Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

Cited by (254)

Items 101–200 of 254

1. Retinal vascular biomarkers for early detection and monitoring of Alzheimer’s disease
   Frost, S, Kanagasingam, Y, Sohrabi, H, Vignarajan, J, Bourgeat, P, Salvado, O, Villemagne, V, Rowe, C C, Lance Macaulay, S, Szoeke, C et al. · 2013 · Translational Psychiatry
2. Glial activation and inflammation along the Alzheimer’s disease continuum
   Nordengen, Kaja, Kirsebom, Bjørn-Eivind, Henjum, Kristi, Selnes, Per, Gísladóttir, Berglind, Wettergreen, Marianne, Torsetnes, Silje Bøen, Grøntvedt, Gøril Rolfseng, Waterloo, Knut K., Aarsland, Dag et al. · 2019 · Journal of Neuroinflammation
3. The low-density lipoprotein receptor-related protein 1 and amyloid-β clearance in Alzheimer’s disease
   Kanekiyo, Takahisa, Bu, Guojun · 2014 · Frontiers in Aging Neuroscience
4. Microglial genes regulating neuroinflammation in the progression of Alzheimer's disease
   Villegas-Llerena, Claudio, Phillips, Alexandra, Garcia-Reitboeck, Pablo, Hardy, John, Pocock, Jennifer M · 2016 · Current Opinion in Neurobiology
5. Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation
   Bis, Joshua C., Jian, Xueqiu, Kunkle, Brian W., Chen, Yuning, Hamilton-Nelson, Kara L., Bush, William S., Salerno, William J., Lancour, Daniel, Ma, Yiyi, Renton, Alan E. et al. · 2020 · Molecular Psychiatry
6. Risk prediction of late-onset Alzheimer’s disease implies an oligogenic architecture
   Zhang, Qian, Sidorenko, Julia, Couvy-Duchesne, Baptiste, Marioni, Riccardo E., Wright, Margaret J., Goate, Alison M., Marcora, Edoardo, Huang, Kuan-lin, Porter, Tenielle, Laws, Simon M. et al. · 2020 · Nature Communications
7. WNT signaling in neuronal maturation and synaptogenesis
   Rosso, Silvana B., Inestrosa, Nibaldo C. · 2013 · Frontiers in Cellular Neuroscience
8. Mosaic Loss of Chromosome y in Blood Is Associated with Alzheimer Disease
   Dumanski, Jan P., Lambert, Jean-Charles, Rasi, Chiara, Giedraitis, Vilmantas, Davies, Hanna, Grenier-Boley, Benjamin, Lindgren, Cecilia M., Campion, Dominique, Dufouil, Carole, Pasquier, Florence et al. · 2016 · The American Journal of Human Genetics
9. CD33 Alzheimer’s risk-altering polymorphism, CD33 expression, and exon 2 splicing
   Malik, Manasi, Simpson, James F., Parikh, Ishita, Wilfred, Bernard R., Fardo, David W., Nelson, Peter T., Estus, Steven · 2013 · The Journal of Neuroscience
10. Epigenetic regulation in the pathophysiology of Alzheimer's disease
    Chouliaras, Leonidas, Rutten, Bart P.F., Kenis, Gunter, Peerbooms, Odette, Visser, Pieter Jelle, Verhey, Frans, van Os, Jim, Steinbusch, Harry W.M., van den Hove, Daniel L.A. · 2010 · Progress in Neurobiology
11. Low‐density lipoprotein receptor‐related protein‐1: a serial clearance homeostatic mechanism controlling Alzheimer’s amyloid β‐peptide elimination from the brain
    Zlokovic, Berislav V., Deane, Rashid, Sagare, Abhay P., Bell, Robert D., Winkler, Ethan A. · 2010 · Journal of Neurochemistry
12. Genetics of familial and sporadic Alzheimer s disease
    Piaceri, Irene · 2013 · Frontiers in Bioscience
13. Lipid and Lipoprotein Metabolism in Microglia
    Loving, Bailey A., Bruce, Kimberley D. · 2020 · Frontiers in Physiology
14. Neurovascular Dysfunction and Faulty Amyloid  -Peptide Clearance in Alzheimer Disease
    Sagare, A. P., Bell, R. D., Zlokovic, B. V. · 2012 · Cold Spring Harbor Perspectives in Medicine
