Human Genome Epidemiology Literature Finder
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Records 1 - 24 (of 24 Records) |
| Query Trace: Amyotrophic Lateral Sclerosis and GRN[original query] |
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| Genetic studies of GRN and IFT74 in amyotrophic lateral sclerosis. Neurobiology of aging 2008 Aug 29 (8): 1279-82. Xiao Shangxi, Sato Christine, Kawarai Toshitaka, Goodall Emily F, Pall Hardev S, Zinman Lorne H, Robertson Janice, Morrison Karen, Rogaeva Ekateri |
| Screening for C9ORF72 repeat expansion in FTLD. Neurobiology of aging 2012 Mar . Ferrari R, Mok K, Moreno JH, Cosentino S, Goldman J, Pietrini P, Mayeux R, Tierney MC, Kapogiannis D, Jicha GA, Murrell JR, Ghetti B, Wassermann EM, Grafman J, Hardy J, Huey ED, Momeni P |
| Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort. JAMA neurology 2013 Mar 70 (3): 365-73. Van Langenhove Tim, van der Zee Julie, Gijselinck Ilse, Engelborghs Sebastiaan, Vandenberghe Rik, Vandenbulcke Mathieu, De Bleecker Jan, Sieben Anne, Versijpt Jan, Ivanoiu Adrian, Deryck Olivier, Willems Christiana, Dillen Lubina, Philtjens Stéphanie, Maes Githa, Bäumer Veerle, Van Den Broeck Marleen, Mattheijssens Maria, Peeters Karin, Martin Jean-Jacques, Michotte Alex, Santens Patrick, De Jonghe Peter, Cras Patrick, De Deyn Peter P, Cruts Marc, Van Broeckhoven Christi |
| Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansions. Neurobiology of aging 2014 Nov 35 (11): 2658.e1-5. Lattante Serena, Le Ber Isabelle, Galimberti Daniela, Serpente Maria, Rivaud-Péchoux Sophie, Camuzat Agnès, Clot Fabienne, Fenoglio Chiara, , Scarpini Elio, Brice Alexis, Kabashi Ed |
| PLD3 is accumulated on neuritic plaques in Alzheimer's disease brains. Alzheimer's research & therapy 2014 6 (9): 70. Satoh Jun-Ichi, Kino Yoshihiro, Yamamoto Yoji, Kawana Natsuki, Ishida Tsuyoshi, Saito Yuko, Arima Kunima |
| Clinical and genetic analysis of MAPT, GRN, and C9orf72 genes in Korean patients with frontotemporal dementia. Neurobiology of aging 2014 May 35 (5): 1213.e13-7. Kim Eun-Joo, Kwon Jay C, Park Kee Hyung, Park Kyung-Won, Lee Jae-Hong, Choi Seong Hye, Jeong Jee H, Kim Byeong C, Yoon Soo Jin, Yoon Young Chul, Kim Sangyun, Park Key-Chung, Choi Byung-Ok, Na Duk L, Ki Chang-Seok, Kim Seung Hy |
| TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions. Acta neuropathologica 2014 Mar 127 (3): 407-18. Gallagher Michael D, Suh Eunran, Grossman Murray, Elman Lauren, McCluskey Leo, Van Swieten John C, Al-Sarraj Safa, Neumann Manuela, Gelpi Ellen, Ghetti Bernardino, Rohrer Jonathan D, Halliday Glenda, Van Broeckhoven Christine, Seilhean Danielle, Shaw Pamela J, Frosch Matthew P, Alafuzoff Irina, Antonell Anna, Bogdanovic Nenad, Brooks William, Cairns Nigel J, Cooper-Knock Johnathan, Cotman Carl, Cras Patrick, Cruts Marc, De Deyn Peter P, DeCarli Charles, Dobson-Stone Carol, Engelborghs Sebastiaan, Fox Nick, Galasko Douglas, Gearing Marla, Gijselinck Ilse, Grafman Jordan, Hartikainen Päivi, Hatanpaa Kimmo J, Highley J Robin, Hodges John, Hulette Christine, Ince Paul G, Jin Lee-Way, Kirby Janine, Kofler Julia, Kril Jillian, Kwok John B J, Levey Allan, Lieberman Andrew, Llado Albert, Martin Jean-Jacques, Masliah Eliezer, McDermott Christopher J, McKee Ann, McLean Catriona, Mead Simon, Miller Carol A, Miller Josh, Munoz David G, Murrell Jill, Paulson Henry, Piguet Olivier, Rossor Martin, Sanchez-Valle Raquel, Sano Mary, Schneider Julie, Silbert Lisa C, Spina Salvatore, van der Zee Julie, Van Langenhove Tim, Warren Jason, Wharton Stephen B, White Charles L, Woltjer Randall L, Trojanowski John Q, Lee Virginia M Y, Van Deerlin Vivianna, Chen-Plotkin Alice |
| Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease. Acta neuropathologica 2015 Jul 130 (1): 77-92. Pottier Cyril, Bieniek Kevin F, Finch NiCole, van de Vorst Maartje, Baker Matt, Perkersen Ralph, Brown Patricia, Ravenscroft Thomas, van Blitterswijk Marka, Nicholson Alexandra M, DeTure Michael, Knopman David S, Josephs Keith A, Parisi Joseph E, Petersen Ronald C, Boylan Kevin B, Boeve Bradley F, Graff-Radford Neill R, Veltman Joris A, Gilissen Christian, Murray Melissa E, Dickson Dennis W, Rademakers Ro |
| Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort. Brain : a journal of neurology 2015 Dec . Van Mossevelde Sara, van der Zee Julie, Gijselinck Ilse, Engelborghs Sebastiaan, Sieben Anne, Van Langenhove Tim, De Bleecker Jan, Baets Jonathan, Vandenbulcke Mathieu, Van Laere Koen, Ceyssens Sarah, Van den Broeck Marleen, Peeters Karin, Mattheijssens Maria, Cras Patrick, Vandenberghe Rik, De Jonghe Peter, Martin Jean-Jacques, De Deyn Peter P, Cruts Marc, Van Broeckhoven Christine, |
| Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains. Acta neuropathologica communications 2015 3 68. Janssens Jonathan, Philtjens Stéphanie, Kleinberger Gernot, Van Mossevelde Sara, van der Zee Julie, Cacace Rita, Engelborghs Sebastiaan, Sieben Anne, Banzhaf-Strathmann Julia, Dillen Lubina, Merlin Céline, Cuijt Ivy, Robberecht Caroline, Schmid Bettina, Santens Patrick, Ivanoiu Adrian, Vandenbulcke Mathieu, Vandenberghe Rik, Cras Patrick, De Deyn Peter P, Martin Jean-Jacques, Maudsley Stuart, Haass Christian, Cruts Marc, Van Broeckhoven Christine, |
| Genetic compendium of 1511 human brains available through the UK Medical Research Council Brain Banks Network Resource. Genome research 2016 Dec . Keogh Michael J, Wei Wei, Wilson Ian, Coxhead Jon, Ryan Sarah, Rollinson Sara, Griffin Helen, Kurzawa-Akanbi Marzena, Santibanez-Koref Mauro, Talbot Kevin, Turner Martin R, McKenzie Chris-Anne, Troakes Claire, Attems Johannes, Smith Colin, Al Sarraj Safa, Morris Chris M, Ansorge Olaf, Pickering-Brown Stuart, Ironside James W, Chinnery Patrick |
| Sex differences in the prevalence of genetic mutations in FTD and ALS: A meta-analysis. Neurology 2017 9 89 (15): 1633-1642. Curtis Ashley F, Masellis Mario, Hsiung Ging-Yuek Robin, Moineddin Rahim, Zhang Kathy, Au Bonnie, Millett Geneva, Mackenzie Ian, Rogaeva Ekaterina, Tierney Mary |
| Factors influencing the age at onset in familial frontotemporal lobar dementia: Important weight of genetics. Neurology. Genetics 2017 12 3 (6): e203. Barbier Mathieu, Camuzat Agnès, Houot Marion, Clot Fabienne, Caroppo Paola, Fournier Clémence, Rinaldi Daisy, Pasquier Florence, Hannequin Didier, Pariente Jérémie, Larcher Kathy, , , Brice Alexis, Génin Emmanuelle, Sabbagh Audrey, Le Ber Isabel |
| Three VCP Mutations in Patients with Frontotemporal Dementia. Journal of Alzheimer's disease : JAD 2018 8 65 (4): 1139-1146. Wong Tsz Hang, Pottier Cyril, Hondius David C, Meeter Lieke H H, van Rooij Jeroen G J, Melhem Shami, , van Minkelen Rick, van Duijn Cornelia M, Rozemuller Annemieke J M, Seelaar Harro, Rademakers Rosa, van Swieten John |
| Analysis of frontotemporal dementia, amyotrophic lateral sclerosis, and other dementia-related genes in 107 Korean patients with frontotemporal dementia. Neurobiology of aging 2018 7 72 186.e1-186.e7. Kim Eun-Joo, Kim Young-Eun, Jang Ja-Hyun, Cho Eun-Hae, Na Duk L, Seo Sang Won, Jung Na-Yeon, Jeong Jee H, Kwon Jay C, Park Kee Hyung, Park Kyung Won, Lee Jae-Hong, Roh Jee Hoon, Kim Hee-Jin, Yoon Soo Jin, Choi Seong Hye, Jang Jae-Won, Ki Chang-Seok, Kim Seung Hy |
| Frontotemporal dementia spectrum: first genetic screen in a Greek cohort. Neurobiology of aging 2018 12 75 224.e1-224.e8. Ramos Eliana Marisa, Koros Christos, Dokuru Deepika Reddy, Van Berlo Victoria, Kroupis Christos, Wojta Kevin, Wang Qing, Andronas Nikolaos, Matsi Stavroula, Beratis Ion N, Huang Alden Y, Lee Suzee E, Bonakis Anastasios, Florou-Hatziyiannidou Chryseis, Fragkiadaki Stella, Kontaxopoulou Dionysia, Agiomyrgiannakis Dimitrios, Kamtsadeli Vasiliki, Tsinia Niki, Papastefanopoulou Vasiliki, Stamelou Maria, Miller Bruce L, Stefanis Leonidas, Papatriantafyllou John D, Papageorgiou Sokratis G, Coppola Giovan |
