Angela D'eustacchio

Trieste, Italy

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 14 publications

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

Journal: Nature genetics

Published: June 05, 2019

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

Journal: Nature genetics

Published: March 18, 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

Journal: Nature genetics

Published: March 18, 2018

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

Journal: Nature genetics

Published: August 14, 2017

Subclinical alteration of the cervical-vaginal microbiome in women with idiopathic infertility.

Subclinical alteration of the cervical-vaginal microbiome in women with idiopathic infertility.

Journal: Journal of cellular physiology

Published: November 11, 2016

A technical application of quantitative next generation sequencing for chimerism evaluation.

A technical application of quantitative next generation sequencing for chimerism evaluation.

Journal: Molecular medicine reports

Published: March 23, 2016

Identification of point mutations and large intragenic deletions in Fanconi anemia using next-generation sequencing technology.

Identification of point mutations and large intragenic deletions in Fanconi anemia using next-generation sequencing technology.

Journal: Molecular genetics & genomic medicine

Published: March 25, 2015

Usher syndrome: an effective sequencing approach to establish a genetic and clinical diagnosis.

Usher syndrome: an effective sequencing approach to establish a genetic and clinical diagnosis.

Journal: Hearing research

Published: August 30, 2014

A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta.

A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta.

Journal: Gene

Published: January 12, 2014

Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients.

Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients.

Journal: Gene

Published: December 06, 2013

Insight into genetic determinants of resting heart rate.

Insight into genetic determinants of resting heart rate.

Journal: Gene

Published: November 06, 2013

Association analysis of bitter receptor genes in five isolated populations identifies a significant correlation between TAS2R43 variants and coffee liking.

Association analysis of bitter receptor genes in five isolated populations identifies a significant correlation between TAS2R43 variants and coffee liking.

Journal: PloS one

Published: October 03, 2013

Showing 1-12 of 14

Last Updated: 09/26/2026