| Year |
Citation |
Score |
| 2016 |
Xie N, Gong H, Suhl JA, Chopra P, Wang T, Warren ST. Reactivation of FMR1 by CRISPR/Cas9-Mediated Deletion of the Expanded CGG-Repeat of the Fragile X Chromosome. Plos One. 11: e0165499. PMID 27768763 DOI: 10.1371/Journal.Pone.0165499 |
0.657 |
|
| 2016 |
Anderson BR, Chopra P, Suhl JA, Warren ST, Bassell GJ. Identification of consensus binding sites clarifies FMRP binding determinants. Nucleic Acids Research. PMID 27378784 DOI: 10.1093/Nar/Gkw593 |
0.521 |
|
| 2016 |
Hestand MS, Nowakowska BA, Vergaelen E, Van Houdt J, Dehaspe L, Suhl JA, Del-Favero J, Mortier G, Zackai E, Swillen A, Devriendt K, Gur RE, McDonald-McGinn DM, Warren ST, Emanuel BS, et al. A catalog of hemizygous variation in 127 22q11 deletion patients. Human Genome Variation. 3: 15065. PMID 27274857 DOI: 10.1038/Hgv.2015.65 |
0.595 |
|
| 2015 |
Suhl JA, Warren ST. Single-Nucleotide Mutations in FMR1 Reveal Novel Functions and Regulatory Mechanisms of the Fragile X Syndrome Protein FMRP. Journal of Experimental Neuroscience. 9: 35-41. PMID 26819560 DOI: 10.4137/Jen.S25524 |
0.674 |
|
| 2015 |
Suhl JA, Muddashetty RS, Anderson BR, Ifrim MF, Visootsak J, Bassell GJ, Warren ST. A 3' untranslated region variant in FMR1 eliminates neuronal activity-dependent translation of FMRP by disrupting binding of the RNA-binding protein HuR. Proceedings of the National Academy of Sciences of the United States of America. PMID 26554012 DOI: 10.1073/Pnas.1514260112 |
0.639 |
|
| 2015 |
Myrick LK, Deng PY, Hashimoto H, Oh YM, Cho Y, Poidevin MJ, Suhl JA, Visootsak J, Cavalli V, Jin P, Cheng X, Warren ST, Klyachko VA. Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures. Proceedings of the National Academy of Sciences of the United States of America. 112: 949-56. PMID 25561520 DOI: 10.1073/Pnas.1423094112 |
0.555 |
|
| 2014 |
Suhl JA, Chopra P, Anderson BR, Bassell GJ, Warren ST. Analysis of FMRP mRNA target datasets reveals highly associated mRNAs mediated by G-quadruplex structures formed via clustered WGGA sequences. Human Molecular Genetics. 23: 5479-91. PMID 24876161 DOI: 10.1093/Hmg/Ddu272 |
0.575 |
|
| 2013 |
McDonald-McGinn DM, Fahiminiya S, Revil T, Nowakowska BA, Suhl J, Bailey A, Mlynarski E, Lynch DR, Yan AC, Bilaniuk LT, Sullivan KE, Warren ST, Emanuel BS, Vermeesch JR, Zackai EH, et al. Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS. Journal of Medical Genetics. 50: 80-90. PMID 23231787 DOI: 10.1136/Jmedgenet-2012-101320 |
0.561 |
|
| 2010 |
Collins SC, Bray SM, Suhl JA, Cutler DJ, Coffee B, Zwick ME, Warren ST. Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males. American Journal of Medical Genetics. Part A. 152: 2512-20. PMID 20799337 DOI: 10.1002/Ajmg.A.33626 |
0.666 |
|
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