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ResearcherID: AAA-5555-2020
Scopus Author ID: 57201501260

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Employment (1)

IRCCS Istituto Auxologico Italiano: Milan, IT

Cytogenetic Biologist (Laboratory of Medical Cytogenetics and Molecular Genetics)
Employment
Source: Self-asserted source
ALESSANDRA SIRONI

Works (12)

Long-read sequencing reveals chromothripsis in a molecularly unsolved case of Cornelia de Lange syndrome

Frontiers in Genetics
2024 | Journal article
DOI: 10.3389/fgene.2024.1358334
EID:

2-s2.0-85188558393

Part of ISSN: 16648021
Contributors: Bestetti, I.; Crippa, M.; Sironi, A.; Bellini, M.; Tumiatti, F.; Ballabio, S.; Ceriotti, F.; Memo, L.; Iascone, M.; Larizza, L. et al.
Source: Self-asserted source
ALESSANDRA SIRONI via Scopus - Elsevier

A unique Smith-Magenis patient with a de novo intragenic deletion on the maternally inherited overexpressed RAI1 allele

European Journal of Human Genetics
2022 | Journal article
DOI: 10.1038/s41431-022-01143-5
EID:

2-s2.0-85134033741

Part of ISSN: 14765438 10184813
Contributors: Sironi, A.; Bestetti, I.; Masciadri, M.; Tumiatti, F.; Crippa, M.; Pantaleoni, C.; Russo, S.; D’Arrigo, S.; Milani, D.; Larizza, L. et al.
Source: Self-asserted source
ALESSANDRA SIRONI via Scopus - Elsevier

Expanding the Molecular Spectrum of ANKRD11 Gene Defects in 33 Patients with a Clinical Presentation of KBG Syndrome

International Journal of Molecular Sciences
2022 | Journal article
DOI: 10.3390/ijms23115912
EID:

2-s2.0-85130794381

Part of ISSN: 14220067 16616596
Contributors: Bestetti, I.; Crippa, M.; Sironi, A.; Tumiatti, F.; Masciadri, M.; Smeland, M.F.; Naik, S.; Murch, O.; Bonati, M.T.; Spano, A. et al.
Source: Self-asserted source
ALESSANDRA SIRONI via Scopus - Elsevier
grade
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Smith-Magenis Syndrome—Clinical Review, Biological Background and Related Disorders

Genes
2022 | Journal article
DOI: 10.3390/genes13020335
EID:

2-s2.0-85124821415

Part of ISSN: 20734425
Contributors: Rinaldi, B.; Villa, R.; Sironi, A.; Garavelli, L.; Finelli, P.; Bedeschi, M.F.
Source: Self-asserted source
ALESSANDRA SIRONI via Scopus - Elsevier
grade
Preferred source (of 2)‎

Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency

Human Reproduction
2021-10-18 | Journal article
DOI: 10.1093/humrep/deab192
Source: Self-asserted source
ALESSANDRA SIRONI
grade
Preferred source (of 2)‎

9q34.3 microduplications lead to neurodevelopmental disorders through EHMT1 overexpression

Neurogenetics
2019 | Journal article
DOI: 10.1007/s10048-019-00581-6
EID:

2-s2.0-85067700919
Contributors: Bonati, M.T.; Castronovo, C.; Sironi, A.; Zimbalatti, D.; Bestetti, I.; Crippa, M.; Novelli, A.; Loddo, S.; Dentici, M.L.; Taylor, J. et al.
Source: Self-asserted source
ALESSANDRA SIRONI via Scopus - Elsevier

High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function

Human Reproduction
2019 | Journal article
DOI: 10.1093/humrep/dey389
EID:

2-s2.0-85062173089
Contributors: Bestetti, I.; Castronovo, C.; Sironi, A.; Caslini, C.; Sala, C.; Rossetti, R.; Crippa, M.; Ferrari, I.; Pistocchi, A.; Toniolo, D. et al.
Source: Self-asserted source
ALESSANDRA SIRONI via Scopus - Elsevier

Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes

Frontiers in Genetics
2019 | Journal article
DOI: 10.3389/fgene.2019.00955
EID:

2-s2.0-85074284179
Contributors: Crippa, M.; Bonati, M.T.; Calzari, L.; Picinelli, C.; Gervasini, C.; Sironi, A.; Bestetti, I.; Guzzetti, S.; Bellone, S.; Selicorni, A. et al.
Source: Self-asserted source
ALESSANDRA SIRONI via Scopus - Elsevier

13q mosaic deletion including RB1 associated to mild phenotype and no cancer outcome-case report and review of the literature 06 Biological Sciences 0604 Genetics

Molecular Cytogenetics
2018 | Journal article
DOI: 10.1186/s13039-018-0401-5
EID:

2-s2.0-85053706222
Contributors: Bestetti, I.; Sironi, A.; Catusi, I.; Mariani, M.; Giardino, D.; Manoukian, S.; Milani, D.; Larizza, L.; Castronovo, C.; Finelli, P.
Source: Self-asserted source
ALESSANDRA SIRONI via Scopus - Elsevier

iPSC-derived neurons of CREBBP- and EP300-mutated Rubinstein-Taybi syndrome patients show morphological alterations and hypoexcitability

Stem Cell Research
2018 | Journal article
DOI: 10.1016/j.scr.2018.05.019
EID:

2-s2.0-85048473649
Contributors: Alari, V.; Russo, S.; Terragni, B.; Ajmone, P.F.; Sironi, A.; Catusi, I.; Calzari, L.; Concolino, D.; Marotta, R.; Milani, D. et al.
Source: Self-asserted source
ALESSANDRA SIRONI via Scopus - Elsevier

Rothmund-Thomson syndrome: Insights from new patients on the genetic variability underpinning clinical presentation and cancer outcome

International Journal of Molecular Sciences
2018 | Journal article
DOI: 10.3390/ijms19041103
EID:

2-s2.0-85045150517
Contributors: Colombo, E.A.; Locatelli, A.; Sánchez, L.C.; Romeo, S.; Elcioglu, N.H.; Maystadt, I.; Martínez, A.E.; Sironi, A.; Fontana, L.; Finelli, P. et al.
Source: Self-asserted source
ALESSANDRA SIRONI via Scopus - Elsevier

Segmental Maternal UPD of Chromosome 7q in a Patient With Pendred and Silver Russell Syndromes-Like Features.

Frontiers in genetics
2018-11-30 | Journal article
DOI: 10.3389/fgene.2018.00600
PMID: 30555519
PMC: PMC6284021
Source: Self-asserted source
ALESSANDRA SIRONI
grade
Preferred source (of 2)‎

Peer review (1 review for 1 publication/grant)

Review activity for Journal of pediatric genetics. (1)
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