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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 - 7 (of 7 Records)

Query Trace: Disease and SCFD1[original query]
An association study between SCFD1 rs10139154 variant and amyotrophic lateral sclerosis in a Chinese cohort.
Amyotrophic lateral sclerosis & frontotemporal degeneration 2017 Dec 1-6.
Chen Yongping, Zhou Qingqing, Gu Xiaojing, Wei Qianqian, Cao Bei, Liu Hui, Hou Yanbing, Shang Huifa
Does SCFD1 rs10139154 Polymorphism Decrease Alzheimer's Disease Risk?
Journal of molecular neuroscience : MN 2019 Jul .
Stamati Polyxeni, Siokas Vasileios, Aloizou Athina-Maria, Karampinis Emmanouil, Arseniou Stylianos, Rakitskii Valerii N, Tsatsakis Aristidis, Spandidos Demetrios A, Gozes Illana, Mitsias Panayiotis D, Bogdanos Dimitrios P, Hadjigeorgiou Georgios M, Dardiotis Efthimi
Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease Genetics.
Cell reports 2020 Oct 33 (4): 108323.
Iacoangeli Alfredo, Lin Tian, Al Khleifat Ahmad, Jones Ashley R, Opie-Martin Sarah, Coleman Jonathan R I, Shatunov Aleksey, Sproviero William, Williams Kelly L, Garton Fleur, Restuadi Restuadi, Henders Anjali K, Mather Karen A, Needham Merilee, Mathers Susan, Nicholson Garth A, Rowe Dominic B, Henderson Robert, McCombe Pamela A, Pamphlett Roger, Blair Ian P, Schultz David, Sachdev Perminder S, Newhouse Stephen J, Proitsi Petroula, Fogh Isabella, Ngo Shyuan T, Dobson Richard J B, Wray Naomi R, Steyn Frederik J, Al-Chalabi Amm
Genome-wide Meta-analysis Identifies Novel Genes Associated with Recurrence and Progression in Non-muscle-invasive Bladder Cancer. GWAS Catalog
European urology oncology 2021 Aug .
Galesloot Tessel E, Grotenhuis Anne J, Kolev Dimitar, Aben Katja K, Bryan Richard T, Catto James W F, Cheng Kar K, Conroy Samantha, Dyrskjøt Lars, Fleshner Neil E, James Nicholas D, Lamy Philippe, Lindskrog Sia Viborg, Malats Núria, Mengual Lourdes, Verhaegh Gerald, Zeegers Maurice P, Kiemeney Lambertus A L M, Vermeulen Sita
SCFD1 expression quantitative trait loci in amyotrophic lateral sclerosis are differentially expressed.
Brain communications 2021 3 (4): fcab236.
Iacoangeli Alfredo, Fogh Isabella, Selvackadunco Sashika, Topp Simon D, Shatunov Aleksey, van Rheenen Wouter, Al-Khleifat Ahmad, Opie-Martin Sarah, Ratti Antonia, Calvo Andrea, , Van Damme Philip, Robberecht Wim, Chio Adriano, Dobson Richard J, Hardiman Orla, Shaw Christopher E, van den Berg Leonard H, Andersen Peter M, Smith Bradley N, Silani Vincenzo, Veldink Jan H, Breen Gerome, Troakes Claire, Al-Chalabi Ammar, Jones Ashley
Genetic analysis of ALS cases in the isolated island population of Malta.
European journal of human genetics : EJHG 2021 1 29 (4): 604-614.
Borg Rebecca, Farrugia Wismayer Maia, Bonavia Karl, Farrugia Wismayer Andrew, Vella Malcolm, van Vugt Joke J F A, Kenna Brendan J, Kenna Kevin P, Vassallo Neville, Veldink Jan H, Cauchi Ruben
Lack of an association between SCFD1 rs10139154 polymorphism and amyotrophic lateral sclerosis.
Molecular medicine reports 2022 Apr 25 (4): .
Siokas Vasileios, Aloizou Athina-Maria, Liampas Ioannis, Bakirtzis Christos, Nasios Grigorios, Paterakis Konstantinos, Sgantzos Markos, Bogdanos Dimitrios P, Spandidos Demetrios A, Tsatsakis Aristidis, Mitsias Panayiotis D, Dardiotis Efthimi
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