المؤلفون: van der Lee, Sven J, Conway, Olivia J, Jansen, Iris, Carrasquillo, Minerva M, Kleineidam, Luca, van den Akker, Erik, Hernández, Isabel, van Eijk, Kristel R, Stringa, Najada, Chen, Jason A, Zettergren, Anna, Andlauer, Till FM, Diez-Fairen, Monica, Simon-Sanchez, Javier, Lleó, Alberto, Zetterberg, Henrik, Nygaard, Marianne, Blauwendraat, Cornelis, Savage, Jeanne E, Mengel-From, Jonas, Moreno-Grau, Sonia, Wagner, Michael, Fortea, Juan, Keogh, Michael J, Blennow, Kaj, Skoog, Ingmar, Friese, Manuel A, Pletnikova, Olga, Zulaica, Miren, Lage, Carmen, de Rojas, Itziar, Riedel-Heller, Steffi, Illán-Gala, Ignacio, Wei, Wei, Jeune, Bernard, Orellana, Adelina, Then Bergh, Florian, Wang, Xue, Hulsman, Marc, Beker, Nina, Tesi, Niccolo, Morris, Christopher M, Indakoetxea, Begoña, Collij, Lyduine E, Scherer, Martin, Morenas-Rodríguez, Estrella, Ironside, James W, van Berckel, Bart NM, Alcolea, Daniel, Wiendl, Heinz, Strickland, Samantha L, Pastor, Pau, Rodríguez Rodríguez, Eloy, DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementia), Netherlands Brain Bank (NBB), Boeve, Bradley F, Petersen, Ronald C, Ferman, Tanis J, van Gerpen, Jay A, Reinders, Marcel JT, Uitti, Ryan J, Tárraga, Lluís, Maier, Wolfgang, Dols-Icardo, Oriol, Kawalia, Amit, Dalmasso, Maria Carolina, Boada, Mercè, Zettl, Uwe K, van Schoor, Natasja M, Beekman, Marian, Allen, Mariet, Masliah, Eliezer, de Munain, Adolfo López, Pantelyat, Alexander, Wszolek, Zbigniew K, Ross, Owen A, Dickson, Dennis W, Graff-Radford, Neill R, Knopman, David, Rademakers, Rosa, Lemstra, Afina W, Pijnenburg, Yolande AL, Scheltens, Philip, Gasser, Thomas, Chinnery, Patrick F, Hemmer, Bernhard, Huisman, Martijn A, Troncoso, Juan, Moreno, Fermin, Nohr, Ellen A, Sørensen, Thorkild IA, Heutink, Peter, Sánchez-Juan, Pascual, Posthuma, Danielle, GIFT (Genetic Investigation in Frontotemporal Dementia and Alzheimer’s Disease) Study Group, Clarimón, Jordi

المصدر: Acta neuropathologica. 139(5)

مصطلحات موضوعية: DESGESCO, EADB, IFGC, IPDGC, RiMod-FTD, Netherlands Brain Bank, GIFT (Genetic Investigation in Frontotemporal Dementia and Alzheimer’s Disease) Study Group, Acquired Cognitive Impairment, Brain Disorders, Neurodegenerative, Alzheimer's Disease, Dementia, Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), Neurosciences, Aging, Parkinson's Disease, Genetics, 2.1 Biological and endogenous factors, Neurological, Neurology & Neurosurgery, Clinical Sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/6np4j59kTest

المؤلفون: Ayer, Ariane H, Wojta, Kevin, Ramos, Eliana Marisa, Dokuru, Deepika, Chen, Jason A, Karydas, Anna M, Papatriantafyllou, John D, Agiomyrgiannakis, Dimitrios, Kamtsadeli, Vasiliki, Tsinia, Niki, Sali, Dimitra, Gylys, Karen H, Agosta, Federica, Filippi, Massimo, Small, Gary W, Bennett, David A, Gearing, Marla, Juncos, Jorge L, Kramer, Joel, Lee, Suzee E, Yokoyama, Jennifer S, Mendez, Mario F, Chui, Helena, Zarow, Chris, Ringman, John M, Kilic, Ulkan, Babacan-Yildiz, Gülsen, Levey, Allan, DeCarli, Charles S, Cotman, Carl W, Boxer, Adam L, Miller, Bruce L, Coppola, Giovanni

