Human Genome Epidemiology Literature Finder
|
Records 1 - 17 (of 17 Records) |
| Query Trace: Cognition and C9orf72[original query] |
|---|
| C9orf72 hexanucleotide repeat expansion and Guam amyotrophic lateral sclerosis-Parkinsonism-dementia complex. JAMA neurology 2013 Jun 70 (6): 742-5. Dombroski Beth A, Galasko Douglas R, Mata Ignacio F, Zabetian Cyrus P, Craig Ulla-Katrina, Garruto Ralph M, Oyanagi Kiyomitsu, Schellenberg Gerard |
| Serum neurofilament light chain protein is a measure of disease intensity in frontotemporal dementia. Neurology 2016 Aug . Rohrer Jonathan D, Woollacott Ione O C, Dick Katrina M, Brotherhood Emilie, Gordon Elizabeth, Fellows Alexander, Toombs Jamie, Druyeh Ronald, Cardoso M Jorge, Ourselin Sebastien, Nicholas Jennifer M, Norgren Niklas, Mead Simon, Andreasson Ulf, Blennow Kaj, Schott Jonathan M, Fox Nick C, Warren Jason D, Zetterberg Henr |
| The Role of APOE in the Occurrence of Frontotemporal Dementia in Amyotrophic Lateral Sclerosis. JAMA neurology 2016 Feb . Chiò Adriano, Brunetti Maura, Barberis Marco, Iazzolino Barbara, Montuschi Anna, Ilardi Antonio, Cammarosano Stefania, Canosa Antonio, Moglia Cristina, Calvo Andr |
| C9orf72 hexanucleotide repeat length in older population: normal variation and effects on cognition. Neurobiology of aging 2019 4 84 242.e7-242.e12. Kaivola Karri, Kiviharju Anna, Jansson Lilja, Rantalainen Ville, Eriksson Johan G, Strandberg Timo E, Laaksovirta Hannu, Renton Alan E, Traynor Bryan J, Myllykangas Liisa, Tienari Pentti |
| The Distinct Traits of the UNC13A Polymorphism in Amyotrophic Lateral Sclerosis. Annals of neurology 2020 7 88 (4): 796-806. Tan Harold H G, Westeneng Henk-Jan, van der Burgh Hannelore K, van Es Michael A, Bakker Leonhard A, van Veenhuijzen Kevin, van Eijk Kristel R, van Eijk Ruben P A, Veldink Jan H, van den Berg Leonard |
| Multimodal longitudinal study of structural brain involvement in amyotrophic lateral sclerosis. Neurology 2020 5 94 (24): e2592-e2604. van der Burgh Hannelore K, Westeneng Henk-Jan, Walhout Renée, van Veenhuijzen Kevin, Tan Harold H G, Meier Jil M, Bakker Leonhard A, Hendrikse Jeroen, van Es Michael A, Veldink Jan H, van den Heuvel Martijn P, van den Berg Leonard |
| A modified Camel and Cactus Test detects presymptomatic semantic impairment in genetic frontotemporal dementia within the GENFI cohort. Applied neuropsychology. Adult 2020 2 29 (1): 112-119. Moore Katrina, Convery Rhian, Bocchetta Martina, Neason Mollie, Cash David M, Greaves Caroline, Russell Lucy L, Clarke Mica T M, Peakman Georgia, van Swieten John, Jiskoot Lize, Moreno Fermin, Barandiaran Myriam, Sanchez-Valle Raquel, Borroni Barbara, Laforce Robert, Doré Marie-Claire, Masellis Mario, Tartaglia Maria Carmela, Graff Caroline, Galimberti Daniela, Rowe James B, Finger Elizabeth, Synofzik Matthis, Karnath Hans-Otto, Vandenberghe Rik, de Mendonça Alexandre, Maruta Carolina, Tagliavini Fabrizio, Santana Isabel, Ducharme Simon, Butler Chris, Gerhard Alex, Levin Johannes, Danek Adrian, Otto Markus, Warren Jason D, Rohrer Jonathan D, |
