Margaret Kenna
17PUBLICATIONS
95CO-AUTHORS
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Publications (17)
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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
|Apr 25, 2024
Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules.Daniel O Dodd, Sabrina Mechaussier, Patricia L Yeyati
|Mar 08, 2024
PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss.Shelby E Redfield, Pedro De-la-Torre, Mina Zamani
|Aug 16, 2023
Vestibular Preservation in Pediatric Cochlear Implantation.Greg R Licameli, Alicia Wang, Guangwei Zhou
|May 09, 2023
Otolaryngologic Manifestations of Trisomy 13 and Trisomy 18 in Pediatric Patients.Jalen Benson, Candace Stewart, Margaret A Kenna
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Frequent Collaborators
5 joint publications
Eliot Shearer
3 joint publications
Julia Perry
3 joint publications
Greg R Licameli
2 joint publications
Judith E C Lieu
2 joint publications
Michael S Cohen
2 joint publications
Shelby Redfield
2 joint publications
Sami S Amr
2 joint publications
Elijah L Mena
2 joint publications
Abna Ajeesh
2 joint publications
Rebecca E Andersen
