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Jacque L Duncan

6PUBLICATIONS

185CO-AUTHORS

Sensory systemsNeurology and neuromuscular diseasesGene mappingPhotography, video and lens-based practiceGenetic immunology

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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 <i>BBS1</i> deletion and <i>BBS9</i> 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 <i>RHO</i> 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

Frequent Collaborators

3 joint publications

Elise Héon

2 joint publications

Kelly A Frazer

2 joint publications

Sandro Banfi

2 joint publications

K Bailey Freund

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