These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

227 related articles for article (PubMed ID: 23786467)

  • 1. A family with two female siblings with compound heterozygous FMR1 premutation alleles.
    Basuta K; Lozano R; Schneider A; Yrigollen CM; Hessl D; Hagerman RJ; Tassone F
    Clin Genet; 2014 May; 85(5):458-63. PubMed ID: 23786467
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical phenotypes of a juvenile sibling pair carrying the fragile X premutation.
    Basuta K; Narcisa V; Chavez A; Kumar M; Gane L; Hagerman R; Tassone F
    Am J Med Genet A; 2011 Mar; 155A(3):519-25. PubMed ID: 21344625
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Maternal FMR1 premutation allele expansion and contraction in fraternal twins.
    Alfaro MP; Cohen M; Vnencak-Jones CL
    Am J Med Genet A; 2013 Oct; 161A(10):2620-5. PubMed ID: 23949867
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fragile X-associated tremor/ataxia syndrome: influence of the FMR1 gene on motor fiber tracts in males with normal and premutation alleles.
    Wang JY; Hessl D; Schneider A; Tassone F; Hagerman RJ; Rivera SM
    JAMA Neurol; 2013 Aug; 70(8):1022-9. PubMed ID: 23753897
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Psychological status in female carriers of premutation FMR1 allele showing a complex relationship with the size of CGG expansion.
    Loesch DZ; Bui MQ; Hammersley E; Schneider A; Storey E; Stimpson P; Burgess T; Francis D; Slater H; Tassone F; Hagerman RJ; Hessl D
    Clin Genet; 2015 Feb; 87(2):173-8. PubMed ID: 24428240
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The role of AGG interruptions in the transcription of FMR1 premutation alleles.
    Yrigollen CM; Tassone F; Durbin-Johnson B; Tassone F
    PLoS One; 2011; 6(7):e21728. PubMed ID: 21818263
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles.
    Nolin SL; Brown WT; Glicksman A; Houck GE; Gargano AD; Sullivan A; Biancalana V; Bröndum-Nielsen K; Hjalgrim H; Holinski-Feder E; Kooy F; Longshore J; Macpherson J; Mandel JL; Matthijs G; Rousseau F; Steinbach P; Väisänen ML; von Koskull H; Sherman SL
    Am J Hum Genet; 2003 Feb; 72(2):454-64. PubMed ID: 12529854
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Immune dysregulation as a cause of autoinflammation in fragile X premutation carriers: link between FMRI CGG repeat number and decreased cytokine responses.
    Careaga M; Rose D; Tassone F; Berman RF; Hagerman R; Ashwood P
    PLoS One; 2014; 9(4):e94475. PubMed ID: 24718368
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Study of telomere length in men who carry a fragile X premutation or full mutation allele.
    Albizua I; Chopra P; Allen EG; He W; Amin AS; Sherman SL
    Hum Genet; 2020 Dec; 139(12):1531-1539. PubMed ID: 32533363
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prevalence and instability of fragile X alleles: implications for offering fragile X prenatal diagnosis.
    Cronister A; Teicher J; Rohlfs EM; Donnenfeld A; Hallam S
    Obstet Gynecol; 2008 Mar; 111(3):596-601. PubMed ID: 18310361
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Screening for the presence of FMR1 premutation alleles in women with parkinsonism.
    Cilia R; Kraff J; Canesi M; Pezzoli G; Goldwurm S; Amiri K; Tang HT; Pan R; Hagerman PJ; Tassone F
    Arch Neurol; 2009 Feb; 66(2):244-9. PubMed ID: 19204162
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Expansion of an FMR1 grey-zone allele to a full mutation in two generations.
    Fernandez-Carvajal I; Lopez Posadas B; Pan R; Raske C; Hagerman PJ; Tassone F
    J Mol Diagn; 2009 Jul; 11(4):306-10. PubMed ID: 19525339
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Inhibition deficits are modulated by age and CGG repeat length in carriers of the FMR1 premutation allele who are mothers of children with fragile X syndrome.
    Klusek J; Hong J; Sterling A; Berry-Kravis E; Mailick MR
    Brain Cogn; 2020 Mar; 139():105511. PubMed ID: 31887710
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evaluation of the human fragile X mental retardation 1 polymerase chain reaction reagents to amplify the FMR1 gene: testing in a clinical diagnostic laboratory.
    Nahhas FA; Monroe TJ; Prior TW; Botma PI; Fang J; Snyder PJ; Talbott SL; Feldman GL
    Genet Test Mol Biomarkers; 2012 Mar; 16(3):187-92. PubMed ID: 21992462
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Size bias of fragile X premutation alleles in late-onset movement disorders.
    Jacquemont S; Leehey MA; Hagerman RJ; Beckett LA; Hagerman PJ
    J Med Genet; 2006 Oct; 43(10):804-9. PubMed ID: 16723388
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program.
    Jarmolowicz AI; Baker EK; Bartlett E; Francis D; Ling L; Gamage D; Delatycki MB; Godler DE
    Am J Med Genet A; 2021 May; 185(5):1498-1503. PubMed ID: 33544979
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Static and dynamic postural control deficits in aging fragile X mental retardation 1 (FMR1) gene premutation carriers.
    Wang Z; Khemani P; Schmitt LM; Lui S; Mosconi MW
    J Neurodev Disord; 2019 Jan; 11(1):2. PubMed ID: 30665341
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles.
    Nolin SL; Glicksman A; Tortora N; Allen E; Macpherson J; Mila M; Vianna-Morgante AM; Sherman SL; Dobkin C; Latham GJ; Hadd AG
    Am J Med Genet A; 2019 Jul; 179(7):1148-1156. PubMed ID: 31050164
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fragile X carrier screening and FMR1 allele distribution in the Japanese population.
    Otsuka S; Sakamoto Y; Siomi H; Itakura M; Yamamoto K; Matumoto H; Sasaki T; Kato N; Nanba E
    Brain Dev; 2010 Feb; 32(2):110-4. PubMed ID: 19211207
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Improved Assays for AGG Interruptions in Fragile X Premutation Carriers.
    Hayward BE; Usdin K
    J Mol Diagn; 2017 Nov; 19(6):828-835. PubMed ID: 28818679
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.