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 *

150 related articles for article (PubMed ID: 21046216)

  • 1. Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia.
    Marino C; Mascheretti S; Riva V; Cattaneo F; Rigoletto C; Rusconi M; Gruen JR; Giorda R; Lazazzera C; Molteni M
    Behav Genet; 2011 Jan; 41(1):67-76. PubMed ID: 21046216
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.
    Schumacher J; Anthoni H; Dahdouh F; König IR; Hillmer AM; Kluck N; Manthey M; Plume E; Warnke A; Remschmidt H; Hülsmann J; Cichon S; Lindgren CM; Propping P; Zucchelli M; Ziegler A; Peyrard-Janvid M; Schulte-Körne G; Nöthen MM; Kere J
    Am J Hum Genet; 2006 Jan; 78(1):52-62. PubMed ID: 16385449
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Moving closer to a public health model of language and learning disabilities: the role of genetics and the search for etiologies.
    Miller B; McCardle P
    Behav Genet; 2011 Jan; 41(1):1-5. PubMed ID: 21229298
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colors.
    Rubenstein KB; Raskind WH; Berninger VW; Matsushita MM; Wijsman EM
    Am J Med Genet B Neuropsychiatr Genet; 2014 Jun; 165B(4):345-56. PubMed ID: 24807833
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Developmental dyslexia susceptibility genes DNAAF4, DCDC2, and NRSN1 are associated with brain function in fluently reading adolescents and young adults.
    Rinne N; Wikman P; Sahari E; Salmi J; Einarsdóttir E; Kere J; Alho K
    Cereb Cortex; 2024 Apr; 34(4):. PubMed ID: 38610086
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 63(1):47-58. PubMed ID: 17230025
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genome-wide association study of shared components of reading disability and language impairment.
    Eicher JD; Powers NR; Miller LL; Akshoomoff N; Amaral DG; Bloss CS; Libiger O; Schork NJ; Darst BF; Casey BJ; Chang L; Ernst T; Frazier J; Kaufmann WE; Keating B; Kenet T; Kennedy D; Mostofsky S; Murray SS; Sowell ER; Bartsch H; Kuperman JM; Brown TT; Hagler DJ; Dale AM; Jernigan TL; St Pourcain B; Davey Smith G; Ring SM; Gruen JR;
    Genes Brain Behav; 2013 Nov; 12(8):792-801. PubMed ID: 24024963
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Quantitative genetics in the era of molecular genetics: learning abilities and disabilities as an example.
    Haworth CM; Plomin R
    J Am Acad Child Adolesc Psychiatry; 2010 Aug; 49(8):783-93. PubMed ID: 20643312
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Human-specific insights into candidate genes and boosted discoveries of novel loci illuminate roles of neuroglia in reading disorders.
    Wei WH; Ma S; Fu B; Song R; Guo H
    Genes Brain Behav; 2024 Jun; 23(3):e12899. PubMed ID: 38752599
    [TBL] [Abstract][Full Text] [Related]  

  • 10. DCDC2, KIAA0319 and CMIP are associated with reading-related traits.
    Scerri TS; Morris AP; Buckingham LL; Newbury DF; Miller LL; Monaco AP; Bishop DV; Paracchini S
    Biol Psychiatry; 2011 Aug; 70(3):237-45. PubMed ID: 21457949
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.
    Newbury DF; Paracchini S; Scerri TS; Winchester L; Addis L; Richardson AJ; Walter J; Stein JF; Talcott JB; Monaco AP
    Behav Genet; 2011 Jan; 41(1):90-104. PubMed ID: 21165691
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The Association of Dyslexia and Developmental Speech and Language Disorder Candidate Genes with Reading and Language Abilities in Adults.
    Doust C; Gordon SD; Garden N; Fisher SE; Martin NG; Bates TC; Luciano M
    Twin Res Hum Genet; 2020 Feb; 23(1):23-32. PubMed ID: 32248883
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genome-wide screening for DNA variants associated with reading and language traits.
    Gialluisi A; Newbury DF; Wilcutt EG; Olson RK; DeFries JC; Brandler WM; Pennington BF; Smith SD; Scerri TS; Simpson NH; ; Luciano M; Evans DM; Bates TC; Stein JF; Talcott JB; Monaco AP; Paracchini S; Francks C; Fisher SE
    Genes Brain Behav; 2014 Sep; 13(7):686-701. PubMed ID: 25065397
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The correlation between reading and mathematics ability at age twelve has a substantial genetic component.
    Davis OS; Band G; Pirinen M; Haworth CM; Meaburn EL; Kovas Y; Harlaar N; Docherty SJ; Hanscombe KB; Trzaskowski M; Curtis CJ; Strange A; Freeman C; Bellenguez C; Su Z; Pearson R; Vukcevic D; Langford C; Deloukas P; Hunt S; Gray E; Dronov S; Potter SC; Tashakkori-Ghanbaria A; Edkins S; Bumpstead SJ; Blackwell JM; Bramon E; Brown MA; Casas JP; Corvin A; Duncanson A; Jankowski JA; Markus HS; Mathew CG; Palmer CN; Rautanen A; Sawcer SJ; Trembath RC; Viswanathan AC; Wood NW; Barroso I; Peltonen L; Dale PS; Petrill SA; Schalkwyk LS; Craig IW; Lewis CM; Price TS; ; Donnelly P; Plomin R; Spencer CC
    Nat Commun; 2014 Jul; 5():4204. PubMed ID: 25003214
    [TBL] [Abstract][Full Text] [Related]  

