Jacque L Duncan
6PUBLICATIONS
185CO-AUTHORS
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Publications (6)
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|Jan 09, 2026
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova
|Jan 20, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova
|Dec 02, 2024
Novel BBS1 deletion and BBS9 nonsense pathogenic variant in Bardet-Biedl syndrome.Janice Min Li, Erika Tavares, Jacque L Duncan
|Apr 25, 2024
Disease modeling and pharmacological rescue of autosomal dominant retinitis pigmentosa associated with RHO copy number variation.Sangeetha Kandoi, Cassandra Martinez, Kevin Xu Chen
|Oct 18, 2021
Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis.Pooja Biswas, Adda L Villanueva, Angel Soto-Hermida
|Oct 26, 2017
Correction: Gustafson et al., Whole Genome Sequencing Revealed Mutations in Two Independent Genes as the Underlying Cause of Retinal Degeneration in an Ashkenazi Jewish Pedigree. Genes 2017, 8, 210.Kevin Gustafson, Jacque L Duncan, Pooja Biswas
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Frequent Collaborators
3 joint publications
Elise Héon
2 joint publications
Kelly A Frazer
2 joint publications
Sandro Banfi
2 joint publications
K Bailey Freund
2 joint publications
Suzanne E de Bruijn
2 joint publications
Carmen Ayuso
2 joint publications
Kim Rodenburg
2 joint publications
Manir Ali
2 joint publications
Lara K Holtes
2 joint publications
Radha Ayyagari
