Systematic Review and UK-Based Study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease
Kilarski, Laura L., Pearson, Justin P., Newsway, Victoria, Majounie, Elisa, Knipe, M. Duleeka W., Misbahuddin, Anjum, Chinnery, Patrick F., Burn, David J., Clarke, Carl E., Marion, Marie-Helene, Lewthwaite, Alistair J., Nicholl, David J., Wood, Nicholas W., Morrison, Karen E., Williams-Gray, Caroline H., Evans, Jonathan R., Sawcer, Stephen J., Barker, Roger A., Wickremaratchi, Mirdhu M., Ben-Shlomo, Yoav, Williams, Nigel M., Morris, Huw R.
Published in Movement disorders (01.10.2012)
Published in Movement disorders (01.10.2012)
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A New Intervention for Implementation of Pharmacogenetics in Psychiatry: A Description of the PSY-PGx Clinical Study
Pelgrim, Teuntje A D, Philipsen, Alexandra, Young, Allan H, Juruena, Mario, Jimenez, Ester, Vieta, Eduard, Jukić, Marin, Van der Eycken, Erik, Heilbronner, Urs, Moldovan, Ramona, Kas, Martien J H, Jagesar, Raj R, Nöthen, Markus M, Hoffmann, Per, Shomron, Noam, Kilarski, Laura L, van Amelsvoort, Thérèse, Campforts, Bea, The Psy-PGx Consortium, van Westrhenen, Roos
Published in Pharmaceuticals (Basel, Switzerland) (2024)
Published in Pharmaceuticals (Basel, Switzerland) (2024)
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Differential effects of severe vs mild GBA mutations on Parkinson disease
Gan-Or, Ziv, Amshalom, Idan, Kilarski, Laura L, Bar-Shira, Anat, Gana-Weisz, Mali, Mirelman, Anat, Marder, Karen, Bressman, Susan, Giladi, Nir, Orr-Urtreger, Avi
Published in Neurology (03.03.2015)
Published in Neurology (03.03.2015)
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Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease
Simón-Sánchez, Javier, Kilarski, Laura L, Nalls, Michael A, Martinez, Maria, Schulte, Claudia, Holmans, Peter, Gasser, Thomas, Hardy, John, Singleton, Andrew B, Wood, Nicholas W, Brice, Alexis, Heutink, Peter, Williams, Nigel, Morris, Huw R
Published in PloS one (12.03.2012)
Published in PloS one (12.03.2012)
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Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12
Kilarski, Laura L, Achterberg, Sefanja, Devan, William J, Traylor, Matthew, Malik, Rainer, Lindgren, Arne, Pare, Guillame, Sharma, Pankaj, Slowik, Agniesczka, Thijs, Vincent, Walters, Matthew, Worrall, Bradford B, Sale, Michele M, Algra, Ale, Kappelle, L Jaap, Wijmenga, Cisca, Norrving, Bo, Sandling, Johanna K, Rönnblom, Lars, Goris, An, Franke, Andre, Sudlow, Cathie, Rothwell, Peter M, Levi, Christopher, Holliday, Elizabeth G, Fornage, Myriam, Psaty, Bruce, Gretarsdottir, Solveig, Thorsteinsdottir, Unnar, Seshadri, Sudha, Mitchell, Braxton D, Kittner, Steven, Clarke, Robert, Hopewell, Jemma C, Bis, Joshua C, Boncoraglio, Giorgio B, Meschia, James, Ikram, M Arfan, Hansen, Bjorn M, Montaner, Joan, Thorleifsson, Gudmar, Stefanson, Kari, Rosand, Jonathan, de Bakker, Paul I W, Farrall, Martin, Dichgans, Martin, Markus, Hugh S, Bevan, Steve
Published in Neurology (19.08.2014)
Published in Neurology (19.08.2014)
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Genetic diagnostics of mental health disorders in adulthood
Kilarski, Laura L, Claus, Isabelle, Binder, Elisabeth B, Degenhardt, Franziska, Domschke, Katharina, Forstner, Andreas J, Grabe, Hans J, Heilbronner, Urs, Müller, Daniel, Nöthen, Markus M, Radtke, Franziska, Rietschel, Marcella, Schulze, Thomas G, Streit, Fabian, Tebartz van Elst, Ludger, Tüscher, Oliver, Deckert, Jürgen, Schulte, Eva C
Published in Nervenarzt (24.09.2024)
Published in Nervenarzt (24.09.2024)
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A novel MMP12 locus is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approach
Traylor, Matthew, Mäkelä, Kari-Matti, Kilarski, Laura L, Holliday, Elizabeth G, Devan, William J, Nalls, Mike A, Wiggins, Kerri L, Zhao, Wei, Cheng, Yu-Ching, Achterberg, Sefanja, Malik, Rainer, Sudlow, Cathie, Bevan, Steve, Raitoharju, Emma, Oksala, Niku, Thijs, Vincent, Lemmens, Robin, Lindgren, Arne, Slowik, Agnieszka, Maguire, Jane M, Walters, Matthew, Algra, Ale, Sharma, Pankaj, Attia, John R, Boncoraglio, Giorgio B, Rothwell, Peter M, de Bakker, Paul I W, Bis, Joshua C, Saleheen, Danish, Kittner, Steven J, Mitchell, Braxton D, Rosand, Jonathan, Meschia, James F, Levi, Christopher, Dichgans, Martin, Lehtimäki, Terho, Lewis, Cathryn M, Markus, Hugh S
Published in PLoS genetics (01.07.2014)
Published in PLoS genetics (01.07.2014)