| Comprehensive Genetic Analysis of a Hungarian Amyotrophic Lateral Sclerosis Cohort. Frontiers in genetics 2019 10 732. Tripolszki Kornélia, Gampawar Piyush, Schmidt Helena, Nagy Zsófia F, Nagy Dóra, Klivényi Péter, Engelhardt József I, Széll Már |
| Genetics of frontotemporal dementia in China. Amyotrophic lateral sclerosis & frontotemporal degeneration 2021 2 22 (5-6): 321-335. Jiang Yaling, Jiao Bin, Xiao Xuewen, Shen |
| Differences in Motor Features of C9orf72, MAPT, or GRN Variant Carriers With Familial Frontotemporal Lobar Degeneration. Neurology 2022 7 99 (11): e1154-e1167. Tipton Philip Wade, Deutschlaender Angela B, Savica Rodolfo, Heckman Michael G, Brushaber Danielle E, Dickerson Bradford C, Gavrilova Ralitza H, Geschwind Daniel H, Ghoshal Nupur, Graff-Radford Jonathan, Graff-Radford Neill R, Grossman Murray, Hsiung Ging-Yuek R, Huey Edward D, Irwin David John, Jones David T, Knopman David S, McGinnis Scott M, Rademakers Rosa, Ramos Eliana Marisa, Forsberg Leah K, Heuer Hilary W, Onyike Chiadi, Tartaglia Carmela, Domoto-Reilly Kimiko, Roberson Erik D, Mendez Mario F, Litvan Irene, Appleby Brian S, Grant Ian, Kaufer Daniel, Boxer Adam L, Rosen Howard J, Boeve Brad F, Wszolek Zbigniew K, |
| Exome Sequencing of a Portuguese Cohort of Frontotemporal Dementia Patients: Looking Into the ALS-FTD Continuum. Frontiers in neurology 2022 13 886379. Tábuas-Pereira Miguel, Santana Isabel, Gibbons Elizabeth, Paquette Kimberly, Almeida Maria Rosário, Baldeiras Inês, Bras Jose, Guerreiro Ri |
| Examining empathy deficits across familial forms of frontotemporal dementia within the GENFI cohort. Cortex; a journal devoted to the study of the nervous system and behavior 2022 3 150 12-28. Foster Phoebe H, Russell Lucy L, Peakman Georgia, Convery Rhian S, Bouzigues Arabella, Greaves Caroline V, Bocchetta Martina, Cash David M, van Swieten John C, Jiskoot Lize C, Moreno Fermin, Sanchez-Valle Raquel, Laforce Robert, Graff Caroline, Masellis Mario, Tartaglia Carmela, Rowe James B, Borroni Barbara, Finger Elizabeth, Synofzik Matthis, Galimberti Daniela, Vandenberghe Rik, de Mendonça Alexandre, Butler Chris R, Gerhard Alex, Ducharme Simon, Le Ber Isabelle, Tagliavini Fabrizio, Santana Isabel, Pasquier Florence, Levin Johannes, Danek Adrian, Otto Markus, Sorbi Sandro, Rohrer Jonathan D, |
| Genetic Screening in Korean Patients with Frontotemporal Dementia Syndrome. Journal of Alzheimer's disease reports 2022 11 6 (1): 651-662. Kim Eun-Joo, Na Duk L, Kim Hee-Jin, Park Kyung Won, Lee Jae-Hong, Roh Jee Hoon, Kwon Jay C, Yoon Soo Jin, Jung Na-Yeon, Jeong Jee Hyang, Jang Jae-Won, Kim Hee-Jin, Park Kee Hyung, Choi Seong Hye, Kim SangYun, Park Young Ho, Kim Byeong C, Youn Young Chul, Ki Chang-Seok, Kim Seung Hyun, Seo Sang Won, Kim Young-E |
| MicroRNA signatures in genetic frontotemporal dementia and amyotrophic lateral sclerosis. Annals of clinical and translational neurology 2022 10 9 (11): 1778-1791. Kmetzsch Virgilio, Latouche Morwena, Saracino Dario, Rinaldi Daisy, Camuzat Agnès, Gareau Thomas, , Le Ber Isabelle, Colliot Olivier, Becker Emmanuel |
| Novel data-driven subtypes and stages of brain atrophy in the ALS-FTD spectrum. Research square 2023 8 . Ting Shen, Jacob W Vogel, Jeffrey Duda, Jeffrey S Phillips, Philip A Cook, James Gee, Lauren Elman, Colin Quinn, Defne A Amado, Michael Baer, Lauren Massimo, Murray Grossman, David J Irwin, Corey T McMill |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 29, 2023
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