Plaster N, Sonntag C, Schilling T, and Hammerschmidt M. (2007) REREa/Atrophin-2 interacts with Histone Deacetylase and Fgf8 signaling to regulate multiple processes of zebrafish development. Developmental Dynamics 236(7):1891-1904. (pdf)

Plaster N, Sonntag C, Busse C, and Hammerschmidt M. (2006) p53 deficiency rescues
apoptosis and differentiation of multiple cell types in zebrafish flathead mutants deficient
for zygotic DNA polymerase delta 1.  Cell Death and Differentiation 13: 223-35. (pdf)

Bendahou S, Donaldson MR, Plaster NM, Tristani-Firouzi RM, Fu YH, and Ptacek LJ.
(2003)  Defective potassium channel Kir2.1 trafficking underlies Andersen-Tawil
syndrome.  Journal of  Biological Chemistry 278(51):51779-85. (pdf)

Tristani-Firouzi RM, Jensen JL, Donaldson MR, Sansone V, Meola G, Hahn A, Bendahou
S, Kwiecinski H, Fidzianska A, Plaster NM, Fu YH, Ptacek LJ, and Tawil R.  (2002)
Functional and clinical characterization of KCNJ2 mutations associated with LQT7
(Andersen syndrome). Journal of  Clinical Investigation 110(3):381-8. (pdf)

Plaster NM, Tawil R, Tristani-Firouzi RM, et al.  (2001) Mutations in Kir2.1 cause the
developmental and episodic electrical phenotypes of Andersen’s syndrome.   Cell
105:511-19. (pdf)

Coffeen CM, McKenna CE, Koeppen A, Plaster NM, Maragakis N, Mihalopoulos J,
Schwankhaus JD, Flanigan KM, Gregg R, and Ptacek LJ. (2000) Genetic localization of
an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis
to chromosome 5q31.  Human Molecular Genetics 9(5):787-793. (pdf)

Plaster N, Uyama E, Uchino M, Ikeda T, Flanigan KM, Kondo I, and Ptacek LJ. (1999)
Genetic localization of the familial adult myoclonic epilepsy (fame) gene to chromosome
8q24.  Neuology 53:1180-1183. (abstract)