Stephan Eliez
2PUBLICATIONS
39CO-AUTHORS
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Publications (2)
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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
|Jul 01, 2022
Altered developmental trajectories of verbal learning skills in 22q11.2DS: associations with hippocampal development and psychosis.Caren Latrèche, Johanna Maeder, Valentina Mancini
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Frequent Collaborators
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Maude Schneider
2 joint publications
Bernice E Morrow
1 joint publications
Caren Latrèche
1 joint publications
Johanna Maeder
1 joint publications
Valentina Mancini
1 joint publications
Jhih-Rong Lin
1 joint publications
Daniella Miller
1 joint publications
T Blaine Crowley
1 joint publications
Amirhossein Hajianpour
1 joint publications
Tiffany Busa
