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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 1, 2023. (Total: 221588Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Cognition 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
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
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
FMR1 locus isoforms: potential biomarker candidates in fragile X-associated tremor/ataxia syndrome (FXTAS).
Scientific reports 2020 Jul 10 (1): 11099.
Zafarullah Marwa, Tang Hiu-Tung, Durbin-Johnson Blythe, Fourie Emily, Hessl David, Rivera Susan M, Tassone Flo
Metabolomic Biomarkers Are Associated With Area of the Pons in Fragile X Premutation Carriers at Risk for Developing FXTAS.
Frontiers in psychiatry 2021 9 12 691717.
Zafarullah Marwa, Durbin-Johnson Blythe, Fourie Emily S, Hessl David R, Rivera Susan M, Tassone Flo
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