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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 9, 2023. (Total: 217811Documents)
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Records 1 - 13 (of 13 Records)

Query Trace: Memory and FMR1[original query]
Age-dependent cognitive changes in carriers of the fragile X syndrome.
Cortex; a journal devoted to the study of the nervous system and behavior 2008 Jun 44 (6): 628-36.
Cornish Kim M, Li Lexin, Kogan Cary S, Jacquemont Sebastien, Turk Jeremy, Dalton Ann, Hagerman Randi J, Hagerman Paul
No evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50.
American journal of human genetics 2008 Dec 83 (6): 692-702.
Hunter Jessica Ezzell, Allen Emily Graves, Abramowitz Ann, Rusin Michele, Leslie Mary, Novak Gloria, Hamilton Debra, Shubeck Lisa, Charen Krista, Sherman Stephanie
Impact of the Fragile X mental retardation 1 (FMR1) gene premutation on neuropsychiatric functioning in adult males without fragile X-associated Tremor/Ataxia syndrome: a controlled study.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Sep 147B (6): 859-72.
Kogan Cary S, Turk Jeremy, Hagerman Randi J, Cornish Kim
Screening for the presence of FMR1 premutation alleles in women with parkinsonism.
Archives of neurology 2009 Feb 66 (2): 244-9.
Cilia Roberto, Kraff Jeremy, Canesi Margherita, Pezzoli Gianni, Goldwurm Stefano, Amiri Khalid, Tang Hiu-Tung, Pan Ruiqin, Hagerman Paul J, Tassone Flo
An fMRI study of the prefrontal activity during the performance of a working memory task in premutation carriers of the fragile X mental retardation 1 gene with and without fragile X-associated tremor/ataxia syndrome (FXTAS).
Journal of psychiatric research 2011 Jan 45 (1): 36-43.
Hashimoto Ryu-ichiro, Backer Kristina C, Tassone Flora, Hagerman Randi J, Rivera Susan
Confirmed rare copy number variants implicate novel genes in schizophrenia.
Biochemical Society transactions 2010 Apr 38 (2): 445-51.
Tam Gloria W C, van de Lagemaat Louie N, Redon Richard, Strathdee Karen E, Croning Mike D R, Malloy Mary P, Muir Walter J, Pickard Ben S, Deary Ian J, Blackwood Douglas H R, Carter Nigel P, Grant Seth G
Neuropsychological findings from older premutation carrier males and their noncarrier siblings from families with fragile X syndrome.
Neuropsychology 2011 May 25 (3): 404-11.
Allen Emily Graves, Hunter Jessica E, Rusin Michele, Juncos Jorge, Novak Gloria, Hamilton Debra, Shubeck Lisa, Charen Krista, Sherman Stephanie
Low-normal FMR1 CGG repeat length: phenotypic associations.
Frontiers in genetics 2014 5 309.
Mailick Marsha R, Hong Jinkuk, Rathouz Paul, Baker Mei W, Greenberg Jan S, Smith Leann, Maenner Matth
Investigation of memory, executive functions, and anatomic correlates in asymptomatic FMR1 premutation carriers.
Neurobiology of aging 2014 Aug 35 (8): 1939-46.
Hippolyte Loyse, Battistella Giovanni, Perrin Aline G, Fornari Eleonora, Cornish Kim M, Beckmann Jacques S, Niederhauser Julien, Vingerhoets François J G, Draganski Bogdan, Maeder Philippe, Jacquemont Sébasti
Temporal dynamics of attentional selection in adult male carriers of the fragile X premutation allele and adult controls.
Frontiers in human neuroscience 2015 9 37.
Wong Ling M, Tassone Flora, Rivera Susan M, Simon Tony
ß-glucuronidase mRNA levels are correlated with gait and working memory in premutation females: understanding the role of FMR1 premutation alleles.
Scientific reports 2016 6 29366.
Kraan C M, Cornish K M, Bui Q M, Li X, Slater H R, Godler D
Working memory and arithmetic impairments in children with FMR1 premutation and gray zone alleles.
Dementia & neuropsychologia 2022 6 16 (1): 105-114.
Martins Aline Aparecida Silva, Paiva Giulia Moreira, Matosinho Carolina Guimarães Ramos, Coser Elisângela Monteiro, Fonseca Pablo Augusto de Souza, Haase Vitor Geraldi, Carvalho Maria Raquel Sant
Evaluation of AQP4 functional variants and its association with fragile X-associated tremor/ataxia syndrome.
Frontiers in aging neuroscience 2023 1 14 1073258.
Elias-Mas Andrea, Potrony Miriam, Bague Jaume, Cutler David J, Alvarez-Mora Maria Isabel, Torres Teresa, Barcos Tamara, Puig-Butille Joan Anton, Rubio Marta, Madrigal Irene, Puig Susana, Allen Emily G, Rodriguez-Revenga La
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