Moroni A - Search Results

1

Reduced folate carrier polymorphism (80A-->G) and neural tube defects.

De Marco P, Calevo MG, Moroni A, Merello E, Raso A, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V. De Marco P, et al. Among authors: moroni a. Eur J Hum Genet. 2003 Mar;11(3):245-52. doi: 10.1038/sj.ejhg.5200946. Eur J Hum Genet. 2003. PMID: 12673279

2

Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population.

De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V. De Marco P, et al. Among authors: moroni a. J Hum Genet. 2002;47(6):319-24. doi: 10.1007/s100380200043. J Hum Genet. 2002. PMID: 12111380

3

Molecular genetic analysis of human homologs of Caenorhabditis elegans mab-21-like 1 gene in patients with neural tube defects.

Merello E, De Marco P, Moroni A, Raso A, Calevo MG, Consalez GG, Cama A, Capra V. Merello E, et al. Among authors: moroni a. Birth Defects Res A Clin Mol Teratol. 2004 Nov;70(11):885-8. doi: 10.1002/bdra.20084. Birth Defects Res A Clin Mol Teratol. 2004. PMID: 15526290

4

Folate pathway gene alterations in patients with neural tube defects.

De Marco P, Moroni A, Merello E, de Franchis R, Andreussi L, Finnell RH, Barber RC, Cama A, Capra V. De Marco P, et al. Among authors: moroni a. Am J Med Genet. 2000 Nov 27;95(3):216-23. doi: 10.1002/1096-8628(20001127)95:3<216::aid-ajmg6>3.0.co;2-f. Am J Med Genet. 2000. PMID: 11102926

5

Polymorphisms in genes involved in folate metabolism as risk factors for NTDs.

De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Cama A, Finnell RH, Andreussi L, Capra V. De Marco P, et al. Among authors: moroni a. Eur J Pediatr Surg. 2001 Dec;11 Suppl 1:S14-7. doi: 10.1055/s-2001-19739. Eur J Pediatr Surg. 2001. PMID: 11813127

6

Schizencephaly: surgical features and new molecular genetic results.

Capra V, De Marco P, Moroni A, Faiella A, Brunelli S, Tortori-Donati P, Andreussi I, Boncinelli E, Cama A. Capra V, et al. Among authors: moroni a. Eur J Pediatr Surg. 1996 Dec;6 Suppl 1:27-9. doi: 10.1055/s-2008-1071034. Eur J Pediatr Surg. 1996. PMID: 9008816

7

Surnames in Sardinia. III. The spatial distribution of surnames for testing neutrality of genes.

Zei G, Piazza A, Moroni A, Cavalli-Sforza LL. Zei G, et al. Among authors: moroni a. Ann Hum Genet. 1986 May;50(2):169-80. doi: 10.1111/j.1469-1809.1986.tb01036.x. Ann Hum Genet. 1986. PMID: 3435046

8

The human gene coding for HCN2, a pacemaker channel of the heart.

Vaccari T, Moroni A, Rocchi M, Gorza L, Bianchi ME, Beltrame M, DiFrancesco D. Vaccari T, et al. Among authors: moroni a. Biochim Biophys Acta. 1999 Sep 3;1446(3):419-25. doi: 10.1016/s0167-4781(99)00092-5. Biochim Biophys Acta. 1999. PMID: 10524219

9

Migration rates of human populations from surname distributions.

Piazza A, Rendine S, Zei G, Moroni A, Cavalli-Sforza LL. Piazza A, et al. Among authors: moroni a. Nature. 1987 Oct 22-28;329(6141):714-6. doi: 10.1038/329714a0. Nature. 1987. PMID: 3670373

10

Surnames in Sardinia. I. Fit of frequency distributions for neutral alleles and genetic population structure.

Zei G, Guglielmino Matessi R, Siri E, Moroni A, Cavalli-Sforza L. Zei G, et al. Among authors: moroni a. Ann Hum Genet. 1983 Oct;47(4):329-52. doi: 10.1111/j.1469-1809.1983.tb01003.x. Ann Hum Genet. 1983. PMID: 6651221

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