Silvia Maria Sirchia
Silvia Maria Sirchia
Associate Professor of Medical Genetics, UniversitÓ degli Studi di Milano
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TitleCited byYear
Evidence of epigenetic changes affecting the chromatin state of the retinoic acid receptor β2 promoter in breast cancer cells
SM Sirchia, AT Ferguson, E Sironi, S Subramanyan, R Orlandi, ...
Oncogene 19 (12), 1556, 2000
Endogenous reactivation of the RARβ2 tumor suppressor gene epigenetically silenced in breast cancer
SM Sirchia, M Ren, R Pili, E Sironi, G Somenzi, R Ghidoni, S Toma, ...
Cancer research 62 (9), 2455-2461, 2002
Role of epigenetics in human aging and longevity: genome-wide DNA methylation profile in centenarians and centenarians’ offspring
D Gentilini, D Mari, D Castaldi, D Remondini, G Ogliari, R Ostan, L Bucci, ...
Age 35 (5), 1961-1973, 2013
Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosis
M Miozzo, C Selmi, B Gentilin, FR Grati, S Sirchia, S Oertelt, M Zuin, ...
Hepatology 46 (2), 456-462, 2007
Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction
S Tabano, P Colapietro, I Cetin, FR Grati, S Zanutto, C Mand˛, ...
Epigenetics 5 (4), 313-324, 2010
Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cells
SM Sirchia, L Ramoscelli, FR Grati, F Barbera, D Coradini, F Rossella, ...
Cancer research 65 (6), 2139-2146, 2005
Blood fetal microchimerism in primary biliary cirrhosis
P Invernizzi, C De Andreis, SM Sirchia, PM Battezzati, M Zuin, F Rossella, ...
Clinical & Experimental Immunology 122 (3), 418-422, 2000
Misbehaviour of XIST RNA in breast cancer cells
SM Sirchia, S Tabano, L Monti, MP Recalcati, M Gariboldi, FR Grati, ...
PloS one 4 (5), e5559, 2009
Genome‐wide analysis of primary plasma cell leukemia identifies recurrent imbalances associated with changes in transcriptional profiles
L Mosca, P Musto, K Todoerti, M Barbieri, L Agnelli, S Fabris, G Tuana, ...
American journal of hematology 88 (1), 16-23, 2013
Confined placental mosaicism
G Simoni, SM Sirchia
Prenatal diagnosis 14 (13), 1185-1189, 1994
Increased loss of the Y chromosome in peripheral blood cells in male patients with autoimmune thyroiditis
L Persani, M Bonomi, A Lleo, S Pasini, F Civardi, I Bianchi, I Campi, ...
Journal of autoimmunity 38 (2-3), J193-J196, 2012
Loss of heterozygosity on chromosome 4q32–35 in sporadic basal cell carcinomas: evidence for the involvement of p33ING2/ING1L and SAP30 genes
E Sironi, A Cerri, D Tomasini, SM Sirchia, G Porta, F Rossella, FR Grati, ...
Journal of cutaneous pathology 31 (4), 318-322, 2004
Losses of heterozygosity in oral and oropharyngeal epithelial carcinomas
FR Grati, SM Sirchia, I Garagiola, E Sironi, S Galioto, F Rossella, ...
Cancer genetics and cytogenetics 118 (1), 57-61, 2000
Chromosome 14 maternal uniparental disomy in the euploid cell line of a fetus with mosaic 46, XX/47, XX,+ 14 karyotype
SM Sirchia, C De Andreis, S Pariani, MG Grimoldi, A Molinari, ...
Human genetics 94 (4), 355-358, 1994
The methylation of the TSC2 promoter underlies the abnormal growth of TSC2 angiomyolipoma-derived smooth muscle cells
E Lesma, SM Sirchia, S Ancona, S Carelli, S Bosari, F Ghelma, ...
The American journal of pathology 174 (6), 2150-2159, 2009
Loss of heterozygosity of the NOS3 dinucleotide repeat marker in atherosclerotic plaques of human carotid arteries
FR Grati, G Ghilardi, SM Sirchia, F Massaro, B Cassani, R Scorza, ...
Atherosclerosis 159 (2), 261-267, 2001
Losses of heterozygosity in endometrial adenocarcinomas: positive correlations with histopathological parameters
SM Sirchia, E Sironi, FR Grati, P Serafini, I Garagiola, F Rossella, ...
Cancer genetics and cytogenetics 121 (2), 156-162, 2000
Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms
E Salsano, S Tabano, SM Sirchia, P Colapietro, B Castellotti, C Gellera, ...
Orphanet journal of rare diseases 7 (1), 10, 2012
Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome
M Calvello, S Tabano, P Colapietro, S Maitz, A Pansa, C Augello, ...
Epigenetics 8 (10), 1053-1060, 2013
DNA methylation and histone modifications modulate the β1, 3 galactosyltransferase β3Gal-T5 native promoter in cancer cells
A Caretti, SM Sirchia, S Tabano, A Zulueta, F Dall’Olio, M Trinchera
The international journal of biochemistry & cell biology 44 (1), 84-90, 2012
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