المؤلفون: Gao, Yixin, Wang, Ting, Yu, Xinghao, International FTD-Genomics Consortium (IFGC), Zhao, Huashuo, Zeng, Ping

المصدر: Scientific reports. 10(1)

مصطلحات موضوعية: International FTD-Genomics Consortium

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/9db5p2hb

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

URL الوصول: https://escholarship.org/uc/item/6np4j59k

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), EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease 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. 138(2)

مصطلحات موضوعية: 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, Amyotrophic lateral sclerosis, Dementia with Lewy bodies, Frontotemporal dementia, Longevity, Multiple sclerosis, Neurodegenerative disease, PLCG2, Parkinson’s disease, Phospholipase C Gamma 2, Progressive supranuclear palsy, Alzheimer's disease, Parkinson's disease, Alzheimer's Disease, frontotemporal dementia, dementia with Lewy-bodies, progressive suprauclear palsy, Parkinson's Disease, amyotrophic lateral sclerosis, multiple sclerosis, neurodegenerative disease, longevity, Clinical Sciences, Neurosciences, Neurology & Neurosurgery

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/4w15z00t

المؤلفون: Bonham, Luke W, Steele, Natasha ZR, Karch, Celeste M, Broce, Iris, Geier, Ethan G, Wen, Natalie L, Momeni, Parastoo, Hardy, John, Miller, Zachary A, Gorno-Tempini, Maria Luisa, Hess, Christopher P, Lewis, Patrick, Miller, Bruce L, Seeley, William W, Manzoni, Claudia, Desikan, Rahul S, Baranzini, Sergio E, Ferrari, Raffaele, Yokoyama, Jennifer S, International FTD-Genomics Consortium (IFGC)

المصدر: Scientific reports. 9(1)

مصطلحات موضوعية: International FTD-Genomics Consortium, Humans, DNA-Binding Proteins, RNA, Risk Factors, Cohort Studies, Apoptosis, Transcription, Genetic, Gene Expression Regulation, Polymorphism, Single Nucleotide, Databases, Genetic, Gene Regulatory Networks, Genome-Wide Association Study, Primary Progressive Nonfluent Aphasia, Protein Interaction Maps, Frontotemporal Dementia (FTD), Human Genome, Dementia, Aphasia, Rare Diseases, Neurodegenerative, Neurosciences, Genetics, Brain Disorders, Biotechnology, Aging, Acquired Cognitive Impairment, 2.1 Biological and endogenous factors, Neurological

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/6q81z06n

المؤلفون: Zhang, Ming, Ferrari, Raffaele, Tartaglia, Maria Carmela, Keith, Julia, Surace, Ezequiel I, Wolf, Uri, Sato, Christine, Grinberg, Mark, Liang, Yan, Xi, Zhengrui, Dupont, Kyle, McGoldrick, Philip, Weichert, Anna, McKeever, Paul M, Schneider, Raphael, McCorkindale, Michael D, Manzoni, Claudia, Rademakers, Rosa, Graff-Radford, Neill R, Dickson, Dennis W, Parisi, Joseph E, Boeve, Bradley F, Petersen, Ronald C, Miller, Bruce L, Seeley, William W, van Swieten, John C, van Rooij, Jeroen, Pijnenburg, Yolande, van der Zee, Julie, Van Broeckhoven, Christine, Le Ber, Isabelle, Van Deerlin, Vivianna, Suh, EunRan, Rohrer, Jonathan D, Mead, Simon, Graff, Caroline, Öijerstedt, Linn, Pickering-Brown, Stuart, Rollinson, Sara, Rossi, Giacomina, Tagliavini, Fabrizio, Brooks, William S, Dobson-Stone, Carol, Halliday, Glenda M, Hodges, John R, Piguet, Olivier, Binetti, Giuliano, Benussi, Luisa, Ghidoni, Roberta, Nacmias, Benedetta, Sorbi, Sandro, Bruni, Amalia C, Galimberti, Daniela, Scarpini, Elio, Rainero, Innocenzo, Rubino, Elisa, Clarimon, Jordi, Lleó, Alberto, Ruiz, Agustin, Hernández, Isabel, Pastor, Pau, Diez-Fairen, Monica, Borroni, Barbara, Pasquier, Florence, Deramecourt, Vincent, Lebouvier, Thibaud, Perneczky, Robert, Diehl-Schmid, Janine, Grafman, Jordan, Huey, Edward D, Mayeux, Richard, Nalls, Michael A, Hernandez, Dena, Singleton, Andrew, Momeni, Parastoo, Zeng, Zhen, Hardy, John, Robertson, Janice, Zinman, Lorne, Rogaeva, Ekaterina, International FTD-Genomics Consortium (IFGC)

