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Silvana Beri
Observed names:
Beri S,
Beri, Silvana,
S Beri,
S. Beri
Institution:
IRCCS Eugenio Medea
Observed institution:
IRCCS Eugenio Medea
OpenAlex ID:
A5030344080
Molecular Mechanisms Generating and Stabilizing Terminal 22q13 Deletions in 44 Subjects with Phelan/McDermid Syndrome
2011
·
Maria Clara Bonaglia
, Roberto Giorda
, et al.
·
PLoS Genetics
·
230
PDF
SLC6A4 methylation as an epigenetic marker of life adversity exposures in humans: A systematic review of literature
2016
·
Livio Provenzi
, Roberto Giorda
, et al.
·
Neuroscience & Biobehavioral Reviews
·
146
Overexpression of the C-type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocation
2007
·
Renata Bocciardi
, Roberto Giorda
, et al.
·
Human Mutation
·
131
PDF
Genotype–phenotype relationship in three cases with overlapping 19p13.12 microdeletions
2010
·
Maria C Bonaglia
, Susan Marelli
, et al.
·
European Journal of Human Genetics
·
126
PDF
Testis development in the absence of SRY: chromosomal rearrangements at SOX9 and SOX3
2014
·
Annalisa Vetro
, Mohammad Reza Dehghani
, et al.
·
European Journal of Human Genetics
·
124
PDF
Refining the phenotype associated with MEF2C haploinsufficiency
2010
·
F Novara
, S Beri
, et al.
·
Clinical Genetics
·
93
Pain-related stress during the Neonatal Intensive Care Unit stay and SLC6A4 methylation in very preterm infants
2015
·
Livio Provenzi
, Monica Fumagalli
, et al.
·
Frontiers in Behavioral Neuroscience
·
90
PDF
A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia
2005
·
Cecilia Marino
, Roberto Giorda
, et al.
·
European Journal of Human Genetics
·
89
Molecular and cytogenetic analysis of the spreading of X inactivation in a girl with microcephaly, mild dysmorphic features and t(X;5)(q22.1;q31.1)
2008
·
Roberto Giorda
, M Clara Bonaglia
, et al.
·
European Journal of Human Genetics
·
86
Serotonin Transporter Gene ( SLC6A4 ) Methylation Associates With Neonatal Intensive Care Unit Stay and 3-Month-Old Temperament in Preterm Infants
2016
·
Rosario Montirosso
, Livio Provenzi
, et al.
·
Child Development
·
85
An Assessment of Gene-by-Environment Interactions in Developmental Dyslexia-Related Phenotypes
2012
·
S. Mascheretti
, A. Bureau
, et al.
·
Genes Brain & Behavior
·
81
DNA methylation regulates tissue‐specific expression of Shank3
2007
·
Silvana Beri
, Noemi Tonna
, et al.
·
Journal of Neurochemistry
·
79
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
2009
·
Roberto Giorda
, M. Clara Bonaglia
, et al.
·
The American Journal of Human Genetics
·
78
PDF
Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract
2010
·
Stefania Gimelli
, Gianluca Caridi
, et al.
·
Human Mutation
·
76
PDF
KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia
2014
·
Sara Mascheretti
, Valentina Riva
, et al.
·
Journal of Human Genetics
·
61
A 46,X,inv(Y) young woman with gonadal dysgenesis and gonadoblastoma: Cytogenetics, molecular, and methylation studies
2005
·
Giorgio Gimelli
, Roberto Giorda
, et al.
·
American Journal of Medical Genetics Part A
·
57
5p13 microduplication syndrome: A new case and better clinical definition of the syndrome
2012
·
Francesca Novara
, Enrico Alfei
, et al.
·
European Journal of Medical Genetics
·
48
Different molecular mechanisms causing 9p21 deletions in acute lymphoblastic leukemia of childhood
2009
·
Francesca Novara
, Silvana Beri
, et al.
·
Human Genetics
·
43
PDF
Two classes of low-copy repeats comediate a new recurrent rearrangement consisting of duplication at 8p23.1 and triplication at 8p23.2
2007
·
Roberto Giorda
, Roberto Ciccone
, et al.
·
Human Mutation
·
42
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
2009
·
Roberto Giorda
, M. Clara Bonaglia
, et al.
·
The American Journal of Human Genetics
·
41
PDF
GRIN2B mediates susceptibility to intelligence quotient and cognitive impairments in developmental dyslexia
2014
·
Sara Mascheretti
, Andrea Facoetti
, et al.
·
Psychiatric Genetics
·
36
Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome)
2018
·
Nehir Kurtas
, Filippo Arrigoni
, et al.
·
Journal of Medical Genetics
·
33
PDF
De novo unbalanced translocations have a complex history/aetiology
2018
·
Maria Clara Bonaglia
, Nehir Edibe Kurtas
, et al.
·
Human Genetics
·
27
PDF
Breakpoint determination of 15 large deletions in Peutz–Jeghers subjects
2010
·
Nicoletta Resta
, Roberto Giorda
, et al.
·
Human Genetics
·
27
Complex pathogenesis of Hirschsprung's disease in a patient with hydrocephalus, vesico-ureteral reflux and a balanced translocation t(3;17)(p12;q11)
2008
·
Paola Griseri
, Yvonne Vos
, et al.
·
European Journal of Human Genetics
·
27
PDF
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Works count:
43
Citation count:
2,120
H-index:
26
I10-index:
31
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