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List of works by Lorenzo Sinibaldi

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

scientific article published on 03 March 2015

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

scientific article

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

scientific article published on 14 February 2018

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

scientific article published on July 2004

BDNF rs6265 methylation and genotype interact on risk for schizophrenia

scientific article published on 18 February 2016

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

scientific article

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.

scientific article published on 13 December 2010

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

scientific article published on 03 August 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

scientific article

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.

scientific article published in February 2007

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

scientific article published on 01 April 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.

scientific article published on January 2009

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

scientific article

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

scientific article published on 27 May 2013

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

scientific article published on 28 March 2013

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

scientific article published on March 2015

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

scientific article published on 05 August 2014

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

scientific article published in April 2005

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

scientific article published in May 2011

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

scientific article published in January 2013

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