1. The molecular genetic basis of atrial fibrillation

   • Xin Huang
   • Yuhui Li
   • Guowei Li

   Review 02 July 2020 Pages: 1485 - 1498

   

2. A novel variant in GPAA1, encoding a GPI transamidase complex protein, causes inherited vascular anomalies with various phenotypes

   • Yongyun Li
   • Liu Yang
   • Renbing Jia

   Original Investigation 12 June 2020 Pages: 1499 - 1511

   

3. The necdin interactome: evaluating the effects of amino acid substitutions and cell stress using proximity-dependent biotinylation (BioID) and mass spectrometry

   • Matthea R. Sanderson
   • Katherine E. Badior
   • Rachel Wevrick

   Original Investigation 11 June 2020 Pages: 1513 - 1529

   

4. Study of telomere length in men who carry a fragile X premutation or full mutation allele

   • Igor Albizua
   • Pankaj Chopra
   • Stephanie L. Sherman

   Original Investigation 12 June 2020 Pages: 1531 - 1539

   

5. The cataract-linked RNA-binding protein Celf1 post-transcriptionally controls the spatiotemporal expression of the key homeodomain transcription factors Pax6 and Prox1 in lens development

   • Sandeep Aryal
   • Justine Viet
   • Salil A. Lachke

   Original Investigation 27 June 2020 Pages: 1541 - 1554

   

6. Complex chromosomal rearrangements of human chromosome 21 in a patient manifesting clinical features partially overlapped with that of Down syndrome

   • Taichi Imaizumi
   • Keiko Yamamoto-Shimojima
   • Toshiyuki Yamamoto

   Original Investigation 13 June 2020 Pages: 1555 - 1563

   

7. Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing loss

   • Kevin T. Booth
   • Amama Ghaffar
   • Saima Riazuddin

   Original Investigation 19 June 2020 Pages: 1565 - 1574

   

8. Severe DNM1 encephalopathy with dysmyelination due to recurrent splice site pathogenic variant

   • Ahmed N. Sahly
   • Eric Krochmalnek
   • Kenneth A. Myers

   Letter to the Editor 09 September 2020 Pages: 1575 - 1578