Sheila Ulivi

Trieste, Italy

Last Updated: 09/26/2026

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Found 49 publications

Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

Journal: Nature genetics

Published: July 09, 2024

Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

Journal: medRxiv : the preprint server for health sciences

Published: July 28, 2023

Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

Journal: Nature genetics

Published: June 12, 2023

Case Report: Two cases of apparent discordance between non-invasive prenatal testing (NIPT) and amniocentesis resulting in feto-placental mosaicism of trisomy 21. Issues in diagnosis, investigation and counselling.

Case Report: Two cases of apparent discordance between non-invasive prenatal testing (NIPT) and amniocentesis resulting in feto-placental mosaicism of trisomy 21. Issues in diagnosis, investigation and counselling.

Journal: Frontiers in genetics

Published: June 30, 2022

Genetic insights into resting heart rate and its role in cardiovascular disease.

Genetic insights into resting heart rate and its role in cardiovascular disease.

Journal: Nature communications

Published: June 06, 2022

Genome-wide association studies on Northern Italy isolated populations provide further support concerning genetic susceptibility for major depressive disorder.

Genome-wide association studies on Northern Italy isolated populations provide further support concerning genetic susceptibility for major depressive disorder.

Journal: The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry

Published: May 26, 2022

Identification of a New Mutation in RSK2, the Gene for Coffin-Lowry Syndrome (CLS), in Two Related Patients with Mild and Atypical Phenotypes.

Identification of a New Mutation in RSK2, the Gene for Coffin-Lowry Syndrome (CLS), in Two Related Patients with Mild and Atypical Phenotypes.

Journal: Brain sciences

Published: July 28, 2021

Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin.

Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin.

Journal: Journal of the American Society of Nephrology : JASN

Published: April 11, 2021

Genetic insights into biological mechanisms governing human ovarian ageing.

Genetic insights into biological mechanisms governing human ovarian ageing.

Journal: Nature

Published: August 24, 2020

Genetic determinants of circulating VEGF levels in major depressive disorder and electroconvulsive therapy response.

Genetic determinants of circulating VEGF levels in major depressive disorder and electroconvulsive therapy response.

Journal: Drug development research

Published: January 29, 2020

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.

Journal: Nature communications

Published: August 02, 2019

Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6.

Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6.

Journal: Genome biology

Published: March 02, 2018

Showing 1-12 of 49

Last Updated: 09/26/2026