London Health Sciences Foundation

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SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile

2022 · Reem Al-Jawahiri, Aidin Foroutan, et al. · Genetics in Medicine · 41

DNA methylation episignature for Witteveen-Kolk syndrome due to SIN3A haploinsufficiency

2022 · Jet Coenen-van der Spek, Raissa Relator, et al. · Genetics in Medicine · 17

Anticytokine Therapies in Severe Coronavirus Disease 2019 Should Be Informed by Detailed Inflammatory Profiling and Specific Therapeutic Targets

2020 · Marat Slessarev, Douglas D. Fraser · Critical Care Explorations · 4

Works count: 3

Citation count: 421