Concepedia

Author

Giancarlo Deidda

Institute of Cell Biology and NeurobiologyORCID

Also Known As

G Deidda, G. C. Deidda, G. Deidda, Giancarlo Deidda

35

Publications

1.3K

Citations

17

H-Index

43

Concepts

All Affiliations

Institute of Cell Biology and NeurobiologyUniversità Cattolica del Sacro CuoreUniversity of Rome Tor VergataIstituti di Ricovero e Cura a Carattere ScientificoFondazione Santa Lucia
GD

About

Giancarlo Deidda is an author at Institute of Cell Biology and Neurobiology specializing in medicine, genetics, and molecular genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

10

10

925

2

Biology

3

3

179

3

Natural Sciences

2

2

45

4

Public Health

2

2

361

5

Biochemistry

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1

26

Giancarlo Deidda

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19

Publications

1.2K

Citations

16

H-Index

YearCitations

Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number ofKpnI repeats at the 4q35 locus and clinical phenotype

Enzo Ricci, Giuliana Galluzzi, Giancarlo Deidda,

Annals of Neurology

1999

296

De Novo Facioscapulohumeral Muscular Dystrophy: Frequent Somatic Mosaicism, Sex-Dependent Phenotype, and the Role of Mitotic Transchromosomal Repeat Interaction between Chromosomes 4 and 10

Silvère M. van der Maarel, Giancarlo Deidda, Richard J.L.F. Lemmers,

The American Journal of Human Genetics

2000

162

Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD).

Giancarlo Deidda, S. Cacurri, N. Piazzo,

Journal of Medical Genetics

1996

142

Physical Mapping Evidence for a Duplicated Region on Chromosome 10qter Showing High Homology with the Facioscapulohumeral Muscular Dystrophy Locus on Chromosome 4qter

Giancarlo Deidda, S. Cacurri, Paola Grisanti,

European Journal of Human Genetics

1995

102

Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2

Patrizia Calandra, Isabella Cascino, Richard J.L.F. Lemmers,

Journal of Medical Genetics

2016

71

Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity

Emanuela Teveroni, Marsha Pellegrino, Sabrina Sacconi,

Journal of Clinical Investigation

2017

65

Sequence Homology between 4qter and 10qter Loci Facilitates the Instability of Subtelomeric KpnI Repeat Units Implicated in Facioscapulohumeral Muscular Dystrophy

S. Cacurri, N. Piazzo, Giancarlo Deidda,

The American Journal of Human Genetics

1998

58

Detection of alpha-globin gene disorders by a simple PCR methodology.

Enrica Foglietta, Giancarlo Deidda, B Graziani,

PubMed

1997

51

Silent thalassemias: genotypes and phenotypes.

I Bianco, Maria Pia Cappabianca, Enrica Foglietta,

PubMed

1997

46

Molecular characterization of β-thalassemia mutations in Egypt

Andrea Novelletto, Mohamed Hafez, Giancarlo Deidda,

Human Genetics

1990

42

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