Reus, L M, Pasaniuc, B, Posthuma, D, Boltz, T, Pijnenburg, Y A L, Ophoff, R A & International FTD-Genomics Consortium 2021, ' Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes ', Biological Psychiatry, vol. 89, no. 8, pp. 825-835 . https://doi.org/10.1016/j.biopsych.2020.12.023 Reus, L M, Pasaniuc, B, Posthuma, D, Boltz, T, International FTD-Genomics Consortium, Ferrari, R, Hernandez, D G, Nalls, M A, Rohrer, J D, Ramasamy, A, Kwok, J B J, Dobson-Stone, C, Brooks, W S, Schofield, P R, Halliday, G M, Hodges, J R, Piguet, O, Bartley, L, Thompson, E, Hernández, I, Ruiz, A, Boada, M, Borroni, B, Padovani, A, Cruchaga, C, Cairns, N J, Benussi, L, Binetti, G, Ghidoni, R, Forloni, G, Galimberti, D, Fenoglio, C, Serpente, M, Scarpini, E, Clarimón, J, Lleó, A, Blesa, R, Waldö, M L, Nilsson, K, Nilsson, C, Mackenzie, I R A, Hsiung, G-Y R, Mann, D M A, Grafman, J, Morris, C M, Attems, J, Griffiths, T D, McKeith, I G, Thomas, A J, Pietrini, P, Huey, E D, Wassermann, E M, Baborie, A, Jaros, E, Tierney, M C, Pastor, P, Razquin, C, Ortega-Cubero, S, Alonso, E, Perneczky, R, Diehl-Schmid, J, Alexopoulos, P, Kurz, A, Rainero, I, Rubino, E, Pinessi, L, Rogaeva, E, St. George-Hyslop, P, Rossi, G, Tagliavini, F, Giaccone, G, Rowe, J B, Schlachetzki, J C M, Uphill, J, Collinge, J, Mead, S, Danek, A, van Deerlin, V M, Grossman, M, Trojanowski, J Q, van der Zee, J, van Broeckhoven, C, Cappa, S F, le Ber, I, Hannequin, D, Golfier, V R, Vercelletto, M, Brice, A, Nacmias, B, Sorbi, S, Bagnoli, S, Piaceri, I, Nielsen, J R E, Hjermind, L E, Riemenschneider, M, Mayhaus, M, Ibach, B, Gasparoni, G, Pichler, S, Gu, W, Rossor, M N, Fox, N C, Warren, J D, Spillantini, M G, Morris, H R, Rizzu, P, Heutink, P, Snowden, J S, Rollinson, S, Richardson, A, Gerhard, A, Bruni, A C, Maletta, R, Frangipane, F, Cupidi, C, Bernardi, L, Anfossi, M, Gallo, M, Conidi, M E, Smirne, N, Rademakers, R, Baker, M, Dickson, D W, Graff-Radford, N R, Petersen, R C, Knopman, D, Josephs, K A, Boeve, B F, Parisi, J E, Seeley, W W, Miller, B L, Karydas, A M, Rosen, H, van Swieten, J C, Dopper, E G P, Seelaar, H, Pijnenburg, Y A L, Scheltens, P, Logroscino, G, Capozzo, R, Novelli, V, Puca, A A, Franceschi, M, Postiglione, A, Milan, G, Sorrentino, P, Kristiansen, M, Chiang, H-H, Graff, C, Pasquier, F, Rollin, A, Deramecourt, V, Lebert, F, Kapogiannis, D, Ferrucci, L, Pickering-Brown, S, Singleton, A B, Hardy, J, Momeni, P & Ophoff, R A 2021, ' Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes ', Biological Psychiatry, vol. 89, no. 8, pp. 825-835 . https://doi.org/10.1016/j.biopsych.2020.12.023 Biological Psychiatry, 89(8), 825-835. Elsevier USA Reus, L M, Pasaniuc, B, Posthuma, D, Boltz, T, Ferrari, R, Hernandez, D G, Nalls, M A, Rohrer, J D, Ramasamy, A, Kwok, J B J, Dobson-Stone, C, Brooks, W S, Schofield, P R, Halliday, G