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Cited by in CrossRef
For: Toral-Lopez J, González Huerta LM, Messina-Baas O, Cuevas-Covarrubias SA. Submicroscopic 11p13 deletion including the elongator acetyltransferase complex subunit 4 gene in a girl with language failure, intellectual disability and congenital malformations: A case report . World J Clin Cases 2020; 8(21): 5296-5303 [PMID: 33269262 DOI: 10.12998/wjcc.v8.i21.5296]
URL: https://www.wjgnet.com/2307-8960/full/v8/i21/5296.htm
Number Citing Articles
1
Kaan Okay, Pelin Ünal Varış, Süha Miral, Athanasia Pavlopoulou, Yavuz Oktay, Gökhan Karakülah. Whole Genome Analysis of Dizygotic Twins With Autism Reveals Prevalent Transposon Insertion Within Neuronal Regulatory Elements: Potential Implications for Disease Etiology and Clinical AssessmentJournal of Autism and Developmental Disorders 2023; 53(3): 1091 doi: 10.1007/s10803-022-05636-6
2
Marija Kojic, Nour E. H. Abbassi, Ting-Yu Lin, Alun Jones, Emma L. Wakeling, Emma Clement, Vasiliki Nakou, Matthew Singleton, Dominika Dobosz, Marios Kaliakatsos, Sebastian Glatt, Brandon J. Wainwright. A novel ELP1 mutation impairs the function of the Elongator complex and causes a severe neurodevelopmental phenotypeJournal of Human Genetics 2023; 68(7): 445 doi: 10.1038/s10038-023-01135-3
3
Monika Gaik, Marija Kojic, Megan R Stegeman, Tülay Öncü‐Öner, Anna Kościelniak, Alun Jones, Ahmed Mohamed, Pak Yan Stefanie Chau, Sazia Sharmin, Andrzej Chramiec‐Głąbik, Paulina Indyka, Michał Rawski, Anna Biela, Dominika Dobosz, Amanda Millar, Vann Chau, Aycan Ünalp, Michael Piper, Mark C Bellingham, Evan E Eichler, Deborah A Nickerson, Handan Güleryüz, Nour El Hana Abbassi, Konrad Jazgar, Melissa J Davis, Saadet Mercimek‐Andrews, Sultan Cingöz, Brandon J Wainwright, Sebastian Glatt. Functional divergence of the two Elongator subcomplexes during neurodevelopmentEMBO Molecular Medicine 2022; 14(7) doi: 10.15252/emmm.202115608
4
Ikram Toudji, Asmaa Toumi, Émile Chamberland, Elsa Rossignol. Interneuron odyssey: molecular mechanisms of tangential migrationFrontiers in Neural Circuits 2023; 17 doi: 10.3389/fncir.2023.1256455
5
Yinwen Li, Jieqiong Chen, Ying Zheng, Zhixuan Chen, Tao Wang, Qian Sun, Xiaoling Wan, Haiyun Liu, Xiaodong Sun. A novel microdeletion of 517 kb downstream of the PAX6 gene in a Chinese family with congenital aniridiaBMC Ophthalmology 2023; 23(1) doi: 10.1186/s12886-023-03147-1
6
Marija Kojic, Tomasz Gawda, Monika Gaik, Alexander Begg, Anna Salerno-Kochan, Nyoman D. Kurniawan, Alun Jones, Katarzyna Drożdżyk, Anna Kościelniak, Andrzej Chramiec-Głąbik, Soroor Hediyeh-Zadeh, Maria Kasherman, Woo Jun Shim, Enakshi Sinniah, Laura A. Genovesi, Rannvá K. Abrahamsen, Christina D. Fenger, Camilla G. Madsen, Julie S. Cohen, Ali Fatemi, Zornitza Stark, Sebastian Lunke, Joy Lee, Jonas K. Hansen, Martin F. Boxill, Boris Keren, Isabelle Marey, Margarita S. Saenz, Kathleen Brown, Suzanne A. Alexander, Sergey Mureev, Alina Batzilla, Melissa J. Davis, Michael Piper, Mikael Bodén, Thomas H. J. Burne, Nathan J. Palpant, Rikke S. Møller, Sebastian Glatt, Brandon J. Wainwright. Elp2 mutations perturb the epitranscriptome and lead to a complex neurodevelopmental phenotypeNature Communications 2021; 12(1) doi: 10.1038/s41467-021-22888-5