Jun Liao
5PUBLICATIONS
28CO-AUTHORS
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Publications (5)
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|Feb 17, 2025
RNA methyltransferase SPOUT1/CENP-32 links mitotic spindle organization with the neurodevelopmental disorder SpADMiSS.Avinash V Dharmadhikari, Maria Alba Abad, Sheraz Khan
|Jan 23, 2024
RNA methyltransferase SPOUT1/CENP-32 links mitotic spindle organization with the neurodevelopmental disorder SpADMiSS.Avinash V Dharmadhikari, Maria Alba Abad, Sheraz Khan
|Sep 28, 2023
3' UTR Deletion of FBXO28 in a Patient with Brain Abnormalities and Developmental Delay.Xin Bi, Maureen S Mulhern, Erica Spiegel
|Mar 04, 2022
3q27.1 microdeletion causes prenatal and postnatal growth restriction and neurodevelopmental abnormalities.Subit Barua, Elaine M Pereira, Vaidehi Jobanputra
|Mar 05, 2021
Deletion of conserved non-coding sequences downstream from NKX2-1: A novel disease-causing mechanism for benign hereditary chorea.Jun Liao, Keith A Coffman, Joseph Locker
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Frequent Collaborators
1 joint publications
Quasar S Padiath
1 joint publications
Jennifer M Bain
1 joint publications
Avinash V Dharmadhikari
1 joint publications
Maria Alba Abad
1 joint publications
Reza Maroofian
1 joint publications
Elena Kondakova
1 joint publications
Rami Abou Jamra
1 joint publications
Pengfei Liu
1 joint publications
Dana Marafi
1 joint publications
Jennifer E Posey
