of aging (01.09.2017)
Published in Neurobiology of aging (01.09.2017)
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De novo mutations in HCN1 cause early infantile epileptic encephalopathy
Nava, Caroline, Dalle, Carine, Rastetter, Agnès, Striano, Pasquale, de Kovel, Carolien G F, Nabbout, Rima, Cancès, Claude, Ville, Dorothée, Brilstra, Eva H, Gobbi, Giuseppe, Raffo, Emmanuel, Bouteiller, Delphine, Marie, Yannick, Trouillard, Oriane, Robbiano, Angela, Keren, Boris, Agher, Dahbia, Roze, Emmanuel, Lesage, Suzanne, Nicolas, Aude, Brice, Alexis, Baulac, Michel, Vogt, Cornelia, El Hajj, Nady, Schneider, Eberhard, Suls, Arvid, Weckhuysen, Sarah, Gormley, Padhraig, Lehesjoki, Anna-Elina, De Jonghe, Peter, Helbig, Ingo, Baulac, Stéphanie, Zara, Federico, Koeleman, Bobby P C, Haaf, Thomas, LeGuern, Eric, Depienne, Christel
Published in Nature genetics (01.06.2014)
Published in Nature genetics (01.06.2014)
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Mendelian randomization study shows no causal relationship between circulating urate levels and Parkinson's disease
Kia, Demis A., Noyce, Alastair J., White, Jon, Speed, Doug, Nicolas, Aude, Burgess, Stephen, Lawlor, Debbie A., Davey Smith, George, Singleton, Andrew, Nalls, Mike A., Sofat, Reecha, Wood, Nicholas W.
Published in Annals of neurology (01.08.2018)
Published in Annals of neurology (01.08.2018)
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Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders
Mencacci, Niccolò E, Reynolds, Regina, Ruiz, Sonia Garcia, Vandrovcova, Jana, Forabosco, Paola, Sánchez-Ferrer, Alvaro, Volpato, Viola, Weale, Michael E, Bhatia, Kailash P, Webber, Caleb, Hardy, John, Botía, Juan A, Ryten, Mina
Published in Brain (London, England : 1878) (01.09.2020)
Published in Brain (London, England : 1878) (01.09.2020)
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Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance
Lubbe, Steven J, Escott-Price, Valentina, Gibbs, J Raphael, Nalls, Mike A, Bras, Jose, Price, T Ryan, Nicolas, Aude, Jansen, Iris E, Mok, Kin Y, Pittman, Alan M, Tomkins, James E, Lewis, Patrick A, Noyce, Alastair J, Lesage, Suzanne, Sharma, Manu, Schiff, Elena R, Levine, Adam P, Brice, Alexis, Gasser, Thomas, Hardy, John, Heutink, Peter, Wood, Nicholas W, Singleton, Andrew B, Williams, Nigel M, Morris, Huw R
Published in Human molecular genetics (15.12.2016)
Published in Human molecular genetics (15.12.2016)
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