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 *

254 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. KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia.
    Mascheretti S; Riva V; Giorda R; Beri S; Lanzoni LF; Cellino MR; Marino C
    J Hum Genet; 2014 Apr; 59(4):189-97. PubMed ID: 24430574
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association of short-term memory with a variant within DYX1C1 in developmental dyslexia.
    Marino C; Citterio A; Giorda R; Facoetti A; Menozzi G; Vanzin L; Lorusso ML; Nobile M; Molteni M
    Genes Brain Behav; 2007 Oct; 6(7):640-6. PubMed ID: 17309662
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Complex effects of dyslexia risk factors account for ADHD traits: evidence from two independent samples.
    Mascheretti S; Trezzi V; Giorda R; Boivin M; Plourde V; Vitaro F; Brendgen M; Dionne G; Marino C
    J Child Psychol Psychiatry; 2017 Jan; 58(1):75-82. PubMed ID: 27501527
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. DCDC2 genetic variants and susceptibility to developmental dyslexia.
    Marino C; Meng H; Mascheretti S; Rusconi M; Cope N; Giorda R; Molteni M; Gruen JR
    Psychiatr Genet; 2012 Feb; 22(1):25-30. PubMed ID: 21881542
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The influence of DCDC2 risk genetic variants on reading: Testing main and haplotypic effects.
    Riva V; Mozzi A; Forni D; Trezzi V; Giorda R; Riva S; Villa M; Sironi M; Cagliani R; Mascheretti S
    Neuropsychologia; 2019 Jul; 130():52-58. PubMed ID: 29803723
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association study of developmental dyslexia candidate genes DCDC2 and KIAA0319 in Chinese population.
    Sun Y; Gao Y; Zhou Y; Chen H; Wang G; Xu J; Xia J; Huen MS; Siok WT; Jiang Y; Tan LH
    Am J Med Genet B Neuropsychiatr Genet; 2014 Dec; 165B(8):627-34. PubMed ID: 25230923
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region.
    Wigg KG; Feng Y; Crosbie J; Tannock R; Kennedy JL; Ickowicz A; Malone M; Schachar R; Barr CL
    Genes Brain Behav; 2008 Nov; 7(8):877-86. PubMed ID: 19076634
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia.
    Marino C; Giorda R; Luisa Lorusso M; Vanzin L; Salandi N; Nobile M; Citterio A; Beri S; Crespi V; Battaglia M; Molteni M
    Eur J Hum Genet; 2005 Apr; 13(4):491-9. PubMed ID: 15702132
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population.
    Venkatesh SK; Siddaiah A; Padakannaya P; Ramachandra NB
    J Hum Genet; 2013 Aug; 58(8):531-8. PubMed ID: 23677054
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Effect of READ1 on latent profiles of reading disorder and comorbid attention and language impairment subtypes.
    Li M; Truong DT; DeMille M; Malins JG; Lovett MW; Bosson-Heenan J; Gruen JR; Frijters JC
    Child Neuropsychol; 2020 Feb; 26(2):145-169. PubMed ID: 31411106
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia.
    Brkanac Z; Chapman NH; Matsushita MM; Chun L; Nielsen K; Cochrane E; Berninger VW; Wijsman EM; Raskind WH
    Am J Med Genet B Neuropsychiatr Genet; 2007 Jun; 144B(4):556-60. PubMed ID: 17450541
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children.
    Eicher JD; Montgomery AM; 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; Gruen JR;
    Brain Imaging Behav; 2016 Mar; 10(1):272-82. PubMed ID: 25953057
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypes.
    Mascheretti S; Bureau A; Battaglia M; Simone D; Quadrelli E; Croteau J; Cellino MR; Giorda R; Beri S; Maziade M; Marino C
    Genes Brain Behav; 2013 Feb; 12(1):47-55. PubMed ID: 23176554
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial dyslexia in a large Swedish family: a whole genome linkage scan.
    Svensson I; Nilsson S; Wahlström J; Jernås M; Carlsson LM; Hjelmquist E
    Behav Genet; 2011 Jan; 41(1):43-9. PubMed ID: 20862559
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia.
    Mascheretti S; Bureau A; Trezzi V; Giorda R; Marino C
    Hum Genet; 2015 Jul; 134(7):749-60. PubMed ID: 25916574
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Further evidence for DYX1C1 as a susceptibility factor for dyslexia.
    Dahdouh F; Anthoni H; Tapia-Páez I; Peyrard-Janvid M; Schulte-Körne G; Warnke A; Remschmidt H; Ziegler A; Kere J; Müller-Myhsok B; Nöthen MM; Schumacher J; Zucchelli M
    Psychiatr Genet; 2009 Apr; 19(2):59-63. PubMed ID: 19240663
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic and protein interaction studies between the ciliary dyslexia candidate genes DYX1C1 and DCDC2.
    Bieder A; Chandrasekar G; Wason A; Erkelenz S; Gopalakrishnan J; Kere J; Tapia-Páez I
    BMC Mol Cell Biol; 2023 May; 24(1):20. PubMed ID: 37237337
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A theoretical molecular network for dyslexia: integrating available genetic findings.
    Poelmans G; Buitelaar JK; Pauls DL; Franke B
    Mol Psychiatry; 2011 Apr; 16(4):365-82. PubMed ID: 20956978
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.