Ishida, Miho

The role and interaction of imprinted genes in human fetal growth

Moore, G. E., Ishida, M., Demetriou, C., Al-Olabi, L., Leon, L. J., Thomas, A. C., Abu-Amero, S., Frost, J. M., Stafford, J. L., Chaoqun, Y., et al. (2015) · Philosophical Transactions of the Royal Society B: Biological Sciences

Genetic Syndromes and ImprintingBirth, Development, and Health

Cited by 155

Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome

Sousa, S. B., Jenkins, D., Chanudet, E., Tasseva, G., Ishida, M., Anderson, G., Docker, J., Ryten, M., Sa, J., Saraiva, J. M., et al. (2014) · Nature Genetics

Dermatological and Skeletal DisordersGenomics and Rare Diseases

Cited by 115

QSOX2 Deficiency-induced short stature, gastrointestinal dysmotility and immune dysfunction

Maharaj, A. V., Ishida, M., Rybak, A., Elfeky, R., Andrews, A., Joshi, A., Elmslie, F., Joensuu, A., Kantojärvi, K., Jia, R. Y., et al. (2024) · Nature Communications

Growth Hormone and Insulin-like Growth FactorsImmunodeficiency and Autoimmune Disorders

Cited by 9