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 *

162 related articles for article (PubMed ID: 31993931)

  • 21. Health problems in females carriers of premutation in the FMR1 gene.
    Lisik MZ
    Psychiatr Pol; 2017 Oct; 51(5):899-907. PubMed ID: 29289969
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population.
    Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; Levine RA; Brunberg JA; Zhang L; Jardini T; Gane LW; Harris SW; Herman K; Grigsby J; Greco CM; Berry-Kravis E; Tassone F; Hagerman PJ
    JAMA; 2004 Jan; 291(4):460-9. PubMed ID: 14747503
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Misunderstood terms and concepts identified through user testing of educational materials for fragile X premutation: "Not weak or fragile?".
    Lincoln-Boyea B; Moultrie RR; Biesecker BB; Underwood M; Duparc M; Wheeler AC; Peay HL
    J Genet Couns; 2024 Apr; 33(2):341-351. PubMed ID: 37232511
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation.
    Hessl D; Tassone F; Loesch DZ; Berry-Kravis E; Leehey MA; Gane LW; Barbato I; Rice C; Gould E; Hall DA; Grigsby J; Wegelin JA; Harris S; Lewin F; Weinberg D; Hagerman PJ; Hagerman RJ
    Am J Med Genet B Neuropsychiatr Genet; 2005 Nov; 139B(1):115-21. PubMed ID: 16184602
    [TBL] [Abstract][Full Text] [Related]  

  • 25. X chromosome inactivation does not define the development of premature ovarian failure in fragile X premutation carriers.
    Spath MA; Nillesen WN; Smits AP; Feuth TB; Braat DD; van Kessel AG; Yntema HG
    Am J Med Genet A; 2010 Feb; 152A(2):387-93. PubMed ID: 20101683
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mapping self-reports of working memory deficits to executive dysfunction in Fragile X Mental Retardation 1 (FMR1) gene premutation carriers asymptomatic for FXTAS.
    Kogan CS; Cornish KM
    Brain Cogn; 2010 Aug; 73(3):236-43. PubMed ID: 20573435
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Fragile X premutation in women: recognizing the health challenges beyond primary ovarian insufficiency.
    Hoyos LR; Thakur M
    J Assist Reprod Genet; 2017 Mar; 34(3):315-323. PubMed ID: 27995424
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Data-driven phenotype discovery of
    Movaghar A; Page D; Brilliant M; Baker MW; Greenberg J; Hong J; DaWalt LS; Saha K; Kuusisto F; Stewart R; Berry-Kravis E; Mailick MR
    Sci Adv; 2019 Aug; 5(8):eaaw7195. PubMed ID: 31457090
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Neurological and endocrine phenotypes of fragile X carrier women.
    Hall D; Todorova-Koteva K; Pandya S; Bernard B; Ouyang B; Walsh M; Pounardjian T; Deburghraeve C; Zhou L; Losh M; Leehey M; Berry-Kravis E
    Clin Genet; 2016 Jan; 89(1):60-7. PubMed ID: 26212380
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Carriage of One or Two FMR1 Premutation Alleles Seems to Have No Effect on Illness Severity in a FXTAS Female with an Autozygous FMR1 Premutation Allele.
    Rodriguez-Revenga L; Pagonabarraga J; Gómez-Anson B; López-Mourelo O; Izquierdo S; Alvarez-Mora MI; Granell E; Madrigal I; Milà M
    Cerebellum; 2016 Oct; 15(5):570-7. PubMed ID: 27315125
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Exploring inhibitory deficits in female premutation carriers of fragile X syndrome: through eye movements.
    Shelton AL; Cornish K; Kraan C; Georgiou-Karistianis N; Metcalfe SA; Bradshaw JL; Hocking DR; Archibald AD; Cohen J; Trollor JN; Fielding J
    Brain Cogn; 2014 Mar; 85():201-8. PubMed ID: 24424424
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation.
    Farzin F; Perry H; Hessl D; Loesch D; Cohen J; Bacalman S; Gane L; Tassone F; Hagerman P; Hagerman R
    J Dev Behav Pediatr; 2006 Apr; 27(2 Suppl):S137-44. PubMed ID: 16685180
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Preimplantation genetic diagnosis versus prenatal diagnosis-decision-making among pregnant FMR1 premutation carriers.
    Haham LM; Avrahami I; Domniz N; Ries-Levavi L; Berkenstadt M; Orvieto R; Cohen Y; Elizur SE
    J Assist Reprod Genet; 2018 Nov; 35(11):2071-2075. PubMed ID: 30136016
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Preliminary evidence of an effect of cerebellar volume on postural sway in FMR1 premutation males.
    Birch RC; Hocking DR; Cornish KM; Menant JC; Georgiou-Karistianis N; Godler DE; Wen W; Hackett A; Rogers C; Trollor JN
    Genes Brain Behav; 2015 Mar; 14(3):251-9. PubMed ID: 25689687
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Premature ovarian failure: a phenotypic expression of fragile X premutation.
    Holoch K; Stein Q; Flanagan J; Hansen K
    S D Med; 2008 Jan; 61(1):13, 15. PubMed ID: 18323308
    [TBL] [Abstract][Full Text] [Related]  

  • 38. DNA testing for fragile X syndrome: implications for parents and family.
    van Rijn MA; de Vries BB; Tibben A; van den Ouweland AM; Halley DJ; Niermeijer MF
    J Med Genet; 1997 Nov; 34(11):907-11. PubMed ID: 9391884
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Amygdala dysfunction in men with the fragile X premutation.
    Hessl D; Rivera S; Koldewyn K; Cordeiro L; Adams J; Tassone F; Hagerman PJ; Hagerman RJ
    Brain; 2007 Feb; 130(Pt 2):404-16. PubMed ID: 17166860
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Broad autism spectrum and obsessive-compulsive symptoms in adults with the fragile X premutation.
    Schneider A; Johnston C; Tassone F; Sansone S; Hagerman RJ; Ferrer E; Rivera SM; Hessl D
    Clin Neuropsychol; 2016 Aug; 30(6):929-43. PubMed ID: 27355445
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.