Ballon, N., Leroy, S., Roy, C., Bourdel, M.C., Olie, J.P., Charles-Nicolas, A., Krebs, M.O. and Poirier, M.F. (2007) Polymorphisms TaqI A of the DRD2, BalI of the DRD3, Exon III Repeat of the DRD4, and 3’ UTR VNTR of the DAT: Association with Childhood ADHD in Male African-Caribbean Cocaine Dependents? American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 144B, 1034-1041.
https://doi.org/10.1002/ajmg.b.30540

has been cited by the following article:

• TITLE: Whole Exome Sequencing: Novel Genetic Polymorphisms in Saudi Arabian Attention Deficit Hyperactivity Disorder (ADHD) Children

  AUTHORS: Neda Mostafa Bogari, Amr Ahmed Amin, Ashwag Aljohani, Ghida Dairi, Mahmoud Zaki El-Readi, Anas Dannoun, Udaya Raja, Mohammad Adil, Nermeen Qutub, Suhair Alhelfawi, Amal Alobaidi, Derar Alqudah, Hussain Banni, Safaa Yehia Eid, Huda Balto, Faisal Al-Allaf, Mohiuddin Taher, Hiba Saed Al-Amoodi, Ahmed Fawzy

  KEYWORDS: Next Generation DNA Sequencing, Single Nucleotide Polymorphisms, Saudi Children, Attention-Deficit Hyperactivity Disorder, ADHD

  JOURNAL NAME: Natural Science, Vol.11 No.2, February 28, 2019

  ABSTRACT: Background: Attention-deficit hyperactivity disorder (ADHD) is a widespread and debilitating disorder with relatively high prevalence in Saudi Arabia. Neuropsychological and radiological investigations have revealed that there are some differences in the components of the brain regions in children with and without ADHD. In this study we have performed whole exome sequencing (WES) in four non-familial cases of ADHD from Makkah Region to identify the genetic polymorphisms associated with the disease in our Saudi population. Methods: Exome sequencing was carried out using Ion Proton with AmpliSeq Exome library methods, and the data were analysed by Ion Reporter 5.6 software. Results: A total of 33 variants were identified from 222 genes selected from the GWAS catalogue for ADHD associated genes. However, the SNPs we identified in these genes were not reported to be associated with ADHD in previous studies. We have identified 2 novel missense variants; one in c.3451G > T; p. (Ala1151Ser) in ITGA1 gene and another is c.988G > A; p. (Ala330Thr) in SPATA13 genes. The variants rs928661, rs11150370 and rs386792899 were the only three variants that appeared on all the 4 patients studied. Six missense variants, rs16841277, rs2228209, rs2230283, rs3741883, rs1716 and rs2272606, were found in 3 different patients, respectively. However, the three documented variants are rs13166360 with bipolar disorder, rs920829 with neuropathic pain, and rs6558702 with schizophrenia. Conclusion: We have identified 2 novel variants in ADHD children. SIFT score of all variants indicates that these substitutions have damaging effects on the protein function. Further screening studies are recommended for confirmation.