15. Age-related macular degeneration (AMD): Alzheimer's disease in the eye?
    Kaarniranta, Kai, Salminen, Antero, Haapasalo, Annakaisa, Soininen, Hilkka, Hiltunen, Mikko · 2011 · Journal of Alzheimer s Disease
16. Wnt signaling deregulation in the aging and Alzheimer’s brain
    Palomer, Ernest, Buechler, Johanna, Salinas, Patricia C. · 2019 · Frontiers in Cellular Neuroscience
17. Concerted changes in transcripts in the prefrontal cortex precede neuropathology in Alzheimer's disease
    Bossers, Koen, Wirz, Kerstin T.S., Meerhoff, Gideon F., Essing, Anke H.W., van Dongen, Jeroen W., Houba, Pieter, Kruse, Chris G., Verhaagen, Joost, Swaab, Dick F. · 2010 · Brain
18. Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals
    Corneveaux, Jason J., Myers, Amanda J., Allen, April N., Pruzin, Jeremy J., Ramirez, Manuel, Engel, Anzhelika, Nalls, Michael A., Chen, Kewei, Lee, Wendy, Chewning, Kendria et al. · 2010 · Human Molecular Genetics
19. Untangling Genetic Risk for Alzheimer’s Disease
    Pimenova, Anna A., Raj, Towfique, Goate, Alison M. · 2018 · Biological Psychiatry
20. Targeting the Synapse in Alzheimer’s Disease
    Jackson, Johanna, Jambrina, Enrique, Li, Jennifer, Marston, Hugh, Menzies, Fiona, Phillips, Keith, Gilmour, Gary · 2019 · Frontiers in Neuroscience
21. Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites
    Brouwers, N, Van Cauwenberghe, C, Engelborghs, S, Lambert, J-C, Bettens, K, Le Bastard, N, Pasquier, F, Montoya, A Gil, Peeters, K, Mattheijssens, M et al. · 2012 · Molecular Psychiatry
22. Is Alzheimer’s disease a systemic disease?
    Morris, Jill K., Honea, Robyn A., Vidoni, Eric D., Swerdlow, Russell H., Burns, Jeffrey M. · 2014 · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
