Concepedia

Author

Michele Valiante

Carlo Forlanini Hospital

Also Known As

M Valiante, M. Valiante, Michele Valiante

28

Publications

343

Citations

9

H-Index

14

Concepts

All Affiliations

Carlo Forlanini HospitalSapienza University of RomeAzienda Socio Sanitaria Territoriale degli Spedali Civili di BresciaUniversity of BresciaPoliclinico Umberto I
MV

About

Michele Valiante is an author at Carlo Forlanini Hospital specializing in medicine, pathology, and cancer genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

2

2

80

2

Pathology

2

2

80

3

Cancer Genetics

1

1

61

4

Genetic Epidemiology

1

1

19

5

Genetics

1

1

61

Michele Valiante

×

6

Publications

224

Citations

6

H-Index

YearCitations

Nosology and inheritance pattern(s) of joint hypermobility syndrome and Ehlers‐Danlos syndrome, hypermobility type: A study of intrafamilial and interfamilial variability in 23 Italian pedigrees

Marco Castori, Chiara Dordoni, Michele Valiante,

American Journal of Medical Genetics Part A

2014

79

Sensitivity to asbestos is increased in patients with mesothelioma and pathogenic germline variants in <i>BAP1</i> or other DNA repair genes

Marta Betti, Anna Aspesi, Daniela Ferrante,

Genes Chromosomes and Cancer

2018

61

Spectrum of mucocutaneous manifestations in 277 patients with joint hypermobility syndrome/Ehlers‐Danlos syndrome, hypermobility type

Marco Castori, Chiara Dordoni, Silvia Morlino,

American Journal of Medical Genetics Part C Seminars in Medical Genetics

2015

37

TFR2-related hereditary hemochromatosis as a frequent cause of primary iron overload in patients from Central-Southern Italy

Francesca Clementina Radio, Silvia Majore, Francesco Binni,

Blood Cells Molecules and Diseases

2013

19

Elsahy–Waters syndrome: Evidence for autosomal recessive inheritance

Marco Castori, Piero Cascone, Michele Valiante,

American Journal of Medical Genetics Part A

2010

14

Clinical presentation and molecular characterization of a novel patient with variant <i> <scp>POC1A</scp> ‐ </i> related syndrome

Silvia Majore, Emanuele Agolini, Lucia Micale,

Clinical Genetics

2020

14

Page 1