Aurora Arghir

5PUBLICATIONS
8CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Child and adolescent development
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Publications (5)

|Aug 28, 2025
FMR1 Methylation Pattern and Repeat Expansion Screening in a Cohort of Boys with Autism Spectrum Disorders: Correlation of Genetic Findings with Clinical Presentations.

Maria Dobre, Gisela Gaina, Alina Erbescu

|Sep 28, 2024
A rare cause of epileptic encephalopathy: case report of a novel patient with PEHO-like phenotype and CCDC88A gene pathogenic variants.

Sorina-Mihaela Papuc, Adelina Glangher, Alina Erbescu

|Feb 25, 2023
Autistic Behavior as Novel Clinical Finding in OFD1 Syndrome.

Sorina Mihaela Papuc, Alina Erbescu, Adelina Glangher

|Aug 06, 2021
The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 Patients.

Magdalena Budisteanu, Sorina Mihaela Papuc, Ioana Streata

|Jan 28, 2021
Autism and severe clinical phenotype in a patient with 8p21.2p11.21 deletion: Case report and literature review.

Aurora Arghir, Sorina Mihaela Papuc, Andreea-Cristina Tutulan-Cunita

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Frequent Collaborators

4 joint publications

Sorina-Mihaela Papuc

1 joint publications

Laura Bernardini

1 joint publications

Alina Erbescu

1 joint publications

Magdalena Budisteanu