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Molecular Mechanisms Generating and Stabilizing Terminal 22q13 Deletions in 44 Subjects with Phelan/McDermid Syndrome
55 auth.
M. Bonaglia,
R. Giorda,
Silvana Beri,
Cristina De Agostini,
F. Novara,
M. Fichera,
L. Grillo,
O. Galesi,
A. Vetro,
R. Ciccone,
M. Bonati,
S. Giglio,
R. Guerrini,
S. Osimani,
S. Marelli,
...
C. Zucca,
Rita Grasso,
R. Borgatti,
E. Mani,
Cristina Motta,
M. Molteni,
C. Romano,
D. Greco,
S. Reitano,
A. Baroncini,
E. Lapi,
A. Cecconi,
G. Arrigo,
M. Patricelli,
C. Pantaleoni,
S. D'Arrigo,
D. Riva,
F. Sciacca,
B. dalla Bernardina,
L. Zoccante,
F. Darra,
C. Termine,
E. Maserati,
S. Bigoni,
Emanuela Priolo,
A. Bottani,
S. Gimelli,
F. Béna,
A. Brusco,
E. di Gregorio,
Irene Bagnasco,
U. Giussani,
L. Nitsch,
P. Politi,
M. Martínez‐Frías,
M. Martínez-Fernández,
N. Martínez Guardia,
A. Bremer,
B. Anderlid,
O. Zuffardi
|
7 |
2011 |
7
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Overexpression of the C‐type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocation
13 auth.
R. Bocciardi,
R. Giorda,
Jens Buttgereit,
S. Gimelli,
M. T. Divizia,
Silvana Beri,
S. Garofalo,
S. Tavella,
M. Lerone,
O. Zuffardi,
...
M. Bader,
R. Ravazzolo,
G. Gimelli
|
7 |
2007 |
7
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🐬
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SLC6A4 methylation as an epigenetic marker of life adversity exposures in humans: A systematic review of literature
L. Provenzi,
R. Giorda,
Silvana Beri,
R. Montirosso
|
6 |
2016 |
6
🐬
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🐜
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Refining the phenotype associated with MEF2C haploinsufficiency
9 auth.
F. Novara,
Silvana Beri,
R. Giorda,
E. Ortibus,
S. Nageshappa,
F. Darra,
...
B. Bernardina,
O. Zuffardi,
H. Esch
|
6 |
2010 |
6
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🐜
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A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia
11 auth.
C. Marino,
R. Giorda,
M. Lorusso,
L. Vanzin,
Nello Salandi,
M. Nobile,
...
A. Citterio,
Silvana Beri,
Valentina Crespi,
M. Battaglia,
M. Molteni
|
6 |
2005 |
6
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|
|
🐜
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Pain-related stress during the Neonatal Intensive Care Unit stay and SLC6A4 methylation in very preterm infants
11 auth.
L. Provenzi,
M. Fumagalli,
I. Sirgiovanni,
R. Giorda,
U. Pozzoli,
F. Morandi,
...
Silvana Beri,
G. Menozzi,
F. Mosca,
R. Borgatti,
R. Montirosso
|
6 |
2015 |
6
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Complex segmental duplications mediate a recurrent dup(X)(p11.22-p11.23) associated with mental retardation, speech delay, and EEG anomalies in males and females.
34 auth.
R. Giorda,
M. Bonaglia,
Silvana Beri,
M. Fichera,
F. Novara,
P. Magini,
J. Urquhart,
F. Sharkey,
C. Zucca,
Rita Grasso,
S. Marelli,
L. Castiglia,
D. Di Benedetto,
S. Musumeci,
G. Vitello,
...
P. Failla,
S. Reitano,
E. Avola,
F. Bisulli,
P. Tinuper,
M. Mastrangelo,
I. Fiocchi,
L. Spaccini,
C. Torniero,
E. Fontana,
S. Lynch,
J. Clayton-Smith,
G. Black,
P. Jonveaux,
B. Leheup,
M. Seri,
C. Romano,
B. dalla Bernardina,
O. Zuffardi
|
6 |
2009 |
6
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|
|
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Serotonin Transporter Gene (SLC6A4) Methylation Associates With Neonatal Intensive Care Unit Stay and 3-Month-Old Temperament in Preterm Infants.
12 auth.
R. Montirosso,
L. Provenzi,
M. Fumagalli,
I. Sirgiovanni,
R. Giorda,
U. Pozzoli,
...
Silvana Beri,
G. Menozzi,
E. Tronick,
F. Morandi,
F. Mosca,
R. Borgatti
|
6 |
2016 |
6
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|
|
🦁
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DNA methylation regulates tissue‐specific expression of Shank3
Silvana Beri,
N. Tonna,
G. Menozzi,
M. Bonaglia,
C. Sala,
R. Giorda
|
6 |
2007 |
6
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