23. Genetic Variation and Neuroimaging Measures in Alzheimer Disease
    Biffi, Alessandro · 2010 · Archives of Neurology
24. Microglia and Astrocytes in Disease: Dynamic Duo or Partners in Crime?
    Liddelow, Shane A., Marsh, Samuel E., Stevens, Beth · 2020 · Trends in Immunology
25. Genetics of Alzheimer’s disease: where we are, and where we are going
    Bellenguez, Céline, Grenier-Boley, Benjamin, Lambert, Jean-Charles · 2020 · Current Opinion in Neurobiology
26. Alzheimer’s disease is associated with altered expression of genes involved in immune response and mitochondrial processes in astrocytes
    Sekar, Shobana, McDonald, Jacquelyn, Cuyugan, Lori, Aldrich, Jessica, Kurdoglu, Ahmet, Adkins, Jonathan, Serrano, Geidy, Beach, Thomas G., Craig, David W., Valla, Jonathan et al. · 2015 · Neurobiology of Aging
27. Plasma clusterin and the risk of Alzheimer disease
    Schrijvers, Elisabeth M. C. · 2011 · JAMA
28. Vascular disruption and blood–brain barrier dysfunction in intracerebral hemorrhage
    Keep, Richard F, Zhou, Ningna, Xiang, Jianming, Andjelkovic, Anuska V, Hua, Ya, Xi, Guohua · 2014 · Fluids and Barriers of the CNS
29. Gene–environment interactions in Alzheimer disease: the emerging role of epigenetics
    Migliore, Lucia, Coppedè, Fabio · 2022 · Nature Reviews Neurology
30. Complement in the pathogenesis of Alzheimer’s disease
    Morgan, B. Paul · 2018 · Seminars in Immunopathology
31. Microglial Phagocytosis: A Disease-Associated Process Emerging from Alzheimer’s Disease Genetics
    Podleśny-Drabiniok, Anna, Marcora, Edoardo, Goate, Alison M. · 2020 · Trends in Neurosciences
32. Replication of CLU, CR1, and PICALM Associations With Alzheimer Disease
    Carrasquillo, Minerva M., Belbin, Olivia, Hunter, Talisha A., Ma, Li, Bisceglio, Gina D., Zou, Fanggeng, Crook, Julia E., Pankratz, V. Shane, Dickson, Dennis W., Graff-Radford, Neill R. et al. · 2010 · Archives of Neurology
33. Molecular Mechanisms and Genetics of Oxidative Stress in Alzheimer’s Disease
    Cioffi, Federica, Adam, Rayan Hassan Ibrahim, Broersen, Kerensa · 2019 · Journal of Alzheimer s Disease
34. <i>Porphyromonas gingivalis</i> Periodontal Infection and Its Putative Links with Alzheimer’s Disease
    Singhrao, Sim K., Harding, Alice, Poole, Sophie, Kesavalu, Lakshmyya, Crean, StJohn · 2015 · Mediators of Inflammation
35. Genome-wide association study of the rate of cognitive decline in Alzheimer’s disease
    Sherva, Richard, Tripodis, Yorghos, Bennett, David A., Chibnik, Lori B., Crane, Paul K., de Jager, Philip L., Farrer, Lindsay A., Saykin, Andrew J., Shulman, Joshua M., Naj, Adam et al. · 2014 · Alzheimer's &amp; Dementia
36. Next generation transcriptomics and genomics elucidate biological complexity of microglia in health and disease
    Wes, Paul D., Holtman, Inge R., Boddeke, Erik W.G.M., Möller, Thomas, Eggen, Bart J.L. · 2016 · Glia
37. Psychedelic N,N-Dimethyltryptamine and 5-Methoxy-N,N-Dimethyltryptamine Modulate Innate and Adaptive Inflammatory Responses through the Sigma-1 Receptor of Human Monocyte-Derived Dendritic Cells
    Szabo, Attila, Kovacs, Attila, Frecska, Ede, Rajnavolgyi, Eva · 2014 · PLoS ONE
38. Identification of novel loci for Alzheimer disease and replication of CLU, PICALM, and BIN1 in Caribbean Hispanic individuals
    Lee, Joseph H., Cheng, Rong, Barral, Sandra, Reitz, Christiane, Medrano, Martin, Lantigua, Rafael, Jiménez-Velazquez, Ivonne Z., Rogaeva, Ekaterina, St. George-Hyslop, Peter H., Mayeux, Richard · 2011 · Archives of Neurology
