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Journal Abstract Search

170 related items for PubMed ID: 22517379

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Whole Genome Analysis in Consanguineous Families Reveals New Loci for Speech Sound Disorder (SSD).
    Yasmin T, Sadia A, Nadeem L, Basra MAR, Rice ML, Raza MH.
    Genes (Basel); 2024 Aug 13; 15(8):. PubMed ID: 39202429
    [Abstract] [Full Text] [Related]

  • 3. Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders.
    Truong DT, Shriberg LD, Smith SD, Chapman KL, Scheer-Cohen AR, DeMille MM, Adams AK, Nato AQ, Wijsman EM, Eicher JD, Gruen JR.
    Hum Genet; 2016 Dec 13; 135(12):1329-1341. PubMed ID: 27535846
    [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 13; 74(2):283-97. PubMed ID: 14740317
    [Abstract] [Full Text] [Related]

  • 5. 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 13; 54(6):1628-43. PubMed ID: 21930616
    [Abstract] [Full Text] [Related]

  • 6. Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36.
    Field LL, Shumansky K, Ryan J, Truong D, Swiergala E, Kaplan BJ.
    Genes Brain Behav; 2013 Feb 13; 12(1):56-69. PubMed ID: 23190410
    [Abstract] [Full Text] [Related]

  • 7. Speech sound disorder influenced by a locus in 15q14 region.
    Stein CM, Millard C, Kluge A, Miscimarra LE, Cartier KC, Freebairn LA, Hansen AJ, Shriberg LD, Taylor HG, Lewis BA, Iyengar SK.
    Behav Genet; 2006 Nov 13; 36(6):858-68. PubMed ID: 16786424
    [Abstract] [Full Text] [Related]

  • 8. 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 13; 24(5):191-200. PubMed ID: 24849541
    [Abstract] [Full Text] [Related]

  • 9. Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family.
    Carrion-Castillo A, Estruch SB, Maassen B, Franke B, Francks C, Fisher SE.
    Hum Genet; 2021 Aug 13; 140(8):1183-1200. PubMed ID: 34076780
    [Abstract] [Full Text] [Related]

  • 10. A multigenerational family study of oral and hand motor sequencing ability provides evidence for a familial speech sound disorder subtype.
    Peter B, Raskind WH.
    Top Lang Disord; 2011 Apr 13; 31(2):145-167. PubMed ID: 21909176
    [Abstract] [Full Text] [Related]

  • 11. Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech.
    Peter B, Button L, Stoel-Gammon C, Chapman K, Raskind WH.
    Clin Linguist Phon; 2013 Mar 13; 27(3):163-91. PubMed ID: 23339324
    [Abstract] [Full Text] [Related]

  • 12. Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech.
    Peter B, Wijsman EM, Nato AQ, University of Washington Center for Mendelian Genomics, Matsushita MM, Chapman KL, Stanaway IB, Wolff J, Oda K, Gabo VB, Raskind WH.
    PLoS One; 2016 Mar 13; 11(4):e0153864. PubMed ID: 27120335
    [Abstract] [Full Text] [Related]

  • 13. Further evidence of pleiotropy influencing speech and language: analysis of the DYX8 region.
    Miscimarra L, Stein C, Millard C, Kluge A, Cartier K, Freebairn L, Hansen A, Shriberg L, Taylor HG, Lewis B, Iyengar SK.
    Hum Hered; 2007 Mar 13; 63(1):47-58. PubMed ID: 17230025
    [Abstract] [Full Text] [Related]

  • 14. 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 16; 5():4831. PubMed ID: 25226531
    [Abstract] [Full Text] [Related]

  • 15. Neuropsychological endophenotype approach to genome-wide linkage analysis identifies susceptibility loci for ADHD on 2q21.1 and 13q12.11.
    Rommelse NN, Arias-Vásquez A, Altink ME, Buschgens CJ, Fliers E, Asherson P, Faraone SV, Buitelaar JK, Sergeant JA, Oosterlaan J, Franke B.
    Am J Hum Genet; 2008 Jul 16; 83(1):99-105. PubMed ID: 18599010
    [Abstract] [Full Text] [Related]

  • 16. Taiwan Schizophrenia Linkage Study: lessons learned from endophenotype-based genome-wide linkage scans and perspective.
    Chen WJ.
    Am J Med Genet B Neuropsychiatr Genet; 2013 Oct 16; 162B(7):636-47. PubMed ID: 24132895
    [Abstract] [Full Text] [Related]

  • 17. Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families.
    Simpson CL, Musolf AM, Li Q, Portas L, Murgia F, Cordero RY, Cordero JB, Moiz BA, Holzinger ER, Middlebrooks CD, Lewis DD, Bailey-Wilson JE, Stambolian D.
    BMC Med Genet; 2019 Jan 31; 20(1):27. PubMed ID: 30704416
    [Abstract] [Full Text] [Related]

  • 18. Pleiotropic effects of the 11p13 locus on developmental verbal dyspraxia and EEG centrotemporal sharp waves.
    Pal DK, Li W, Clarke T, Lieberman P, Strug LJ.
    Genes Brain Behav; 2010 Nov 31; 9(8):1004-12. PubMed ID: 20825490
    [Abstract] [Full Text] [Related]

  • 19. 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 31; 14(4):377-85. PubMed ID: 25778907
    [Abstract] [Full Text] [Related]

  • 20. A genome-wide linkage search for bipolar disorder susceptibility loci in a large and complex pedigree from the eastern part of Cuba.
    Marcheco-Teruel B, Flint TJ, Wikman FP, Torralbas M, González L, Blanco L, Tan Q, Ewald H, Orntoft T, Kruse TA, Børglum AD, Mors O.
    Am J Med Genet B Neuropsychiatr Genet; 2006 Dec 05; 141B(8):833-43. PubMed ID: 16917938
    [Abstract] [Full Text] [Related]

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