M, Hodges, J R, Piguet, O, Bartley, L, Thompson, E, Hernández, I, Ruiz, A, Boada, M, Borroni, B, Padovani, A, Cruchaga, C, Cairns, N J, Benussi, L, Binetti, G, Ghidoni, R, Forloni, G, Galimberti, D, Fenoglio, C, Serpente, M, Scarpini, E, Clarimón, J, Lleó, A, Blesa, R, Waldö, M L, Nilsson, K, Nilsson, C, Mackenzie, I R A, Hsiung, G Y R, Mann, D M A, Grafman, J, Morris, C M, Attems, J, Griffiths, T D, McKeith, I G, Thomas, A J, Pietrini, P, Huey, E D, Wassermann, E M, Baborie, A, Jaros, E, Tierney, M C, Pastor, P, Razquin, C, Ortega-Cubero, S, Alonso, E, Perneczky, R, Diehl-Schmid, J, Alexopoulos, P, Kurz, A, Rainero, I, Rubino, E, Pinessi, L, Rogaeva, E, St. George-Hyslop, P, Rossi, G, Tagliavini, F, Giaccone, G, Rowe, J B, Schlachetzki, J C M, Uphill, J, Collinge, J, Mead, S, Danek, A, Van Deerlin, V M, Grossman, M, Trojanowski, J Q, van der Zee, J, Van Broeckhoven, C, Cappa, S F, Le Ber, I, Hannequin, D, Golfier, V, Vercelletto, M, Brice, A, Nacmias, B, Sorbi, S, Bagnoli, S, Piaceri, I, Nielsen, J E, Hjermind, L E, Riemenschneider, M, Mayhaus, M, Ibach, B, Gasparoni, G, Pichler, S, Gu, W, Rossor, M N, Fox, N C, Warren, J D, Spillantini, M G, Morris, H R, Rizzu, P, Heutink, P, Snowden, J S, Rollinson, S, Richardson, A, Gerhard, A, Bruni, A C, Maletta, R, Frangipane, F, Cupidi, C, Bernardi, L, Anfossi, M, Gallo, M, Conidi, M E, Smirne, N, Rademakers, R, Baker, M, Dickson, D W, Graff-Radford, N R, Petersen, R C, Knopman, D, Josephs, K A, Boeve, B F, Parisi, J E, Seeley, W W, Miller, B L, Karydas, A M, Rosen, H, van Swieten, J C, Dopper, E G P, Seelaar, H, Pijnenburg, Y A L, Scheltens, P, Logroscino, G, Capozzo, R, Novelli, V, Puca, A A, Franceschi, M, Postiglione, A, Milan, G, Sorrentino, P, Kristiansen, M, Chiang, H H, Graff, C, Pasquier, F, Rollin, A, Deramecourt, V, Lebert, F, Kapogiannis, D, Ferrucci, L, Pickering-Brown, S, Singleton, A B, Hardy, J, Momeni, P & Ophoff, R A 2021, ' Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes ', Biological Psychiatry, bind 89, nr. 8, s. 825-835 . https://doi.org/10.1016/j.biopsych.2020.12.023 Biological Psychiatry, 89(8), 825-835. Elsevier Inc.
Scientific reports, vol 10, iss 1 Scientific Reports, 10(1):12184. Nature Publishing Group Scientific reports 10(1), 12184 (2020). doi:10.1038/s41598-020-68848-9 Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020) Gao, Y, Wang, T, Yu, X, Ferrari, R, Hernandez, D G, Nalls, M A, Rohrer, J D, Ramasamy, A, Kwok, J B J, Dobson-Stone, C, Brooks, W S, Schofield, P R, Halliday, G M, Hodges, J R, Piguet, O, Bartley, L, Thompson, E, Haan, E, Hernández, I, Ruiz, A, Boada, M, Borroni, B, Padovani, A, Cruchaga, C, Cairns, N J, Benussi, L, Binetti, G, Ghidoni, R, Forloni, G, Albani, D, Galimberti, D, Fenoglio, C, Serpente, M, Scarpini, E, Clarimón, J, Lleó, A, Blesa, R, Waldö, M L, Nilsson, K, Nilsson, C, Mackenzie, I