1. A review of migraine genetics: gathering genomic and transcriptomic factors

   • Andreia Dias
   • Tiago Mariz
   • Miguel Alves-Ferreira

   Review 22 October 2021 Pages: 1 - 14

   

2. PRNCR1: a long non-coding RNA with a pivotal oncogenic role in cancer

   • Abhishek Bardhan
   • Anwesha Banerjee
   • Amlan Ghosh

   Review 02 November 2021 Pages: 15 - 29

   

3. Differential fates of introns in gene expression due to global alternative splicing

   • Anjani Kumari
   • Saam Sedehizadeh
   • Marzena Wojciechowska

   Review Open access 14 December 2021 Pages: 31 - 47

   

4. ASTL is mutated in female infertility

   • Sateesh Maddirevula
   • Serdar Coskun
   • Fowzan S. Alkuraya

   Original Investigation 26 October 2021 Pages: 49 - 54

   

5. Mitochondrial “dysmorphology” in variant classification

   • Hanan E. Shamseldin
   • Amal Alhashem
   • Fowzan S. Alkuraya

   Original Investigation 08 November 2021 Pages: 55 - 64

   

6. MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects

   • Juliette Coursimault
   • Anne-Marie Guerrot
   • François Lecoquierre

   Original Investigation 08 November 2021 Pages: 65 - 80

   

7. SLC gene mutations and pediatric neurological disorders: diverse clinical phenotypes in a Saudi Arabian population

   • Ali Mir
   • Montaha Almudhry
   • Yousef Housawi

   Original Investigation 19 November 2021 Pages: 81 - 99

   

8. Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes

   • Mohamed H. Al-Hamed
   • Wesam Kurdi
   • Faiqa Imtiaz

   Original Investigation 01 December 2021 Pages: 101 - 126

   

9. Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation

   • R. J. Longchamps
   • S. Y. Yang
   • D. E. Arking

   Original Investigation Open access 02 December 2021 Pages: 127 - 146

   

10. Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity

    • Chiara Fallerini
    • Nicola Picchiotti
    • Simone Furini

    Original Investigation Open access 10 December 2021 Pages: 147 - 173

    

11. Retraction Note to: Revisiting the male genetic landscape of China: a multi-center study of almost 38,000 Y-STR haplotypes

    • Michael Nothnagel
    • Guangyao Fan
    • Lutz Roewer

    Retraction Note 11 December 2021 Pages: 175 - 176