Beverly S Emanuel
9PUBLICATIONS
86CO-AUTHORS
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Publications (9)
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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 05, 2024
Tbx1 haploinsufficiency leads to local skull deformity, paraflocculus and flocculus dysplasia, and motor-learning deficit in 22q11.2 deletion syndrome.Tae-Yeon Eom, J Eric Schmitt, Yiran Li
|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
|Apr 02, 2024
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion Syndrome.Lisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos
|Jul 18, 2023
Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS.Yingjie Zhao, Yujue Wang, Lijie Shi
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