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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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57. GENETICS MEETS TRANSCRIPTOMICS: EXPRESSION AND SPLICING OUTLIER ANALYSIS IN WHOLE TRANSCRIPTOMES OF INDIVIDUALS WITH SCHIZOPHRENIA
Schulte, Eva, Yepez, Vicente A, Kilarski, Laura L, Claus, Isabelle, Degenhardt, Franziska, Adorjan, Kristina, Budde, Monika, Kalman, Janos L., Papiol, Sergi, Senner, Fanny, Forstner, Andreas J., Heilbronner, Urs, Nöthen, Markus, Gagneur, Julien, Schulze, Thomas
Published in European neuropsychopharmacology (01.10.2024)
Published in European neuropsychopharmacology (01.10.2024)
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Influence of CYP2C19 and CYP2D6 on side effects of aripiprazole and risperidone: A systematic review
de Brabander, Emma, Kleine Schaars, Kristian, van Amelsvoort, Therese, Budde, Monika, Heilbronner, Urs, Young, Allan H., Juruena, Mario, Vieta, Eduard, Fares-Otero, Natalia E., Kas, Martien J., Nöthen, Markus, Philipsen, Alexandra, Kilarski, Laura L., Laatsch, Jonathan, Rossner, Moritz J., Wichert, Sven P., Moldovan, Ramona, Shomron, Noam, Schulze, Thomas G., King Ng, Roger Man, Olisa, Nigel, Van der Eycken, Erik, Pelgrim, Teuntje A.D., van Westrhenen, Roos
Published in Journal of psychiatric research (01.06.2024)
Published in Journal of psychiatric research (01.06.2024)
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Shared genetic contribution to ischemic stroke and Alzheimer's disease
Traylor, Matthew, Adib-Samii, Poneh, Harold, Denise, Dichgans, Martin, Williams, Julie, Lewis, Cathryn M., Markus, Hugh S.
Published in Annals of neurology (01.05.2016)
Published in Annals of neurology (01.05.2016)
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Genetische Diagnostik bei psychischen Erkrankungen im Erwachsenenalter
Kilarski, Laura L., Claus, Isabelle, Binder, Elisabeth B., Degenhardt, Franziska, Domschke, Katharina, Forstner, Andreas J., Grabe, Hans J., Heilbronner, Urs, Müller, Daniel, Nöthen, Markus M., Radtke, Franziska, Rietschel, Marcella, Schulze, Thomas G., Streit, Fabian, Tebartz van Elst, Ludger, Tüscher, Oliver, Deckert, Jürgen, Schulte, Eva C.
Published in Nervenarzt (24.09.2024)
Published in Nervenarzt (24.09.2024)
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A Novel MMP12 Locus Is Associated with Large Artery Atherosclerotic Stroke Using a Genome-Wide Age-at-Onset Informed Approach: e1004469
Traylor, Matthew, Mäkelä, Kari-Matti, Kilarski, Laura L, Holliday, Elizabeth G, Devan, William J, Nalls, Mike A, Wiggins, Kerri L, Zhao, Wei, Cheng, Yu-Ching, Achterberg, Sefanja, Malik, Rainer, Sudlow, Cathie, Bevan, Steve, Raitoharju, Emma, Oksala, Niku, Thijs, Vincent, Lemmens, Robin, Lindgren, Arne, Slowik, Agnieszka, Maguire, Jane M, Walters, Matthew, Algra, Ale, Sharma, Pankaj, Attia, John R, Boncoraglio, Giorgio B, Rothwell, Peter M, Bakker, I Wde, Bis, Joshua C, Saleheen, Danish, Kittner, Steven J, Mitchell, Braxton D, Rosand, Jonathan, Meschia, James F, Levi, Christopher, Dichgans, Martin, Lehtimäki, Terho, Lewis, Cathryn M, Markus, Hugh S, Consortium, International StrokeGenetics
Published in PLoS genetics (01.07.2014)
Published in PLoS genetics (01.07.2014)
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Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
Keller, M. F., Saad, M., Bras, J., Bettella, F., Nicolaou, N., Simon-Sanchez, J., Mittag, F., Buchel, F., Sharma, M., Gibbs, J. R., Schulte, C., Moskvina, V., Durr, A., Holmans, P., Kilarski, L. L., Guerreiro, R., Hernandez, D. G., Brice, A., Ylikotila, P., Stefansson, H., Majamaa, K., Morris, H. R., Williams, N., Gasser, T., Heutink, P., Wood, N. W., Hardy, J., Martinez, M., Singleton, A. B., Nalls, M. A.
Published in Human molecular genetics (15.04.2013)
Published in Human molecular genetics (15.04.2013)
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Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
Keller, M. F., Saad, M., Bras, J., Bettella, F., Nicolaou, N., Simon-Sanchez, J., Mittag, F., chel, F. B., Sharma, M., Gibbs, J. R., Schulte, C., Moskvina, V., Durr, A., Holmans, P., Kilarski, L. L., Guerreiro, R., Hernandez, D. G., Brice, A., Ylikotila, P., Stefansson, H., Majamaa, K., Morris, H. R., Williams, N., Gasser, T., Heutink, P., Wood, N. W., Hardy, J., Martinez, M., Singleton, A. B., Nalls, M. A.
Published in Human molecular genetics (15.07.2013)
Published in Human molecular genetics (15.07.2013)
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