39. Young microglia restore amyloid plaque clearance of aged microglia
    Daria, Anna, Colombo, Alessio, Llovera, Gemma, Hampel, Heike, Willem, Michael, Liesz, Arthur, Haass, Christian, Tahirovic, Sabina · 2017 · The EMBO Journal
40. Targeting microglia for the treatment of Alzheimer’s Disease
    Wes, Paul D., Sayed, Faten A., Bard, Frédérique, Gan, Li · 2016 · Glia
41. NEBULA is a fast negative binomial mixed model for differential or co-expression analysis of large-scale multi-subject single-cell data
    He, Liang, Davila-Velderrain, Jose, Sumida, Tomokazu S., Hafler, David A., Kellis, Manolis, Kulminski, Alexander M. · 2021 · Communications Biology
42. Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls
    Bellenguez, Céline, Charbonnier, Camille, Grenier-Boley, Benjamin, Quenez, Olivier, Le Guennec, Kilan, Nicolas, Gaël, Chauhan, Ganesh, Wallon, David, Rousseau, Stéphane, Richard, Anne Claire et al. · 2017 · Neurobiology of Aging
43. TREM2 in CNS homeostasis and neurodegenerative disease
    Painter, Meghan M., Atagi, Yuka, Liu, Chia-Chen, Rademakers, Rosa, Xu, Huaxi, Fryer, John D., Bu, Guojun · 2015 · Molecular Neurodegeneration
44. <i>CR1</i> is associated with amyloid plaque burden and age‐related cognitive decline
    Chibnik, Lori B., Shulman, Joshua M., Leurgans, Sue E., Schneider, Julie A., Wilson, Robert S., Tran, Dong, Aubin, Cristin, Buchman, Aron S., Heward, Christopher B., Myers, Amanda J. et al. · 2011 · Annals of Neurology
45. Effect of the Mediterranean diet on cognition and brain morphology and function: a systematic review of randomized controlled trials
    Radd-Vagenas, Sue, Duffy, Shantel L, Naismith, Sharon L, Brew, Bruce J, Flood, Victoria M, Fiatarone Singh, Maria A · 2018 · The American Journal of Clinical Nutrition
46. Developing novel blood‐based biomarkers for Alzheimer's disease
    Snyder, Heather M., Carrillo, Maria C., Grodstein, Francine, Henriksen, Kim, Jeromin, Andreas, Lovestone, Simon, Mielke, Michelle M., O'Bryant, Sid, Sarasa, Manual, Sj⊘gren, Magnus et al. · 2014 · Alzheimer's &amp; Dementia
47. Transcriptomics Profiling of Alzheimer’s Disease Reveal Neurovascular Defects, Altered Amyloid-β Homeostasis, and Deregulated Expression of Long Noncoding RNAs
    Magistri, Marco, Velmeshev, Dmitry, Makhmutova, Madina, Faghihi, Mohammad Ali · 2015 · Journal of Alzheimer's Disease
48. Correlating familial Alzheimer’s disease gene mutations with clinical phenotype
    Ryan, Natalie S, Rossor, Martin N · 2010 · Biomarkers in Medicine
49. Defining Alzheimer as a common age-related neurodegenerative process not inevitably leading to dementia
    Ferrer, Isidro · 2012 · Progress in Neurobiology
50. PU.1 regulates Alzheimer’s disease-associated genes in primary human microglia
    Rustenhoven, Justin, Smith, Amy M., Smyth, Leon C., Jansson, Deidre, Scotter, Emma L., Swanson, Molly E. V., Aalderink, Miranda, Coppieters, Natacha, Narayan, Pritika, Handley, Renee et al. · 2018 · Molecular Neurodegeneration
51. APOE-related risk of mild cognitive impairment and dementia for prevention trials: An analysis of four cohorts
    Qian, Jing, Wolters, Frank J., Beiser, Alexa, Haan, Mary, Ikram, M. Arfan, Karlawish, Jason, Langbaum, Jessica B., Neuhaus, John M., Reiman, Eric M., Roberts, J. Scott et al. · 2017 · PLOS Medicine
52. The new genetic landscape of Alzheimer’s disease: from amyloid cascade to genetically driven synaptic failure hypothesis?
