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 *

108 related articles for article (PubMed ID: 25339756)

  • 1. DCDC2 polymorphism is associated with left temporoparietal gray and white matter structures during development.
    Darki F; Peyrard-Janvid M; Matsson H; Kere J; Klingberg T
    J Neurosci; 2014 Oct; 34(43):14455-62. PubMed ID: 25339756
    [TBL] [Abstract][Full Text] [Related]  

  • 2. White matter maturation is associated with the emergence of Theory of Mind in early childhood.
    Grosse Wiesmann C; Schreiber J; Singer T; Steinbeis N; Friederici AD
    Nat Commun; 2017 Mar; 8():14692. PubMed ID: 28322222
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association of DCDC2 Polymorphisms with Normal Variations in Reading Abilities in a Chinese Population.
    Zhang Y; Li J; Song S; Tardif T; Burmeister M; Villafuerte SM; Su M; McBride C; Shu H
    PLoS One; 2016; 11(4):e0153603. PubMed ID: 27100778
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Neuroimaging genetic associations between
    Thomas T; Perdue MV; Khalaf S; Landi N; Hoeft F; Pugh K; Grigorenko EL
    J Clin Exp Neuropsychol; 2021 Apr; 43(3):276-289. PubMed ID: 33960276
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Common functional polymorphisms of DISC1 and cortical maturation in typically developing children and adolescents.
    Raznahan A; Lee Y; Long R; Greenstein D; Clasen L; Addington A; Rapoport JL; Giedd JN
    Mol Psychiatry; 2011 Sep; 16(9):917-26. PubMed ID: 20628343
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Animal models of developmental dyslexia.
    Galaburda AM
    Front Neurosci; 2022; 16():981801. PubMed ID: 36452335
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A systematic review and meta-analysis of imaging genetics studies of specific reading disorder.
    Thomas T; Khalaf S; Grigorenko EL
    Cogn Neuropsychol; 2021 May; 38(3):179-204. PubMed ID: 34529546
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Mediation Role of Dynamic Multisensory Processing Using Molecular Genetic Data in Dyslexia.
    Mascheretti S; Riva V; Feng B; Trezzi V; Andreola C; Giorda R; Villa M; Dionne G; Gori S; Marino C; Facoetti A
    Brain Sci; 2020 Dec; 10(12):. PubMed ID: 33339203
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dyslexia Candidate Gene and Ciliary Gene Expression Dynamics During Human Neuronal Differentiation.
    Bieder A; Yoshihara M; Katayama S; Krjutškov K; Falk A; Kere J; Tapia-Páez I
    Mol Neurobiol; 2020 Jul; 57(7):2944-2958. PubMed ID: 32445086
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Neuroimaging genetics studies of specific reading disability and developmental language disorder: A review.
    Landi N; Perdue M
    Lang Linguist Compass; 2019 Sep; 13(9):. PubMed ID: 31844423
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Patterns of biomarkers for three phenotype profiles of persisting specific learning disabilities during middle childhood and early adolescence: A preliminary study.
    Abbott RD; Raskind WH; Matsushita M; Price ND; Richards T; Berninger VW
    Biomark Genes; 2017 Dec; 1(1):. PubMed ID: 30854516
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Neurobiological Sex Differences in Developmental Dyslexia.
    Krafnick AJ; Evans TM
    Front Psychol; 2018; 9():2669. PubMed ID: 30687153
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A molecular-genetic and imaging-genetic approach to specific comprehension difficulties in children.
    Li M; Malins JG; DeMille MMC; Lovett MW; Truong DT; Epstein K; Lacadie C; Mehta C; Bosson-Heenan J; Gruen JR; Frijters JC;
    NPJ Sci Learn; 2018; 3():20. PubMed ID: 30631481
    [TBL] [Abstract][Full Text] [Related]  

  • 15. White matter network connectivity deficits in developmental dyslexia.
    Lou C; Duan X; Altarelli I; Sweeney JA; Ramus F; Zhao J
    Hum Brain Mapp; 2019 Feb; 40(2):505-516. PubMed ID: 30251768
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of NCAN as a candidate gene for developmental dyslexia.
    Einarsdottir E; Peyrard-Janvid M; Darki F; Tuulari JJ; Merisaari H; Karlsson L; Scheinin NM; Saunavaara J; Parkkola R; Kantojärvi K; Ämmälä AJ; Yiu-Lin Yu N; Matsson H; Nopola-Hemmi J; Karlsson H; Paunio T; Klingberg T; Leinonen E; Kere J
    Sci Rep; 2017 Aug; 7(1):9294. PubMed ID: 28839234
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neural Noise Hypothesis of Developmental Dyslexia.
    Hancock R; Pugh KR; Hoeft F
    Trends Cogn Sci; 2017 Jun; 21(6):434-448. PubMed ID: 28400089
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dyslexia risk gene relates to representation of sound in the auditory brainstem.
    Neef NE; Müller B; Liebig J; Schaadt G; Grigutsch M; Gunter TC; Wilcke A; Kirsten H; Skeide MA; Kraft I; Kraus N; Emmrich F; Brauer J; Boltze J; Friederici AD
    Dev Cogn Neurosci; 2017 Apr; 24():63-71. PubMed ID: 28182973
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms.
    Mascheretti S; De Luca A; Trezzi V; Peruzzo D; Nordio A; Marino C; Arrigoni F
    Transl Psychiatry; 2017 Jan; 7(1):e987. PubMed ID: 28045463
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.