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Lista de obras de Lorenzo Sinibaldi

A de novo proximal 3q29 chromosome microduplication in a patient with oculo auriculo vertebral spectrum

artículo científico publicado en 2015

Additive effects of genetic variation in dopamine regulating genes on working memory cortical activity in human brain.

artículo científico publicado en 2006

Attention-deficit/hyperactivity disorder, joint hypermobility-related disorders and pain: expanding body-mind connections to the developmental age.

artículo científico publicado en 2018

Autosomal dominant Brody disease cosegregates with a chromosomal (2;7)(p11.2;p12.1) translocation in an Italian family

artículo científico

BDNF rs6265 methylation and genotype interact on risk for schizophrenia

artículo científico publicado en 2016

Brain derived neurotrophic factor (BDNF) expression is regulated by microRNAs miR-26a and miR-26b allele-specific binding.

artículo científico publicado en 2011

COMT Val158Met polymorphism predicts negative symptoms response to treatment with olanzapine in schizophrenia

article

Catechol-O-methyltransferase Val(158)Met association with parahippocampal physiology during memory encoding in schizophrenia.

artículo científico publicado en 2010

Craniosynostosis-microphthalmia syndrome belongs to the spectrum of BCOR-related disorders

artículo científico publicado en 2020

DAT by perceived MC interaction on human prefrontal activity and connectivity during emotion processing.

scientific article published on 27 July 2012

Deletions of NF1 gene and exons detected by multiplex ligation-dependent probe amplification

artículo científico publicado en 2007

Delineation of MidXq28-duplication syndrome distal to MECP2 and proximal to RAB39B genes

scientific article published on 17 June 2019

Duplication 18q21.31-q22.2.

artículo científico publicado en 2007

Fluorescence in situ hybridization analysis of allelic losses involving the long arm of chromosome 17 in NF1-associated neurofibromas

artículo científico publicado en 2004

Further insight into the neurobehavioral pattern of children carrying the 2p16.3 heterozygous deletion involving NRXN1: report of five new cases

scientific article published on 13 July 2020

Genetically determined interaction between the dopamine transporter and the D2 receptor on prefronto-striatal activity and volume in humans.

artículo científico publicado en 2009

HDR (Hypoparathyroidism, Deafness, Renal dysplasia) syndrome associated to GATA3 gene duplication

artículo científico publicado en 2009

Interstitial 4q deletion associated with a mosaic complementary supernumerary marker chromosome in prenatal diagnosis

artículo científico publicado en 2013

Neurocognitive effects of methylphenidate on ADHD children with different DAT genotypes: a longitudinal open label trial.

artículo científico publicado en 2013

Psychopathological manifestations of joint hypermobility and joint hypermobility syndrome/ Ehlers-Danlos syndrome, hypermobility type: The link between connective tissue and psychological distress revised.

artículo científico

Quantitative ultrasound at the phalanges in a cohort of monozygotic twins of different ages

artículo científico publicado en 2014

Reproductive history of a healthy woman with mosaic duplication of chromosome 4p.

artículo científico publicado en 2005

Stress-related methylation of the catechol-O-methyltransferase Val 158 allele predicts human prefrontal cognition and activity.

artículo científico publicado en 2011

The clinical utility and indications of chromosomal microarray analysis in prenatal diagnosis.

artículo científico publicado en 2013

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