Concepedia

Author

Antonio Romito

Telethon Institute Of Genetics And Medicine

Also Known As

Antonio Romito

17

Publications

796

Citations

10

H-Index

24

Concepts

All Affiliations

Telethon Institute Of Genetics And MedicineCentre National de la Recherche ScientifiqueUniversity of GenevaCentogene (Germany)Inserm
AR

About

Antonio Romito is an author at Telethon Institute Of Genetics And Medicine specializing in medicine, developmental biology, and cardiac reprogramming.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

4

4

240

2

Cell Biology

2

2

92

3

Cardiac Reprogramming

2

2

92

4

Molecular Genetics

1

1

114

5

Cell Development

1

1

27

Antonio Romito

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8

Publications

527

Citations

8

H-Index

YearCitations

Ftx is a non-coding RNA which affects Xist expression and chromatin structure within the X-inactivation center region

Corinne Chureau, Sophie Chantalat, Antonio Romito,

Human Molecular Genetics

2010

244

The Ftx Noncoding Locus Controls X Chromosome Inactivation Independently of Its RNA Products

Giulia Furlan, Nancy Gutierrez Hernandez, Christophe Huret,

Molecular Cell

2018

114

Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modifications

Antonietta Coppola, Antonio Romito, Christelle Borel,

Stem Cell Research

2013

65

Energy biogenesis: one key for coordinating two genomes

Marco Sardiello, Gaetano Tripoli, Antonio Romito,

Trends in Genetics

2004

34

Lack of Sik1 in Mouse Embryonic Stem Cells Impairs Cardiomyogenesis by Down-Regulating the Cyclin-Dependent Kinase Inhibitor p57kip2

Antonio Romito, Enza Lonardo, Guglielmo Roma,

PLoS ONE

2010

27

A mouse embryonic stem cell bank for inducible overexpression of human chromosome 21 genes

Rossella De Cegli, Antonio Romito, Simona Iacobacci,

Genome Biology

2010

18

CLEC16A interacts with retromer and TRIM27, and its loss impairs endosomal trafficking and neurodevelopment

Daphne J. Smits, Jordy Dekker, Rachel Schot,

Human Genetics

2022

14

Biallelic variants in HECT E3 paralogs, HECTD4 and UBE3C, encoding ubiquitin ligases cause neurodevelopmental disorders that overlap with Angelman syndrome

Eissa Faqeih, Malak Alghamdi, Marwa A. Almahroos,

Genetics in Medicine

2022

11

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