Concepedia

Author

Angelo Notarangelo

Istituti di Ricovero e Cura a Carattere ScientificoORCID

Also Known As

A Notarangelo, A. Notarangelo, ANGELANTONIO NOTARANGELO, Angelantonio Notarangelo, Angelo Notarangelo

35

Publications

1.1K

Citations

13

H-Index

66

Concepts

All Affiliations

Istituti di Ricovero e Cura a Carattere ScientificoCasa Sollievo della SofferenzaNuovo Ospedale San Giovanni di DioTelethon Institute Of Genetics And MedicineUniversity of Turin
AN

About

Angelo Notarangelo is an author at Istituti di Ricovero e Cura a Carattere Scientifico specializing in medicine, genetics, and obstetrics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

9

9

582

2

Natural Sciences

2

2

116

3

Arts

1

1

238

4

Health Sciences

1

1

10

5

Public Health

1

1

12

Angelo Notarangelo

×

13

Publications

884

Citations

12

H-Index

YearCitations

MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss

Salvatore Melchionda, Nadav Ahituv, Luigi Bisceglia,

The American Journal of Human Genetics

2001

238

Sedlin Controls the ER Export of Procollagen by Regulating the Sar1 Cycle

Rossella Venditti, Tiziana Scanu, Michele Santoro,

Science

2012

171

Ring chromosome 21 in healthy persons: different consequencies in females and in males

Bruno Dallapiccola, V De Filippis, Angelo Notarangelo,

Human Genetics

1986

109

Regulation of<i>KEAP1</i>expression by promoter methylation in malignant gliomas and association with patient’s outcome

Lucia Anna Muscarella, Raffaela Barbano, Vincenzo D’Angelo,

Epigenetics

2011

104

Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneity.

Paolo Gasparini, Marı́a Julia Calonge, Luigi Bisceglia,

PubMed

1995

87

Fine Exon–Intron Structure of the Fanconi Anemia Group A (FAA) Gene and Characterization of Two Genomic Deletions

Marta Centra, Elena Memeo, Maria D’Apolito,

Genomics

1998

50

High Specificity of Quantitative Methylation‐Specific PCR Analysis for <i>MGMT</i> Promoter Hypermethylation Detection in Gliomas

Paola Parrella, Antonella la Torre, Massimiliano Copetti,

BioMed Research International

2009

28

On the parental origin of the X's in a prenatally diagnosed 49,XXXXX syndrome

G. A. Martini, Gerardo Andrés Obeso Carillo, F. Catizone,

Prenatal Diagnosis

1993

27

Translocation of the proto-oncogene Bcl-6 in human glioblastoma multiforme

Simona Ruggieri, Roberto Tamma, Andrea Marzullo,

Cancer Letters

2014

20

Dp71 Expression in Human Glioblastoma

Simona Ruggieri, Michelina De Giorgis, Tiziana Annese,

International Journal of Molecular Sciences

2019

16

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