R A, Hsiung, G Y R, Mann, D M A, Grafman, J, Morris, C M, Attems, J, Griffiths, T D, McKeith, I G, Thomas, A J, Pietrini, P, Huey, E D, Wassermann, E M, Baborie, A, Jaros, E, Tierney, M C, Pastor, P, Razquin, C, Ortega-Cubero, S, Alonso, E, Perneczky, R, Diehl-Schmid, J, Alexopoulos, P, Kurz, A, Rainero, I, Rubino, E, Pinessi, L, Rogaeva, E, George-Hyslop, P S, Rossi, G, Tagliavini, F, Giaccone, G, Rowe, J B, Schlachetzki, J C M, Uphill, J, Collinge, J, Mead, S, Danek, A, Van Deerlin, V M, Grossman, M, Trojanowski, J Q, van der Zee, J, Cruts, M, Van Broeckhoven, C, Cappa, S F, Leber, I, Hannequin, D, Golfier, V, Vercelletto, M, Brice, A, Nacmias, B, Sorbi, S, Bagnoli, S, Piaceri, I, Nielsen, J E, Hjermind, L E, Riemenschneider, M, Mayhaus, M, Ibach, B, Gasparoni, G, Pichler, S, Gu, W, Rossor, M N, Fox, N C, Warren, J D, Spillantini, M G, Morris, H R, Rizzu, P, Heutink, P, Snowden, J S, Rollinson, S, Richardson, A, Gerhard, A, Bruni, A C, Maletta, R, Frangipane, F, Cupidi, C, Bernardi, L, Anfossi, M, Gallo, M, Conidi, M E, Smirne, N, Rademakers, R, Baker, M, Dickson, D W, Graff-Radford, N R, Petersen, R C, Knopman, D, Josephs, K A, Boeve, B F, Parisi, J E, Seeley, W W, Miller, B L, Karydas, A M, Rosen, H, van Swieten, J C, Dopper, E G P, Seelaar, H, Pijnenburg, Y A L, Scheltens, P, Logroscino, G, Capozzo, R, Novelli, V, Puca, A A, Franceschi, M, Postiglione, A, Milan, G, Sorrentino, P, Kristiansen, M, Chiang, H H, Graff, C, Pasquier, F, Rollin, A, Deramecourt, V, Lebouvier, T, Kapogiannis, D, Ferrucci, L, Pickering-Brown, S, Singleton, A B, Hardy, J, Momeni, P, Zhao, H, Zeng, P & International FTD-Genomics Consortium (IFGC) 2020, ' Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis ', Scientific Reports, vol. 10, no. 1, 12184 . https://doi.org/10.1038/s41598-020-68848-9 Scientific Reports r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau instname Gao, Y, Wang, T, Yu, X, Ferrari, R, Hernandez, D G, Nalls, M A, Rohrer, J D, Ramasamy, A, Kwok, J B J, Dobson-Stone, C, Brooks, W S, Schofield, P R, Halliday, G M, Hodges, J R, Piguet, O, Bartley, L, Thompson, E, Haan, E, Hernández, I, Ruiz, A, Boada, M, Borroni, B, Padovani, A, Cruchaga, C, Cairns, N J, Benussi, L, Binetti, G, Ghidoni, R, Forloni, G, Albani, D, Galimberti, D, Fenoglio, C, Serpente, M, Scarpini, E, Clarimón, J, Lleó, A, Blesa, R, Waldö, M L, Nilsson, K, Nilsson, C, Mackenzie, I R A, Hsiung, G Y R, Mann, D M A, Grafman, J, Morris, C M, Attems, J, Griffiths, T D, Rowe, J B, Nielsen, J E, Hjermind, L E & International FTD-Genomics Consortium (IFGC) 2020, ' Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis ', Scientific Reports, vol. 10, no. 1, 12184 . https://doi.org/10.1038/s41598-020-68848-9 Scientific reports