    Dourlen, Pierre, Kilinc, Devrim, Malmanche, Nicolas, Chapuis, Julien, Lambert, Jean-Charles · 2019 · Acta Neuropathologica
53. A review of quality of life after predictive testing for and earlier identification of neurodegenerative diseases
    Paulsen, Jane S., Nance, Martha, Kim, Ji-In, Carlozzi, Noelle E., Panegyres, Peter K., Erwin, Cheryl, Goh, Anita, McCusker, Elizabeth, Williams, Janet K. · 2013 · Progress in Neurobiology
54. Glycoprotein NMB: a novel Alzheimer’s disease associated marker expressed in a subset of activated microglia
    Hüttenrauch, Melanie, Ogorek, Isabella, Klafki, Hans, Otto, Markus, Stadelmann, Christine, Weggen, Sascha, Wiltfang, Jens, Wirths, Oliver · 2018 · Acta Neuropathologica Communications
55. Role of Phosphatidylinositol Clathrin Assembly Lymphoid-Myeloid Leukemia (PICALM) in Intracellular Amyloid Precursor Protein (APP) Processing and Amyloid Plaque Pathogenesis
    Xiao, Qingli, Gil, So-Chon, Yan, Ping, Wang, Yan, Han, Sharon, Gonzales, Ernie, Perez, Ronaldo, Cirrito, John R., Lee, Jin-Moo · 2012 · Journal of Biological Chemistry
56. Wnts in adult brain: from synaptic plasticity to cognitive deficiencies
    Oliva, Carolina A., Vargas, Jessica Y., Inestrosa, Nibaldo C. · 2013 · Frontiers in Cellular Neuroscience
57. More than cholesterol transporters: lipoprotein receptors in CNS function and neurodegeneration
    Lane-Donovan, Courtney, Philips, Gary T., Herz, Joachim · 2014 · Neuron
58. Genetics ignite focus on microglial inflammation in Alzheimer’s disease
    Malik, Manasi, Parikh, Ishita, Vasquez, Jared B., Smith, Conor, Tai, Leon, Bu, Guojun, LaDu, Mary Jo, Fardo, David W., Rebeck, G. William, Estus, Steven · 2015 · Molecular Neurodegeneration
59. Prostaglandin signaling suppresses beneficial microglial function in Alzheimer’s disease models
    Johansson, Jenny U., Woodling, Nathaniel S., Wang, Qian, Panchal, Maharshi, Liang, Xibin, Trueba-Saiz, Angel, Brown, Holden D., Mhatre, Siddhita D., Loui, Taylor, Andreasson, Katrin I. · 2015 · Journal of Clinical Investigation
60. Microglial TYROBP/DAP12 in Alzheimer's Disease: Transduction of Physiological and Pathological Signals Across TREM2
    Haure-Mirande, Jean-Vianney, Audrain, Mickael, Ehrlich, Michelle E., Gandy, Sam · 2022 · Molecular Neurodegeneration
61. Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer’s disease
    Furney, S J, Simmons, A, Breen, G, Pedroso, I, Lunnon, K, Proitsi, P, Hodges, A, Powell, J, Wahlund, L-O, Kloszewska, I et al. · 2011 · Molecular Psychiatry
62. Plasma levels of apolipoprotein <scp>E</scp> and risk of dementia in the general population
    Rasmussen, Katrine L., Tybjærg‐Hansen, Anne, Nordestgaard, Børge G., Frikke‐Schmidt, Ruth · 2015 · Annals of Neurology
63. New roles for Fc receptors in neurodegeneration-the impact on Immunotherapy for Alzheimer's Disease
    Fuller, James P., Stavenhagen, Jeffrey B., Teeling, Jessica L. · 2014 · Frontiers in Neuroscience
64. Inflammatory pathways in Alzheimer’s disease mediated by gut microbiota
    Qian, Xiao-hang, Song, Xiao-xuan, Liu, Xiao-li, Chen, Sheng-di, Tang, Hui-dong · 2021 · Ageing Research Reviews
