Andrea Riccio Selected Research

Beckwith-Wiedemann Syndrome (Exomphalos Macroglossia Gigantism Syndrome)

10/2016	EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome.
1/2016	Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes.
1/2016	Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol.
1/2012	The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases.
9/2004	Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.

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Andrea Riccio Research Topics

Disease

5	Beckwith-Wiedemann Syndrome (Exomphalos Macroglossia Gigantism Syndrome) 10/2016 - 09/2004
4	Neoplasms (Cancer) 01/2016 - 10/2008
3	Imprinting Disorders 01/2020 - 01/2016
2	Uniparental Disomy 02/2016 - 01/2016
2	Silver-Russell Syndrome 01/2016 - 01/2012
1	Triploidy 11/2021
1	Female Infertility 01/2020
1	Hydatidiform Mole (Molar Pregnancy) 01/2020
1	Genomic Instability 01/2019
1	Breast Neoplasms (Breast Cancer) 01/2014
1	Type 1 Diabetes Mellitus (Autoimmune Diabetes) 05/2013
1	Adenoma (Adenomas) 10/2008
1	Carcinoma (Carcinomatosis) 10/2008
1	Growth Disorders 03/2008

Drug/Important Bio-Agent (IBA)

2	SilverIBA 10/2016 - 03/2008
2	Cyclin-Dependent Kinase Inhibitor p57IBA 02/2016 - 01/2016
2	DNA (Deoxyribonucleic Acid)IBA 05/2013 - 10/2008
1	CyclinsIBA 11/2021
1	Proteins (Proteins, Gene)FDA Link 01/2020
1	CateninsIBA 01/2019
1	ORALIT (ORS)IBA 01/2016
1	Insulin-Like PeptidesIBA 01/2016
1	human PMS2 proteinIBA 01/2014
1	Untranslated RNA (Noncoding RNA)IBA 01/2012
1	ElementsIBA 09/2004

Therapy/Procedure

1	Precision Medicine 01/2016
1	Segmental Mastectomy (Lumpectomy) 01/2014