The lancet / Neurology 19(10), 840-848 (2020). doi:10.1016/S1474-4422(20)30273-8 Lancet Neurol 2020; 19: 840?48 UCrea Repositorio Abierto de la Universidad de Cantabria instname Lancet Neurology, 19(10), 840-848. Lancet Publishing Group The Lancet Neurology, 19(10), 840-848. Lancet Publishing Group Jones, E, Hummerich, H, Viré, E, Uphill, J, Dimitriadis, A, Speedy, H, Campbell, T, Norsworthy, P, Quinn, L, Whitfield, J, Linehan, J, Jaunmuktane, Z, Brandner, S, Jat, P, Nihat, A, How Mok, T, Ahmed, P, Collins, S, Stehmann, C, Sarros, S, Kovacs, G G, Geschwind, M D, Golubjatnikov, A, Frontzek, K, Budka, H, Aguzzi, A, Karamujić-Čomić, H, van der Lee, S J, Ibrahim-Verbaas, C A, van Duijn, C M, Sikorska, B, Golanska, E, Liberski, P P, Calero, M, Calero, O, Sanchez-Juan, P, Salas, A, Martinón-Torres, F, Bouaziz-Amar, E, Haïk, S, Laplanche, J-L, Brandel, J-P, Amouyel, P, Lambert, J-C, Parchi, P, Bartoletti-Stella, A, Capellari, S, Poleggi, A, Ladogana, A, Pocchiari, M, Aneli, S, Matullo, G, Knight, R, Zafar, S, Zerr, I, Booth, S, Coulthart, M B, Jansen, G H, Glisic, K, Blevins, J, Gambetti, P, Safar, J, Appleby, B, Collinge, J & Mead, S 2020, ' Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease : a genome-wide association study ', Lancet Neurology, vol. 19, no. 10, pp. 840-848 . https://doi.org/10.1016/S1474-4422(20)30273-8
Nature Genetics Nature Genetics, Nature Publishing Group, 2017, 49 (9), pp.1373-1384. ⟨10.1038/ng.3916⟩ Nature Genetics, 2017, 49 (9), pp.1373-1384. ⟨10.1038/ng.3916⟩ Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid Consejería de Sanidad de la Comunidad de Madrid Sims, R, Van Der Lee, S J, Naj, A C, Bellenguez, C, Badarinarayan, N, Jakobsdottir, J, Kunkle, B W, Boland, A, Raybould, R, Bis, J C, Martin, E R, Grenier-Boley, B, Heilmann-Heimbach, S, Chouraki, V, Kuzma, A B, Sleegers, K, Vronskaya, M, Ruiz, A, Graham, R R, Olaso, R, Hoffmann, P, Grove, M L, Vardarajan, B N, Hiltunen, M, Nöthen, M M, White, C C, Hamilton-Nelson, K L, Epelbaum, J, Maier, W, Choi, S H, Beecham, G W, Dulary, C, Herms, S, Smith, A V, Funk, C C, Derbois, C, Forstner, A J, Ahmad, S, Li, H, Bacq, D, Harold, D, Satizabal, C L, Valladares, O, Squassina, A, Thomas, R, Brody, J A, Qu, L, Sánchez-Juan, P, Morgan, T, Wolters, F J, Zhao, Y, Garcia, F S, Denning, N, Fornage, M, Malamon, J, Naranjo, M C D, Majounie, E, Mosley, T H, Dombroski, B, Wallon, D, Lupton, M K, Dupuis, J, Whitehead, P, Fratiglioni, L, Medway, C, Jian, X, Mukherjee, S, Keller, L, Brown, K, Lin, H, Cantwell, L B, Panza, F, McGuinness, B, Moreno-Grau, S, Burgess, J D, Solfrizzi, V, Proitsi, P, Adams, H H, Allen, M, Seripa, D, Pastor, P, Cupples, L A, Price, N D, Hannequin, D, Frank-García, A, Levy, D, Chakrabarty, P, Caffarra, P, Giegling, I, Beiser, A S, Giedraitis, V, Hampel, H, Garcia, M E, Wang, X, Lannfelt, L, Mecocci, P, Eiriksdottir, G, Crane, P K, Pasquier, F, Boccardi, V, Henández, I, Barber, R