Author:
Elsayed Liena Elbaghir Omer,AlHarbi Norah Ayed,Alqarni Ashwaq Mohammed,Eltayeb Huda Hussein Elwasila,Mostafa Noura Mostafa Mohamed,Abdulrahim Maha Mohammed,Zaid Hadeel Ibrahim Bin,Alanzi Latifah Mansour,Ababtain Sarah Abdullah,Aldulaijan Khawlah,Aloyouni Sheka Yagub,Othman Moneeb Abdullah Kassem,Alkheilewi Mohammad Abdullah,Binduraihem Adel Mohammed,Alrukban Hadeel Abdollah,Ahmed Hiba Yousif,AlRadini Faten Abdullah,Alahdal Hadil Mohammad,Mushiba Aziza Mufareh,Alzaher Omaima Abdulazeem
Funder
This research was funded by the Deanship of Scientific Research at Princess Nourah bint Abdulrahman University, through the Research Funding Program
Publisher
Springer Science and Business Media LLC
Reference49 articles.
1. Aguirre M, Rivas MA, Priest J. Phenome-wide Burden of Copy-number variation in the UK Biobank. Am J Hum Genet. 2019;105:373–83.
2. Kaminsky EB, Kaul V, Paschall J, Church DM, Bunke B, Kunig D, et al. An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities. Genet Med off J Am Coll Med Genet. 2011;13:777–84.
3. Auwerx C, Lepamets M, Sadler MC, Patxot M, Stojanov M, Baud D, et al. The individual and global impact of copy-number variants on complex human traits. Am J Hum Genet. 2022;109:647–68.
4. Smajlagić D, Lavrichenko K, Berland S, Helgeland Ø, Knudsen GP, Vaudel M, et al. Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents. Eur J Hum Genet. 2021;29:205–15.
5. Oliva-Teles N, de Stefano MC, Gallagher L, Rakic S, Jorge P, Cuturilo G, et al. Rare pathogenic Copy Number Variation in the 16p11.2 (BP4-BP5) Region Associated with Neurodevelopmental and Neuropsychiatric disorders: a review of the literature. Int J Environ Res Public Health. 2020;17:9253.