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Rahul N. Kanadia, Ph.D. - Publications

Affiliations: 
2004 University of Florida, Gainesville, Gainesville, FL, United States 
Area:
Genetics
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25 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
2023 Girardini KN, Olthof AM, Kanadia RN. Introns: the "dark matter" of the eukaryotic genome. Frontiers in Genetics. 14: 1150212. PMID 37260773 DOI: 10.3389/fgene.2023.1150212  0.777
2022 Olthof AM, White AK, Kanadia RN. The emerging significance of splicing in vertebrate development. Development (Cambridge, England). 149. PMID 36178052 DOI: 10.1242/dev.200373  0.78
2021 White AK, Baumgartner M, Lee MF, Drake KD, Aquino GS, Kanadia RN. Trp53 ablation fails to prevent microcephaly in mouse pallium with impaired minor intron splicing. Development (Cambridge, England). PMID 34557915 DOI: 10.1242/dev.199591  0.608
2021 Olthof AM, White AK, Mieruszynski S, Doggett K, Lee MF, Chakroun A, Abdel Aleem AK, Rousseau J, Magnani C, Roifman CM, Campeau PM, Heath JK, Kanadia RN. Disruption of exon-bridging interactions between the minor and major spliceosomes results in alternative splicing around minor introns. Nucleic Acids Research. PMID 33660780 DOI: 10.1093/nar/gkab118  0.779
2020 Soto-Perez J, Baumgartner M, Kanadia RN. Role of in the Development and Evolution of the Gyrified Cortex. Frontiers in Neuroscience. 14: 617513. PMID 33390896 DOI: 10.3389/fnins.2020.617513  0.636
2020 Drake KD, Lemoine C, Aquino GS, Vaeth AM, Kanadia RN. Loss of U11 small nuclear RNA in the developing mouse limb results in micromelia. Development (Cambridge, England). PMID 32665241 DOI: 10.1242/Dev.190967  0.502
2020 Olthof AM, Rasmussen JS, Campeau PM, Kanadia RN. Disrupted minor intron splicing is prevalent in Mendelian disorders. Molecular Genetics & Genomic Medicine. e1374. PMID 32573973 DOI: 10.1002/Mgg3.1374  0.781
2020 Cheng SY, Cipi J, Ma S, Hafler BP, Kanadia RN, Brush RS, Agbaga MP, Punzo C. Altered photoreceptor metabolism in mouse causes late stage age-related macular degeneration-like pathologies. Proceedings of the National Academy of Sciences of the United States of America. PMID 32434914 DOI: 10.1073/Pnas.2000339117  0.36
2019 Baumgartner M, Drake K, Kanadia RN. An Integrated Model of Minor Intron Emergence and Conservation. Frontiers in Genetics. 10: 1113. PMID 31798628 DOI: 10.3389/Fgene.2019.01113  0.716
2019 Olthof AM, Hyatt KC, Kanadia RN. Minor intron splicing revisited: identification of new minor intron-containing genes and tissue-dependent retention and alternative splicing of minor introns. Bmc Genomics. 20: 686. PMID 31470809 DOI: 10.1186/S12864-019-6046-X  0.775
2018 Baumgartner M, Olthof AM, Aquino GS, Hyatt KC, Lemoine C, Drake K, Sturrock N, Nguyen N, Al Seesi S, Kanadia RN. Minor spliceosome inactivation causes microcephaly due to cell cycle defects and death of self-amplifying radial glial cells. Development (Cambridge, England). PMID 30093551 DOI: 10.1242/Dev.166322  0.734
2017 Karunakaran DKP, Kanadia R. In Vivo and Explant Electroporation of Morpholinos in the Developing Mouse Retina. Methods of Molecular Biology. 1565: 215-227. PMID 28364246 DOI: 10.1007/978-1-4939-6817-6_18  0.411
2016 Karunakaran DK, Al Seesi S, Banday AR, Baumgartner M, Olthof A, Lemoine C, Măndoiu II, Kanadia RN. Network-based bioinformatics analysis of spatio-temporal RNA-Seq data reveals transcriptional programs underpinning normal and aberrant retinal development. Bmc Genomics. 17: 495. PMID 27586787 DOI: 10.1186/S12864-016-2822-Z  0.75
