Publications by authors named "Victoria Giunta"

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Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22-23 Deletions.
Tanner J Nelson, Daniel E McGinn, T Blaine Crowley, Lydia Rockart, Audrey Green, Victoria Giunta

Clin Genet· December 2025

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ZNF280A links DNA double-strand break repair to human 22q11.2 distal deletion syndrome.
Thomas L Clarke, Hyo Min Cho, Ilaria Ceppi, Boya Gao, Tribhuwan Yadav, Victoria Giunta

Nat Cell Biol· June 2025

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Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications.
Ruben C Gur, Carrie E Bearden, Sebastien Jacquemont, Ann Swillen, Therese van Amelsvoort, Victoria Giunta

Mol Psychiatry· February 2025

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Hearing Loss in Children with 22q11.2 Deletion Syndrome.
Jill Arganbright, Terrence Blaine Crowley, Meghan Tracy, Janelle Noel-MacDonnell, Kim Gaiser, Victoria Giunta

Laryngoscope· February 2025

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Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications.
Ruben Gur, Carrie Bearden, Sébastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Victoria Giunta

Res Sq· December 2023

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Immunologic, Molecular, and Clinical Profile of Patients with Chromosome 22q11.2 Duplications.
Dharmagat Bhattarai, Daniel E McGinn, T Blaine Crowley, Victoria Giunta, Kimberly Gaiser

J Clin Immunol· May 2023

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Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants.
Jente Verbesselt, Cynthia B Solot, Ellen Van Den Heuvel, T Blaine Crowley, Victoria Giunta

Genes (Basel)· March 2023

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Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome.
Marta Smyk, Maciej Geremek, Kamila Ziemkiewicz, Tomasz Gambin, Anna Kutkowska-Kaźmierczak, Victoria Giunta

Genes (Basel)· March 2023

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