المصدر: Alzheimer Disease & Associated Disorders. 33(4)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Biological Psychology, Clinical Sciences, Neurosciences, Psychology, Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), Alzheimer's Disease Related Dementias (ADRD), Neurodegenerative, Brain Disorders, Alzheimer's Disease, Acquired Cognitive Impairment, Dementia, Rare Diseases, Frontotemporal Dementia (FTD), Aging, Aetiology, 2.1 Biological and endogenous factors, Neurological, Aged, Alzheimer Disease, Amyotrophic Lateral Sclerosis, Cognitive Dysfunction, Cohort Studies, Female, Frontotemporal Dementia, Genetic Predisposition to Disease, Genetic Variation, Genotype, Humans, Internationality, Male, Membrane Glycoproteins, Neurodegenerative Diseases, Receptors, Immunologic, Alzheimer disease, frontotemporal dementia, genetics, TREM2, progressive supranuclear palsy, mild cognitive impairment, corticobasal syndrome, amyotrophic lateral sclerosis, association study, Cognitive Sciences, Geriatrics, Clinical sciences, Biological psychology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/0xx7h0m7Test
https://escholarship.org/content/qt0xx7h0m7/qt0xx7h0m7.pdfTest

المؤلفون: van der Lee, Sven J, Conway, Olivia J, Jansen, Iris, Carrasquillo, Minerva M, Kleineidam, Luca, van den Akker, Erik, Hernández, Isabel, van Eijk, Kristel R, Stringa, Najada, Chen, Jason A, Zettergren, Anna, Andlauer, Till FM, Diez-Fairen, Monica, Simon-Sanchez, Javier, Lleó, Alberto, Zetterberg, Henrik, Nygaard, Marianne, Blauwendraat, Cornelis, Savage, Jeanne E, Mengel-From, Jonas, Moreno-Grau, Sonia, Wagner, Michael, Fortea, Juan, Keogh, Michael J, Blennow, Kaj, Skoog, Ingmar, Friese, Manuel A, Pletnikova, Olga, Zulaica, Miren, Lage, Carmen, de Rojas, Itziar, Riedel-Heller, Steffi, Illán-Gala, Ignacio, Wei, Wei, Jeune, Bernard, Orellana, Adelina, Then Bergh, Florian, Wang, Xue, Hulsman, Marc, Beker, Nina, Tesi, Niccolo, Morris, Christopher M, Indakoetxea, Begoña, Collij, Lyduine E, Scherer, Martin, Morenas-Rodríguez, Estrella, Ironside, James W, van Berckel, Bart NM, Alcolea, Daniel, Wiendl, Heinz, Strickland, Samantha L, Pastor, Pau, Rodríguez Rodríguez, Eloy, Boeve, Bradley F, Petersen, Ronald C, Ferman, Tanis J, van Gerpen, Jay A, Reinders, Marcel JT, Uitti, Ryan J, Tárraga, Lluís, Maier, Wolfgang, Dols-Icardo, Oriol, Kawalia, Amit, Dalmasso, Maria Carolina, Boada, Mercè, Zettl, Uwe K, van Schoor, Natasja M, Beekman, Marian, Allen, Mariet, Masliah, Eliezer, de Munain, Adolfo López, Pantelyat, Alexander, Wszolek, Zbigniew K, Ross, Owen A, Dickson, Dennis W, Graff-Radford, Neill R, Knopman, David, Rademakers, Rosa, Lemstra, Afina W, Pijnenburg, Yolande AL, Scheltens, Philip, Gasser, Thomas, Chinnery, Patrick F, Hemmer, Bernhard, Huisman, Martijn A, Troncoso, Juan, Moreno, Fermin, Nohr, Ellen A, Sørensen, Thorkild IA, Heutink, Peter, Sánchez-Juan, Pascual, Posthuma, Danielle, Clarimón, Jordi, Christensen, Kaare, Ertekin-Taner, Nilüfer, Scholz, Sonja W, Ramirez, Alfredo, Ruiz, Agustín, Slagboom, Eline, van der Flier, Wiesje M

