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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Disease and STMN2[original query]
Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. GWAS Catalog
The Lancet. Neurology 2009 Jan 8 (1): 57-66.
Mead Simon, Poulter Mark, Uphill James, Beck John, Whitfield Jerome, Webb Thomas E F, Campbell Tracy, Adamson Gary, Deriziotis Pelagia, Tabrizi Sarah J, Hummerich Holger, Verzilli Claudio, Alpers Michael P, Whittaker John C, Collinge Jo
RARB and STMN2 polymorphisms are not associated with sporadic Creutzfeldt-Jakob disease (CJD) in the Korean population.
Molecular biology reports 2014 41 (4): 2389-95.
Jeong Byung-Hoon, Kim Hae-Jung, Lee Kyung-Hee, Carp Richard I, Kim Yong-S
Truncated stathmin-2 is a marker of TDP-43 pathology in frontotemporal dementia.
The Journal of clinical investigation 2020 Aug .
Prudencio Mercedes, Humphrey Jack, Pickles Sarah, Brown Anna-Leigh, Hill Sarah E, Kachergus Jennifer M, Shi J, Heckman Michael G, Spiegel Matthew R, Cook Casey, Song Yuping, Yue Mei, Daughrity Lillian M, Carlomagno Yari, Jansen-West Karen, de Castro Cristhoper Fernandez, DeTure Michael, Koga Shunsuke, Wang Ying-Chih, Sivakumar Prasanth, Bodo Cristian, Candalija Ana, Talbot Kevin, Selvaraj Bhuvaneish T, Burr Karen, Chandran Siddharthan, Newcombe Jia, Lashley Tammaryn, Hubbard Isabel, Catalano Demetra, Kim Duyang, Propp Nadia, Fennessey Samantha, , Fagegaltier Delphine, Phatnani Hemali, Secrier Maria, Fisher Elizabeth Mc, Oskarsson Björn, van Blitterswijk Marka, Rademakers Rosa, Graff-Radford Neil R, Boeve Bradley F, Knopman David S, Petersen Ronald C, Josephs Keith A, Thompson E Aubrey, Raj Towfique, Ward Michael, Dickson Dennis W, Gendron Tania F, Fratta Pietro, Petrucelli Leona
Analysis of STMN2 CA repeats in italian ALS patients shows no association.
Amyotrophic lateral sclerosis & frontotemporal degeneration 2022 Jul 1-3.
Doronzio Paolo Niccolò, Lattante Serena, Marangi Giuseppe, Martello Francesco, Conte Amelia, Bisogni Giulia, Bernardo Daniela, Patanella Agata Katia, Meleo Emiliana, Zollino Marcella, Sabatelli Mar
NEK1 and STMN2 short tandem repeat lengths are not associated with Australian amyotrophic lateral sclerosis risk.
Neurobiology of aging 2022 Aug 116 92-95.
Grima Natalie, Henden Lyndal, Fearnley Liam G, Rowe Dominic B, D'Silva Susan, Pamphlett Roger, Adams Lorel, Kiernan Matthew C, Mazumder Srestha, Timmins Hannah C, Zoing Margaret, Bahlo Melanie, Blair Ian P, Williams Kelly
Analysis of Structural Variants Previously Associated With ALS in Europeans Highlights Genomic Architectural Differences in Africans.
Neurology. Genetics 2023 6 9 (4): e200077.
Nomakhosazana R Monnakgotla, Amokelani C Mahungu, Jeannine M Heckmann, Gerrit Botha, Nicola J Mulder, Gang Wu, Evadnie Rampersaud, Jason Myers, Marka Van Blitterswijk, Rosa Rademakers, J Paul Taylor, Joanne Wuu, Michael Benatar, Melissa N
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