about
HDR (Hypoparathyroidism, Deafness, Renal dysplasia) syndrome associated to GATA3 gene duplicationDeletions of NF1 gene and exons detected by multiplex ligation-dependent probe amplificationBrain derived neurotrophic factor (BDNF) expression is regulated by microRNAs miR-26a and miR-26b allele-specific binding.BDNF rs6265 methylation and genotype interact on risk for schizophreniaGenetically determined interaction between the dopamine transporter and the D2 receptor on prefronto-striatal activity and volume in humans.DAT by perceived MC interaction on human prefrontal activity and connectivity during emotion processing.Psychopathological manifestations of joint hypermobility and joint hypermobility syndrome/ Ehlers-Danlos syndrome, hypermobility type: The link between connective tissue and psychological distress revised.Autosomal dominant Brody disease cosegregates with a chromosomal (2;7)(p11.2;p12.1) translocation in an Italian family.The clinical utility and indications of chromosomal microarray analysis in prenatal diagnosis.Additive effects of genetic variation in dopamine regulating genes on working memory cortical activity in human brain.Attention-deficit/hyperactivity disorder, joint hypermobility-related disorders and pain: expanding body-mind connections to the developmental age.Neurocognitive effects of methylphenidate on ADHD children with different DAT genotypes: a longitudinal open label trial.Stress-related methylation of the catechol-O-methyltransferase Val 158 allele predicts human prefrontal cognition and activity.Catechol-O-methyltransferase Val(158)Met association with parahippocampal physiology during memory encoding in schizophrenia.Duplication 18q21.31-q22.2.Reproductive history of a healthy woman with mosaic duplication of chromosome 4p.A de novo proximal 3q29 chromosome microduplication in a patient with oculo auriculo vertebral spectrumCOMT Val158Met polymorphism predicts negative symptoms response to treatment with olanzapine in schizophreniaFluorescence in situ hybridization analysis of allelic losses involving the long arm of chromosome 17 in NF1-associated neurofibromasInterstitial 4q deletion associated with a mosaic complementary supernumerary marker chromosome in prenatal diagnosisQuantitative ultrasound at the phalanges in a cohort of monozygotic twins of different agesDelineation of MidXq28-duplication syndrome distal to MECP2 and proximal to RAB39B genes
P50
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P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Lorenzo Sinibaldi
@ast
Lorenzo Sinibaldi
@en
Lorenzo Sinibaldi
@es
Lorenzo Sinibaldi
@nl
type
label
Lorenzo Sinibaldi
@ast
Lorenzo Sinibaldi
@en
Lorenzo Sinibaldi
@es
Lorenzo Sinibaldi
@nl
prefLabel
Lorenzo Sinibaldi
@ast
Lorenzo Sinibaldi
@en
Lorenzo Sinibaldi
@es
Lorenzo Sinibaldi
@nl
P106
P21
P31
P496
0000-0002-1371-936X