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International Journal of Cancer|December 20, 2018
Relationship of DNA methylation to mutational changes and transcriptional organization in fusion-positive and fusion-negative rhabdomyosarcomaWenyue Sun, Bishwanath Chatterjee, Jack F Shern, et al.
Human Molecular Genetics|April 17, 2015
Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomaliesRama Rao Damerla, Cheng Cui, George C Gabriel, et al.
Journal of Cardiovascular Disease Research|December 3, 2011
Evaluating the role of connexin43 in congenital heart disease: Screening for mutations in patients with outflow tract anomalies and the analysis of knock-in mouse modelsGuo-Ying Huang, Li-Jian Xie, Kaari L Linask, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 17, 2009
Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxyZhen Zhang, Deanne Alpert, Richard Francis, et al.
Plos Biology|December 5, 2013
Wdpcp, a PCP protein required for ciliogenesis, regulates directional cell migration and cell polarity by direct modulation of the actin cytoskeletonCheng Cui, Bishwanath Chatterjee, Thomas P Lozito, et al.
Circulation|April 14, 2012
High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxyNader Nakhleh, Richard Francis, Rachel A Giese, et al.
Nature|March 26, 2015
Global genetic analysis in mice unveils central role for cilia in congenital heart diseaseYou Li, Nikolai T Klena, George C Gabriel, et al.
Nature Genetics|May 23, 2017
The complex genetics of hypoplastic left heart syndromeXiaoqin Liu, Hisato Yagi, Shazina Saeed, et al.
Science Signaling|November 22, 2018
The HDAC3-SMARCA4-miR-27a axis promotes expression of the PAX3:FOXO1 fusion oncogene in rhabdomyosarcomaNarendra Bharathy, Noah E Berlow, Eric Wang, et al.
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