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David R Murdock

4PUBLICATIONS

108CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Neurosciences not elsewhere classifiedGene mapping

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Publications (4)

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|Feb 06, 2026

Genome and Transcriptome-Wide Analyses Identify Multiple Candidate Genes and a Significant Polygenic Contribution in Bicuspid Aortic Valve.

Sébastien Thériault, Jacob A Holdcraft, Dinara Sharipova

|Mar 18, 2024

Novel syndromic neurodevelopmental disorder caused by <i>de novo</i> deletion of <i>CHASERR</i>, a long noncoding RNA.

Vijay S Ganesh, Kevin Riquin, Nicolas Chatron

|Mar 02, 2023

An FBN1 deep intronic variant is associated with pseudoexon formation and a variable Marfan phenotype in a five generation family.

Dong-Chuan Guo, Xueyan Duan, Kathleen Mimnagh

|Sep 02, 2022

Long read sequencing and expression studies of AHDC1 deletions in Xia-Gibbs syndrome reveal a novel genetic regulatory mechanism.

Varuna Chander, Medhat Mahmoud, Jianhong Hu

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Frequent Collaborators

2 joint publications

Dianna Milewicz

2 joint publications

Dongchuan Guo

1 joint publications

Varuna Chander

1 joint publications

Medhat Mahmoud

1 joint publications

Zain Dardas

1 joint publications

Christopher M Grochowski

1 joint publications

Michael M Khayat

1 joint publications

He Li

1 joint publications

Simon Body

1 joint publications

Qingchang Meng

Frequent Collaborators

2 joint publications

Dianna Milewicz

2 joint publications

Dongchuan Guo

1 joint publications

Varuna Chander

1 joint publications

Medhat Mahmoud

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