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Jun Shen, Ph.D. - Publications

Affiliations: 
Harvard University, Cambridge, MA, United States 
Area:
Genes involved in the development and function of the cerebral cortex
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10 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2017 Evrony GD, Cordero DR, Shen J, Partlow JN, Yu TW, Rodin RE, Hill RS, Coulter ME, Lam AN, Jayaraman D, Gerrelli D, Diaz DG, Santos C, Morrison V, Galli A, et al. Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome. Genome Research. PMID 28630177 DOI: 10.1101/Gr.219899.116  0.689
2015 Lin SY, Vollrath MA, Mangosing S, Shen J, Cardenas E, Corey DP. The zebrafish pinball wizard gene encodes WRB, a tail-anchored-protein receptor essential for inner-ear hair cells and retinal photoreceptors. The Journal of Physiology. PMID 26593130 DOI: 10.1113/Jp271437  0.729
2015 Shen J, Scheffer DI, Kwan KY, Corey DP. SHIELD: an integrative gene expression database for inner ear research. Database : the Journal of Biological Databases and Curation. 2015: bav071. PMID 26209310 DOI: 10.1093/Database/Bav071  0.706
2015 Scheffer DI, Shen J, Corey DP, Chen ZY. Gene Expression by Mouse Inner Ear Hair Cells during Development. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 6366-80. PMID 25904789 DOI: 10.1523/Jneurosci.5126-14.2015  0.594
2015 Scheffer DI, Zhang DS, Shen J, Indzhykulian A, Karavitaki KD, Xu YJ, Wang Q, Lin JJ, Chen ZY, Corey DP. XIRP2, an actin-binding protein essential for inner ear hair-cell stereocilia. Cell Reports. 10: 1811-8. PMID 25772365 DOI: 10.1016/J.Celrep.2015.02.042  0.694
2015 Kwan KY, Shen J, Corey DP. C-MYC transcriptionally amplifies SOX2 target genes to regulate self-renewal in multipotent otic progenitor cells. Stem Cell Reports. 4: 47-60. PMID 25497456 DOI: 10.1016/J.Stemcr.2014.11.001  0.717
2010 Shen J, Gilmore EC, Marshall CA, Haddadin M, Reynolds JJ, Eyaid W, Bodell A, Barry B, Gleason D, Allen K, Ganesh VS, Chang BS, Grix A, Hill RS, Topcu M, et al. Mutations in PNKP cause microcephaly, seizures and defects in DNA repair. Nature Genetics. 42: 245-9. PMID 20118933 DOI: 10.1038/Ng.526  0.705
2010 Powers SE, Taniguchi K, Yen W, Melhuish TA, Shen J, Walsh CA, Sutherland AE, Wotton D. Tgif1 and Tgif2 regulate Nodal signaling and are required for gastrulation. Development (Cambridge, England). 137: 249-59. PMID 20040491 DOI: 10.1242/Dev.040782  0.482
2005 Shen J, Eyaid W, Mochida GH, Al-Moayyad F, Bodell A, Woods CG, Walsh CA. ASPM mutations identified in patients with primary microcephaly and seizures. Journal of Medical Genetics. 42: 725-9. PMID 16141009 DOI: 10.1136/Jmg.2004.027706  0.458
2005 Shen J, Walsh CA. Targeted disruption of Tgif, the mouse ortholog of a human holoprosencephaly gene, does not result in holoprosencephaly in mice. Molecular and Cellular Biology. 25: 3639-47. PMID 15831469 DOI: 10.1128/Mcb.25.9.3639-3647.2005  0.481
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