Items where authors include "Ikegawa, S"

Article

Al-Jawahiri, R orcid.org/0000-0002-5689-3368, Foroutan, A, Kerkhof, J et al. (111 more authors) (2022) SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile. Genetics in Medicine, 24 (6). pp. 1261-1273. ISSN 1098-3600

Bjornsdottir, G, Stefansdottir, L, Thorleifsson, G et al. (119 more authors) (2022) Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology. Nature Communications, 13 (1). 634. ISSN 2041-1723

Boer, CG, Hatzikotoulas, K, Southam, L et al. (63 more authors) (2021) Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Cell, 184 (18). 4784-4818.e17. ISSN 0092-8674