C, Scherer, M, Tarraga, L, Adams, P M, Leber, M, Chen, Y, Albert, M S, Riedel-Heller, S, Emilsson, V, Beekly, D, Braae, A, Schmidt, R, Blacker, D, Masullo, C, Schmidt, H, Doody, R S, Spalletta, G, Jr, W T L, Fairchild, T J, Bossù, P, Lopez, O L, Frosch, M P, Sacchinelli, E, Ghetti, B, Yang, Q, Huebinger, R M, Jessen, F, Li, S, Kamboh, M I, Morris, J C, Sotolongo-Grau, O, Katz, M J, Corcoran, C, Dunstan, M, Braddel, A, Thomas, C, Meggy, A, Marshall, R, Gerrish, A, Chapman, J, Aguilar, M, Taylor, S, Hill, M, Fairén, M D, Hodges, A, Vellas, B, Soininen, H, Kloszewska, I, Daniilidou, M, Uphill, J, Patel, Y, Hughes, J T, Lord, J, Turton, J, Hartmann, A M, Cecchetti, R, Fenoglio, C, Serpente, M, Arcaro, M, Caltagirone, C, Orfei, M D, Ciaramella, A, Pichler, S, Mayhaus, M, Gu, W, Lleó, A, Fortea, J, Blesa, R, Barber, I S, Brookes, K, Cupidi, C, Maletta, R G, Carrell, D, Sorbi, S, Moebus, S, Urbano, M, Pilotto, A, Kornhuber, J, Bosco, P, Todd, S, Craig, D, Johnston, J, Gill, M, Lawlor, B, Lynch, A, Fox, N C, Hardy, J, Albin, R L, Apostolova, L G, Arnold, S E, Asthana, S, Atwood, C S, Baldwin, C T, Barnes, L L, Barral, S, Beach, T G, Becker, J T, Bigio, E H, Bird, T D, Boeve, B F, Bowen, J D, Boxer, A, Burke, J R, Burns, J M, Buxbaum, J D, Cairns, N J, Cao, C, Carlson, C S, Carlsson, C M, Carney, R M, Carrasquillo, M M, Carroll, S L, Diaz, C C, Chui, H C, Clark, D G, Cribbs, D H, Crocco, E A, Decarli, C, Dick, M, Duara, R, Evans, D A, Faber, K M, Fallon, K B, Fardo, D W, Farlow, M R, Ferris, S, Foroud, T M, Galasko, D R, Gearing, M, Geschwind, D H, Gilbert, J R, Graff-Radford, N R, Green, R C, Growdon, J H, Hamilton, R L, Harrell, L E, Honig, L S, Huentelman, M J, Hulette, C M, Hyman, B T, Jarvik, G P, Abner, E, Jin, L W, Jun, G, Karydas, A, Kaye, J A, Kim, R, Kowall, N W, Kramer, J H, Laferla, F M, Lah, J J, Leverenz, J B, Levey, A I, Li, G, Lieberman, A P, Lunetta, K L, Lyketsos, C G, Marson, D C, Martiniuk, F, Mash, D C, Masliah, E, McCormick, W C, McCurry, S M, McDavid, A N, McKee, A C, Mesulam, M, Miller, B L, Miller, C A, Miller, J W, Morris, J C, Murrell, J R, Myers, A J, O'Bryant, S, Olichney, J M, Pankratz, V S, Parisi, J E, Paulson, H L, Perry, W, Peskind, E, Pierce, A, Poon, W W, Potter, H, Quinn, J F, Raj, A, Raskind, M, Reisberg, B, Reitz, C, Ringman, J M, Roberson, E D, Rogaeva, E, Rosen, H J, Rosenberg, R N, Sager, M A, Saykin, A J, Schneider, J A, Schneider, L S, Seeley, W W, Smith, A G, Sonnen, J A, Spina, S, Stern, R A, Swerdlow, R H, Tanzi, R E, Thornton-Wells, T A, Trojanowski, J Q, Troncoso, J C, Van Deerlin, V M, Van Eldik, L J, Vinters, H V, Vonsattel, J P, Weintraub, S, Welsh-Bohmer, K A, Wilhelmsen, K C, Williamson, J, Wingo, T S, Woltjer, R L, Wright, C B, Yu, C E, Yu, L, Garzia, F, Golamaully, F, Septier, G, Engelborghs, S, Vandenberghe, R, De Deyn, P