Alessandro Vimercati
Milan, 20145, Italy
Last Updated: 09/26/2026
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Found 8 publications
Hypomethylation of the MEG8:Int2-DMR in patients with pathogenic PLAG1 variants suggests new role of the chr14q32 imprinting cluster in Silver-Russell syndrome.
Journal: Clinical epigenetics
Published: September 23, 2025
PEG10 loss of function causes Silver-Russell syndrome: a familial case with paternal deletion.
Journal: Scientific reports
Published: September 09, 2025
Distinguishing Genetic Alterations Versus (Epi)Mutations in Silver-Russell Syndrome and Focus on the IGF1R Gene.
Journal: The Journal of clinical endocrinology and metabolism
Published: June 26, 2024
A long way to syndromic short stature.
Journal: Italian journal of pediatrics
Published: October 18, 2023
Case report: atypical Silver-Russell syndrome patient with hand dystonia: the valuable support of the consensus statement to the wide syndromic spectrum.
Journal: Frontiers in genetics
Published: April 03, 2023
Modeling RTT Syndrome by iPSC-Derived Neurons from Male and Female Patients with Heterogeneously Severe Hot-Spot MECP2 Variants.
Journal: International journal of molecular sciences
Published: October 11, 2022
Germline variants in genes of the subcortical maternal complex and Multilocus Imprinting Disturbance are associated with miscarriage/infertility or Beckwith-Wiedemann progeny.
Journal: Clinical epigenetics
Published: January 11, 2022
Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases.
Journal: Genes
Published: March 15, 2021
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Last Updated: 09/26/2026