| Apathy in presymptomatic genetic frontotemporal dementia predicts cognitive decline and is driven by structural brain changes. Alzheimer's & dementia : the journal of the Alzheimer's Association 2020 12 17 (6): 969-983. Malpetti Maura, Jones P Simon, Tsvetanov Kamen A, Rittman Timothy, van Swieten John C, Borroni Barbara, Sanchez-Valle Raquel, Moreno Fermin, Laforce Robert, Graff Caroline, Synofzik Matthis, Galimberti Daniela, Masellis Mario, Tartaglia Maria Carmela, Finger Elizabeth, Vandenberghe Rik, de Mendonça Alexandre, Tagliavini Fabrizio, Santana Isabel, Ducharme Simon, Butler Chris R, Gerhard Alexander, Levin Johannes, Danek Adrian, Otto Markus, Frisoni Giovanni B, Ghidoni Roberta, Sorbi Sandro, Heller Carolin, Todd Emily G, Bocchetta Martina, Cash David M, Convery Rhian S, Peakman Georgia, Moore Katrina M, Rohrer Jonathan D, Kievit Rogier A, Rowe James B, |
| Assessment of executive function declines in presymptomatic and mildly symptomatic familial frontotemporal dementia: NIH-EXAMINER as a potential clinical trial endpoint. Alzheimer's & dementia : the journal of the Alzheimer's Association 2020 1 16 (1): 11-21. Staffaroni Adam M, Bajorek Lynn, Casaletto Kaitlin B, Cobigo Yann, Goh Sheng-Yang M, Wolf Amy, Heuer Hilary W, Elahi Fanny M, Ljubenkov Peter A, Dever Reilly, Kornak John, Appleby Brian, Bove Jessica, Bordelon Yvette, Brannelly Patrick, Brushaber Danielle, Caso Christina, Coppola Giovanni, Dheel Christina, Dickerson Bradford C, Dickinson Susan, Dominguez Sophia, Domoto-Reilly Kimiko, Faber Kelly, Ferrall Jessica, Fields Julie A, Fishman Ann, Fong Jamie, Foroud Tatiana, Forsberg Leah K, Gavrilova Ralitza, Gearhart Debra, Ghazanfari Behnaz, Ghoshal Nupur, Goldman Jill, Graff-Radford Jonathan, Graff-Radford Neill, Grant Ian, Grossman Murray, Haley Dana, Hsiung Ging-Yuek, Huey Edward D, Irwin David J, Jones David T, Jones Lynne, Kantarci Kejal, Karydas Anna, Kaufer Daniel I, Kerwin Diana R, Knopman David S, Kraft Ruth, Kremers Walter K, Kukull Walter A, Litvan Irene, Lucente Diane, Lungu Codrin, Mackenzie Ian R, Maldonado Miranda, Manoochehri Masood, McGinnis Scott M, McKinley Emily, Mendez Mario F, Miller Bruce L, Multani Namita, Onyike Chiadi, Padmanabhan Jaya, Pantelyat Alex, Pearlman Rodney, Petrucelli Len, Potter Madeline, Rademakers Rosa, Ramos Eliana Marisa, Rankin Katherine P, Rascovsky Katya, Roberson Erik D, Rogalski Emily, Sengdy Pheth, Shaw Leslie M, Syrjanen Jeremy, Tartaglia M Carmela, Tatton Nadine, Taylor Joanne, Toga Arthur, Trojanowski John Q, Weintraub Sandra, Wang Ping, Wong Bonnie, Wszolek Zbigniew, Boxer Adam L, Boeve Brad F, Kramer Joel H, Rosen Howard J, |
| Role of genetics in amyotrophic lateral sclerosis: a large cohort study in Chinese mainland population. Journal of medical genetics 2021 Sep . Chen Yong-Ping, Yu Shi-Hui, Wei Qian-Qian, Cao Bei, Gu Xiao-Jing, Chen Xue-Ping, Song Wei, Zhao Bi, Wu Ying, Sun Ming-Ming, Liu Fei-Fei, Hou Yan-Bing, Ou Ru-Wei, Zhang Ling-Yu, Liu Kun-Cheng, Lin Jun-Yu, Xu Xin-Ran, Li Chun-Yu, Yang Jing, Jiang Zheng, Liu Jiao, Cheng Yang-Fan, Xiao Yi, Chen Ke, Feng Fei, Cai Ying-Ying, Li Shi-Rong, Hu Tao, Yuan Xiao-Qin, Guo Xiao-Yan, Liu Hui, Han Qing, Zhou Qing-Qing, Shao Na, Li Jian-Peng, Pan Ping-Lei, Ma Sha, Shang Hui-Fa |
