Lantieri F - Search Results

1

Analysis of GWAS top hits in ADHD suggests association to two polymorphisms located in genes expressed in the cerebellum.

Lantieri F, Glessner JT, Hakonarson H, Elia J, Devoto M. Lantieri F, et al. Am J Med Genet B Neuropsychiatr Genet. 2010 Sep;153B(6):1127-33. doi: 10.1002/ajmg.b.31110. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 20607790

2

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.

Elia J, Gai X, Xie HM, Perin JC, Geiger E, Glessner JT, D'arcy M, deBerardinis R, Frackelton E, Kim C, Lantieri F, Muganga BM, Wang L, Takeda T, Rappaport EF, Grant SF, Berrettini W, Devoto M, Shaikh TH, Hakonarson H, White PS. Elia J, et al. Among authors: lantieri f. Mol Psychiatry. 2010 Jun;15(6):637-46. doi: 10.1038/mp.2009.57. Epub 2009 Jun 23. Mol Psychiatry. 2010. PMID: 19546859 Free PMC article.

3

Candidate gene analysis in an on-going genome-wide association study of attention-deficit hyperactivity disorder: suggestive association signals in ADRA1A.

Elia J, Capasso M, Zaheer Z, Lantieri F, Ambrosini P, Berrettini W, Devoto M, Hakonarson H. Elia J, et al. Among authors: lantieri f. Psychiatr Genet. 2009 Jun;19(3):134-41. doi: 10.1097/YPG.0b013e32832a5043. Psychiatr Genet. 2009. PMID: 19352218

4

Nocturnal enuresis: a suggestive endophenotype marker for a subgroup of inattentive attention-deficit/hyperactivity disorder.

Elia J, Takeda T, Deberardinis R, Burke J, Accardo J, Ambrosini PJ, Blum NJ, Brown LW, Lantieri F, Berrettini W, Devoto M, Hakonarson H. Elia J, et al. Among authors: lantieri f. J Pediatr. 2009 Aug;155(2):239-44.e5. doi: 10.1016/j.jpeds.2009.02.031. Epub 2009 May 15. J Pediatr. 2009. PMID: 19446845

5

Comparative analysis of different approaches for dealing with candidate regions in the context of a genome-wide association study.

Lantieri F, Jhun MA, Park J, Park T, Devoto M. Lantieri F, et al. BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S93. doi: 10.1186/1753-6561-3-s7-s93. BMC Proc. 2009. PMID: 20018090 Free PMC article.

6

A common haplotype at the 5' end of the RET proto-oncogene, overrepresented in Hirschsprung patients, is associated with reduced gene expression.

Griseri P, Bachetti T, Puppo F, Lantieri F, Ravazzolo R, Devoto M, Ceccherini I. Griseri P, et al. Among authors: lantieri f. Hum Mutat. 2005 Feb;25(2):189-95. doi: 10.1002/humu.20135. Hum Mutat. 2005. PMID: 15643606

7

Incorporating prior biological information in linkage studies increases power and limits multiple testing.

Lantieri F, Rydbeck H, Griseri P, Ceccherini I, Devoto M. Lantieri F, et al. BMC Proc. 2007;1 Suppl 1(Suppl 1):S89. doi: 10.1186/1753-6561-1-s1-s89. Epub 2007 Dec 18. BMC Proc. 2007. PMID: 18466592 Free PMC article.

8

Haplotypes of the human RET proto-oncogene associated with Hirschsprung disease in the Italian population derive from a single ancestral combination of alleles.

Lantieri F, Griseri P, Puppo F, Campus R, Martucciello G, Ravazzolo R, Devoto M, Ceccherini I. Lantieri F, et al. Ann Hum Genet. 2006 Jan;70(Pt 1):12-26. doi: 10.1111/j.1529-8817.2005.00196.x. Ann Hum Genet. 2006. PMID: 16441254

9

Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.

Tang CS, Gui H, Kapoor A, Kim JH, Luzón-Toro B, Pelet A, Burzynski G, Lantieri F, So MT, Berrios C, Shin HD, Fernández RM, Le TL, Verheij JB, Matera I, Cherny SS, Nandakumar P, Cheong HS, Antiñolo G, Amiel J, Seo JM, Kim DY, Oh JT, Lyonnet S, Borrego S, Ceccherini I, Hofstra RM, Chakravarti A, Kim HY, Sham PC, Tam PK, Garcia-Barceló MM. Tang CS, et al. Among authors: lantieri f. Hum Mol Genet. 2016 Dec 1;25(23):5265-5275. doi: 10.1093/hmg/ddw333. Hum Mol Genet. 2016. PMID: 27702942 Free PMC article.

10

Inclusion of a priori information in genome-wide association analysis.

Tintle N, Lantieri F, Lebrec J, Sohns M, Ballard D, Bickeböller H. Tintle N, et al. Among authors: lantieri f. Genet Epidemiol. 2009;33 Suppl 1(Suppl 1):S74-80. doi: 10.1002/gepi.20476. Genet Epidemiol. 2009. PMID: 19924705 Free PMC article.

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