65. Mutations in ABCA7 in a Belgian cohort of Alzheimer's disease patients: a targeted resequencing study
    Cuyvers, Elise, De Roeck, Arne, Van den Bossche, Tobi, Van Cauwenberghe, Caroline, Bettens, Karolien, Vermeulen, Steven, Mattheijssens, Maria, Peeters, Karin, Engelborghs, Sebastiaan, Vandenbulcke, Mathieu et al. · 2015 · The Lancet Neurology
66. Rare coding mutations identified by sequencing of <scp>A</scp>lzheimer disease genome‐wide association studies loci
    Vardarajan, Badri N., Ghani, Mahdi, Kahn, Amanda, Sheikh, Stephanie, Sato, Christine, Barral, Sandra, Lee, Joseph H., Cheng, Rong, Reitz, Christiane, Lantigua, Rafael et al. · 2015 · Annals of Neurology
67. Post-mortem analysis of neuroinflammatory changes in human Alzheimer’s disease
    Gomez-Nicola, Diego, Boche, Delphine · 2015 · Alzheimer's Research &amp; Therapy
68. Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer’s disease
    Stein, Jason L., Hua, Xue, Morra, Jonathan H., Lee, Suh, Hibar, Derrek P., Ho, April J., Leow, Alex D., Toga, Arthur W., Sul, Jae Hoon, Kang, Hyun Min et al. · 2010 · NeuroImage
69. Implication of the Immune System in Alzheimer's Disease: Evidence from Genome-Wide Pathway Analysis
    Lambert, Jean-Charles, Grenier-Boley, Benjamin, Chouraki, Vincent, Heath, Simon, Zelenika, Diana, Fievet, Nathalie, Hannequin, Didier, Pasquier, Florence, Hanon, Olivier, Brice, Alexis et al. · 2010 · Journal of Alzheimer's Disease
70. Human iPSC‐derived microglia: A growing toolset to study the brain's innate immune cells
    Hasselmann, Jonathan, Blurton‐Jones, Mathew · 2020 · Glia
71. ATP-binding cassette transporter A1: From metabolism to neurodegeneration
    Koldamova, Radosveta, Fitz, Nicholas F., Lefterov, Iliya · 2014 · Neurobiology of Disease
72. Microglial complement receptor 3 regulates brain Aβ levels through secreted proteolytic activity
    Czirr, Eva, Castello, Nicholas A., Mosher, Kira I., Castellano, Joseph M., Hinkson, Izumi V., Lucin, Kurt M., Baeza-Raja, Bernat, Ryu, Jae Kyu, Li, Lulin, Farina, Sasha N. et al. · 2017 · Journal of Experimental Medicine
73. Higher CSF sTREM2 and microglia activation are associated with slower rates of beta-amyloid accumulation
    Ewers, Michael, Biechele, Gloria, Suárez‐Calvet, Marc, Sacher, Christian, Blume, Tanja, Morenas‐Rodriguez, Estrella, Deming, Yuetiva, Piccio, Laura, Cruchaga, Carlos, Kleinberger, Gernot et al. · 2020 · EMBO Molecular Medicine
74. Complement receptor 1 (CR1) and Alzheimer's disease
    Crehan, Helen, Holton, Patrick, Wray, Selina, Pocock, Jennifer, Guerreiro, Rita, Hardy, John · 2012 · Immunobiology
75. DAP12 stabilizes the C-terminal fragment of the triggering receptor expressed on myeloid cells-2 (TREM2) and protects against LPS-induced pro-inflammatory response
    Zhong, Li, Chen, Xiao-Fen, Zhang, Zhen-Lian, Wang, Zhe, Shi, Xin-Zhen, Xu, Kai, Zhang, Yun-Wu, Xu, Huaxi, Bu, Guojun · 2015 · Journal of Biological Chemistry
76. Sex differences in metabolic aging of the brain: insights into female susceptibility to Alzheimer's disease
