Donna McDonald-McGinn
25PUBLICATIONS
165CO-AUTHORS
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Publications (25)
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|Mar 27, 2026
Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.Jhih-Rong Lin, Daniella Miller, Dana Luong
|Jan 28, 2026
22q11.2 Deletion Syndrome in Offspring Conceived via Assisted Reproductive Technology Versus Spontaneously.Jennifer Borowka, Terrence Blaine Crowley, Ashika Mani
|Dec 08, 2025
Charting Brain Structure in 22q11.2 Deletion Syndrome with Clinical Neuroimaging.Benjamin Jung, J Eric Schmitt, Jakob Seidlitz
|Jun 16, 2025
ZNF280A links DNA double-strand break repair to human 22q11.2 distal deletion syndrome.Thomas L Clarke, Hyo Min Cho, Ilaria Ceppi
|Nov 13, 2024
Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndrome.Lisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos
|Jul 27, 2024
Expanding Genetic Counselor Roles: A Model for Global Research Development.Colleen C Muraresku, Elizabeth M McCormick, Lydia Rockart
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Frequent Collaborators
16 joint publications
Terrence Blaine Crowley
11 joint publications
Anne S Bassett
9 joint publications
Ann Swillen
8 joint publications
Elaine Zackai
8 joint publications
Carrie E Bearden
6 joint publications
Beverly S Emanuel
6 joint publications
Jacob Vorstman
5 joint publications
Michael J Owen
5 joint publications
Jeroen Breckpot
4 joint publications
Stephen W Scherer
