1. Peter S. Harper: obituary

   • Angus J. Clarke
   • Julian R. Sampson

   Obituary 17 March 2021 Pages: 981 - 983

   

2. Admixture mapping identifies African and Amerindigenous local ancestry loci associated with fetal growth

   • Fasil Tekola-Ayele
   • Marion Ouidir
   • Cuilin Zhang

   Original Investigation 15 February 2021 Pages: 985 - 997

   

3. Insights into the pathogenicity of missense variants in the forkhead domain of FOX proteins underlying Mendelian disorders

   • Luis Bermúdez-Guzmán
   • Reiner A. Veitia

   Original Investigation 27 February 2021 Pages: 999 - 1010

   

4. Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland

   • Irma Järvelä
   • Tuomo Määttä
   • Isabelle Schrauwen

   Original Investigation Open access 12 March 2021 Pages: 1011 - 1029

5. A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet–Biedl syndrome

   • Patrick Lorès
   • Zine-Eddine Kherraf
   • Aminata Touré

   Original Investigation 10 March 2021 Pages: 1031 - 1043

   

6. Correction to: A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet–Biedl syndrome

   • Patrick Lorès
   • Zine-Eddine Kherraf
   • Aminata Touré

   Correction 26 March 2021 Pages: 1045 - 1045

7. A missense variant in NUF2, a component of the kinetochore NDC80 complex, causes impaired chromosome segregation and aneuploidy associated with microcephaly and short stature

   • Daniela Tiaki Uehara
   • Hiroshi Mitsubuchi
   • Johji Inazawa

   Original Investigation 15 March 2021 Pages: 1047 - 1060

   

8. Pathogenic variants in CDH11 impair cell adhesion and cause Teebi hypertelorism syndrome

   • Dong Li
   • Michael E. March
   • Elizabeth J. Bhoj

   Original Investigation 03 April 2021 Pages: 1061 - 1076

   

9. Okur-Chung neurodevelopmental syndrome-linked CK2α variants have reduced kinase activity

   • I. Dominguez
   • J. M. Cruz-Gamero
   • H. Rebholz

   Original Investigation 04 May 2021 Pages: 1077 - 1096

   

10. Geographic variation in the polygenic score of height in Japan

    • Mariko Isshiki
    • Yusuke Watanabe
    • Jun Ohashi

    Original Investigation 26 April 2021 Pages: 1097 - 1108

    

11. Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy

    • Ilaria Parenti
    • Daphné Lehalle
    • Cyril Mignot

    Original Investigation Open access 04 May 2021 Pages: 1109 - 1120