Structure and Expression Analyses of SVA Elements in Relation to Functional Genes
Yun-Jeong Kwon, Yuri Choi, Jungwoo Eo, Yu-Na Noh, Jeong-An Gim, Yi-Deun Jung, Ja-Rang Lee, Heui-Soo Kim
Genomics Inform. 2013;11(3):142-148.   Published online 2013 Sep 30     DOI: https://doi.org/10.5808/GI.2013.11.3.142
Citations to this article as recorded by Crossref logo
A Genome-Wide Screen for the Exonisation of Reference SINE-VNTR-Alus and Their Expression in CNS Tissues of Individuals with Amyotrophic Lateral Sclerosis
Abigail L. Pfaff, Vivien J. Bubb, John P. Quinn, Sulev Koks
International Journal of Molecular Sciences.2023; 24(14): 11548.     CrossRef
Regulation of expression quantitative trait loci by SVA retrotransposons within the major histocompatibility complex
Jerzy K Kulski, Abigail L Pfaff, Luke D Marney, Alexander Fröhlich, Vivien J Bubb, John P Quinn, Sulev Koks
Experimental Biology and Medicine.2023;[Epub]     CrossRef
Integrating whole-genome sequencing with multi-omic data reveals the impact of structural variants on gene regulation in the human brain
Ricardo A. Vialle, Katia de Paiva Lopes, David A. Bennett, John F. Crary, Towfique Raj
Nature Neuroscience.2022; 25(4): 504.     CrossRef
Human Retrotransposons and Effective Computational Detection Methods for Next-Generation Sequencing Data
Haeun Lee, Jun Won Min, Seyoung Mun, Kyudong Han
Life.2022; 12(10): 1583.     CrossRef
A BBS1 SVA F retrotransposon insertion is a frequent cause of Bardet‐Biedl syndrome
Clarisse Delvallée, Samuel Nicaise, Manuela Antin, Anne‐Sophie Leuvrey, Elsa Nourisson, Carmen C. Leitch, Georgios Kellaris, Corinne Stoetzel, Véronique Geoffroy, Sophie Scheidecker, Boris Keren, Christel Depienne, Joakim Klar, Niklas Dahl, Jean‐François
Clinical Genetics.2021; 99(2): 318.     CrossRef
Contribution of unfixed transposable element insertions to human regulatory variation
Clément Goubert, Nicolas Arce Zevallos, Cédric Feschotte
Philosophical Transactions of the Royal Society B: Biological Sciences.2020; 375(1795): 20190331.     CrossRef
SVA insertion in X-linked Dystonia Parkinsonism alters histone H3 acetylation associated with TAF1 gene
Tiziana Petrozziello, Amanda M. Dios, Kaly A. Mueller, Christine A. Vaine, William T. Hendriks, Kelly E. Glajch, Alexandra N. Mills, Kotchaphorn Mangkalaphiban, Ellen B. Penney, Naoto Ito, Cara Fernandez-Cerado, Gierold Paul A. Legarda, M. Salvie Velasco-
PLOS ONE.2020; 15(12): e0243655.     CrossRef
The Role of SINE-VNTR-Alu (SVA) Retrotransposons in Shaping the Human Genome
Olympia Gianfrancesco, Bethany Geary, Abigail L. Savage, Kimberley J. Billingsley, Vivien J. Bubb, John P. Quinn
International Journal of Molecular Sciences.2019; 20(23): 5977.     CrossRef
Identification of polymorphic SVA retrotransposons using a mobile element scanning method for SVA (ME-Scan-SVA)
Hongseok Ha, Jui Wan Loh, Jinchuan Xing
Mobile DNA.2016;[Epub]     CrossRef
Decreased N-TAF1 expression in X-Linked Dystonia-Parkinsonism patient-specific neural stem cells
Naoto Ito, William T. Hendriks, Jyotsna Dhakal, Christine A. Vaine, Christina Liu, David Shin, Kyle Shin, Noriko Wakabayashi-Ito, Marisela Dy, Trisha Multhaupt-Buell, Nutan Sharma, Xandra O. Breakefield, D. Cristopher Bragg
Disease Models & Mechanisms.2016;[Epub]     CrossRef
Composite non-LTR retrotransposons in hominoid primates
Annette Damert
Mobile Genetic Elements.2015; 5(5): 67.     CrossRef