المصدر: Brain : a journal of neurology. 141(10)

مصطلحات موضوعية: International FTD-Genomics Consortium, Humans, Amyotrophic Lateral Sclerosis, Age of Onset, DNA Methylation, Gene Expression Regulation, CpG Islands, Genotype, Heterozygote, Polymorphism, Single Nucleotide, Aged, Middle Aged, Female, Male, Frontotemporal Dementia, C9orf72 Protein, C9orf72, genetic association, age of onset, amyotrophic lateral sclerosis, frontotemporal dementia, Polymorphism, Single Nucleotide, Neurology & Neurosurgery, Medical and Health Sciences, Psychology and Cognitive Sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/1qp1x4zx

المؤلفون: Bonham, Luke W, Steele, Natasha ZR, Karch, Celeste M, Manzoni, Claudia, Geier, Ethan G, Wen, Natalie, Ofori-Kuragu, Aaron, Momeni, Parastoo, Hardy, John, Miller, Zachary A, Hess, Christopher P, Lewis, Patrick, Miller, Bruce L, Seeley, William W, Baranzini, Sergio E, Desikan, Rahul S, Ferrari, Raffaele, Yokoyama, Jennifer S, International FTD-Genomics Consortium (IFGC)

المصدر: Neurology. Genetics. 4(5)

مصطلحات موضوعية: International FTD-Genomics Consortium, Neurodegenerative, Brain Disorders, Acquired Cognitive Impairment, Genetics, Dementia, Rare Diseases, Frontotemporal Dementia (FTD), Alzheimer's Disease Related Dementias (ADRD), Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), Biotechnology, Neurosciences, Human Genome, Aging, 2.1 Biological and endogenous factors, Neurological

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/9mn3k1r0

المؤلفون: Bonham, Luke W, Karch, Celeste M, Fan, Chun C, Tan, Chin, Geier, Ethan G, Wang, Yunpeng, Wen, Natalie, Broce, Iris J, Li, Yi, Barkovich, Matthew J, Ferrari, Raffaele, Hardy, John, Momeni, Parastoo, Höglinger, Günter, Müller, Ulrich, Hess, Christopher P, Sugrue, Leo P, Dillon, William P, Schellenberg, Gerard D, Miller, Bruce L, Andreassen, Ole A, Dale, Anders M, Barkovich, A James, Yokoyama, Jennifer S, Desikan, Rahul S, International FTD-Genomics Consortium (IFGC), International Parkinson’s Disease Genetics Consortium (IPDGC), International Genomics of Alzheimer’s Project (IGAP)

المصدر: Translational psychiatry. 8(1)

مصطلحات موضوعية: International FTD-Genomics Consortium, International Parkinson’s Disease Genetics Consortium, International Genomics of Alzheimer’s Project, Brain, Microglia, Animals, Mice, Transgenic, Humans, Neurodegenerative Diseases, Genetic Predisposition to Disease, Receptors, CXCR4, Risk Factors, Gene Expression, Polymorphism, Single Nucleotide, Gene Regulatory Networks, Genome-Wide Association Study, Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), Brain Disorders, Alzheimer's Disease Related Dementias (ADRD), Aging, Genetics, Rare Diseases, Parkinson's Disease, Neurosciences, Frontotemporal Dementia (FTD), Acquired Cognitive Impairment, Alzheimer's Disease, Neurodegenerative, Dementia, 2.1 Biological and endogenous factors, Neurological, Clinical Sciences, Public Health and Health Services, Psychology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/3br131m2