P, Fernadez, C M, Benito, Y A, Thonberg, H, Forsell, C, Lilius, L, Kinhult-Stählbom, A, Kilander, L, Brundin, R, Concari, L, Helisalmi, S, Koivisto, A M, Haapasalo, A, Dermecourt, V, Fievet, N, Hanon, O, Dufouil, C, Brice, A, Ritchie, K, Dubois, B, Himali, J J, Keene, C D, Tschanz, J, Fitzpatrick, A L, Kukull, W A, Norton, M, Aspelund, T, Larson, E B, Munger, R, Rotter, J I, Lipton, R B, Bullido, M J, Hofman, A, Montine, T J, Coto, E, Boerwinkle, E, Petersen, R C, Alvarez, V, Rivadeneira, F, Reiman, E M, Gallo, M, O'Donnell, C J, Reisch, J S, Bruni, A C, Royall, D R, Dichgans, M, Sano, M, Galimberti, D, St George-Hyslop, P, Scarpini, E, Tsuang, D W, Mancuso, M, Bonuccelli, U, Winslow, A R, Daniele, A, Wu, C K, Peters, O, Nacmias, B, Riemenschneider, M, Heun, R, Brayne, C, Rubinsztein, D C, Bras, J, Guerreiro, R, Al-Chalabi, A, Shaw, C E, Collinge, J, Mann, D, Tsolaki, M, Clarimón, J, Sussams, R, Lovestone, S, O'Donovan, M C, Owen, M J, Behrens, T W, Mead, S, Goate, A M, Uitterlinden, A G, Holmes, C, Cruchaga, C, Ingelsson, M, Bennett, D A, Powell, J, Golde, T E, Graff, C, De Jager, P L, Morgan, K, Ertekin-Taner, N, Combarros, O, Psaty, B M, Passmore, P, Younkin, S G, Berr, C, Gudnason, V, Rujescu, D, Dickson, D W, Dartigues, J F, Destefano, A L, Ortega-Cubero, S, Hakonarson, H, Campion, D, Boada, M, Kauwe, J K, Farrer, L A, Van Broeckhoven, C, Ikram, M A, Jones, L, Haines, J L, Tzourio, C, Launer, L J, Escott-Price, V, Mayeux, R, Deleuze, J F, Amin, N, Holmans, P A, Pericak-Vance, M A, Amouyel, P, Van Duijn, C M, Ramirez, A, Wang, L S, Lambert, J C, Seshadri, S, Williams, J & Schellenberg, G D 2017, ' Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease ', Nature Genetics, vol. 49, no. 9, pp. 1373-1384 . https://doi.org/10.1038/ng.3916 Nature Genetics, 49(9), 1373-+. Nature Publishing Group Nature genetics 49(9), 1373-1384 (2017). doi:10.1038/ng.3916 Sims, R, van der Lee, S J, Naj, A C, Bellenguez, C, Badarinarayan, N, Jakobsdottir, J, Kunkle, B W, Boland, A, Raybould, R, Bis, J C, Martin, E R, Grenier-Boley, B, Heilmann-Heimbach, S, Chouraki, V, Kuzma, A B, Sleegers, K, Vronskaya, M, Ruiz, A, Graham, R R, Olaso, R, Hoffmann, P, Grove, M L, Vardarajan, B N, Hiltunen, M, Nöthen, M M, White, C C, Hamilton-Nelson, K L, Epelbaum, J, Maier, W, Choi, S-H, Beecham, G W, Dulary, C, Herms, S, Smith, A V, Funk, C C, Derbois, C, Forstner, A J, Ahmad, S, Li, H, Bacq, D, Harold, D, Satizabal, C L, Valladares, O, Lupton, M K, Proitsi, P, Hodges, A, Patel, Y, Al-Chalabi, A, Shaw, C E, Powell, J 2017, ' Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease ', Nature Genetics, vol. 49, pp. 1373-1384 . https://doi.org/10.1038/ng.3916 Nature genetics Nature Genetics, 49(9), 1373-1384. Nature Publishing Group NATURE GENETICS r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau instname