    Zhao, Liqin, Mao, Zisu, Woody, Sarah K., Brinton, Roberta D. · 2016 · Neurobiology of Aging
77. The pursuit of susceptibility genes for Alzheimer's disease: progress and prospects
    Sleegers, Kristel, Lambert, Jean-Charles, Bertram, Lars, Cruts, Marc, Amouyel, Philippe, Van Broeckhoven, Christine · 2010 · Trends in Genetics
78. Targeting innate immunity for neurodegenerative disorders of the central nervous system
    Andreasson, Katrin I., Bachstetter, Adam D., Colonna, Marco, Ginhoux, Florent, Holmes, Clive, Lamb, Bruce, Landreth, Gary, Lee, Daniel C., Low, Donovan, Lynch, Marina A. et al. · 2016 · Journal of Neurochemistry
79. Opposing Effects of Membrane-Anchored CX3CL1 on Amyloid and Tau Pathologies via the p38 MAPK Pathway
    Lee, Sungho, Xu, Guixiang, Jay, Taylor R., Bhatta, Sabina, Kim, Ki-Wook, Jung, Steffen, Landreth, Gary E., Ransohoff, Richard M., Lamb, Bruce T. · 2014 · The Journal of Neuroscience
80. Genetic architecture of Alzheimer's disease
    Neuner, Sarah M., TCW, Julia, Goate, Alison M. · 2020 · Neurobiology of Disease
81. Tracking neuroinflammation in Alzheimer’s disease: the role of positron emission tomography imaging
    Zimmer, Eduardo Rigon, Leuzy, Antoine, Benedet, Andréa Lessa, Breitner, John, Gauthier, Serge, Rosa-Neto, Pedro · 2014 · Journal of Neuroinflammation
82. APOE genotype and sex affect microglial interactions with plaques in Alzheimer’s disease mice
    Stephen, T. L., Cacciottolo, M., Balu, D., Morgan, T. E., LaDu, M. J., Finch, C. E., Pike, C. J. · 2019 · Acta Neuropathologica Communications
83. Roles of Microglial and Monocyte Chemokines and Their Receptors in Regulating Alzheimer's Disease-Associated Amyloid-β and Tau Pathologies
    Guedes, Joana R., Lao, Taotao, Cardoso, Ana L., El Khoury, Joseph · 2018 · Frontiers in Neurology
84. Distribution and Expression of Picalm in Alzheimer Disease
    Baig, Shabnam, Joseph, Sally A., Tayler, Hannah, Abraham, Richard, Owen, Michael J., Williams, Julie, Kehoe, Patrick G., Love, Seth · 2010 · Journal of Neuropathology &amp; Experimental Neurology
85. Alzheimer’s disease risk polymorphisms regulate gene expression in the ZCWPW1 and the CELF1 loci
    Karch, Celeste M., Ezerskiy, Lubov A., Bertelsen, Sarah, Alzheimer’s Disease Genetics Consortium (ADGC), Goate, Alison M. · 2016 · PLoS ONE
86. Transcriptome-wide piRNA profiling in human brains of Alzheimer's disease
    Qiu, Wenying, Guo, Xiaoyun, Lin, Xiandong, Yang, Qian, Zhang, Wanying, Zhang, Yong, Zuo, Lingjun, Zhu, Yong, Li, Chiang-Shan R., Ma, Chao et al. · 2017 · Neurobiology of Aging
87. PICALM and Alzheimer’s Disease: An Update and Perspectives
    Ando, Kunie, Nagaraj, Siranjeevi, Küçükali, Fahri, de Fisenne, Marie-Ange, Kosa, Andreea-Claudia, Doeraene, Emilie, Lopez Gutierrez, Lidia, Brion, Jean-Pierre, Leroy, Karelle · 2022 · Cells
88. Apolipoprotein E isoforms and regulation of the innate immune response in brain of patients with Alzheimer's disease
    Keene, C Dirk, Cudaback, Eiron, Li, Xianwu, Montine, Kathleen S, Montine, Thomas J · 2011 · Current Opinion in Neurobiology
89. Neuroinflammation in Alzheimer’s disease wanes with age
