Vanesa Lotersztein
B, Argentina
Last Updated: 09/26/2026
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Found 13 publications
Investigation of multilocus imprinting disturbance (MLID) in 101 Beckwith-Wiedemann spectrum patients.
Journal: Clinical epigenetics
Published: April 29, 2025
Contribution of large genomic rearrangements in BRCA1/2 genes and CHEK2 1100delC allele variant to the development of breast/ovarian cancer in Argentinian population.
Journal: Breast cancer research and treatment
Published: October 23, 2024
In silico and in vivo analyses of a novel variant in MYO6 identified in a family with postlingual non-syndromic hearing loss from Argentina.
Journal: NAR genomics and bioinformatics
Published: September 17, 2024
Comprehensive Approach for the Genetic Diagnosis of Patients with Waardenburg Syndrome.
Journal: Journal of personalized medicine
Published: August 01, 2024
Identification of copy-number variants in patients with overgrowth disorders.
Journal: Clinical genetics
Published: June 17, 2024
Nationwide genetic analysis of more than 600 families with inherited eye diseases in Argentina.
Journal: NPJ genomic medicine
Published: December 12, 2022
GJB2 and GJB6 Genetic Variant Curation in an Argentinean Non-Syndromic Hearing-Impaired Cohort.
Journal: Genes
Published: September 18, 2020
Implementation of chromosomal microarrays in a cohort of patients with intellectual disability at the Argentinean public health system.
Journal: Molecular biology reports
Published: February 03, 2020
Inflammatory cutaneous lesions and pulmonary manifestations in a new patient with autosomal recessive ISG15 deficiency case report.
Journal: Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology
Published: January 16, 2020
Last Updated: 09/26/2026