Angela Barnicoat

Disruption of the bipartite imprinting center in a family with Angelman syndrome.

M. Pembrey, S. Malcolm, B. Horsthemke, 2001, American journal of human genetics.

Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13).

R. Regan, J. Flint, R. Winter, 2001, American journal of medical genetics.

A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp

B. Horsthemke, A. Barnicoat, K. Buiting, 1999, Human Genetics.

Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study

Joshua C Randall, Tomas W. Fitzgerald, G. J. Swaminathan, 2016, bioRxiv.

Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia (vol 49, pg 223, 2017)

D. Grozeva, H. Bergman, D. Arkadir, 2017 .