    Hoozemans, Jeroen JM, Rozemuller, Annemieke JM, van Haastert, Elise S, Eikelenboom, Piet, van Gool, Willem A · 2011 · Journal of Neuroinflammation
90. Genome-wide association analysis of age-at-onset in Alzheimer's disease
    Kamboh, M I, Barmada, M M, Demirci, F Y, Minster, R L, Carrasquillo, M M, Pankratz, V S, Younkin, S G, Saykin, A J, The Alzheimer's Disease Neuroimaging Initiative, Sweet, R A et al. · 2012 · Molecular Psychiatry
91. Amyloid PET in clinical practice: Its place in the multidimensional space of Alzheimer's disease
    Vandenberghe, Rik, Adamczuk, Katarzyna, Dupont, Patrick, Laere, Koen Van, Chételat, Gaël · 2013 · NeuroImage: Clinical
92. Blockage of CR1 prevents activation of rodent microglia
    Crehan, Helen, Hardy, John, Pocock, Jennifer · 2013 · Neurobiology of Disease
93. Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer’s disease resilience
    for the Alzheimer’s Disease Neuroimaging Initiative, Ridge, Perry G., Karch, Celeste M., Hsu, Simon, Arano, Ivan, Teerlink, Craig C., Ebbert, Mark T. W., Gonzalez Murcia, Josue D., Farnham, James M., Damato, Anna R. et al. · 2017 · Genome Medicine
94. Effect of Complement CR1 on Brain Amyloid Burden During Aging and Its Modification by APOE Genotype
    Thambisetty, Madhav, An, Yang, Nalls, Michael, Sojkova, Jitka, Swaminathan, Shanker, Zhou, Yun, Singleton, Andrew B., Wong, Dean F., Ferrucci, Luigi, Saykin, Andrew J. et al. · 2013 · Biological Psychiatry
95. Follow-up of loci from the International Genomics of Alzheimer’s Disease Project identifies TRIP4 as a novel susceptibility gene
    Ruiz, A, Heilmann, S, Becker, T, Hernández, I, Wagner, H, Thelen, M, Mauleón, A, Rosende-Roca, M, Bellenguez, C, Bis, J C et al. · 2014 · Translational Psychiatry
96. Reelin protects against amyloid β toxicity in vivo
    Lane-Donovan, Courtney, Philips, Gary T., Wasser, Catherine R., Durakoglugil, Murat S., Masiulis, Irene, Upadhaya, Ajeet, Pohlkamp, Theresa, Coskun, Cagil, Kotti, Tiina, Steller, Laura et al. · 2015 · Science Signaling
97. Lesions without symptoms: understanding resilience to Alzheimer disease neuropathological changes
    Gómez-Isla, Teresa, Frosch, Matthew P. · 2022 · Nature Reviews Neurology
98. Analysis of the Putative Role of CR1 in Alzheimer’s Disease: Genetic Association, Expression and Function
    Fonseca, Maria I., Chu, Shuhui, Pierce, Aimee L., Brubaker, William D., Hauhart, Richard E., Mastroeni, Diego, Clarke, Elizabeth V., Rogers, Joseph, Atkinson, John P., Tenner, Andrea J. · 2016 · PLOS ONE
99. An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer’s disease
    On Behalf of the BELNEU Consortium, De Roeck, Arne, Duchateau, Lena, Van Dongen, Jasper, Cacace, Rita, Bjerke, Maria, Van den Bossche, Tobi, Cras, Patrick, Vandenberghe, Rik, De Deyn, Peter P. et al. · 2018 · Acta Neuropathologica
100. Genome-wide association reveals genetic effects on human Aβ 42 and τ protein levels in cerebrospinal fluids: a case control study
     Han, Mi-Ryung, Schellenberg, Gerard D, Wang, Li-San, the Alzheimer's Disease Neuroimaging Initiative · 2010 · BMC Neurology