Beri S - Search Results

1

GRIN2B mediates susceptibility to intelligence quotient and cognitive impairments in developmental dyslexia.

Mascheretti S, Facoetti A, Giorda R, Beri S, Riva V, Trezzi V, Cellino MR, Marino C. Mascheretti S, et al. Among authors: beri s. Psychiatr Genet. 2015 Feb;25(1):9-20. doi: 10.1097/YPG.0000000000000068. Psychiatr Genet. 2015. PMID: 25426763

2

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. Marino C, et al. Among authors: beri s. Eur J Hum Genet. 2005 Apr;13(4):491-9. doi: 10.1038/sj.ejhg.5201356. Eur J Hum Genet. 2005. PMID: 15702132

3

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. Mascheretti S, et al. Among authors: beri s. J Hum Genet. 2014 Apr;59(4):189-97. doi: 10.1038/jhg.2013.141. Epub 2014 Jan 16. J Hum Genet. 2014. PMID: 24430574

4

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. Mascheretti S, et al. Among authors: beri s. Genes Brain Behav. 2013 Feb;12(1):47-55. doi: 10.1111/gbb.12000. Epub 2012 Nov 24. Genes Brain Behav. 2013. PMID: 23176554 Free article.

5

Low-copy repeats at the human VIPR2 gene predispose to recurrent and nonrecurrent rearrangements.

Beri S, Bonaglia MC, Giorda R. Beri S, et al. Eur J Hum Genet. 2013 Jul;21(7):757-61. doi: 10.1038/ejhg.2012.235. Epub 2012 Oct 17. Eur J Hum Genet. 2013. PMID: 23073313 Free PMC article.

6

Genotype-phenotype relationship in a child with 2.3 Mb de novo interstitial 12p13.33-p13.32 deletion.

Fanizza I, Bertuzzo S, Beri S, Scalera E, Massagli A, Sali ME, Giorda R, Bonaglia MC. Fanizza I, et al. Among authors: beri s. Eur J Med Genet. 2014 Jul;57(7):334-8. doi: 10.1016/j.ejmg.2014.04.009. Epub 2014 Apr 26. Eur J Med Genet. 2014. PMID: 24780630

7

Effect of family structure and TPH2 G-703T on the stability of dysregulation profile throughout adolescence.

Nobile M, Bianchi V, Monzani D, Beri S, Bellina M, Greco A, Colombo P, Tesei A, Caldirola D, Giorda R, Perna G, Molteni M. Nobile M, et al. Among authors: beri s. J Affect Disord. 2016 Jan 15;190:576-584. doi: 10.1016/j.jad.2015.10.057. Epub 2015 Nov 4. J Affect Disord. 2016. PMID: 26583347

8

Concurrent transposition of distal 6p and 20q to the 22q telomere: a recurrent benign chromosomal variant.

Bonaglia MC, Giorda R, Beri S, Peters GB, Kirk EP, Hung D, Ciccone R, Gottardi G, Zuffardi O. Bonaglia MC, et al. Among authors: beri s. Eur J Med Genet. 2008 Mar-Apr;51(2):148-55. doi: 10.1016/j.ejmg.2007.11.005. Epub 2007 Dec 8. Eur J Med Genet. 2008. PMID: 18226592

9

Molecular and cytogenetic analysis of the spreading of X inactivation in a girl with microcephaly, mild dysmorphic features and t(X;5)(q22.1;q31.1).

Giorda R, Bonaglia MC, Milani G, Baroncini A, Spada F, Beri S, Menozzi G, Rusconi M, Zuffardi O. Giorda R, et al. Among authors: beri s. Eur J Hum Genet. 2008 Aug;16(8):897-905. doi: 10.1038/ejhg.2008.28. Epub 2008 Feb 27. Eur J Hum Genet. 2008. PMID: 18301446

10

SLC6A4 methylation as an epigenetic marker of life adversity exposures in humans: A systematic review of literature.

Provenzi L, Giorda R, Beri S, Montirosso R. Provenzi L, et al. Among authors: beri s. Neurosci Biobehav Rev. 2016 Dec;71:7-20. doi: 10.1016/j.neubiorev.2016.08.021. Epub 2016 Aug 24. Neurosci Biobehav Rev. 2016. PMID: 27565518 Review.

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