2015 Karunakaran DK, Chhaya N, Lemoine C, Congdon S, Black A, Kanadia R. Loss of citron kinase affects a subset of progenitor cells that alters late but not early neurogenesis in the developing rat retina. Investigative Ophthalmology & Visual Science. 56: 787-98. PMID 25593024 DOI: 10.1167/Iovs.14-15272  0.364
2015 Baumgartner M, Lemoine C, Al Seesi S, Karunakaran DK, Sturrock N, Banday AR, Kilcollins AM, Mandoiu I, Kanadia RN. Minor splicing snRNAs are enriched in the developing mouse CNS and are crucial for survival of differentiating retinal neurons. Developmental Neurobiology. 75: 895-907. PMID 25492806 DOI: 10.1002/Dneu.22257  0.72
2014 Banday AR, Baumgartner M, Al Seesi S, Karunakaran DK, Venkatesh A, Congdon S, Lemoine C, Kilcollins AM, Mandoiu I, Punzo C, Kanadia RN. Replication-dependent histone genes are actively transcribed in differentiating and aging retinal neurons. Cell Cycle (Georgetown, Tex.). 13: 2526-41. PMID 25486194 DOI: 10.4161/15384101.2015.941757  0.684
2013 Karunakaran DK, Banday AR, Wu Q, Kanadia R. Expression analysis of an evolutionarily conserved alternative splicing factor, Sfrs10, in age-related macular degeneration. Plos One. 8: e75964. PMID 24098751 DOI: 10.1371/Journal.Pone.0075964  0.441
2013 Karunakaran DKP, Congdon S, Guerrette T, Banday AR, Lemoine C, Chhaya N, Kanadia R. The expression analysis of Sfrs10 and Celf4 during mouse retinal development. Gene Expression Patterns. 13: 425-436. PMID 23932931 DOI: 10.1016/J.Gep.2013.07.009  0.493
2011 Huynh MA, Ikeuchi Y, Netherton S, de la Torre-Ubieta L, Kanadia R, Stegmüller J, Cepko C, Bonni S, Bonni A. An isoform-specific SnoN1-FOXO1 repressor complex controls neuronal morphogenesis and positioning in the mammalian brain. Neuron. 69: 930-44. PMID 21382553 DOI: 10.1016/J.Neuron.2011.02.008  0.556
2010 Kanadia RN, Cepko CL. Alternative splicing produces high levels of noncoding isoforms of bHLH transcription factors during development. Genes & Development. 24: 229-34. PMID 20080942 DOI: 10.1101/Gad.1847110  0.635
2008 Kanadia RN, Clark VE, Punzo C, Trimarchi JM, Cepko CL. Temporal requirement of the alternative-splicing factor Sfrs1 for the survival of retinal neurons. Development (Cambridge, England). 135: 3923-33. PMID 18987029 DOI: 10.1242/Dev.024620  0.742
2006 Kanadia RN, Shin J, Yuan Y, Beattie SG, Wheeler TM, Thornton CA, Swanson MS. Reversal of RNA missplicing and myotonia after muscleblind overexpression in a mouse poly(CUG) model for myotonic dystrophy. Proceedings of the National Academy of Sciences of the United States of America. 103: 11748-53. PMID 16864772 DOI: 10.1073/Pnas.0604970103  0.767
2006 Lin X, Miller JW, Mankodi A, Kanadia RN, Yuan Y, Moxley RT, Swanson MS, Thornton CA. Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy. Human Molecular Genetics. 15: 2087-97. PMID 16717059 DOI: 10.1093/Hmg/Ddl132  0.648
2003 Kanadia RN, Johnstone KA, Mankodi A, Lungu C, Thornton CA, Esson D, Timmers AM, Hauswirth WW, Swanson MS. A muscleblind knockout model for myotonic dystrophy. Science (New York, N.Y.). 302: 1978-80. PMID 14671308 DOI: 10.1126/Science.1088583  0.665
2003 Kanadia RN, Urbinati CR, Crusselle VJ, Luo D, Lee YJ, Harrison JK, Oh SP, Swanson MS. Developmental expression of mouse muscleblind genes Mbnl1, Mbnl2 and Mbnl3. Gene Expression Patterns : Gep. 3: 459-62. PMID 12915312 DOI: 10.1016/S1567-133X(03)00064-4  0.696
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