Items where authors include "Gardner, E.J."

Article

Kentistou, K.A. orcid.org/0000-0002-5816-664X, Kaisinger, L.R. orcid.org/0000-0002-0849-3191, Stankovic, S. orcid.org/0000-0002-6602-1379 et al. (220 more authors) (2024) Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nature Genetics, 56 (7). pp. 1397-1411. ISSN 1061-4036

Leeson-Payne, A. orcid.org/0000-0002-1823-2913, Iyinikkel, J., Malcolm, C. et al. (16 more authors) (2024) Loss of GPR75 protects against non-alcoholic fatty liver disease and body fat accumulation. Cell Metabolism, 36 (5). pp. 1076-1087. ISSN 1550-4131

Wright, C.F., Quaife, N.M., Ramos-Hernández, L. et al. (31 more authors) (2021) Non-coding region variants upstream of MEF2C cause severe developmental disorder through three distinct loss-of-function mechanisms. American Journal of Human Genetics, 108 (6). pp. 1083-1094. ISSN 0002-9297

Martin, H.C., Gardner, E.J., Samocha, K.E. et al. (13 more authors) (2021) The contribution of X-linked coding variation to severe developmental disorders. Nature Communications, 12. 627. ISSN 2041-1723

Kaplanis, J., Samocha, K.E., Wiel, L. et al. (30 more authors) (2020) Evidence for 28 genetic disorders discovered by combining healthcare and research data. Nature, 586 (7831). pp. 757-762. ISSN 0028-0836