Paola Primignani

Lodi, 26900, Italy

Last Updated: 09/26/2026

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Found 18 publications

Sex-specific cardiometabolic remodeling induced by DPP-4 inhibition under high-fat diet: insights from cardiac proteomics.

Sex-specific cardiometabolic remodeling induced by DPP-4 inhibition under high-fat diet: insights from cardiac proteomics.

Journal: Nutrition, metabolism, and cardiovascular diseases : NMCD

Published: April 08, 2026

Chemical investigation of biological trace evidence; toxicological screening of waste residues obtained from DNA extraction processes.

Chemical investigation of biological trace evidence; toxicological screening of waste residues obtained from DNA extraction processes.

Journal: International journal of legal medicine

Published: March 04, 2023

SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa.

SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa.

Journal: Frontiers in genetics

Published: September 15, 2020

Ocular swabs on exhumed bodies: An alternative to the collection of "classical" tissue samples in forensic genetics.

Ocular swabs on exhumed bodies: An alternative to the collection of "classical" tissue samples in forensic genetics.

Journal: Forensic science international. Genetics

Published: December 27, 2018

Workload measurement for molecular genetics laboratory: A survey study.

Workload measurement for molecular genetics laboratory: A survey study.

Journal: PloS one

Published: May 11, 2018

Clinical evaluation and molecular screening of a large consecutive series of albino patients.

Clinical evaluation and molecular screening of a large consecutive series of albino patients.

Journal: Journal of human genetics

Published: March 22, 2016

Screening of PAX6 gene in Italian congenital aniridia patients revealed four novel mutations.

Screening of PAX6 gene in Italian congenital aniridia patients revealed four novel mutations.

Journal: Ophthalmic genetics

Published: February 06, 2016

Detection of the first OCA6 Italian patient in a large cohort of albino subjects.

Detection of the first OCA6 Italian patient in a large cohort of albino subjects.

Journal: Journal of dermatological science

Published: October 31, 2015

A novel OTX2 gene frameshift mutation in a child with microphthalmia, ectopic pituitary and growth hormone deficiency.

A novel OTX2 gene frameshift mutation in a child with microphthalmia, ectopic pituitary and growth hormone deficiency.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: October 28, 2015

A Novel MGC4607/CCM2 Gene Mutation Associated with Cerebral Spinal and Cutaneous Cavernous Angiomas.

A Novel MGC4607/CCM2 Gene Mutation Associated with Cerebral Spinal and Cutaneous Cavernous Angiomas.

Journal: Journal of molecular neuroscience : MN

Published: March 09, 2015

Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites.

Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites.

Journal: Journal of human genetics

Published: March 05, 2015

SOX2, OTX2 and PAX6 analysis in subjects with anophthalmia and microphthalmia.

SOX2, OTX2 and PAX6 analysis in subjects with anophthalmia and microphthalmia.

Journal: European journal of medical genetics

Published: May 14, 2014

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Last Updated: 09/26/2026