Giorda R - Search Results

1

Maternal and infant NR3C1 and SLC6A4 epigenetic signatures of the COVID-19 pandemic lockdown: when timing matters.

Nazzari S, Grumi S, Mambretti F, Villa M, Giorda R, Provenzi L; MOM-COPE Study Group. Nazzari S, et al. Among authors: giorda r. Transl Psychiatry. 2022 Sep 16;12(1):386. doi: 10.1038/s41398-022-02160-0. Transl Psychiatry. 2022. PMID: 36114180 Free PMC article.

2

Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome.

Bonaglia MC, Giorda R, Borgatti R, Felisari G, Gagliardi C, Selicorni A, Zuffardi O. Bonaglia MC, et al. Among authors: giorda r. Am J Hum Genet. 2001 Aug;69(2):261-8. doi: 10.1086/321293. Epub 2001 Jun 18. Am J Hum Genet. 2001. PMID: 11431708 Free PMC article.

3

20-Mb duplication of chromosome 9p in a girl with minimal physical findings and normal IQ: narrowing of the 9p duplication critical region to 6 Mb.

Bonaglia MC, Giorda R, Carrozzo R, Roncoroni ME, Grasso R, Borgatti R, Zuffardi O. Bonaglia MC, et al. Among authors: giorda r. Am J Med Genet. 2002 Oct 1;112(2):154-9. doi: 10.1002/ajmg.10699. Am J Med Genet. 2002. PMID: 12244548

4

A 2.3 Mb duplication of chromosome 8q24.3 associated with severe mental retardation and epilepsy detected by standard karyotype.

Bonaglia MC, Giorda R, Tenconi R, Pessina M, Pramparo T, Borgatti R, Zuffardi O. Bonaglia MC, et al. Among authors: giorda r. Eur J Hum Genet. 2005 May;13(5):586-91. doi: 10.1038/sj.ejhg.5201369. Eur J Hum Genet. 2005. PMID: 15657611

5

Subtelomeric trisomy 21q: a new benign chromosomal variant.

Bonaglia MC, Marelli S, Gottardi G, Zucca C, Pramparo T, Giorda R, Grasso R, Borgatti R, Zuffardi O. Bonaglia MC, et al. Among authors: giorda r. Eur J Med Genet. 2007 Jan-Feb;50(1):54-9. doi: 10.1016/j.ejmg.2006.07.001. Epub 2006 Sep 10. Eur J Med Genet. 2007. PMID: 17055792

6

Provenzi L, Fumagalli M, Sirgiovanni I, Giorda R, Pozzoli U, Morandi F, Beri S, Menozzi G, Mosca F, Borgatti R, Montirosso R. Provenzi L, et al. Among authors: giorda r. Front Behav Neurosci. 2015 Apr 21;9:99. doi: 10.3389/fnbeh.2015.00099. eCollection 2015. Front Behav Neurosci. 2015. PMID: 25941480 Free PMC article.

7

Serotonin Transporter Gene (SLC6A4) Methylation Associates With Neonatal Intensive Care Unit Stay and 3-Month-Old Temperament in Preterm Infants.

Montirosso R, Provenzi L, Fumagalli M, Sirgiovanni I, Giorda R, Pozzoli U, Beri S, Menozzi G, Tronick E, Morandi F, Mosca F, Borgatti R. Montirosso R, et al. Among authors: giorda r. Child Dev. 2016 Jan-Feb;87(1):38-48. doi: 10.1111/cdev.12492. Child Dev. 2016. PMID: 26822441

8

SLC6A4 promoter region methylation and socio-emotional stress response in very preterm and full-term infants.

Montirosso R, Provenzi L, Giorda R, Fumagalli M, Morandi F, Sirgiovanni I, Pozzoli U, Grunau R, Oberlander TF, Mosca F, Borgatti R. Montirosso R, et al. Among authors: giorda r. Epigenomics. 2016 Jul;8(7):895-907. doi: 10.2217/epi-2016-0010. Epub 2016 Jul 6. Epigenomics. 2016. PMID: 27381173

9

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: giorda r. 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.

10

Clinical Characterization, Genetics, and Long-Term Follow-up of a Large Cohort of Patients With Agenesis of the Corpus Callosum.

Romaniello R, Marelli S, Giorda R, Bedeschi MF, Bonaglia MC, Arrigoni F, Triulzi F, Bassi MT, Borgatti R. Romaniello R, et al. Among authors: giorda r. J Child Neurol. 2017 Jan;32(1):60-71. doi: 10.1177/0883073816664668. Epub 2016 Sep 29. J Child Neurol. 2017. PMID: 27683483

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