Simoni G - Search Results

1

Post-zygotic origin of complete maternal chromosome 7 isodisomy and consequent loss of placental PEG1/MEST expression.

Miozzo M, Grati FR, Bulfamante G, Rossella F, Cribiù M, Radaelli T, Cassani B, Persico T, Cetin I, Pardi G, Simoni G. Miozzo M, et al. Among authors: simoni g. Placenta. 2001 Nov;22(10):813-21. doi: 10.1053/plac.2001.0728. Placenta. 2001. PMID: 11718568

2

Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnancies.

Grati FR, Miozzo M, Cassani B, Rossella F, Antonazzo P, Gentilin B, Sirchia SM, Mori L, Rigano S, Bulfamante G, Cetin I, Simoni G. Grati FR, et al. Among authors: simoni g. Placenta. 2005 Jan;26(1):10-8. doi: 10.1016/j.placenta.2004.04.009. Placenta. 2005. PMID: 15664406

3

The role of imprinted genes in fetal growth.

Miozzo M, Simoni G. Miozzo M, et al. Among authors: simoni g. Biol Neonate. 2002;81(4):217-28. doi: 10.1159/000056752. Biol Neonate. 2002. PMID: 12011565 Review.

4

Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies.

Grati FR, Sirchia SM, Gentilin B, Rossella F, Ramoscelli L, Antonazzo P, Cavallari U, Bulfamante G, Cetin I, Simoni G, Miozzo M. Grati FR, et al. Among authors: simoni g. Eur J Hum Genet. 2004 Apr;12(4):272-8. doi: 10.1038/sj.ejhg.5201121. Eur J Hum Genet. 2004. PMID: 14673477

5

Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cells.

Sirchia SM, Ramoscelli L, Grati FR, Barbera F, Coradini D, Rossella F, Porta G, Lesma E, Ruggeri A, Radice P, Simoni G, Miozzo M. Sirchia SM, et al. Among authors: simoni g. Cancer Res. 2005 Mar 15;65(6):2139-46. doi: 10.1158/0008-5472.CAN-04-3465. Cancer Res. 2005. PMID: 15781624 Free article.

6

Three cases with de novo 6q imbalance and variable prenatal phenotype.

Grati FR, Lalatta F, Turolla L, Cavallari U, Gentilin B, Rossella F, Cetin I, Antonazzo P, Bellotti M, Dulcetti F, Baldo D, Tenconi R, Simoni G, Miozzo M. Grati FR, et al. Among authors: simoni g. Am J Med Genet A. 2005 Jul 30;136(3):254-8. doi: 10.1002/ajmg.a.30837. Am J Med Genet A. 2005. PMID: 15957159

7

Direct chromosome preparation and culture using chorionic villi: an evaluation of the two techniques.

Simoni G, Terzoli G, Rossella F. Simoni G, et al. Am J Med Genet. 1990 Feb;35(2):181-3. doi: 10.1002/ajmg.1320350208. Am J Med Genet. 1990. PMID: 2309755

8

Losses of heterozygosity in endometrial adenocarcinomas: positive correlations with histopathological parameters.

Sirchia SM, Sironi E, Grati FR, Serafini P, Garagiola I, Rossella F, Dulcetti F, Pardi G, Garsia S, Simoni G. Sirchia SM, et al. Among authors: simoni g. Cancer Genet Cytogenet. 2000 Sep;121(2):156-62. doi: 10.1016/s0165-4608(00)00240-5. Cancer Genet Cytogenet. 2000. PMID: 11063800

9

Chromosome 11 segmental paternal isodisomy in amniocytes from two fetuses with omphalocoele: new highlights on phenotype-genotype correlations in Beckwith-Wiedemann syndrome.

Grati FR, Turolla L, D'Ajello P, Ruggeri A, Miozzo M, Bracalente G, Baldo D, Laurino L, Boldorini R, Frate E, Surico N, Larizza L, Maggi F, Simoni G. Grati FR, et al. Among authors: simoni g. J Med Genet. 2007 Apr;44(4):257-63. doi: 10.1136/jmg.2006.046854. Epub 2007 Jan 26. J Med Genet. 2007. PMID: 17259293 Free PMC article.

10

Frequency of monosomy X in women with primary biliary cirrhosis.

Invernizzi P, Miozzo M, Battezzati PM, Bianchi I, Grati FR, Simoni G, Selmi C, Watnik M, Gershwin ME, Podda M. Invernizzi P, et al. Among authors: simoni g. Lancet. 2004 Feb 14;363(9408):533-5. doi: 10.1016/S0140-6736(04)15541-4. Lancet. 2004. PMID: 14975617

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