المؤلفون: Yokoyama, Jennifer S, Karch, Celeste M, Fan, Chun C, Bonham, Luke W, Kouri, Naomi, Ross, Owen A, Rademakers, Rosa, Kim, Jungsu, Wang, Yunpeng, Höglinger, Günter U, Müller, Ulrich, Ferrari, Raffaele, Hardy, John, International FTD-Genomics Consortium (IFGC), Momeni, Parastoo, Sugrue, Leo P, Hess, Christopher P, James Barkovich, A, Boxer, Adam L, Seeley, William W, Rabinovici, Gil D, Rosen, Howard J, Miller, Bruce L, Schmansky, Nicholas J, Fischl, Bruce, Hyman, Bradley T, Dickson, Dennis W, Schellenberg, Gerard D, Andreassen, Ole A, Dale, Anders M, Desikan, Rahul S

المصدر: Acta Neuropathologica. 133(5)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Neurosciences, Human Genome, Alzheimer's Disease Related Dementias (ADRD), Pick's Disease, Rare Diseases, Brain Disorders, Dementia, Genetics, Neurodegenerative, Aging, Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), Frontotemporal Dementia (FTD), Acquired Cognitive Impairment, 2.1 Biological and endogenous factors, Neurological, Basal Ganglia Diseases, Frontotemporal Dementia, Humans, Inclusion Bodies, Neurons, Risk Factors, Supranuclear Palsy, Progressive, Tauopathies, tau Proteins, International FTD-Genomics Consortium, Clinical Sciences, Neurology & Neurosurgery

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/78j6x9mk
https://escholarship.org/content/qt78j6x9mk/qt78j6x9mk.pdf

المؤلفون: Ferrari, Raffaele, Wang, Yunpeng, Vandrovcova, Jana, Guelfi, Sebastian, Witeolar, Aree, Karch, Celeste M, Schork, Andrew J, Fan, Chun C, Brewer, James B, International FTD-Genomics Consortium (IFGC),, International Parkinson's Disease Genomics Consortium (IPDGC),, International Genomics of Alzheimer's Project (IGAP),, Momeni, Parastoo, Schellenberg, Gerard D, Dillon, William P, Sugrue, Leo P, Hess, Christopher P, Yokoyama, Jennifer S, Bonham, Luke W, Rabinovici, Gil D, Miller, Bruce L, Andreassen, Ole A, Dale, Anders M, Hardy, John, Desikan, Rahul S

المصدر: Journal of neurology, neurosurgery, and psychiatry. 88(2)

مصطلحات موضوعية: International FTD-Genomics Consortium (IFGC), International Parkinson's Disease Genomics Consortium (IPDGC), International Genomics of Alzheimer's Project (IGAP), Humans, Parkinson Disease, Alzheimer Disease, Genetic Predisposition to Disease, Genotype, Polymorphism, Single Nucleotide, Alleles, Genome-Wide Association Study, Frontotemporal Dementia, Acquired Cognitive Impairment, Genetics, Parkinson's Disease, Biotechnology, Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), Human Genome, Dementia, Prevention, Aging, Alzheimer's Disease, Neurosciences, Neurodegenerative, Brain Disorders, Aetiology, 2.1 Biological and endogenous factors, Neurological, Medical and Health Sciences, Psychology and Cognitive Sciences, Neurology & Neurosurgery

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/09r1w13w

المؤلفون: Jiang, Shan^{Aff1, Aff2}, Wen, Natalie^{Aff1, Aff2}, Li, Zeran^{Aff1, Aff2}, Dube, Umber^{Aff1, Aff2}, Del Aguila, Jorge^{Aff1, Aff2}, Budde, John^{Aff1, Aff2}, Martinez, Rita^{Aff1, Aff2}, Hsu, Simon^{Aff1, Aff2}, Fernandez, Maria V.^{Aff1, Aff2}, Cairns, Nigel J., Dominantly Inherited Alzheimer Network (DIAN), International FTD-Genomics Consortium (IFGC), Harari, Oscar^{Aff1, Aff2}, Cruchaga, Carlos^{Aff1, Aff2}, Karch, Celeste M.^{Aff1, Aff2}

المصدر: Translational Psychiatry. 8(1)