Fragile X syndrome: a review of clinical and molecular diagnoses
2017 · The Italian Journal of Pediatrics/Italian journal of pediatrics · 160 citations
https://doi.org/10.1186/s13052-017-0355-y
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Silvia Tabano
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico(IT)
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Silvia Tabano is an academic researcher from Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico. The author has contributed to research in topics: Epigenetics and DNA Methylation & Genetic Syndromes and Imprinting & Pregnancy and preeclampsia studies. The author has an h-index of 31, co-authored 100 publications.
ORCID: 0000-0002-5260-6691Papers by this author
worksMesenchymal stem cells: potential for therapy and treatment of chronic non-healing skin wounds
2015 · Organogenesis · 122 citations
https://doi.org/10.1080/15476278.2015.1126018
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes
2016 · Clinical Epigenetics · 68 citations
https://doi.org/10.1186/s13148-016-0183-8
Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms
2012 · Orphanet Journal of Rare Diseases · 31 citations
https://doi.org/10.1186/1750-1172-7-10
Mental health and the effects on methylation of stress-related genes in front-line versus other health care professionals during the second wave of COVID-19 pandemic: an Italian pilot study
2022 · European Archives of Psychiatry and Clinical Neuroscience · 19 citations
https://doi.org/10.1007/s00406-022-01472-y
MassARRAY-based simultaneous detection of hotspot somatic mutations and recurrent fusion genes in papillary thyroid carcinoma: the PTC-MA assay
2017 · Endocrine · 18 citations
https://doi.org/10.1007/s12020-017-1483-2
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