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Records 1-6

Query Trace: Amyotrophic Lateral Sclerosis and TMEM106B[original query]

A novel temporal-predominant neuro-astroglial tauopathy associated with TMEM106B gene polymorphism in FTLD/ALS-TDP. Brain pathology (Zurich, Switzerland) 2020 Dec e12924. Llibre-Guerra Jorge J, Lee Suzee E, Suemoto Claudia K, Ehrenberg Alexander J, Kovacs Gabor G, Karydas Anna, Staffaroni Adam, De Paula Franca Resende Elisa, Kim Eun-Joo, Hwang Ji-Hye, Ramos Eliana Marisa, Wojta Kevin J, Pasquini Lorenzo, Pang Shirley Yin-Yu, Spina Salvatore, Allen Isabel E, Kramer Joel, Miller Bruce L, Seeley William W, Grinberg Lea Similar articles in PubMed
Association analysis of polymorphisms in VMAT2 and TMEM106B genes for Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy. Journal of the neurological sciences 2017 Jun 377 65-71. Hu Tao, Chen Yongping, Ou Ruwei, Wei Qianqian, Cao Bei, Zhao Bi, Wu Ying, Song Wei, Chen Xueping, Shang Hui-Fa Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
Frontotemporal lobar degeneration genome wide association study replication confirms a risk locus shared with amyotrophic lateral sclerosis. Neurobiology of aging 2011 Apr 32 (4): 758.e1-7. Rollinson Sara, Mead Simon, Snowden Julie, Richardson Anna, Rohrer Jonathan, Halliwell Nicola, Usher Suzanne, Neary David, Mann David, Hardy John, Pickering-Brown Stua Similar articles in PubMed
Risk genotypes at TMEM106B are associated with cognitive impairment in amyotrophic lateral sclerosis. Acta neuropathologica 2011 Mar 121 (3): 373-80. Vass Ryan, Ashbridge Emily, Geser Felix, Hu William T, Grossman Murray, Clay-Falcone Dana, Elman Lauren, McCluskey Leo, Lee Virginia M Y, Van Deerlin Vivianna M, Trojanowski John Q, Chen-Plotkin Alice Similar articles in PubMed

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