  • 15. DYX1C1 is required for axonemal dynein assembly and ciliary motility.
    Tarkar A; Loges NT; Slagle CE; Francis R; Dougherty GW; Tamayo JV; Shook B; Cantino M; Schwartz D; Jahnke C; Olbrich H; Werner C; Raidt J; Pennekamp P; Abouhamed M; Hjeij R; Köhler G; Griese M; Li Y; Lemke K; Klena N; Liu X; Gabriel G; Tobita K; Jaspers M; Morgan LC; Shapiro AJ; Letteboer SJ; Mans DA; Carson JL; Leigh MW; Wolf WE; Chen S; Lucas JS; Onoufriadis A; Plagnol V; Schmidts M; Boldt K; ; Roepman R; Zariwala MA; Lo CW; Mitchison HM; Knowles MR; Burdine RD; Loturco JJ; Omran H
    Nat Genet; 2013 Sep; 45(9):995-1003. PubMed ID: 23872636
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A genome-wide association study for reading and language abilities in two population cohorts.
    Luciano M; Evans DM; Hansell NK; Medland SE; Montgomery GW; Martin NG; Wright MJ; Bates TC
    Genes Brain Behav; 2013 Aug; 12(6):645-52. PubMed ID: 23738518
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia.
    Gialluisi A; Andlauer TFM; Mirza-Schreiber N; Moll K; Becker J; Hoffmann P; Ludwig KU; Czamara D; Pourcain BS; Honbolygó F; Tóth D; Csépe V; Huguet G; Chaix Y; Iannuzzi S; Demonet JF; Morris AP; Hulslander J; Willcutt EG; DeFries JC; Olson RK; Smith SD; Pennington BF; Vaessen A; Maurer U; Lyytinen H; Peyrard-Janvid M; Leppänen PHT; Brandeis D; Bonte M; Stein JF; Talcott JB; Fauchereau F; Wilcke A; Kirsten H; Müller B; Francks C; Bourgeron T; Monaco AP; Ramus F; Landerl K; Kere J; Scerri TS; Paracchini S; Fisher SE; Schumacher J; Nöthen MM; Müller-Myhsok B; Schulte-Körne G
    Mol Psychiatry; 2021 Jul; 26(7):3004-3017. PubMed ID: 33057169
    [TBL] [Abstract][Full Text] [Related]  

  • 18. From BDNF to reading: Neural activation and phonological processing as multiple mediators.
    Mascheretti S; Perdue MV; Feng B; Andreola C; Dionne G; Jasińska KK; Pugh KR; Grigorenko EL; Landi N
    Behav Brain Res; 2021 Jan; 396():112859. PubMed ID: 32810467
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genome-wide association study of word reading: Overlap with risk genes for neurodevelopmental disorders.
    Price KM; Wigg KG; Feng Y; Blokland K; Wilkinson M; He G; Kerr EN; Carter TC; Guger SL; Lovett MW; Strug LJ; Barr CL
    Genes Brain Behav; 2020 Jul; 19(6):e12648. PubMed ID: 32108986
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders.
    ;
    Cell; 2019 Dec; 179(7):1469-1482.e11. PubMed ID: 31835028
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.