المؤلفون: van Rheenen, Wouter, Shatunov, Aleksey, Dekker, Annelot M, McLaughlin, Russell L, Diekstra, Frank P, Pulit, Sara L, van der Spek, Rick AA, Võsa, Urmo, de Jong, Simone, Robinson, Matthew R, Yang, Jian, Fogh, Isabella, van Doormaal, Perry Tc, Tazelaar, Gijs HP, Koppers, Max, Blokhuis, Anna M, Sproviero, William, Jones, Ashley R, Kenna, Kevin P, van Eijk, Kristel R, Harschnitz, Oliver, Schellevis, Raymond D, Brands, William J, Medic, Jelena, Menelaou, Androniki, Vajda, Alice, Ticozzi, Nicola, Lin, Kuang, Rogelj, Boris, Vrabec, Katarina, Ravnik-Glavač, Metka, Koritnik, Blaž, Zidar, Janez, Leonardis, Lea, Grošelj, Leja Dolenc, Millecamps, Stéphanie, Salachas, François, Meininger, Vincent, de Carvalho, Mamede, Pinto, Susana, Mora, Jesus S, Rojas-García, Ricardo, Polak, Meraida, Chandran, Siddharthan, Colville, Shuna, Swingler, Robert, Morrison, Karen E, Shaw, Pamela J, Hardy, John, Orrell, Richard W, Pittman, Alan, Sidle, Katie, Fratta, Pietro, Malaspina, Andrea, Topp, Simon, Petri, Susanne, Abdulla, Susanne, Drepper, Carsten, Sendtner, Michael, Meyer, Thomas, Ophoff, Roel A, Staats, Kim A, Wiedau-Pazos, Martina, Lomen-Hoerth, Catherine, Van Deerlin, Vivianna M, Trojanowski, John Q, Elman, Lauren, McCluskey, Leo, Basak, A Nazli, Tunca, Ceren, Hamzeiy, Hamid, Parman, Yesim, Meitinger, Thomas, Lichtner, Peter, Radivojkov-Blagojevic, Milena, Andres, Christian R, Maurel, Cindy, Bensimon, Gilbert, Landwehrmeyer, Bernhard, Brice, Alexis, Payan, Christine AM, Saker-Delye, Safaa, Dürr, Alexandra, Wood, Nicholas W, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Rietschel, Marcella, Cichon, Sven, Nöthen, Markus M, Amouyel, Philippe, Tzourio, Christophe, Dartigues, Jean-François, Uitterlinden, Andre G, Rivadeneira, Fernando, Estrada, Karol, Hofman, Albert, Curtis, Charles, Blauw, Hylke M

المصدر: Nature genetics. 48(9)

مصطلحات موضوعية: PARALS Registry, SLALOM Group, SLAP Registry, FALS Sequencing Consortium, SLAGEN Consortium, NNIPPS Study Group, Humans, Amyotrophic Lateral Sclerosis, Genetic Predisposition to Disease, Proteins, Cytoskeletal Proteins, Myelin Proteins, Case-Control Studies, Cohort Studies, Mutation, Netherlands, Munc18 Proteins, Genome-Wide Association Study, Neurosciences, Rare Diseases, Brain Disorders, Biotechnology, Prevention, Human Genome, Neurodegenerative, Genetics, ALS, Aetiology, 2.1 Biological and endogenous factors, Biological Sciences, Medical and Health Sciences, Developmental Biology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/22r175sv

المؤلفون: Schijven, Dick, Geuze, Elbert, Vinkers, Christiaan H., Pulit, Sara L., Schür, Remmelt R., Malgaz, Marie, Bekema, Erwin, Medic, Jelena, van der Kust, Kendrick E., Veldink, Jan H., Boks, Marco P., Vermetten, Eric, Luykx, Jurjen J.

المصدر: In European Neuropsychopharmacology December 2019 29(12):1354-1364

المؤلفون: Lin, Bochao Danae^{Aff1, Aff2, Aff3}, Colas, Fabrice, Nijman, Isaac J., Medic, Jelena, Brands, William, Parr, Jeremy R., van Eijk, Kristel R.^{Aff1, Aff3}, Klauck, Sabine M., Chiocchetti, Andreas G., Freitag, Christine M., Maestrini, Elena, Bacchelli, Elena, Coon, Hilary, Vicente, Astrid, Oliveira, Guiomar, Pagnamenta, Alistair T., Gallagher, Louise, Ennis, Sean, Anney, Richard, Bourgeron, Thomas, Luykx, Jurjen J.^{Aff1, Aff3, Aff17}, Vorstman, Jacob^{Aff1, Aff18, Aff19}

المصدر: Translational Psychiatry. 10(1)

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المؤلفون: Medic, Jelena, Atkinson, Christine, Hurburgh, Jr., Charles R.

المصدر: Journal of the American Oil Chemists' Society. March 2014 91(3):363-384

المؤلفون: Harakalova, Magdalena, Nijman, Isaäc J., Medic, Jelena, Mokry, Michal, Renkens, Ivo, Blankensteijn, Jan D., Kloosterman, Wigard, Baas, Annette F., Cuppen, Edwin

المصدر: Journal of Cardiovascular Translational Research. June 2011 4(3):271-280

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المؤلفون: Okhuijsen-Pfeifer, Cynthia, Ayhan, Yavuz, Lin, Bochao D., van Eijk, Kristel R., Bekema, Erwin, Kool, Lindy J. G. B., Bogers, Jan P. A. M., Muderrisoglu, Ahmet, Babaoglu, Melih O., Van Assche, Evelien, Medic, Jelena, Veerman, Selene, Cohen, Dan, van Beek, Hanneke, de Jonge, Annemieke A. M., Beld, Edwin, Yağcıoğlu, A. Elif Anıl, Luykx, Jurjen J.

المصدر: Schizophrenia Bulletin Open; Jan2020, Vol. 2 Issue 1, p1-9, 9p

مصطلحات موضوعية: CLOZAPINE, ANTIPSYCHOTIC agents, NEUTROPENIA, AGRANULOCYTOSIS, PHARMACOGENOMICS, INDIVIDUALIZED medicine

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