Similar articles for PMID: 27307794

Year	Number of Results
1999	1
2000	1
2001	1
2002	3
2003	1
2004	3
2005	1
2007	3
2008	3
2009	7
2010	8
2011	12
2012	10
2013	6
2014	15
2015	4
2016	6
2017	2
2018	3
2019	3
2020	7
2021	3
2022	9
2023	7
2024	3

1

Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes.

Pettigrew KA, Frinton E, Nudel R, Chan MTM, Thompson P, Hayiou-Thomas ME, Talcott JB, Stein J, Monaco AP, Hulme C, Snowling MJ, Newbury DF, Paracchini S. Pettigrew KA, et al. J Neurodev Disord. 2016 Jun 14;8:24. doi: 10.1186/s11689-016-9157-6. eCollection 2016. J Neurodev Disord. 2016. PMID: 27307794 Free PMC article.

2

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.

Nudel R, Simpson NH, Baird G, O'Hare A, Conti-Ramsden G, Bolton PF, Hennessy ER; SLI Consortium; Ring SM, Davey Smith G, Francks C, Paracchini S, Monaco AP, Fisher SE, Newbury DF. Nudel R, et al. Genes Brain Behav. 2014 Apr;13(4):418-29. doi: 10.1111/gbb.12127. Epub 2014 Mar 24. Genes Brain Behav. 2014. PMID: 24571439 Free PMC article.

3

Pedigree-Based Gene Mapping Supports Previous Loci and Reveals Novel Suggestive Loci in Specific Language Impairment.

Andres EM, Earnest KK, Smith SD, Rice ML, Raza MH. Andres EM, et al. J Speech Lang Hear Res. 2020 Dec 14;63(12):4046-4061. doi: 10.1044/2020_JSLHR-20-00102. Epub 2020 Nov 13. J Speech Lang Hear Res. 2020. PMID: 33186502 Free PMC article.

4

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. Scerri TS, et al. Biol Psychiatry. 2011 Aug 1;70(3):237-45. doi: 10.1016/j.biopsych.2011.02.005. Epub 2011 Mar 31. Biol Psychiatry. 2011. PMID: 21457949 Free PMC article.

5

Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study.

Nudel R, Christiani CAJ, Ohland J, Uddin MJ, Hemager N, Ellersgaard D, Spang KS, Burton BK, Greve AN, Gantriis DL, Bybjerg-Grauholm J, Jepsen JRM, Thorup AAE, Mors O, Werge T, Nordentoft M. Nudel R, et al. BMC Neurosci. 2020 Jul 7;21(1):30. doi: 10.1186/s12868-020-00581-5. BMC Neurosci. 2020. PMID: 32635940 Free PMC article.

6

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.

Scerri TS, Darki F, Newbury DF, Whitehouse AJ, Peyrard-Janvid M, Matsson H, Ang QW, Pennell CE, Ring S, Stein J, Morris AP, Monaco AP, Kere J, Talcott JB, Klingberg T, Paracchini S. Scerri TS, et al. PLoS One. 2012;7(11):e50321. doi: 10.1371/journal.pone.0050321. Epub 2012 Nov 28. PLoS One. 2012. PMID: 23209710 Free PMC article.

7

Intergenerational longitudinal associations between parental reading/musical traits, infants' auditory processing, and later phonological awareness skills.

Cantiani C, Dondena C, Molteni M, Riva V, Lorusso ML. Cantiani C, et al. Front Neurosci. 2023 Jul 19;17:1201997. doi: 10.3389/fnins.2023.1201997. eCollection 2023. Front Neurosci. 2023. PMID: 37539387 Free PMC article.

8

A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures.

Martinelli A, Rice ML, Talcott JB, Diaz R, Smith S, Raza MH, Snowling MJ, Hulme C, Stein J, Hayiou-Thomas ME, Hawi Z, Kent L, Pitt SJ, Newbury DF, Paracchini S. Martinelli A, et al. Hum Mol Genet. 2021 Jun 9;30(12):1160-1171. doi: 10.1093/hmg/ddab111. Hum Mol Genet. 2021. PMID: 33864365 Free PMC article.

9

Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits.

Bates TC, Luciano M, Medland SE, Montgomery GW, Wright MJ, Martin NG. Bates TC, et al. Behav Genet. 2011 Jan;41(1):50-7. doi: 10.1007/s10519-010-9402-9. Epub 2010 Oct 15. Behav Genet. 2011. PMID: 20949370

10

Phonological processing in children with specific language impairment with and without reading difficulties.

Loucas T, Baird G, Simonoff E, Slonims V. Loucas T, et al. Int J Lang Commun Disord. 2016 Sep;51(5):581-8. doi: 10.1111/1460-6984.12225. Epub 2016 Mar 17. Int J Lang Commun Disord. 2016. PMID: 26992032

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