Giorda R - Search Results

1

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: giorda r. Eur J Hum Genet. 2005 Apr;13(4):491-9. doi: 10.1038/sj.ejhg.5201356. Eur J Hum Genet. 2005. PMID: 15702132

2

Effects of serotonin transporter promoter genotype on platelet serotonin transporter functionality in depressed children and adolescents.

Nobile M, Begni B, Giorda R, Frigerio A, Marino C, Molteni M, Ferrarese C, Battaglia M. Nobile M, et al. Among authors: giorda r. J Am Acad Child Adolesc Psychiatry. 1999 Nov;38(11):1396-402. doi: 10.1097/00004583-199911000-00014. J Am Acad Child Adolesc Psychiatry. 1999. PMID: 10560226

3

Inverted duplications are recurrent rearrangements always associated with a distal deletion: description of a new case involving 2q.

Bonaglia MC, Giorda R, Poggi G, Raggi ME, Rossi E, Baroncini A, Giglio S, Borgatti R, Zuffardi O. Bonaglia MC, et al. Among authors: giorda r. Eur J Hum Genet. 2000 Aug;8(8):597-603. doi: 10.1038/sj.ejhg.5200509. Eur J Hum Genet. 2000. PMID: 10951522

4

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.

5

Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spot.

Sironi M, Pozzoli U, Cagliani R, Giorda R, Comi GP, Bardoni A, Menozzi G, Bresolin N. Sironi M, et al. Among authors: giorda r. Hum Genet. 2003 Mar;112(3):272-88. doi: 10.1007/s00439-002-0881-5. Epub 2002 Dec 19. Hum Genet. 2003. PMID: 12596052

6

No evidence for association and linkage disequilibrium between dyslexia and markers of four dopamine-related genes.

Marino C, Giorda R, Vanzin L, Molteni M, Lorusso ML, Nobile M, Baschirotto C, Alda M, Battaglia M. Marino C, et al. Among authors: giorda r. Eur Child Adolesc Psychiatry. 2003 Aug;12(4):198-202. doi: 10.1007/s00787-003-0332-4. Eur Child Adolesc Psychiatry. 2003. PMID: 14505070

7

A locus on 15q15-15qter influences dyslexia: further support from a transmission/disequilibrium study in an Italian speaking population.

Marino C, Giorda R, Vanzin L, Nobile M, Lorusso ML, Baschirotto C, Riva L, Molteni M, Battaglia M. Marino C, et al. Among authors: giorda r. J Med Genet. 2004 Jan;41(1):42-6. doi: 10.1136/jmg.2003.010603. J Med Genet. 2004. PMID: 14729831 Free PMC article. No abstract available.

8

A case-control and family-based association study of the 5-HTTLPR in pediatric-onset depressive disorders.

Nobile M, Cataldo MG, Giorda R, Battaglia M, Baschirotto C, Bellina M, Marino C, Molteni M. Nobile M, et al. Among authors: giorda r. Biol Psychiatry. 2004 Aug 15;56(4):292-5. doi: 10.1016/j.biopsych.2004.05.018. Biol Psychiatry. 2004. PMID: 15312818

9

An assessment of transmission disequilibrium between quantitative measures of childhood problem behaviors and DRD2/Taql and DRD4/48bp-repeat polymorphisms.

Marino C, Vanzin L, Giorda R, Frigerio A, Lorusso ML, Nobile M, Molteni M, Battaglia M. Marino C, et al. Among authors: giorda r. Behav Genet. 2004 Sep;34(5):495-502. doi: 10.1023/B:BEGE.0000038487.80597.7e. Behav Genet. 2004. PMID: 15319572

10

Influence of the serotonin transporter promoter gene and shyness on children's cerebral responses to facial expressions.

Battaglia M, Ogliari A, Zanoni A, Citterio A, Pozzoli U, Giorda R, Maffei C, Marino C. Battaglia M, et al. Among authors: giorda r. Arch Gen Psychiatry. 2005 Jan;62(1):85-94. doi: 10.1001/archpsyc.62.1.85. Arch Gen Psychiatry. 2005. PMID: 15630076

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