المصدر: Acta Neuropathologica. 138(2)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Neurosciences, Rare Diseases, Acquired Cognitive Impairment, Alzheimer's Disease, Neurodegenerative, Alzheimer's Disease Related Dementias (ADRD), Brain Disorders, Dementia, Clinical Research, Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), Prevention, Aging, Genetics, Aetiology, 2.1 Biological and endogenous factors, Neurological, Alleles, Alzheimer Disease, Amyotrophic Lateral Sclerosis, Brain, Frontotemporal Dementia, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Lewy Body Disease, Longevity, Microglia, Multiple Sclerosis, Mutation, Neuroimaging, Parkinson Disease, Phospholipase C gamma, Risk, Alzheimer's disease, Frontotemporal dementia, Dementia with Lewy bodies, Progressive supranuclear palsy, Parkinson's disease, Amyotrophic lateral sclerosis, Multiple sclerosis, Neurodegenerative disease, PLCG2, Phospholipase C Gamma 2, DESGESCO (Dementia Genetics Spanish Consortium), EADB, EADB, IFGC (International FTD-Genomics Consortium), IPDGC, IPDGC, RiMod-FTD, Netherlands Brain Bank, GIFT (Genetic Investigation in Frontotemporal Dementia and Alzheimer’s Disease) Study Group, Alzheimer’s disease, Parkinson’s disease, frontotemporal dementia, dementia with Lewy-bodies, progressive suprauclear palsy, Parkinson's Disease, amyotrophic lateral sclerosis, multiple sclerosis, neurodegenerative disease, longevity, Clinical Sciences, Neurology & Neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/4w15z00tTest

المؤلفون: Chen, Zhongbo, Chen, Jason A, Shatunov, Aleksey, Jones, Ashley R, Kravitz, Stephanie N, Huang, Alden Y, Lawrence, Lauren, Lowe, Jennifer K, Lewis, Cathryn M, Payan, Christine AM, Lieb, Wolfgang, Franke, Andre, Deloukas, Panagiotis, Amouyel, Philippe, Tzourio, Christophe, Dartigues, Jean‐François, Groups, NNIPPS and BBBIPPS Study, Ludolph, Albert, Bensimon, Gilbert, Leigh, P Nigel, Bronstein, Jeff M, Coppola, Giovanni, Geschwind, Daniel H, Al‐Chalabi, Ammar

المصدر: Movement Disorders. 34(7)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Neurosciences, Clinical Sciences, Prevention, Clinical Research, Neurodegenerative, Genetics, Brain Disorders, Rare Diseases, Genetic Testing, Human Genome, Aetiology, 2.1 Biological and endogenous factors, Neurological, Adult, Age of Onset, Aged, Aged, 80 and over, DNA Copy Number Variations, Female, Genome-Wide Association Study, Genotype, Humans, Male, Middle Aged, Polymorphism, Single Nucleotide, Supranuclear Palsy, Progressive, tau Proteins, copy number variation, genome-wide association study, progressive supranuclear palsy, NNIPPS and BBBIPPS Study Groups, Human Movement and Sports Sciences, Neurology & Neurosurgery, Clinical sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/1fg3g3t6Test

