Cynthia Morton
15PUBLICATIONS
136CO-AUTHORS
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Publications (15)
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|Jul 26, 2024
Chromosomal structural rearrangements implicate long non-coding RNAs in rare germline disorders.Rebecca E Andersen, Ibrahim F Alkuraya, Abna Ajeesh
|Jul 01, 2024
Rare germline disorders implicate long non-coding RNAs disrupted by chromosomal structural rearrangements.Rebecca E Andersen, Ibrahim F Alkuraya, Abna Ajeesh
|Jun 23, 2022
The Burden and Benefits of Knowledge: Ethical Considerations Surrounding Population-Based Newborn Genome Screening for Hearing.Calli O Mitchell, Greysha Rivera-Cruz, Matthew Hoi Kin Chau
|May 28, 2022
Experience of Low-Pass Whole-Genome Sequencing-Based Copy Number Variant Analysis: A Survey of Chinese Tertiary Hospitals.Yu Zheng, Baosheng Zhu, Jichun Tan
|Jan 05, 2021
A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing.Yoel Hirsch, Chayada Tangshewinsirikul, Kevin T Booth
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Frequent Collaborators
4 joint publications
Sami S Amr
3 joint publications
Felix R Day
3 joint publications
Marjo-Riitta Jarvelin
2 joint publications
O Uimari
2 joint publications
T L Edwards
2 joint publications
Z Ruhioglu
2 joint publications
C M Becker
2 joint publications
S D Gordon
2 joint publications
S E Medland
2 joint publications
G W Montgomery
