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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2010 | 4 |
2011 | 1 |
2022 | 2 |
2024 | 0 |
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6 results
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Page 1
The dyslexia-associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage.
J Biol Chem. 2010 Dec 17;285(51):40148-62. doi: 10.1074/jbc.M110.145961. Epub 2010 Oct 13.
J Biol Chem. 2010.
PMID: 20943657
Free PMC article.
A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3.
Addis L, Friederici AD, Kotz SA, Sabisch B, Barry J, Richter N, Ludwig AA, Rübsamen R, Albert FW, Pääbo S, Newbury DF, Monaco AP.
Addis L, et al.
Genes Brain Behav. 2010 Aug;9(6):545-61. doi: 10.1111/j.1601-183X.2010.00583.x. Epub 2010 Mar 25.
Genes Brain Behav. 2010.
PMID: 20345892
Free PMC article.
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PCSK6 is associated with handedness in individuals with dyslexia.
Scerri TS, Brandler WM, Paracchini S, Morris AP, Ring SM, Richardson AJ, Talcott JB, Stein J, Monaco AP.
Scerri TS, et al.
Hum Mol Genet. 2011 Feb 1;20(3):608-14. doi: 10.1093/hmg/ddq475. Epub 2010 Nov 4.
Hum Mol Genet. 2011.
PMID: 21051773
Free PMC article.
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An allele-specific gene expression assay to test the functional basis of genetic associations.
Paracchini S, Monaco AP, Knight JC.
Paracchini S, et al.
J Vis Exp. 2010 Nov 3;(45):2279. doi: 10.3791/2279.
J Vis Exp. 2010.
PMID: 21085102
Free PMC article.
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Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.
Eising E, Mirza-Schreiber N, de Zeeuw EL, Wang CA, Truong DT, Allegrini AG, Shapland CY, Zhu G, Wigg KG, Gerritse ML, Molz B, Alagöz G, Gialluisi A, Abbondanza F, Rimfeld K, van Donkelaar M, Liao Z, Jansen PR, Andlauer TFM, Bates TC, Bernard M, Blokland K, Bonte M, Børglum AD, Bourgeron T, Brandeis D, Ceroni F, Csépe V, Dale PS, de Jong PF, DeFries JC, Démonet JF, Demontis D, Feng Y, Gordon SD, Guger SL, Hayiou-Thomas ME, Hernández-Cabrera JA, Hottenga JJ, Hulme C, Kere J, Kerr EN, Koomar T, Landerl K, Leonard GT, Lovett MW, Lyytinen H, Martin NG, Martinelli A, Maurer U, Michaelson JJ, Moll K, Monaco AP, Morgan AT, Nöthen MM, Pausova Z, Pennell CE, Pennington BF, Price KM, Rajagopal VM, Ramus F, Richer L, Simpson NH, Smith SD, Snowling MJ, Stein J, Strug LJ, Talcott JB, Tiemeier H, van der Schroeff MP, Verhoef E, Watkins KE, Wilkinson M, Wright MJ, Barr CL, Boomsma DI, Carreiras M, Franken MJ, Gruen JR, Luciano M, Müller-Myhsok B, Newbury DF, Olson RK, Paracchini S, Paus T, Plomin R, Reilly S, Schulte-Körne G, Tomblin JB, van Bergen E, Whitehouse AJO, Willcutt EG, St Pourcain B, Francks C, Fisher SE.
Eising E, et al.
Proc Natl Acad Sci U S A. 2022 Aug 30;119(35):e2202764119. doi: 10.1073/pnas.2202764119. Epub 2022 Aug 23.
Proc Natl Acad Sci U S A. 2022.
PMID: 35998220
Free PMC article.
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Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities.
Price KM, Wigg KG, Eising E, Feng Y, Blokland K, Wilkinson M, Kerr EN, Guger SL; Quantitative Trait Working Group of the GenLang Consortium; Fisher SE, Lovett MW, Strug LJ, Barr CL.
Price KM, et al.
Transl Psychiatry. 2022 Nov 29;12(1):495. doi: 10.1038/s41398-022-02250-z.
Transl Psychiatry. 2022.
PMID: 36446759
Free PMC article.
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