المؤلفون: Chen, Jason A, Chen, Zhongbo, Won, Hyejung, Huang, Alden Y, Lowe, Jennifer K, Wojta, Kevin, Yokoyama, Jennifer S, Bensimon, Gilbert, Leigh, P Nigel, Payan, Christine, Shatunov, Aleksey, Jones, Ashley R, Lewis, Cathryn M, Deloukas, Panagiotis, Amouyel, Philippe, Tzourio, Christophe, Dartigues, Jean-Francois, Ludolph, Albert, Boxer, Adam L, Bronstein, Jeff M, Al-Chalabi, Ammar, Geschwind, Daniel H, Coppola, Giovanni

المصدر: Molecular neurodegeneration. 13(1)

مصطلحات موضوعية: Humans, Supranuclear Palsy, Progressive, Neurodegenerative Diseases, Genetic Predisposition to Disease, Genotype, Polymorphism, Single Nucleotide, Female, Male, Genome-Wide Association Study, Genome-wide association study, Neurodegeneration, Progressive supranuclear palsy, Supranuclear Palsy, Progressive, Polymorphism, Single Nucleotide, Prevention, Clinical Trials and Supportive Activities, Neurodegenerative, Rare Diseases, Genetics, Human Genome, Clinical Research, 2.1 Biological and endogenous factors, Neurological, Clinical Sciences, Neurosciences, Neurology & Neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/79n4d1xnTest

المؤلفون: Chen, Jason A, Fears, Scott C, Jasinska, Anna J, Huang, Alden, Al‐Sharif, Noor B, Scheibel, Kevin E, Dyer, Thomas D, Fagan, Anne M, Blangero, John, Woods, Roger, Jorgensen, Matthew J, Kaplan, Jay R, Freimer, Nelson B, Coppola, Giovanni

المصدر: Brain and Behavior. 8(2)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Biological Psychology, Clinical Sciences, Neurosciences, Psychology, Aging, Genetics, Acquired Cognitive Impairment, Dementia, Human Genome, Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), Biotechnology, Brain Disorders, Alzheimer's Disease, Neurodegenerative, Aetiology, 2.1 Biological and endogenous factors, Neurological, Alzheimer Disease, Amyloid beta-Peptides, Animals, Biomarkers, Brain, Cerebral Amyloid Angiopathy, Chlorocebus aethiops, Chromosomes, Mammalian, Female, Genetic Linkage, Genome-Wide Association Study, Male, Models, Animal, Monkey Diseases, Neurodegenerative Diseases, Neuroimaging, Organ Size, Pedigree, Peptide Fragments, tau Proteins, Alzheimer's disease, amyloid beta, cerebral amyloid angiopathy, cerebrospinal fluid, tau, vervet, Cognitive Sciences, Clinical sciences, Biological psychology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/9d54j8gxTest

المؤلفون: Lopez, Ana, Lee, Suzee E, Wojta, Kevin, Ramos, Eliana Marisa, Klein, Eric, Chen, Jason, Boxer, Adam L, Gorno-Tempini, Maria Luisa, Geschwind, Daniel H, Schlotawa, Lars, Ogryzko, Nikolay V, Bigio, Eileen H, Rogalski, Emily, Weintraub, Sandra, Mesulam, Marsel M, Consortium, Tauopathy Genetics, Fleming, Angeleen, Coppola, Giovanni, Miller, Bruce L, Rubinsztein, David C

المصدر: Brain. 140(4)

مصطلحات موضوعية: Health Sciences, Neurosciences, Dementia, Alzheimer's Disease, Rare Diseases, Frontotemporal Dementia (FTD), Acquired Cognitive Impairment, Aging, Brain Disorders, Neurodegenerative, Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), Genetics, Aetiology, 2.1 Biological and endogenous factors, Neurological, Alleles, Animals, Autophagy, Autophagy-Related Protein 5, Behavior, Animal, Disease Models, Animal, Embryo, Nonmammalian, Frontotemporal Dementia, Heredodegenerative Disorders, Nervous System, Humans, Kinetics, Polymorphism, Single Nucleotide, Proteasome Endopeptidase Complex, RNA, Supranuclear Palsy, Progressive, Tauopathies, Zebrafish, Zebrafish Proteins, tau Proteins, neurodegeneration, tauopathy, autophagy, proteasome, Tauopathy Genetics Consortium, Medical and Health Sciences, Psychology and Cognitive Sciences, Neurology & Neurosurgery, Biomedical and clinical sciences, Health sciences, Psychology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/3p51f6zmTest

