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 *

184 related articles for article (PubMed ID: 24849541)

  • 1. Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders.
    Stein CM; Truitt B; Deng F; Ciesla AA; Qiu F; Joseph P; Raghavendra R; Fondran J; Igo RP; Tag J; Freebairn L; Taylor HG; Lewis BA; Iyengar SK
    Psychiatr Genet; 2014 Oct; 24(5):191-200. PubMed ID: 24849541
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Literacy outcomes of children with early childhood speech sound disorders: impact of endophenotypes.
    Lewis BA; Avrich AA; Freebairn LA; Hansen AJ; Sucheston LE; Kuo I; Taylor HG; Iyengar SK; Stein CM
    J Speech Lang Hear Res; 2011 Dec; 54(6):1628-43. PubMed ID: 21930616
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains.
    Eicher JD; Stein CM; Deng F; Ciesla AA; Powers NR; Boada R; Smith SD; Pennington BF; Iyengar SK; Lewis BA; Gruen JR
    Genes Brain Behav; 2015 Apr; 14(4):377-85. PubMed ID: 25778907
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading.
    Stein CM; Schick JH; Gerry Taylor H; Shriberg LD; Millard C; Kundtz-Kluge A; Russo K; Minich N; Hansen A; Freebairn LA; Elston RC; Lewis BA; Iyengar SK
    Am J Hum Genet; 2004 Feb; 74(2):283-97. PubMed ID: 14740317
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits.
    Bates TC; Luciano M; Medland SE; Montgomery GW; Wright MJ; Martin NG
    Behav Genet; 2011 Jan; 41(1):50-7. PubMed ID: 20949370
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Common variation near ROBO2 is associated with expressive vocabulary in infancy.
    St Pourcain B; Cents RA; Whitehouse AJ; Haworth CM; Davis OS; O'Reilly PF; Roulstone S; Wren Y; Ang QW; Velders FP; Evans DM; Kemp JP; Warrington NM; Miller L; Timpson NJ; Ring SM; Verhulst FC; Hofman A; Rivadeneira F; Meaburn EL; Price TS; Dale PS; Pillas D; Yliherva A; Rodriguez A; Golding J; Jaddoe VW; Jarvelin MR; Plomin R; Pennell CE; Tiemeier H; Davey Smith G
    Nat Commun; 2014 Sep; 5():4831. PubMed ID: 25226531
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Replicative genetic association study between functional polymorphisms in
    Yang SY; Kim SA; Hur GM; Park M; Park JE; Yoo HJ
    Mol Autism; 2017; 8():44. PubMed ID: 28808521
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Contribution of Genetic Polymorphisms and Haplotypes in DRD2, BDNF, and Opioid Receptors to Heroin Dependence and Endophenotypes Among the Han Chinese.
    Gao X; Wang Y; Lang M; Yuan L; Reece AS; Wang W
    OMICS; 2017 Jul; 21(7):404-412. PubMed ID: 28692418
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Musical aptitude is associated with AVPR1A-haplotypes.
    Ukkola LT; Onkamo P; Raijas P; Karma K; Järvelä I
    PLoS One; 2009 May; 4(5):e5534. PubMed ID: 19461995
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family.
    Peter B; Matsushita M; Raskind WH
    Psychiatr Genet; 2012 Oct; 22(5):226-34. PubMed ID: 22517379
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Subtyping Children With Speech Sound Disorders by Endophenotypes.
    Lewis BA; Avrich AA; Freebairn LA; Taylor HG; Iyengar SK; Stein CM
    Top Lang Disord; 2011; 31(2):112-127. PubMed ID: 22844175
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The Speech "Bamana": Using the Syllable Repetition Task to Identify Underlying Phonological Deficits in Children With Speech and Language Impairments.
    Roepke E; Bower KE; Miller CA; Brosseau-Lapré F
    J Speech Lang Hear Res; 2020 Jul; 63(7):2229-2244. PubMed ID: 32640178
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phonological processing and reading in children with speech sound disorders.
    Rvachew S
    Am J Speech Lang Pathol; 2007 Aug; 16(3):260-70. PubMed ID: 17666551
    [TBL] [Abstract][Full Text] [Related]  

  • 14. DRD2 and PPP1R1B (DARPP-32) polymorphisms independently confer increased risk for autism spectrum disorders and additively predict affected status in male-only affected sib-pair families.
    Hettinger JA; Liu X; Hudson ML; Lee A; Cohen IL; Michaelis RC; Schwartz CE; Lewis SM; Holden JJ
    Behav Brain Funct; 2012 May; 8():19. PubMed ID: 22559203
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Heritability estimation for speech-sound traits with developmental trajectories.
    Stein CM; Lu Q; Elston RC; Freebairn LA; Hansen AJ; Shriberg LD; Taylor HG; Lewis BA; Iyengar SK
    Behav Genet; 2011 Mar; 41(2):184-91. PubMed ID: 20623172
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Examination of AVPR1a as an autism susceptibility gene.
    Wassink TH; Piven J; Vieland VJ; Pietila J; Goedken RJ; Folstein SE; Sheffield VC
    Mol Psychiatry; 2004 Oct; 9(10):968-72. PubMed ID: 15098001
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Reading Outcomes for Individuals With Histories of Suspected Childhood Apraxia of Speech.
    Miller GJ; Lewis B; Benchek P; Freebairn L; Tag J; Budge K; Iyengar SK; Voss-Hoynes H; Taylor HG; Stein C
    Am J Speech Lang Pathol; 2019 Nov; 28(4):1432-1447. PubMed ID: 31419159
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Morphological Awareness Skills of Second- and Third-Grade Students With and Without Speech Sound Disorders.
    Apel K; Henbest VS
    Lang Speech Hear Serv Sch; 2020 Jul; 51(3):603-616. PubMed ID: 32692964
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association and Promoter Analysis of AVPR1A in Finnish Autism Families.
    Kantojärvi K; Oikkonen J; Kotala I; Kallela J; Vanhala R; Onkamo P; Järvelä I
    Autism Res; 2015 Oct; 8(5):634-9. PubMed ID: 25707602
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association between the arginine vasopressin 1a receptor (AVPR1a) gene and autism in a family-based study: mediation by socialization skills.
    Yirmiya N; Rosenberg C; Levi S; Salomon S; Shulman C; Nemanov L; Dina C; Ebstein RP
    Mol Psychiatry; 2006 May; 11(5):488-94. PubMed ID: 16520824
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.