Admixture mapping identifies African and Amerindigenous local ancestry loci associated with fetal growth Fasil Tekola-AyeleMarion OuidirCuilin Zhang Original Investigation 15 February 2021 Pages: 985 - 997
Insights into the pathogenicity of missense variants in the forkhead domain of FOX proteins underlying Mendelian disorders Luis Bermúdez-GuzmánReiner A. Veitia Original Investigation 27 February 2021 Pages: 999 - 1010
Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland Irma JärveläTuomo MäättäIsabelle Schrauwen Original Investigation Open access 12 March 2021 Pages: 1011 - 1029
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 LorèsZine-Eddine KherrafAminata Touré Original Investigation 10 March 2021 Pages: 1031 - 1043
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 LorèsZine-Eddine KherrafAminata Touré Correction 26 March 2021 Pages: 1045 - 1045
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 UeharaHiroshi MitsubuchiJohji Inazawa Original Investigation 15 March 2021 Pages: 1047 - 1060
Pathogenic variants in CDH11 impair cell adhesion and cause Teebi hypertelorism syndrome Dong LiMichael E. MarchElizabeth J. Bhoj Original Investigation 03 April 2021 Pages: 1061 - 1076
Okur-Chung neurodevelopmental syndrome-linked CK2α variants have reduced kinase activity I. DominguezJ. M. Cruz-GameroH. Rebholz Original Investigation 04 May 2021 Pages: 1077 - 1096
Geographic variation in the polygenic score of height in Japan Mariko IsshikiYusuke WatanabeJun Ohashi Original Investigation 26 April 2021 Pages: 1097 - 1108
Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy Ilaria ParentiDaphné LehalleCyril Mignot Original Investigation Open access 04 May 2021 Pages: 1109 - 1120