المؤلفون: Chen, Jason, Yu, Jin-Tai, Wojta, Kevin, Wang, Hui-Fu, Zetterberg, Henrik, Blennow, Kaj, Yokoyama, Jennifer S, Weiner, Michael W, Kramer, Joel H, Rosen, Howard, Miller, Bruce L, Coppola, Giovanni, Boxer, Adam L

المصدر: Neurology. 88(7)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Neurosciences, Clinical Sciences, Aging, Alzheimer's Disease, Human Genome, Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), Brain Disorders, Prevention, Neurodegenerative, Genetics, Frontotemporal Dementia (FTD), Dementia, Acquired Cognitive Impairment, Aetiology, 2.1 Biological and endogenous factors, Neurological, Aged, Aged, 80 and over, Alzheimer Disease, Apolipoprotein E4, Biomarkers, Cognitive Dysfunction, Cohort Studies, Endophenotypes, Female, Genetic Loci, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Interleukin-2 Receptor alpha Subunit, Male, Middle Aged, Polymorphism, Single Nucleotide, Ubiquitin-Protein Ligases, United States, White People, tau Proteins, Alzheimer's Disease Neuroimaging Initiative, Cognitive Sciences, Neurology & Neurosurgery, Clinical sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/6743d7z9Test

المؤلفون: Cho, Seo-Hyun, Chen, Jason A, Sayed, Faten, Ward, Michael E, Gao, Fuying, Nguyen, Thi A, Krabbe, Grietje, Sohn, Peter Dongmin, Lo, Iris, Minami, Sakura, Devidze, Nino, Zhou, Yungui, Coppola, Giovanni, Gan, Li

المصدر: Journal of Neuroscience. 35(2)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Neurosciences, Aging, Neurodegenerative, Brain Disorders, Acquired Cognitive Impairment, Dementia, Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), Alzheimer's Disease, Genetics, Aetiology, 2.1 Biological and endogenous factors, Inflammatory and immune system, Neurological, Animals, Case-Control Studies, Cognition, DNA Methylation, Epigenesis, Genetic, Humans, Interleukin-1beta, Mice, Microglia, Sirtuin 1, Tauopathies, Up-Regulation, epigenetic, innate immunity, interleukin, memory deficits, neuroinflammation, NF-kappa B, NF-κ B, Medical and Health Sciences, Psychology and Cognitive Sciences, Neurology & Neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/4w97s39wTest

المؤلفون: Li, Yun, Chen, Jason A, Sears, Renee L, Gao, Fuying, Klein, Eric D, Karydas, Anna, Geschwind, Michael D, Rosen, Howard J, Boxer, Adam L, Guo, Weilong, Pellegrini, Matteo, Horvath, Steve, Miller, Bruce L, Geschwind, Daniel H, Coppola, Giovanni

المصدر: PLOS Genetics. 10(3)

مصطلحات موضوعية: Biological Sciences, Genetics, Neurosciences, Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), Frontotemporal Dementia (FTD), Clinical Research, Prevention, Rare Diseases, Alzheimer's Disease, Acquired Cognitive Impairment, Dementia, Aging, Neurodegenerative, Brain Disorders, Human Genome, Alzheimer's Disease Related Dementias (ADRD), Aetiology, 2.1 Biological and endogenous factors, Neurological, Brain, Chromosomes, Human, Pair 17, DNA Methylation, Epigenesis, Genetic, Frontotemporal Dementia, Genetic Association Studies, Genetic Predisposition to Disease, Haplotypes, Humans, Neurodegenerative Diseases, Risk Factors, Supranuclear Palsy, Progressive, Tauopathies, tau Proteins, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/96z3f279Test