Anna C. Thomas

Clinical and genetic heterogeneity of erythrokeratoderma variabilis.

D. Kelsell, I. Leigh, V. Venning, 2005, The Journal of investigative dermatology.

A Deafness-Associated Mutant Human Connexin 26 Improves the Epithelial Barrier In Vitro

Daniel J. Jagger, David P. Kelsell, Michael A. Curtis, 2007, Journal of Membrane Biology.

Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS

N. Sebire, E. Healy, V. Kinsler, 2013, The Journal of investigative dermatology.

Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis

R. Happle, C. Chiaverini, J. Rivière, 2016, The Journal of investigative dermatology.

Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy

Julie C. Sapp, L. Biesecker, M. Topf, 2018, The Journal of clinical investigation.

Paternally Expressed, Imprinted Insulin-Like Growth Factor-2 in Chorionic Villi Correlates Significantly with Birth Weight

K. Nicolaides, D. Peebles, P. Stanier, 2013, PloS one.