Daniela Francesca Giachino

Associate Professor of Medical Genetics

University of Turin

Italy

Research Interests

Explore related searches

Professors in Italy Professors in Medical Science Medical Science professors in Italy

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

Articles (9)

Year:

2024

Year:

2023

Year:

2022

Year:

2022

Year:

2021

Year:

2021

Year:

2021

Year:

2020

Year:

2020

Collaborators (12)

Caroline Schluth-Bolard

University of Lyon

FRANCE

View details

Barbara Mognetti

Università degli Studi di Torino

ITALY

View details

Giuseppe Matullo

ITALY

View details

Fabio Luigi Massimo Ricciardolo

Professore Ordinario già Professore Associato e già Ricercatore Universitario

Università degli Studi di Torino

ITALY

View details

Carloalberto Biole'

Azienda Ospedaliero Universitaria Città della Salute e della Scienza di Torino

ITALY

View details

Sebastian Clauss

GERMANY

View details

Gianluca Witel

Candiolo Cancer Institute

ITALY

View details

Annika Winbo

University of Auckland

NEW ZEALAND

View details

Giorgio V Scagliotti

University of Turin

ITALY

View details

Mirco Dindo

Assistant Professor

University of Perugia

ITALY

View details

Monica Pentenero

Associate Professor

University of Turin

ITALY

View details

Silvia Deaglio

University of Turin

ITALY

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Daniela Francesca Giachino

Research Interests

Explore related searches

Contact this professor

Articles (9)

Genetic Testing for Patients with Cardiomyopathies: The INDACO Study—Towards a Cardiogenetic Clinic

Glucocorticoid Receptor Polymorphism A3669G Is Associated with Airflow Obstruction in Mild-to-Severe Asthma

Gingival Overgrowths Revealing PTEN Hamartoma Tumor Syndrome: Report of Novel PTEN Pathogenic Variants

Diagnostics of <i>BAP1</i>-Tumor Predisposition Syndrome by a Multitesting Approach: A Ten-Year-Long Experience

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

Clinical exome sequencing is a powerful tool in the diagnostic flow of monogenic kidney diseases: an Italian experience

Effects of eight neuropsychiatric copy number variants on human brain structure

The ILE56 mutation on different genetic backgrounds of alanine:glyoxylate aminotransferase: Clinical features and biochemical characterization

Ventricular conduction delay as marker of risk in Brugada Syndrome. Results from the analysis of clinical and electrocardiographic features of a large cohort of patients

Collaborators (12)

Caroline Schluth-Bolard

Barbara Mognetti

Giuseppe Matullo

Fabio Luigi Massimo Ricciardolo

Carloalberto Biole'

Sebastian Clauss

Gianluca Witel

Annika Winbo

Giorgio V Scagliotti

Mirco Dindo

Monica Pentenero

Silvia Deaglio

Make your next move.