| Anomia is present pre-symptomatically in frontotemporal dementia due to MAPT mutations. Journal of neurology 2022 3 269 (8): 4322-4332. Bouzigues Arabella, Russell Lucy L, Peakman Georgia, Bocchetta Martina, Greaves Caroline V, Convery Rhian S, Todd Emily, Rowe James B, Borroni Barbara, Galimberti Daniela, Tiraboschi Pietro, Masellis Mario, Tartaglia Maria Carmela, Finger Elizabeth, van Swieten John C, Seelaar Harro, Jiskoot Lize, Sorbi Sandro, Butler Chris R, Graff Caroline, Gerhard Alexander, Langheinrich Tobias, Laforce Robert, Sanchez-Valle Raquel, de Mendonça Alexandre, Moreno Fermin, Synofzik Matthis, Vandenberghe Rik, Ducharme Simon, Le Ber Isabelle, Levin Johannes, Danek Adrian, Otto Markus, Pasquier Florence, Santana Isabel, Rohrer Jonathan D, |
| Thalamic and Cerebellar Regional Involvement across the ALS-FTD Spectrum and the Effect of C9orf72. Brain sciences 2022 3 12 (3): . Bocchetta Martina, Todd Emily G, Tse Nga Yan, Devenney Emma M, Tu Sicong, Caga Jashelle, Hodges John R, Halliday Glenda M, Irish Muireann, Piguet Olivier, Kiernan Matthew C, Rohrer Jonathan D, Ahmed Rebekah |
| Cerebellar integrity and contributions to cognition in C9orf72-mediated frontotemporal dementia. Cortex; a journal devoted to the study of the nervous system and behavior 2022 2 149 73-84. Chen Yu, Landin-Romero Ramon, Kumfor Fiona, Irish Muireann, Dobson-Stone Carol, Kwok John B, Halliday Glenda M, Hodges John R, Piguet Olivi |
| The severity of behavioural symptoms in FTD is linked to the loss of GABRQ-expressing VENs and pyramidal neurons. Neuropathology and applied neurobiology 2022 2 48 (4): e12798. Gami-Patel Priya, Scarioni Marta, Bouwman Femke H, Boon Baayla D C, van Swieten John C, Brain Bank Netherlands, Rozemuller Annemieke J M, Smit August B, Pijnenburg Yolande A L, Hoozemans Jeroen J M, Dijkstra Anke |
| Clinical and Metabolic Signature of UNC13A rs12608932 Variant in Amyotrophic Lateral Sclerosis. Neurology. Genetics 2022 10 8 (6): e200033. Calvo Andrea, Canosa Antonio, Moglia Cristina, Manera Umberto, Grassano Maurizio, Vasta Rosario, Palumbo Francesca, Cugnasco Paolo, Gallone Salvatore, Brunetti Maura, De Marchi Fabiola, Arena Vincenzo, Pagani Marco, Dalgard Clifton, Scholz Sonja W, Chia Ruth, Corrado Lucia, Dalfonso Sandra, Mazzini Letizia, Traynor Bryan J, Chio Adria |
| 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 |
| Cerebellar and subcortical atrophy contribute to psychiatric symptoms in frontotemporal dementia. Human brain mapping 2023 3 . Bussy Aurélie, Levy Jake P, Best Tristin, Patel Raihaan, Cupo Lani, Van Langenhove Tim, Nielsen Jørgen E, Pijnenburg Yolande, Waldö Maria Landqvist, Remes Anne M, Schroeter Matthias L, Santana Isabel, Pasquier Florence, Otto Markus, Danek Adrian, Levin Johannes, Le Ber Isabelle, Vandenberghe Rik, Synofzik Matthis, Moreno Fermin, de Mendonça Alexandre, Sanchez-Valle Raquel, Laforce Robert, Langheinrich Tobias, Gerhard Alexander, Graff Caroline, Butler Chris R, Sorbi Sandro, Jiskoot Lize, Seelaar Harro, van Swieten John C, Finger Elizabeth, Tartaglia Maria Carmela, Masellis Mario, Tiraboschi Pietro, Galimberti Daniela, Borroni Barbara, Rowe James B, Bocchetta Martina, Rohrer Jonathan D, Devenyi Gabriel A, Chakravarty M Mallar, Ducharme Simon, |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 18, 2023
- Content source: